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  • Question 1 - A 32-year-old man who drinks 6 cans of soda a day would like...

    Incorrect

    • A 32-year-old man who drinks 6 cans of soda a day would like to stop his habit. He is considering taking varenicline (Champix®) to help him quit smoking and wants to learn about its potential side effects.
      What is the most common side effect associated with orlistat?

      Your Answer: Increased intraocular pressure

      Correct Answer: Abnormal dreams

      Explanation:

      Understanding the Side Effects of Varenicline

      Varenicline is a medication commonly used to help people quit smoking. However, like any medication, it can have side effects. One of the most common side effects is abnormal dreams and sleep disorders. While eye pain, lacrimation, and visual disturbances can occur, increased intraocular pressure is not a known side effect. Menorrhagia and vaginal discharge may occur, but amenorrhoea and galactorrhoea are not associated with varenicline. It’s important to note that nicotine withdrawal symptoms can occur as early as 4 hours after the last cigarette and peak around 48 hours after quitting. These symptoms can include headache, anxiety, tobacco cravings, appetite changes, nausea, paraesthesiae, sleep disturbance, sweating, and low mood.

    • This question is part of the following fields:

      • Pharmacology/Therapeutics
      24.3
      Seconds
  • Question 2 - A 26-year-old woman comes in for her routine medical check-up before starting her...

    Incorrect

    • A 26-year-old woman comes in for her routine medical check-up before starting her new job as a soccer player. She reports feeling healthy and has no notable medical history in her family.

      During the physical examination, her lungs sound clear and her heart has a normal rhythm. Her pulse rate is 62 beats per minute. However, her ECG reveals sinus rhythm with a prolonged PR interval of 215ms.

      What is the appropriate course of action for managing her ECG results?

      Your Answer: Routine referral to cardiology

      Correct Answer: No intervention needed

      Explanation:

      First-degree heart block is a common occurrence in athletes and does not require any intervention. This patient’s ECG shows a prolonged PR interval, which is the defining characteristic of first-degree heart block. As it is a normal variant, there is no need for any referral or further investigations. The patient can continue to play football without any concerns.

      Normal Variants in Athlete ECGs

      Athletes may exhibit certain ECG changes that are considered normal variants. These include sinus bradycardia, junctional rhythm, first degree heart block, and Mobitz type 1 (Wenckebach phenomenon). Sinus bradycardia refers to a slower than normal heart rate originating from the sinus node, which is the natural pacemaker of the heart. Junctional rhythm occurs when the heart’s electrical impulses originate from the junction between the atria and ventricles, rather than the sinus node. First degree heart block is a delay in the electrical conduction between the atria and ventricles, resulting in a prolonged PR interval on the ECG. Mobitz type 1, also known as Wenckebach phenomenon, is a type of heart block where there is a progressive lengthening of the PR interval until a beat is dropped. These ECG changes are considered normal in athletes and do not necessarily indicate any underlying cardiac pathology.

    • This question is part of the following fields:

      • Cardiovascular
      15.5
      Seconds
  • Question 3 - A 10-year-old boy is brought to surgery as his father is worried about...

    Incorrect

    • A 10-year-old boy is brought to surgery as his father is worried about his weight. This has been a concern for more than three years and dad believes it is affecting his son's performance in school. What is the best way to determine the extent of his obesity?

      Your Answer: Weight plotted on percentile chart

      Correct Answer: Body mass index percentile adjusted to age and gender

      Explanation:

      Understanding Obesity in Children

      Childhood obesity is a complex issue that requires careful assessment and management. Unlike adults, defining obesity in children is more challenging as body mass index (BMI) varies with age. To accurately assess BMI, percentile charts are needed. According to recent guidelines by the National Institute for Health and Care Excellence (NICE), the UK 1990 BMI charts should be used to provide age- and gender-specific information.

      NICE recommends tailored clinical intervention if BMI is at the 91st centile or above. If BMI is at the 98th centile or above, assessing for comorbidities is necessary. Lifestyle factors are the most common cause of obesity in childhood. However, other factors such as growth hormone deficiency, hypothyroidism, Down’s syndrome, Cushing’s syndrome, and Prader-Willi syndrome can also contribute to obesity in children.

      Obesity in children can lead to various consequences, including orthopaedic problems such as slipped upper femoral epiphyses and Blount’s disease, musculoskeletal pains, psychological consequences like poor self-esteem and bullying, sleep apnoea, and benign intracranial hypertension. Moreover, obesity in childhood can increase the risk of developing type 2 diabetes mellitus, hypertension, and ischaemic heart disease in the long run. Therefore, it is crucial to identify and manage obesity in children to prevent these adverse outcomes.

    • This question is part of the following fields:

      • Paediatrics
      17.5
      Seconds
  • Question 4 - A 55-year-old woman presents with a 4-week history of proximal muscle weakness. She...

    Incorrect

    • A 55-year-old woman presents with a 4-week history of proximal muscle weakness. She has a significant history of alcohol and smoking. Her blood tests reveal macrocytosis, abnormal liver function tests, elevated TSH (thyroid-stimulating hormone) and normal free thyroxine (fT4) levels.
      Which of the following is the most likely cause of her symptoms & blood results?

      Your Answer: Pernicious anaemia

      Correct Answer: Alcohol excess

      Explanation:

      Differential diagnosis of a patient with alcohol excess, elevated liver function tests, macrocytosis, and compensated hypothyroidism

      Chronic excess alcohol consumption can lead to a variety of health problems, including liver disease, neurological damage, and endocrine dysfunction. In this case, the patient presents with elevated liver function tests and macrocytosis, which are consistent with alcohol excess. The thyroid function tests show compensated hypothyroidism, which can also be caused by alcohol-related liver damage. However, the proximal myopathy is not typical of hypothyroidism, which usually causes muscle weakness in a more diffuse pattern. Cushing’s syndrome, pernicious anaemia, and thyrotoxicosis are less likely diagnoses based on the absence of specific clinical features and laboratory findings. Therefore, the most likely explanation for this patient’s presentation is alcohol excess, which may require further evaluation and management to prevent further complications.

    • This question is part of the following fields:

      • Endocrinology/Metabolic Disease
      64.1
      Seconds
  • Question 5 - A toddler is due his measles, mumps and rubella (MMR) vaccine. The toddler's...

    Incorrect

    • A toddler is due his measles, mumps and rubella (MMR) vaccine. The toddler's mother wants to have a bit of information regarding the vaccine. What type of vaccine is the MMR?

      Your Answer: A conjugate vaccine

      Correct Answer: A live attenuated vaccine

      Explanation:

      Types of Vaccines and Their Definitions

      Live Attenuated Vaccine:
      This type of vaccine involves injecting a small sample of the virus into the body, allowing the immune system to fight it and create an immune response against it for future attacks. The MMR vaccine is an example of a live attenuated vaccine.

      Conjugate Vaccine:
      Conjugate vaccines are created by combining a weak antigen with a strong antigen to produce a stronger immune response. Typically, a polysaccharide is joined with a strong protein to create this type of vaccine.

      Inactivated Vaccine:
      Inactivated vaccines, such as the pertussis and hepatitis A vaccines, contain dead pathogens that cannot cause disease but still stimulate an immune response.

      Subunit Vaccine:
      Subunit vaccines only contain the antigenic component of the pathogen. However, there is no guarantee that immunological memory will be achieved appropriately. The pneumococcal vaccine is an example of a subunit vaccine.

      Toxoid Vaccine:
      Toxoid vaccines are toxins that have been deactivated but still stimulate an immune response from the immune system. Examples include the diphtheria and tetanus vaccines.

      Understanding the Different Types of Vaccines

    • This question is part of the following fields:

      • Immunology/Allergy
      10.2
      Seconds
  • Question 6 - An 80-year-old man presents with leg swelling and nocturnal dyspnea. His BNP levels...

    Incorrect

    • An 80-year-old man presents with leg swelling and nocturnal dyspnea. His BNP levels are elevated and an echocardiogram confirms heart failure with reduced ejection fraction. He has a history of diabetes and is currently on metformin. Besides furosemide, what other medication should be initiated for his heart failure management?

      Your Answer: Aspirin

      Correct Answer: Ramipril

      Explanation:

      When treating heart failure patients, it is recommended to initiate therapy with either an angiotensin-converting enzyme (ACE) inhibitor or a beta-blocker licensed for heart failure treatment, but not both simultaneously. If the patient exhibits signs of fluid overload or has diabetes mellitus, an ACE inhibitor like ramipril is preferred. On the other hand, if the patient has angina, a beta-blocker such as bisoprolol, carvedilol, or nebivolol is preferred.

      Drug Management for Chronic Heart Failure: NICE Guidelines

      Chronic heart failure is a serious condition that requires proper management to improve patient outcomes. In 2018, the National Institute for Health and Care Excellence (NICE) updated their guidelines on drug management for chronic heart failure. The guidelines recommend first-line therapy with both an ACE-inhibitor and a beta-blocker, with clinical judgement used to determine which one to start first. Second-line therapy involves the use of aldosterone antagonists, which should be monitored for hyperkalaemia. SGLT-2 inhibitors are also increasingly being used to manage heart failure with a reduced ejection fraction. Third-line therapy should be initiated by a specialist and may include ivabradine, sacubitril-valsartan, hydralazine in combination with nitrate, digoxin, or cardiac resynchronisation therapy. Other treatments such as annual influenza and one-off pneumococcal vaccines are also recommended.

      Overall, the NICE guidelines provide a comprehensive approach to drug management for chronic heart failure. It is important to note that loop diuretics have not been shown to reduce mortality in the long-term, and that ACE-inhibitors and beta-blockers have no effect on mortality in heart failure with preserved ejection fraction. Healthcare professionals should carefully consider the patient’s individual needs and circumstances when determining the appropriate drug therapy for chronic heart failure.

    • This question is part of the following fields:

      • Cardiovascular
      15.1
      Seconds
  • Question 7 - A 52-year-old woman had a anterior myocardial infarction (MI) three weeks ago and...

    Incorrect

    • A 52-year-old woman had a anterior myocardial infarction (MI) three weeks ago and has been prescribed various drugs by the cardiology team.
      Which of the following medications is most likely to decrease this patient’s mortality post-MI?

      Your Answer: Isosorbide mononitrate

      Correct Answer: Bisoprolol

      Explanation:

      Common Medications for Cardiovascular Conditions

      Bisoprolol is a beta-blocker that specifically targets the heart, reducing strain by decreasing pre-load and after-load. It has been found to be effective in reducing mortality after a heart attack, especially in patients with heart failure.

      Amiodarone is an anti-arrhythmic drug that can be used to prevent irregular heartbeats. However, it does not improve mortality rates in post-heart attack patients.

      Isosorbide mononitrate is a medication that helps lower blood pressure and can alleviate chest pain in stable angina. It does not improve mortality rates and should be used with caution when taken with sildenafil.

      Nicorandil works by dilating the coronary arteries, reducing chest pain in stable angina. While it does not improve prognostic outcomes, it can improve symptoms.

      Patients who have experienced a myocardial infarction (MI) should be started on a combination of medications to improve their outcomes. The following medications are recommended for post-MI patients:

      1. Statin: This medication helps to lower cholesterol levels and reduce the risk of future cardiovascular events.

      2. ACE inhibitor: This medication helps to lower blood pressure and reduce the risk of heart failure.

      3. Beta blocker: This medication helps to reduce the workload on the heart and improve its function.

      4. Aspirin: This medication helps to prevent blood clots and reduce the risk of future cardiovascular events.

      Other medications may be used to relieve symptoms, such as ISMN and nicorandil, but they do not offer any mortality benefit. It is important for post-MI patients to take their medications as prescribed and to follow up with their healthcare provider regularly to monitor their progress.

    • This question is part of the following fields:

      • Pharmacology/Therapeutics
      15
      Seconds
  • Question 8 - A 50-year-old woman presents with complaints of hot flashes that occur randomly and...

    Incorrect

    • A 50-year-old woman presents with complaints of hot flashes that occur randomly and are affecting her work as a lawyer, especially during court sessions. She is hesitant to try hormone replacement therapy due to its side effects and is seeking alternative options. What medication can be prescribed to alleviate her symptoms?

      Your Answer: Oestrogen cream

      Correct Answer: Fluoxetine

      Explanation:

      According to NICE guidelines, women experiencing vasomotor symptoms during menopause can be prescribed fluoxetine, a selective serotonin uptake inhibitor (SSRI). While clonidine is also approved for treating these symptoms, its effectiveness is not well-established and it can cause side effects such as dry mouth, sedation, depression, and fluid retention. Gabapentin is being studied for its potential to reduce hot flushes, but more research is needed.

      Managing Menopause: Lifestyle Modifications, Hormone Replacement Therapy, and Non-Hormone Replacement Therapy

      Menopause is a natural biological process that marks the end of a woman’s reproductive years. It is diagnosed when a woman has not had a period for 12 consecutive months. Menopausal symptoms are common and can last for up to 7 years, with varying degrees of severity and duration. The management of menopause can be divided into three categories: lifestyle modifications, hormone replacement therapy (HRT), and non-hormone replacement therapy.

      Lifestyle modifications can help manage menopausal symptoms such as hot flushes, sleep disturbance, mood changes, and cognitive symptoms. Regular exercise, weight loss, stress reduction, and good sleep hygiene are recommended. For women who cannot or do not want to take HRT, non-hormonal treatments such as fluoxetine, citalopram, or venlafaxine for vasomotor symptoms, vaginal lubricants or moisturizers for vaginal dryness, and cognitive behavior therapy or antidepressants for psychological symptoms can be prescribed.

      HRT is a treatment option for women with moderate to severe menopausal symptoms. However, it is contraindicated in women with current or past breast cancer, any estrogen-sensitive cancer, undiagnosed vaginal bleeding, or untreated endometrial hyperplasia. HRT brings certain risks, including venous thromboembolism, stroke, coronary heart disease, breast cancer, and ovarian cancer. Women should be advised of these risks and the fact that symptoms typically last for 2-5 years.

      When stopping HRT, it is important to gradually reduce the dosage to limit recurrence of symptoms in the short term. However, in the long term, there is no difference in symptom control. Women who experience ineffective treatment, ongoing side effects, or unexplained bleeding should be referred to secondary care. Overall, managing menopause requires a personalized approach that takes into account a woman’s medical history, preferences, and individual symptoms.

    • This question is part of the following fields:

      • Reproductive Medicine
      56.2
      Seconds
  • Question 9 - A 56-year-old man has just been diagnosed with type 2 diabetes after a...

    Incorrect

    • A 56-year-old man has just been diagnosed with type 2 diabetes after a routine blood test. He has a history of myocardial infarction and chronic left ventricular systolic dysfunction. The patient is started on metformin and titrated to the maximum tolerated dose. The following are the results of his blood tests:
      - Na+ 138 mmol/L (135 - 145)
      - K+ 3.9 mmol/L (3.5 - 5.0)
      - Urea 4.0 mmol/L (2.0 - 7.0)
      - Creatinine 75 µmol/L (55 - 120)
      - eGFR >90 mL/min (>90)
      - Hba1c 62 mmol/mol (7.8%) (20-41)

      What is the most appropriate medication to initiate for this patient?

      Your Answer: Insulin

      Correct Answer: Empagliflozin

      Explanation:

      For this patient with type 2 diabetes mellitus (T2DM) and cardiac comorbidity, the most appropriate medication would be an SGLT-2 inhibitor. This is especially true for patients with established cardiovascular disease (CVD) or those under 40 with one or more cardiovascular risk factors. Studies have shown that SGLT-2 inhibitors have a cardioprotective effect, with the greatest benefit seen in those with CVD. Additionally, these medications have been associated with reduced hospital admissions and mortality in patients with heart failure.

      Gliclazide is not the best option for this patient as there is no evidence that it would have a beneficial effect on their cardiac comorbidity, unlike SGLT-2 inhibitors. While gliclazide is effective at lowering HbA1c, it can cause weight gain. In some cases, gliclazide may be used as rescue therapy for patients with T2DM who have very poor glycemic control and are symptomatic, but this is not the case for this patient.

      Insulin is not necessary at this stage, as there are many other medications available to optimize glycemic control before insulin should be considered. In some cases, insulin may be used as short-term rescue therapy for patients with T2DM who have very poor glycemic control and are symptomatic, but this is not the case for this patient.

      Pioglitazone is not a suitable option for this patient, as it is contraindicated in patients with heart failure due to its potential to worsen fluid retention and edema. Additionally, pioglitazone is associated with an increased risk of fractures. However, pioglitazone does have benefits such as safety in renal impairment and a low risk of hypoglycemia.

      NICE updated its guidance on the management of type 2 diabetes mellitus (T2DM) in 2022, reflecting advances in drug therapy and improved evidence regarding newer therapies such as SGLT-2 inhibitors. The first-line drug of choice remains metformin, which should be titrated up slowly to minimize gastrointestinal upset. HbA1c targets should be agreed upon with patients and checked every 3-6 months until stable, with consideration for relaxing targets on a case-by-case basis. Dietary advice includes encouraging high fiber, low glycemic index sources of carbohydrates and controlling intake of foods containing saturated fats and trans fatty acids. Blood pressure targets are the same as for patients without type 2 diabetes, and antiplatelets should not be offered unless a patient has existing cardiovascular disease. Only patients with a 10-year cardiovascular risk > 10% should be offered a statin, with atorvastatin 20mg as the first-line choice.

    • This question is part of the following fields:

      • Endocrinology/Metabolic Disease
      21.7
      Seconds
  • Question 10 - Sarah is a 44-year-old hairdresser who contacts her GP due to a 2-day...

    Incorrect

    • Sarah is a 44-year-old hairdresser who contacts her GP due to a 2-day history of cough and fever. Her Covid-19 test is negative and she does not sound breathless on the phone. Sarah has been taking paracetamol regularly but despite this, she is still feeling feverish; she has recorded her temperature as 37.8ºC. She has a past medical history of eczema, gilbert's syndrome and adrenal insufficiency. She takes hydrocortisone 15 mg in the morning and 10mg at lunchtime, and also takes fludrocortisone 200 micrograms once a day.
      What is the most appropriate management plan for Sarah?

      Your Answer: Double the dose of both his hydrocortisone and fludrocortisone

      Correct Answer: Double the dose of his hydrocortisone

      Explanation:

      To manage an Addison’s patient with an intercurrent illness, it is recommended to double the dose of their glucocorticoids, specifically hydrocortisone, while keeping the fludrocortisone dose the same. This is because the patient’s fever >37.5 indicates a moderate intercurrent illness. Continuing paracetamol regularly is not the main priority in this situation. Advising the patient to call 999 for admission is unnecessary unless there are severe symptoms such as vomiting or persistent diarrhea. Doubling the dose of fludrocortisone is not recommended as it is a mineralocorticoid with weak glucocorticoid activity, and increasing the glucocorticoid is necessary to mimic a stress response.

      Addison’s disease is a condition that requires patients to undergo both glucocorticoid and mineralocorticoid replacement therapy. This treatment usually involves taking a combination of hydrocortisone and fludrocortisone. Hydrocortisone is typically given in 2 or 3 divided doses, with patients requiring 20-30 mg per day, mostly in the first half of the day. Patient education is crucial, and it is essential to emphasize the importance of not missing glucocorticoid doses. Additionally, patients should consider wearing MedicAlert bracelets and steroid cards, and they should be provided with hydrocortisone for injection with needles and syringes to treat an adrenal crisis.

      During an intercurrent illness, it is crucial to manage the glucocorticoid dose properly. In simple terms, the glucocorticoid dose should be doubled, while the fludrocortisone dose should remain the same. The Addison’s Clinical Advisory Panel has produced guidelines that detail specific scenarios, and patients should refer to these guidelines for more information. It is essential to discuss how to adjust the glucocorticoid dose during an intercurrent illness with a healthcare professional. Proper management of Addison’s disease is crucial to ensure that patients can lead healthy and fulfilling lives.

    • This question is part of the following fields:

      • Infectious Diseases
      35.5
      Seconds
  • Question 11 - An 80-year-old man is admitted to the orthogeriatric ward following a femoral fracture...

    Incorrect

    • An 80-year-old man is admitted to the orthogeriatric ward following a femoral fracture from a fall. He has a medical history of diabetes mellitus type 2, benign prostate hyperplasia, and severe hay fever. After a few days, the patient reports experiencing suprapubic discomfort and difficulty urinating. Which medication is the most probable cause of his symptoms?

      Your Answer: Doxazosin

      Correct Answer: Codeine

      Explanation:

      Urinary retention is a common side effect of opioid analgesia, including the use of codeine. Other medications that can cause this issue include tricyclic antidepressants, anticholinergics, and NSAIDs. Doxazosin, an alpha-blocker, is often prescribed to improve symptoms of benign prostatic hyperplasia and reduce resistance to bladder outflow. Duloxetine, an SSRI used to treat diabetic neuropathy, does not typically cause urinary retention. Finasteride, a 5-alpha reductase inhibitor, is a second-line treatment for benign prostatic hyperplasia when alpha-blockers are not effective, as it reduces prostatic bulk.

      Drugs that can cause urinary retention

      Urinary retention is a condition where a person is unable to empty their bladder completely. This can be caused by various factors, including certain medications. Some drugs that may lead to urinary retention include tricyclic antidepressants like amitriptyline, anticholinergics such as antipsychotics and antihistamines, opioids, NSAIDs, and disopyramide. These drugs can affect the muscles that control the bladder, making it difficult to urinate.

    • This question is part of the following fields:

      • Pharmacology/Therapeutics
      12.5
      Seconds
  • Question 12 - A 32-year-old woman presents with back pain that shoots down her right leg,...

    Incorrect

    • A 32-year-old woman presents with back pain that shoots down her right leg, which she experienced suddenly while picking up her child. During examination, she can only raise her right leg to 30 degrees due to shooting pains down her leg. There is reduced sensation on the dorsum of her right foot, especially around the big toe, and weak foot dorsiflexion. The ankle and knee reflexes seem intact, and a diagnosis of disc prolapse is suspected. Which nerve root is most likely affected?

      Your Answer: L3

      Correct Answer: L5

      Explanation:

      The characteristics of a L5 lesion include the absence of dorsiflexion in the foot and a lack of sensation on the top of the foot.

      Understanding Prolapsed Disc and its Features

      A prolapsed lumbar disc is a common cause of lower back pain that can lead to neurological deficits. It is characterized by clear dermatomal leg pain, which is usually worse than the back pain. The pain is often aggravated when sitting. The features of the prolapsed disc depend on the site of compression. For instance, L3 nerve root compression can cause sensory loss over the anterior thigh, weak quadriceps, reduced knee reflex, and a positive femoral stretch test. On the other hand, L4 nerve root compression can lead to sensory loss in the anterior aspect of the knee, weak quadriceps, reduced knee reflex, and a positive femoral stretch test.

      The management of prolapsed disc is similar to that of other musculoskeletal lower back pain. It involves analgesia, physiotherapy, and exercises. According to NICE, the first-line treatment for back pain without sciatica symptoms is NSAIDs +/- proton pump inhibitors, rather than neuropathic analgesia. If the symptoms persist after 4-6 weeks, referral for consideration of MRI is appropriate. Understanding the features of prolapsed disc can help in the diagnosis and management of this condition.

    • This question is part of the following fields:

      • Musculoskeletal
      25.5
      Seconds
  • Question 13 - A 35-year-old woman comes to the GP clinic for preconception counseling. She plans...

    Incorrect

    • A 35-year-old woman comes to the GP clinic for preconception counseling. She plans to conceive within the next 6 months. She has never been pregnant before and has a medical history of Type 1 diabetes mellitus and irritable bowel syndrome. She is currently taking insulin and has no known drug allergies. Her BMI is 22 kg/m2, and she does not smoke or drink alcohol. There is no family history of neural tube defects, and her partner has no history of neural tube defects. What is the recommended folic acid dosage for her?

      Your Answer: Folic acid 5 mg once a day from now to the end of pregnancy

      Correct Answer: Folic acid 5 mg once a day from now to 12 weeks of pregnancy

      Explanation:

      If a woman has Type 1 diabetes mellitus, she is at a high risk of having a baby with neural tube defects. To prevent this, she should take 5mg of folic acid daily for three months before getting pregnant until the first 12 weeks of pregnancy. Any other dosage or duration of the regime would be incorrect for her.

      Folic Acid: Importance, Deficiency, and Prevention

      Folic acid is a vital nutrient that is converted to tetrahydrofolate (THF) in the body. It is found in green, leafy vegetables and plays a crucial role in the transfer of 1-carbon units to essential substrates involved in the synthesis of DNA and RNA. However, certain factors such as phenytoin, methotrexate, pregnancy, and alcohol excess can cause a deficiency in folic acid. This deficiency can lead to macrocytic, megaloblastic anemia and neural tube defects.

      To prevent neural tube defects during pregnancy, it is recommended that all women take 400mcg of folic acid until the 12th week of pregnancy. Women at higher risk of conceiving a child with a neural tube defect should take 5mg of folic acid from before conception until the 12th week of pregnancy. Women are considered higher risk if they or their partner has a neural tube defect, they have had a previous pregnancy affected by a neural tube defect, or they have a family history of a neural tube defect. Additionally, women with certain medical conditions such as coeliac disease, diabetes, or thalassaemia trait, or those taking antiepileptic drugs, or who are obese (BMI of 30 kg/m2 or more) are also considered higher risk.

      In summary, folic acid is an essential nutrient that plays a crucial role in DNA and RNA synthesis. Deficiency in folic acid can lead to serious health consequences, including neural tube defects. However, taking folic acid supplements during pregnancy can prevent these defects and ensure a healthy pregnancy.

    • This question is part of the following fields:

      • Reproductive Medicine
      56.5
      Seconds
  • Question 14 - A 35-year-old female patient arrives at the emergency department complaining of diplopia that...

    Correct

    • A 35-year-old female patient arrives at the emergency department complaining of diplopia that has been ongoing for 2 months. She reports feeling more fatigued and weak towards the end of the day. Upon examination, anti-acetylcholine receptor antibodies are detected in her blood. A CT scan of her chest is ordered and reveals the presence of an anterior mediastinal mass. What is the most probable diagnosis for this mass?

      Your Answer: Thymoma

      Explanation:

      The most common causes of a mass in the anterior mediastinum are referred to as the 4 T’s: teratoma, terrible lymphadenopathy, thymic mass, and thyroid mass. The woman’s symptoms and positive anti-AChR suggest that she may have myasthenia gravis, which requires a CT chest to check for a thymoma. Other conditions that may show up on a CT chest, such as benign lung nodules, lung tumors, sarcoidosis, and tuberculosis, are unlikely given her presentation. It is important to note that the mediastinum is not the same as the lungs, and therefore, all other answer options are incorrect as the question specifically asks for an anterior mediastinal mass.

      The Mediastinum and its Regions

      The mediastinum is the area located between the two pulmonary cavities and is covered by the mediastinal pleura. It extends from the thoracic inlet at the top to the diaphragm at the bottom. The mediastinum is divided into four regions: the superior mediastinum, middle mediastinum, posterior mediastinum, and anterior mediastinum.

      The superior mediastinum is located between the manubriosternal angle and T4/5 and contains important structures such as the superior vena cava, brachiocephalic veins, arch of aorta, thoracic duct, trachea, oesophagus, thymus, vagus nerve, left recurrent laryngeal nerve, and phrenic nerve.

      The anterior mediastinum contains thymic remnants, lymph nodes, and fat. The middle mediastinum contains the pericardium, heart, aortic root, arch of azygos vein, and main bronchi. The posterior mediastinum contains the oesophagus, thoracic aorta, azygos vein, thoracic duct, vagus nerve, sympathetic nerve trunks, and splanchnic nerves.

      In summary, the mediastinum is a crucial area of the chest that contains many important structures and is divided into four distinct regions.

    • This question is part of the following fields:

      • Respiratory Medicine
      22.7
      Seconds
  • Question 15 - A 65-year-old man presents with palpitations and is found to have a regular,...

    Correct

    • A 65-year-old man presents with palpitations and is found to have a regular, monomorphic, broad complex tachycardia on cardiac monitoring. He has a history of type 2 diabetes mellitus and has undergone percutaneous coronary intervention for his left anterior descending, right coronary, and circumflex arteries. Physical examination is unremarkable except for tachycardia, and there are no signs of myocardial ischemia on a 12-lead electrocardiogram. Which of the following management options should be avoided in this case?

      Your Answer: Verapamil

      Explanation:

      Verapamil is contraindicated in ventricular tachycardia, which is the most probable diagnosis.

      Managing Ventricular Tachycardia

      Ventricular tachycardia is a type of rapid heartbeat that originates in the ventricles of the heart. In a peri-arrest situation, it is assumed to be ventricular in origin. If the patient shows adverse signs such as low blood pressure, chest pain, heart failure, or syncope, immediate cardioversion is necessary. However, in the absence of such signs, antiarrhythmic drugs may be used. If drug therapy fails, electrical cardioversion may be needed with synchronised DC shocks.

      There are several drugs that can be used to manage ventricular tachycardia, including amiodarone, lidocaine, and procainamide. Amiodarone is ideally administered through a central line, while lidocaine should be used with caution in severe left ventricular impairment. Verapamil should not be used in VT. If drug therapy fails, an electrophysiological study (EPS) may be conducted, or an implantable cardioverter-defibrillator (ICD) may be implanted. The ICD is particularly indicated in patients with significantly impaired LV function.

    • This question is part of the following fields:

      • Cardiovascular
      21.6
      Seconds
  • Question 16 - A 60-year-old woman presents after collapsing at home. She has diplopia on right...

    Incorrect

    • A 60-year-old woman presents after collapsing at home. She has diplopia on right gaze, right-sided facial weakness and left flaccid hemiparesis.
      Which of the following is the most likely site for her lesion?

      Your Answer: Right cerebral hemisphere

      Correct Answer: Right pons

      Explanation:

      Lesions in different areas of the brainstem can cause specific neurological symptoms. A lesion in the right pons can result in left-sided weakness, right-sided facial paralysis, and double vision when looking towards the lesion. This is known as Millard-Gubler syndrome and is caused by a blockage in the penetrating branches of the basilar artery. A lesion in the right midbrain can affect cranial nerves III and IV, while a lesion in the left midbrain can cause contralateral hemiparesis, contralateral hypoglossal nerve palsy, and ipsilateral oculomotor nerve palsy. A lesion in the left pons can cause contralateral hemiparesis, ipsilateral lateral gaze palsy, and ipsilateral paralysis of the upper and lower face. Lesions in the cerebral hemisphere produce purely contralateral and upper motor neuron signs. The insertion site, cranial nerves, and skull base associated with each area of the brainstem are also important to consider.

    • This question is part of the following fields:

      • Neurology
      64.4
      Seconds
  • Question 17 - A 62-year-old woman presents to the General Practitioner. She has a past medical...

    Incorrect

    • A 62-year-old woman presents to the General Practitioner. She has a past medical history of hypertension, diabetes mellitus type II, peripheral vascular disease and ischaemic heart disease. The patient had an episode of retinal artery occlusion (RAO) and had to go to the Eye Hospital as an emergency.
      After many investigations, the Ophthalmologist stated that the cause of her RAO is atherosclerosis of her central retinal artery (CRA). The patient is worried about her eyesight becoming worse and asks about long-term management plans for RAO.
      Which of the following is considered part of the long-term management plan for RAO?
      Select the SINGLE most appropriate management from the list below.

      Your Answer: Firm routine ocular massages

      Correct Answer: Prophylaxis with an antiplatelet agent

      Explanation:

      Retinal artery occlusion is a condition that increases the risk of ischemic end-organ damage, such as stroke. Long-term management involves identifying and addressing underlying causes, reducing risk factors for atherosclerosis, and considering carotid endarterectomy if necessary. Ophthalmic follow-up and referral to low-vision-aid clinics may also be necessary. Acute treatment options include ocular massage, intra-arterial fibrinolysis, and lowering intraocular pressure with anterior chamber paracentesis. Atherosclerosis and embolism are the main causes of RAO, and prophylaxis with an antiplatelet or anticoagulation agent may be necessary for long-term management. However, even with early treatment, the prognosis is generally poor, and only about one-third of patients show any improvement.

    • This question is part of the following fields:

      • Ophthalmology
      60.7
      Seconds
  • Question 18 - A 33-year-old man who is HIV positive comes to the clinic complaining of...

    Correct

    • A 33-year-old man who is HIV positive comes to the clinic complaining of shortness of breath and a dry cough. He has been homeless and has not been keeping up with his outpatient appointments or taking his antiretroviral medication. Upon examination, his respiratory rate is 24 breaths per minute and there are scattered crackles in his chest. His oxygen saturation is 96% on room air but drops quickly after walking. Based on the likely diagnosis of Pneumocystis jiroveci pneumonia, what is the most appropriate first-line treatment?

      Your Answer: Co-trimoxazole

      Explanation:

      The treatment for Pneumocystis jiroveci pneumonia involves the use of co-trimoxazole, a combination of trimethoprim and sulfamethoxazole.

      Pneumocystis jiroveci Pneumonia in HIV Patients

      Pneumocystis jiroveci pneumonia (formerly known as Pneumocystis carinii pneumonia) is a common opportunistic infection in individuals with AIDS. Pneumocystis jiroveci is an organism that is classified as a fungus by some and a protozoa by others. Patients with a CD4 count below 200/mm³ should receive prophylaxis for PCP. Symptoms of PCP include dyspnea, dry cough, fever, and few chest signs. Pneumothorax is a common complication of PCP, and extrapulmonary manifestations are rare.

      Chest X-rays typically show bilateral interstitial pulmonary infiltrates, but other findings such as lobar consolidation may also be present. Sputum tests often fail to show PCP, and bronchoalveolar lavage (BAL) is often necessary to demonstrate the presence of the organism. Treatment for PCP includes co-trimoxazole and IV pentamidine in severe cases. Aerosolized pentamidine is an alternative treatment but is less effective and carries a risk of pneumothorax. Steroids may be used if the patient is hypoxic, as they can reduce the risk of respiratory failure and death.

      In summary, PCP is a common opportunistic infection in individuals with AIDS, and prophylaxis should be given to those with a CD4 count below 200/mm³. Symptoms include dyspnea, dry cough, and fever, and chest X-rays typically show bilateral interstitial pulmonary infiltrates. Treatment includes co-trimoxazole, IV pentamidine, and steroids if the patient is hypoxic.

    • This question is part of the following fields:

      • Respiratory Medicine
      21.3
      Seconds
  • Question 19 - A 27-year-old female is brought in under Section 2 of the Mental Health...

    Correct

    • A 27-year-old female is brought in under Section 2 of the Mental Health Act. She was discovered at home, sitting on her bedroom floor in filthy clothes and in unsanitary conditions. Her attire indicated significant weight loss and she appeared severely dehydrated. She did not cooperate with the evaluation, seeming to ignore the team.

      Upon admission, her blood tests revealed hyperkalaemia and an acute kidney injury. While receiving treatment for this, she made no effort to eat or drink, remove her cannula, or leave the ward, nor did she show any signs of distress. She did not communicate with any staff, instead spending hours lying in bed staring into space.

      According to her GP, she has no prior medical history and has never been prescribed psychiatric medication before. What is the most appropriate course of treatment?

      Your Answer: Electroconvulsive therapy

      Explanation:

      When a patient is suffering from life-threatening major depressive disorder and is exhibiting catatonia, ECT is recommended. In this case, the patient is experiencing severe dehydration, suicidal thoughts, and catatonia, indicating the need for urgent treatment. While the patient has not previously taken any psychiatric medication, an SSRI like citalopram, even with augmentation, would not be suitable due to the severity of the illness. ECT is the best option for achieving rapid results.

      Electroconvulsive therapy (ECT) is a viable treatment option for patients who suffer from severe depression that does not respond to medication, such as catatonia, or those who experience psychotic symptoms. The only absolute contraindication for ECT is when a patient has raised intracranial pressure.

      Short-term side effects of ECT include headaches, nausea, short-term memory impairment, memory loss of events prior to the therapy, and cardiac arrhythmia. However, these side effects are typically temporary and resolve quickly.

      Long-term side effects of ECT are less common, but some patients have reported impaired memory. It is important to note that the benefits of ECT often outweigh the potential risks, and it can be a life-changing treatment for those who have not found relief from other forms of therapy.

    • This question is part of the following fields:

      • Psychiatry
      23
      Seconds
  • Question 20 - A 30-year-old female patient visits the clinic as she has not had a...

    Incorrect

    • A 30-year-old female patient visits the clinic as she has not had a menstrual period for 5 months. She has had regular periods since she was 12 years old. After conducting a negative urinary pregnancy test, the doctor ordered some blood tests. The results are as follows:
      FSH 4.2 IU/L (4.5 - 22.5)
      LH 0.5 IU/L (0.5 - 50.0)
      Oestradiol 110 pmol/L (100 - 1000)
      Testosterone 1.2 nmol/L (0.8-3.1)
      Prolactin 280 IU/mL (60-600)
      T4 11.5 pmol/l (9-18)

      What is the most probable diagnosis?

      Your Answer: Hyperprolactinaemia

      Correct Answer: Hypothalamic amenorrhoea

      Explanation:

      If a woman experiences secondary amenorrhoea and has low levels of gonadotrophins, it suggests that the cause is related to the hypothalamus. High levels of gonadotrophins would indicate premature ovarian failure, while high levels of LH and androgens would suggest polycystic ovarian syndrome. Normal levels of prolactin and thyroxine have been observed in this woman.

      Understanding Amenorrhoea: Causes, Investigations, and Management

      Amenorrhoea is a condition characterized by the absence of menstrual periods in women. It can be classified into two types: primary and secondary. Primary amenorrhoea occurs when menstruation fails to start by the age of 15 in girls with normal secondary sexual characteristics or by the age of 13 in girls with no secondary sexual characteristics. On the other hand, secondary amenorrhoea is the cessation of menstruation for 3-6 months in women with previously normal and regular menses or 6-12 months in women with previous oligomenorrhoea.

      There are various causes of amenorrhoea, including gonadal dysgenesis, testicular feminization, congenital malformations of the genital tract, functional hypothalamic amenorrhoea, congenital adrenal hyperplasia, imperforate hymen, hypothalamic amenorrhoea, polycystic ovarian syndrome, hyperprolactinemia, premature ovarian failure, Sheehan’s syndrome, Asherman’s syndrome, and thyrotoxicosis. To determine the underlying cause of amenorrhoea, initial investigations such as full blood count, urea & electrolytes, coeliac screen, thyroid function tests, gonadotrophins, prolactin, and androgen levels are necessary.

      The management of amenorrhoea depends on the underlying cause. For primary amenorrhoea, it is important to investigate and treat any underlying cause. Women with primary ovarian insufficiency due to gonadal dysgenesis may benefit from hormone replacement therapy to prevent osteoporosis. For secondary amenorrhoea, it is important to exclude pregnancy, lactation, and menopause in women 40 years of age or older and treat the underlying cause accordingly. It is important to note that hypothyroidism may also cause amenorrhoea.

    • This question is part of the following fields:

      • Reproductive Medicine
      17.3
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  • Question 21 - A 35-year-old man presents to his General Practitioner (GP) with concerns about a...

    Incorrect

    • A 35-year-old man presents to his General Practitioner (GP) with concerns about a mole on his leg. He has noticed over the past few months that it has increased in size. On examination, the mole is 7 mm in diameter and has an irregular border but is a consistent colour.
      What is the most appropriate management option for this patient?

      Your Answer: Removal in primary care minor surgery clinic

      Correct Answer: 2-week wait referral to dermatology

      Explanation:

      Understanding Referral Guidelines for Suspicious Pigmented Lesions

      When assessing pigmented lesions, the National Institute of Health and Care Excellence (NICE) recommends using the 7-point scoring system.
      The 7-point checklist includes:
      Major features (2 points each):
      change in size
      irregular shape or border
      irregular colour.
      Minor features (1 point each):
      > 7 mm at greatest diameter
      inflammation
      oozing or crusting
      change in sensation including itch.

      Lesions scoring 3 or more or with other suspicious features of melanoma should be referred urgently via the cancer fast-track pathway to dermatology.

      For lesions with a low suspicion of melanoma, a photo should be taken with a ruler and the patient advised to return in eight weeks for review. However, lesions scoring 5 on the checklist, like those with a change in size, irregular shape or border, and irregular color, should be referred urgently to a dermatologist to avoid any delay in diagnosis and subsequent treatment.

      Excision of lesions suspicious of melanoma should be avoided in primary care as this can delay treatment, and incomplete excision is more common. Routine referral to dermatology would be suitable for a pigmented lesion which scores less than 3 on the 7-point checklist if there are no other features to suggest melanoma. Referral to genetics is recommended if three or more family members have been diagnosed with melanoma.

      It is important to understand these referral guidelines to ensure timely and appropriate management of suspicious pigmented lesions.

    • This question is part of the following fields:

      • Dermatology
      29.5
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  • Question 22 - You are taking the history of an Emergency Department patient who was assaulted....

    Correct

    • You are taking the history of an Emergency Department patient who was assaulted. The victim is a 20-year-old female who has a deep laceration on her thigh caused by a rusty machete. The wound has exposed tendon, muscle, and subcutaneous fat. According to her medical records, she received all her childhood immunizations on schedule, including 5 doses of tetanus vaccine, with the last one administered when she was 16 years old.

      What is the appropriate management for tetanus risk in this patient?

      Your Answer: No tetanus vaccine booster and no immunoglobulins required

      Explanation:

      If a patient has received 5 doses of the tetanus vaccine, with the most recent dose administered less than 10 years ago, they do not need a booster vaccine or immunoglobulins, regardless of the severity of the wound. This is the correct course of action. The patient’s childhood vaccinations would have included 5 doses of the tetanus vaccine, with the last dose given at age 14 or later. Therefore, the patient is already adequately protected and does not require a booster or immunoglobulin, regardless of the severity of the wound.

      The option of administering a tetanus vaccine booster with antibiotics is not the correct course of action. While antibiotics may be considered for protection against other bacteria, the patient already has sufficient protection against tetanus and does not require vaccination.

      Similarly, administering a tetanus vaccine booster with tetanus immunoglobulin is not necessary. As previously mentioned, the patient already has adequate protection from previous vaccinations. Immunoglobulin would only be necessary if the patient had an incomplete or unknown vaccine history or if it had been more than 10 years since the last vaccine.

      Lastly, administering a tetanus vaccine booster alone is not necessary. The patient already has protection from previous vaccinations and does not require a booster.

      Tetanus Vaccination and Management of Wounds

      The tetanus vaccine is a purified toxin that is given as part of a combined vaccine. In the UK, it is given as part of the routine immunisation schedule at 2, 3, and 4 months, 3-5 years, and 13-18 years, providing a total of 5 doses for long-term protection against tetanus.

      When managing wounds, the first step is to classify them as clean, tetanus-prone, or high-risk tetanus-prone. Clean wounds are less than 6 hours old and have negligible tissue damage, while tetanus-prone wounds include puncture-type injuries acquired in a contaminated environment or wounds containing foreign bodies. High-risk tetanus-prone wounds include wounds or burns with systemic sepsis, certain animal bites and scratches, heavy contamination with material likely to contain tetanus spores, wounds or burns with extensive devitalised tissue, and wounds or burns that require surgical intervention.

      If the patient has had a full course of tetanus vaccines with the last dose less than 10 years ago, no vaccine or tetanus immunoglobulin is required regardless of the wound severity. If the patient has had a full course of tetanus vaccines with the last dose more than 10 years ago, a reinforcing dose of vaccine is required for tetanus-prone wounds, and a reinforcing dose of vaccine plus tetanus immunoglobulin is required for high-risk wounds. If the vaccination history is incomplete or unknown, a reinforcing dose of vaccine is required regardless of the wound severity, and a reinforcing dose of vaccine plus tetanus immunoglobulin is required for tetanus-prone and high-risk wounds.

      Overall, proper vaccination and wound management are crucial in preventing tetanus infection.

    • This question is part of the following fields:

      • Infectious Diseases
      84.6
      Seconds
  • Question 23 - A 36-year-old female patient complains of various symptoms that have persisted for the...

    Incorrect

    • A 36-year-old female patient complains of various symptoms that have persisted for the last four months. These symptoms include weight gain, especially around the abdomen, with noticeable purplish stretch marks, thin skin, and easy bruising. She has also been experiencing increased swelling in her ankles and a low mood. As part of the diagnostic process, a series of laboratory tests are conducted.
      What electrolyte abnormality is anticipated in this patient?

      Your Answer: Hyperkalaemic metabolic acidosis

      Correct Answer: Hypokalaemic metabolic alkalosis

      Explanation:

      The patient is suffering from Cushing’s syndrome, which is characterized by an excess of cortisol. This can be caused by exogenous glucocorticoid therapy, autonomous overproduction by the adrenal glands, or increased production of adrenocorticotrophic hormone. High levels of cortisol can mimic the effects of aldosterone, leading to increased sodium and water retention and increased potassium excretion, resulting in hypokalemia. The increased resorption of bicarbonate in the tubules due to potassium depletion causes metabolic alkalosis. Hyperkalemic metabolic acidosis is not expected because cortisol’s effect on the mineralocorticoid receptor causes a loss of potassium. Hyperkalemic respiratory alkalosis is also not expected because cortisol’s effect on the mineralocorticoid receptor leads to potassium excretion. Additionally, any acid-base disturbance in Cushing’s syndrome is likely to be metabolically mediated rather than respiratory. Hypokalemic metabolic acidosis is not expected because the concomitant loss of potassium and reabsorption of bicarbonate causes metabolic alkalosis.

      Investigations for Cushing’s Syndrome

      Cushing’s syndrome is a condition caused by excessive cortisol production in the body. There are various causes of Cushing’s syndrome, including iatrogenic, ACTH-dependent, and ACTH-independent causes. To diagnose Cushing’s syndrome, doctors typically perform tests to confirm the condition and determine its underlying cause.

      General lab findings consistent with Cushing’s syndrome include hypokalaemic metabolic alkalosis and impaired glucose tolerance. Ectopic ACTH secretion, which is often associated with small cell lung cancer, is characterized by very low potassium levels.

