To improve control of hypertension in patients who are already taking an ACE inhibitor or an angiotensin receptor blocker, the 2019 NICE guidelines recommend adding either a calcium channel blocker (such as amlodipine) or a thiazide-like diuretic (such as indapamide). This is a change from previous guidelines, which only recommended adding a calcium channel blocker in this situation.

Hypertension, or high blood pressure, is a common condition that can lead to serious health problems if left untreated. The National Institute for Health and Care Excellence (NICE) has published updated guidelines for the management of hypertension in 2019. Some of the key changes include lowering the threshold for treating stage 1 hypertension in patients under 80 years old, allowing the use of angiotensin receptor blockers instead of ACE inhibitors, and recommending the use of calcium channel blockers or thiazide-like diuretics in addition to ACE inhibitors or angiotensin receptor blockers.

Lifestyle changes are also important in managing hypertension. Patients should aim for a low salt diet, reduce caffeine intake, stop smoking, drink less alcohol, eat a balanced diet rich in fruits and vegetables, exercise more, and lose weight.

Treatment for hypertension depends on the patient’s blood pressure classification. For stage 1 hypertension with ABPM/HBPM readings of 135/85 mmHg or higher, treatment is recommended for patients under 80 years old with target organ damage, established cardiovascular disease, renal disease, diabetes, or a 10-year cardiovascular risk equivalent to 10% or greater. For stage 2 hypertension with ABPM/HBPM readings of 150/95 mmHg or higher, drug treatment is recommended regardless of age.

The first-line treatment for patients under 55 years old or with a background of type 2 diabetes mellitus is an ACE inhibitor or angiotensin receptor blocker. Calcium channel blockers are recommended for patients over 55 years old or of black African or African-Caribbean origin. If a patient is already taking an ACE inhibitor or angiotensin receptor blocker, a calcium channel blocker or thiazide-like diuretic can be added.

If blood pressure remains uncontrolled with the optimal or maximum tolerated doses of four drugs, NICE recommends seeking expert advice or adding a fourth drug. Blood pressure targets vary depending on age, with a target of 140/90 mmHg for patients under 80 years old and 150/90 mmHg for patients over 80 years old. Direct renin inhibitors, such as Aliskiren, may be used in patients who are intolerant of other antihypertensive drugs, but their role is currently limited.

The definition of a TIA has been updated to focus on the affected tissue rather than the duration of symptoms. It is now defined as a temporary episode of neurological dysfunction resulting from restricted blood flow to the brain, spinal cord, or retina, without causing acute tissue damage. An ischaemic stroke, on the other hand, is characterized by neurological dysfunction caused by cerebral infarction, while multiple sclerosis is defined by neurological dysfunction caused by demyelination. Finally, a functional neurological disorder is characterized by transient symptoms of psychological origin.

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, sudden transient loss of vision in one eye (amaurosis fugax), diplopia, and homonymous hemianopia.

NICE recommends immediate antithrombotic therapy, giving aspirin 300 mg immediately unless the patient has a bleeding disorder or is taking an anticoagulant. If aspirin is contraindicated, management should be discussed urgently with the specialist team. Specialist review is necessary if the patient has had more than one TIA or has a suspected cardioembolic source or severe carotid stenosis. Urgent assessment within 24 hours by a specialist stroke physician is required if the patient has had a suspected TIA in the last 7 days. Referral for specialist assessment should be made as soon as possible within 7 days if the patient has had a suspected TIA more than a week previously. The person should be advised not to drive until they have been seen by a specialist.

Neuroimaging should be done on the same day as specialist assessment if possible. MRI is preferred to determine the territory of ischaemia or to detect haemorrhage or alternative pathologies. Carotid imaging is necessary as atherosclerosis in the carotid artery may be a source of emboli in some patients. All patients should have an urgent carotid doppler unless they are not a candidate for carotid endarterectomy.

Antithrombotic therapy is recommended, with clopidogrel being the first-line treatment. Aspirin + dipyridamole should be given to patients who cannot tolerate clopidogrel. Carotid artery endarterectomy should only be considered if the patient has suffered a stroke or TIA in the carotid territory and is not severely disabled. It should only be recommended if carotid stenosis is greater

The Importance of Non-HDL Cholesterol in Statin Treatment

NICE guidelines recommend that high-intensity statin treatment for both primary and secondary prevention of cardiovascular disease should aim for a greater than 40% reduction in non-HDL cholesterol. Non-HDL cholesterol includes LDL, IDL, and VLDL cholesterol. In the past, LDL reduction has been used as a marker of statin effect. However, non-HDL reduction is more useful as it takes into account the atherogenic properties of IDL and VLDL cholesterol, which may be raised even in the presence of normal LDL levels.

