Pregnancy Complications: Placental Abruption, Uterine Rupture, Placenta Previa, and Placenta Accreta

During pregnancy, there are several complications that can occur, including placental abruption, uterine rupture, placenta previa, and placenta accreta.

Placental abruption happens when part of the placenta separates prematurely from the uterus. Symptoms include abdominal or back pain, vaginal bleeding (although there may be no bleeding in concealed abruption), a hard abdomen, and eventually shock. Treatment involves hospitalization, resuscitation, and delivery of the baby.

Uterine rupture is rare and usually occurs during labor, especially in women who have had previous uterine surgery. Symptoms include abdominal pain and tenderness, vaginal bleeding, fetal heart rate deterioration, and hypovolemic shock. Emergency exploratory laparotomy with Caesarean section and fluid resuscitation is necessary.

Placenta previa occurs when the placenta attaches to the lower uterine segment and often presents with painless vaginal bleeding after the 28th week. However, severe pain is not a typical symptom. The location of the placenta can be determined through scans.

Placenta accreta happens when the placenta attaches to the myometrium instead of just the endometrium. This can lead to failure of the placenta to separate after delivery, resulting in significant postpartum bleeding.

Immediate Management of Stridor Following Thyroidectomy

An unrecognised or rapidly expanding haematoma can lead to airway compromise and asphyxiation after thyroidectomy. Therefore, it is crucial to take immediate action in case of stridor. The first step is to remove the skin clips and sutures to relieve pressure on the trachea. Failure to do so can result in tracheal occlusion and death. It is important to act quickly and avoid delays in getting the patient to the operating theatre, as this may lead to an avoidable death.

Once the neck has been opened on the ward, the patient should be transferred to the operating theatre for a thorough examination of the neck and meticulous control of bleeding before closing the neck wound. This is necessary to ensure that any bleeding is properly managed and the wound is closed without any complications. By following these steps, the risk of airway compromise and asphyxiation can be minimized, and the patient can recover safely from the surgery.

Topical Treatments for Chronic Plaque Psoriasis: NICE Recommendations

Chronic plaque psoriasis is a common skin condition that can be managed with topical treatments. The National Institute for Health and Care Excellence (NICE) recommends a stepwise approach to treatment, with different options depending on the severity of the condition and the response to previous therapies.

First-line treatment for chronic plaque psoriasis is a potent corticosteroid applied once daily, combined with a vitamin D analogue, for up to 4 weeks. This combination therapy has been shown to be effective in reducing inflammation and improving symptoms.

If there is no improvement with both steroid and calcipotriol after 8 weeks, topical calcipotriol alone can be used as a second-line management option. However, it is insufficient to prescribe alone as a first-line treatment.

Topical steroid alone is a third-line management option for psoriasis if there is no improvement after 8-12 weeks. This is because long-term use of topical steroids can have side effects such as skin thinning and increased risk of infection.

Short-acting dithranol could be used as a fourth-line option, but not as initial management. Topical coal tar is also part of third-line management for psoriasis.

In summary, the NICE recommendations for topical treatments for chronic plaque psoriasis involve a stepwise approach, with combination therapy as the first-line option and other treatments used if there is no improvement or if side effects occur. It is important to work with a healthcare provider to find the most effective and safe treatment plan for each individual.

NICE Recommendations for Topical Treatments for Chronic Plaque Psoriasis

According to RCOG guidelines, women typically feel fetal movements by 20 weeks of gestation. However, if no movements are felt by 24 weeks, it is recommended to refer the woman to a maternal fetal medicine unit to assess for potential neuromuscular conditions.

Understanding Reduced Fetal Movements

Introduction:
Reduced fetal movements can indicate fetal distress and are a response to chronic hypoxia in utero. This can lead to stillbirth and fetal growth restriction. It is believed that placental insufficiency may also be linked to reduced fetal movements.

Physiology:
Quickening is the first onset of fetal movements, which usually occurs between 18-20 weeks gestation and increases until 32 weeks gestation. Multiparous women may experience fetal movements sooner. Fetal movements should not reduce towards the end of pregnancy. There is no established definition for what constitutes reduced fetal movements, but less than 10 movements within 2 hours (in pregnancies past 28 weeks gestation) is an indication for further assessment.

Epidemiology:
Reduced fetal movements affect up to 15% of pregnancies, with 3-5% of pregnant women having recurrent presentations with RFM. Fetal movements should be established by 24 weeks gestation.

Risk factors for reduced fetal movements:
Posture, distraction, placental position, medication, fetal position, body habitus, amniotic fluid volume, and fetal size can all affect fetal movement awareness.

Investigations:
Fetal movements are usually based on maternal perception, but can also be objectively assessed using handheld Doppler or ultrasonography. Investigations are dependent on gestation at onset of RFM. If concern remains, despite normal CTG, urgent (within 24 hours) ultrasound can be used.