      The two most commonly used tests to confirm Cushing’s syndrome are the overnight dexamethasone suppression test and the 24-hour urinary free cortisol test. The overnight dexamethasone suppression test is the most sensitive test and is used first-line to test for Cushing’s syndrome. Patients with Cushing’s syndrome do not have their morning cortisol spike suppressed. The 24-hour urinary free cortisol test measures the amount of cortisol in the urine over a 24-hour period.

      To localize the cause of Cushing’s syndrome, doctors may perform additional tests such as high-dose dexamethasone suppression test, CRH stimulation, and petrosal sinus sampling of ACTH. An insulin stress test may also be used to differentiate between true Cushing’s and pseudo-Cushing’s. Overall, a combination of these tests can help diagnose Cushing’s syndrome and determine its underlying cause.

    • This question is part of the following fields:

      • Endocrinology/Metabolic Disease
      19.2
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  • Question 24 - A 68-year-old woman visits her GP with a complaint of urine leakage when...

    Incorrect

    • A 68-year-old woman visits her GP with a complaint of urine leakage when she coughs, sneezes, or laughs. She has been experiencing this for the past year intermittently, but it has become more severe over the last two months. She has no dysuria or haematuria and is in good health with no abdominal symptoms. All three of her children were delivered vaginally. A urine dip and culture test came back negative. What is the probable diagnosis?

      Your Answer: Detrusor instability

      Correct Answer: Stress incontinence

      Explanation:

      The most probable cause of urinary incontinence while coughing is stress incontinence. This occurs when the bladder neck drops below the levator ani sling, which can happen when there is increased intra-abdominal pressure, such as when coughing, laughing, or sneezing. Stress incontinence is characterized by leakage of urine during these activities. Neurogenic bladder, on the other hand, typically presents with overflow incontinence or retention, which is not limited to increased intra-abdominal pressure. Detrusor instability is associated with urgency and increased urinary frequency. Urinary tract infections and pyelonephritis are characterized by increased frequency, dysuria, pyrexia, and loin pain. In this case, the negative urine dip makes infection an unlikely cause.

      Understanding Urinary Incontinence: Causes, Classification, and Management

      Urinary incontinence (UI) is a common condition that affects around 4-5% of the population, with elderly females being more susceptible. Several risk factors contribute to UI, including advancing age, previous pregnancy and childbirth, high body mass index, hysterectomy, and family history. UI can be classified into different types, such as overactive bladder (OAB)/urge incontinence, stress incontinence, mixed incontinence, overflow incontinence, and functional incontinence.

      Initial investigation of UI involves completing bladder diaries for at least three days, vaginal examination, urine dipstick and culture, and urodynamic studies. Management of UI depends on the predominant type of incontinence. For urge incontinence, bladder retraining and bladder stabilizing drugs such as antimuscarinics are recommended. For stress incontinence, pelvic floor muscle training and surgical procedures such as retropubic mid-urethral tape procedures may be offered. Duloxetine, a combined noradrenaline and serotonin reuptake inhibitor, may also be used as an alternative to surgery.

      In summary, understanding the causes, classification, and management of UI is crucial in providing appropriate care for patients. Early diagnosis and intervention can significantly improve the quality of life for those affected by this condition.

    • This question is part of the following fields:

      • Renal Medicine/Urology
      62.7
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  • Question 25 - A 63-year-old woman presents to her General Practitioner concerned about a lesion to...

    Incorrect

    • A 63-year-old woman presents to her General Practitioner concerned about a lesion to her right temple. It has been there for several months. Examination reveals a round lesion, 1 cm in diameter, with rolled edges and a pearly appearance.
      Which of the following, from the history, is the most likely diagnosis?
      Select the SINGLE most likely diagnosis from the list below. Select ONE option only.

      Your Answer: Squamous cell carcinoma (SCC)

      Correct Answer: Basal cell carcinoma (BCC)

      Explanation:

      Skin cancer can take on different forms, including basal cell carcinoma (BCC), actinic keratosis, herpes zoster infection, melanoma, and squamous cell carcinoma (SCC). BCCs can appear on any part of the body and often produce a bloody crust. AKs are scaly or hyperkeratotic lesions that can become malignant and are common in individuals over 60 years old. Herpes zoster infection causes a rash that is usually unilateral and follows a dermatomal distribution. Melanoma is a malignant tumour that arises from cutaneous melanocytes and can take on different types. SCC is the second most common type of skin cancer and arises from the keratinocytes of the epidermis. It predominantly affects sun-exposed sites and has a firm, indurated appearance with surrounding inflammation. BCCs are commonly found in sun-exposed areas and have a pearly appearance with rolled edges and surrounding telangiectasia. Management for skin cancer varies depending on the type and severity, but removal through curettage or excision is common for BCCs.

    • This question is part of the following fields:

      • Dermatology
      64.2
      Seconds
  • Question 26 - A 2-year-old girl is brought to her pediatrician by her father. He has...

    Incorrect

    • A 2-year-old girl is brought to her pediatrician by her father. He has a photograph and is worried about the different appearances of her eyes. One eye shows a normal red reflex while the other appears white. He wants to know if this is normal.

      What is your advice for him?

      Your Answer: Routinely refer to ophthalmology

      Correct Answer: Urgent referral to ophthalmology

      Explanation:

      If a newborn lacks red reflex, it is important to consider the possibility of retinoblastoma. Other causes should also be evaluated, but urgent referral to an ophthalmologist for a comprehensive, dilated eye examination is necessary.

      Retinoblastoma is a prevalent type of eye cancer that is commonly found in children, with an average age of diagnosis at 18 months. It is caused by a loss of function of the retinoblastoma tumor suppressor gene on chromosome 13, which is inherited in an autosomal dominant pattern. About 10% of cases are hereditary. The most common presenting symptom is the absence of red-reflex, which is replaced by a white pupil (leukocoria). Other possible features include strabismus and visual problems.

      When it comes to managing retinoblastoma, enucleation is not the only option. Depending on how advanced the tumor is, other treatment options include external beam radiation therapy, chemotherapy, and photocoagulation. The prognosis for retinoblastoma is excellent, with over 90% of patients surviving into adulthood.

    • This question is part of the following fields:

      • Paediatrics
      55.4
      Seconds
  • Question 27 - A 56-year-old man with a history of type 2 diabetes mellitus complains of...

    Incorrect

    • A 56-year-old man with a history of type 2 diabetes mellitus complains of right shoulder pain and limited movement in all directions. What is the probable diagnosis?

      Your Answer: Diabetic amyotrophy

      Correct Answer: Adhesive capsulitis

      Explanation:

      The development of adhesive capsulitis is more likely in individuals with diabetes mellitus.

      Understanding Adhesive Capsulitis (Frozen Shoulder)

      Adhesive capsulitis, commonly known as frozen shoulder, is a prevalent cause of shoulder pain that primarily affects middle-aged women. The exact cause of this condition is not yet fully understood. However, studies have shown that up to 20% of diabetics may experience an episode of frozen shoulder. Symptoms typically develop over several days, with external rotation being more affected than internal rotation or abduction. Both active and passive movement are affected, and patients usually experience a painful freezing phase, an adhesive phase, and a recovery phase. In some cases, the condition may affect both shoulders, which occurs in up to 20% of patients. The episode typically lasts between 6 months and 2 years.

      Diagnosis of adhesive capsulitis is usually clinical, although imaging may be necessary for atypical or persistent symptoms. Unfortunately, no single intervention has been proven to improve the outcome in the long-term. However, there are several treatment options available, including nonsteroidal anti-inflammatory drugs (NSAIDs), physiotherapy, oral corticosteroids, and intra-articular corticosteroids.

    • This question is part of the following fields:

      • Musculoskeletal
      40.2
      Seconds
  • Question 28 - A 67-year-old man attending the respiratory clinic receives a suspected diagnosis of chronic...

    Incorrect

    • A 67-year-old man attending the respiratory clinic receives a suspected diagnosis of chronic obstructive pulmonary disease.
      Which of the following is the most appropriate investigation to confirm diagnosis?

      Your Answer: Electrocardiograph (ECG)

      Correct Answer: Spirometry

      Explanation:

      Investigations for COPD: Spirometry is Key

      COPD is a chronic obstructive airway disease that is diagnosed through a combination of clinical history, signs, and investigations. While several investigations may be used to support a diagnosis of COPD, spirometry is the most useful and important tool. A spirometer is used to measure functional lung volumes, including forced expiratory volume in 1 s (FEV1) and forced vital capacity (FVC). The FEV1:FVC ratio provides an estimate of the severity of airflow obstruction, with a normal ratio being 75-80%. In patients with COPD, the ratio is typically <0.7 and FEV1 <80% predicted. Spirometry is essential for establishing a baseline for disease severity, monitoring disease progression, and assessing the effects of treatment. Other investigations, such as echocardiography, chest radiography, ECG, and peak flow, may be used to exclude other pathologies or assess comorbidities, but spirometry remains the key investigation for diagnosing and managing COPD.

    • This question is part of the following fields:

      • Respiratory Medicine
      26.2
      Seconds
  • Question 29 - A 27-year-old woman comes in for her 8th week of pregnancy and reports...

    Incorrect

    • A 27-year-old woman comes in for her 8th week of pregnancy and reports an uncomplicated pregnancy thus far. She is currently in good health and not experiencing any symptoms. However, she expresses concern about not being vaccinated against rubella as a child due to her parents' anti-vaccine beliefs. She is aware of the potential harm rubella can cause to her developing fetus and blood tests confirm that she is not immune to the virus.

      What advice should be given to her?

      Your Answer: She can have the MMR vaccine now

      Correct Answer: She can have the MMR vaccine postnatally

      Explanation:

      In the case of a pregnant woman who is not immune to rubella, it is recommended to offer the MMR vaccination after giving birth. Rubella can cause severe harm to the developing foetus, especially during the first 8-10 weeks of pregnancy. Although congenital rubella syndrome is now rare due to widespread MMR vaccination, there has been a resurgence of measles, mumps, and rubella outbreaks in developed countries due to the anti-vaccination movement. The woman should avoid contact with individuals who may have rubella and cannot receive the vaccine while pregnant. Referral to an obstetrician is not necessary at this time since the woman is asymptomatic and in good health. The MMR vaccine should not be administered at 20 weeks of pregnancy, and if the woman is not immune, it should be offered postnatally. If there is a suspicion of rubella based on the woman’s clinical presentation, the local Health Protection Team should be notified, but this is not necessary in this case since there is no suspicion.

      Rubella and Pregnancy: Risks, Features, Diagnosis, and Management

      Rubella, also known as German measles, is a viral infection caused by the togavirus. Thanks to the introduction of the MMR vaccine, it is now rare. However, if contracted during pregnancy, there is a risk of congenital rubella syndrome, which can cause serious harm to the fetus. It is important to note that the incubation period is 14-21 days, and individuals are infectious from 7 days before symptoms appear to 4 days after the onset of the rash.

      The risk of damage to the fetus is highest in the first 8-10 weeks of pregnancy, with a risk as high as 90%. However, damage is rare after 16 weeks. Features of congenital rubella syndrome include sensorineural deafness, congenital cataracts, congenital heart disease (e.g. patent ductus arteriosus), growth retardation, hepatosplenomegaly, purpuric skin lesions, ‘salt and pepper’ chorioretinitis, microphthalmia, and cerebral palsy.

      If a suspected case of rubella in pregnancy arises, it should be discussed immediately with the local Health Protection Unit (HPU) as type/timing of investigations may vary. IgM antibodies are raised in women recently exposed to the virus. It should be noted that it is very difficult to distinguish rubella from parvovirus B19 clinically. Therefore, it is important to also check parvovirus B19 serology as there is a 30% risk of transplacental infection, with a 5-10% risk of fetal loss.

      If a woman is tested at any point and no immunity is demonstrated, they should be advised to keep away from people who might have rubella. Non-immune mothers should be offered the MMR vaccination in the post-natal period. However, MMR vaccines should not be administered to women known to be pregnant or attempting to become pregnant.

    • This question is part of the following fields:

      • Reproductive Medicine
      18.5
      Seconds
  • Question 30 - Which one of the following statements regarding juvenile idiopathic arthritis is accurate? ...

    Incorrect

    • Which one of the following statements regarding juvenile idiopathic arthritis is accurate?

      Your Answer:

      Correct Answer: Achilles tendonitis is a recognised association

      Explanation:

      Ankylosing spondylitis is a type of spondyloarthropathy that is associated with HLA-B27. It is more commonly seen in young males, with a sex ratio of 3:1, and typically presents with lower back pain and stiffness that develops gradually. The stiffness is usually worse in the morning and improves with exercise, while pain at night may improve upon getting up. Clinical examination may reveal reduced lateral and forward flexion, as well as reduced chest expansion. Other features associated with ankylosing spondylitis include apical fibrosis, anterior uveitis, aortic regurgitation, Achilles tendonitis, AV node block, amyloidosis, cauda equina syndrome, and peripheral arthritis (more common in females).

    • This question is part of the following fields:

      • Musculoskeletal
      0
      Seconds
  • Question 31 - A 72-year-old man presents to your clinic complaining of left nostril blockage and...

    Incorrect

    • A 72-year-old man presents to your clinic complaining of left nostril blockage and frequent nosebleeds for the past 4 weeks. He has a medical history of well-controlled diabetes and hypertension and has a smoking history of 20 cigarettes per day since he was 18. He used to work in construction. During the examination, you observe a nasal polyp on the left side. What would be the most suitable course of action?

      Your Answer:

      Correct Answer: 2 week-wait referral

      Explanation:

      Unilateral nasal polyps are a cause for concern and should be promptly referred to an ENT specialist as they may indicate nasal cancer. However, they can also be caused by other factors such as nose picking, foreign bodies, misapplication of nasal spray or cystic fibrosis. Treatment with antibiotics, oral steroids, nasal drops or cautery is unlikely to be effective and may delay the diagnosis of a serious condition.

      Understanding Nasal Polyps

      Nasal polyps are a relatively uncommon condition affecting around 1% of adults in the UK. They are more commonly seen in men and are not typically found in children or the elderly. There are several associations with nasal polyps, including asthma (particularly late-onset asthma), aspirin sensitivity, infective sinusitis, cystic fibrosis, Kartagener’s syndrome, and Churg-Strauss syndrome. When asthma, aspirin sensitivity, and nasal polyposis occur together, it is known as Samter’s triad.

      The symptoms of nasal polyps include nasal obstruction, rhinorrhoea, sneezing, and a poor sense of taste and smell. It is important to note that any unusual symptoms, such as unilateral symptoms or bleeding, require further investigation. If nasal polyps are suspected, patients should be referred to an ear, nose, and throat (ENT) specialist for a full examination.

      The management of nasal polyps typically involves the use of topical corticosteroids, which can shrink polyp size in around 80% of patients. Overall, understanding nasal polyps and their associations can help with early detection and appropriate management.

    • This question is part of the following fields:

      • ENT
      0
      Seconds
  • Question 32 - A Foundation Year 1 doctor stops you in the corridor to ask for...

    Incorrect

    • A Foundation Year 1 doctor stops you in the corridor to ask for some advice about prescribing and unwanted pharmacological effects of drugs in pregnancy.
      Which of the following list of potential pharmacological risks of drugs in pregnancy is true?

      Your Answer:

      Correct Answer: Aspirin : kernicterus

      Explanation:

      Various drugs can have negative effects on pregnancy beyond the risk of birth defects. For example, aspirin should be used with caution in the third trimester due to the potential for impaired platelet function, hemorrhage, and increased blood loss during labor. High doses of aspirin may also lead to intrauterine growth restriction, closure of the fetal ductus arteriosus, and persistent pulmonary hypertension in newborns. Similarly, ACE inhibitors should be avoided during pregnancy unless absolutely necessary, as they can negatively impact fetal and neonatal blood pressure control and renal function. Thiazide diuretics should not be used to treat gestational hypertension, as they can cause neonatal thrombocytopenia, bone marrow suppression, jaundice, electrolyte imbalances, and hypoglycemia. NSAIDs should also be avoided during pregnancy unless the potential benefits outweigh the risks, as they can lead to closure of the fetal ductus arteriosus and delayed onset and increased duration of labor. Other drugs, such as b-blockers and carbimazole, can also have negative effects on pregnancy and should be used with caution.

    • This question is part of the following fields:

      • Pharmacology/Therapeutics
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  • Question 33 - A 50-year-old man visits the Gastroenterology Clinic with concerns about his tongue. He...

    Incorrect

    • A 50-year-old man visits the Gastroenterology Clinic with concerns about his tongue. He has noticed unusual patterns on his tongue that have been present for a while, but he is worried about tongue cancer as he has been a heavy smoker for the past 20 years. What is the most suitable initial management option for this patient?

      Your Answer:

      Correct Answer: None

      Explanation:

      Geographic Tongue: A Benign Condition Requiring No Medical Intervention

      Geographic tongue, also known as benign migratory glossitis, is a common condition that affects up to 3% of the general population. While some patients may experience a burning sensation when consuming hot or spicy foods, most are asymptomatic. The diagnosis of geographic tongue can usually be confirmed from history and physical examination alone, and no medical intervention is required.

      Surgical correction is not warranted for geographic tongue, as it is a benign condition of no clinical significance. Aspiration for cytology is also not appropriate, as the diagnosis can be made without further investigation. Excision biopsy may actually cause harm, as histological findings are identical to those seen in pustular psoriasis.

      A full blood count is not necessary for the diagnosis of geographic tongue. Instead, the condition can be identified through the elongation of rete ridges, hyperparakeratosis and acanthosis at the periphery, loss of filiform papillae, and migration and clustering of neutrophils within the epithelium towards the centre of the lesions. The predominant inflammatory infiltrates in the lamina propria is neutrophils with an admixture of chronic inflammatory cells.

      In summary, geographic tongue is a benign condition that requires no medical intervention. Diagnosis can be made through history and physical examination alone, and further investigation may cause harm.

    • This question is part of the following fields:

      • Gastroenterology/Nutrition
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  • Question 34 - A 28-year-old woman visits the GP clinic as she hasn't had her menstrual...

    Incorrect

    • A 28-year-old woman visits the GP clinic as she hasn't had her menstrual period for 3 months. Upon conducting a urinary pregnancy test, it comes out positive. A dating scan is scheduled, which shows a gestational sac with a nonviable foetus. What could be the possible diagnosis?

      Your Answer:

      Correct Answer: Missed miscarriage

      Explanation:

      Miscarriage is a common complication that can occur in up to 25% of all pregnancies. There are different types of miscarriage, each with its own set of symptoms and characteristics. Threatened miscarriage is painless vaginal bleeding that occurs before 24 weeks, typically at 6-9 weeks. The bleeding is usually less than menstruation, and the cervical os is closed. Missed or delayed miscarriage is when a gestational sac containing a dead fetus is present before 20 weeks, without the symptoms of expulsion. The mother may experience light vaginal bleeding or discharge, and the symptoms of pregnancy may disappear. Pain is not usually a feature, and the cervical os is closed. Inevitable miscarriage is characterized by heavy bleeding with clots and pain, and the cervical os is open. Incomplete miscarriage occurs when not all products of conception have been expelled, and there is pain and vaginal bleeding. The cervical os is open in this type of miscarriage.

    • This question is part of the following fields:

      • Reproductive Medicine
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  • Question 35 - At what point in the childhood immunisation schedule is the Meningitis B vaccine...

    Incorrect

    • At what point in the childhood immunisation schedule is the Meningitis B vaccine administered?

      Your Answer:

      Correct Answer: 2, 4, and 12 months

      Explanation:

      The most prevalent cause of meningococcal disease in children in the UK is currently Meningitis B. In 2015, the Meningitis B vaccination was added to the NHS routine childhood immunisation schedule. It is administered at 2, 4, and 12 months of age, in conjunction with other immunisations in the schedule. If given at a different time, doses must be spaced at least 2 months apart. For children over one year old, only two doses are necessary.

      Meningitis B Vaccine Now Part of Routine NHS Immunisation

      Children in the UK have been vaccinated against meningococcus serotypes A and C for many years, leaving meningococcal B as the most common cause of bacterial meningitis in the country. However, a new vaccine called Bexsero has been developed to combat this strain. Initially, the Joint Committee on Vaccination and Immunisation (JCVI) rejected the use of Bexsero due to a cost-benefit analysis. However, the decision was eventually reversed, and the vaccine has been added to the routine NHS immunisation schedule.

      The vaccine is administered in three doses at 2 months, 4 months, and 12-13 months. Additionally, Bexsero will be available on the NHS for individuals at high risk of meningococcal disease, such as those with asplenia, splenic dysfunction, or complement disorder. This new vaccine is a significant step in protecting children and vulnerable individuals from meningitis B.

    • This question is part of the following fields:

      • Paediatrics
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  • Question 36 - A 25-year-old man is brought to the emergency department by his colleagues 30...

    Incorrect

    • A 25-year-old man is brought to the emergency department by his colleagues 30 minutes after being hit in the head with a falling object at a construction site. He did not lose consciousness, has had no problems with memory before or after the injury, and has not had any seizures. Since the injury, he has vomited 3 times but does not currently feel nauseous. The patient has no past medical history. He is responsive to commands, is aware of his surroundings, and his eye movements are normal. There is no visible bruising or fluid discharge from the ear or nose. No delays in investigations are expected. What is the most suitable course of action to take next?

      Your Answer:

      Correct Answer: Arrange CT head within 1 hour

      Explanation:

      If a patient experiences more than one episode of vomiting following a head injury, it is necessary to arrange a CT head within one hour. This is because persistent vomiting can indicate the development of neurological complications, such as intracranial bleeds, which can initially present as vomiting. Although the patient in this scenario has a Glasgow coma score of 15 and no other neurological symptoms, the presence of multiple episodes of vomiting warrants urgent imaging. Admitting the patient and arranging neurological observations would not be appropriate unless there was equipment failure preventing the CT scan. Similarly, arranging a CT head within four or eight hours is not appropriate, as the recommended timeframe for imaging in cases of head injury is within one hour for patients with persistent vomiting.

      NICE Guidelines for Investigating Head Injuries in Adults

      Head injuries can be serious and require prompt medical attention. The National Institute for Health and Care Excellence (NICE) has provided clear guidelines for healthcare professionals to determine which adult patients need further investigation with a CT head scan. Patients who require immediate CT head scans include those with a Glasgow Coma Scale (GCS) score of less than 13 on initial assessment, suspected open or depressed skull fractures, signs of basal skull fractures, post-traumatic seizures, focal neurological deficits, and more than one episode of vomiting.

      For patients with any loss of consciousness or amnesia since the injury, a CT head scan within 8 hours is recommended for those who are 65 years or older, have a history of bleeding or clotting disorders, experienced a dangerous mechanism of injury, or have more than 30 minutes of retrograde amnesia of events immediately before the head injury. Additionally, patients on warfarin who have sustained a head injury with no other indications for a CT head scan should also receive a scan within 8 hours of the injury.

      It is important for healthcare professionals to follow these guidelines to ensure that patients receive appropriate and timely care for their head injuries. By identifying those who require further investigation, healthcare professionals can provide the necessary treatment and support to prevent further complications and improve patient outcomes.

    • This question is part of the following fields:

      • Neurology
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  • Question 37 - A 25-year-old woman presents to the Genitourinary Medicine Clinic with a 1-week history...

    Incorrect

    • A 25-year-old woman presents to the Genitourinary Medicine Clinic with a 1-week history of lower abdominal pain and deep dyspareunia. She has also noticed a creamy foul-smelling vaginal discharge. There is no past medical history of note and she takes no regular medications.
      On examination, her temperature is 38.1 °C. The remainder of her observations are within normal limits. There is palpable lower abdominal tenderness and guarding in the left iliac fossa. Bimanual examination elicits bilateral adnexal tenderness. There is no inguinal lymphadenopathy.
      Given the likely diagnosis, what is the most appropriate investigation to confirm the causative organism?

      Select ONE option only

      Your Answer:

      Correct Answer: Nucleic acid amplification testing (NAAT)

      Explanation:

      Investigations for Pelvic Inflammatory Disease

      Pelvic inflammatory disease (PID) is a condition that can cause deep dyspareunia and lower abdominal and adnexal tenderness. The most common cause of PID is Chlamydia trachomatis, which can be diagnosed through nucleic acid amplification testing (NAAT). This involves taking a urine sample and a swab from the vagina or cervix to test for the organism. While a blood culture may be considered for a febrile patient, it is not routinely used for diagnosing C. trachomatis. Vaginal microscopy and culture used to be the preferred method for diagnosis, but NAAT is now recommended. Testing vaginal pH is commonly used for vaginal infections, but is not useful for PID. Urine microscopy and culture is used for UTIs, but the presence of vaginal discharge and deep dyspareunia suggests PID instead.

    • This question is part of the following fields:

      • Infectious Diseases
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  • Question 38 - A 5-year-old boy presents to the Paediatric Emergency Department with a fever and...

    Incorrect

    • A 5-year-old boy presents to the Paediatric Emergency Department with a fever and a rash. He has been feeling sick for 5 days with persistent high temperatures. During the examination, he displays cracked lips, a bright red tongue, a widespread erythematous maculopapular rash, and peeling of the skin on his hands and feet. Additionally, he has bilateral conjunctivitis. What is the necessary investigation to screen for a potential complication, given the most probable diagnosis?

      Your Answer:

      Correct Answer: Echocardiogram

      Explanation:

      Kawasaki disease can lead to coronary artery aneurysms, which can be detected through an echocardiogram. To diagnose Kawasaki disease, the patient must have a fever for more than 5 days and at least 4 of the following symptoms: bilateral conjunctivitis, cervical lymphadenopathy, polymorphic rash, cracked lips/strawberry tongue, and oedema/desquamation of the hands/feet. This patient has a rash, conjunctivitis, mucosal involvement, and desquamation of the hands and feet, indicating Kawasaki disease. While cardiac magnetic resonance angiography is a non-invasive alternative to coronary angiography, it is not first-line due to its cost and limited availability. A chest x-ray may be considered to check for cardiomegaly, but it is not necessary as echocardiography can diagnose pericarditis or myocarditis without radiation. Coronary angiography is invasive and carries risks, so it is not first-line unless large coronary artery aneurysms are seen on echocardiography. A lumbar puncture is not necessary at this stage unless the patient displays symptoms of meningitis.

      Understanding Kawasaki Disease

      Kawasaki disease is a rare type of vasculitis that primarily affects children. It is important to identify this disease early on as it can lead to serious complications, such as coronary artery aneurysms. The disease is characterized by a high-grade fever that lasts for more than five days and is resistant to antipyretics. Other symptoms include conjunctival injection, bright red, cracked lips, strawberry tongue, cervical lymphadenopathy, and red palms and soles that later peel.

      Diagnosis of Kawasaki disease is based on clinical presentation as there is no specific diagnostic test available. Management of the disease involves high-dose aspirin, which is one of the few indications for aspirin use in children. Intravenous immunoglobulin is also used as a treatment option. Echocardiogram is the initial screening test for coronary artery aneurysms, rather than angiography.

      Complications of Kawasaki disease can be serious, with coronary artery aneurysm being the most common. It is important to recognize the symptoms of Kawasaki disease early on and seek medical attention promptly to prevent potential complications.

    • This question is part of the following fields:

      • Paediatrics
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  • Question 39 - A 32-year-old man has had severe left-sided facial pain with purulent nasal discharge...

    Incorrect

    • A 32-year-old man has had severe left-sided facial pain with purulent nasal discharge for ten days. He describes how he initially felt 'okay' with milder symptoms, but noticed a sudden deterioration in his symptoms a few days ago.
      Which of the following treatments would be the treatment of choice?

      Your Answer:

      Correct Answer: Phenoxymethylpenicillin

      Explanation:

      Treatment Options for Acute Sinusitis: Antibiotics, Decongestants, and Antihistamines

      Acute bacterial sinusitis is a common condition that can cause severe symptoms such as discolored or purulent discharge, severe localized pain, and fever. Antibiotics are prescribed only if the patient has a co-morbidity or if acute bacterial sinusitis is clinically suspected. The antibiotics of choice include amoxicillin, phenoxymethylpenicillin, doxycycline, or erythromycin. Second-line treatments include co-amoxiclav and azithromycin.

      Decongestants such as ephedrine can be used to relieve nasal congestion, but they should not be used for more than seven days to avoid rebound congestion. Antihistamines such as chlorpheniramine are not recommended unless there is a coexisting allergic rhinitis.

      It is important to note that flucloxacillin and metronidazole are not the antibiotics of choice for acute sinusitis. Doxycycline or erythromycin are acceptable alternatives. Treatment should be used only for persistent symptoms or purulent nasal discharge lasting at least 7 days, or if the symptoms are severe.

    • This question is part of the following fields:

      • ENT
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  • Question 40 - A 28-year-old woman comes in for a check-up. She reports having 'IBS' and...

    Incorrect

    • A 28-year-old woman comes in for a check-up. She reports having 'IBS' and experiencing occasional episodes of abdominal pain, bloating, and loose stools for the past two years. However, her symptoms have worsened significantly over the past two weeks. She is now having 3-4 watery, grey, 'frothy' stools per day, along with increased abdominal bloating, cramps, and flatulence. She also feels that she has lost weight based on the fit of her clothes. The following blood tests are ordered:
      Hb 10.9 g/dl
      Platelets 199 * 109/l
      WBC 7.2 * 109/l
      Ferritin 15 ng/ml
      Vitamin B12 225 ng/l
      Folate 2.1 nmol/l
      What is the most likely diagnosis?

      Your Answer:

      Correct Answer: Coeliac disease

      Explanation:

      The key indicators in this case are the presence of anaemia and low levels of ferritin and folate, which are all typical of coeliac disease. The description of the diarrhoea also matches the usual symptoms, although some patients may have stools that are visibly fatty.

      While irritable bowel syndrome is a common condition, it is unlikely to be the cause in this case due to the abnormal blood test results. Low levels of ferritin and folate would not typically be associated with IBS or gastroenteritis. Even if the patient had menorrhagia, this would not explain the low folate levels, although it could account for the anaemia and low ferritin.

      Coeliac disease is much more common than Crohn’s disease, with a prevalence that is around 100 times higher. In an exam scenario, there would typically be more clues pointing towards a diagnosis of Crohn’s disease, such as the presence of mouth ulcers.

      Understanding Coeliac Disease

      Coeliac disease is an autoimmune disorder that affects approximately 1% of the UK population. It is caused by sensitivity to gluten, a protein found in wheat, barley, and rye. Repeated exposure to gluten leads to villous atrophy, which causes malabsorption. Coeliac disease is associated with various conditions, including dermatitis herpetiformis and autoimmune disorders such as type 1 diabetes mellitus and autoimmune hepatitis. It is strongly linked to HLA-DQ2 and HLA-DQ8.

      To diagnose coeliac disease, NICE recommends screening patients who exhibit signs and symptoms such as chronic or intermittent diarrhea, unexplained gastrointestinal symptoms, sudden weight loss, and autoimmune thyroid disease. Other conditions associated with coeliac disease include irritable bowel syndrome, dermatitis herpetiformis, and type 1 diabetes. First-degree relatives of patients with coeliac disease should also be screened.

      Complications of coeliac disease include anemia, hyposplenism, osteoporosis, lactose intolerance, and enteropathy-associated T-cell lymphoma of the small intestine. In rare cases, coeliac disease may lead to esophageal cancer or other malignancies.

      Overall, understanding coeliac disease is crucial for early diagnosis and management of the condition. Screening for coeliac disease in patients with relevant symptoms and conditions can help prevent complications and improve quality of life.

    • This question is part of the following fields:

      • Gastroenterology/Nutrition
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  • Question 41 - A 63-year-old woman who is undergoing treatment for bladder cancer presents to the...

    Incorrect

    • A 63-year-old woman who is undergoing treatment for bladder cancer presents to the Emergency Department because she has noticed that the urine in her catheter is blood-stained.
      On examination, the urine is pink in colour. Her observations are normal.
      What would be the next most appropriate step in this patient’s management?
      Select the SINGLE most likely option.

      Your Answer:

      Correct Answer: Arrange a full blood count

      Explanation:

      Management of a Patient with Suspected Bladder Tumour and Bleeding

      When managing a patient with suspected bladder tumour and bleeding, it is important to consider the appropriate steps to take. Here are some options and their potential outcomes:

      1. Arrange a full blood count: This test can help assess the degree of blood loss and guide the urgency of treatment.

      2. Transfuse two units of O-negative blood: While patients with bladder tumours can bleed extensively, it is important to first assess the need for transfusion through a full blood count.

      3. Flush the urinary catheter using normal saline: This step is appropriate for a blocked catheter, but not for a patient with active bleeding.

      4. Remove the urinary catheter: This step can cause blood clots and urinary retention, and is not indicated for this patient.

      5. Transfer to theatre for resection of tumour: While this may be necessary in cases of catastrophic bleeding, it is important to first assess the patient’s stability and obtain blood tests before planning definitive management.

      In summary, careful consideration of the appropriate steps is crucial in managing a patient with suspected bladder tumour and bleeding.

    • This question is part of the following fields:

      • Renal Medicine/Urology
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  • Question 42 - A 42-year-old female presents to her primary care physician with a 2-month history...

    Incorrect

    • A 42-year-old female presents to her primary care physician with a 2-month history of progressive fatigue. She has a medical history of type-1 diabetes mellitus. Her doctor orders a full blood count, which reveals a low Hb and high mean cell volume. The platelet and WBC counts are within normal limits. Which antibody test should be performed to assist in the diagnosis?

      Your Answer:

      Correct Answer: Intrinsic-factor antibodies

      Explanation:

      When investigating vitamin B12 deficiency, intrinsic factor antibodies are more useful than gastric parietal cell antibodies due to the low specificity of the latter. Megaloblastic anaemia, characterized by low haemoglobin and raised mean cell volume, can be caused by B12 or folate deficiency and may indicate pernicious anaemia, an autoimmune condition that impairs B12 uptake. Intrinsic factor antibodies are more specific for pernicious anaemia and are commonly used to confirm the diagnosis along with a blood test. Anti-histone antibodies are involved in drug-induced lupus caused by certain drugs. Anti-TTG antibodies are used to screen for coeliac disease, which can cause microcytic anaemia due to iron deficiency from malabsorption. While gastric parietal cell antibodies are linked to pernicious anaemia, their low specificity makes them less reliable for diagnosis compared to intrinsic factor antibodies.

      Understanding Pernicious Anaemia

      Pernicious anaemia is a condition that results in vitamin B12 deficiency due to an autoimmune disorder affecting the gastric mucosa. The term pernicious means causing harm in a gradual or subtle way, and this is reflected in the often subtle symptoms and delayed diagnosis of the condition. While pernicious anaemia is the most common cause of vitamin B12 deficiency, other causes include atrophic gastritis, gastrectomy, and malnutrition.

      The pathophysiology of pernicious anaemia involves antibodies to intrinsic factor and/or gastric parietal cells. These antibodies can bind to intrinsic factor, blocking the vitamin B12 binding site, or reduce acid production and cause atrophic gastritis. This leads to reduced intrinsic factor production and reduced vitamin B12 absorption, which can result in megaloblastic anaemia and neuropathy.

      Risk factors for pernicious anaemia include being female, middle to old age, and having other autoimmune disorders such as thyroid disease, type 1 diabetes mellitus, Addison’s, rheumatoid arthritis, and vitiligo. It is also more common in individuals with blood group A.

      Symptoms of pernicious anaemia include anaemia features such as lethargy, pallor, and dyspnoea, as well as neurological features such as peripheral neuropathy and subacute combined degeneration of the spinal cord. Neuropsychiatric features such as memory loss, poor concentration, confusion, depression, and irritability may also be present, along with mild jaundice and glossitis.

      Diagnosis of pernicious anaemia involves a full blood count, vitamin B12 and folate levels, and testing for antibodies such as anti intrinsic factor antibodies and anti gastric parietal cell antibodies. Treatment involves vitamin B12 replacement, usually given intramuscularly, and folic acid supplementation may also be required. Complications of pernicious anaemia include an increased risk of gastric cancer.

    • This question is part of the following fields:

      • Haematology/Oncology
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  • Question 43 - A 55-year-old woman has been asked to come back for a follow-up cervical...

    Incorrect

    • A 55-year-old woman has been asked to come back for a follow-up cervical smear by her GP. She had a cervical smear done 18 months ago which revealed the presence of high-risk HPV but no abnormal cytology. The follow-up cervical smear has returned negative for high-risk HPV. What is the best course of action for managing this patient?

      Your Answer:

      Correct Answer: Repeat cervical smear in 5 years

      Explanation:

      If the 1st repeat smear at 12 months for cervical cancer screening is now negative for hrHPV, the patient should return to routine recall, which is repeating the cervical smear in 5 years. Cytological examination of the smear is not necessary as the NHS now follows an HPV first system. Referral for colposcopy is also not indicated unless there is evidence of dyskaryosis or inadequate smears. Repeating the cervical smear in 3 years is not appropriate for a 50-year-old patient, and repeating the smear after 12 months is only necessary if the most recent smear is positive for hrHPV with no cytological abnormalities.

      The cervical cancer screening program has evolved to include HPV testing, which allows for further risk stratification. A negative hrHPV result means a return to normal recall, while a positive result requires cytological examination. Abnormal cytology results lead to colposcopy, while normal cytology results require a repeat test at 12 months. Inadequate samples require a repeat within 3 months, and two consecutive inadequate samples lead to colposcopy. Treatment for CIN typically involves LLETZ or cryotherapy. Individuals who have been treated for CIN should be invited for a test of cure repeat cervical sample 6 months after treatment.

    • This question is part of the following fields:

      • Reproductive Medicine
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  • Question 44 - A 12-year-old boy has been under the care of the Paediatrics Team since...

    Incorrect

    • A 12-year-old boy has been under the care of the Paediatrics Team since birth and is attending the Paediatric Clinic for a follow-up appointment. His mother reports that he is struggling at school due to his learning and behavioural difficulties. He has a large jaw, hyper-extensible joints and macroorchidism.
      Which of the following is the most likely syndrome?

      Your Answer:

      Correct Answer: Fragile X syndrome

      Explanation:

      Genetic Conditions and Their Phenotypic Features

      Fragile X Syndrome, Down Syndrome, Edwards Syndrome, Noonan Syndrome, and Pierre-Robin Syndrome are genetic conditions that have distinct phenotypic features. Fragile X Syndrome is an X-linked form of learning disability and autism that mainly presents after puberty. Down Syndrome is characterized by brachycephaly, prominent epicanthal folds, and small nose and mouth with protruding tongue, among others, and is usually diagnosed at birth. Edwards Syndrome has a life expectancy of days to weeks and is characterized by neonatal hypotonia, apnea, and seizures. Noonan Syndrome is inherited in an autosomal-dominant pattern and is characterized by distinctive facial features, congenital heart defects, and skeletal malformations. Pierre-Robin Syndrome results in facial abnormalities, respiratory and feeding difficulties, and cleft palate. Understanding the phenotypic features of these genetic conditions is crucial for early diagnosis and management.

    • This question is part of the following fields:

      • Paediatrics
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  • Question 45 - A 54-year-old man presents to his General Practitioner with a three-day history of...

    Incorrect

    • A 54-year-old man presents to his General Practitioner with a three-day history of blurring of vision. He has a past medical history of hypertension, managed with amlodipine, ramipril, and indapamide, and type II diabetes mellitus, which is well controlled with metformin.
      On examination, his visual acuity is 6/18 in both eyes with a reduction in colour vision. There is no relative afferent pupillary defect. On direct fundoscopy, the optic disc's margins are ill-defined and seem to be raised in both eyes. There are also some cotton-wool spots scattered around the retina in both eyes.
      What is the most likely diagnosis?

      Your Answer:

      Correct Answer: Hypertensive retinopathy

      Explanation:

      Differentiating Hypertensive Retinopathy from Other Eye Conditions

      Hypertensive retinopathy is a serious condition that can lead to vision loss if left untreated. A grade 4 hypertensive retinopathy, as classified by the Keith-Wagener-Barker system, is characterized by bilateral optic disc swelling and cotton-wool spots. This condition can cause a reduction in visual acuity and color vision due to optic neuropathy secondary to hypertension.

      It is important to differentiate hypertensive retinopathy from other eye conditions that may present with similar symptoms. Proliferative diabetic retinopathy, for example, is unlikely if the patient’s type II diabetes is well-controlled. The presence of cotton-wool spots does not indicate diabetic retinopathy.

      An intracranial space-occupying lesion is also not indicated in the patient’s history. Optic neuritis, while it can present with loss of optic nerve function, is more likely to present unilaterally and without cotton-wool spots.

      Pre-proliferative diabetic retinopathy is also unlikely in this case, as the patient’s diabetes is well-controlled. In diabetic retinopathy, optic discs will not be raised.

      In summary, a thorough understanding of the patient’s medical history and symptoms is necessary to accurately diagnose hypertensive retinopathy and differentiate it from other eye conditions.

    • This question is part of the following fields:

      • Ophthalmology
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  • Question 46 - A 5-year-old child is brought to the Paediatric department by his grandmother. He...

    Incorrect

    • A 5-year-old child is brought to the Paediatric department by his grandmother. He has developed a very high fever and is breathing with a high-pitched sound. His grandmother is very worried as she has tried to get him to drink some water and take paracetamol this morning, but he is drooling and refuses to take anything orally. The child is Spanish speaking, however, his grandmother translates that he feels too hot and his chest hurts.

      What is the most suitable initial step in managing this child's condition?

      Your Answer:

      Correct Answer: Call anaesthetics

      Explanation:

      Acute epiglottitis is characterized by the sudden onset of fever, drooling, and stridor in a child. It is important to immediately call anaesthetics as there is a high risk of airway obstruction if the child becomes upset. The Hib vaccination is widely available and subsidized in many countries, including Poland where it has been available since the 1990s.

      Humidified oxygen is commonly used to manage bronchiolitis, but it should be avoided in patients with suspected epiglottitis as it may cause distress and worsen the airway obstruction. IV hydrocortisone is not a first-line treatment for epiglottitis and cannulating a patient before securing their airway or having anaesthetics present is not recommended.

      Nebulized salbutamol is useful for treating viral wheezing or asthma exacerbations, which present with an expiratory wheeze and fever, but not drooling. However, it should not be administered to a child with suspected epiglottitis until their airway is secured by anaesthetics to prevent further complications.

      Acute epiglottitis is a rare but serious infection caused by Haemophilus influenzae type B. It is important to recognize and treat it promptly as it can lead to airway obstruction. Although it was once considered a disease of childhood, it is now more common in adults in the UK due to the immunization program. The incidence of epiglottitis has decreased since the introduction of the Hib vaccine. Symptoms include a rapid onset, high temperature, stridor, drooling of saliva, and a tripod position where the patient leans forward and extends their neck to breathe easier. Diagnosis is made by direct visualization, but x-rays may be done to rule out a foreign body.

      Immediate senior involvement is necessary, including those who can provide emergency airway support such as anaesthetics or ENT. Endotracheal intubation may be necessary to protect the airway. It is important not to examine the throat if epiglottitis is suspected due to the risk of acute airway obstruction. The diagnosis is made by direct visualization, but only senior staff who are able to intubate if necessary should perform this. Treatment includes oxygen and intravenous antibiotics.

    • This question is part of the following fields:

      • Paediatrics
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  • Question 47 - A 14-year-old girl arrives at the clinic with her mother. She is asking...

    Incorrect

    • A 14-year-old girl arrives at the clinic with her mother. She is asking for the combined oral contraceptive (COC) pill as she has recently started a relationship with a 19-year-old man whom she met at a local coffee shop, but they have not yet engaged in sexual activity. During the consultation, you discuss the age difference, but the mother assures you that she has met the boyfriend and believes he treats her daughter well. Both the girl and her mother insist that they do not want anyone else involved. What is the most appropriate course of action?

      Your Answer:

      Correct Answer: Immediately phone local child protection lead and refer to social services

      Explanation:

      According to the GMC guidelines, sexual intercourse with children below the age of 13 cannot be considered consensual, and therefore, any sexual activity would be classified as rape. In such cases, breaking confidentiality is mandatory.

      Guidelines for Obtaining Consent in Children

      The General Medical Council has provided guidelines for obtaining consent in children. According to these guidelines, young people who are 16 years or older can be treated as adults and are presumed to have the capacity to make decisions. However, for children under the age of 16, their ability to understand what is involved determines whether they have the capacity to decide. If a competent child refuses treatment, a person with parental responsibility or the court may authorize investigation or treatment that is in the child’s best interests.

      When it comes to providing contraceptives to patients under 16 years of age, the Fraser Guidelines must be followed. These guidelines state that the young person must understand the professional’s advice, cannot be persuaded to inform their parents, is likely to begin or continue having sexual intercourse with or without contraceptive treatment, and will suffer physical or mental health consequences without contraceptive treatment. Additionally, the young person’s best interests require them to receive contraceptive advice or treatment with or without parental consent.

      Some doctors use the term Fraser competency when referring to contraception and Gillick competency when referring to general issues of consent in children. However, rumors that Victoria Gillick removed her permission to use her name or applied copyright have been debunked. It is important to note that in Scotland, those with parental responsibility cannot authorize procedures that a competent child has refused.

    • This question is part of the following fields:

      • Paediatrics
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  • Question 48 - A 32-year-old woman at 28 weeks gestation reports decreased fetal movements. Upon ultrasound,...

    Incorrect

    • A 32-year-old woman at 28 weeks gestation reports decreased fetal movements. Upon ultrasound, it is discovered that the fetus is hydropic. Her 5-year-old child had a fever and redness on the cheeks recently. What is the probable infectious agent responsible for this?

      Your Answer:

      Correct Answer: Parvovirus B19

      Explanation:

      The symptoms exhibited by the child indicate erythema infectiosum, which is caused by an infection with parvovirus B19. Most pregnant women have immunity to this virus and it typically does not pose a risk. However, in rare cases, infection during the first trimester has been associated with hydrops fetalis, which can lead to miscarriage.

      Parvovirus B19: A Virus with Various Clinical Presentations

      Parvovirus B19 is a DNA virus that can cause different clinical presentations. One of the most common is erythema infectiosum, also known as fifth disease or slapped-cheek syndrome. This illness may manifest as a mild feverish condition or a noticeable rash that appears after a few days. The rash is characterized by rose-red cheeks, which is why it is called slapped-cheek syndrome. It may spread to the rest of the body but rarely involves the palms and soles. The rash usually peaks after a week and then fades, but for some months afterwards, a warm bath, sunlight, heat, or fever may trigger a recurrence of the bright red cheeks and rash. Most children recover without specific treatment, and school exclusion is unnecessary as the child is not infectious once the rash emerges. However, in adults, the virus may cause acute arthritis.