Using non-HDL cholesterol also has other benefits. Hypertriglyceridaemia can interfere with lab-based LDL calculations, but it doesn’t impact non-HDL calculation, which is measured by a different method. Additionally, a fasting sample is not required to measure non-HDL cholesterol, making sampling and monitoring easier. Overall, non-HDL cholesterol is an important marker to consider in statin treatment for cardiovascular disease prevention.

When it comes to reducing the risk of stroke in individuals with atrial fibrillation and a CHA2DS2VASc score of 2 or higher, the first-line option should be anticoagulation with a direct-acting oral anticoagulant (DOAC) such as apixaban, dabigatran, edoxaban, or rivaroxaban. In a primary care setting, it is important to use the CHA2DS2VASc assessment tool to evaluate the person’s stroke risk, as well as assess the risk of bleeding and work to mitigate any current risk factors such as uncontrolled hypertension, concurrent medication, harmful alcohol consumption, and reversible causes of anemia.

Atrial fibrillation (AF) is a condition that requires careful management, including the use of anticoagulation therapy. The latest guidelines from NICE recommend assessing the need for anticoagulation in all patients with a history of AF, regardless of whether they are currently experiencing symptoms. The CHA2DS2-VASc scoring system is used to determine the most appropriate anticoagulation strategy, with a score of 2 or more indicating the need for anticoagulation. However, it is important to ensure a transthoracic echocardiogram has been done to exclude valvular heart disease, which is an absolute indication for anticoagulation.

When considering anticoagulation therapy, doctors must also assess the patient’s bleeding risk. NICE recommends using the ORBIT scoring system to formalize this risk assessment, taking into account factors such as haemoglobin levels, age, bleeding history, renal impairment, and treatment with antiplatelet agents. While there are no formal rules on how to act on the ORBIT score, individual patient factors should be considered. The risk of bleeding increases with a higher ORBIT score, with a score of 4-7 indicating a high risk of bleeding.

For many years, warfarin was the anticoagulant of choice for AF. However, the development of direct oral anticoagulants (DOACs) has changed this. DOACs have the advantage of not requiring regular blood tests to check the INR and are now recommended as the first-line anticoagulant for patients with AF. The recommended DOACs for reducing stroke risk in AF are apixaban, dabigatran, edoxaban, and rivaroxaban. Warfarin is now used second-line, in patients where a DOAC is contraindicated or not tolerated. Aspirin is not recommended for reducing stroke risk in patients with AF.

Treatment options for resistant hypertension

Resistant hypertension can be a challenging condition to manage, and the National Institute for Health and Care Excellence (NICE) has provided guidelines to help healthcare professionals make informed decisions. In step 4 of the guidelines, NICE recommends a combination of ACE inhibitor, calcium channel blocker, and diuretic therapy, with the addition of further diuretic or alpha or beta blocker if necessary.

If further diuretic therapy is required, NICE suggests a higher-dose thiazide-like diuretic or spironolactone, depending on the patient’s serum potassium level. However, if spironolactone is not licensed for use or not tolerated, increasing the dose of indapamide is a suitable alternative. It’s important to note that the maximum dose of modified-release indapamide is 1.5mg daily.

If further diuretic therapy is not tolerated or contraindicated, NICE recommends considering an alpha or beta blocker. In cases of resistant hypertension, seeking expert advice may also be beneficial. By following these guidelines, healthcare professionals can provide effective treatment options for patients with resistant hypertension.

Differential Diagnosis for a Young Patient with Cardiomyopathy and Recent Travel History

Cardiomyopathy is a myocardial disorder that can range from asymptomatic to life-threatening. It is important to consider this diagnosis in young patients presenting with heart failure, arrhythmias, or thromboembolism. While recent travel history may be relevant to other potential diagnoses, such as atypical pneumonia or thromboembolism, neither of these fully fit the patient’s history and examination. Rheumatic heart disease, pericarditis, and pulmonary embolus can also be ruled out based on the patient’s symptoms. The underlying cause and type of cardiomyopathy in this case are unknown but could be multiple.

NICE Guidance on Antihypertensive Treatment for People Over 55 and Black People of African or Caribbean Family Origin

According to the latest NICE guidance, people aged over 55 years and black people of African or Caribbean family origin of any age should be offered step 1 antihypertensive treatment with a CCB. If a CCB is not suitable due to oedema or intolerance, or if there is evidence of heart failure or a high risk of heart failure, a thiazide-like diuretic should be offered instead.

This guidance aims to provide effective treatment options for hypertension in these specific populations, taking into account individual circumstances and potential side effects. It is important for healthcare professionals to follow these recommendations to ensure the best possible outcomes for their patients.