Prognosis:
Reduced fetal movements can represent fetal distress, but in 70% of pregnancies with a single episode of reduced fetal movement, there is no onward complication. However, between 40-55% of women who suffer from stillbirth experience reduced fetal movements prior to diagnosis. Recurrent RFM requires further investigations to consider structural or genetic fetal abnormalities.

The T wave on an ECG indicates ventricular repolarisation and is typically positive in all leads except AvR and V1. Abnormal T wave findings may suggest strain, bundle branch block, ischaemia/infarction, hyperkalaemia, Prinzmetal angina, or early STEMI. The P wave represents atrial depolarisation, while atrial repolarisation is hidden by the QRS complex. The PR interval is determined by the duration of conduction delay through the atrioventricular node. Finally, the QRS complex indicates ventricular depolarisation.

Acute epididymo-orchitis cases are commonly caused by enteric organisms (such as Escherichia coli or Enterococcus faecalis) in men aged 35 years and above. This type of infection is often linked to urinary tract infections and may be related to structural issues in the urinary tract.

Epididymo-orchitis is a condition where the epididymis and/or testes become infected, leading to pain and swelling. It is commonly caused by infections spreading from the genital tract or bladder, with Chlamydia trachomatis and Neisseria gonorrhoeae being the usual culprits in sexually active younger adults, while E. coli is more commonly seen in older adults with a low-risk sexual history. Symptoms include unilateral testicular pain and swelling, with urethral discharge sometimes present. Testicular torsion, which can cause ischaemia of the testicle, is an important differential diagnosis and needs to be excluded urgently, especially in younger patients with severe pain and an acute onset.

Investigations are guided by the patient’s age, with sexually transmitted infections being assessed in younger adults and a mid-stream urine (MSU) being sent for microscopy and culture in older adults with a low-risk sexual history. Management guidelines from the British Association for Sexual Health and HIV (BASHH) recommend ceftriaxone 500 mg intramuscularly as a single dose, plus doxycycline 100 mg orally twice daily for 10-14 days if the organism causing the infection is unknown. Further investigations are recommended after treatment to rule out any underlying structural abnormalities.

Hormones and their Effects on Digestion

Cholecystokinin is a hormone that helps neutralize partially digested food by causing the gallbladder to contract and the pancreas to release alkaline pancreatic fluid. This helps to counteract the acidity of the food and aids in digestion. Gastrin, on the other hand, increases the production of stomach acid and speeds up the rate at which food is emptied from the stomach. This hormone is important for breaking down food and preparing it for further digestion. Secretin, another hormone, works to reduce the production of stomach acid, which can be helpful in preventing acid reflux and other digestive issues. Finally, leptin is a hormone that helps to suppress appetite, which can be useful in maintaining a healthy weight and preventing overeating. By the effects of these hormones on digestion, we can better understand how our bodies process food and maintain overall health.

Common Complications of Suxamethonium Administration

Suxamethonium is a commonly used muscle relaxant during anesthesia. However, it can lead to several complications, including malignant hyperthermia, raised intraocular pressure, anaphylaxis, prolonged paralysis, and hyperkalemia.

Malignant hyperthermia is a genetic myopathy that causes a hypermetabolic state, leading to circulatory collapse and death. Treatment involves recognition, removal of stimuli, continuation of anesthesia with intravenous agents, cooling, and administration of dantrolene.

Raised intraocular pressure and intracranial pressure can occur after suxamethonium administration, but this is only relevant to patients with ocular and intracranial diseases.

Anaphylaxis is a severe allergic reaction that can occur after suxamethonium administration. Diagnosis is based on signs and symptoms.

Prolonged paralysis can occur in patients with abnormal pseudocholinesterase level or function, which is generally due to inherited genetic alleles. Diagnosis is by blood test.

Hyperkalemia can occur after suxamethonium administration, especially in patients with severe muscle damage or recent burns. Diagnosis does not require a muscle biopsy.

When treating patients with clozapine, it is important to monitor for agranulocytosis, a rare but potentially fatal side-effect. Patients should report flu-like symptoms and undergo regular blood tests. In this case, the patient’s sore throat and fever may indicate agranulocytosis, so a full blood count is necessary. While an ECG should be done before starting antipsychotic treatment, it is not the most important test in this scenario. Blood glucose should be monitored to exclude organic causes and hyperglycemia caused by antipsychotics. Liver function and urea/electrolytes should also be monitored regularly, but are not the most important tests to conduct immediately in this case.

The knife likely cut the right gastro-omental artery, which is a branch of the gastroduodenal artery. This artery runs along the greater curvature of the stomach within the superior border of the greater omentum and anastomoses with the left gastro-omental artery, a branch of the splenic artery. The coeliac trunk, which supplies blood to the foregut, is not related to the greater omentum but to the lesser omentum. The hepatic artery proper, one of the terminal branches of the common hepatic artery, courses towards the liver in the free edge of the lesser omentum. The splenic artery, a tortuous branch of the coeliac trunk, supplies blood to the spleen and gives off the left gastro-omental artery. The short gastric artery, on the other hand, supplies blood to the fundus of the stomach and branches off the splenic artery.