      Aside from erythema infectiosum, parvovirus B19 can also present as asymptomatic, pancytopenia in immunosuppressed patients, aplastic crises in sickle-cell disease, and hydrops fetalis. The virus suppresses erythropoiesis for about a week, so aplastic anemia is rare unless there is a chronic hemolytic anemia. In pregnant women, the virus can cross the placenta and cause severe anemia due to viral suppression of fetal erythropoiesis, which can lead to heart failure secondary to severe anemia and the accumulation of fluid in fetal serous cavities (e.g. ascites, pleural and pericardial effusions). This condition is treated with intrauterine blood transfusions.

      It is important to note that the virus can affect an unborn baby in the first 20 weeks of pregnancy. If a woman is exposed early in pregnancy (before 20 weeks), she should seek prompt advice from her antenatal care provider as maternal IgM and IgG will need to be checked. The virus is spread by the respiratory route, and a person is infectious 3 to 5 days before the appearance of the rash. Children are no longer infectious once the rash appears, and there is no specific treatment. Therefore, the child need not be excluded from school as they are no longer infectious by the time the rash occurs.

    • This question is part of the following fields:

      • Paediatrics
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  • Question 49 - A 35-year-old man presents with symptoms of depression, difficulty sleeping, and a strong...

    Incorrect

    • A 35-year-old man presents with symptoms of depression, difficulty sleeping, and a strong desire for sugary foods during the winter months. He reports that his symptoms are more severe in the winter than in the summer. He has no history of other mental health issues or physical problems. What is the most probable diagnosis?

      Your Answer:

      Correct Answer: Seasonal affective disorder (SAD)

      Explanation:

      Differentiating Seasonal Affective Disorder from Other Depressive Disorders

      Seasonal affective disorder (SAD) is a type of depression that occurs in a regular temporal pattern, typically beginning in autumn or winter and ending in spring or summer. Unlike classic major depression, SAD is characterized by symptoms of hyperphagia, hypersomnia, and weight gain. The cause of SAD is believed to be a malfunction of the light-sensitive hormone melatonin during winter. Treatment involves phototherapy, which exposes individuals to bright light for several hours a day.

      Reactive depression, on the other hand, is a subtype of major depression that occurs as a result of an external event, such as a relationship breakdown or bereavement. There is no indication of a stressful life event in the presented vignette.

      Bipolar affective disorder is characterized by distinct episodes of depression and mania, which is not evident in the vignette. Dysthymia is a persistent depression of mood that does not fully meet the criteria for a diagnosis of major depression and does not have a definite seasonal variation like SAD.

      Finally, double depression occurs when one or more episodes of major depression occur on a background of dysthymia. It is important to differentiate SAD from other depressive disorders to provide appropriate treatment and management.

    • This question is part of the following fields:

      • Psychiatry
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  • Question 50 - A 47-year-old man presents with complaints of fever, back pain, and painful urination....

    Incorrect

    • A 47-year-old man presents with complaints of fever, back pain, and painful urination. Upon examination, suprapubic tenderness and tender prostate are noted. The diagnosis of acute prostatitis is suspected. What is the most suitable treatment for this patient?

      Your Answer:

      Correct Answer: Ciprofloxacin

      Explanation:

      Immediate antibiotic therapy should be initiated for men suspected of having prostatitis. While urine cultures and sexual health screening are important, treatment should not be delayed. According to NICE, quinolone antibiotics such as ciprofloxacin 500 mg twice daily or ofloxacin 200 mg twice daily should be administered for 28 days to treat acute prostatitis. If these antibiotics are not suitable, trimethoprim 200 mg twice daily for 28 days is recommended. Pain management through analgesia should also be provided, and patients should be reevaluated within 24 to 48 hours.

      Antibiotic Guidelines for Common Infections

      Respiratory infections, urinary tract infections, skin infections, ear, nose, and throat infections, genital infections, and gastrointestinal infections are some of the most common infections that require antibiotic treatment. The British National Formulary (BNF) provides guidelines for the appropriate use of antibiotics for these infections.

      For respiratory infections such as chronic bronchitis, community-acquired pneumonia, and hospital-acquired pneumonia, antibiotics such as amoxicillin, tetracycline, clarithromycin, co-amoxiclav, cefuroxime, piperacillin with tazobactam, ceftazidime, or ciprofloxacin are recommended depending on the severity and type of infection.

      For urinary tract infections, lower urinary tract infections can be treated with trimethoprim or nitrofurantoin, while acute pyelonephritis requires broad-spectrum cephalosporin or quinolone. Acute prostatitis can be treated with quinolone or trimethoprim.

      Skin infections such as impetigo, cellulitis, erysipelas, and animal or human bites require antibiotics such as topical hydrogen peroxide, oral flucloxacillin, erythromycin, doxycycline, clarithromycin, or metronidazole depending on the severity and type of infection.

      Ear, nose, and throat infections such as throat infections, sinusitis, otitis media, otitis externa, periapical or periodontal abscess, and acute necrotising ulcerative gingivitis require antibiotics such as phenoxymethylpenicillin, amoxicillin, erythromycin, or flucloxacillin depending on the severity and type of infection.

      Genital infections such as gonorrhoea, chlamydia, pelvic inflammatory disease, syphilis, and bacterial vaginosis require antibiotics such as intramuscular ceftriaxone, doxycycline, azithromycin, ofloxacin, metronidazole, or benzathine benzylpenicillin depending on the severity and type of infection.

      Gastrointestinal infections such as Clostridioides difficile, Campylobacter enteritis, Salmonella (non-typhoid), and Shigellosis require antibiotics such as oral vancomycin, oral fidaxomicin, clarithrom

    • This question is part of the following fields:

      • Renal Medicine/Urology
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  • Question 51 - A 23 year old woman has been admitted to the obstetrics ward for...

    Incorrect

    • A 23 year old woman has been admitted to the obstetrics ward for 2 days due to preterm premature rupture of membranes (PPROM). She is now experiencing abdominal pain, uterine contractions, and symptoms similar to the flu. Prior to this admission, she had no complications and is currently 24 weeks pregnant. During examination, she appears ill with a fever of 39 degrees. A gynecological exam reveals a malodorous discharge originating from the cervix, which is collected and sent for analysis. What is the most probable diagnosis at this stage?

      Your Answer:

      Correct Answer: Chorioamnionitis

      Explanation:

      Understanding Chorioamnionitis

      Chorioamnionitis is a serious medical condition that can affect both the mother and the foetus during pregnancy. It is caused by a bacterial infection that affects the amniotic fluid, membranes, and placenta. This condition is considered a medical emergency and can be life-threatening if not treated promptly. It is more likely to occur when the membranes rupture prematurely, but it can also happen when the membranes are still intact.

      Prompt delivery of the foetus is crucial in treating chorioamnionitis, and a cesarean section may be necessary. Intravenous antibiotics are also administered to help fight the infection. This condition affects up to 5% of all pregnancies, and it is important for pregnant women to be aware of the symptoms and seek medical attention immediately if they suspect they may have chorioamnionitis.

    • This question is part of the following fields:

      • Reproductive Medicine
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  • Question 52 - A 50-year-old woman is discovered in cardiac arrest and her blood test shows:
    Sodium...

    Incorrect

    • A 50-year-old woman is discovered in cardiac arrest and her blood test shows:
      Sodium 130 mmol/l (135-145)
      Potassium 7.3mmol/l (3.5-5.0)
      Urea 9.1mmol/l (2.5-7.0)
      Creatinine 167 mmol/l (60-110)
      To begin with, she is administered IV calcium gluconate.
      What effect does this medication have on the electrolyte levels?

      Your Answer:

      Correct Answer: No change

      Explanation:

      To stabilize the cardiac membrane in cases of hyperkalemia with ECG changes, IV calcium gluconate is administered. This is done to prevent further increase in potassium levels. The removal of potassium from the extracellular space to the intracellular space is achieved through a combination of insulin and dextrose or nebulized salbutamol. Calcium resonium is then used to excrete potassium from the body.

      Managing Hyperkalaemia

      Hyperkalaemia, if left untreated, can lead to life-threatening arrhythmias. It is important to address any precipitating factors, such as acute kidney injury, and stop any aggravating drugs, such as ACE inhibitors. The management of hyperkalaemia can be categorised by the aims of treatment, which include stabilising the cardiac membrane, shifting potassium from extracellular to intracellular fluid compartments, and removing potassium from the body.

      The severity of hyperkalaemia can be classified as mild, moderate, or severe, with the latter being defined as a serum potassium level of 6.5 mmol/L or higher. It is important to note that the presence of ECG changes is crucial in determining the appropriate management. ECG changes associated with hyperkalaemia include peaked or ‘tall-tented’ T waves, loss of P waves, broad QRS complexes, and a sinusoidal wave pattern.

      The principles of treatment modalities for hyperkalaemia involve stabilising the cardiac membrane with IV calcium gluconate, shifting potassium from extracellular to intracellular fluid compartments with a combined insulin/dextrose infusion or nebulised salbutamol, and removing potassium from the body with calcium resonium, loop diuretics, or dialysis. In practical treatment, all patients with severe hyperkalaemia or ECG changes should receive emergency treatment with IV calcium gluconate, insulin/dextrose infusion, and other temporary measures to lower serum potassium levels. Further management involves stopping exacerbating drugs, treating any underlying cause, and lowering total body potassium with calcium resonium, loop diuretics, or dialysis.

    • This question is part of the following fields:

      • Renal Medicine/Urology
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  • Question 53 - You encounter a 50-year-old female patient during a clinic visit who had a...

    Incorrect

    • You encounter a 50-year-old female patient during a clinic visit who had a cholecystectomy six months ago. She reports experiencing persistent diarrhea since the surgery, which appears to float in the toilet. What medication would you suggest to alleviate these symptoms?

      Your Answer:

      Correct Answer: Cholestyramine

      Explanation:

      Cholestyramine is an effective treatment for bile-acid malabsorption. It functions by binding to bile acids in the small intestine and facilitating their reabsorption into the bile acid production cycle. This approach addresses the root cause of diarrhea in patients with this condition. In the case of the patient described, the removal of her gallbladder likely disrupted the normal cycle of bile release and reabsorption, leading to excessive bile in the large intestine and resulting in increased water and salt loss in the stool and faster transit time of stool through the intestines. While bismuth may be useful in preventing symptoms during infectious diarrhea, it is not a long-term solution. Creon is typically used to replace pancreatic enzymes in conditions such as cystic fibrosis, where there is a reduction in pancreatic enzymes reaching the intestine. Loperamide may be effective in preventing diarrhea in the short term, but it does not address the underlying cause of the patient’s condition.

      Understanding Bile-Acid Malabsorption

      Bile-acid malabsorption is a condition that can cause chronic diarrhea. It can be primary, which means that it is caused by excessive production of bile acid, or secondary, which is due to an underlying gastrointestinal disorder that reduces bile acid absorption. This condition can lead to steatorrhea and malabsorption of vitamins A, D, E, and K. Secondary causes are often seen in patients with ileal disease, such as Crohn’s disease, as well as those who have undergone cholecystectomy, have coeliac disease, or have small intestinal bacterial overgrowth.

      To diagnose bile-acid malabsorption, the test of choice is SeHCAT, a nuclear medicine test that uses a gamma-emitting selenium molecule in selenium homocholic acid taurine or tauroselcholic acid. Scans are done 7 days apart to assess the retention or loss of radiolabeled 75SeHCAT.

      The management of bile-acid malabsorption involves the use of bile acid sequestrants, such as cholestyramine. These medications work by binding to bile acids in the intestine, preventing their reabsorption and promoting their excretion. With proper management, the symptoms of bile-acid malabsorption can be controlled, and patients can lead a normal life.

    • This question is part of the following fields:

      • Gastroenterology/Nutrition
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  • Question 54 - A 7-year-old girl is seen in clinic for nocturnal enuresis. Despite her mother's...

    Incorrect

    • A 7-year-old girl is seen in clinic for nocturnal enuresis. Despite her mother's attempts at using a reward system, there has been no improvement. What is the best initial approach to management?

      Your Answer:

      Correct Answer: Enuresis alarm

      Explanation:

      If general advice has not been effective, an enuresis alarm is typically the initial treatment for nocturnal enuresis. It is not advisable to limit fluid intake. According to Clinical Knowledge Summaries, children should consume approximately eight drinks per day, evenly distributed throughout the day, with the last one consumed approximately one hour before bedtime.

      Nocturnal enuresis, or bedwetting, is when a child involuntarily urinates during the night. Most children achieve continence by the age of 3 or 4, so enuresis is defined as the involuntary discharge of urine in a child aged 5 or older without any underlying medical conditions. Enuresis can be primary, meaning the child has never achieved continence, or secondary, meaning the child has been dry for at least 6 months before.

      When managing bedwetting, it’s important to look for any underlying causes or triggers, such as constipation, diabetes mellitus, or recent onset UTIs. General advice includes monitoring fluid intake and encouraging regular toileting patterns, such as emptying the bladder before sleep. Reward systems, like star charts, can also be helpful, but should be given for agreed behavior rather than dry nights.

      The first-line treatment for bedwetting is an enuresis alarm, which has a high success rate. These alarms have sensor pads that detect wetness and wake the child up to use the toilet. If short-term control is needed, such as for sleepovers, or if the alarm is ineffective or not acceptable to the family, desmopressin may be prescribed. Overall, managing bedwetting involves identifying any underlying causes and implementing strategies to promote continence.

    • This question is part of the following fields:

      • Paediatrics
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  • Question 55 - A 19-year-old woman goes to a family planning clinic to talk about contraception...

    Incorrect

    • A 19-year-old woman goes to a family planning clinic to talk about contraception options. She has been experiencing migraine with aura for the past year and a half. According to the UK Medical Eligibility Criteria, which contraceptive method is considered safe to use without caution or contraindication in this situation?

      Your Answer:

      Correct Answer: Copper intrauterine device

      Explanation:

      The use of combined oral contraceptive pills is completely contraindicated in patients with migraine with aura due to an increased risk of ischaemic stroke (UKMEC class 4). However, progestogen-based contraception methods and the levonorgestrel-releasing intrauterine device are considered safe (UKMEC 2) as the benefits of using these methods outweigh the potential risks. The copper intrauterine device is the only form of contraception recommended by UKMEC as having no contraindication in this condition (UKMEC 1).

      Intrauterine contraceptive devices include copper IUDs and levonorgestrel-releasing IUS. Both are over 99% effective. The IUD prevents fertilization by decreasing sperm motility, while the IUS prevents endometrial proliferation and thickens cervical mucus. Potential problems include heavier periods with IUDs and initial bleeding with the IUS. There is a small risk of uterine perforation, ectopic pregnancy, and infection. New IUS systems, such as Jaydess® and Kyleena®, have smaller frames and less levonorgestrel, resulting in lower serum levels and different rates of amenorrhea.

    • This question is part of the following fields:

      • Reproductive Medicine
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  • Question 56 - A 45-year-old woman presents to her General Practitioner with right lower-limb pain. This...

    Incorrect

    • A 45-year-old woman presents to her General Practitioner with right lower-limb pain. This is mainly localised over a red patch that has recently developed on the inner part of her thigh.
      On examination, there is a well-demarcated area of erythematous skin on the patient’s thigh, which is warm and tender to touch. There are no other rashes or skin changes present in the rest of her body. Her temperature is 37.5°C and the rest of her parameters are within normal limits.
      Which of the following is the most likely diagnosis?

      Your Answer:

      Correct Answer: Cellulitis

      Explanation:

      Differential Diagnosis for a Lower Limb Rash: Cellulitis, Atopic Dermatitis, Contact Dermatitis, Necrobiosis Lipoidica, and Pretibial Myxedema

      The patient in question is most likely suffering from cellulitis, as evidenced by the presence of erythema, warmth, tenderness, and swelling in the affected area. Cellulitis typically presents as a unilateral rash in the lower limbs, with a well-defined margin and potential skin breakdown or ulceration in severe cases. Localized lymph node swelling may also occur, and systemic symptoms such as tachycardia, fever, confusion, or respiratory distress may be present in more severe cases. It is important to examine the skin carefully for potential points of entry for pathogens, such as wounds, local skin infections, or recent injection sites.

      Atopic dermatitis, on the other hand, typically presents as an itchy rash in a flexural distribution, with a history of atopy and episodic flares starting from a young age. Contact dermatitis, which can be either irritant or allergic, is characterized by erythema and may present with crusting or vesicles in rare cases. Necrobiosis lipoidica is a condition that typically occurs in diabetic patients, presenting as shiny, painless areas of yellow or red skin on the shins, often with telangiectasia. Pretibial myxedema, which occurs in patients with Graves’ disease, presents as a shiny, waxy, orange-peel texture on the shins.

      In summary, a lower limb rash can have various causes, and a careful examination of the skin and consideration of the patient’s medical history can help narrow down the differential diagnosis.

    • This question is part of the following fields:

      • Dermatology
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  • Question 57 - You are seeing a 5-year-old boy in your clinic who has a history...

    Incorrect

    • You are seeing a 5-year-old boy in your clinic who has a history of multiple wheezy episodes over the past 4 years and was diagnosed with asthma. He was admitted to the hospital 5 months ago with shortness-of-breath and wheeze and was diagnosed with a viral exacerbation of asthma. The paediatric team prescribed him a Clenil (beclometasone dipropionate) inhaler 50mcg bd and salbutamol 100mcg prn via a spacer before his discharge. His mother reports that he has a persistent night-time cough and is regularly using his salbutamol inhaler. On clinical examination, his chest appears normal. What would be the most appropriate next step in managing this patient?

      Your Answer:

      Correct Answer: Add a leukotriene receptor antagonist

      Explanation:

      Managing Asthma in Children: NICE Guidelines

      Asthma management in children has been updated by NICE in 2017, following the 2016 BTS guidelines. The new guidelines for children aged 5-16 are similar to those for adults, with a stepwise approach for treatment. For newly-diagnosed asthma, short-acting beta agonist (SABA) is recommended. If symptoms persist, a combination of SABA and paediatric low-dose inhaled corticosteroid (ICS) is used. Leukotriene receptor antagonist (LTRA) is added if symptoms still persist, followed by long-acting beta agonist (LABA) if necessary. Maintenance and reliever therapy (MART) is used as a combination of ICS and LABA for daily maintenance therapy and symptom relief. For children under 5 years old, clinical judgement plays a greater role in diagnosis. The stepwise approach is similar to that for older children, with an 8-week trial of paediatric moderate-dose ICS before adding LTRA. If symptoms persist, referral to a paediatric asthma specialist is recommended.

      It should be noted that NICE does not recommend changing treatment for well-controlled asthma patients simply to adhere to the latest guidelines. The definitions of low, moderate, and high-dose ICS have also changed, with different definitions for adults and children. For children, <= 200 micrograms budesonide or equivalent is considered a paediatric low dose, 200-400 micrograms is a moderate dose, and > 400 micrograms is a high dose. Overall, the new NICE guidelines provide a clear and concise approach to managing asthma in children.

    • This question is part of the following fields:

      • Paediatrics
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  • Question 58 - A 78-year-old man visits his GP complaining of a cough that has been...

    Incorrect

    • A 78-year-old man visits his GP complaining of a cough that has been producing green sputum and shortness of breath for the past three days. During the examination, the GP detects the presence of rhonchi. The patient's vital signs are stable. Given his medical history of type 2 diabetes, which is being managed with metformin, and heart failure, for which he is taking ramipril, bisoprolol, and furosemide, the GP suspects acute bronchitis. What is the most appropriate course of action?

      Your Answer:

      Correct Answer: Oral doxycycline

      Explanation:

      Antibiotics may be prescribed for acute bronchitis if the patient has co-existing co-morbidities or is at high risk of complications. NICE guidelines advise against the use of antibiotics for those who are not systemically very unwell and not at high risk of complications. However, if the patient is very unwell or at risk of complications, antibiotics should be offered. In this case, the patient’s age, diabetes, and heart failure put him at high risk, so antibiotics should be offered in accordance with NICE guidelines. While local guidelines should be consulted, NICE recommends oral doxycycline as the first-line treatment. Inhaled bronchodilators should not be offered unless the patient has an underlying airway disease such as asthma. Oral flucloxacillin is not commonly used for respiratory tract infections, and IV co-amoxiclav is not necessary in this stable patient who can be managed without admission.

      Acute bronchitis is a chest infection that typically resolves on its own within three weeks. It occurs when the trachea and major bronchi become inflamed, leading to swollen airways and the production of sputum. The primary cause of acute bronchitis is viral infection, with most cases occurring in the autumn or winter. Symptoms include a sudden onset of cough, sore throat, runny nose, and wheezing. While most patients have a normal chest examination, some may experience a low-grade fever or wheezing. It is important to differentiate acute bronchitis from pneumonia, which presents with different symptoms and chest examination findings.

      Diagnosis of acute bronchitis is typically based on clinical presentation, but CRP testing may be used to determine if antibiotic therapy is necessary. Management involves pain relief and ensuring adequate fluid intake. Antibiotics may be considered for patients who are systemically unwell, have pre-existing health conditions, or have a CRP level between 20-100mg/L. Doxycycline is the recommended first-line treatment, but it cannot be used in children or pregnant women. Alternatives include amoxicillin.

    • This question is part of the following fields:

      • Respiratory Medicine
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  • Question 59 - A 27 year old pregnant woman is currently experiencing a prolonged second stage...

    Incorrect

    • A 27 year old pregnant woman is currently experiencing a prolonged second stage of labour due to cephalopelvic disproportion. The midwife is aware of the potential risks to both the mother and foetus and calls for an obstetrician. The obstetrician performs a perineal incision in a mediolateral direction. What is the name of this procedure?

      Your Answer:

      Correct Answer: Episiotomy

      Explanation:

      The procedure being performed is called an episiotomy, which can be done using various techniques. In this case, the medio-lateral approach is being used, which involves making a cut at either the 7 o’clock or 5 o’clock positions. The main reasons for performing this procedure are twofold. Firstly, it helps to prevent the vagina from tearing during childbirth, particularly in cases where the baby’s head is too large for the mother’s pelvis. By making a controlled incision, the risk of the tear extending towards the anus and surrounding muscles is reduced, which could lead to long-term problems such as fecal incontinence. Secondly, the episiotomy creates more space for the baby to pass through, making delivery easier and safer for both the mother and child.

      Understanding Episiotomy

      Episiotomy is a surgical procedure that involves making an incision in the posterior wall of the vagina and perineum during the second stage of labor. This procedure is done to make it easier for the baby to pass through the birth canal. The incision is made in the area between the vagina and anus, and it can be either midline or mediolateral.

      Episiotomy is usually performed when the baby is in distress, and there is a need to speed up the delivery process. It can also be done to prevent tearing of the perineum, which can be more difficult to repair than an episiotomy. However, the procedure is not without risks, and it can lead to complications such as pain, infection, and bleeding.

      In recent years, there has been a decline in the use of episiotomy, as studies have shown that it does not necessarily reduce the risk of tearing or improve healing time. Many healthcare providers now only perform episiotomy when it is medically necessary. It is important for expectant mothers to discuss the use of episiotomy with their healthcare provider and understand the risks and benefits before making a decision.

    • This question is part of the following fields:

      • Reproductive Medicine
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  • Question 60 - A 28-year-old woman is experiencing dysuria, dyspareunia, and abnormal vaginal discharge during her...

    Incorrect

    • A 28-year-old woman is experiencing dysuria, dyspareunia, and abnormal vaginal discharge during her 16th week of pregnancy. She is concerned as she has had unprotected sex with multiple partners. Her medical history is unremarkable except for a penicillin allergy. Nucleic acid amplification tests (NAAT) confirm a Chlamydia infection. What is the recommended treatment?

      Your Answer:

      Correct Answer: Azithromycin

      Explanation:

      Azithromycin or erythromycin are appropriate options for treating Chlamydia in a pregnant patient who is allergic to penicillin. In this case, the patient’s NAAT testing confirmed the presence of Chlamydia, but doxycycline is contraindicated due to the patient’s pregnancy. Amoxicillin is not an option due to the patient’s penicillin allergy. Ceftriaxone is not indicated for Chlamydia, and doxycycline is contraindicated in pregnancy. Therefore, azithromycin or erythromycin are the most appropriate treatment options.

      Chlamydia is a common sexually transmitted infection caused by Chlamydia trachomatis. It is prevalent in the UK, with approximately 1 in 10 young women affected. The incubation period is around 7-21 days, but many cases are asymptomatic. Symptoms in women include cervicitis, discharge, and bleeding, while men may experience urethral discharge and dysuria. Complications can include epididymitis, pelvic inflammatory disease, and infertility.

      Traditional cell culture is no longer widely used for diagnosis, with nuclear acid amplification tests (NAATs) being the preferred method. Testing can be done using urine, vulvovaginal swab, or cervical swab. Screening is recommended for sexually active individuals aged 15-24 years, and opportunistic testing is common.

      Doxycycline is the first-line treatment for Chlamydia, with azithromycin as an alternative if doxycycline is contraindicated or not tolerated. Pregnant women may be treated with azithromycin, erythromycin, or amoxicillin. Patients diagnosed with Chlamydia should be offered partner notification services, with all contacts since the onset of symptoms or within the last six months being notified and offered treatment.

    • This question is part of the following fields:

      • Reproductive Medicine
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  • Question 61 - You are an F2 treating an elderly patient with acute epiglottitis in the...

    Incorrect

    • You are an F2 treating an elderly patient with acute epiglottitis in the emergency department.
      Which is the most appropriate initial management?

      Your Answer:

      Correct Answer: Call for an anaesthetist

      Explanation:

      Management of Acute Epiglottitis

      Acute epiglottitis is a medical emergency that requires prompt management to prevent airway obstruction. It is caused by inflammation of the epiglottis and is most common in children. Symptoms include fever, sore throat, difficulty swallowing, and respiratory distress. The most severe cases can lead to complete airway obstruction, which can be fatal.

      The most important initial step in management is to call for an anaesthetist to intubate the child. Attempting to administer treatment via a facemask or examining the child’s throat can cause distress and increase the risk of complete airway obstruction. The anaesthetist should be present during any examination or treatment to ensure the safety of the child.

      In summary, acute epiglottitis is a medical emergency that requires prompt management to prevent airway obstruction. Calling for an anaesthetist to intubate the child is the most important initial step in management. Any examination or treatment should be done with the anaesthetist present to ensure the safety of the child.

    • This question is part of the following fields:

      • Paediatrics
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  • Question 62 - A 67-year-old man complains of lower urinary tract symptoms. He has been experiencing...

    Incorrect

    • A 67-year-old man complains of lower urinary tract symptoms. He has been experiencing urinary urgency and occasional incontinence for the past few months. He reports no difficulty with urinary flow, hesitancy, or straining. Prostate examination and urinalysis reveal no abnormalities. What medication is most likely to relieve his symptoms?

      Your Answer:

      Correct Answer: Antimuscarinic

      Explanation:

      Patients with an overactive bladder can benefit from antimuscarinic drugs. Oxybutynin, tolterodine, and darifenacin are some examples of effective medications. However, before resorting to medication, it is important to discuss conservative measures with the patient and offer bladder training.

      Lower urinary tract symptoms (LUTS) are a common issue in men over the age of 50, with benign prostatic hyperplasia being the most common cause. However, other causes such as prostate cancer should also be considered. These symptoms can be classified into three groups: voiding, storage, and post-micturition. To properly manage LUTS, it is important to conduct a urinalysis to check for infection and haematuria, perform a digital rectal examination to assess the size and consistency of the prostate, and possibly conduct a PSA test after proper counselling. Patients should also complete a urinary frequency-volume chart and an International Prostate Symptom Score to guide management.

      For predominantly voiding symptoms, conservative measures such as pelvic floor muscle training, bladder training, and prudent fluid intake can be helpful. If symptoms are moderate or severe, an alpha-blocker may be offered. If the prostate is enlarged and the patient is at high risk of progression, a 5-alpha reductase inhibitor should be offered. If there are mixed symptoms of voiding and storage not responding to an alpha-blocker, an antimuscarinic drug may be added. For predominantly overactive bladder symptoms, moderating fluid intake and bladder retraining should be offered, and antimuscarinic drugs may be prescribed if symptoms persist. Mirabegron may be considered if first-line drugs fail. For nocturia, moderating fluid intake at night, furosemide 40mg in the late afternoon, and desmopressin may be helpful.

    • This question is part of the following fields:

      • Renal Medicine/Urology
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  • Question 63 - A 32-week pregnant woman presents to the early pregnancy unit with a concern...

    Incorrect

    • A 32-week pregnant woman presents to the early pregnancy unit with a concern that her uterus is small for this stage of pregnancy. Upon ultrasound, she is diagnosed with oligohydramnios. What could be a potential cause of oligohydramnios?

      Your Answer:

      Correct Answer: Renal agenesis

      Explanation:

      Oligohydramnios is a condition that occurs during pregnancy when there is a shortage of amniotic fluid. This can result in a smaller symphysiofundal height.

      Oligohydramnios is a condition characterized by a decrease in the amount of amniotic fluid present in the womb. The definition of oligohydramnios varies, but it is generally considered to be present when there is less than 500ml of amniotic fluid at 32-36 weeks of gestation or an amniotic fluid index (AFI) that falls below the 5th percentile.

      There are several potential causes of oligohydramnios, including premature rupture of membranes, Potter sequence, bilateral renal agenesis with pulmonary hypoplasia, intrauterine growth restriction, post-term gestation, and pre-eclampsia. These conditions can all contribute to a reduction in the amount of amniotic fluid present in the womb, which can have significant implications for fetal development and health. It is important for healthcare providers to monitor amniotic fluid levels and identify any potential causes of oligohydramnios in order to provide appropriate care and support for both the mother and the developing fetus.

    • This question is part of the following fields:

      • Reproductive Medicine
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  • Question 64 - A 25-year-old man presents to your GP clinic with concerns of a possible...

    Incorrect

    • A 25-year-old man presents to your GP clinic with concerns of a possible urinary tract infection. He reports experiencing burning sensations during urination for the past two weeks, particularly in the morning. Additionally, he has noticed some itching around his penis. The patient has no significant medical history. During the examination, you observe that his abdomen is soft and nontender. Upon performing a urine dip, you find that it is positive for leukocytes. What is the most probable cause of his symptoms?

      Your Answer:

      Correct Answer: Urethritis due to a sexually transmitted infection

      Explanation:

      The BASH guidelines for Sexually Transmitted Infections in Primary Care state that in young men, urethritis is typically caused by an STI. Men under the age of 35 rarely experience urine infections, so any sexually active man experiencing dysuria should be screened for STIs. The presence of leukocytes in the urine indicates the presence of pus cells, which are a result of an STI. Chlamydia is the most prevalent STI in the UK.

      Chlamydia is a common sexually transmitted infection caused by Chlamydia trachomatis. It is prevalent in the UK, with approximately 1 in 10 young women affected. The incubation period is around 7-21 days, but many cases are asymptomatic. Symptoms in women include cervicitis, discharge, and bleeding, while men may experience urethral discharge and dysuria. Complications can include epididymitis, pelvic inflammatory disease, and infertility.

      Traditional cell culture is no longer widely used for diagnosis, with nuclear acid amplification tests (NAATs) being the preferred method. Testing can be done using urine, vulvovaginal swab, or cervical swab. Screening is recommended for sexually active individuals aged 15-24 years, and opportunistic testing is common.

      Doxycycline is the first-line treatment for Chlamydia, with azithromycin as an alternative if doxycycline is contraindicated or not tolerated. Pregnant women may be treated with azithromycin, erythromycin, or amoxicillin. Patients diagnosed with Chlamydia should be offered partner notification services, with all contacts since the onset of symptoms or within the last six months being notified and offered treatment.

    • This question is part of the following fields:

      • Renal Medicine/Urology
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  • Question 65 - A 45-year-old woman, with a history of gallstones, arrives at the emergency department...

    Incorrect

    • A 45-year-old woman, with a history of gallstones, arrives at the emergency department complaining of central abdominal pain that radiates to her back. Upon conducting blood tests, you observe the following result:
      Amylase 480 U/L (30 - 110). The patient is diagnosed with acute pancreatitis and inquires about the severity of her condition. What is the primary factor in determining the clinical severity of acute pancreatitis?

      Your Answer:

      Correct Answer: Presence of any systemic or local complications

      Explanation:

      When determining the severity of pancreatitis, the presence of systemic or local complications is the most important factor to consider. Mild acute pancreatitis is characterized by the absence of both organ failure and local complications. Local complications in severe cases may include peripancreatic fluid collections, pancreatic or peripancreatic necrosis, pseudocysts, and walled-off areas of necrosis. The Atlanta classification system categorizes acute pancreatitis as mild, moderate, or severe. Mild cases have no organ failure, local or systemic complications, and typically resolve within a week. Pain level and initial CRP levels are not used to classify severity, but a high white blood cell count may indicate an increased risk of severe pancreatitis. Serum amylase levels and pancreatic calcification on CT scans are also not reliable indicators of severity.

      Managing Acute Pancreatitis in a Hospital Setting

      Acute pancreatitis is a serious condition that requires management in a hospital setting. The severity of the condition can be stratified based on the presence of organ failure and local complications. Key aspects of care include fluid resuscitation, aggressive early hydration with crystalloids, and adequate pain management with intravenous opioids. Patients should not be made ‘nil-by-mouth’ unless there is a clear reason, and enteral nutrition should be offered within 72 hours of presentation. Antibiotics should not be used prophylactically, but may be indicated in cases of infected pancreatic necrosis. Surgery may be necessary for patients with acute pancreatitis due to gallstones or obstructed biliary systems, and those with infected necrosis may require radiological drainage or surgical necrosectomy.

    • This question is part of the following fields:

      • Gastroenterology/Nutrition
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  • Question 66 - Generalised myositis is a known side effect of certain drugs. Among the options...

    Incorrect

    • Generalised myositis is a known side effect of certain drugs. Among the options listed below, which drug is most likely to cause this side effect?

      Your Answer:

      Correct Answer: Simvastatin

      Explanation:

      Muscle Effects of Common Medications

      Many medications can have effects on muscles, including statins, metoclopramide, amitriptyline, cyclizine, and venlafaxine. Statins can increase the risk of muscle toxicity, especially in patients with a history of muscular disorders, high alcohol intake, renal impairment, or hypothyroidism. Metoclopramide is associated with extrapyramidal symptoms and acute dystonic reactions, but not generalised myositis. Amitriptyline and cyclizine are rarely associated with extrapyramidal symptoms and tremor, and amitriptyline may cause myalgia on drug withdrawal. Venlafaxine commonly causes hypertonia and tremor, and more rarely myoclonus, but not generalised myositis. It is important to be aware of these potential muscle effects when prescribing and monitoring these medications.

      Muscle Effects of Commonly Prescribed Medications

    • This question is part of the following fields:

      • Pharmacology/Therapeutics
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  • Question 67 - What is the cause of scarlet fever? ...

    Incorrect

    • What is the cause of scarlet fever?

      Your Answer:

      Correct Answer: Group A haemolytic streptococci

      Explanation:

      Scarlet fever is a condition caused by erythrogenic toxins produced by Group A haemolytic streptococci, usually Streptococcus pyogenes. It is more prevalent in children aged 2-6 years, with the highest incidence at 4 years. The disease spreads through respiratory droplets or direct contact with nose and throat discharges, especially during sneezing and coughing. The incubation period is 2-4 days, and symptoms include fever, malaise, headache, nausea/vomiting, sore throat, ‘strawberry’ tongue, and a rash that appears first on the torso and spares the palms and soles. The rash has a rough ‘sandpaper’ texture and desquamination occurs later in the course of the illness, particularly around the fingers and toes.

      To diagnose scarlet fever, a throat swab is usually taken, but antibiotic treatment should be initiated immediately, rather than waiting for the results. Management involves administering oral penicillin V for ten days, while patients with a penicillin allergy should be given azithromycin. Children can return to school 24 hours after commencing antibiotics, and scarlet fever is a notifiable disease. Although usually a mild illness, scarlet fever may be complicated by otitis media, rheumatic fever, acute glomerulonephritis, or rare invasive complications such as bacteraemia, meningitis, or necrotizing fasciitis, which may present acutely with life-threatening illness.

    • This question is part of the following fields:

      • Paediatrics
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  • Question 68 - A 28-year-old man presents to the colorectal surgeons with recurrent episodes of bright...

    Incorrect

    • A 28-year-old man presents to the colorectal surgeons with recurrent episodes of bright red rectal bleeding over the past 5 months. During examination, a muco-epithelial defect is observed in the posterior midline of the anus. However, a complete digital rectal exam (DRE) could not be performed due to severe pain. Despite trying bulk-forming laxatives, lubricants, and topical glyceryl trinitrate (GTN), the patient has experienced little relief. What is the recommended next step in managing this likely diagnosis?

      Your Answer:

      Correct Answer: Sphincterotomy

      Explanation:

      For cases of anal fissures that do not respond to conservative management, sphincterotomy may be considered as the next step. This is likely the case for the patient in question, who has not seen improvement with laxatives, lubricants, and topical GTN. While a high-fibre diet is important in managing anal fissures, it should be initiated alongside other conservative measures. If the patient had a perianal abscess, incision and drainage would be the appropriate treatment. For haemorrhoids, rubber band ligation would be the management, while anal fistulae would require seton insertion.

      Understanding Anal Fissures: Causes, Symptoms, and Treatment

      Anal fissures are tears in the lining of the distal anal canal that can be either acute or chronic. Acute fissures last for less than six weeks, while chronic fissures persist for more than six weeks. The most common risk factors for anal fissures include constipation, inflammatory bowel disease, and sexually transmitted infections such as HIV, syphilis, and herpes.

      Symptoms of anal fissures include painful, bright red rectal bleeding, with around 90% of fissures occurring on the posterior midline. If fissures are found in other locations, underlying causes such as Crohn’s disease should be considered.

      Management of acute anal fissures involves softening stool, dietary advice, bulk-forming laxatives, lubricants, topical anaesthetics, and analgesia. For chronic anal fissures, the same techniques should be continued, and topical glyceryl trinitrate (GTN) is the first-line treatment. If GTN is not effective after eight weeks, surgery (sphincterotomy) or botulinum toxin may be considered, and referral to secondary care is recommended.

      In summary, anal fissures can be a painful and uncomfortable condition, but with proper management, they can be effectively treated. It is important to identify and address underlying risk factors to prevent the development of chronic fissures.

    • This question is part of the following fields:

      • Gastroenterology/Nutrition
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  • Question 69 - An 80-year-old man visits his GP complaining of a painful lesion on his...

    Incorrect

    • An 80-year-old man visits his GP complaining of a painful lesion on his ear that has been bothering him for a year. The lesion has remained the same for several months but is causing him significant discomfort when he lies down. He reports no other symptoms.
      Upon examination, the doctor observes a well-defined, 10mm, flesh-colored nodule on the superior helix of the ear. The nodule is firm, very tender to touch, and covered with some scales.
      What is the most probable diagnosis?

      Your Answer:

      Correct Answer: Chondrodermatitis nodularis helicis

      Explanation:

      Chondrodermatitis nodularis helicis is a painful, non-cancerous nodule that commonly occurs on the ear, particularly in men. Based on the patient’s level of pain and the stable nature of the lesion, this is the most likely diagnosis. While squamous cell carcinoma is a possible differential, it typically progresses more rapidly than this lesion. Similarly, basal cell carcinoma usually develops gradually and is not typically associated with significant pain. Although actinic keratosis can cause a scaly lesion on the ear, it is usually not as painful as chondrodermatitis nodularis helicis and tends to progress slowly over time.

      Understanding Chondrodermatitis Nodularis Helicis

      Chondrodermatitis nodularis helicis (CNH) is a harmless condition that is characterized by the formation of a painful nodule on the ear. It is believed to be caused by various factors such as continuous pressure on the ear, trauma, or exposure to cold. This condition is more prevalent in men and tends to occur more frequently as one ages.

      To manage CNH, it is essential to reduce pressure on the ear. This can be achieved by using foam ear protectors while sleeping. Other treatment options include cryotherapy, steroid injection, and collagen injection. However, surgical treatment may be necessary in some cases, although there is a high likelihood of recurrence.

      Overall, understanding CNH is crucial in managing this condition effectively. By taking the necessary precautions and seeking appropriate treatment, individuals can alleviate the pain and discomfort associated with CNH.

    • This question is part of the following fields:

      • Dermatology
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  • Question 70 - Amiodarone is known to cause which side effect? Choose ONE option from the...

    Incorrect

    • Amiodarone is known to cause which side effect? Choose ONE option from the list provided.

      Your Answer:

      Correct Answer: Hyperthyroidism

      Explanation:

      Understanding the Side Effects of Amiodarone: A Comprehensive Overview

      Amiodarone is a medication commonly used to treat cardiac arrhythmias. However, it is important to be aware of its potential side effects. Here is a breakdown of some of the most important things to know:

      Hyperthyroidism: Amiodarone can cause both hypo and hyperthyroidism. Patients taking this medication should have their thyroid function checked regularly.

      COPD: While amiodarone is not known to cause COPD, it can lead to pulmonary toxicity, including pneumonitis and fibrosis. Patients should have yearly chest x-rays.

      Drug-induced diabetes mellitus: There is no known association between amiodarone and the development of diabetes mellitus.

      Drug-induced pemphigus: Long-term use of amiodarone can cause phototoxicity and skin discoloration. Patients should protect their skin from light during treatment. However, it is not known to cause drug-induced pemphigus.

      Renal calculi: There is no known association between amiodarone and the development of kidney disease, including renal calculi.

      Other important side effects of amiodarone include hepatotoxicity, bradycardia, phototoxicity, and development of corneal deposits. If you are taking amiodarone, it is important to be aware of these potential side effects and to discuss any concerns with your healthcare provider.

    • This question is part of the following fields:

      • Pharmacology/Therapeutics
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  • Question 71 - A 60-year-old man presents with a sudden onset of vision loss in his...

    Incorrect

    • A 60-year-old man presents with a sudden onset of vision loss in his left eye upon waking up this morning. He reports no pain in his eye. His medical history includes diabetes mellitus and hypertension. Upon fundoscopic examination, the right eye appears normal, but the left eye shows multiple retinal haemorrhages. What is the most probable diagnosis?

      Your Answer:

      Correct Answer: Central retinal vein occlusion

      Explanation:

      The sudden painless loss of vision and severe retinal haemorrhages observed on fundoscopy in this patient are indicative of central retinal vein occlusion. Amaurosis fugax, which is caused by atheroembolism from the carotid arteries, results in temporary vision loss that resolves within a few minutes. In contrast, this patient’s vision loss is persistent. While central retinal artery occlusion also causes acute painless vision loss, it is characterized by a loss of relative afferent pupillary defect, a cherry-red macula, and a white/pale retina on fundoscopy. Hypertensive retinopathy may cause flame-shaped haemorrhages and cotton wool spots on the retina, but it does not result in sudden vision loss.

      Understanding Central Retinal Vein Occlusion

      Central retinal vein occlusion (CRVO) is a possible cause of sudden, painless loss of vision. It is more common in older individuals and those with hypertension, cardiovascular disease, glaucoma, or polycythemia. The condition is characterized by a sudden reduction or loss of visual acuity, usually affecting only one eye. Fundoscopy reveals widespread hyperemia and severe retinal hemorrhages, which are often described as a stormy sunset.

      Branch retinal vein occlusion (BRVO) is a similar condition that affects a smaller area of the fundus. It occurs when a vein in the distal retinal venous system is blocked, usually at arteriovenous crossings.

      Most patients with CRVO are managed conservatively, but treatment may be necessary in some cases. For instance, intravitreal anti-vascular endothelial growth factor (VEGF) agents may be used to manage macular edema, while laser photocoagulation may be necessary to treat retinal neovascularization.

      Overall, understanding the risk factors, features, and management options for CRVO is essential for prompt diagnosis and appropriate treatment. Proper management can help prevent further vision loss and improve the patient’s quality of life.

    • This question is part of the following fields:

      • Ophthalmology
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  • Question 72 - You are clerking a 26-year-old in the emergency department. He reports experiencing painful...

    Incorrect

    • You are clerking a 26-year-old in the emergency department. He reports experiencing painful prolonged erection of the penis for the third time. What could be the probable cause of his recurrent presentations?

      Your Answer:

      Correct Answer: Sickle cell disease

      Explanation:

      Recurrent priapism is a common occurrence in individuals with sickle cell disease, while alcohol and drug abuse may also lead to this condition. Balanitis, on the other hand, is an inflammation that affects the head of the penis and is not associated with priapism. Paraphimosis, however, can be caused by the inability to retract the foreskin.

      Sickle-cell anaemia is a genetic disorder that occurs when abnormal haemoglobin, known as HbS, is produced due to an autosomal recessive condition. This condition is more common in individuals of African descent, as the heterozygous condition provides some protection against malaria. About 10% of UK Afro-Caribbean’s are carriers of HbS, and they only experience symptoms if they are severely hypoxic. Homozygotes tend to develop symptoms between 4-6 months when the abnormal HbSS molecules replace fetal haemoglobin.

      The pathophysiology of sickle-cell anaemia involves the substitution of the polar amino acid glutamate with the non-polar valine in each of the two beta chains (codon 6) of haemoglobin. This substitution decreases the water solubility of deoxy-Hb, causing HbS molecules to polymerise and sickle RBCs in the deoxygenated state. HbAS patients sickle at p02 2.5 – 4 kPa, while HbSS patients sickle at p02 5 – 6 kPa. Sickle cells are fragile and haemolyse, blocking small blood vessels and causing infarction.

      The definitive diagnosis of sickle-cell anaemia is through haemoglobin electrophoresis.

    • This question is part of the following fields:

      • Renal Medicine/Urology
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  • Question 73 - A 55-year-old male patient visits the GP clinic complaining of weakness in his...

    Incorrect

    • A 55-year-old male patient visits the GP clinic complaining of weakness in his right leg for the past three days. During the examination, it was observed that there was a weakness in the right knee flexion, but the knee extension was intact. Additionally, there was a weakness in the dorsal and plantar flexion of the right ankle, as well as the right flexor hallucis longus. The right ankle jerk was lost, but the knee-jerk was intact, and the plantar response was downgoing. Based on the most probable nerve that is damaged in this patient, what are the nerve roots that supply this nerve?

      Your Answer:

      Correct Answer: L4-5, S1-3

      Explanation:

      The sciatic nerve is innervated by spinal nerves L4-5, S1-3. The patient exhibits weakness in all muscle groups below the knee, with an intact knee jerk but weak ankle jerk, indicating damage to the sciatic nerve. The iliohypogastric nerve is supplied by T12-L1, while the genitofemoral nerve is supplied by L1-2.

      Understanding Sciatic Nerve Lesion

      The sciatic nerve is a major nerve in the body that is supplied by the L4-5, S1-3 vertebrae. It divides into two branches, the tibial and common peroneal nerves, which supply the hamstring and adductor muscles. A sciatic nerve lesion can cause paralysis of knee flexion and all movements below the knee, as well as sensory loss below the knee. However, knee jerk reflexes remain intact while ankle and plantar reflexes are lost.

      There are several causes of sciatic nerve lesions, including fractures of the neck of the femur, posterior hip dislocation, and trauma.

    • This question is part of the following fields:

      • Neurology
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  • Question 74 - An 85-year-old woman and her daughter visit your clinic to inquire about the...

    Incorrect

    • An 85-year-old woman and her daughter visit your clinic to inquire about the need for bone protection medication. The patient has a medical history of a fractured neck of femur 12 months ago, chronic kidney disease stage IV, hypertension, and ischaemic heart disease. She was prescribed alendronic acid after her fracture, but it was discontinued six months ago due to reflux issues. Risedronate was also not tolerated due to the same reason. Her DEXA scan after the fracture revealed a T score of -4.2. What is the most appropriate course of action?

      Your Answer:

      Correct Answer: Refer for consideration of denosumab

      Explanation:

      The situation is complex as the patient requires bone protection due to her low T score and previous hip fracture. However, bisphosphonates are not suitable for her as they are contraindicated in patients with an eGFR below 35 mL/minute/1.73m(2), which she has due to her stage IV chronic kidney disease. Therefore, reintroducing alendronate or using IV zoledronate infusion is not an option. Repeating her DEXA scan at this point would not provide any additional information. While calcium and vitamin D supplementation should continue, they are not sufficient for her bone protection needs. The best option is denosumab, which would require administration in a secondary care setting and close monitoring of her calcium levels due to her renal disease.

      The NICE guidelines for managing osteoporosis in postmenopausal women include offering vitamin D and calcium supplementation, with alendronate being the first-line treatment. If a patient cannot tolerate alendronate, risedronate or etidronate may be given as second-line drugs, with strontium ranelate or raloxifene as options if those cannot be taken. Treatment criteria for patients not taking alendronate are based on age, T-score, and risk factors. Bisphosphonates have been shown to reduce the risk of fractures, with alendronate and risedronate being superior to etidronate in preventing hip fractures. Other treatments include selective estrogen receptor modulators, strontium ranelate, denosumab, teriparatide, and hormone replacement therapy. Hip protectors and falls risk assessment may also be considered in management.

    • This question is part of the following fields:

      • Musculoskeletal
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  • Question 75 - A 25-year-old woman has a Nexplanon implanted on day 20 of her 30...

    Incorrect

    • A 25-year-old woman has a Nexplanon implanted on day 20 of her 30 day cycle. When can she trust the Nexplanon to prevent pregnancy?

      Your Answer:

      Correct Answer: After 7 days

      Explanation:

      Contraceptives – Time to become effective (if not used on the first day of period):
      Immediate: IUD
      2 days: Progestin-only pill (POP)
      7 days: Combined oral contraceptive (COC), injection, implant, intrauterine system (IUS)

      Implanon and Nexplanon are subdermal contraceptive implants that slowly release the progestogen hormone etonogestrel to prevent ovulation and thicken cervical mucus. Nexplanon is the newer version and has a redesigned applicator to prevent deep insertions and is radiopaque for easier location. It is highly effective with a failure rate of 0.07/100 women-years and lasts for 3 years. It does not contain estrogen, making it suitable for women with a past history of thromboembolism or migraine. It can be inserted immediately after a termination of pregnancy. However, a trained professional is needed for insertion and removal, and additional contraceptive methods are required for the first 7 days if not inserted on days 1 to 5 of a woman’s menstrual cycle.

      The main disadvantage of these implants is irregular and heavy bleeding, which can be managed with a co-prescription of the combined oral contraceptive pill. Other adverse effects include headache, nausea, and breast pain. Enzyme-inducing drugs such as certain antiepileptic and rifampicin may reduce the efficacy of Nexplanon, and women should switch to a method unaffected by enzyme-inducing drugs or use additional contraception until 28 days after stopping the treatment.

      There are also contraindications for using these implants, such as ischaemic heart disease/stroke, unexplained, suspicious vaginal bleeding, past breast cancer, severe liver cirrhosis, and liver cancer. Current breast cancer is a UKMEC 4 condition, which represents an unacceptable risk if the contraceptive method is used. Overall, these implants are a highly effective and long-acting form of contraception, but they require careful consideration of the potential risks and contraindications.

    • This question is part of the following fields:

      • Reproductive Medicine
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  • Question 76 - A 32-year-old female sex worker presents to the emergency department complaining of a...

    Incorrect

    • A 32-year-old female sex worker presents to the emergency department complaining of a high fever and severe headache. During the physical examination, you observe neck stiffness and mild photophobia, prompting you to perform a lumbar puncture. The results of the lumbar puncture reveal the presence of a yeast and a capsule in the CSF stained with India ink.
      What is the most probable diagnosis?

      Your Answer:

      Correct Answer: Cryptococcal meningitis

      Explanation:

      Cryptococcus neoformans is a yeast that has a protective capsule and requires oxygen to survive. It can thrive in both plants and animals, and when it infects humans, it causes cryptococcosis. While the infection typically affects the lungs, it can also lead to fungal meningitis and encephalitis in individuals with weakened immune systems. HIV-positive patients are particularly susceptible to this infection, and given the patient’s history as a sex worker, it’s possible that they have an undiagnosed HIV infection that has progressed to AIDS. Additionally, cryptococcus neoformans can be detected through india ink staining during a lumbar puncture.

      The investigation and management of suspected bacterial meningitis are intertwined due to the potential negative impact of delayed antibiotic treatment. Patients should be urgently transferred to the hospital, and an ABC approach should be taken initially. A lumbar puncture should be delayed in certain circumstances, and IV antibiotics should be given as a priority if there is any doubt. The bloods and CSF should be tested for various parameters, and prophylaxis should be offered to households and close contacts of patients affected with meningococcal meningitis.

    • This question is part of the following fields:

      • Infectious Diseases
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  • Question 77 - A 65-year-old woman is discharged following an uncomplicated renal transplant for end-stage renal...

    Incorrect

    • A 65-year-old woman is discharged following an uncomplicated renal transplant for end-stage renal failure from hypertension. She received a kidney with 4 out of 6 mismatched human leukocyte antigen (HLA) and is taking the appropriate medications. Thirty days postoperatively, she developed watery loose stools, followed by a skin rash that is itchy, painful and red. On examination, she has a red-violet rash affecting her hands and feet.
      Investigations reveal the following:
      Investigation Result Normal value
      Haemoglobin (Hb) 131 g/l 115–155 g/l
      White cell count (WCC) 5.4 × 109/l 4.0–11.0 × 109/l
      Platelets (PLT) 280 ×109/l 150–400 × 109/l
      Sodium (Na+) 139 mmol/l 135–145 mmol/l
      Potassium (K+) 4.0 mmol/l 3.5–5.0 mmol/l
      Urea 15.1 mmol/l 2.5–6.5 mmol/l
      Creatinine (Cr) 170 μmol/l 50–120 µmol/l
      Alanine aminotransferase (ALT) 54 IU/l 7–55 IU/l
      Alkaline phosphatase (ALP) 165 IU/l 30–130 IU/l
      Bilirubin 62 µmol/l 2–17 µmol/l
      Which of the following is the most likely diagnosis?

      Your Answer:

      Correct Answer: Graft-versus-host disease

      Explanation:

      Differential Diagnosis for a Patient with Watery Diarrhea and Rash after Renal Transplantation

      Graft-versus-host disease (GVHD) is a potential complication of solid organ transplantation, with a mortality rate of 75%. It typically presents with watery diarrhea, a painful red-violet rash, and raised bilirubin. Diagnosis is obtained through biopsy, and treatment involves immunosuppressants such as tacrolimus and methylprednisolone.

      Acute viral hepatitis is another possible cause of diarrhea and jaundice, but the patient’s normal ALT and atypical symptoms make it unlikely. Azathioprine toxicity can cause bone marrow suppression, while Sjögren syndrome causes dry eyes and xerostomia, neither of which fit this patient’s presentation.

      Viral gastroenteritis is a consideration, but the presence of a painful/itchy rash and raised bilirubin suggests a need for further investigation. Given the recent renal transplant, a high degree of suspicion for GVHD and other potential complications is warranted.

    • This question is part of the following fields:

      • Renal Medicine/Urology
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  • Question 78 - A 48-year-old man suffers an Achilles tendon rupture while playing basketball. He has...

    Incorrect

    • A 48-year-old man suffers an Achilles tendon rupture while playing basketball. He has never had any medical issues related to his muscles or bones. He recently began taking antibiotics for an infection and has been on them for the past week. What type of antibiotic is he likely taking?

      Your Answer:

      Correct Answer: Ciprofloxacin

      Explanation:

      New-onset Achilles tendon disorders, including tendinitis and tendon rupture, are likely caused by ciprofloxacin, a medication with important side effects to consider.

      Achilles tendon disorders are a common cause of pain in the back of the heel. These disorders can include tendinopathy, partial tears, and complete ruptures of the Achilles tendon. Certain factors, such as the use of quinolone antibiotics and high cholesterol levels, can increase the risk of developing these disorders. Symptoms of Achilles tendinopathy typically include gradual onset of pain that worsens with activity, as well as morning stiffness. Treatment for this condition usually involves pain relief, reducing activities that exacerbate the pain, and performing calf muscle eccentric exercises.

      In contrast, an Achilles tendon rupture is a more serious condition that requires immediate medical attention. This type of injury is often caused by sudden, forceful movements during sports or running. Symptoms of an Achilles tendon rupture include an audible popping sound, sudden and severe pain in the calf or ankle, and an inability to walk or continue the activity. To help diagnose an Achilles tendon rupture, doctors may use Simmond’s triad, which involves examining the foot for abnormal angles and feeling for a gap in the tendon. Ultrasound is typically the first imaging test used to confirm a diagnosis of Achilles tendon rupture. If a rupture is suspected, it is important to seek medical attention from an orthopaedic specialist as soon as possible.

    • This question is part of the following fields:

      • Musculoskeletal
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  • Question 79 - A 68-year-old woman with isolated systolic hypertension, who also has urinary tract infections,...

    Incorrect

    • A 68-year-old woman with isolated systolic hypertension, who also has urinary tract infections, osteoporosis and diabetes, attends outpatients with a blood pressure reading of 192/88 mmHg. Which of the following medications would you prescribe for this patient?

      Your Answer:

      Correct Answer: Valsartan

      Explanation:

      Choosing the Right Medication for Hypertension: A Guide

      When it comes to treating hypertension, there are several medications to choose from. The National Institute for Health and Care Excellence (NICE) recommends an angiotensin-converting enzyme (ACE) inhibitor or an angiotensin receptor blocker (ARB) as first-line treatment for those under 55, while calcium channel blockers (CCBs) are preferred for patients over 55 and those of Afro-Caribbean origin. Beta blockers, once a common choice, are no longer recommended as first-line treatment.

      If initial treatment is not effective, a thiazide diuretic can be added to an ACE inhibitor or ARB and CCB. Alpha blockers, such as doxazosin, are no longer commonly used for hypertension and are contraindicated in patients with urinary incontinence. Valsartan, an ARB, is an alternative for patients who cannot tolerate an ACE inhibitor.

      For elderly patients with isolated systolic hypertension, a dihydropyridine CCB like amlodipine is the drug of choice, especially if thiazides are not an option. Beta blockers should be used with caution in patients with asthma and are not indicated in this case. By carefully considering the patient’s age, ethnicity, and medical history, healthcare providers can choose the most appropriate medication for treating hypertension.

    • This question is part of the following fields:

      • Cardiovascular
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  • Question 80 - A 30-year-old female arrives at the Emergency Department after intentionally overdosing on paracetamol....

    Incorrect

    • A 30-year-old female arrives at the Emergency Department after intentionally overdosing on paracetamol. What is the most significant indicator of an ongoing high risk of suicide?

      Your Answer:

      Correct Answer: Made efforts to avoid herself being found by friends and family

      Explanation:

      Although deliberate self-harm is more prevalent among females, completed suicide is more prevalent among males.

      Suicide Risk Factors and Protective Factors

      Suicide risk assessment is a common practice in psychiatric care, with patients being stratified into high, medium, or low risk categories. However, there is a lack of evidence on the positive predictive value of individual risk factors. A review in the BMJ concluded that such assessments may not be useful in guiding decision-making, as 50% of suicides occur in patients deemed low risk. Nevertheless, certain factors have been associated with an increased risk of suicide, including male sex, history of deliberate self-harm, alcohol or drug misuse, mental illness, depression, schizophrenia, chronic disease, advancing age, unemployment or social isolation, and being unmarried, divorced, or widowed.

      If a patient has attempted suicide, there are additional risk factors to consider, such as efforts to avoid discovery, planning, leaving a written note, final acts such as sorting out finances, and using a violent method. On the other hand, there are protective factors that can reduce the risk of suicide, such as family support, having children at home, and religious belief. It is important to consider both risk and protective factors when assessing suicide risk and developing a treatment plan.

    • This question is part of the following fields:

      • Psychiatry
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  • Question 81 - A 67-year-old man presents for a review of his chronic obstructive pulmonary disease....

    Incorrect

    • A 67-year-old man presents for a review of his chronic obstructive pulmonary disease. He reports experiencing constant shortness of breath during physical activity, which has remained stable over the past year. He has a history of asbestos exposure and is currently under the care of a respiratory physician. During the examination, no abnormalities are detected, but a chest X-ray reveals the presence of pleural plaques. The patient expresses concern that these plaques may develop into cancer. What advice do you offer this patient regarding his test results?

      Your Answer:

      Correct Answer: Benign and do not require follow-up

      Explanation:

      Pleural plaques are benign and do not develop into cancerous growths, so there is no need for any follow-up. These plaques are the most common form of lung disease caused by asbestos exposure, but they do not increase the risk of lung cancer or mesothelioma. While ongoing monitoring of the patient’s lung disease is recommended, there is no need to specifically monitor the pleural plaques. It is important to note that pleural plaques are a sign of past asbestos exposure, which could increase the risk of mesothelioma, but the plaques themselves are not a cause for concern. Therefore, the patient does not require a specialist referral for the pleural plaques alone. However, if the patient experiences worsening shortness of breath or frequent exacerbations, a specialist referral may be necessary to assess for disease progression or malignancy.

      Asbestos-Related Lung Diseases

      Asbestos exposure can lead to various lung diseases, ranging from benign pleural plaques to malignant mesothelioma. Pleural plaques are non-cancerous and do not require any follow-up, but they are the most common form of asbestos-related lung disease and typically appear after a latent period of 20-40 years. Asbestos exposure may also cause diffuse pleural thickening, which is similar to the pattern seen after an empyema or haemothorax, but the underlying pathophysiology is not fully understood.

      Asbestosis is a lung disease that is related to the length of exposure to asbestos. It causes lower lobe fibrosis and is typically characterized by dyspnea, reduced exercise tolerance, clubbing, bilateral end-inspiratory crackles, and a restrictive pattern with reduced gas transfer on lung function tests. Asbestosis is treated conservatively, as no interventions offer significant benefits. The latent period for asbestosis is typically 15-30 years.

      Mesothelioma is a malignant disease of the pleura that is caused by asbestos exposure, with crocidolite (blue) asbestos being the most dangerous form. Possible features of mesothelioma include progressive shortness-of-breath, chest pain, and pleural effusion. Patients are usually offered palliative chemotherapy, and there is a limited role for surgery and radiotherapy. Unfortunately, the prognosis for mesothelioma is very poor, with a median survival from diagnosis of 8-14 months.

      Although mesothelioma is often associated with asbestos exposure, lung cancer is actually the most common form of cancer related to asbestos exposure. It has a synergistic effect with cigarette smoke, which increases the risk of developing lung cancer.

    • This question is part of the following fields:

      • Respiratory Medicine
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  • Question 82 - A 27-year-old man with a medical history of sickle cell disease presents with...

    Incorrect

    • A 27-year-old man with a medical history of sickle cell disease presents with intense pain in his left hip. He mentions having received antibiotics from his general practitioner for a chest infection. How would you categorize this sickle cell crisis?

      Your Answer:

      Correct Answer: Thrombotic crises

      Explanation:

      Sickle cell patients may experience thrombotic crises due to factors such as infection, dehydration, or deoxygenation. In this case, the patient’s severe pain and recent infection suggest a thrombotic crisis. Other types of crises, such as sequestration crises that present with acute chest syndrome, aplastic crises caused by parvovirus infection, or haemolytic crises with increased haemolysis, may have different symptoms. A thyrotoxic crisis would not be related to sickle cell disease.

      Sickle cell anaemia is a condition that involves periods of good health with intermittent crises. There are several types of crises that can occur, including thrombotic or painful crises, sequestration, acute chest syndrome, aplastic, and haemolytic. Thrombotic crises, also known as painful crises or vaso-occlusive crises, are triggered by factors such as infection, dehydration, and deoxygenation. These crises are diagnosed clinically and can result in infarcts in various organs, including the bones, lungs, spleen, and brain.

      Sequestration crises occur when sickling occurs within organs such as the spleen or lungs, leading to pooling of blood and worsening of anaemia. This type of crisis is associated with an increased reticulocyte count. Acute chest syndrome is caused by vaso-occlusion within the pulmonary microvasculature, resulting in infarction in the lung parenchyma. Symptoms include dyspnoea, chest pain, pulmonary infiltrates on chest x-ray, and low pO2. Management involves pain relief, respiratory support, antibiotics, and transfusion.

      Aplastic crises are caused by infection with parvovirus and result in a sudden fall in haemoglobin. Bone marrow suppression leads to a reduced reticulocyte count. Haemolytic crises are rare and involve a fall in haemoglobin due to an increased rate of haemolysis. It is important to recognise and manage these crises promptly, as they can lead to serious complications and even death.

    • This question is part of the following fields:

      • Haematology/Oncology
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  • Question 83 - You assess a 45-year-old male with Marfan's syndrome. What is the probable reason...

    Incorrect

    • You assess a 45-year-old male with Marfan's syndrome. What is the probable reason for mortality in individuals with this condition?

      Your Answer:

      Correct Answer: Aortic dissection

      Explanation:

      Aortic dissection may be more likely to occur in individuals with Marfan’s syndrome due to the dilation of the aortic sinuses.

      Understanding Marfan’s Syndrome

      Marfan’s syndrome is a genetic disorder that affects the connective tissue in the body. It is caused by a defect in the FBN1 gene on chromosome 15, which codes for the protein fibrillin-1. This disorder is inherited in an autosomal dominant pattern, meaning that a person only needs to inherit one copy of the defective gene from one parent to develop the condition. Marfan’s syndrome affects approximately 1 in 3,000 people.

      The features of Marfan’s syndrome include a tall stature with an arm span to height ratio greater than 1.05, a high-arched palate, arachnodactyly (long, slender fingers), pectus excavatum (sunken chest), pes planus (flat feet), and scoliosis (curvature of the spine). In addition, individuals with Marfan’s syndrome may experience cardiovascular problems such as dilation of the aortic sinuses, mitral valve prolapse, and aortic aneurysm. They may also have lung issues such as repeated pneumothoraces. Eye problems are also common, including upwards lens dislocation, blue sclera, and myopia. Finally, dural ectasia, or ballooning of the dural sac at the lumbosacral level, may also occur.

      In the past, the life expectancy of individuals with Marfan’s syndrome was around 40-50 years. However, with regular echocardiography monitoring and the use of beta-blockers and ACE inhibitors, this has improved significantly in recent years. Despite these improvements, aortic dissection and other cardiovascular problems remain the leading cause of death in individuals with Marfan’s syndrome.

    • This question is part of the following fields:

      • Musculoskeletal
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  • Question 84 - A 45-year old woman became pregnant unexpectedly. She had given birth to five...

    Incorrect

    • A 45-year old woman became pregnant unexpectedly. She had given birth to five healthy children in her 20s and 30s with her now 47-year-old husband. Chorionic villus biopsy and karyotype analysis revealed that she was carrying a fetus with trisomy 21 (Down syndrome).
      What is the most likely cause of the condition?

      Your Answer:

      Correct Answer: The mother’s age

      Explanation:

      Down syndrome is a genetic condition that is caused by three mechanisms. The most common cause is Trisomy 21, which occurs when there is a non-separation of the homologous chromosomes during meiosis. This risk increases with advancing maternal age, with a likelihood of 1 in 1500 at age 20 and 1 in 50 at age 45 or older. Translocation, where part of chromosome 21 attaches to another chromosome, accounts for about 4% of cases. Mosaicism, where only some cells carry the extra copy of chromosome 21, is the rarest type. Paternal age is not a significant factor, but if either parent is a translocation carrier, there is a 1 in 2 chance of passing it on to their offspring. A spontaneous mutation in the fetus is not a cause of Down syndrome.

    • This question is part of the following fields:

      • Genetics
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  • Question 85 - A 67-year-old man presents to the Emergency Department with pleuritic chest pain that...

    Incorrect

    • A 67-year-old man presents to the Emergency Department with pleuritic chest pain that started two hours ago. He has a history of lung cancer with bony metastases and has recently started treatment with erlotinib.

      His vital signs are as follows: temperature 37.2ºC; oxygen saturation 92% on room air; respiratory rate 20 breaths per minute; heart rate 98 beats per minute; blood pressure 140/86 mmHg.

      A chest X-ray is performed, which shows no abnormalities. He is started on supplemental oxygen therapy, and a CT pulmonary angiogram (CTPA) is ordered.

      While waiting for the CTPA results, what is the most appropriate next step in management?

      Your Answer:

      Correct Answer: Commence rivaroxaban

      Explanation:

      The recommended initial management for patients with suspected pulmonary embolism (PE) is to ensure they are haemodynamically stable before starting anticoagulation. According to the latest NICE Guidelines (2020), a direct oral anticoagulant (DOAC) such as apixaban or rivaroxaban should be started unless there are contraindications. In this case, the patient is stable and can be started on rivaroxaban. It is important to note that starting prophylactic dose LMWH is not appropriate for suspected PE, and commencing warfarin at loading dose is also not recommended due to its delayed anticoagulant effects. Thrombolytic agents such as alteplase are only appropriate for haemodynamically unstable patients. Dabigatran is an alternative option for patients who cannot take apixaban or rivaroxaban, but it too requires a bridging dose of LMWH.

      Management of Pulmonary Embolism: NICE Guidelines

      Pulmonary embolism (PE) is a serious condition that requires prompt management. The National Institute for Health and Care Excellence (NICE) updated their guidelines on the management of venous thromboembolism (VTE) in 2020, with some key changes. One of the significant changes is the recommendation to use direct oral anticoagulants (DOACs) as the first-line treatment for most people with VTE, including those with active cancer. Another change is the increasing use of outpatient treatment for low-risk PE patients, determined by a validated risk stratification tool.

      Anticoagulant therapy is the cornerstone of VTE management, and the guidelines recommend using apixaban or rivaroxaban as the first-line treatment following the diagnosis of a PE. If neither of these is suitable, LMWH followed by dabigatran or edoxaban or LMWH followed by a vitamin K antagonist (VKA) can be used. For patients with active cancer, DOACs are now recommended instead of LMWH. The length of anticoagulation is determined by whether the VTE was provoked or unprovoked, with treatment typically stopped after 3-6 months for provoked VTE and continued for up to 6 months for unprovoked VTE.

      In cases of haemodynamic instability, thrombolysis is recommended as the first-line treatment for massive PE with circulatory failure. Patients who have repeat pulmonary embolisms, despite adequate anticoagulation, may be considered for inferior vena cava (IVC) filters. However, the evidence base for IVC filter use is weak.

      Overall, the updated NICE guidelines provide clear recommendations for the management of PE, including the use of DOACs as first-line treatment and outpatient management for low-risk patients. The guidelines also emphasize the importance of individualized treatment based on risk stratification and balancing the risks of VTE recurrence and bleeding.

    • This question is part of the following fields:

      • Respiratory Medicine
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  • Question 86 - A 67-year-old man presents to you with complaints of increasing shortness of breath....

    Incorrect

    • A 67-year-old man presents to you with complaints of increasing shortness of breath. He reports having to use 3 or 4 pillows to sleep at night and feeling more breathless after climbing just one flight of stairs. His medical history includes a previous myocardial infarction and high cholesterol. During examination, you observe bibasal crepitations and notice swelling in his ankles. What is the most suitable next investigation to perform?

      Your Answer:

      Correct Answer: B-type Natriuretic Peptide (BNP)

      Explanation:

      According to the updated 2018 NICE guidelines, the initial test for patients with suspected chronic heart failure should be an NT-proBNP test, regardless of their history of myocardial infarction. Additionally, all patients should undergo a 12-lead ECG. While a CT chest is typically not necessary, a chest x-ray may be performed to rule out other potential conditions.

      Chronic heart failure is a condition that requires proper diagnosis and management. In 2018, NICE updated their guidelines on the diagnosis and management of this condition. Previously, the first-line investigation was determined by whether the patient had previously had a myocardial infarction or not. However, this is no longer the case. All patients should now have an N-terminal pro-B-type natriuretic peptide (NT‑proBNP) blood test as the first-line investigation.

      Interpreting the NT-proBNP blood test is crucial in determining the severity of the condition. If the levels are high, specialist assessment, including transthoracic echocardiography, should be arranged within two weeks. If the levels are raised, specialist assessment, including echocardiogram, should be arranged within six weeks. B-type natriuretic peptide (BNP) is a hormone produced mainly by the left ventricular myocardium in response to strain. Very high levels of BNP are associated with a poor prognosis.

      There are different levels of BNP, and each level indicates a different severity of the condition. High levels of BNP are greater than 400 pg/ml (116 pmol/litre) for BNP and greater than 2000 pg/ml (236 pmol/litre) for NTproBNP. Raised levels of BNP are between 100-400 pg/ml (29-116 pmol/litre) for BNP and between 400-2000 pg/ml (47-236 pmol/litre) for NTproBNP. Normal levels of BNP are less than 100 pg/ml (29 pmol/litre) for BNP and less than 400 pg/ml (47 pmol/litre) for NTproBNP.

      It is important to note that several factors can alter the BNP level. Factors that increase BNP levels include left ventricular hypertrophy, ischaemia, tachycardia, right ventricular overload, hypoxaemia (including pulmonary embolism), GFR < 60 ml/min, sepsis, COPD, diabetes, and age > 70. On the other hand, factors that decrease BNP levels include diuretics, ACE inhibitors, beta-blockers, angiotensin 2 receptor blockers, and aldosterone antagonists.

    • This question is part of the following fields:

      • Respiratory Medicine
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  • Question 87 - A 70-year-old man is brought to the Emergency Department by his wife who...

    Incorrect

    • A 70-year-old man is brought to the Emergency Department by his wife who reports that he has been feeling down lately. She also mentions that he ingested 30 atenolol 50mg tablets about four hours ago. Upon assessment, his pulse is recorded at 42 beats per minute and his blood pressure is 98/62 mmHg. What is the initial treatment option that should be considered?

      Your Answer:

      Correct Answer: Intravenous atropine

      Explanation:

      If gastric lavage is to be attempted, it should only be done within 1-2 hours of the patient taking the overdose.

      Managing Beta-Blocker Overdose

      Beta-blocker overdose can lead to various symptoms such as bradycardia, hypotension, heart failure, and syncope. To manage these symptoms, it is important to first identify if the patient is bradycardic. If so, atropine can be administered. However, in cases where atropine is not effective, glucagon may be used as an alternative. It is important to note that haemodialysis is not an effective treatment for beta-blocker overdose. Proper management of beta-blocker overdose is crucial in preventing further complications and ensuring the patient’s safety.

    • This question is part of the following fields:

      • Pharmacology/Therapeutics
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  • Question 88 - A 50-year-old male presents for a routine check-up and his blood pressure is...

    Incorrect

    • A 50-year-old male presents for a routine check-up and his blood pressure is found to be 170/100 mmHg (and high blood pressure is confirmed during home blood pressure readings.) He is investigated for secondary causes, none are found, and a diagnosis of primary hypertension is made. His GP starts him on 5mg lisinopril. Two weeks later, his kidney function results show:
      Na+ 140 mmol/L (135 - 145)
      K+ 4.5 mmol/L (3.5 - 5.0)
      Bicarbonate 28 mmol/L (22 - 29)
      Urea 7 mmol/L (2.0 - 7.0)
      Creatinine 200 µmol/L (55 - 120)

      Which of the following is the most likely explanation for the improvement in his renal function?

      Your Answer:

      Correct Answer: Renal artery stenosis

      Explanation:

      Undiagnosed bilateral renal artery stenosis can lead to significant renal impairment after starting an ACE inhibitor. This condition is commonly caused by atherosclerosis, but young females may also develop it due to fibromuscular dysplasia. As it often lacks symptoms, it can go unnoticed. While ACE inhibitors may cause a slight rise in serum creatinine, they usually only mildly affect renal function. Therefore, it is crucial to monitor renal function two weeks after initiating ramipril and other ACE inhibitors. Glomerulonephritis, which refers to inflammation of the glomeruli, has multiple causes and typically results in gradual renal function decline, not rapid worsening after ACE inhibitor initiation. Although renal calculi and renal artery thrombosis can cause acute kidney injury, the patient in this question lacks pain and thrombosis risk factors. Chronic, untreated hypertension can also affect renal function, but it progresses slowly over years, and the patient’s renal function was normal before starting ramipril.

      Angiotensin-converting enzyme (ACE) inhibitors are commonly used as the first-line treatment for hypertension and heart failure in younger patients. However, they may not be as effective in treating hypertensive Afro-Caribbean patients. These inhibitors are also used to treat diabetic nephropathy and for secondary prevention of ischaemic heart disease. The mechanism of action of ACE inhibitors is to inhibit the conversion of angiotensin I to angiotensin II. They are metabolized in the liver through phase 1 metabolism.

      ACE inhibitors may cause side effects such as cough, which occurs in around 15% of patients and may occur up to a year after starting treatment. This is thought to be due to increased bradykinin levels. Angioedema may also occur up to a year after starting treatment. Hyperkalaemia and first-dose hypotension are other potential side effects, especially in patients taking diuretics. ACE inhibitors should be avoided during pregnancy and breastfeeding, and caution should be exercised in patients with renovascular disease, aortic stenosis, or hereditary or idiopathic angioedema.

      Patients receiving high-dose diuretic therapy (more than 80 mg of furosemide a day) are at an increased risk of hypotension when taking ACE inhibitors. Before initiating treatment, urea and electrolytes should be checked, and after increasing the dose, a rise in creatinine and potassium may be expected. Acceptable changes include an increase in serum creatinine up to 30% from baseline and an increase in potassium up to 5.5 mmol/l. Patients with undiagnosed bilateral renal artery stenosis may experience significant renal impairment. The current NICE guidelines provide a flow chart for the management of hypertension.

    • This question is part of the following fields:

      • Renal Medicine/Urology
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  • Question 89 - A 47-year-old man is seen by his General Practitioner for his annual hypertension...

    Incorrect

    • A 47-year-old man is seen by his General Practitioner for his annual hypertension review. He agrees to be referred to the local smoking cessation service, as he is currently experiencing chest pain.
      Which of the following medications will need to be monitored closely on cessation of smoking?

      Your Answer:

      Correct Answer: Theophylline

      Explanation:

      The Effect of Smoking Cessation on Asthma Medications

      Smoking cessation can have a significant impact on the management of asthma and the use of certain medications. Here is a breakdown of how smoking cessation affects different asthma medications:

      Theophylline: Smoking induces the hepatic enzyme CYP1A2, which plays a major role in metabolizing theophylline. Therefore, quitting smoking can lead to higher plasma levels of theophylline and potentially fatal arrhythmias. Patients need to have their plasma theophylline concentration levels monitored closely and may require a reduced dose after quitting smoking.

      Budesonide/formoterol: Neither budesonide nor formoterol are metabolized by CYP1A2, so there is no need for close monitoring following smoking cessation. Asthma control should improve after quitting smoking, and the inhaler dose should be reviewed as part of stepwise management.

      Montelukast: Montelukast is metabolized by the cytochrome P450 system but not CYP1A2, so smoking cessation does not affect its level.

      Prednisolone: Prednisolone is metabolized by the cytochrome P450 system, but CYP1A2 is not involved. Therefore, smoking cessation does not affect its metabolism.

      Salbutamol: Smoking cessation can improve asthma control, leading to less frequent use of salbutamol or other reliever inhalers. There is no need to monitor this closely as reducing the as-required use of this medication poses no risk.

    • This question is part of the following fields:

      • Haematology/Oncology
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  • Question 90 - A 60-year-old African American male presents with widespread bone pain and muscle weakness....

    Incorrect

    • A 60-year-old African American male presents with widespread bone pain and muscle weakness. Upon investigation, the following results were obtained:
      Calcium 2.05 mmol/l
      Phosphate 0.68 mmol/l
      ALP 340 U/l
      What is the probable diagnosis?

      Your Answer:

      Correct Answer: Osteomalacia

      Explanation:

      Osteomalacia may be indicated by bone pain, tenderness, and proximal myopathy (resulting in a waddling gait), as well as low levels of calcium and phosphate and elevated alkaline phosphatase.

      Understanding Osteomalacia

      Osteomalacia is a condition that occurs when the bones become soft due to low levels of vitamin D, which leads to a decrease in bone mineral content. This condition is commonly seen in adults, while in growing children, it is referred to as rickets. The causes of osteomalacia include vitamin D deficiency, malabsorption, lack of sunlight, chronic kidney disease, drug-induced factors, inherited conditions, liver disease, and coeliac disease.

      The symptoms of osteomalacia include bone pain, muscle tenderness, fractures, especially in the femoral neck, and proximal myopathy, which may lead to a waddling gait. To diagnose osteomalacia, blood tests are conducted to check for low vitamin D levels, low calcium and phosphate levels, and raised alkaline phosphatase levels. X-rays may also show translucent bands known as Looser’s zones or pseudofractures.

      The treatment for osteomalacia involves vitamin D supplementation, with a loading dose often needed initially. Calcium supplementation may also be necessary if dietary calcium intake is inadequate. Understanding the causes, symptoms, and treatment options for osteomalacia is crucial in managing this condition effectively.

    • This question is part of the following fields:

      • Musculoskeletal
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  • Question 91 - A 42-year-old man visits his GP complaining of a headache and thick nasal...

    Incorrect

    • A 42-year-old man visits his GP complaining of a headache and thick nasal discharge that has persisted for six days. He reports the headache as a frontal pressure pain that worsens when he bends forward. He denies experiencing cough or general malaise. His vital signs are heart rate 62/min, respiratory rate 13/min, blood pressure 127/63 mmHg, and temperature 36.2 ºC. He has a medical history of asthma, which he manages with his salbutamol inhaler. What is the appropriate management plan for the most likely diagnosis?

      Your Answer:

      Correct Answer: Analgesia and abundant fluids

      Explanation:

      For uncomplicated acute sinusitis, antibiotics are not necessary. Instead, the recommended treatment is pain relief and staying hydrated. The patient in this scenario has typical symptoms of acute sinusitis, such as facial pain, nasal discharge, and difficulty breathing. Antibiotics are only prescribed in severe cases or when the patient is at high risk of complications. Co-amoxiclav is an example of an antibiotic that may be used in these situations. Intranasal corticosteroids may be prescribed if the condition lasts longer than ten days. Intranasal decongestants and oral corticosteroids are not effective treatments for acute sinusitis and should not be used.

      Acute sinusitis is a condition where the mucous membranes of the paranasal sinuses become inflamed. This inflammation is usually caused by infectious agents such as Streptococcus pneumoniae, Haemophilus influenzae, and rhinoviruses. Certain factors can predispose individuals to this condition, including nasal obstruction, recent local infections, swimming/diving, and smoking. Symptoms of acute sinusitis include facial pain, nasal discharge, and nasal obstruction. Treatment options include analgesia, intranasal decongestants or nasal saline, and intranasal corticosteroids. Oral antibiotics may be prescribed for severe presentations, but they are not typically required. In some cases, an initial viral sinusitis can worsen due to secondary bacterial infection, which is known as double-sickening.

    • This question is part of the following fields:

      • ENT
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  • Question 92 - A 7 year-old girl from Sierra Leone presents with a 2 week history...

    Incorrect

    • A 7 year-old girl from Sierra Leone presents with a 2 week history of painful left leg. She is homozygous for sickle cell disease. On examination the child is febrile at 39.8ºC and there is bony tenderness over the left tibial shaft. Investigations are:
      Hb 6.9 g/dL
      Blood culture Gram positive cocci
      X-ray left tibia: Osteomyelitis - destruction of bony cortex with periosteal reaction.
      What is the most likely responsible pathogen?

      Your Answer:

      Correct Answer: Non-typhi Salmonella

      Explanation:

      Non-typhi salmonella (NTS) is known to cause blood and bone infections, particularly in children with sickle cell disease and malaria. The exact reason for this susceptibility is not fully understood, but it may be due to the bacteria’s affinity for iron, which is made available through haemolysis. Other bacteria such as E.coli and P. aeruginosa are not commonly associated with sickle cell disease, and Staphylococcus aureus is a gram-positive coccus. Aplastic anaemia and parvovirus can be ruled out as causes, as the child’s haemoglobin level is normal and parvovirus does not cause osteomyelitis.

      Understanding Osteomyelitis: Types, Causes, and Treatment

      Osteomyelitis is a bone infection that can be classified into two types: haematogenous and non-haematogenous. Haematogenous osteomyelitis is caused by bacteria that enter the bloodstream and is usually monomicrobial. It is more common in children, with vertebral osteomyelitis being the most common form in adults. Risk factors include sickle cell anaemia, intravenous drug use, immunosuppression, and infective endocarditis. On the other hand, non-haematogenous osteomyelitis results from the spread of infection from adjacent soft tissues or direct injury to the bone. It is often polymicrobial and more common in adults, with risk factors such as diabetic foot ulcers, pressure sores, diabetes mellitus, and peripheral arterial disease.

      Staphylococcus aureus is the most common cause of osteomyelitis, except in patients with sickle-cell anaemia where Salmonella species predominate. To diagnose osteomyelitis, MRI is the imaging modality of choice, with a sensitivity of 90-100%. Treatment for osteomyelitis involves a six-week course of flucloxacillin. Clindamycin is an alternative for patients who are allergic to penicillin.

      In summary, osteomyelitis is a bone infection that can be caused by bacteria entering the bloodstream or spreading from adjacent soft tissues or direct injury to the bone. It is more common in children and adults with certain risk factors. Staphylococcus aureus is the most common cause, and MRI is the preferred imaging modality for diagnosis. Treatment involves a six-week course of flucloxacillin or clindamycin for penicillin-allergic patients.

    • This question is part of the following fields:

      • Musculoskeletal
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  • Question 93 - A 25-year-old Asian woman presents with completely depigmented patches of skin on her...

    Incorrect

    • A 25-year-old Asian woman presents with completely depigmented patches of skin on her arms and legs.
      What is the most likely diagnosis?

      Your Answer:

      Correct Answer: Vitiligo

      Explanation:

      Common Skin Pigmentation Disorders

      Skin pigmentation disorders are conditions that affect the color of the skin. Here are some of the most common ones:

      Vitiligo: This rare condition is believed to be caused by the immune system attacking melanocytes, resulting in patches of skin with no pigment. It is more common in people of African descent.

      Albinism: This genetic disorder reduces the activity of tyrosinase in melanocytes, resulting in a complete lack of pigment in the skin, hair, and eyes.

      Melanoma: This is a type of skin cancer that develops from melanocytes. It is characterized by irregular, highly pigmented moles.

      Melasma: This condition causes increased pigmentation, usually under the eyes. It is common in pregnant women and users of oral contraceptives.

      Pityriasis alba: This condition causes white, scaly patches on the face, and is most commonly seen in children.

      Understanding these skin pigmentation disorders can help individuals identify and manage them effectively.

    • This question is part of the following fields:

      • Dermatology
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  • Question 94 - A 47-year-old man visits his doctor for a routine follow-up blood test that...

    Incorrect

    • A 47-year-old man visits his doctor for a routine follow-up blood test that reveals elevated levels of a tumour marker in his blood. Which of the following is most commonly linked to increased levels of serum alpha-fetoprotein (AFP)?

      Your Answer:

      Correct Answer: Hepatocellular carcinoma

      Explanation:

      Tumour Markers for Common Cancers

      Tumour markers are substances produced by cancer cells that can be detected in the blood. They are used to help diagnose and monitor the progression of cancer. Here are the most common tumour markers associated with some of the most prevalent cancers:

      Hepatocellular carcinoma: Alpha-fetoprotein (AFP) is the most likely tumour marker associated with this type of liver cancer, which often develops in people with chronic liver diseases.

      Breast cancer: Cancer antigen 15-3 (CA 15-3) is the most likely tumour marker associated with breast cancer, which affects both men and women.

      Colorectal cancer: Carcinoembryonic antigen (CEA) is the most likely tumour marker associated with colorectal cancer, which can develop from polyps in the colon or rectum.

      Pancreatic cancer: CA 19-9 is the most likely tumour marker associated with pancreatic cancer, which is often difficult to detect in its early stages.

      Prostate cancer: Prostate-specific antigen (PSA) is the most likely tumour marker associated with prostate cancer, which is the most common cancer in men.

    • This question is part of the following fields:

      • Haematology/Oncology
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  • Question 95 - A 75-year-old man complains of persistent ringing in his left ear for the...

    Incorrect

    • A 75-year-old man complains of persistent ringing in his left ear for the past 4 months. He has also noticed a decline in hearing from his left ear over the past 2 weeks. During the examination, Rinne's test reveals that air conduction is louder than bone conduction in the left ear, and Weber's test shows lateralisation to the right ear. Which of the following conditions is likely to present with unilateral tinnitus and hearing loss?

      Your Answer:

      Correct Answer: Acoustic neuroma

      Explanation:

      The traditional presentation of vestibular schwannoma involves a blend of symptoms such as vertigo, hearing impairment, tinnitus, and a missing corneal reflex.

      An acoustic neuroma is typically linked to one-sided tinnitus and hearing loss.

      Tinnitus and deafness are not commonly associated with multiple sclerosis (MS), which is a condition characterized by demyelination.

      Chronic otitis media is a persistent inflammation of the middle ear and mastoid cavity, which is marked by recurring otorrhoea and conductive hearing loss.

      Understanding Vestibular Schwannoma (Acoustic Neuroma)

      Vestibular schwannoma, also known as acoustic neuroma, is a type of brain tumor that accounts for 5% of intracranial tumors and 90% of cerebellopontine angle tumors. The condition is characterized by a combination of symptoms such as vertigo, hearing loss, tinnitus, and an absent corneal reflex. The affected cranial nerves can predict the features of the condition. For instance, cranial nerve VIII can cause vertigo, unilateral sensorineural hearing loss, and unilateral tinnitus. On the other hand, cranial nerve V can lead to an absent corneal reflex, while cranial nerve VII can cause facial palsy.

      Bilateral vestibular schwannomas are often seen in neurofibromatosis type 2. The diagnosis of vestibular schwannoma is made through an MRI of the cerebellopontine angle, and audiometry is also important since only 5% of patients have a normal audiogram.

      The management of vestibular schwannoma involves surgery, radiotherapy, or observation. The choice of treatment depends on the size and location of the tumor, the patient’s age and overall health, and the severity of symptoms. In conclusion, understanding vestibular schwannoma is crucial in managing the condition effectively.

    • This question is part of the following fields:

      • ENT
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  • Question 96 - A 67-year-old male presents to an urgent care centre with concerns about decreased...

    Incorrect

    • A 67-year-old male presents to an urgent care centre with concerns about decreased frequency of urination. He reports only urinating once in the past 12 hours and feels unable to urinate despite the urge to do so. The patient has a medical history of diabetes mellitus managed with metformin and chronic back pain managed with ibuprofen and PPI cover. He has no known allergies. Blood tests reveal the following results: Na+ 139 mmol/L (135 - 145), K+ 4.8 mmol/L (3.5 - 5.0), Bicarbonate 22 mmol/L (22 - 29), Urea 7.1 mmol/L (2.0 - 7.0), and Creatinine 200 µmol/L (55 - 120). The patient's previous creatinine level was 119 µmol/L. The general practitioner refers the patient to the emergency department for further investigation. What is the correct classification?

      Your Answer:

      Correct Answer: Acute Kidney Injury stage 1

      Explanation:

      The patient in this vignette meets the criteria for AKI Stage 1, which is characterized by a moderate increase in serum creatinine (1.5-1.9 times the baseline) or reduced urine output (<0.5 mL/kg/hr) for at least 6 hours. The patient has risk factors such as age, diabetes mellitus, and NSAID use for back pain, which can contribute to AKI. It is important to note that AKI is a classification and not a diagnosis. AKI Stage 2 is characterized by a more significant increase in serum creatinine (2-2.9 times the baseline) or reduced urine output for at least 12 hours. The vignette does not show renal function that is severe enough to meet this classification. AKI Stage 3 is the most severe stage, with a serum creatinine increase of 3 times or more from baseline or reduced urine output for at least 24 hours. Again, the patient’s renal function is not severe enough to meet this classification. There is no AKI Stage 4 or 5. Chronic kidney disease is classified from stages 1-5 based on the patient’s estimated glomerular filtration rate (eGFR). A patient with CKD Stage 4 would have an eGFR of 15-29 ml/min/1.73m², while a patient with CKD Stage 5 would have end-stage renal disease with an eGFR <15 ml/min/1.73m² or be receiving renal replacement therapy. The NICE guidelines for acute kidney injury (AKI) identify risk factors such as emergency surgery, CKD, diabetes, and use of nephrotoxic drugs. Diagnostic criteria include a rise in creatinine, fall in urine output, or fall in eGFR. The KDIGO criteria are used to stage AKI, with stage 3 indicating the most severe cases. Referral to a nephrologist is recommended for certain cases, such as AKI with no known cause or inadequate response to treatment. Complications of AKI include CKD, hyperkalaemia, metabolic acidosis, and fluid overload.

    • This question is part of the following fields:

      • Renal Medicine/Urology
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  • Question 97 - A new father is curious as to when his toddler will be receiving...

    Incorrect

    • A new father is curious as to when his toddler will be receiving her vaccines. He is particularly interested in the six-in-one vaccine which he has heard about from some friends at playgroup. When is the six-in-one vaccine given to toddlers?

      Your Answer:

      Correct Answer: 8, 12, and 16 weeks

      Explanation:

      Childhood Vaccination Schedule in the UK

      In the UK, childhood vaccinations are an important part of ensuring the health and wellbeing of children. Here is a breakdown of the vaccination schedule:

      8, 12, and 16 weeks: The 6-in-1 vaccine is given as a single injection to protect against diphtheria, hepatitis B, Haemophilus influenza B, polio, tetanus, and pertussis. This vaccine is given at eight, 12, and 16 weeks old.

      One year: At one year, children receive the MMR vaccine, Hib/Men C vaccine, and third dose of the meningitis B and pneumococcal vaccines.

      8, 12, and 16 months: There are three doses given, however at eight, 12, and 16 weeks of age, not months.

      24 months: From 2-9 years old, children will receive the annual flu vaccine via nasal spray.

      It is important to follow the vaccination schedule to ensure that children are protected against serious illnesses. Talk to your healthcare provider for more information.

    • This question is part of the following fields:

      • Immunology/Allergy
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  • Question 98 - A 28-year-old female patient visits your clinic with a complaint of fishy-smelling vaginal...

    Incorrect

    • A 28-year-old female patient visits your clinic with a complaint of fishy-smelling vaginal discharge. You suspect bacterial vaginosis and decide to prescribe metronidazole. The patient has no known drug allergies and is generally healthy, except for taking the combined oral contraceptive pill (COCP). What is the most crucial advice you should provide her regarding the potential side effects of metronidazole?

      Your Answer:

      Correct Answer: She should abstain from alcohol whilst taking metronidazole

      Explanation:

      Taking metronidazole and alcohol together can result in a disulfiram-like reaction, so patients should be cautioned against consuming alcohol while on the medication. Metronidazole is not associated with cholestasis, hepatotoxicity, or QT prolongation. As an enzyme inhibitor, metronidazole enhances the efficacy of the COCP. While Stevens-Johnson syndrome is a rare side effect of metronidazole, a photosensitive rash is not typically observed.

      Metronidazole is an antibiotic that functions by producing reactive cytotoxic metabolites within bacteria. This medication can cause adverse effects such as a disulfiram-like reaction when combined with alcohol and an increased anticoagulant effect when taken with warfarin.

    • This question is part of the following fields:

      • Reproductive Medicine
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  • Question 99 - A 67-year-old man with worsening dyspnea is suspected to have idiopathic pulmonary fibrosis....

    Incorrect

    • A 67-year-old man with worsening dyspnea is suspected to have idiopathic pulmonary fibrosis. What is the preferred diagnostic test to confirm the diagnosis?

      Your Answer:

      Correct Answer: High-resolution CT scan

      Explanation:

      Understanding Idiopathic Pulmonary Fibrosis

      Idiopathic pulmonary fibrosis (IPF) is a chronic lung condition that causes progressive fibrosis of the interstitium of the lungs. Unlike other causes of lung fibrosis, IPF has no underlying cause. It is typically seen in patients aged 50-70 years and is more common in men.

      The symptoms of IPF include progressive exertional dyspnoea, dry cough, clubbing, and bibasal fine end-inspiratory crepitations on auscultation. Diagnosis is made through spirometry, impaired gas exchange tests, and imaging such as chest x-rays and high-resolution CT scans.

      Management of IPF includes pulmonary rehabilitation, but very few medications have been shown to be effective. Some evidence suggests that pirfenidone, an antifibrotic agent, may be useful in selected patients. Many patients will eventually require supplementary oxygen and a lung transplant.

      The prognosis for IPF is poor, with an average life expectancy of around 3-4 years. CT scans can show advanced pulmonary fibrosis, including honeycombing. While there is no cure for IPF, early diagnosis and management can help improve quality of life and potentially prolong survival.

    • This question is part of the following fields:

      • Respiratory Medicine
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  • Question 100 - As a junior doctor in an inpatient psychiatric unit, you have assessed a...

    Incorrect

    • As a junior doctor in an inpatient psychiatric unit, you have assessed a 25-year-old patient who has recently been diagnosed with paranoid schizophrenia. Your consultant has initiated treatment with olanzapine and baseline blood tests have been conducted. According to NICE guidelines, what further investigation is recommended for this patient?

      Your Answer:

      Correct Answer: ECG

      Explanation:

      Patients starting antipsychotic medications should have a baseline ECG, along with weight, waist circumference, pulse and BP measurements, blood tests (including fasting glucose, HbA1c, lipids and prolactin), assessment of movement disorders and nutritional status. An ECG may also be necessary if the medication’s summary of product characteristics recommends it, if the patient has a high risk of cardiovascular disease, has a personal history of cardiovascular disease, or is being admitted as an inpatient. As olanzapine is a second-generation antipsychotic that can cause QT prolongation, an ECG is particularly important for this patient because she is currently hospitalized.

      Monitoring patients who are taking antipsychotic medication is a crucial aspect of their treatment. In addition to regular clinical follow-ups, extensive monitoring is required to ensure the safety and effectiveness of the medication. The British National Formulary (BNF) recommends a range of tests and assessments to be carried out at various intervals. At the start of therapy, a full blood count (FBC), urea and electrolytes (U&E), and liver function tests (LFT) should be conducted. Clozapine, in particular, requires more frequent monitoring of FBC, initially on a weekly basis. Lipids and weight should be measured at the start of therapy, after three months, and annually thereafter. Fasting blood glucose and prolactin levels should be checked at the start of therapy, after six months, and annually thereafter. Blood pressure should be measured at baseline and frequently during dose titration. An electrocardiogram should be conducted at baseline, and cardiovascular risk assessment should be carried out annually. For more detailed information, please refer to the BNF, which also provides specific recommendations for individual drugs.

    • This question is part of the following fields:

      • Psychiatry
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  • Question 101 - What is the likelihood of a 44-year-old mother having a child with Down's...

    Incorrect

    • What is the likelihood of a 44-year-old mother having a child with Down's syndrome?

      Your Answer:

      Correct Answer: 1 in 50

      Explanation:

      The risk of Down’s syndrome is 1 in 1,000 at the age of 30, and this risk decreases by a factor of 3 for every 5 years.

      Down’s Syndrome: Epidemiology and Genetics

      Down’s syndrome is a genetic disorder that occurs when there is an extra copy of chromosome 21. The risk of having a child with Down’s syndrome increases with maternal age. At 20 years old, the risk is 1 in 1,500, but by 45 years old, the risk increases to 1 in 50 or greater. To remember this, one can start with a risk of 1/1,000 at 30 years old and divide the denominator by 3 for every extra 5 years of age.

      There are three main types of Down’s syndrome: nondisjunction, Robertsonian translocation, and mosaicism. Nondisjunction accounts for 94% of cases and occurs when the chromosomes fail to separate properly during cell division. The risk of recurrence is 1 in 100 if the mother is under 35 years old. Robertsonian translocation occurs when part of chromosome 21 attaches to another chromosome, usually chromosome 14. This accounts for 5% of cases and has a higher risk of recurrence if the mother or father is a carrier. Mosaicism accounts for 1% of cases and occurs when there are two genetically different populations of cells in the body.

      In summary, Down’s syndrome is a genetic disorder that is more common with increasing maternal age. The risk of recurrence depends on the type of Down’s syndrome and whether the parents are carriers. It is important for individuals to understand the genetics and epidemiology of Down’s syndrome to make informed decisions about family planning.

    • This question is part of the following fields:

      • Paediatrics
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  • Question 102 - A 26-year-old woman is recuperating from a kidney transplant. Within 24 hours of...

    Incorrect

    • A 26-year-old woman is recuperating from a kidney transplant. Within 24 hours of the surgery, she complains of increased discomfort at the transplant site. Upon examination, she has a fever, tenderness at the transplant site, and has not produced urine since the procedure. Her creatinine levels have significantly increased in the past 24 hours. What is the fundamental mechanism behind her rejection?

      Your Answer:

      Correct Answer: Pre-existing antibodies against ABO or HLA antigens

      Explanation:

      Understanding HLA Typing and Graft Failure in Renal Transplants

      The human leucocyte antigen (HLA) system, also known as the major histocompatibility complex (MHC), is located on chromosome 6 and plays a crucial role in renal transplants. The HLA system includes class 1 antigens (A, B, and C) and class 2 antigens (DP, DQ, and DR), with DR being the most important for HLA matching in renal transplants. Graft survival rates for cadaveric transplants are 90% at 1 year and 60% at 10 years, while living-donor transplants have a 95% survival rate at 1 year and 70% at 10 years.

      Post-operative problems may include acute tubular necrosis of the graft, vascular thrombosis, urine leakage, and urinary tract infections. Hyperacute rejection, which occurs within minutes to hours, is caused by pre-existing antibodies against ABO or HLA antigens and leads to widespread thrombosis of graft vessels, resulting in the need for graft removal. Acute graft failure, which occurs within 6 months, is usually due to mismatched HLA and is picked up by a rising creatinine, pyuria, and proteinuria. Chronic graft failure, which occurs after 6 months, is caused by both antibody and cell-mediated mechanisms and leads to fibrosis of the transplanted kidney, with recurrence of the original renal disease being a common cause.

      In summary, understanding the HLA system and its role in renal transplants is crucial for successful outcomes. Monitoring for post-operative problems and early detection of graft failure can help improve long-term survival rates.

    • This question is part of the following fields:

      • Renal Medicine/Urology
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  • Question 103 - A patient who has recently returned from a camping trip is worried about...

    Incorrect

    • A patient who has recently returned from a camping trip is worried about having contracted Lyme disease. She has developed a rash and feels fatigued and achy. What is the most suitable test to investigate Lyme disease in a patient like her?

      Your Answer:

      Correct Answer: Blood test for serology

      Explanation:

      When there is no history of erythema migrans, ELISA is the primary test used to investigate suspected cases of Lyme disease.

      Understanding Lyme Disease

      Lyme disease is a bacterial infection caused by Borrelia burgdorferi and is transmitted through tick bites. The early symptoms of Lyme disease include erythema migrans, a characteristic bulls-eye rash that appears at the site of the tick bite. This rash is painless, slowly increases in size, and can be more than 5 cm in diameter. Other early symptoms include headache, lethargy, fever, and joint pain.

      If erythema migrans is present, Lyme disease can be diagnosed clinically, and antibiotics should be started immediately. The first-line test for Lyme disease is an enzyme-linked immunosorbent assay (ELISA) to detect antibodies to Borrelia burgdorferi. If the ELISA is negative but Lyme disease is still suspected, it should be repeated 4-6 weeks later. If Lyme disease is suspected in patients who have had symptoms for 12 weeks or more, an immunoblot test should be done.

      Tick bites can cause significant anxiety, but routine antibiotic treatment is not recommended by NICE. If the tick is still present, it should be removed using fine-tipped tweezers, and the area should be washed. In cases of suspected or confirmed Lyme disease, doxycycline is the preferred treatment for early disease, while ceftriaxone is used for disseminated disease. A Jarisch-Herxheimer reaction may occur after initiating therapy, which can cause fever, rash, and tachycardia.

      In summary, Lyme disease is a bacterial infection transmitted through tick bites. Early symptoms include erythema migrans, headache, lethargy, fever, and joint pain. Diagnosis is made through clinical presentation and ELISA testing, and treatment involves antibiotics. Tick bites do not require routine antibiotic treatment, and ticks should be removed using fine-tipped tweezers.

    • This question is part of the following fields:

      • Infectious Diseases
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  • Question 104 - A 7-year-old girl is seen in clinic after falling off her scooter two...

    Incorrect

    • A 7-year-old girl is seen in clinic after falling off her scooter two hours ago. She fell forward and used her right arm to break her fall. Upon examination, she has minor scrapes on her right forearm but no indication of a fracture. Her nose is red and has some scrapes. Upon examination of her nostrils, there is a bilateral red swelling in the middle that is slightly soft. There are no other indications of a head injury. What is the best course of action?

      Your Answer:

      Correct Answer: Arrange an urgent ENT review

      Explanation:

      Nasal Septal Haematoma: A Complication of Nasal Trauma

      Nasal septal haematoma is a serious complication that can occur after even minor nasal trauma. It is characterized by the accumulation of blood between the septal cartilage and the surrounding perichondrium. The most common symptom is nasal obstruction, but pain and rhinorrhoea may also be present. On examination, a bilateral, red swelling arising from the nasal septum is typically seen. It is important to differentiate this from a deviated septum, which will be firm to the touch.

      If left untreated, nasal septal haematoma can lead to irreversible septal necrosis within just a few days. This occurs due to pressure-related ischaemia of the cartilage, which can result in necrosis and a saddle-nose deformity. To prevent this, surgical drainage and intravenous antibiotics are necessary. It is important to be vigilant for this complication after any nasal trauma, no matter how minor.

    • This question is part of the following fields:

      • ENT
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  • Question 105 - A 17-year-old female patient presents with concerns about her acne and its impact...

    Incorrect

    • A 17-year-old female patient presents with concerns about her acne and its impact on her self-esteem. She has been experiencing acne for a few years and is currently taking the combined oral contraceptive pill, which has provided some relief. After a thorough discussion, you decide to initiate treatment with topical isotretinoin. What other side effect, in addition to its teratogenic effects, should you inform her about?

      Your Answer:

      Correct Answer: Erythema

      Explanation:

      The initial approach to treating acne involves the use of a topical retinoid (such as tretinoin, isotretinoin, or adapalene) or benzoyl peroxide, particularly if there are papules and pustules present. Patients should be informed of the potential side effects of topical retinoids, which may include burning, redness, and dryness of the skin, as well as eye irritation and swelling. However, topical retinoids are not associated with aggravating acne, causing headaches or nausea, or leading to yellowing of the skin.

      Acne vulgaris is a common skin condition that typically affects adolescents, with the face, neck, and upper trunk being the most commonly affected areas. It is characterized by the obstruction of hair follicles with keratin plugs, leading to the formation of comedones, inflammation, and pustules. The severity of acne can be classified as mild, moderate, or severe, depending on the presence and extent of inflammatory lesions, papules, and pustules.

      The management of acne vulgaris typically involves a step-up approach, starting with single topical therapy such as topical retinoids or benzoyl peroxide. If this is not effective, topical combination therapy may be used, which includes a topical antibiotic, benzoyl peroxide, and topical retinoid. Oral antibiotics such as tetracyclines may also be prescribed, but they should be avoided in pregnant or breastfeeding women and children under 12 years of age. Erythromycin may be used in pregnancy, while minocycline is now considered less appropriate due to the possibility of irreversible pigmentation. Oral antibiotics should be used for a maximum of three months and always co-prescribed with a topical retinoid or benzoyl peroxide to reduce the risk of antibiotic resistance.

      Combined oral contraceptives (COCP) are an alternative to oral antibiotics in women, and Dianette (co-cyrindiol) may be used as it has anti-androgen properties. However, it has an increased risk of venous thromboembolism compared to other COCPs, so it should generally be used second-line and for only three months. Oral isotretinoin is a potent medication that should only be used under specialist supervision, and it is contraindicated in pregnancy. Finally, there is no evidence to support dietary modification in the management of acne vulgaris.

    • This question is part of the following fields:

      • Dermatology
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  • Question 106 - A 48-year-old man visits his doctor with worries about a discharge coming from...

    Incorrect

    • A 48-year-old man visits his doctor with worries about a discharge coming from his nipples. Which medication is the most probable cause for this symptom?

      Your Answer:

      Correct Answer: Chlorpromazine

      Explanation:

      Gynaecomastia may be linked to each of the remaining four drugs instead of galactorrhoea.

      Understanding Prolactin and Galactorrhoea

      Prolactin is a hormone produced by the anterior pituitary gland, and its release is regulated by various physiological factors. Dopamine is the primary inhibitor of prolactin release, and dopamine agonists like bromocriptine can be used to manage galactorrhoea. Galactorrhoea is a condition characterized by the production of breast milk in individuals who are not breastfeeding. It is important to distinguish the causes of galactorrhoea from those of gynaecomastia, which is the enlargement of male breast tissue.

      Excess prolactin can lead to different symptoms in men and women. Men may experience impotence, loss of libido, and galactorrhoea, while women may have amenorrhoea and galactorrhoea. Several factors can cause raised prolactin levels, including prolactinoma, pregnancy, oestrogens, stress, exercise, sleep, acromegaly, polycystic ovarian syndrome, and primary hypothyroidism. Additionally, certain medications like metoclopramide, domperidone, phenothiazines, haloperidol, SSRIs, and opioids can also increase prolactin levels.

      In summary, understanding prolactin and its effects on the body is crucial in diagnosing and managing conditions like galactorrhoea. Identifying the underlying causes of raised prolactin levels is essential in providing appropriate treatment and improving patient outcomes.

    • This question is part of the following fields:

      • Reproductive Medicine
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  • Question 107 - A 35-year-old woman presents to her GP with complaints of excessive thirst and...

    Incorrect

    • A 35-year-old woman presents to her GP with complaints of excessive thirst and frequent urination. She is currently 20 weeks pregnant and this is her first pregnancy. Her BMI is 30 kg/m². The GP decides to conduct an oral glucose tolerance test to investigate the possibility of gestational diabetes.
      What finding would confirm the suspicion of gestational diabetes in this case?

      Your Answer:

      Correct Answer: Fasting glucose 5.9 mmol/L

      Explanation:

      To diagnose gestational diabetes, a fasting glucose level of >= 5.6 mmol/L or a 2-hour glucose level of >= 7.8 mmol/L can be used. A patient with a BMI of >30 kg/m² and symptoms of polydipsia and polyuria should undergo an oral glucose tolerance test during 24-28 weeks of pregnancy. In this test, the patient fasts for 8-10 hours, then drinks a glucose solution and has blood samples taken before and 2 hours after. A fasting glucose level of 5.9mmol/L or higher confirms the diagnosis of gestational diabetes.

      Gestational diabetes is a common medical disorder affecting around 4% of pregnancies. Risk factors include a high BMI, previous gestational diabetes, and family history of diabetes. Screening is done through an oral glucose tolerance test, and diagnostic thresholds have recently been updated. Management includes self-monitoring of blood glucose, diet and exercise advice, and medication if necessary. For pre-existing diabetes, weight loss and insulin are recommended, and tight glycemic control is important. Targets for self-monitoring include fasting glucose of 5.3 mmol/l and 1-2 hour post-meal glucose levels.

    • This question is part of the following fields:

      • Endocrinology/Metabolic Disease
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  • Question 108 - A 58-year-old woman develops a red and hot right shin. She is afebrile...

    Incorrect

    • A 58-year-old woman develops a red and hot right shin. She is afebrile and otherwise well. She has no known allergies. Her Wells' score is -2.
      Which of the following would be the best option?
      Select the SINGLE best option from the list below. Select ONE option only.

      Your Answer:

      Correct Answer: Oral flucloxacillin

      Explanation:

      Treatment Options for Cellulitis and the Use of Doppler Ultrasound for DVT Diagnosis

      Cellulitis is a common bacterial skin infection that can be treated with oral flucloxacillin, according to UK antimicrobial guidelines. Hospital admission for cellulitis treatment is only necessary for febrile and ill patients or those with comorbidities. Oral co-amoxiclav is recommended for facial cellulitis, but not for cellulitis in other locations. Oral vancomycin is used for Clostridium difficile infection, not cellulitis.

      A Doppler ultrasound scan can be useful in diagnosing deep venous thrombosis (DVT), but it is unlikely to be necessary for a patient with cellulitis who is otherwise well and has a low Wells’ score. The Wells’ score is a tool used to assess the likelihood of DVT based on clinical features.

    • This question is part of the following fields:

      • Dermatology
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  • Question 109 - Which one of the following statement regarding the 1977 Abortion Act is true?...

    Incorrect

    • Which one of the following statement regarding the 1977 Abortion Act is true?

      Your Answer:

      Correct Answer: It states that an abortion may be performed if the pregnancy presents a risk to the physical or mental health of any existing children

      Explanation:

      Termination of Pregnancy in the UK

      The UK’s current abortion law is based on the 1967 Abortion Act, which was amended in 1990 to reduce the upper limit for termination from 28 weeks to 24 weeks gestation. To perform an abortion, two registered medical practitioners must sign a legal document, except in emergencies where only one is needed. The procedure must be carried out by a registered medical practitioner in an NHS hospital or licensed premise.

      The method used to terminate a pregnancy depends on the gestation period. For pregnancies less than nine weeks, mifepristone (an anti-progestogen) is administered, followed by prostaglandins 48 hours later to stimulate uterine contractions. For pregnancies less than 13 weeks, surgical dilation and suction of uterine contents is used. For pregnancies more than 15 weeks, surgical dilation and evacuation of uterine contents or late medical abortion (inducing ‘mini-labour’) is used.

      The 1967 Abortion Act outlines the circumstances under which a person shall not be guilty of an offence under the law relating to abortion. These include if two registered medical practitioners are of the opinion, formed in good faith, that the pregnancy has not exceeded its 24th week and that the continuance of the pregnancy would involve risk, greater than if the pregnancy were terminated, of injury to the physical or mental health of the pregnant woman or any existing children of her family. The limits do not apply in cases where it is necessary to save the life of the woman, there is evidence of extreme fetal abnormality, or there is a risk of serious physical or mental injury to the woman.

    • This question is part of the following fields:

      • Reproductive Medicine
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  • Question 110 - A 70-year-old male has been admitted to the cardiology ward following his presentation...

    Incorrect

    • A 70-year-old male has been admitted to the cardiology ward following his presentation to the emergency department with palpitations and dyspnoea. After further investigations, he was diagnosed with atrial fibrillation and prescribed digoxin for rate control. What is the recommended frequency for routine drug monitoring in this case?

      Your Answer:

      Correct Answer: No routine monitoring required

      Explanation:

      Digoxin levels do not require regular monitoring, unless there is suspicion of toxicity. As this patient is commencing digoxin and has no signs of toxicity, routine monitoring is unnecessary. It is not necessary to measure digoxin levels every month until they have stabilized, nor is it appropriate to monitor the drug every 2 weeks for the first 3 months. Routine monitoring is also not required annually throughout the course of treatment.

      Understanding Digoxin and Its Toxicity

      Digoxin is a medication used for rate control in atrial fibrillation and for improving symptoms in heart failure patients. It works by decreasing conduction through the atrioventricular node and increasing the force of cardiac muscle contraction. However, it has a narrow therapeutic index and requires monitoring for toxicity.

      Toxicity may occur even when the digoxin concentration is within the therapeutic range. Symptoms of toxicity include lethargy, nausea, vomiting, anorexia, confusion, yellow-green vision, arrhythmias, and gynaecomastia. Hypokalaemia is a classic precipitating factor, as it allows digoxin to more easily bind to the ATPase pump and increase its inhibitory effects. Other factors that may contribute to toxicity include increasing age, renal failure, myocardial ischaemia, electrolyte imbalances, hypoalbuminaemia, hypothermia, hypothyroidism, and certain medications such as amiodarone, quinidine, and verapamil.

      Management of digoxin toxicity involves the use of Digibind, correction of arrhythmias, and monitoring of potassium levels. It is important to recognize the potential for toxicity and monitor patients accordingly to prevent adverse outcomes.

    • This question is part of the following fields:

      • Pharmacology/Therapeutics
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  • Question 111 - As a foundation doctor on the neonatal ward, you are updating a prescription...

    Incorrect

    • As a foundation doctor on the neonatal ward, you are updating a prescription chart for a premature baby born at twenty-seven weeks who is in poor condition. While reviewing the chart, you come across caffeine as one of the medications prescribed. Can you explain the purpose of caffeine in neonatal care?

      Your Answer:

      Correct Answer: Aiding weaning off a ventilator

      Explanation:

      Newborn babies can benefit from caffeine as it acts as a respiratory stimulant. It is also used to help neonates transition off a ventilator. Sildenafil, known as Viagra, is typically used to treat erectile dysfunction in adults, but it can also be used to treat pulmonary hypertension in neonates. The approach to addressing distress in newborns depends on the underlying cause, which is often related to respiratory or pain issues. Gaviscon and ranitidine are sometimes used to treat gastro-oesophageal reflux, although this is not an approved use. Necrotising enterocolitis is more prevalent in premature babies and can be treated through medical interventions, such as resting the gut, or surgical interventions, such as resection.

      Surfactant Deficient Lung Disease in Premature Infants

      Surfactant deficient lung disease (SDLD), previously known as hyaline membrane disease, is a condition that affects premature infants. It occurs due to the underproduction of surfactant and the immaturity of the lungs’ structure. The risk of SDLD decreases with gestation, with 50% of infants born at 26-28 weeks and 25% of infants born at 30-31 weeks being affected. Other risk factors include male sex, diabetic mothers, Caesarean section, and being the second born of premature twins.

      The clinical features of SDLD are similar to those of respiratory distress in newborns, including tachypnea, intercostal recession, expiratory grunting, and cyanosis. Chest x-rays typically show a ground-glass appearance with an indistinct heart border.

      Prevention during pregnancy involves administering maternal corticosteroids to induce fetal lung maturation. Management of SDLD includes oxygen therapy, assisted ventilation, and exogenous surfactant given via an endotracheal tube. With proper management, the prognosis for infants with SDLD is generally good.

    • This question is part of the following fields:

      • Paediatrics
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  • Question 112 - A 56-year-old woman with COPD has been recommended an inhaled corticosteroid. What is...

    Incorrect

    • A 56-year-old woman with COPD has been recommended an inhaled corticosteroid. What is the primary advantage of using inhaled corticosteroids for treating COPD patients?

      Your Answer:

      Correct Answer: Reduced frequency of exacerbations

      Explanation:

      Inhaled corticosteroids are used to decrease the frequency of exacerbations in patients with COPD.

      NICE guidelines recommend smoking cessation advice, annual influenza and one-off pneumococcal vaccinations, and pulmonary rehabilitation for COPD patients. Bronchodilator therapy is first-line treatment, with the addition of LABA and LAMA for patients without asthmatic features and LABA, ICS, and LAMA for those with asthmatic features. Theophylline is recommended after trials of bronchodilators or for patients who cannot use inhaled therapy. Azithromycin prophylaxis is recommended in select patients. Mucolytics should be considered for patients with a chronic productive cough. Loop diuretics and long-term oxygen therapy may be used for cor pulmonale. Smoking cessation and long-term oxygen therapy may improve survival in stable COPD patients. Lung volume reduction surgery may be considered in selected patients.

    • This question is part of the following fields:

      • Respiratory Medicine
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  • Question 113 - A 45-year-old woman had an anterior myocardial infarction. She has a body mass...

    Incorrect

    • A 45-year-old woman had an anterior myocardial infarction. She has a body mass index (BMI) of 30 kg/m2, smokes 10 cigarettes per day and admits to a high-sugar diet and minimal exercise.
      Which of the following non-pharmacological interventions will be most helpful in reducing her risk for a future ischaemic event?

      Your Answer:

      Correct Answer: Stopping smoking

      Explanation:

      Reducing the Risk of Vascular Events: Lifestyle Interventions

      Smoking, high salt intake, poor diet, lack of exercise, and obesity are all risk factors for vascular events such as heart attacks and strokes. However, making lifestyle changes can significantly reduce the risk of these events.

      Stopping smoking is the most effective non-pharmacological intervention, as it reduces the risk of heart disease by 2-3 times compared to those who continue to smoke.

      Reducing salt intake to 3-6 g/day can also help, as both high and low salt intake can increase the risk of vascular events.

      Improving diet by controlling calorie intake can lead to weight loss, improved blood sugar control, and better lipid profiles.

      Regular exercise, such as 30 minutes of activity five times a week, can lower the risk of vascular events by 30%.

      Finally, weight reduction is important, as obesity increases the risk of heart attacks and strokes at a younger age and can lead to higher mortality rates.

      Overall, making these lifestyle changes can significantly reduce the risk of vascular events and improve overall health.

    • This question is part of the following fields:

      • Cardiovascular
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  • Question 114 - A 36-year-old woman comes to the clinic with a lump in her left...

    Incorrect

    • A 36-year-old woman comes to the clinic with a lump in her left breast. She has recently lost approximately 1.5 stone in weight by attending a weight loss program. During the examination, a firm lump is detected in her left breast that is not mobile but not attached to the underlying muscle. She recalls being hit by a squash ball in this area a few months ago. What is the probable reason for her lump?

      Your Answer:

      Correct Answer: Fat necrosis

      Explanation:

      When a woman presents with a breast lump, fat necrosis should be considered as a possible diagnosis if there is a history of trauma to the area. This condition typically presents as a firm lump that may be accompanied by bruising. Fibroadenomas, on the other hand, are more commonly seen in younger women and present as a mobile but firm lump that can be easily moved during examination. Breast cysts are fluid-filled masses that may be detected if they are large enough and can fluctuate or transilluminate. Breast abscesses are typically seen in breastfeeding women and present as a hot, tender swelling. While breast cancer is unlikely based on the clinical history, all women with a breast lump should be referred to a specialist for confirmation of diagnosis through triple assessment. It is important to note that intentional weight loss, as in this case, should not be considered a factor in the diagnosis.

      Understanding Fat Necrosis of the Breast

      Fat necrosis of the breast is a condition that affects up to 40% of cases and is often caused by trauma. This condition can be mistaken for breast cancer due to its physical features, such as a mass that may initially increase in size. It is important to understand that fat necrosis is not cancerous and can be treated with proper care.

    • This question is part of the following fields:

      • Haematology/Oncology
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  • Question 115 - A 48-year-old man comes to the General Practitioner complaining of feeling dizzy and...

    Incorrect

    • A 48-year-old man comes to the General Practitioner complaining of feeling dizzy and experiencing shortness of breath during physical activity. He has a bicuspid aortic valve and is waiting for valve replacement surgery.
      Which of the following murmurs would be the most likely to occur in this patient?

      Your Answer:

      Correct Answer: Ejection systolic murmur loudest over the 2nd intercostal space, right sternal edge

      Explanation:

      Differentiating Heart Murmurs Based on Location and Type

      Heart murmurs are abnormal sounds heard during a heartbeat and can indicate various cardiac conditions. The location and type of murmur can help differentiate between different conditions.

      Ejection systolic murmur loudest over the 2nd intercostal space, right sternal edge: This is typical for aortic stenosis, which is more likely to occur in a bicuspid aortic valve. The murmur may radiate to the carotids. Pulmonary stenosis, hypertrophic obstructive cardiomyopathy, and atrial septal defect can also cause this type of murmur, but the location would be different.

      Ejection systolic murmur loudest over the 2nd intercostal space, left sternal edge: This location is typical for pulmonary stenosis, not aortic stenosis. The patient’s history indicates symptomatic aortic stenosis, making this finding inconsistent.

      Early diastolic murmur loudest over the 3rd intercostal space, left sternal edge: This type and location of murmur is typical for aortic regurgitation, not aortic stenosis. The location is Erb’s point, where S1 and S2 should both be heard.

      Mid-diastolic murmur loudest over the apex: This type and location of murmur is typical for mitral stenosis, not aortic stenosis. The apex is the mitral area, located at the 5th intercostal space in the midclavicular line.

      Pansystolic murmur loudest over the apex: This type and location of murmur is typical for mitral regurgitation, not aortic stenosis. The apex is the mitral area, located at the 5th intercostal space in the midclavicular line.

    • This question is part of the following fields:

      • Cardiovascular
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  • Question 116 - An 80-year-old man arrives at the Emergency Department after experiencing a 3-hour episode...

    Incorrect

    • An 80-year-old man arrives at the Emergency Department after experiencing a 3-hour episode of right facial weakness with forehead sparing. He has a medical history of polymyalgia rheumatica and haemophilia B and takes low dose prednisolone as his only regular medication. He has been a smoker for the past 20 years, consuming 20 cigarettes a day. Upon examination, he reports that his neurological symptoms have resolved 30 minutes ago. What is the best initial course of action?

      Your Answer:

      Correct Answer: Admit and arrange a CT head

      Explanation:

      If a patient with a bleeding disorder or on anticoagulants such as warfarin or DOACs is suspected of having a TIA, immediate admission for imaging is necessary to rule out a hemorrhage. In this case, the patient’s age, sex, smoking history, and bleeding disorder increase the likelihood of a TIA. The patient’s history of polymyalgia rheumatica and low dose prednisolone management are not relevant to the diagnosis or management of TIA.

      Admission and a CT head are necessary due to the patient’s history of haemophilia B, which increases the risk of hemorrhagic causes of stroke-like symptoms. Aspirin should not be given immediately as it may worsen bleeding in patients with bleeding disorders or on anticoagulants. Reassuring and managing as an outpatient is not appropriate for either hemorrhagic or ischemic causes of TIA, both of which are possible in this case. Thrombectomy is not the appropriate management for this patient as he is at high risk of hemorrhagic stroke, and imaging is necessary to rule out a bleed.

      A transient ischaemic attack (TIA) is a brief period of neurological deficit caused by a vascular issue, lasting less than an hour. The original definition of a TIA was based on time, but it is now recognized that even short periods of ischaemia can result in pathological changes to the brain. Therefore, a new ’tissue-based’ definition is now used. The clinical features of a TIA are similar to those of a stroke, but the symptoms resolve within an hour. Possible features include unilateral weakness or sensory loss, aphasia or dysarthria, ataxia, vertigo, or loss of balance, visual problems, and sudden transient loss of vision in one eye (amaurosis fugax).

      NICE recommends immediate antithrombotic therapy with aspirin 300 mg unless the patient has a bleeding disorder or is taking an anticoagulant. If the patient has had more than one TIA or has a suspected cardioembolic source or severe carotid stenosis, specialist review is necessary. Urgent assessment is required within 24 hours for patients who have had a suspected TIA in the last 7 days. Referral for specialist assessment is necessary as soon as possible within 7 days for patients who have had a suspected TIA more than a week previously. Neuroimaging and carotid imaging are recommended, and antithrombotic therapy is necessary. Carotid artery endarterectomy should only be considered if the carotid stenosis is greater than 70% according to ECST criteria or greater than 50% according to NASCET criteria.

    • This question is part of the following fields:

      • Neurology
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  • Question 117 - A 32-year-old man is brought to the emergency department by his physician due...

    Incorrect

    • A 32-year-old man is brought to the emergency department by his physician due to bone pain, weakness, and splenomegaly. He has been experiencing increasing fatigue and weakness while performing his daily tasks over the past few weeks. During the examination, he appears extremely pale and has petechiae on his lower limbs. After a bone marrow sample is taken, he is diagnosed with acute promyelocytic leukemia (APML). What is the most probable finding on his blood film?

      Your Answer:

      Correct Answer: Auer rods

      Explanation:

      A finding of Auer rods on a blood film strongly indicates the presence of acute promyelocytic leukemia.

      The correct answer is ‘Auer rods’. This patient has been diagnosed with APML, and the most common finding on a blood film associated with this is Auer rods. These are needle-like structures that are large, pink or red stained and can be seen within the cytoplasm of myeloid blast cells.

      ‘Tear-drop’ poikilocytes are typically found in myelofibrosis, which is characterized by flat, elongated red blood cells that resemble a tear-drop in shape. This occurs due to the squeezing of cells through fibrotic tissue in bone marrow in myelofibrotic disorders.

      Smear cells are usually seen in chronic lymphocytic leukemia (CLL), which are remnants of cells that lack identifiable plasma membrane or nuclear structure.

      Spherocytes are generally found in hereditary spherocytosis or autoimmune hemolytic anemia, which are red blood cells that are sphere-shaped and more fragile than normal red blood cells due to abnormalities in the red cell membrane.

      Acute myeloid leukaemia is a common form of acute leukaemia in adults that may occur as a primary disease or following a myeloproliferative disorder. Symptoms are related to bone marrow failure and include anaemia, neutropenia, thrombocytopenia, splenomegaly, and bone pain. Poor prognostic features include age over 60, >20% blasts after first course of chemo, and deletions of chromosome 5 or 7. Acute promyelocytic leukaemia M3 is associated with t(15;17) and has a good prognosis. The French-American-British classification system includes seven subtypes.

    • This question is part of the following fields:

      • Haematology/Oncology
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  • Question 118 - A 28-year-old pregnant woman is brought into the Emergency Department with acute confusion...

    Incorrect

    • A 28-year-old pregnant woman is brought into the Emergency Department with acute confusion and abnormal behaviour. Her husband says she has been well till today. There is no past medical history of note and she takes no regular medication.
      On examination, she is febrile with a temperature of 38.7 °C. Her heart rate is 125 bpm with a blood pressure of 115/95 mmHg. Chest sounds are clear and heart sounds are normal. She has a soft abdomen with a palpable uterus in keeping with 16 weeks’ gestation.
      Investigations:
      Investigation Result Normal value
      Haemoglobin (Hb) 92 g/l 115–155 g/l
      White cell count (WCC) 10.3 × 109/l 4.0–11.0 × 109/l
      Neutrophils 7.1 × 109/l 2.5–7.5 × 109/l
      Lymphocytes 0.9 × 109/l 0.8–5.0 × 109/l
      Platelets (PLT) 57 × 109/l 150–400 × 109/l
      Sodium (Na+) 136 mmol/l 135–145 mmol/l
      Potassium (K+) 4.5 mmol/l 3.5–5.0 mmol/l
      Urea 17.3 mmol/l 1.8–7.1 mmol/l
      Creatinine (Cr) 225µmol/l 50–120 µmol/l
      Estimated glomerular filtration rate (eGFR) 34 60+
      Bilirubin 20µmol/l 1–22 µmol/l
      Alanine aminotransferase (ALT) 35 U/l 7–55 U/l
      Alkaline phosphatase (ALP) 85 U/l 30–150 U/l
      Albumin 40 g/l 35–55 g/l
      C-reactive protein (CRP) 9 mg/l < 10 mg/l
      Which of the following is the best investigation to confirm the likely diagnosis?

      Select ONE option only

      Your Answer:

      Correct Answer: Blood film

      Explanation:

      Investigations for Thrombotic Thrombocytopenic Purpura in a Pregnant Patient with Fever and Confusion

      Thrombotic thrombocytopenic purpura (TTP) should be considered in a pregnant patient presenting with fever, acute kidney injury, cerebral dysfunction, thrombocytopenia, and microangiopathic hemolytic anemia. To confirm the diagnosis, a blood film is needed to show the presence of schistocytes from the destruction of red blood cells. An abdominal ultrasound may be considered, but it will not aid in identifying the underlying diagnosis. Although a blood culture is appropriate, it would not confirm the diagnosis. A CT head or lumbar puncture may be useful in excluding visible organic pathology, but they do not play a role in the diagnosis of TTP.

    • This question is part of the following fields:

      • Haematology/Oncology
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  • Question 119 - A 25-year-old student presents to his General Practitioner with symptoms of a flu-like...

    Incorrect

    • A 25-year-old student presents to his General Practitioner with symptoms of a flu-like illness. He reports not having eaten for the past 48 hours. During examination, mild jaundice is observed, but no other significant physical findings are noted. The patient's total serum bilirubin level is elevated at 60 μmol/l (reference range < 20 μmol/l), while the other liver function tests (LFTs) are normal. Full blood count (FBC), urea and electrolytes, and haptoglobins are within normal limits. What is the most likely diagnosis for this clinical presentation?

      Your Answer:

      Correct Answer: Gilbert syndrome

      Explanation:

      Differential Diagnosis: Jaundice and Abdominal Symptoms

      Gilbert Syndrome:
      Gilbert syndrome is an inherited condition that can manifest as jaundice on clinical examination. Patients may also experience non-specific symptoms such as abdominal cramps, fatigue, and malaise. Fasting, febrile illness, alcohol, or exercise can exacerbate jaundice in patients with Gilbert syndrome. Diagnosis is based on a thorough history and physical examination, as well as blood tests that show unconjugated hyperbilirubinaemia.

      Haemolytic Anaemia:
      Haemolysis is the premature destruction of erythrocytes, which can lead to anaemia if bone marrow activity cannot compensate for erythrocyte loss. Mild haemolysis can be asymptomatic, while severe haemolysis can cause life-threatening symptoms such as angina and cardiopulmonary decompensation. Changes in lactate dehydrogenase and serum haptoglobin levels are the most sensitive general tests for haemolytic anaemia.

      Hepatitis A:
      Hepatitis A is a viral infection that results almost exclusively from ingestion, typically through faecal-oral transmission. Symptoms include fatigue, anorexia, nausea, and vomiting. LFT abnormalities are common, and diagnosis is based on serologic testing for immunoglobulin M (IgM) antibody to HAV.

      Hepatitis B:
      Hepatitis B is a viral infection that is transmitted haematogenously and sexually. Symptoms include fatigue, anorexia, nausea, and vomiting. LFT abnormalities are common, and diagnosis is based on serologic testing for hepatitis B surface antigen (HBsAg).

      Cholecystitis:
      Cholecystitis is inflammation of the gall bladder that occurs most commonly because of an obstruction of the cystic duct by gallstones arising from the gall bladder. Symptoms include upper abdominal pain, nausea, vomiting, and fever. Signs of peritoneal irritation may also be present.

      Conclusion:
      In summary, the differential diagnosis of jaundice and abdominal symptoms includes Gilbert syndrome, haemolytic anaemia, hepatitis A, hepatitis B, and cholecystitis. Diagnosis is based on a thorough history and physical examination, as well as blood tests and serologic testing as appropriate. Treatment

    • This question is part of the following fields:

      • Gastroenterology/Nutrition
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  • Question 120 - A 50-year-old woman presents to the Emergency Department with sudden, painless loss of...

    Incorrect

    • A 50-year-old woman presents to the Emergency Department with sudden, painless loss of vision in her right eye. On examination, fundoscopy reveals a pale retina with a cherry-red spot at the macula in her right eye. Her left eye is normal.
      What is the most likely diagnosis?

      Your Answer:

      Correct Answer: Central retinal-artery occlusion (CRAO)

      Explanation:

      Differentiating Eye Conditions: A Brief Overview

      Central retinal-artery occlusion (CRAO) is characterized by a sudden loss of vision due to the lack of blood supply to the inner layer of the retina. On fundoscopy, the retina appears pale with a ‘cherry-red spot’ at the macula.

      Age-related macular degeneration (AMD) is the most common cause of irreversible vision loss in the developed world. However, deterioration in vision is usually gradual in AMD unless there is a retinal haemorrhage, which would be seen on fundoscopy.

      Central retinal-vein occlusion (CRVO) results in retinal hypoxia and is characterized by tortuous vessels, retinal-vein engorgement, haemorrhages, cotton-wool spots, and optic disc swelling.

      Glaucoma is a progressive optic neuropathy that can result in irreversible loss of nerve fibres if left untreated. On fundoscopy, you may see ‘cupping of the optic disc or an increased cup-to-disc ratio.

      Retinal detachment refers to the separation of the inner layers of the retina from the underlying retinal pigment epithelium. It may present with four Fs: floaters, flashing lights (photopsia), field loss, and fall in visual acuity. Retinal detachment is one of the most time-critical eye emergencies encountered in the emergency setting.

      In summary, understanding the different presentations and fundoscopic findings of these eye conditions is crucial in making an accurate diagnosis and providing appropriate management.

    • This question is part of the following fields:

      • Ophthalmology
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  • Question 121 - During your FY2 rotation in General Practice, you saw a 75-year-old man in...

    Incorrect

    • During your FY2 rotation in General Practice, you saw a 75-year-old man in your GP clinic who complained of blurred vision in his right eye for the past 4 months. He finally decided to come to see you because he felt his vision was now very distorted. On dilated fundoscopy, the left eye appeared normal, but you could see drusen at the macula in the right eye. You suspect age-related macular degeneration.
      What is the ONE next step in management for this patient?

      Your Answer:

      Correct Answer: Refer to ophthalmology urgently within 1 week

      Explanation:

      It is essential to refer patients suspected of having AMD to ophthalmology urgently within 1 week for a formal diagnosis. This is because if the diagnosis is wet AMD, anti-VEGF injections can be administered, which will improve the patient’s long-term visual outcome. Even if drusen is present, which is more indicative of dry AMD, an urgent referral should still be made within 1 week. Delaying the referral for a month will postpone the formal diagnosis and treatment commencement for the patient. While multi-vitamins may be beneficial for dry AMD, it is not the next step in management. Atorvastatin is used to lower blood cholesterol levels and is not effective in treating drusen.

      Age-related macular degeneration (ARMD) is a common cause of blindness in the UK, characterized by the degeneration of the central retina (macula) and the formation of drusen. It is more prevalent in females and is strongly associated with advancing age, smoking, family history, and conditions that increase the risk of ischaemic cardiovascular disease. ARMD can be classified into two forms: dry and wet. Dry ARMD is more common and is characterized by drusen, while wet ARMD is characterized by choroidal neovascularisation and carries a worse prognosis. Clinical features of ARMD include subacute onset of visual loss, difficulties in dark adaptation, and visual disturbances such as photopsia and glare.

      To diagnose ARMD, slit-lamp microscopy and color fundus photography are used to identify any pigmentary, exudative, or haemorrhagic changes affecting the retina. Fluorescein angiography and indocyanine green angiography may also be used to visualize changes in the choroidal circulation. Treatment for dry ARMD involves a combination of zinc with anti-oxidant vitamins A, C, and E, which has been shown to reduce disease progression by around one third. For wet ARMD, anti-VEGF agents such as ranibizumab, bevacizumab, and pegaptanib are used to limit disease progression and stabilize or reverse visual loss. Laser photocoagulation may also be used to slow progression, but anti-VEGF therapies are usually preferred due to the risk of acute visual loss after treatment.

      In summary, ARMD is a common cause of blindness in the UK that is strongly associated with advancing age, smoking, and family history. It can be classified into dry and wet forms, with wet ARMD carrying a worse prognosis. Diagnosis involves the use of various imaging techniques, and treatment options include a combination of zinc and anti-oxidant vitamins for dry ARMD and anti-VEGF agents or laser photocoagulation for wet ARMD.

    • This question is part of the following fields:

      • Ophthalmology
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  • Question 122 - A 68-year-old man presents with lower back pain. He has a medical history...

    Incorrect

    • A 68-year-old man presents with lower back pain. He has a medical history of prostate cancer, asthma, diabetes, and hypertension. The pain is radiating down his right leg and he is experiencing reduced power in that leg. Additionally, he has a decreased anal tone. Although the lumbar spine x-ray shows no apparent fracture, what would be the most appropriate next investigation to perform?

      Your Answer:

      Correct Answer: MRI lumbosacral spine

      Explanation:

      Lower back pain accompanied by lower limb pain, limb weakness, numbness or tingling, and decreased perianal tone are red flags that suggest spinal cord compression. In this case, the patient has a history of prostate cancer, which further raises suspicion. Urgent MRI is necessary to rule out spinal cord compression, and the results should be discussed with the on-call neurosurgical team. Additional x-rays or ultrasound would not be helpful, as MRI is the preferred diagnostic tool.

      Neoplastic Spinal Cord Compression: An Oncological Emergency

      Neoplastic spinal cord compression is a medical emergency that affects around 5% of cancer patients. The majority of cases are due to vertebral body metastases, resulting in extradural compression. This condition is more common in patients with lung, breast, and prostate cancer.

      The earliest and most common symptom of neoplastic spinal cord compression is back pain, which may worsen when lying down or coughing. Other symptoms include lower limb weakness and sensory changes such as numbness and sensory loss. The neurological signs depend on the level of the lesion, with lesions above L1 resulting in upper motor neuron signs in the legs and a sensory level. Lesions below L1 usually cause lower motor neuron signs in the legs and perianal numbness. Tendon reflexes tend to be increased below the level of the lesion and absent at the level of the lesion.

      An urgent MRI is recommended within 24 hours of presentation, according to the 2019 NICE guidelines. High-dose oral dexamethasone is used for management, and urgent oncological assessment is necessary for consideration of radiotherapy or surgery.

      In summary, neoplastic spinal cord compression is a serious condition that requires prompt diagnosis and management to prevent further neurological damage.

    • This question is part of the following fields:

      • Neurology
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  • Question 123 - An elderly man, aged 74, with metastatic small cell lung cancer has been...

    Incorrect

    • An elderly man, aged 74, with metastatic small cell lung cancer has been admitted to the hospice for symptom management. He is currently experiencing persistent hiccups that are difficult to control. What is the best course of action for managing this symptom?

      Your Answer:

      Correct Answer: Chlorpromazine

      Explanation:

      Palliative Care Prescribing for Hiccups

      Hiccups can be a distressing symptom for patients receiving palliative care. To manage this symptom, healthcare professionals may prescribe medications such as chlorpromazine, which is licensed for the treatment of intractable hiccups. Other medications that may be used include haloperidol and gabapentin. In cases where there are hepatic lesions, dexamethasone may also be prescribed. It is important to note that the choice of medication will depend on the individual patient’s needs and medical history. Proper management of hiccups can improve the patient’s quality of life and provide relief from discomfort.

    • This question is part of the following fields:

      • Respiratory Medicine
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  • Question 124 - An 85-year-old man complains of increasing back pain and overall weakness. An X-ray...

    Incorrect

    • An 85-year-old man complains of increasing back pain and overall weakness. An X-ray of his back reveals multiple vertebral collapses and lytic lesions.
      What is the most probable diagnosis?

      Your Answer:

      Correct Answer: Multiple myeloma

      Explanation:

      Understanding Multiple Myeloma: A Malignant Disease of Plasma Cells

      Multiple myeloma is a malignant disease of plasma cells that commonly affects adults aged over 60 years. It is characterized by the production of paraproteinaemia in the blood, which can affect multiple organs including the blood, bone, kidneys, and immune system. The most common symptoms of multiple myeloma include unexplained bone pain, hypercalcaemia, weight loss, hyperviscosity symptoms, spinal cord compression, and fever.

      On the other hand, osteoporosis is a condition characterized by low bone mass and deterioration of the structure of the bone tissue, resulting in bone fragility and susceptibility to fracture. Multiple vertebral collapses and lytic lesions are more sinister in nature and are commonly associated with multiple myeloma.

      Osteosarcoma, bone metastases, and chronic myeloblastic leukaemia (CML) are not related to multiple myeloma. Osteosarcoma is characterized by cortical destruction and the presence of a soft-tissue mass, while bone metastases usually lead to destruction of the cortex on plain radiographs. Symptoms of CML include fatigue, night sweats, weight loss, abdominal fullness, and left upper quadrant pain.

      In summary, understanding the symptoms and characteristics of multiple myeloma is crucial in diagnosing and treating this malignant disease of plasma cells.

    • This question is part of the following fields:

      • Haematology/Oncology
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  • Question 125 - You are assessing a 10-month-old infant with a viral upper respiratory tract infection....

    Incorrect

    • You are assessing a 10-month-old infant with a viral upper respiratory tract infection. Despite being clinically stable, the mother inquires about the child's development towards the end of the consultation. The infant is observed to point and babble 'mama' and 'dada', but has not yet developed any other words. She appears to be timid and cries when being examined. The infant has an early pincer grip and can roll from front to back, but is unable to sit without support. How would you evaluate her developmental progress?

      Your Answer:

      Correct Answer: Isolated delay in gross motor skills

      Explanation:

      A delay in gross motor skills is likely as most babies are able to sit without support by 7-8 months, but the other developmental features are normal for her age. If the delay persists at 12 months, referral to a paediatrician should be considered.

      Gross Motor Developmental Milestones

      Gross motor skills refer to the ability to use large muscles in the body for activities such as crawling, walking, running, and jumping. These skills are essential for a child’s physical development and are achieved through a series of developmental milestones.

      At 3 months, a baby should have little or no head lag when pulled to sit and should have good head control when lying on their abdomen. By 6 months, they should be able to lift and grasp their feet when lying on their back, pull themselves to a sitting position, and roll from front to back. At 9 months, they should be able to pull themselves to a standing position and crawl. By 12 months, they should be able to cruise and walk with one hand held. At 18 months, they should be able to walk unsupported and squat to pick up a toy. By 2 years, they should be able to run and walk up and down stairs holding onto a rail. At 3 years, they should be able to ride a tricycle using pedals and walk up stairs without holding onto a rail. By 4 years, they should be able to hop on one leg.

      It is important to note that while the majority of children crawl on all fours before walking, some children may bottom-shuffle, which is a normal variant that runs in families. These milestones serve as a guide for parents and healthcare professionals to monitor a child’s physical development and identify any potential delays or concerns.

    • This question is part of the following fields:

      • Paediatrics
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  • Question 126 - A 65-year-old woman with a history of hypertension and heart failure presents with...

    Incorrect

    • A 65-year-old woman with a history of hypertension and heart failure presents with atrial fibrillation. She is stable with a ventricular rate of 70. Which of the following drug options would be the most suitable for her?

      Your Answer:

      Correct Answer: Warfarin or direct oral anticoagulant (DOAC)

      Explanation:

      Treatment Options for Atrial Fibrillation: Warfarin, DOACs, Aspirin, Digoxin, Furosemide, and Lidocaine

      Patients with atrial fibrillation and a CHA2DS2-VASC score of 4 require anticoagulation to reduce the risk of a CVA. The two main options are warfarin and DOACs, but the choice depends on other co-morbidities and patient preference. Before starting warfarin, patients should be referred to the Anticoagulation Clinic and screened for contraindications.

      Aspirin has no benefit in atrial fibrillation, and digoxin should only be used for short-term rate control due to evidence of increased mortality with long-term use. Furosemide can help with symptoms and edema in heart failure but does not improve mortality. Lidocaine is only appropriate for ventricular arrhythmias in unstable patients and requires specialist support.

      In summary, the treatment options for atrial fibrillation vary depending on the patient’s individual circumstances and should be carefully considered by healthcare professionals.

    • This question is part of the following fields:

      • Cardiovascular
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  • Question 127 - Which one of the following is not a notifiable disease in the United...

    Incorrect

    • Which one of the following is not a notifiable disease in the United Kingdom?

      Your Answer:

      Correct Answer: HIV

      Explanation:

      Notifying authorities about HIV is not required.

      Notifiable Diseases in the UK

      In the UK, certain diseases are considered notifiable, meaning that the Local Health Protection Team must be notified if a case is suspected or confirmed. The Proper Officer at the team will then inform the Health Protection Agency on a weekly basis. Notifiable diseases include acute encephalitis, acute infectious hepatitis, acute meningitis, acute poliomyelitis, anthrax, botulism, brucellosis, cholera, COVID-19, diphtheria, enteric fever, food poisoning, haemolytic uraemic syndrome, infectious bloody diarrhoea, invasive group A streptococcal disease, legionnaires disease, leprosy, malaria, measles, meningococcal septicaemia, mumps, plague, rabies, rubella, severe acute respiratory syndrome, scarlet fever, smallpox, tetanus, tuberculosis, typhus, viral haemorrhagic fever, whooping cough, and yellow fever.

      It is important to note that HIV is not a notifiable disease in the UK, and in April 2010, dysentery, ophthalmia neonatorum, leptospirosis, and relapsing fever were removed from the list of notifiable diseases. The purpose of notifiable diseases is to monitor and control the spread of infectious diseases in the population. By requiring healthcare professionals to report cases, public health officials can track outbreaks and take appropriate measures to prevent further transmission.

    • This question is part of the following fields:

      • Infectious Diseases
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  • Question 128 - A 55-year-old man presented to his GP with two instances of painless visible...

    Incorrect

    • A 55-year-old man presented to his GP with two instances of painless visible haematuria. He was subsequently referred to urology for biopsy and flexible cystoscopy, which revealed a transitional cell carcinoma of the bladder. What is the most significant risk factor associated with this condition?

      Your Answer:

      Correct Answer: Smoking

      Explanation:

      Risk Factors for Bladder Cancer

      Bladder cancer is a type of cancer that affects the bladder, and there are different types of bladder cancer. The most common type is urothelial (transitional cell) carcinoma, and the risk factors for this type of bladder cancer include smoking, exposure to aniline dyes, rubber manufacture, and cyclophosphamide. Smoking is the most important risk factor in western countries, with a hazard ratio of around 4. Exposure to aniline dyes, such as working in the printing and textile industry, can also increase the risk of bladder cancer. Rubber manufacture and cyclophosphamide are also risk factors for urothelial carcinoma.

      On the other hand, squamous cell carcinoma of the bladder has different risk factors. Schistosomiasis and smoking are the main risk factors for this type of bladder cancer. Schistosomiasis is a parasitic infection that can cause inflammation and damage to the bladder, which can increase the risk of developing squamous cell carcinoma. Smoking is also a risk factor for squamous cell carcinoma, as it can cause changes in the cells of the bladder lining that can lead to cancer.

      In summary, the risk factors for bladder cancer depend on the type of cancer. Urothelial carcinoma is mainly associated with smoking, exposure to aniline dyes, rubber manufacture, and cyclophosphamide, while squamous cell carcinoma is mainly associated with schistosomiasis and smoking. It is important to be aware of these risk factors and take steps to reduce your risk of developing bladder cancer.

    • This question is part of the following fields:

      • Renal Medicine/Urology
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  • Question 129 - A 55-year-old male carpenter visits the GP clinic complaining of right foot drop....

    Incorrect

    • A 55-year-old male carpenter visits the GP clinic complaining of right foot drop. He has a medical history of type 2 diabetes mellitus and hypertension. During the examination, the doctor observed weakness in the right foot dorsiflexion and eversion. The patient also reported sensory loss on the dorsum of the right foot and lower lateral part of the right leg. No other neurological deficits were detected. What is the probable diagnosis?

      Your Answer:

      Correct Answer: Common peroneal nerve palsy

      Explanation:

      The patient is likely suffering from common peroneal nerve palsy, which may be caused by diabetes. This condition can result in weakness of foot dorsiflexion and foot eversion. L5 nerve root compression is a possible cause of foot drop, but it does not lead to weakness of foot eversion, so it is not the correct option. Sciatic nerve palsy can also cause foot drop, but it can also affect other nerves, resulting in weakness of foot plantar flexion and sensory loss of the sole of the foot, which is not present in this case. Stroke is a central cause of foot drop, but the absence of upper motor neuron signs suggests common peroneal nerve pathology is more likely. Polyneuropathy involves multiple nerves, so it is not the correct option.

      Understanding Common Peroneal Nerve Lesion

      A common peroneal nerve lesion is a type of nerve injury that often occurs at the neck of the fibula. This nerve is a branch of the sciatic nerve, which divides into the tibial and common peroneal nerves. The most notable symptom of this type of nerve damage is foot drop, which is characterized by weakness or paralysis of the muscles that lift the foot.

      In addition to foot drop, other symptoms of a common peroneal nerve lesion may include weakness in foot dorsiflexion and eversion, as well as the extensor hallucis longus muscle. Sensory loss may also occur over the dorsum of the foot and the lower lateral part of the leg, and there may be wasting of the anterior tibial and peroneal muscles.

      Overall, understanding the symptoms of a common peroneal nerve lesion can help individuals recognize and seek treatment for this type of nerve injury. With proper care and management, it may be possible to improve symptoms and prevent further damage to the affected nerve.

    • This question is part of the following fields:

      • Neurology
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  • Question 130 - A 10-year-old girl presents to the Emergency Department after suffering a head injury...

    Incorrect

    • A 10-year-old girl presents to the Emergency Department after suffering a head injury falling from a tree. She has remained conscious and her Glasgow Coma Score (GCS) has been 15 since the accident. She is not vomiting.
      On examination, there is no focal neurological deficit. An area of bruising is seen behind her left ear and she has a headache. No other injuries are observed.
      What is the most appropriate initial investigation for this patient?

      Your Answer:

      Correct Answer: Computed tomography (CT) head

      Explanation:

      The patient requires a CT head scan within an hour of the accident, as per NICE guidelines. A basal skull fracture, which can be fatal, may be caused by high-impact mechanisms and can present with symptoms such as bruising behind the ear, bruising around the eyes, blood behind the eardrum, or cerebral spinal fluid rhinorrhoea. Optic-nerve entrapment may also occur if the fracture is displaced, leading to changes in vision. Patients are at an increased risk of developing meningitis. An MRI head is not the primary investigation of choice for acute clinically important brain injuries due to safety, logistic, and resource reasons. A lateral cervical spine X-ray may be required for a thorough assessment of the C-spine, but a CT head and neck would be easier to perform if imaging of the neck is necessary. A plain skull X-ray may be used for non-accidental brain injury in children to avoid high-dose radiation from a CT scan, but it should not be used to diagnose brain trauma without consulting a neuroscience unit. If red flags are present, a CT head is necessary to exclude severe intracranial pathology.

    • This question is part of the following fields:

      • Paediatrics
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  • Question 131 - A 54-year-old man with a recent diagnosis of fatty liver disease presents at...

    Incorrect

    • A 54-year-old man with a recent diagnosis of fatty liver disease presents at the clinic. During a liver screen to determine the cause of his condition, his hepatitis B serology is tested and the results are as follows:
      - HBsAg: Negative
      - HBcAg: Negative
      - Anti-HBs IgG: Positive
      - Anti-HBc IgG: Positive

      What is his hepatitis B status?

      Your Answer:

      Correct Answer: Cleared previous infection

      Explanation:

      To determine a patient’s immune status for Hepatitis B, a systematic approach is necessary. First, antigenic results are examined to determine if the virus is present, followed by antibody results to assess the body’s response to the virus. In this case, negative results for both HBsAg and HBcAg indicate no active infection, while the presence of antibodies to both antigens suggests a previous infection that has been cleared, resulting in immunity.

      In acute infection, both HBsAg and HBcAg are positive, with a limited antibody response. Chronic infection is characterized by ongoing viral infection and an inadequate immune response, resulting in the virus not being cleared. Immunization exposes the immune system to purified viral protein, resulting in the production of anti-HBs antibodies and conferring some immunity.

      To distinguish between immunization and previous infection, the absence of anti-HBc antibodies indicates immunization, as there are no viral antigens present. If an individual has never been exposed to any Hepatitis B antigens, all serology tests would be negative.

      Interpreting hepatitis B serology is an important skill that is still tested in medical exams. It is crucial to keep in mind a few key points. The surface antigen (HBsAg) is the first marker to appear and triggers the production of anti-HBs. If HBsAg is present for more than six months, it indicates chronic disease, while its presence for one to six months implies acute disease. Anti-HBs indicates immunity, either through exposure or immunization, and is negative in chronic disease. Anti-HBc indicates previous or current infection, with IgM anti-HBc appearing during acute or recent hepatitis B infection and persisting IgG anti-HBc. HbeAg is a marker of infectivity and HBV replication.

      To illustrate, if someone has been previously immunized, their anti-HBs will be positive, while all other markers will be negative. If they had hepatitis B more than six months ago but are not a carrier, their anti-HBc will be positive, and HBsAg will be negative. However, if they are now a carrier, both anti-HBc and HBsAg will be positive. If HBsAg is present, it indicates an ongoing infection, either acute or chronic if present for more than six months. On the other hand, anti-HBc indicates that the person has caught the virus, and it will be negative if they have been immunized.

    • This question is part of the following fields:

      • Infectious Diseases
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  • Question 132 - A 42-year-old man presents to the Emergency Department. He reports experiencing sudden blurred...

    Incorrect

    • A 42-year-old man presents to the Emergency Department. He reports experiencing sudden blurred vision and difficulty speaking. He denies any history of head injury or trauma and does not have a headache. On examination, he exhibits exaggerated reflexes and upward plantars. Fundoscopy reveals no abnormalities. What is the most probable diagnosis?

      Your Answer:

      Correct Answer: Multiple sclerosis

      Explanation:

      Neurological Conditions and Upper Motor Neurone Signs

      Upper motor neurone signs, such as spasticity, hyperreflexia, clonus, and the Babinski reflex, are indicative of certain neurological conditions. Multiple sclerosis, a demyelinating disease, is one such condition that causes these signs. On the other hand, a stroke in a young person is relatively unlikely to cause upper motor neurone signs. Cerebral venous thrombosis could cause these signs, but it would be highly unlikely without a headache and normal fundoscopy. Guillain–Barré syndrome (GBS) is a relatively symmetrical, ascending lower motor neurone disease that does not typically present with blurred vision and speech disturbances. Poliomyelitis, a lower motor neurone condition, is characterised by hypotonia and hyporeflexia and would not cause the Babinski reflex.

      Understanding Upper Motor Neurone Signs in Neurological Conditions

    • This question is part of the following fields:

      • Neurology
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  • Question 133 - A middle-aged man presents with a round, slowly enlarging erythema on his thigh....

    Incorrect

    • A middle-aged man presents with a round, slowly enlarging erythema on his thigh. He also complains of joint discomfort and fatigue. Lyme disease is suspected.
      Which of the following is the most appropriate laboratory test to confirm this diagnosis?
      Select the SINGLE most appropriate laboratory test from the list below.

      Your Answer:

      Correct Answer: Anti-Borrelia burgdorferi titre

      Explanation:

      Diagnostic Tests for Lyme Disease: Understanding the Results

      Lyme disease is a common illness caused by the spirochaete B. burgdorferi, transmitted to humans via tick bites. Serologic testing is the most frequently used diagnostic tool, but false positives and negatives are common. The enzyme immunoassay (EIA) or enzyme-linked immunosorbent assay (ELISA) is the first step, followed by a western blot if necessary. However, serologic results cannot distinguish active from inactive disease. Antinuclear antibodies and rheumatoid factor test results are negative in B. burgdorferi infection. The erythrocyte sedimentation rate is usually elevated but is not specific to detect infection. Culture of joint fluids can rule out gout and pseudogout, but detection of B. burgdorferi DNA in synovial fluid is not reliable. Blood cultures are impractical. Understanding the limitations of these tests is crucial for accurate diagnosis and treatment of Lyme disease.

    • This question is part of the following fields:

      • Infectious Diseases
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  • Question 134 - You are on-call and reviewing a potassium result. The patient's details are as...

    Incorrect

    • You are on-call and reviewing a potassium result. The patient's details are as follows:
      Na+ 141 mmol/l
      K+ 6.4 mmol/l
      Bicarbonate 16 mmol/l
      Urea 13.1 mmol/l
      Creatinine 195 µmol/l
      You are uncertain about administering calcium gluconate and decide to seek advice from your senior. She advises you to only give calcium gluconate if there are ECG changes. What ECG changes are most indicative of hyperkalaemia in a patient who is 60 years old?

      Your Answer:

      Correct Answer: Widening of the QRS complex

      Explanation:

      ECG characteristics of hypokalaemia include a prolonged QT interval, prolonged PR interval, and the presence of U waves.

      Understanding Hyperkalaemia: Causes and Symptoms

      Hyperkalaemia is a condition characterized by high levels of potassium in the blood. The regulation of plasma potassium levels is influenced by various factors such as aldosterone, insulin levels, and acid-base balance. When metabolic acidosis occurs, hyperkalaemia may develop as hydrogen and potassium ions compete for exchange with sodium ions across cell membranes and in the distal tubule. ECG changes that may be observed in hyperkalaemia include tall-tented T waves, small P waves, widened QRS leading to a sinusoidal pattern, and asystole.

      There are several causes of hyperkalaemia, including acute kidney injury, metabolic acidosis, Addison’s disease, rhabdomyolysis, and massive blood transfusion. Certain drugs such as potassium-sparing diuretics, ACE inhibitors, angiotensin 2 receptor blockers, spironolactone, ciclosporin, and heparin can also cause hyperkalaemia. It is important to note that beta-blockers can interfere with potassium transport into cells and potentially cause hyperkalaemia in renal failure patients. On the other hand, beta-agonists like Salbutamol are sometimes used as emergency treatment.

      Foods that are high in potassium include salt substitutes, bananas, oranges, kiwi fruit, avocado, spinach, and tomatoes. It is essential to monitor potassium levels in the blood to prevent complications associated with hyperkalaemia. If left untreated, hyperkalaemia can lead to serious health problems such as cardiac arrhythmias and even death.

    • This question is part of the following fields:

      • Cardiovascular
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  • Question 135 - You are seeing a 65-year-old patient in the outpatient clinic who complains of...

    Incorrect

    • You are seeing a 65-year-old patient in the outpatient clinic who complains of weight loss and a painless, growing penile sore that has been present for more than two months. The patient has a history of genital warts. What tests would be suitable for this probable diagnosis?

      Your Answer:

      Correct Answer: Immunoassay for Human Immunodeficiency Virus

      Explanation:

      Penile cancer is strongly linked to sexually transmitted diseases, including HIV infection. Therefore, it would be advisable to conduct an HIV test in cases where penile cancer is suspected. Liver function tests may not be as relevant as an HIV test since penile cancer is unlikely to spread to the liver. Instead, it can spread locally to lymph nodes, bones, and even the brain. Herpes is not a likely cause of penile cancer as it typically causes painful lesions that disappear within a week. Chancroid, caused by Haemophilus ducreyi, can cause painful lesions, while syphilis, caused by Treponema pallidum, can cause a painless ulcer known as a chancre. However, a chancre would not cause weight loss, and the lesion typically resolves within six to eight weeks, even without treatment.

      Understanding Penile Cancer: Causes, Symptoms, and Treatment

      Penile cancer is a rare type of cancer that is typically characterized by squamous cell carcinoma. It is a condition that affects the penis and can cause a variety of symptoms, including penile lump and ulceration. There are several risk factors associated with penile cancer, including human immunodeficiency virus infection, human papillomavirus virus infection, genital warts, poor hygiene, phimosis, paraphimosis, balanitis, and age over 50.

      When it comes to treating penile cancer, there are several options available, including radiotherapy, chemotherapy, and surgery. The prognosis for penile cancer can vary depending on the stage of the cancer and the treatment options chosen. However, the overall survival rate for penile cancer is approximately 50% at 5 years.

    • This question is part of the following fields:

      • Renal Medicine/Urology
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  • Question 136 - A 28-year-old woman comes to her GP complaining of pelvic pain and deep...

    Incorrect

    • A 28-year-old woman comes to her GP complaining of pelvic pain and deep dyspareunia that has been ongoing for four days. During the examination, the GP notes a temperature of 37.9 degrees Celsius, lower abdominal tenderness, and cervical motion tenderness. The GP suspects that the woman may have pelvic inflammatory disease. What criteria should the GP use to determine whether antibiotics should be prescribed?

      Your Answer:

      Correct Answer: Clinical evidence - history and examination

      Explanation:

      According to NICE guidelines, clinicians should diagnose pelvic inflammatory disease based on clinical symptoms and start antibiotic treatment promptly. While investigations such as endocervical and high vaginal swabs for microscopy and culture should be performed, they should not delay treatment. Negative swab results do not exclude the possibility of the disease. Blood cultures are not necessary unless the patient shows signs of systemic illness. Transvaginal ultrasound is not the first choice but may be necessary if an abscess is suspected.
      (NICE CKS – Pelvic Inflammatory Disease)

      Understanding Pelvic Inflammatory Disease

      Pelvic inflammatory disease (PID) is a condition that occurs when the female pelvic organs, including the uterus, fallopian tubes, ovaries, and surrounding peritoneum, become infected and inflamed. The most common cause of PID is an ascending infection from the endocervix, often caused by Chlamydia trachomatis. Other causative organisms include Neisseria gonorrhoeae, Mycoplasma genitalium, and Mycoplasma hominis. Symptoms of PID include lower abdominal pain, fever, dyspareunia, dysuria, menstrual irregularities, vaginal or cervical discharge, and cervical excitation.

      To diagnose PID, a pregnancy test should be done to rule out an ectopic pregnancy, and a high vaginal swab should be taken to screen for Chlamydia and Gonorrhoea. However, these tests are often negative, so consensus guidelines recommend having a low threshold for treatment due to the potential complications of untreated PID. Management typically involves a combination of antibiotics, such as oral ofloxacin and oral metronidazole or intramuscular ceftriaxone, oral doxycycline, and oral metronidazole.

      Complications of PID include perihepatitis (Fitz-Hugh Curtis Syndrome), which occurs in around 10% of cases and is characterized by right upper quadrant pain that may be confused with cholecystitis. PID can also lead to infertility, with the risk as high as 10-20% after a single episode, chronic pelvic pain, and ectopic pregnancy. In mild cases of PID, intrauterine contraceptive devices may be left in, but recent guidelines suggest that removal of the IUD should be considered for better short-term clinical outcomes. Understanding PID and its potential complications is crucial for early diagnosis and effective management.

    • This question is part of the following fields:

      • Reproductive Medicine
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  • Question 137 - As a foundation doctor in general practice, you assess a thirty-five-year-old woman who...

    Incorrect

    • As a foundation doctor in general practice, you assess a thirty-five-year-old woman who presents with complaints of dizziness. She reports that the symptoms worsen when she rolls over in bed and are accompanied by nausea. She denies any prior episodes, aural fullness, or nystagmus. What diagnostic measures could be taken to confirm the diagnosis?

      Your Answer:

      Correct Answer: Dix–Hallpike manoeuvre

      Explanation:

      The Dix-Hallpike test involves quickly moving the patient to a supine position with their neck extended to determine if they experience symptoms of benign paroxysmal positional vertigo. A positive result can confirm the diagnosis. Based on the symptoms, it is likely that this patient has this condition.

      Understanding Benign Paroxysmal Positional Vertigo

      Benign paroxysmal positional vertigo (BPPV) is a common condition that causes sudden dizziness and vertigo triggered by changes in head position. It typically affects individuals over the age of 55 and is less common in younger patients. Symptoms include vertigo triggered by movements such as rolling over in bed or looking upwards, and may be accompanied by nausea. Each episode usually lasts between 10-20 seconds and can be diagnosed through a positive Dix-Hallpike manoeuvre, which involves the patient experiencing vertigo and rotatory nystagmus.

      Fortunately, BPPV has a good prognosis and often resolves on its own within a few weeks to months. Treatment options include the Epley manoeuvre, which is successful in around 80% of cases, and vestibular rehabilitation exercises such as the Brandt-Daroff exercises. While medication such as Betahistine may be prescribed, it tends to have limited value. However, it is important to note that around half of people with BPPV will experience a recurrence of symptoms 3-5 years after their initial diagnosis.

      Overall, understanding BPPV and its symptoms can help individuals seek appropriate treatment and manage their condition effectively.

    • This question is part of the following fields:

      • ENT
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  • Question 138 - A 45-year-old man has a 3-month history of weight loss, fatigue and difficulty...

    Incorrect

    • A 45-year-old man has a 3-month history of weight loss, fatigue and difficulty breathing with a 20-pack-year smoking history. A chest X-ray reveals multiple rounded nodules of different sizes spread throughout both lungs.
      What is the most probable diagnosis?

      Your Answer:

      Correct Answer: Pulmonary metastases

      Explanation:

      Differential diagnosis of lung nodules on chest radiograph

      Pulmonary metastases is a likely diagnosis for lung nodules on a chest radiograph, especially in patients with a history of cancer. Other possible causes of lung nodules include infections, such as lung abscesses or tuberculosis, occupational lung diseases, such as silicosis, and traumatic injuries, such as rib fractures. However, the clinical presentation and radiological features of these conditions differ from those of pulmonary metastases. Therefore, a thorough evaluation of the patient’s medical history, physical examination, laboratory tests, and imaging studies is necessary to establish the correct diagnosis and guide the appropriate treatment.

    • This question is part of the following fields:

      • Respiratory Medicine
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  • Question 139 - An 80-year-old man is brought to the emergency department by ambulance after being...

    Incorrect

    • An 80-year-old man is brought to the emergency department by ambulance after being found on the floor at home. He is disoriented and unable to provide a clear history. His relatives are yet to arrive. He has a GCS of 12. On examination you note crackles at the left base on auscultation, an ejection systolic murmur over the left sternal edge, and a soft, nontender abdomen. His right pupil is slightly dilated compared to the left and is sluggish to react to light. He has no obvious injuries.
      What is the most appropriate, immediate source of action to aid in diagnosis?

      Your Answer:

      Correct Answer: CT brain

      Explanation:

      Immediate CT scan is necessary to evaluate for raised intracranial pressure and tentorial herniation in a patient with a sluggishly responsive unilaterally dilated pupil. This is the most pressing concern, given the patient’s reduced GCS. Although other investigations will be necessary, the CT brain is the most critical test, as the patient may require urgent neurosurgical intervention to save their life.

      Patients with head injuries should be managed according to ATLS principles and extracranial injuries should be managed alongside cranial trauma. There are different types of traumatic brain injuries, including extradural hematoma, subdural hematoma, and subarachnoid hemorrhage. Primary brain injury may be focal or diffuse, and secondary brain injury can occur due to cerebral edema, ischemia, infection, or herniation. Management may include IV mannitol/frusemide, decompressive craniotomy, and ICP monitoring. Pupillary findings can provide information on the location and severity of the injury.

    • This question is part of the following fields:

      • Neurology
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  • Question 140 - Which one of the following investigations is essential prior to initiating anti-tuberculosis treatment...

    Incorrect

    • Which one of the following investigations is essential prior to initiating anti-tuberculosis treatment in elderly patients?

      Your Answer:

      Correct Answer: Liver functions tests

      Explanation:

      The management of tuberculosis has been outlined in guidelines by the British Thoracic Society. It is recommended that liver function tests are conducted in all cases and monitored during treatment. Prior to starting ethambutol, it is important to check visual acuity and renal function.

      Side-Effects and Mechanism of Action of Tuberculosis Drugs

      Rifampicin is a drug that inhibits bacterial DNA dependent RNA polymerase, which prevents the transcription of DNA into mRNA. However, it is a potent liver enzyme inducer and can cause hepatitis, orange secretions, and flu-like symptoms.

      Isoniazid, on the other hand, inhibits mycolic acid synthesis. It can cause peripheral neuropathy, which can be prevented with pyridoxine (Vitamin B6). It can also cause hepatitis and agranulocytosis. Additionally, it is a liver enzyme inhibitor.

      Pyrazinamide is converted by pyrazinamidase into pyrazinoic acid, which in turn inhibits fatty acid synthase (FAS) I. However, it can cause hyperuricaemia, leading to gout, as well as arthralgia, myalgia, and hepatitis.

      Lastly, Ethambutol inhibits the enzyme arabinosyl transferase, which polymerizes arabinose into arabinan. It can cause optic neuritis, so it is important to check visual acuity before and during treatment. Additionally, the dose needs adjusting in patients with renal impairment.

      In summary, these tuberculosis drugs have different mechanisms of action and can cause various side-effects. It is important to monitor patients closely and adjust treatment accordingly to ensure the best possible outcomes.

    • This question is part of the following fields:

      • Pharmacology/Therapeutics
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  • Question 141 - At what age would a typical infant develop the capability to sit upright...

    Incorrect

    • At what age would a typical infant develop the capability to sit upright without assistance?

      Your Answer:

      Correct Answer: 6-8 months

      Explanation:

      The answer, which is typically 7-8 months, differs slightly from the 6 months stated in the MRCPCH Development Guide.

      Gross Motor Developmental Milestones

      Gross motor skills refer to the ability to use large muscles in the body for activities such as crawling, walking, running, and jumping. These skills are essential for a child’s physical development and are achieved through a series of developmental milestones.
      At 3 months, a baby should have little or no head lag when pulled to sit and should have good head control when lying on their abdomen. By 6 months, they should be able to lift and grasp their feet when lying on their back, pull themselves to a sitting position, and roll from front to back. At 9 months, they should be able to pull themselves to a standing position and crawl. By 12 months, they should be able to cruise and walk with one hand held. At 18 months, they should be able to walk unsupported and squat to pick up a toy. By 2 years, they should be able to run and walk up and down stairs holding onto a rail. At 3 years, they should be able to ride a tricycle using pedals and walk up stairs without holding onto a rail. By 4 years, they should be able to hop on one leg.

      It is important to note that while the majority of children crawl on all fours before walking, some children may bottom-shuffle, which is a normal variant that runs in families. These milestones serve as a guide for parents and healthcare professionals to monitor a child’s physical development and identify any potential delays or concerns.

    • This question is part of the following fields:

      • Paediatrics
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  • Question 142 - A 70-year-old man is rushed to the hospital due to severe chest pain...

    Incorrect

    • A 70-year-old man is rushed to the hospital due to severe chest pain and nausea. His ECG reveals ST elevation in leads V1, V2, V3, and V4. Following angiography and percutaneous coronary intervention, his left anterior descending coronary artery is stented. The patient admits to avoiding doctors and not seeing his GP for more than two decades. He has been smoking 15 cigarettes daily since he was 18. What are the recommended medications for secondary prevention?

      Your Answer:

      Correct Answer: Aspirin + prasugrel + lisinopril + bisoprolol + atorvastatin

      Explanation:

      Myocardial infarction (MI) is a serious condition that requires proper management to prevent further complications. In 2013, NICE released guidelines on the secondary prevention of MI. One of the key recommendations is the use of four drugs: dual antiplatelet therapy (aspirin plus a second antiplatelet agent), ACE inhibitor, beta-blocker, and statin. Patients are also advised to adopt a Mediterranean-style diet and engage in regular exercise. Sexual activity may resume four weeks after an uncomplicated MI, and PDE5 inhibitors may be used six months after the event.

      Most patients with acute coronary syndrome are now given dual antiplatelet therapy, with ticagrelor and prasugrel being the preferred options. The treatment period for these drugs is 12 months, after which they should be stopped. However, this period may be adjusted for patients at high risk of bleeding or further ischaemic events. Additionally, patients with heart failure and left ventricular systolic dysfunction should be treated with an aldosterone antagonist within 3-14 days of the MI, preferably after ACE inhibitor therapy.

      Overall, the NICE guidelines provide a comprehensive approach to the secondary prevention of MI. By following these recommendations, patients can reduce their risk of further complications and improve their overall health outcomes.

    • This question is part of the following fields:

      • Cardiovascular
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  • Question 143 - A 32-year-old female patient presents to her GP with worries regarding her medication....

    Incorrect

    • A 32-year-old female patient presents to her GP with worries regarding her medication. She was diagnosed with systemic lupus erythematosus 2 years ago and is currently on azathioprine 120mg/day, divided into doses. She recently took a home pregnancy test which came back positive. What is the most appropriate approach to managing her medication?

      Your Answer:

      Correct Answer: Continue azathioprine

      Explanation:

      It is safe to continue using azathioprine during pregnancy, even if on an established dose. Discontinuing or reducing the medication could lead to disease progression and serious health risks for the patient. Therefore, the dose of azathioprine should not be lowered. Switching to corticosteroids would not be appropriate as the patient is already on a safe medication. Infliximab should only be used if necessary during pregnancy, so continuing with azathioprine is a better option. Methotrexate should never be used during pregnancy as it is known to be teratogenic.

      Azathioprine is a medication that is broken down into mercaptopurine, which is an active compound that inhibits the production of purine. To determine if someone is at risk for azathioprine toxicity, a test for thiopurine methyltransferase (TPMT) may be necessary. Adverse effects of this medication include bone marrow depression, which can be detected through a full blood count if there are signs of infection or bleeding, as well as nausea, vomiting, pancreatitis, and an increased risk of non-melanoma skin cancer. It is important to note that there is a significant interaction between azathioprine and allopurinol, so lower doses of azathioprine should be used in conjunction with allopurinol. Despite these potential side effects, azathioprine is generally considered safe to use during pregnancy.

    • This question is part of the following fields:

      • Musculoskeletal
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  • Question 144 - A middle-aged woman comes to you with concerns about skin lesions on her...

    Incorrect

    • A middle-aged woman comes to you with concerns about skin lesions on her chest. Upon examination, you notice two small red papules with visible fine vessels surrounding them. The lesions blanch when pressure is applied. What commonly used medication could be causing these lesions?

      Your Answer:

      Correct Answer: Combined oral contraceptive

      Explanation:

      Spider naevi are a type of skin angioma that are typically found in the distribution of the superior vena cava. While they can occur without any apparent cause, the presence of multiple lesions may indicate an excess of oestrogen in the body. This is often associated with liver cirrhosis, as the liver is responsible for processing oestrogens. However, it can also occur during pregnancy or as a side effect of oestrogen-containing medications.

      Understanding Spider Naevi

      Spider naevi, also known as spider angiomas, are characterized by a central red papule surrounded by capillaries. These lesions can be identified by their ability to blanch upon pressure. Spider naevi are typically found on the upper part of the body and are more common in childhood, affecting around 10-15% of people.

      To differentiate spider naevi from telangiectasia, one can press on the lesion and observe how it fills. Spider naevi fill from the center, while telangiectasia fills from the edge. It is important to note that spider naevi may be associated with liver disease, pregnancy, and the use of combined oral contraceptive pills.

      In summary, understanding spider naevi is important for proper diagnosis and management. By recognizing their distinct characteristics and potential associations, healthcare professionals can provide appropriate care for their patients.

    • This question is part of the following fields:

      • Dermatology
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  • Question 145 - Which of the following is the least commonly associated with cocaine toxicity? ...

    Incorrect

    • Which of the following is the least commonly associated with cocaine toxicity?

      Your Answer:

      Correct Answer: Metabolic alkalosis

      Explanation:

      Understanding Cocaine Toxicity

      Cocaine is a popular recreational stimulant derived from the coca plant. However, its widespread use has resulted in an increase in cocaine toxicity cases. The drug works by blocking the uptake of dopamine, noradrenaline, and serotonin, leading to a variety of adverse effects.

      Cardiovascular effects of cocaine include coronary artery spasm, tachycardia, bradycardia, hypertension, QRS widening, QT prolongation, and aortic dissection. Neurological effects may include seizures, mydriasis, hypertonia, and hyperreflexia. Psychiatric effects such as agitation, psychosis, and hallucinations may also occur. Other complications include ischaemic colitis, hyperthermia, metabolic acidosis, and rhabdomyolysis.

      Managing cocaine toxicity involves using benzodiazepines as a first-line treatment for most cocaine-related problems. For chest pain, benzodiazepines and glyceryl trinitrate may be used, and primary percutaneous coronary intervention may be necessary if myocardial infarction develops. Hypertension can be treated with benzodiazepines and sodium nitroprusside. The use of beta-blockers in cocaine-induced cardiovascular problems is controversial, with some experts warning against it due to the risk of unopposed alpha-mediated coronary vasospasm.

      In summary, cocaine toxicity can lead to a range of adverse effects, and managing it requires careful consideration of the patient’s symptoms and medical history.

    • This question is part of the following fields:

      • Pharmacology/Therapeutics
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  • Question 146 - A 10-year-old child with a history of infective diarrhoea presents with fever, hypertension,...

    Incorrect

    • A 10-year-old child with a history of infective diarrhoea presents with fever, hypertension, haematuria and bloody stools two weeks later. What could be a potential diagnosis?

      Your Answer:

      Correct Answer: Haemolytic uraemic syndrome

      Explanation:

      Haemolytic uraemic syndrome (HUS) is a condition that causes progressive kidney failure and is associated with microangiopathic haemolytic anaemia and thrombocytopenia. There are two main types of HUS, one of which is associated with Shiga-like toxin (Stx) and is commonly seen in children who have had diarrhoea. The classic form of Stx-HUS is often caused by E. coli O157:H7 and is characterized by a history of gastroenteritis, fever, bloody diarrhoea, oedema, and hypertension. Henoch-Schönlein purpura is an acute disorder that affects small blood vessels in various parts of the body, including the skin, gastrointestinal tract, kidneys, and joints. It is characterized by a rash with bullae and ulcers, which typically appears in crops. Post-infectious glomerulonephritis is a condition that occurs after a streptococcal infection and is characterized by haematuria, proteinuria, red blood cell casts in the urine, oedema, and hypertension. Membranoproliferative glomerulonephritis is a rare cause of chronic nephritis that occurs primarily in children and young adults and may be idiopathic or secondary in aetiology. Acute interstitial nephritis is a condition that causes sudden kidney dysfunction, fever, and occasionally a rash, and is often associated with drug use.

    • This question is part of the following fields:

      • Renal Medicine/Urology
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  • Question 147 - You assess a 50-year-old woman who has developed a dependence on temazepam, which...

    Incorrect

    • You assess a 50-year-old woman who has developed a dependence on temazepam, which was initially prescribed as a sleep aid. She expresses a desire to overcome her addiction to temazepam and seeks assistance. Her current dosage is 20 mg per day. What would be the most suitable approach?

      Your Answer:

      Correct Answer: Switch to the equivalent diazepam dose then slowly withdraw over the next 2 months

      Explanation:

      Benzodiazepines are drugs that enhance the effect of the neurotransmitter GABA, which inhibits brain activity. They are used for various purposes, including sedation, anxiety relief, muscle relaxation, and seizure prevention. However, patients can develop a tolerance and dependence on these drugs, so they should only be prescribed for a short period of time. When withdrawing from benzodiazepines, it is important to do so gradually to avoid withdrawal symptoms, which can include insomnia, anxiety, and seizures. Barbiturates are another type of drug that affect GABA, but they work differently than benzodiazepines by increasing the duration of chloride channel opening.

    • This question is part of the following fields:

      • Psychiatry
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  • Question 148 - A 28-year-old female visits her GP with complaints of recurring lower abdominal pain....

    Incorrect

    • A 28-year-old female visits her GP with complaints of recurring lower abdominal pain. The pain occurs every month, around midcycle, and lasts for 1-2 days. She experiences a cramping sensation and there is no associated vaginal bleeding. She reports feeling well otherwise during these episodes and denies any gastrointestinal issues or changes to her menstrual cycle. Physical examination today is unremarkable. What is the probable cause of her symptoms?

      Your Answer:

      Correct Answer: Mittelschmerz

      Explanation:

      If a woman experiences pelvic pain during ovulation but does not have any vaginal bleeding, it may be Mittelschmerz. This type of pain is typically felt in the middle of the menstrual cycle. It is unlikely that a young patient with normal examination and intermittent abdominal pain during ovulation has ovarian malignancy. Additionally, there are no symptoms of hirsutism or changes to periods that suggest PCOS, nor are there any gastrointestinal symptoms that suggest IBS.

      Understanding Mittelschmerz: Abdominal Pain Associated with Ovulation

      Mittelschmerz, which translates to middle pain, is a type of abdominal pain that occurs during ovulation in approximately 20% of women. The exact cause of this mid-cycle pain is not fully understood, but there are several theories. One theory suggests that the pain is caused by the leakage of follicular fluid containing prostaglandins during ovulation. Another theory suggests that the growth of the follicle stretches the surface of the ovary, leading to pain.

      The pain associated with Mittelschmerz typically presents suddenly in either iliac fossa and then spreads to the pelvic area. The pain is usually not severe and can last from minutes to hours. It is self-limiting and resolves within 24 hours of onset. The pain may switch sides from month to month, depending on the site of ovulation.

      There are no specific tests to confirm Mittelschmerz, and it is diagnosed clinically after taking a full history and examination to exclude other conditions. Abdominal and pelvic examinations typically do not reveal any abnormal signs.

      Mittelschmerz is not harmful and can be managed with simple analgesia. Understanding this condition can help women recognize and manage the pain associated with ovulation.

    • This question is part of the following fields:

      • Reproductive Medicine
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  • Question 149 - What advice would you give a young man about his alcohol consumption? ...

    Incorrect

    • What advice would you give a young man about his alcohol consumption?

      Your Answer:

      Correct Answer: No more than 14 units of alcohol per week. If you do drink as much as 14 units per week, it is best to spread this evenly over 3 days or more

      Explanation:

      Please limit your alcohol consumption to a maximum of 21 units per week, with no more than 3 units in a single day.

      Alcohol consumption guidelines were revised in 2016 by the Chief Medical Officer, based on recommendations from an expert group report. The most significant change was a reduction in the recommended maximum number of units of alcohol for men from 21 to 14, aligning with the guidelines for women. The government now advises that both men and women should not exceed 14 units of alcohol per week, and if they do, it is best to spread it evenly over three or more days. Pregnant women are advised not to drink alcohol at all, as it can cause long-term harm to the baby. One unit of alcohol is equivalent to 10 mL of pure ethanol, and the strength of a drink is determined by its alcohol by volume (ABV). Examples of one unit of alcohol include a 25ml single measure of spirits with an ABV of 40%, a third of a pint of beer with an ABV of 5-6%, and half a 175ml standard glass of red wine with an ABV of 12%. To calculate the number of units in a drink, multiply the number of millilitres by the ABV and divide by 1,000.

    • This question is part of the following fields:

      • Gastroenterology/Nutrition
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  • Question 150 - A 35-year-old woman with a history of eczema presents with itchy, red patches...

    Incorrect

    • A 35-year-old woman with a history of eczema presents with itchy, red patches on her inner elbows, back of knees, and thighs. The skin on her right thigh is oozing. She reports feeling fatigued and wonders if she has had a fever. Her vital signs are within normal limits. Based on your assessment, you diagnose her with moderately severe eczema.
      What is the best course of action for managing her condition?

      Your Answer:

      Correct Answer: Regular Diprobase® ointment and once-daily betamethasone valerate 0.025% cream plus 10 days of oral flucloxacillin

      Explanation:

      Treatment Regime for Moderately Severe Eczema with Superimposed Infection

      Moderately severe eczema with evidence of superimposed infection requires a specific treatment regime. The severity of eczema is categorized into four categories: clear, mild, moderate, and severe. In this case, the patient has small areas of dry skin mainly in the flexures, and there is evidence of superimposed infection with the erythematous, weeping patch of skin in the lateral thigh, indicating infected eczema/cellulitis.

      The treatment regime should include a regular emollient ointment, such as Diprobase®, applied generously to the skin multiple times a day. Additionally, a moderately potent topical corticosteroid, such as betamethasone valerate 0.025% or clobetasone butyrate 0.05%, should be used sparingly on the inflamed areas once a day. The patient must be advised to apply the steroid first and allow 15–20 min for it to be absorbed before applying the emollient. Treatment should last 7–14 days and should continue until 48 h after the eczematous patches have cleared.

      Furthermore, oral antibiotics are necessary for the treatment of infected eczema. Oral flucloxacillin is considered first-line, and treatment usually lasts for a 10-day period.

      It is important to note that hydrocortisone 1% cream is only a mild steroid and not indicated in the initial management of moderate eczema. Betamethasone valerate 1% cream is a potent topical corticosteroid and should be reserved for the management of acute flare-ups of severe eczema. Oral flucloxacillin alone is not sufficient for treatment, and there is a need for a moderately potent topical corticosteroid as well to settle the inflammation.

      In conclusion, a combination of regular emollient ointment, moderately potent topical corticosteroid, and oral antibiotics is necessary for the effective treatment of moderately severe eczema with superimposed infection.

    • This question is part of the following fields:

      • Dermatology
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  • Question 151 - A 55-year-old woman has been diagnosed with Bell's palsy. What is the current...

    Incorrect

    • A 55-year-old woman has been diagnosed with Bell's palsy. What is the current evidence-based approach to managing this condition?

      Your Answer:

      Correct Answer: Prednisolone

      Explanation:

      Understanding Bell’s Palsy

      Bell’s palsy is a sudden, one-sided facial nerve paralysis of unknown cause. It is more common in individuals aged 20-40 years and pregnant women. The condition is characterized by lower motor neuron facial nerve palsy, which affects the forehead. Unlike upper motor neuron lesions, the upper face is spared. Patients may also experience post-auricular pain, altered taste, dry eyes, and hyperacusis.

      The management of Bell’s palsy has been a subject of debate. However, it is now widely accepted that all patients should receive oral prednisolone within 72 hours of onset. The addition of antiviral medications is still a matter of discussion, but it may be beneficial for severe facial palsy. Eye care is also crucial to prevent exposure keratopathy, and patients should be prescribed artificial tears and eye lubricants. If they are unable to close their eyes at bedtime, they should tape them closed using microporous tape.

      If the paralysis shows no sign of improvement after three weeks, an urgent referral to ENT is necessary. Patients with long-standing weakness may require a referral to plastic surgery. The prognosis for Bell’s palsy is generally good, with most patients making a full recovery within 3-4 months. However, untreated patients may experience permanent moderate to severe weakness in around 15% of cases.

    • This question is part of the following fields:

      • Neurology
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  • Question 152 - A 28-year-old male with a history of Marfan's syndrome arrives at the emergency...

    Incorrect

    • A 28-year-old male with a history of Marfan's syndrome arrives at the emergency department reporting a sudden, painless loss of vision in his left eye. He did not experience any symptoms beforehand and did not sustain any injuries.

      What is the probable diagnosis?

      Your Answer:

      Correct Answer: Lens dislocation

      Explanation:

      In Marfan’s syndrome, painless loss of vision in one eye may be caused by lens dislocation, which is a common ocular symptom of the condition. The dislocation usually occurs in the upper outer part of the eye and can affect one or both eyes. While retinal detachment can also cause sudden vision loss without pain, it is less common than lens dislocation and is often preceded by visual disturbances such as flashes, floaters, or blind spots.

      Causes of Lens Dislocation

      Lens dislocation can occur due to various reasons. One of the most common causes is Marfan’s syndrome, which causes the lens to dislocate upwards. Homocystinuria is another condition that can lead to lens dislocation, but in this case, the lens dislocates downwards. Ehlers-Danlos syndrome is also a known cause of lens dislocation. Trauma, such as a blow to the eye, can also cause the lens to dislocate. Uveal tumors and autosomal recessive ectopia lentis are other potential causes of lens dislocation. It is important to identify the underlying cause of lens dislocation to determine the appropriate treatment plan. Proper diagnosis and management can help prevent complications and improve outcomes for patients.

    • This question is part of the following fields:

      • Ophthalmology
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  • Question 153 - A 27-year-old female patient who is 10-weeks pregnant visits the GP clinic with...

    Incorrect

    • A 27-year-old female patient who is 10-weeks pregnant visits the GP clinic with a painless rash on her left leg that has been expanding outwardly in a circular pattern. She mentions that the rash appeared 3 weeks after returning from a hiking trip in the western part of the United States. Lyme disease is confirmed through serological testing, but doxycycline cannot be prescribed due to her pregnancy. What is the best alternative treatment option for this patient?

      Your Answer:

      Correct Answer: Amoxicillin

      Explanation:

      Understanding Lyme Disease

      Lyme disease is a bacterial infection caused by Borrelia burgdorferi and is transmitted through tick bites. The early symptoms of Lyme disease include erythema migrans, a characteristic bulls-eye rash that appears at the site of the tick bite. This rash is painless, slowly increases in size, and can be more than 5 cm in diameter. Other early symptoms include headache, lethargy, fever, and joint pain.

      If erythema migrans is present, Lyme disease can be diagnosed clinically, and antibiotics should be started immediately. The first-line test for Lyme disease is an enzyme-linked immunosorbent assay (ELISA) to detect antibodies to Borrelia burgdorferi. If the ELISA is negative but Lyme disease is still suspected, it should be repeated 4-6 weeks later. If Lyme disease is suspected in patients who have had symptoms for 12 weeks or more, an immunoblot test should be done.

      Tick bites can cause significant anxiety, but routine antibiotic treatment is not recommended by NICE. If the tick is still present, it should be removed using fine-tipped tweezers, and the area should be washed. In cases of suspected or confirmed Lyme disease, doxycycline is the preferred treatment for early disease, while ceftriaxone is used for disseminated disease. A Jarisch-Herxheimer reaction may occur after initiating therapy, which can cause fever, rash, and tachycardia.

      In summary, Lyme disease is a bacterial infection transmitted through tick bites. Early symptoms include erythema migrans, headache, lethargy, fever, and joint pain. Diagnosis is made through clinical presentation and ELISA testing, and treatment involves antibiotics. Tick bites do not require routine antibiotic treatment, and ticks should be removed using fine-tipped tweezers.

    • This question is part of the following fields:

      • Reproductive Medicine
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  • Question 154 - A 3-day-old infant is presented to the Emergency Department due to increased irritability,...

    Incorrect

    • A 3-day-old infant is presented to the Emergency Department due to increased irritability, poor feeding, and decreased muscle tone as observed by the mother in the last 24 hours. Meningitis is confirmed through lumbar puncture. What is the probable causative agent in this scenario?

      Your Answer:

      Correct Answer: Group B streptococcus

      Explanation:

      Meningitis poses a higher risk to neonates, particularly those with low birth weight, prematurity, traumatic delivery, fetal hypoxia, and maternal peripartum infection. The initial symptoms are usually vague and may include elevated body temperature, respiratory distress, apnea, episodes of bradycardia, low blood pressure, difficulty feeding, irritability, and decreased activity.

      Organisms causing meningitis in children

      Meningitis is a serious condition that can affect children of all ages. The organisms that cause meningitis vary depending on the age of the child. In neonates up to 3 months old, Group B Streptococcus is the most common cause, which is usually acquired from the mother during birth. E. coli and other Gram-negative organisms, as well as Listeria monocytogenes, can also cause meningitis in this age group.

      From 1 month to 6 years old, Neisseria meningitidis (meningococcus), Streptococcus pneumoniae (pneumococcus), and Haemophilus influenzae are the most common organisms that cause meningitis. In children over 6 years old, Neisseria meningitidis and Streptococcus pneumoniae are the most common causes.

      It is important for parents to be aware of the signs and symptoms of meningitis, such as fever, headache, stiff neck, and sensitivity to light. If a child is showing these symptoms, they should be taken to a doctor immediately for evaluation and treatment. Early diagnosis and treatment can help prevent serious complications and improve outcomes.

    • This question is part of the following fields:

      • Paediatrics
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  • Question 155 - A 28-year-old woman comes in for a check-up. She has a history of...

    Incorrect

    • A 28-year-old woman comes in for a check-up. She has a history of depression and is currently taking citalopram. Despite returning from a recent trip to Italy, she complains of feeling fatigued all the time. During the examination, you notice a slightly raised red rash on the bridge of her nose and cheeks. Although she complains of having 'stiff joints,' you find no evidence of arthritis. You order some basic blood tests:
      Hb 12.5 g/dl
      Platelets 135 * 109/l
      WBC 3.5 * 109/l
      Na+ 140 mmol/l
      K+ 4.2 mmol/l
      Urea 3.2 mmol/l
      Creatinine 80 µmol/l
      Free T4 11.8 pmol/l
      TSH 1.30 mu/l
      CRP 8 mg/l
      What is the most likely diagnosis?

      Your Answer:

      Correct Answer: Systemic lupus erythematosus

      Explanation:

      The presence of a malar rash, arthralgia, lethargy, and a history of mental health issues suggest a possible diagnosis of SLE. It is important to note that the CRP levels are usually within normal range in SLE, unlike the ESR.

      Understanding Systemic Lupus Erythematosus

      Systemic lupus erythematosus (SLE) is an autoimmune disorder that affects multiple systems in the body. It is more common in women and people of Afro-Caribbean origin, and typically presents in early adulthood. The general features of SLE include fatigue, fever, mouth ulcers, and lymphadenopathy.

      SLE can also affect the skin, causing a malar (butterfly) rash that spares the nasolabial folds, discoid rash in sun-exposed areas, photosensitivity, Raynaud’s phenomenon, livedo reticularis, and non-scarring alopecia. Musculoskeletal symptoms include arthralgia and non-erosive arthritis.

      Cardiovascular manifestations of SLE include pericarditis and myocarditis, while respiratory symptoms may include pleurisy and fibrosing alveolitis. Renal involvement can lead to proteinuria and glomerulonephritis, with diffuse proliferative glomerulonephritis being the most common type.

      Finally, neuropsychiatric symptoms of SLE may include anxiety and depression, as well as more severe manifestations such as psychosis and seizures. Understanding the various features of SLE is important for early diagnosis and management of this complex autoimmune disorder.

    • This question is part of the following fields:

      • Musculoskeletal
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  • Question 156 - A boy of 7 presents with a unilateral painless limp. Examination shows limitation...

    Incorrect

    • A boy of 7 presents with a unilateral painless limp. Examination shows limitation of rotation and extension at the affected hip joint, and a radiograph shows a dense flattened and fragmented femoral head on the affected side.
      Which of the following is the most likely diagnosis?

      Your Answer:

      Correct Answer: Perthes' disease

      Explanation:

      Perthes’ Disease: Avascular Necrosis of the Proximal Femoral Head in Children

      Perthes’ disease is a condition that results from avascular necrosis of the proximal femoral head, which is caused by a compromised blood supply. It typically affects children aged 4-10, with boys being affected more frequently than girls. The disease presents with a painless limp and limited range of motion of the affected hip, followed by hip pain as necrosis develops.

      The diagnosis of Perthes’ disease is suspected clinically, and radiographs may be normal initially or show only a non-specific effusion. As the condition progresses, the joint space between the ossified femoral head and acetabulum widens, and narrowing or collapse of the femoral head causes it to appear widened and flattened. Eventually, femoral head collapse may ensue.

      Other conditions that may present similarly to Perthes’ disease include slipped upper femoral epiphysis, septic arthritis, juvenile rheumatoid arthritis, and congenital dislocation of the hip. However, each of these conditions has its own unique features and diagnostic criteria.

      Overall, Perthes’ disease is a generalised disorder of cartilage development that predisposes children to repeated episodes of infarction in the proximal femoral epiphysis. The most significant factors determining prognosis are onset in the older child, epiphyseal protrusion, extensive involvement of the epiphysis, and arrest of subcapital growth.

    • This question is part of the following fields:

      • Paediatrics
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  • Question 157 - A 65-year-old man presents to the emergency department with a 12-day history of...

    Incorrect

    • A 65-year-old man presents to the emergency department with a 12-day history of muscle cramping and fatigue. His blood tests and ECG are as follows:
      - Na+ 140 mmol/L (135 - 145)
      - K+ 3.7 mmol/L (3.5 - 5.0)
      - Bicarbonate 28 mmol/L (22 - 29)
      - Urea 6.2 mmol/L (2.0 - 7.0)
      - Creatinine 95 µmol/L (55 - 120)
      - Calcium 1.7 mmol/L (2.1-2.6)
      - Phosphate 1.3 mmol/L (0.8-1.4)
      - Magnesium 0.62 mmol/L (0.7-1.0)

      The patient's ECG shows a regular sinus rhythm with a rate of 72 BPM and a QTc of 480 ms. What is the most appropriate next step in management?

      Your Answer:

      Correct Answer: Intravenous calcium gluconate

      Explanation:

      A 68-year-old man presents with hypocalcaemia and a prolonged QT interval, which can increase the risk of cardiac arrhythmias such as Torsades de pointes. Urgent intravenous calcium gluconate is the recommended treatment for severe hypocalcaemia, which can cause symptoms such as hand and foot spasming, tetany, and seizures. Checking the vitamin D level is important for identifying the cause of hypocalcaemia, but it is not the next best step in managing this patient’s acute condition. Oral calcium carbonate supplementation may be useful in some cases, but intravenous calcium is the preferred treatment for severe hypocalcaemia. Levothyroxine is not indicated for this patient, as hypothyroidism has not been diagnosed and urgent IV calcium gluconate should be given.

      Understanding Hypocalcaemia: Its Causes and Management

      Hypocalcaemia is a medical condition characterized by low levels of calcium in the blood. It can be caused by various factors such as vitamin D deficiency, chronic kidney disease, hypoparathyroidism, pseudohypoparathyroidism, rhabdomyolysis, magnesium deficiency, massive blood transfusion, and acute pancreatitis. In some cases, contamination of blood samples with EDTA may also lead to falsely low calcium levels.

      To manage severe hypocalcaemia, which may manifest as carpopedal spasm, tetany, seizures, or prolonged QT interval, intravenous calcium replacement is necessary. The preferred method is through the administration of intravenous calcium gluconate, with a recommended dose of 10ml of 10% solution over 10 minutes. However, it is important to note that intravenous calcium chloride may cause local irritation. ECG monitoring is also recommended during the treatment process. Further management of hypocalcaemia depends on the underlying cause.

      In summary, hypocalcaemia is a condition that can be caused by various factors, and its management depends on the severity of the symptoms and the underlying cause. Intravenous calcium replacement is the preferred method for severe cases, and ECG monitoring is recommended during treatment.

    • This question is part of the following fields:

      • Renal Medicine/Urology
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  • Question 158 - A 54-year-old man presents to your clinic after a routine blood test showed...

    Incorrect

    • A 54-year-old man presents to your clinic after a routine blood test showed abnormal liver function tests. He denies any alcohol consumption and his hepatitis screen is negative. His cholesterol level is 4.2 and his HBA1c is 38ml/mol. He has a body mass index of 31 kg/m² and an ultrasound reveals non-alcoholic fatty liver disease. What is the most suitable approach to manage this condition?

      Your Answer:

      Correct Answer: Diet and exercise

      Explanation:

      The primary management approach for NAFLD is weight loss, achieved through diet and exercise. Medications have not shown to be effective in improving the condition’s outcome.

      Non-Alcoholic Fatty Liver Disease: Causes, Features, and Management

      Non-alcoholic fatty liver disease (NAFLD) is a prevalent liver disease in developed countries, primarily caused by obesity. It encompasses a range of conditions, from simple steatosis (fat accumulation in the liver) to steatohepatitis (fat with inflammation) and may progress to fibrosis and liver cirrhosis. Insulin resistance is believed to be the primary mechanism leading to steatosis, making NAFLD a hepatic manifestation of metabolic syndrome. Non-alcoholic steatohepatitis (NASH) is a type of liver damage similar to alcoholic hepatitis but occurs in the absence of alcohol abuse. It affects around 3-4% of the general population and may be responsible for some cases of cryptogenic cirrhosis.

      NAFLD is usually asymptomatic, but hepatomegaly, increased echogenicity on ultrasound, and elevated ALT levels are common features. The enhanced liver fibrosis (ELF) blood test is recommended by NICE to check for advanced fibrosis in patients with incidental NAFLD. If the ELF blood test is not available, non-invasive tests such as the FIB4 score or NAFLD fibrosis score, in combination with a FibroScan, may be used to assess the severity of fibrosis. Patients with advanced fibrosis should be referred to a liver specialist for further evaluation, which may include a liver biopsy to stage the disease more accurately.

      The mainstay of NAFLD treatment is lifestyle changes, particularly weight loss, and monitoring. Research is ongoing into the role of gastric banding and insulin-sensitizing drugs such as metformin and pioglitazone. While there is no evidence to support screening for NAFLD in adults, NICE guidelines recommend the management of incidental NAFLD findings.

    • This question is part of the following fields:

      • Gastroenterology/Nutrition
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  • Question 159 - A 26-year-old woman presents to gastroenterology clinic with severe ulcerative colitis. Before starting...

    Incorrect

    • A 26-year-old woman presents to gastroenterology clinic with severe ulcerative colitis. Before starting azathioprine to improve her symptoms, what potential contraindications should be ruled out?

      Your Answer:

      Correct Answer: Thiopurine methyltransferase deficiency (TPMT)

      Explanation:

      Azathioprine is a medication that is broken down into mercaptopurine, which is an active compound that inhibits the production of purine. To determine if someone is at risk for azathioprine toxicity, a test for thiopurine methyltransferase (TPMT) may be necessary. Adverse effects of this medication include bone marrow depression, which can be detected through a full blood count if there are signs of infection or bleeding, as well as nausea, vomiting, pancreatitis, and an increased risk of non-melanoma skin cancer. It is important to note that there is a significant interaction between azathioprine and allopurinol, so lower doses of azathioprine should be used in conjunction with allopurinol. Despite these potential side effects, azathioprine is generally considered safe to use during pregnancy.

    • This question is part of the following fields:

      • Musculoskeletal
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  • Question 160 - A 38-year-old woman with rheumatoid arthritis visits her doctor every three months for...

    Incorrect

    • A 38-year-old woman with rheumatoid arthritis visits her doctor every three months for blood tests. Which of the following blood tests is necessary for monitoring the use of methotrexate?

      Your Answer:

      Correct Answer: FBC, U&Es, LFTs

      Explanation:

      Importance of Drug Monitoring in Primary Care

      Patients on methotrexate require regular monitoring of their blood tests to prevent severe side effects. The three essential blood tests that need monitoring are FBC, U&Es, and LFTs. Methotrexate can cause blood dyscrasias, liver cirrhosis, and kidney failure, making it crucial to monitor these tests every 2-3 months once therapy has stabilized. Patients should report any symptoms of infection, bruising, mouth ulcers, abdominal discomfort, dark urine, and shortness of breath. They should also avoid self-medication with over-the-counter aspirin or ibuprofen.

      Thyroid function is not affected by methotrexate, and regular monitoring is not necessary unless there is another medical condition that justifies it. However, patients on methotrexate should report any signs of blood disorders such as ecchymosis and telangiectasia.

      Drug monitoring is becoming increasingly common in primary care, especially for patients under shared care with secondary/specialty care. Some examples of drug monitoring in primary care include amiodarone, azathioprine, lithium, and methotrexate. Each drug requires specific blood tests, and the frequency of monitoring varies. For instance, patients on methotrexate require FBC, U&Es, and LFTs every 2-3 months.

    • This question is part of the following fields:

      • Pharmacology/Therapeutics
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  • Question 161 - Which of the following medications is most likely to cause a rash when...

    Incorrect

    • Which of the following medications is most likely to cause a rash when exposed to sunlight?

      Your Answer:

      Correct Answer: Tetracycline

      Explanation:

      Drugs that can cause sensitivity to light

      Photosensitivity is a condition where the skin becomes more sensitive to light, resulting in rashes, blisters, and other skin irritations. Certain drugs can cause photosensitivity, making it important to be aware of the medications that can cause this condition. Some of the drugs that can cause photosensitivity include thiazides, tetracyclines, sulphonamides, ciprofloxacin, amiodarone, NSAIDs like piroxicam, psoralens, and sulphonylureas.

      Thiazides are a type of diuretic that can cause photosensitivity, while tetracyclines, sulphonamides, and ciprofloxacin are antibiotics that can also cause this condition. Amiodarone is a medication used to treat heart rhythm problems, but it can also cause photosensitivity. NSAIDs like piroxicam are pain relievers that can cause photosensitivity, while psoralens are used to treat skin conditions like psoriasis and can also cause photosensitivity. Sulphonylureas are medications used to treat diabetes that can cause photosensitivity as well.

      It is important to note that not everyone who takes these medications will experience photosensitivity, but it is still important to be aware of the potential side effects.

    • This question is part of the following fields:

      • Pharmacology/Therapeutics
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  • Question 162 - A first-time mother brings her daughter, Lily, who is 7-months old, to the...

    Incorrect

    • A first-time mother brings her daughter, Lily, who is 7-months old, to the GP surgery. She is worried about Lily's development as she is still unable to sit without support. However, Lily is able to roll from front to back, sit with back straight if being held, and grasp toys when lying on her back. Can you inform the mother at what age Lily will be able to sit without support?

      Your Answer:

      Correct Answer: 7-8 months, refer if not achieved by 12 months

      Explanation:

      If sitting without support is not achieved by 12 months, referral is necessary, although it should typically be achieved by 7-8 months.

      Gross Motor Developmental Milestones

      Gross motor skills refer to the ability to use large muscles in the body for activities such as crawling, walking, running, and jumping. These skills are essential for a child’s physical development and are achieved through a series of developmental milestones.
      At 3 months, a baby should have little or no head lag when pulled to sit and should have good head control when lying on their abdomen. By 6 months, they should be able to lift and grasp their feet when lying on their back, pull themselves to a sitting position, and roll from front to back. At 9 months, they should be able to pull themselves to a standing position and crawl. By 12 months, they should be able to cruise and walk with one hand held. At 18 months, they should be able to walk unsupported and squat to pick up a toy. By 2 years, they should be able to run and walk up and down stairs holding onto a rail. At 3 years, they should be able to ride a tricycle using pedals and walk up stairs without holding onto a rail. By 4 years, they should be able to hop on one leg.

      It is important to note that while the majority of children crawl on all fours before walking, some children may bottom-shuffle, which is a normal variant that runs in families. These milestones serve as a guide for parents and healthcare professionals to monitor a child’s physical development and identify any potential delays or concerns.

    • This question is part of the following fields:

      • Paediatrics
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  • Question 163 - A 50-year-old woman is undergoing evaluation for hypertension that is not responding to...

    Incorrect

    • A 50-year-old woman is undergoing evaluation for hypertension that is not responding to treatment. She has a medical history of medullary thyroid carcinoma. Her physical examination is unremarkable. During her work-up, she is found to have hypercalcemia with a level of 2.8 mmol/l. Her parathyroid hormone (PTH) is slightly elevated above the normal range. What is the underlying diagnosis?

      Your Answer:

      Correct Answer: Multiple endocrine neoplasia type 2A

      Explanation:

      Differential Diagnosis for Hypercalcaemia with Elevated PTH Levels

      Hypercalcaemia with elevated parathyroid hormone (PTH) levels can be indicative of several conditions. Here are some possible differential diagnoses:

      Multiple Endocrine Neoplasia Type 2A (MEN 2A)
      MEN 2A is caused by a gain in function mutation in the RET proto-oncogene. The classic triad of MEN 2A is medullary thyroid carcinoma, primary hyperparathyroidism, and phaeochromocytoma. Patients with MEN 2A may also have treatment-resistant hypertension.

      Marfan Syndrome
      Marfan syndrome is a hereditary disorder of connective tissue. Patients with Marfan syndrome are typically tall and thin with hyperlax joints, recurrent dislocation of the lens of the eye, and cardiovascular anomalies (particularly aortic regurgitation). However, dysfunction of the parathyroid hormone axis is not usually associated with this condition.

      Multiple Endocrine Neoplasia Type 1 (MEN 1)
      MEN 1 also occurs due to a mutation in the RET gene. However, patients with MEN 1 classically suffer from hyperparathyroidism, pituitary adenomas (typically prolactinomas), and pancreatic islet cell tumors, and not the features described in the case.

      Multiple Myeloma
      Multiple myeloma is also associated with hypercalcaemia, but PTH levels would be appropriately low.

      Neurofibromatosis
      Neurofibromatosis is a disorder caused by a mutation in the neurofibromin gene on chromosome 17. It is associated with multiple neural tumors together with a variety of skin, musculoskeletal, and ocular manifestations, but disruption of the parathyroid hormone axis is not a feature.

    • This question is part of the following fields:

      • Endocrinology/Metabolic Disease
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  • Question 164 - A mother brings in her 3-day-old female baby to the pediatrician's office. She...

    Incorrect

    • A mother brings in her 3-day-old female baby to the pediatrician's office. She noticed a small cyst on the roof of the baby's mouth. Upon examination, a small white cystic vesicle measuring approximately 2 mm in diameter is found on the hard palate near the midline. What is the probable diagnosis?

      Your Answer:

      Correct Answer: Epstein's pearl

      Explanation:

      Epstein’s pearl, a type of congenital cyst found in the mouth, typically does not require any treatment. These cysts are commonly found on the hard palate, but can also be mistaken for a tooth eruption when located on the gums. They usually resolve on their own within a few weeks. Neonatal teeth, on the other hand, are rare and not typically found on the hard palate. Bohn’s nodules are mucous gland cysts that are usually located on the buccal or lingual aspects of the alveolar ridges, and rarely on the palate. A congenital ranula is a papule or nodule that is firm and translucent, and is typically found on the anterior floor of the mouth, lateral to the lingual frenulum.

      Understanding Epstein’s Pearl

      Epstein’s pearl is a type of cyst that is present in the mouth from birth. It is commonly found on the hard palate, but can also be seen on the gums, which may be mistaken for a tooth eruption. The good news is that no treatment is usually required as these cysts tend to disappear on their own within a few weeks.

    • This question is part of the following fields:

      • Paediatrics
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  • Question 165 - A 27-year-old woman is receiving a blood transfusion at the haematology day unit....

    Incorrect

    • A 27-year-old woman is receiving a blood transfusion at the haematology day unit. She has a medical history of acute lymphoblastic leukaemia and her recent haemoglobin level was 69 g/dL. The doctor has prescribed two units of blood for her.

      During the administration of the first unit of blood, the patient experiences difficulty breathing. Upon examination, her vital signs show a temperature of 37.5ºC, heart rate of 99 beats/min, and blood pressure of 90/55 mmHg. Her oxygen saturation level is 96% on air, and she has a respiratory rate of 22 breaths/min. Bilateral wheezing is heard during auscultation.

      What is the most probable cause of this patient's symptoms?

      Your Answer:

      Correct Answer: Anaphylaxis

      Explanation:

      The patient experienced hypotension, dyspnoea, wheezing, and angioedema during a blood transfusion, which indicates anaphylaxis, a severe and life-threatening allergic reaction to the blood product. Treatment involves stopping the transfusion immediately and administering intramuscular adrenaline. Acute haemolytic reaction, bacterial contamination, and minor allergic reaction are not likely explanations for the patient’s symptoms.

      Complications of Blood Product Transfusion: Understanding the Risks

      Blood product transfusion can lead to various complications that can be classified into different categories. Immunological complications include acute haemolytic reactions, non-haemolytic febrile reactions, and allergic/anaphylaxis reactions. Infective complications may also arise, including the transmission of vCJD. Other complications include transfusion-related acute lung injury (TRALI), transfusion-associated circulatory overload (TACO), hyperkalaemia, iron overload, and clotting.

      Non-haemolytic febrile reactions are thought to be caused by antibodies reacting with white cell fragments in the blood product and cytokines that have leaked from the blood cell during storage. On the other hand, allergic reactions to blood transfusions are caused by hypersensitivity reactions to components within the transfusion. TRALI is a rare but potentially fatal complication of blood transfusion, while TACO is a relatively common reaction due to fluid overload resulting in pulmonary oedema.

      It is important to understand the risks associated with blood product transfusion and to be aware of the different types of complications that may arise. Proper management and prompt treatment are crucial in preventing further harm to the patient.

    • This question is part of the following fields:

      • Respiratory Medicine
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  • Question 166 - Which X-ray alteration is not linked to osteoarthritis? ...

    Incorrect

    • Which X-ray alteration is not linked to osteoarthritis?

      Your Answer:

      Correct Answer: Periarticular erosions

      Explanation:

      X-Ray Changes in Osteoarthritis

      Osteoarthritis is a degenerative joint disease that affects millions of people worldwide. One of the most common diagnostic tools used to identify osteoarthritis is an X-ray. X-ray changes in osteoarthritis are characterized by the acronym LOSS, which stands for loss of joint space, osteophytes forming at joint margins, subchondral sclerosis, and subchondral cysts.

      Loss of joint space refers to the narrowing of the space between the bones in a joint. This occurs as the cartilage that cushions the joint wears away, causing the bones to rub against each other. Osteophytes are bony growths that form at the edges of the joint. These growths can cause pain and limit joint movement. Subchondral sclerosis is a hardening of the bone beneath the cartilage. This occurs as the bone tries to compensate for the loss of cartilage. Subchondral cysts are fluid-filled sacs that form in the bone beneath the cartilage. These cysts can cause pain and further damage to the joint.

      In summary, X-ray changes in osteoarthritis are characterized by LOSS: loss of joint space, osteophytes forming at joint margins, subchondral sclerosis, and subchondral cysts. These changes can help doctors diagnose and monitor the progression of osteoarthritis.

    • This question is part of the following fields:

      • Musculoskeletal
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  • Question 167 - A 12-month-old boy is due to receive his vaccinations today.
    Which of the following...

    Incorrect

    • A 12-month-old boy is due to receive his vaccinations today.
      Which of the following vaccines are most likely to be given to a child at 12 months old?

      Your Answer:

      Correct Answer: MMR, Hib/meningitis C, meningitis B and pneumococcal

      Explanation:

      Vaccination Schedule for Infants in the UK

      In the UK, infants are recommended to receive a series of vaccinations to protect them from various diseases. Here is a breakdown of the vaccination schedule and when each vaccine is given.

      UK Infant Vaccination Schedule

      MMR, Hib/Men C, Men B, and Pneumococcal Vaccines

      At one year of age, infants are given the MMR, Hib/Men C, and the third dose of both the Men B and pneumococcal vaccines.

      Pneumococcal, Rotavirus, Men B, and MMR Vaccines

      The pneumococcal and rotavirus vaccines are given at eight weeks, while the Men B vaccine is given at 8 weeks, 16 weeks, and one year. The MMR vaccine is given at 12-14 months.

      MMR, Rotavirus, and Pneumococcal Vaccines

      The MMR vaccine is given at 12-14 months, while the rotavirus and pneumococcal vaccines are given at eight weeks, 16 weeks, and one year.

      Rotavirus, MMR, Six-in-One, and Men B Vaccines

      The rotavirus and six-in-one vaccines are given at eight weeks, while the Men B vaccine is given at 8 weeks, 16 weeks, and one year. The MMR vaccine is given at 12-14 months.

      Six-in-One Vaccine

      The six-in-one vaccine is given at eight weeks, 12 weeks, and 16 weeks.

    • This question is part of the following fields:

      • Immunology/Allergy
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  • Question 168 - A preterm baby boy is found to have meconium ileus shortly after birth.
    Which...

    Incorrect

    • A preterm baby boy is found to have meconium ileus shortly after birth.
      Which of the following conditions is most commonly associated with meconium ileus?

      Your Answer:

      Correct Answer: Cystic fibrosis

      Explanation:

      Common Genetic Conditions and Associated Manifestations

      Cystic Fibrosis, Edward Syndrome, Down Syndrome, Myelomeningocele, and Patau Syndrome are all genetic conditions that can have various manifestations. Cystic Fibrosis affects multiple organ systems, including the lungs, liver, pancreas, and small bowel, leading to progressive organ failure. Edward Syndrome is a trisomy syndrome with a high incidence of major structural anomalies, including congenital heart disease and central nervous system abnormalities. Down Syndrome is the most common trisomy and is associated with characteristic facial features and an increased risk for congenital heart disease and gastrointestinal anomalies. Myelomeningocele is a spinal anomaly that can result in lower limb paralysis and bladder and bowel dysfunction. Patau Syndrome is the least common trisomy syndrome and is associated with congenital heart disease, central nervous system and spinal abnormalities, abnormal facies, and polydactyly. Meconium ileus is a common manifestation associated with Cystic Fibrosis in all of these conditions.

    • This question is part of the following fields:

      • Genetics
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  • Question 169 - A 48-year-old type 2 diabetic man has an annual review; bloods show creatinine...

    Incorrect

    • A 48-year-old type 2 diabetic man has an annual review; bloods show creatinine 109 μmol/l (reference range 53–106 μmol/l) and estimated glomerular filtration rate (eGFR) 64 (reference range >90 ml/min/1.73 m2). Urinary albumin : creatinine ratio (ACR) test = 37 mg/mmol (reference range <3 mg/mmol- 30 mg/mmol). The results are repeated 4 weeks later and the results are very similar.
      Which class of chronic kidney disease (CKD) does this fit?
      Select the SINGLE most appropriate class from the list below.
      Select ONE option only.

      Your Answer:

      Correct Answer: CKD stage 2

      Explanation:

      Understanding the Stages of Chronic Kidney Disease

      Chronic kidney disease (CKD) is a condition in which the kidneys gradually lose function over time. To help diagnose and manage CKD, healthcare professionals use a staging system based on the glomerular filtration rate (GFR), which measures how well the kidneys are filtering waste from the blood.

      The stages of CKD are as follows:

      – Stage 1: GFR >90 ml/min/1.73 m2 (normal or high)
      – Stage 2: GFR 60–89 ml/min/1.73 m2 (mildly decreased)
      – Stage 3a: GFR 45–59 ml/min/1.73 m2 (mildly to moderately decreased)
      – Stage 3b: GFR 30–44 ml/min/1.73 m2 (moderately to severely decreased)
      – Stage 4: GFR 15–29 ml/min/1.73 m2 (severely decreased)
      – Stage 5: GFR <15 ml/min/1.73 m2 (kidney failure) The 2008 National Institute for Health and Care Excellence (NICE) guideline on CKD recommends subdividing stage 3 into 3a and 3b, and adding the suffix P to denote significant proteinuria at any stage. Significant proteinuria is defined as a urinary albumin-to-creatinine ratio (ACR) of 30 mg/mmol or higher. Understanding the stage of CKD can help healthcare professionals determine appropriate treatment and management strategies to slow the progression of the disease and prevent complications.

    • This question is part of the following fields:

      • Renal Medicine/Urology
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  • Question 170 - A 48-year-old woman is referred to the oncology clinic by the local general...

    Incorrect

    • A 48-year-old woman is referred to the oncology clinic by the local general surgeon. She has undergone a mastectomy for carcinoma of the right breast.
      Which of the following factors is associated with a poor prognosis in patients with breast cancer?

      Your Answer:

      Correct Answer: Young age

      Explanation:

      Prognostic Factors in Breast Cancer and Their Impact on Survival

      Breast cancer prognosis is influenced by several factors, including axillary nodal status, tumour type and grade, lymphatic/vascular invasion/proliferation markers, ethnicity, patient age at diagnosis, oestrogen receptor and progesterone receptor status, and HER2/neu overexpression. Younger patients tend to have more aggressive tumours, which increases their risk of recurrence and mortality over their lifetimes.

      Oestrogen receptor-positive tumours have a better prognosis and can be treated with tamoxifen, which increases survival rates. Progesterone receptor-positive tumours also have a good prognosis and can be targeted using HER2 receptor modulators like tamoxifen. On the other hand, oestrogen receptor-negative and progesterone receptor-negative tumours are associated with a poor prognosis.

      Tumour grade is another important prognostic factor, with high-grade tumours being linked to a poorer prognosis. Additionally, a positive lymph node status is a poor prognostic factor, as the risk of recurrence increases with the number of affected nodes.

      In summary, understanding these prognostic factors can help healthcare professionals tailor treatment plans and provide patients with more accurate information about their prognosis and survival.

    • This question is part of the following fields:

      • Haematology/Oncology
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  • Question 171 - A 47-year-old woman presents to the Stroke Clinic for review after experiencing a...

    Incorrect

    • A 47-year-old woman presents to the Stroke Clinic for review after experiencing a transient ischaemic attack (TIA). It is suspected that the patient’s TIA was caused by an issue with her carotid arteries.
      A magnetic resonance angiogram (MRA) is requested followed by catheter angiography. The MRA shows a right internal carotid with narrowed eccentric lumen, surrounded by a crescent-shaped mural thrombus and thin annular enhancement. The catheter angiogram shows a ‘string sign’ in the right internal carotid.
      What internal carotid abnormality is most likely the cause of this patient’s TIA?

      Your Answer:

      Correct Answer: Carotid-artery dissection

      Explanation:

      Cervico-cerebral arterial dissections (CADs) are a common cause of strokes in younger patients, accounting for almost 20% of strokes in those under 45 years old. The majority of cases involve the extracranial internal carotid artery, while extracranial vertebral dissections make up about 15% of cases. A high level of suspicion is necessary to diagnose CAD, and confirmation can be obtained through various imaging techniques such as Doppler ultrasonography, magnetic resonance imaging/magnetic resonance angiography (MRA), computed tomography angiography (CTA), or catheter angiography. CTA can reveal several characteristic features of CAD, including an abnormal vessel contour, enlargement of the dissected artery, an intimal flap, and a dissecting aneurysm. The traditional method of diagnosing arterial dissections is catheter angiography, which typically shows a long segment of narrowed lumen known as the string sign. Other conditions such as carotid-artery pseudoaneurysm, carotid-artery aneurysm, carotid-artery occlusion, and carotid-artery stenosis can also be identified through imaging techniques, but they are not evident in this particular angiogram.

    • This question is part of the following fields:

      • Neurology
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  • Question 172 - A 28-year-old man presents to his General Practitioner with pallor, fatigue, weakness, palpitations...

    Incorrect

    • A 28-year-old man presents to his General Practitioner with pallor, fatigue, weakness, palpitations and dyspnoea on exertion. His symptoms have come on quickly over the last three weeks. A full blood count is ordered and is suggestive of acute lymphoblastic myeloid leukaemia (AML).
      What Is the next most appropriate investigation for this patient?

      Your Answer:

      Correct Answer: Bone marrow biopsy

      Explanation:

      Diagnostic Tests for Acute Myeloid Leukaemia

      Acute myeloid leukaemia (AML) is a type of blood cancer that affects the bone marrow. To diagnose AML, several diagnostic tests may be performed. The most common tests include a bone marrow biopsy, ultrasound scan of the abdomen, chest X-ray, computerised tomography (CT) scan of chest, abdomen and pelvis, and lumbar puncture.

      Bone Marrow Biopsy: This is the most important test for diagnosing AML. It involves extracting cells from the bone marrow and examining them under a microscope. AML is characterised by the presence of primitive myeloblasts and Auer rods in the bone marrow.

      Ultrasound Scan of the Abdomen: This test is used to check for enlarged lymph nodes in the abdomen or spleen. If any enlarged lymph nodes are found, they may be biopsied to determine the extent of the leukaemia.

      Chest X-ray: This test is used to check for enlarged lymph nodes in the mediastinum.

      CT Scan of Chest, Abdomen and Pelvis: This test is not usually used as a first-line investigation for AML. However, once the diagnosis is confirmed, a CT scan may be used to assess for the presence of enlarged lymph nodes or for planning purposes if radiotherapy is going to form part of the treatment.

      Lumbar Puncture: This test is not usually used in the diagnosis of AML unless it is suspected that the leukaemia cells are also present in the cerebrospinal fluid.

      In conclusion, a bone marrow biopsy is the most important test for diagnosing AML. Other tests may be used to determine the extent of the leukaemia or for planning purposes if radiotherapy is going to form part of the treatment.

    • This question is part of the following fields:

      • Haematology/Oncology
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  • Question 173 - A 7-week-old male infant was presented to the GP clinic by his anxious...

    Incorrect

    • A 7-week-old male infant was presented to the GP clinic by his anxious mother. She complains of a 2-week history of inadequate feeding and weight gain, accompanied by fast breathing, especially during feeding. The mother became extremely worried when she observed a bluish tint on her baby's skin this morning.
      What is the probable diagnosis?

      Your Answer:

      Correct Answer: Tetralogy of Fallot

      Explanation:

      TOF is the primary reason for cyanotic congenital heart disease, which usually manifests at 1-2 months of age. While transposition of the great arteries is also a significant cause of this condition, it typically presents within the first 24 hours of life. Ventricular septal defect and atrioventricular septal defect are not associated with cyanotic congenital heart disease.

      Understanding Tetralogy of Fallot

      Tetralogy of Fallot (TOF) is a congenital heart disease that results from the anterior malalignment of the aorticopulmonary septum. It is the most common cause of cyanotic congenital heart disease, and it typically presents at around 1-2 months, although it may not be detected until the baby is 6 months old. The condition is characterized by four features, including ventricular septal defect (VSD), right ventricular hypertrophy, right ventricular outflow tract obstruction, and overriding aorta. The severity of the right ventricular outflow tract obstruction determines the degree of cyanosis and clinical severity.

      Other features of TOF include cyanosis, which may cause episodic hypercyanotic ‘tet’ spells due to near occlusion of the right ventricular outflow tract. These spells are characterized by tachypnea and severe cyanosis that may occasionally result in loss of consciousness. They typically occur when an infant is upset, in pain, or has a fever, and they cause a right-to-left shunt. Additionally, TOF may cause an ejection systolic murmur due to pulmonary stenosis, and a right-sided aortic arch is seen in 25% of patients. Chest x-ray shows a ‘boot-shaped’ heart, while ECG shows right ventricular hypertrophy.

      The management of TOF often involves surgical repair, which is usually undertaken in two parts. Cyanotic episodes may be helped by beta-blockers to reduce infundibular spasm. However, it is important to note that at birth, transposition of the great arteries is the more common lesion as patients with TOF generally present at around 1-2 months. Understanding the features and management of TOF is crucial for healthcare professionals to provide appropriate care and treatment for affected infants.

    • This question is part of the following fields:

      • Paediatrics
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  • Question 174 - A 6-year-old girl is brought to see her GP by her mother. She...

    Incorrect

    • A 6-year-old girl is brought to see her GP by her mother. She is noted to be on the 4th centile for weight. Her mother notes that for the past few months her daughter has been tired and passes greasy foul-smelling stools three times a day. Blood tests reveal mild anaemia, positive serum IgA anti-endomysial antibody (EMA-IgA) and very elevated tissue transglutaminase (tTG) levels.
      Which of the following is the most likely cause of her symptoms?
      Select the SINGLE most likely cause from the list below. Select ONE option only.

      Your Answer:

      Correct Answer: Coeliac disease

      Explanation:

      Understanding Coeliac Disease: Symptoms, Diagnosis, and Treatment

      Coeliac disease (CD) is a common autoimmune disorder that affects almost 1% of individuals in developed countries. It is triggered by gluten and related prolamins present in wheat, rye, and barley, and primarily affects the small intestine, leading to flattening of the small intestinal mucosa. CD can present in various ways, including typical GI symptoms, atypical symptoms, or no symptoms at all. Diagnosis is made through serology tests for specific autoimmune markers, and treatment involves a lifelong avoidance of gluten ingestion.

      Other potential diagnoses, such as travellers’ diarrhoea, growth hormone deficiency, hypothyroidism, and severe combined immunodeficiency, have different clinical presentations and are not consistent with this patient’s symptoms. Understanding the symptoms, diagnosis, and treatment of CD is crucial for proper management and improved quality of life for affected individuals.

    • This question is part of the following fields:

      • Gastroenterology/Nutrition
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  • Question 175 - A 50-year-old woman presents to the GP clinic with complaints of heavy vaginal...

    Incorrect

    • A 50-year-old woman presents to the GP clinic with complaints of heavy vaginal bleeding. She reports having regular menstrual cycles and denies any intermenstrual or postcoital bleeding. The patient has no significant gynaecological history and is not on any regular medications. She is not in a committed relationship and uses condoms for contraception. Additionally, she has no desire to have children. What is the recommended initial treatment option?

      Your Answer:

      Correct Answer: Intrauterine system

      Explanation:

      For the treatment of menorrhagia, the first-line option would be the intrauterine system. Specifically, the Mirena, which contains levonorgestrel, is highly effective in treating menorrhagia and also serves as a long-acting reversible contraceptive. While the combined oral contraceptive pill, tranexamic acid, and mefenamic acid may provide relief from symptoms, they are not the preferred initial treatment. On the other hand, the intrauterine device would not be suitable for addressing this patient’s menorrhagia.

      Managing Heavy Menstrual Bleeding

      Heavy menstrual bleeding, also known as menorrhagia, is a condition where a woman experiences excessive blood loss during her menstrual cycle. While it was previously defined as total blood loss of over 80 ml per cycle, the management of menorrhagia now depends on the woman’s perception of what is excessive. In the past, hysterectomy was a common treatment for heavy periods, but the approach has changed significantly since the 1990s.

      To manage menorrhagia, a full blood count should be performed in all women. If symptoms suggest a structural or histological abnormality, a routine transvaginal ultrasound scan should be arranged. For women who do not require contraception, mefenamic acid or tranexamic acid can be used. If there is no improvement, other drugs can be tried while awaiting referral.

      For women who require contraception, options include the intrauterine system (Mirena), combined oral contraceptive pill, and long-acting progestogens. Norethisterone can also be used as a short-term option to rapidly stop heavy menstrual bleeding. The flowchart below shows the management of menorrhagia.

      [Insert flowchart here]

    • This question is part of the following fields:

      • Reproductive Medicine
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  • Question 176 - A 55-year-old woman had a recent acute myocardial infarction (MI).
    Which medication has been...

    Incorrect

    • A 55-year-old woman had a recent acute myocardial infarction (MI).
      Which medication has been proven to reduce mortality after an MI?

      Your Answer:

      Correct Answer: Bisoprolol

      Explanation:

      Medications for Post-Myocardial Infarction Patients

      Post-myocardial infarction (MI) patients require specific medications to prevent further cardiovascular disease and improve their overall health. One of the most important drugs to offer is a beta-blocker, such as bisoprolol, as soon as the patient is stable. This medication should be continued for at least 12 months after an MI in patients without left ventricular systolic dysfunction or heart failure, and indefinitely in those with left ventricular systolic dysfunction. While beta-blockers can reduce mortality and morbidity for up to a year after an MI, recent studies suggest that continuing treatment beyond a year may not provide any additional benefits. Other medications, such as amiodarone, isosorbide mononitrate, and nicorandil, offer symptom relief but do not reduce mortality or morbidity. Calcium-channel blockers, like diltiazem, may be considered for secondary prevention in patients without pulmonary congestion or left ventricular systolic dysfunction if beta-blockers are contraindicated or discontinued. However, current guidelines recommend offering all post-MI patients an ACE inhibitor, dual antiplatelet therapy, beta-blocker, and statin to improve their long-term health outcomes.

    • This question is part of the following fields:

      • Cardiovascular
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  • Question 177 - A 72-year-old man presents to the cardiology clinic with symptomatic aortic stenosis. Despite...

    Incorrect

    • A 72-year-old man presents to the cardiology clinic with symptomatic aortic stenosis. Despite his overall good health, he is eager for intervention. What intervention is most likely to be recommended for him?

      Your Answer:

      Correct Answer: Bioprosthetic aortic valve replacement

      Explanation:

      Mechanical valves are typically preferred for younger patients as they have a longer lifespan compared to other types of prosthetic heart valves.

      Prosthetic Heart Valves: Options for Replacement

      Prosthetic heart valves are commonly used to replace damaged aortic and mitral valves. There are two main options for replacement: biological (bioprosthetic) or mechanical. Biological valves are usually sourced from bovine or porcine origins and are commonly used in older patients. However, they have a major disadvantage of structural deterioration and calcification over time. On the other hand, mechanical valves have a low failure rate but require long-term anticoagulation due to the increased risk of thrombosis. Warfarin is still the preferred anticoagulant for patients with mechanical heart valves, and the target INR varies depending on the valve type. Aspirin is only given in addition if there is an additional indication, such as ischaemic heart disease. Following the 2008 NICE guidelines, antibiotics are no longer recommended for common procedures such as dental work for prophylaxis of endocarditis.

    • This question is part of the following fields:

      • Cardiovascular
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  • Question 178 - A 21-year-old soccer player comes to you with complaints of shoulder and lower...

    Incorrect

    • A 21-year-old soccer player comes to you with complaints of shoulder and lower back pain. He reports that his back has been getting stiffer over the past few months and has worsened. During the examination, you find out that he is also experiencing enthesitis of the Achilles tendon. You suspect a particular diagnosis and want to confirm it. What antigen's presence would confirm the diagnosis?

      Your Answer:

      Correct Answer: HLA-B27

      Explanation:

      Ankylosing spondylitis is a type of spondyloarthropathy that is associated with HLA-B27. It is more commonly seen in young males, with a sex ratio of 3:1, and typically presents with lower back pain and stiffness that develops gradually. The stiffness is usually worse in the morning and improves with exercise, while pain at night may improve upon getting up. Clinical examination may reveal reduced lateral and forward flexion, as well as reduced chest expansion. Other features associated with ankylosing spondylitis include apical fibrosis, anterior uveitis, aortic regurgitation, Achilles tendonitis, AV node block, amyloidosis, cauda equina syndrome, and peripheral arthritis (more common in females).

    • This question is part of the following fields:

      • Musculoskeletal
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  • Question 179 - A 36-year-old woman presents to her GP with concerns about facial flushing. She...

    Incorrect

    • A 36-year-old woman presents to her GP with concerns about facial flushing. She reports experiencing random episodes of redness on her face, particularly after consuming alcohol. She also mentions an increase in the number of spots on her cheeks and wonders if these symptoms are related. During the examination, the GP observes two small telangiectasia on the nose and left cheek, as well as a few small papules on each cheek. What management options should the GP suggest to alleviate the patient's symptoms?

      Your Answer:

      Correct Answer: Topical metronidazole

      Explanation:

      For the treatment of mild to moderate acne rosacea, topical metronidazole is recommended. This patient’s symptoms, including flushing and papules, suggest acne rosacea, and as they only have a few telangiectasia and papules, topical metronidazole would be the most appropriate treatment. Laser therapy may be considered for persistent telangiectasia, but it is not necessary at this stage and would likely be arranged by a specialist. Oral isotretinoin is not used to treat acne rosacea and is reserved for severe acne vulgaris, and can only be prescribed by a specialist due to potential harmful side effects. Oral oxytetracycline would be appropriate for more severe cases of acne rosacea with troublesome papules and pustules. Topical fusidic acid is not used to treat acne rosacea but can be used for impetigo.

      Understanding Rosacea: Symptoms and Management

      Rosacea, also known as acne rosacea, is a chronic skin condition that has no known cause. It typically affects the nose, cheeks, and forehead, and the first symptom is often flushing. Over time, telangiectasia (visible blood vessels) may appear, followed by persistent redness with papules and pustules. In some cases, rhinophyma (enlarged nose) may develop, and there may be ocular involvement, such as blepharitis. Sunlight can exacerbate symptoms.

      Mild cases of rosacea may be treated with topical metronidazole, while topical brimonidine gel may be used for patients with predominant flushing but limited telangiectasia. More severe cases may require systemic antibiotics like oxytetracycline. Patients are advised to apply high-factor sunscreen daily and use camouflage creams to conceal redness. Laser therapy may be appropriate for those with prominent telangiectasia, and patients with rhinophyma should be referred to a dermatologist.

      Overall, understanding the symptoms and management of rosacea can help individuals manage their condition and improve their quality of life.

    • This question is part of the following fields:

      • Dermatology
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  • Question 180 - A pair in their early 30s visit their GP seeking advice on their...

    Incorrect

    • A pair in their early 30s visit their GP seeking advice on their inability to conceive despite engaging in regular sexual activity for 6 months. What would be the most suitable course of action for you to recommend?

      Your Answer:

      Correct Answer: Wait until they have been having regular intercourse for 12 months

      Explanation:

      Couples are advised to engage in regular sexual intercourse every 2-3 days for a period of 12 months before seeking referral to a specialist. After this time, fertility testing should be conducted, including semen analysis for the male and mid-luteal progesterone level for the female to confirm ovulation. The use of basal body temperature kits is not recommended as they can increase anxiety and have not been proven effective. However, early referral should be considered for females over 35 years of age, those with a history of amenorrhea or pelvic surgery, and those with abnormal genital examinations. Males with a history of genital surgery, STIs, varicocele, or significant systemic illness should also be referred early.

      Infertility is a common issue that affects approximately 1 in 7 couples. It is important to note that around 84% of couples who have regular sexual intercourse will conceive within the first year, and 92% within the first two years. The causes of infertility can vary, with male factor accounting for 30%, unexplained causes accounting for 20%, ovulation failure accounting for 20%, tubal damage accounting for 15%, and other causes accounting for the remaining 15%.

      When investigating infertility, there are some basic tests that can be done. These include a semen analysis and a serum progesterone test. The serum progesterone test is done 7 days prior to the expected next period, typically on day 21 for a 28-day cycle. The interpretation of the serum progesterone level is as follows: if it is less than 16 nmol/l, it should be repeated and if it remains consistently low, referral to a specialist is necessary. If the level is between 16-30 nmol/l, it should be repeated, and if it is greater than 30 nmol/l, it indicates ovulation.

      It is important to counsel patients on lifestyle factors that can impact fertility. This includes taking folic acid, maintaining a healthy BMI between 20-25, and advising regular sexual intercourse every 2 to 3 days. Additionally, patients should be advised to quit smoking and limit alcohol consumption to increase their chances of conceiving.

    • This question is part of the following fields:

      • Reproductive Medicine
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  • Question 181 - A 28-year-old primip nurse has presented to you 5 days after being in...

    Incorrect

    • A 28-year-old primip nurse has presented to you 5 days after being in contact with a child who had a vesicular rash on their face and chest. She is currently 14 weeks pregnant and has been experiencing some morning sickness, but otherwise feels fine. Her blood tests show that she is not immune to varicella zoster virus. What should be the next course of action in your management plan?

      Your Answer:

      Correct Answer: A single dose of varicella-zoster immunoglobulin (VZI)

      Explanation:

      If a pregnant woman is not immune to the varicella zoster virus and has been in close contact with someone who has the virus, it is recommended that she receive varicella-zoster immunoglobulin (VZIG) as soon as possible. VZIG can be effective up to 10 days after contact, or 10 days after the appearance of the rash in the person with the virus if there are continuous exposures.
      For pregnant women who are not immune and have been exposed to chickenpox, they should be considered potentially infectious from 8-28 days after exposure if they receive VZIG, and from 8-21 days after exposure if they do not receive VZIG.
      Source: RCOG

      Chickenpox exposure in pregnancy can pose risks to both the mother and fetus, including fetal varicella syndrome. Post-exposure prophylaxis (PEP) with varicella-zoster immunoglobulin (VZIG) or antivirals should be given to non-immune pregnant women, with timing dependent on gestational age. If a pregnant woman develops chickenpox, specialist advice should be sought and oral aciclovir may be given if she is ≥ 20 weeks and presents within 24 hours of onset of the rash.

    • This question is part of the following fields:

      • Reproductive Medicine
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  • Question 182 - Which of the following is a common feature of ulcerative colitis? ...

    Incorrect

    • Which of the following is a common feature of ulcerative colitis?

      Your Answer:

      Correct Answer: Pseudopolyps

      Explanation:

      Pseudopolyps observed during endoscopy are indicative of ulcerative colitis.

      Crohn’s disease and ulcerative colitis are the two main types of inflammatory bowel disease with many similarities in symptoms and management options. However, there are key differences such as non-bloody diarrhea and upper gastrointestinal symptoms being more common in Crohn’s disease, while bloody diarrhea and abdominal pain in the left lower quadrant are more common in ulcerative colitis. Complications and pathology also differ between the two diseases.

    • This question is part of the following fields:

      • Gastroenterology/Nutrition
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  • Question 183 - A 65-year-old man with a history of Parkinson's disease comes to the clinic...

    Incorrect

    • A 65-year-old man with a history of Parkinson's disease comes to the clinic complaining of an itchy, red rash on his neck, behind his ears, and around the nasolabial folds. He experienced a similar outbreak last year but did not seek medical attention. What is the probable diagnosis?

      Your Answer:

      Correct Answer: Seborrhoeic dermatitis

      Explanation:

      Patients with Parkinson’s disease are more likely to experience seborrhoeic dermatitis.

      Understanding Seborrhoeic Dermatitis in Adults

      Seborrhoeic dermatitis is a chronic skin condition that affects around 2% of the general population. It is caused by an inflammatory reaction related to the overgrowth of a fungus called Malassezia furfur, which is a normal inhabitant of the skin. The condition is characterized by eczematous lesions that appear on the sebum-rich areas of the body, such as the scalp, periorbital, auricular, and nasolabial folds. It can also lead to the development of otitis externa and blepharitis.

      Seborrhoeic dermatitis is often associated with other medical conditions, such as HIV and Parkinson’s disease. The management of the condition depends on the affected area. For scalp disease, over-the-counter preparations containing zinc pyrithione and tar are usually the first-line treatment. If these are not effective, ketoconazole is the preferred second-line agent. Selenium sulphide and topical corticosteroids may also be useful.

      For the face and body, topical antifungals such as ketoconazole and topical steroids are often used. However, it is important to use steroids for short periods only to avoid side effects. Seborrhoeic dermatitis can be difficult to treat, and recurrences are common. Therefore, it is important to work closely with a healthcare provider to manage the condition effectively.

    • This question is part of the following fields:

      • Dermatology
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  • Question 184 - A 45-year-old man with hypertension complains of recurring headaches accompanied by sensitivity to...

    Incorrect

    • A 45-year-old man with hypertension complains of recurring headaches accompanied by sensitivity to light, nausea, and occasional vomiting. The headaches usually affect the right side of his head and sometimes cause temporary vision problems. They last up to 10 hours and occur approximately once every 4-6 weeks. The neurological examination and blood pressure are normal.

      What would be the most suitable initial medical treatment for acute attacks? Choose the ONE most appropriate first-line medical treatment from the options provided.

      Your Answer:

      Correct Answer: Ibuprofen

      Explanation:

      Treatment Options for Migraines: A Comparison of Medications

      Migraines are a recurring type of headache that can last for several hours to a few days. They are often accompanied by symptoms such as sensitivity to light and sound, nausea, and vomiting. There are several medications available for the treatment of migraines, each with its own benefits and drawbacks.

      Ibuprofen is a simple analgesic that is recommended by the National Institute for Health and Care Excellence (NICE) for the treatment of acute migraine attacks. It is safe for patients with ischaemic heart disease, but the daily dose should not exceed 1200 mg.

      Sumatriptan is a serotonin-receptor agonist that causes intracerebral vasoconstriction. It is recommended by NICE for the treatment of acute migraines, but it is contraindicated in patients with a history of ischaemic heart disease.

      Amitriptyline is a tricyclic antidepressant that is used for long-term prophylaxis of migraines. It is recommended by NICE for this use but not for acute treatment.

      Co-codamol, an opiate medication, is not recommended by NICE for the treatment of migraines due to the risk of medication-overuse headache and worsening of nausea and vomiting symptoms.

      Ergotamine tartrate, another medication that was previously used to treat migraines, is now limited in use due to its unpleasant side effects such as nausea and vomiting. NICE advises against its use for the treatment of acute migraines.

      In conclusion, the choice of medication for the treatment of migraines should be based on the patient’s medical history and the severity of their symptoms. Patients should consult with their healthcare provider to determine the best treatment plan for their individual needs.

    • This question is part of the following fields:

      • Neurology
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  • Question 185 - You are conducting an interview with a 24-year-old man who has arrived at...

    Incorrect

    • You are conducting an interview with a 24-year-old man who has arrived at the emergency department after self-harming. As you converse with him, you observe that his facial expression is devoid of emotion, his tone of voice is flat, and his body language lacks any animation. This is evident even when he talks about his traumatic experiences of childhood abuse. How would you record this in your documentation?

      Your Answer:

      Correct Answer: Flattened affect

      Explanation:

      Affect and mood can be easily confused during a mental state exam. Affect refers to the current emotional state that can be observed, while mood is the predominant emotional state over a longer period. It is helpful to think of affect as the weather on a particular day and mood as the overall climate.

      Mood is determined by the patient’s history and can be described as their emotional state over the past month. Symptoms of depression or mania can be used to determine the patient’s mood. On the other hand, affect is the emotional state that is currently being displayed by the patient during the assessment. It is expressed through facial expressions, voice tone, and body movements. Affect can be normal, restricted, blunted, or flat. Labile affect is characterized by abrupt shifts in emotions.

      In the given scenario, the patient is displaying a flattened affect, which means there is no expression of emotion. Apathy may be a symptom present in the patient’s history, but the scenario is specifically referring to the current observed emotional state. Depressed mood may also be present, but it is discussed in the patient’s history and is not the same as affect. Symptoms of depressed mood include anhedonia, low mood, lack of energy, poor concentration, and poor sleep.

      Thought disorders can manifest in various ways, including circumstantiality, tangentiality, neologisms, clang associations, word salad, Knight’s move thinking, flight of ideas, perseveration, and echolalia. Circumstantiality involves providing excessive and unnecessary detail when answering a question, but eventually returning to the original point. Tangentiality, on the other hand, refers to wandering from a topic without returning to it. Neologisms are newly formed words, often created by combining two existing words. Clang associations occur when ideas are related only by their similar sounds or rhymes. Word salad is a type of speech that is completely incoherent, with real words strung together into nonsensical sentences. Knight’s move thinking is a severe form of loosening of associations, characterized by unexpected and illogical leaps from one idea to another. Flight of ideas is a thought disorder that involves jumping from one topic to another, but with discernible links between them. Perseveration is the repetition of ideas or words despite attempts to change the topic. Finally, echolalia is the repetition of someone else’s speech, including the question that was asked.

    • This question is part of the following fields:

      • Psychiatry
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  • Question 186 - A 16-year-old boy presents to you with complaints of excessive sweating in his...

    Incorrect

    • A 16-year-old boy presents to you with complaints of excessive sweating in his hands. He reports feeling embarrassed in social situations, particularly when he has to shake hands with someone. He is also concerned about how this may impact his upcoming A-level exams.

      Which of the following is the most appropriate initial management approach for this condition?

      Your Answer:

      Correct Answer: Aluminium chloride

      Explanation:

      Hyperhidrosis is not treated with beta blockers like propranolol or calcium channel blockers like nifedipine.

      Hyperhidrosis is a condition characterized by the excessive production of sweat. To manage this condition, there are several options available. The first-line treatment is the use of topical aluminium chloride preparations, although it may cause skin irritation as a side effect. Iontophoresis is another option that is particularly useful for patients with palmar, plantar, and axillary hyperhidrosis. Botulinum toxin is also licensed for axillary symptoms. Surgery, such as Endoscopic transthoracic sympathectomy, is another option, but patients should be informed of the risk of compensatory sweating. Overall, there are various management options available for hyperhidrosis, and patients should discuss with their healthcare provider to determine the best course of action.

    • This question is part of the following fields:

      • Dermatology
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  • Question 187 - A 26-year-old man presents to the eye casualty department on his own accord....

    Incorrect

    • A 26-year-old man presents to the eye casualty department on his own accord. He mentions that he rarely visits doctors but decided to seek medical attention for his current issue. The patient has a medical history of ulcerative colitis.
      Upon initial examination, the doctor notes inflammation in either the episclera or the sclera and proceeds to perform a slit lamp examination.
      What is the classic distinguishing feature between the two diagnoses based on the history and examination?

      Your Answer:

      Correct Answer: Pain

      Explanation:

      Distinguishing between scleritis and episcleritis cannot be based solely on the redness of the eyes, as both conditions result in visible redness.

      Rheumatoid Arthritis and Its Effects on the Eyes

      Rheumatoid arthritis is a chronic autoimmune disease that affects various parts of the body, including the eyes. In fact, ocular manifestations of rheumatoid arthritis are quite common, with approximately 25% of patients experiencing eye problems. These eye problems can range from mild to severe and can significantly impact a patient’s quality of life.

      The most common ocular manifestation of rheumatoid arthritis is keratoconjunctivitis sicca, also known as dry eye syndrome. This condition occurs when the eyes do not produce enough tears, leading to discomfort, redness, and irritation. Other ocular manifestations of rheumatoid arthritis include episcleritis, scleritis, corneal ulceration, and keratitis. Episcleritis and scleritis both cause redness in the eyes, with scleritis also causing pain. Corneal ulceration and keratitis both affect the cornea, with corneal ulceration being a more severe condition that can lead to vision loss.

      In addition to these conditions, patients with rheumatoid arthritis may also experience iatrogenic ocular manifestations. These are side effects of medications used to treat the disease. For example, steroid use can lead to cataracts, while the use of chloroquine can cause retinopathy.

      Overall, it is important for patients with rheumatoid arthritis to be aware of the potential ocular manifestations of the disease and to seek prompt medical attention if they experience any eye-related symptoms. Early diagnosis and treatment can help prevent vision loss and improve overall quality of life.

    • This question is part of the following fields:

      • Ophthalmology
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  • Question 188 - A 63-year-old man presents with a complaint of neck and arm pain that...

    Incorrect

    • A 63-year-old man presents with a complaint of neck and arm pain that has been ongoing for four months. He describes the pain as similar to 'electric shocks' and notes that it worsens when he turns his head. There is no history of trauma or any other apparent cause. The patient is in good health and not taking any medications. During the examination, it is noted that he has reduced sensation on the back of his thumb and middle finger. What is the probable underlying diagnosis?

      Your Answer:

      Correct Answer: C6 radiculopathy

      Explanation:

      Understanding Dermatomes: Major Landmarks and Mnemonics

      Dermatomes are areas of skin that are innervated by a single spinal nerve. Understanding dermatomes is important in diagnosing and treating various neurological conditions. The major dermatome landmarks are listed with helpful mnemonics to remember them.

      Starting from the top of the body, the C2 dermatome covers the posterior half of the skull, resembling a cap. Moving down to C3, it covers the area of a high turtleneck shirt. C4 covers the area of a low-collar shirt. The C5 dermatome runs along the ventral axial line of the upper limb, while C6 covers the thumb and index finger. To remember this, make a 6 with your left hand by touching the tip of the thumb and index finger together.

      Moving down to C7, it covers the middle finger and palm of the hand. C8 covers the ring and little finger. The T4 dermatome covers the area of the nipples, while T5 covers the inframammary fold. T6 covers the xiphoid process, and T10 covers the umbilicus. To remember this, think of BellybuT-TEN.

      The L1 dermatome covers the inguinal ligament, which can be remembered by thinking of L for ligament, 1 for 1nguinal. L4 covers the knee caps, and to remember this, think of being down on all fours. L5 covers the big toe and dorsum of the foot (except the lateral aspect), and can be remembered by thinking of it as the largest of the five toes. Finally, the S1 dermatome covers the lateral foot and small toe, while S2 and S3 cover the genitalia.

      Understanding dermatomes and their landmarks can aid in diagnosing and treating various neurological conditions. The mnemonics provided can help in remembering these important landmarks.

    • This question is part of the following fields:

      • Neurology
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  • Question 189 - A 35-year-old man comes to his General Practitioner complaining of an itchy rash...

    Incorrect

    • A 35-year-old man comes to his General Practitioner complaining of an itchy rash on the flexural surface of both his arms that has been present for 1 week. On examination, the rash appears polygonal and shiny with a white lines pattern on the surface. What is the most appropriate next step?

      Your Answer:

      Correct Answer: No further testing required, start treatment

      Explanation:

      Diagnostic Testing for Lichen Planus: Understanding Skin Patch Testing, Skin Prick Testing, and RAST

      Lichen planus is a clinical diagnosis that can be made based on the characteristic appearance of the rash. However, in some cases, a biopsy may be helpful if the presentation is atypical. The diagnosis is typically made without the need for further testing, and treatment can be started promptly.

      Skin patch testing and skin prick testing are not useful for diagnosing lichen planus, as they are mainly used for different types of hypersensitivity reactions. Skin patch testing is used for contact dermatitis and other type IV hypersensitivity reactions, while skin prick testing is used for type I hypersensitivity reactions, such as food allergies and pollen allergies.

      Radioallergosorbent testing (RAST) is also unsuitable for diagnosing lichen planus, as it is used to determine the amount of immunoglobulin E (IgE) that reacts specifically with suspected or known allergens. RAST is useful for food allergies, inhaled allergens (such as pollen), and wasp/bee venom.

      In summary, diagnostic testing is not typically required for lichen planus, as it can be diagnosed clinically. Skin patch testing, skin prick testing, and RAST are not useful for diagnosing lichen planus and are mainly used for different types of hypersensitivity reactions.

    • This question is part of the following fields:

      • Dermatology
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  • Question 190 - A 35-year-old woman has Addison’s disease.
    Which of the following medications is she likely...

    Incorrect

    • A 35-year-old woman has Addison’s disease.
      Which of the following medications is she likely to be taking long term?

      Your Answer:

      Correct Answer: Hydrocortisone and fludrocortisone

      Explanation:

      Common Medications for Adrenal Disorders

      Adrenal disorders such as Addison’s disease and Cushing’s syndrome require specific medications for treatment. Here are some commonly used drugs and their indications:

      Hydrocortisone and Fludrocortisone: These are the mainstays of treatment for Addison’s disease, as they replace the deficient glucocorticosteroids and mineralocorticoids.

      Phenoxybenzamine: This medication is used to treat phaeochromocytoma before surgery.

      Metyrapone: It can be used to diagnose or treat Cushing’s syndrome by reducing the amount of aldosterone and cortisol in the body.

      Prednisolone and Levothyroxine: Prednisolone can be used instead of hydrocortisone in Addison’s disease to avoid peaks and troughs. However, levothyroxine is not used to treat Addison’s disease, but it’s important to check for concurrent thyroid disease.

      Spironolactone: It’s used to treat Conn’s disease, which causes hyperaldosteronism. It’s not appropriate for Addison’s disease treatment, as both can cause hyperkalaemia.

    • This question is part of the following fields:

      • Endocrinology/Metabolic Disease
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  • Question 191 - A 50-year-old known alcoholic presents to the Emergency Department with disorientation. Upon examination,...

    Incorrect

    • A 50-year-old known alcoholic presents to the Emergency Department with disorientation. Upon examination, there is gross distension of the abdomen, shifting dullness, pitting edema to the mid-thigh, and a temperature of 38ºC. What is the probable diagnosis?

      Your Answer:

      Correct Answer: Spontaneous bacterial peritonitis

      Explanation:

      The probable diagnosis in this case is spontaneous bacterial peritonitis, as indicated by the presence of fever and absence of diarrhoea. The patient’s history of chronic alcohol abuse and diffuse oedema also suggests liver failure, which increases the risk of developing spontaneous bacterial peritonitis.

      Understanding Spontaneous Bacterial Peritonitis

      Spontaneous bacterial peritonitis (SBP) is a type of peritonitis that typically affects individuals with ascites caused by liver cirrhosis. The condition is characterized by symptoms such as abdominal pain, fever, and ascites. Diagnosis is usually made through paracentesis, which involves analyzing the ascitic fluid for a neutrophil count of over 250 cells/ul. The most common organism found on ascitic fluid culture is E. coli.

      Management of SBP typically involves the administration of intravenous cefotaxime. Antibiotic prophylaxis is also recommended for patients with ascites who have previously experienced an episode of SBP or have a fluid protein level of less than 15 g/l and a Child-Pugh score of at least 9 or hepatorenal syndrome. NICE recommends prophylactic oral ciprofloxacin or norfloxacin until the ascites has resolved.

      Alcoholic liver disease is a significant predictor of poor prognosis in SBP. Understanding the symptoms, diagnosis, and management of SBP is crucial for healthcare professionals to provide appropriate care and improve patient outcomes.

    • This question is part of the following fields:

      • Gastroenterology/Nutrition
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  • Question 192 - A patient in her late 60s is hospitalized with digoxin toxicity. Which of...

    Incorrect

    • A patient in her late 60s is hospitalized with digoxin toxicity. Which of her medications is the most probable cause of this condition?

      Your Answer:

      Correct Answer: Diltiazem

      Explanation:

      The use of diltiazem can lead to the development of digoxin toxicity.

      Understanding Digoxin and Its Toxicity

      Digoxin is a medication used for rate control in atrial fibrillation and for improving symptoms in heart failure patients. It works by decreasing conduction through the atrioventricular node and increasing the force of cardiac muscle contraction. However, it has a narrow therapeutic index and requires monitoring for toxicity.

      Toxicity may occur even when the digoxin concentration is within the therapeutic range. Symptoms of toxicity include lethargy, nausea, vomiting, anorexia, confusion, yellow-green vision, arrhythmias, and gynaecomastia. Hypokalaemia is a classic precipitating factor, as it allows digoxin to more easily bind to the ATPase pump and increase its inhibitory effects. Other factors that may contribute to toxicity include increasing age, renal failure, myocardial ischaemia, electrolyte imbalances, hypoalbuminaemia, hypothermia, hypothyroidism, and certain medications such as amiodarone, quinidine, and verapamil.

      Management of digoxin toxicity involves the use of Digibind, correction of arrhythmias, and monitoring of potassium levels. It is important to recognize the potential for toxicity and monitor patients accordingly to prevent adverse outcomes.

    • This question is part of the following fields:

      • Pharmacology/Therapeutics
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  • Question 193 - A 75-year-old male has two episodes of weakness affecting the right arm and...

    Incorrect

    • A 75-year-old male has two episodes of weakness affecting the right arm and leg each lasting ten minutes, both within the space of 2 days. He did not attend the emergency department after the first episode. His only significant past medical history is hypertension, for which he takes amlodipine 5mg OD. He has experienced one similar episode to this one year ago, but did not seek medical attention. His son is present who informs you that the patient has lost a significant amount of weight in the last year. On further questioning, he reports some haemoptysis lately. His blood pressure in the department was 170/90 mmHg initially.

      His bloods reveal:
      Hb 115 g/l
      Platelets 149 * 109/l
      WBC 13.1 * 109/l
      Na+ 132 mmol/l
      K+ 5.3 mmol/l
      Creatinine 111 µmol/l
      CRP 15 mg/l
      ECG: Sinus tachycardia, rate 104/min

      What is the most appropriate management for this gentleman?

      Your Answer:

      Correct Answer: Admit for CT head + aspirin

      Explanation:

      This question assesses the candidate’s understanding of TIA risk stratification. The individual meets the criteria for crescendo TIAs, having experienced two TIAs within a week. This necessitates prompt evaluation and imaging. Admission is recommended for any patient with a score of more than 4 on the ABCD2 scale or crescendo TIA.

      A transient ischaemic attack (TIA) is a brief period of neurological deficit caused by a vascular issue, lasting less than an hour. The original definition of a TIA was based on time, but it is now recognized that even short periods of ischaemia can result in pathological changes to the brain. Therefore, a new ’tissue-based’ definition is now used. The clinical features of a TIA are similar to those of a stroke, but the symptoms resolve within an hour. Possible features include unilateral weakness or sensory loss, aphasia or dysarthria, ataxia, vertigo, or loss of balance, visual problems, and sudden transient loss of vision in one eye (amaurosis fugax).

      NICE recommends immediate antithrombotic therapy with aspirin 300 mg unless the patient has a bleeding disorder or is taking an anticoagulant. If the patient has had more than one TIA or has a suspected cardioembolic source or severe carotid stenosis, specialist review is necessary. Urgent assessment is required within 24 hours for patients who have had a suspected TIA in the last 7 days. Referral for specialist assessment is necessary as soon as possible within 7 days for patients who have had a suspected TIA more than a week previously. Neuroimaging and carotid imaging are recommended, and antithrombotic therapy is necessary. Carotid artery endarterectomy should only be considered if the carotid stenosis is greater than 70% according to ECST criteria or greater than 50% according to NASCET criteria.

    • This question is part of the following fields:

      • Neurology
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  • Question 194 - A 39-year-old female patient arrives at the Emergency Department complaining of intense, stabbing...

    Incorrect

    • A 39-year-old female patient arrives at the Emergency Department complaining of intense, stabbing pain in her right flank that spreads to her groin. The pain comes and goes but is excruciating, reaching a severity of 10/10 at its peak. A pregnancy test yields negative results, while a urine dip shows positive for nitrites, leukocytes, and blood.
      What test should be conducted to properly diagnose the condition?

      Your Answer:

      Correct Answer: Non-contrast CTKUB

      Explanation:

      When a patient presents with symptoms of renal colic, such as severe pain that radiates from the loin to the groin, a non-contrast CT-KUB is the preferred imaging test to detect any renal calculi and ensure there is no obstruction caused by them. In cases where an infected, obstructing stone is suspected, urgent nephrostomy may be necessary. Abdominal x-rays are not reliable for detecting calculi and should not be used as an indication for this type of investigation. A CT abdomen and pelvis is unnecessary and may expose the patient to unnecessary radiation. A CTKUB with contrast is also not recommended as it may mask the appearance of calculi. While ultrasound can be used to detect renal calculi, CT is more accurate and is now recommended as the first-line investigation. In cases where infection is suspected, CT is superior in assessing the anatomy and identifying any potential obstruction or collection that may require invasive intervention, such as nephrostomy insertion.

      The management of renal stones involves initial medication and investigations, including an NSAID for analgesia and a non-contrast CT KUB for imaging. Stones less than 5mm may pass spontaneously, but more intensive treatment is needed for ureteric obstruction or renal abnormalities. Treatment options include shockwave lithotripsy, ureteroscopy, and percutaneous nephrolithotomy. Prevention strategies include high fluid intake, low animal protein and salt diet, and medication such as thiazides diuretics for hypercalciuria and allopurinol for uric acid stones.

    • This question is part of the following fields:

      • Renal Medicine/Urology
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  • Question 195 - A 35-year-old woman presents to the Genitourinary Medicine Clinic with an 8-day history...

    Incorrect

    • A 35-year-old woman presents to the Genitourinary Medicine Clinic with an 8-day history of dysuria and lower abdominal pain. She has had two sexual partners over the last three months and uses the combined oral contraceptive pill as contraception. She has noticed some spotting and post-coital bleeding since her last period and a foul-smelling vaginal discharge for the last few days. There is no past medical history of note and no known allergies.
      On examination, she has lower abdominal tenderness but no guarding or palpable organomegaly. On examination, there is a thick yellow vaginal discharge and mildly tender palpable inguinal lymphadenopathy.
      Given the likely diagnosis, what is the most appropriate management for this patient?
      Select the SINGLE most appropriate management from the list below.
      Select ONE option only.

      Your Answer:

      Correct Answer: Doxycycline

      Explanation:

      Treatment Options for Sexually Transmitted Diseases

      Sexually transmitted diseases (STDs) can present with a variety of symptoms and signs. The most common STD is Chlamydia trachomatis, which can be asymptomatic or present with dysuria, abdominal pain, and vaginal discharge. Endocervical and high vaginal swabs should be taken, and a urinalysis and pregnancy test should be completed. The first-line treatment for C. trachomatis is doxycycline.

      Ceftriaxone is indicated for Neisseria gonorrhoeae infections, which can present similarly to chlamydia with discharge and dysuria. However, the most likely diagnosis for this patient is C. trachomatis, making doxycycline the correct answer.

      Benzylpenicillin is used in patients with suspected syphilis infection secondary to the spirochaete Treponema pallidum. Syphilis has primary, secondary, and tertiary stages with primary syphilis presenting as a painless chancre with local, non-tender lymphadenopathy prior to secondary disease with fever and a rash. This is not seen here, making syphilis a less likely diagnosis.

      Metronidazole is the recommended treatment for bacterial vaginosis and Trichomonas vaginalis. However, it is not used in the treatment of C. trachomatis.

      Trimethoprim would be the recommended treatment if this patient was diagnosed with a urinary-tract infection (UTI). While the history of lower abdominal pain and dysuria are suggestive of a UTI, a foul-smelling vaginal discharge points towards an alternative diagnosis.

    • This question is part of the following fields:

      • Infectious Diseases
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  • Question 196 - A 42-year-old woman presents to her General Practitioner with polyuria, weight loss and...

    Incorrect

    • A 42-year-old woman presents to her General Practitioner with polyuria, weight loss and tiredness for six months. Full blood count, urea and electrolytes (U&Es), liver function tests, thyroid function test and calcium are all normal. Glycosylated haemoglobin (HbA1c) is 48 mmol/mol and repeat sample is 50 mmol/mol. On examination, her body mass index is 35 kg/m2, she is normotensive and urinalysis is normal.
      Which of the following investigations should be arranged urgently?
      Select ONE investigation from the list below.

      Your Answer:

      Correct Answer: Computed tomography (CT) abdomen

      Explanation:

      Diagnostic Tests for a Patient with Suspected Type II Diabetes Mellitus

      Computed Tomography (CT) Abdomen:
      A CT abdomen is recommended for any patient over the age of 60 with weight loss combined with a new onset of diabetes or abdominal or back pain, nausea, vomiting or change in bowel habit. This is because new-onset type II diabetes can be a presenting feature of pancreatic cancer in patients over the age of 60, especially those who have also experienced weight loss.

      Pancreatic Autoantibodies:
      Pancreatic autoantibodies include anti-glutamic acid decarboxylase, insulin autoantibodies and islet-cell antibodies, the presence of which would support a diagnosis of type I diabetes. These tests are usually carried out in secondary care for atypical presentations such as suspected type II diabetes in a child or a non-overweight person.

      Glucose Tolerance Test:
      Glucose tolerance test has a limited role in diagnosing type II diabetes now that HbA1c is an accepted diagnostic investigation. It is still used routinely to investigate pregnant women at risk of gestational diabetes.

      Short Synacthen Test:
      A short synacthen test is used to diagnose adrenal insufficiency. The history and investigation results do not suggest this as a likely diagnosis, so this test would not be indicated.

      Ultrasound of the Urinary Tract:
      Ultrasound is not indicated unless a structural problem is suspected. Although this man is experiencing polyuria, his urinalysis and PSA are both normal, which makes a urological cause for his symptoms less likely than the newly diagnosed diabetes. Diabetes can cause renal impairment, but this should be monitored with annual urine albumin : creatinine measurement and regular U&Es blood test.

    • This question is part of the following fields:

      • Endocrinology/Metabolic Disease
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  • Question 197 - A 30-year-old runner complains of anterior groin pain accompanied by hip snapping. The...

    Incorrect

    • A 30-year-old runner complains of anterior groin pain accompanied by hip snapping. The pain is described as sharp and aggravated after prolonged sitting. During the examination, the patient displays limited range of motion and experiences pain when the hip is adducted and internally rotated while flexed to 90 degrees. What is the probable diagnosis?

      Your Answer:

      Correct Answer: Femoroacetabular impingement

      Explanation:

      Anterior groin pain in active young adults is often caused by femoroacetabular impingement (FAI), which is a common condition that can lead to persistent hip pain. Symptoms include hip/groin pain that worsens with prolonged sitting and is often accompanied by snapping, clicking, or locking of the hip. FAI is typically associated with prior hip pathology, such as Perthes disease in childhood, and is caused by an abnormality in hip anatomy that results in abnormal contact between the femur and acetabulum rim. Over time, this can cause soft tissue damage, including labral tears. Snapping hip syndrome, on the other hand, is characterized by a snapping or clunking sound as tendons move over the hip bones during flexion and extension. This condition is usually painless unless there is an associated labral tear. Stress fractures, in contrast, typically improve with rest rather than worsening. Osteonecrosis of the femoral head is usually associated with other risk factors, such as steroid use, alcohol consumption, or autoimmune conditions. Initially, pain occurs during activity, but it can become constant as the condition progresses.

      Causes of Hip Pain in Adults

      Hip pain in adults can be caused by a variety of conditions. Osteoarthritis is a common cause, with pain that worsens with exercise and improves with rest. Reduced internal rotation is often the first sign, and risk factors include age, obesity, and previous joint problems. Inflammatory arthritis can also cause hip pain, with pain typically worse in the morning and accompanied by systemic features and raised inflammatory markers. Referred lumbar spine pain may be caused by femoral nerve compression, which can be tested with a positive femoral nerve stretch test. Greater trochanteric pain syndrome, or trochanteric bursitis, is caused by repeated movement of the iliotibial band and is most common in women aged 50-70 years. Meralgia paraesthetica is caused by compression of the lateral cutaneous nerve of the thigh and typically presents as a burning sensation over the antero-lateral aspect of the thigh. Avascular necrosis may have gradual or sudden onset and may follow high dose steroid therapy or previous hip fracture or dislocation. Pubic symphysis dysfunction is common in pregnancy and presents with pain over the pubic symphysis with radiation to the groins and medial aspects of the thighs, often with a waddling gait. Transient idiopathic osteoporosis is an uncommon condition sometimes seen in the third trimester of pregnancy, with groin pain and limited range of movement in the hip, and patients may be unable to weight bear. ESR may be elevated in this condition.

    • This question is part of the following fields:

      • Musculoskeletal
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  • Question 198 - A 42-year-old woman presents to her General Practitioner with a 4-month history of...

    Incorrect

    • A 42-year-old woman presents to her General Practitioner with a 4-month history of nasal congestion and coughing. Over the previous few days, she has also been experiencing a persistent headache which seems to be worse when she leans forward.
      Which of the following is the most probable diagnosis?

      Your Answer:

      Correct Answer: Chronic rhinosinusitis

      Explanation:

      Differentiating Chronic Rhinosinusitis from Other Headache Disorders

      Chronic rhinosinusitis is a condition characterized by inflammation of the paranasal sinuses and nasal passages that lasts for 12 weeks or longer. Patients with chronic rhinosinusitis typically present with symptoms such as nasal congestion, coughing, persistent headache that worsens on bending forwards, facial pain, nasal discharge, and postnasal drip. Predisposing factors for chronic rhinosinusitis include atopy, nasal obstruction, recent local infection, swimming or diving, and smoking. Management of chronic rhinosinusitis involves avoidance of allergens, intranasal corticosteroids, and nasal irrigation with saline.

      Acute sinusitis shares many features with chronic rhinosinusitis, but the history of symptoms is much shorter. Treatment for acute sinusitis includes analgesia, intranasal decongestants or nasal saline, and intranasal corticosteroids if symptoms persist for more than ten days. Oral antibiotics may be given for severe presentations.

      Cluster headaches are characterized by intense, sharp, stabbing pain around one eye, accompanied by eye redness, lacrimation, lid swelling, nasal stuffiness, skin erythema, miosis or ptosis. Cluster headaches occur in clusters lasting between four and 12 weeks, with patients feeling completely fine in between clusters. Tension headaches are described as a band-like headache that does not impair activities of daily living.

      Postnasal drip (PND) typically presents with a chronic cough and bad breath, unlike the presentation in chronic rhinosinusitis. It is important to differentiate chronic rhinosinusitis from other headache disorders to ensure appropriate management and treatment.

    • This question is part of the following fields:

      • ENT
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  • Question 199 - A 55-year-old man presents with a chronic cough and is diagnosed with lung...

    Incorrect

    • A 55-year-old man presents with a chronic cough and is diagnosed with lung cancer. He asks if his occupation could be a contributing factor. What is the most probable occupational risk factor for developing lung cancer?

      Your Answer:

      Correct Answer: Passive smoking

      Explanation:

      Risk Factors for Lung Cancer

      Lung cancer is a deadly disease that can be caused by various factors. The most significant risk factor for lung cancer is smoking, which increases the risk by a factor of 10. However, other factors such as exposure to asbestos, arsenic, radon, nickel, chromate, and aromatic hydrocarbon can also increase the risk of developing lung cancer. Additionally, cryptogenic fibrosing alveolitis has been linked to an increased risk of lung cancer.

      It is important to note that not all factors are related to lung cancer. For example, coal dust exposure has not been found to increase the risk of lung cancer. However, smoking and asbestos exposure are synergistic, meaning that a smoker who is also exposed to asbestos has a 50 times increased risk of developing lung cancer (10 x 5). Understanding these risk factors can help individuals make informed decisions about their health and take steps to reduce their risk of developing lung cancer.

    • This question is part of the following fields:

      • Respiratory Medicine
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  • Question 200 - An epidemic of diarrhoea and vomiting has broken out on one of the...

    Incorrect

    • An epidemic of diarrhoea and vomiting has broken out on one of the elderly care wards. The catering suppliers assure you that their food is unlikely to be responsible because they follow the strictest hygiene procedures. A total of 15 elderly patients on the ward have become unwell with a sudden onset of diarrhoea and vomiting. Those infected earlier have recovered with rehydration therapy after about 48 hours. Examination of faeces by electron microscopy has revealed circular virus particles with radiating spokes.
      Which virus is most likely to be responsible for this outbreak?

      Your Answer:

      Correct Answer: Rotavirus

      Explanation:

      Common Viruses that Cause Gastroenteritis

      Gastroenteritis is a self-limiting illness caused by several viruses, including rotavirus, enteric adenovirus, small round-structured virus (SRSV), norovirus, and astrovirus. Among these, rotavirus is the most common cause of gastroenteritis in children under 5 years of age, while norovirus affects people of all ages. Rotavirus causes infant deaths worldwide, but acquired immunity develops after one episode. Norovirus is usually transmitted through contaminated food or water, while adenovirus is endemic throughout the year and commonly affects children in daycare settings. SRSV is another name for norovirus, and astrovirus is associated with contaminated food and water. Symptoms of gastroenteritis include anorexia, low-grade fever, vomiting, and watery diarrhea, but most cases do not require medication and can be managed with supportive treatment. Death from dehydration remains common in developing countries.

    • This question is part of the following fields:

      • Infectious Diseases
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SESSION STATS - PERFORMANCE PER SPECIALTY

Haematology/Oncology (1/1) 100%
Paediatrics (1/1) 100%
Gastroenterology/Nutrition (1/3) 33%
Reproductive Medicine (0/3) 0%
Cardiovascular (1/2) 50%
Musculoskeletal (1/2) 50%
Dermatology (1/4) 25%
Neurology (1/3) 33%
Psychiatry (0/1) 0%
Ophthalmology (0/1) 0%
Endocrinology/Metabolic Disease (1/2) 50%
Pharmacology/Therapeutics (0/1) 0%
Renal Medicine/Urology (1/1) 100%
Infectious Diseases (0/2) 0%
ENT (0/1) 0%
Respiratory Medicine (1/1) 100%
Passmed