Renal Function Monitoring for ACE Inhibitor Treatment

Renal function monitoring is crucial before initiating treatment with an ACE inhibitor and one to two weeks after initiation or any subsequent dose increase, according to NICE recommendations. Although ACE inhibitors have a role in managing chronic kidney disease, they can also cause impairment of renal function that may be progressive. The concomitant use of NSAIDs and potassium-sparing diuretics increases the risks of renal side effects and hyperkalaemia, respectively.

In patients with bilateral renal stenosis who are given ACE inhibitors, marked renal failure can occur. Therefore, if there is a significant deterioration in renal function as a result of ACE inhibition, a specialist should be involved. It is important to monitor renal function regularly to ensure the safe and effective use of ACE inhibitors in the management of various conditions.

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. ACE inhibitors are also used to treat diabetic nephropathy and prevent ischaemic heart disease. These drugs work by inhibiting the conversion of angiotensin I to angiotensin II and are metabolized in the liver.

While ACE inhibitors are generally well-tolerated, they can cause side effects such as cough, angioedema, hyperkalaemia, and first-dose hypotension. Patients with certain conditions, such as renovascular disease, aortic stenosis, or hereditary or idiopathic angioedema, should use ACE inhibitors with caution or avoid them altogether. Pregnant and breastfeeding women should also avoid these drugs.

Patients taking high-dose diuretics may be at increased risk of hypotension when using ACE inhibitors. Therefore, it is important to monitor urea and electrolyte levels before and after starting treatment, as well as any changes in creatinine and potassium levels. Acceptable changes include a 30% increase in serum creatinine 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 when using ACE inhibitors.

The current NICE guidelines recommend using a flow chart to manage hypertension, with ACE inhibitors as the first-line treatment for patients under 55 years old. However, individual patient factors and comorbidities should be taken into account when deciding on the best treatment plan.

Beta-blockers are a class of drugs that are primarily used to manage cardiovascular disorders. They have a wide range of indications, including angina, post-myocardial infarction, heart failure, arrhythmias, hypertension, thyrotoxicosis, migraine prophylaxis, and anxiety. Beta-blockers were previously avoided in heart failure, but recent evidence suggests that certain beta-blockers can improve both symptoms and mortality. They have also replaced digoxin as the rate-control drug of choice in atrial fibrillation. However, their role in reducing stroke and myocardial infarction has diminished in recent years due to a lack of evidence.

Examples of beta-blockers include atenolol and propranolol, which was one of the first beta-blockers to be developed. Propranolol is lipid-soluble, which means it can cross the blood-brain barrier.

Like all drugs, beta-blockers have side-effects. These can include bronchospasm, cold peripheries, fatigue, sleep disturbances (including nightmares), and erectile dysfunction. There are also some contraindications to using beta-blockers, such as uncontrolled heart failure, asthma, sick sinus syndrome, and concurrent use with verapamil, which can precipitate severe bradycardia.

Moderate to severe aortic stenosis is a contraindication for ACE inhibitors like ramipril due to the potential risk of reducing coronary perfusion pressure and causing cardiac ischemia. Therefore, the patient should stop taking ramipril until cardiology review. However, bisoprolol, which reduces cardiac workload by inhibiting β1-adrenergic receptors, is safe to use in the presence of aortic stenosis. Digoxin, which improves cardiac contractility, is also safe to use unless there are defects in the cardiac conduction system. Metformin should be used with caution in patients with chronic heart failure but is not contraindicated in those with valvular disease. Quinine is also safe to use in the presence of aortic stenosis but should be stopped if there are defects in the cardiac conduction system.

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. ACE inhibitors are also used to treat diabetic nephropathy and prevent ischaemic heart disease. These drugs work by inhibiting the conversion of angiotensin I to angiotensin II and are metabolized in the liver.

While ACE inhibitors are generally well-tolerated, they can cause side effects such as cough, angioedema, hyperkalaemia, and first-dose hypotension. Patients with certain conditions, such as renovascular disease, aortic stenosis, or hereditary or idiopathic angioedema, should use ACE inhibitors with caution or avoid them altogether. Pregnant and breastfeeding women should also avoid these drugs.

Patients taking high-dose diuretics may be at increased risk of hypotension when using ACE inhibitors. Therefore, it is important to monitor urea and electrolyte levels before and after starting treatment, as well as any changes in creatinine and potassium levels. Acceptable changes include a 30% increase in serum creatinine 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 when using ACE inhibitors.

The current NICE guidelines recommend using a flow chart to manage hypertension, with ACE inhibitors as the first-line treatment for patients under 55 years old. However, individual patient factors and comorbidities should be taken into account when deciding on the best treatment plan.

Ankle swelling is more commonly associated with dihydropyridine calcium channel blockers like amlodipine than with verapamil. Although ankle oedema is a known side effect of all calcium channel blockers, there are differences in the incidence of ankle oedema between the two classes. Therefore, lacidipine, which belongs to the dihydropyridine class, is more likely to cause ankle swelling than verapamil.

Factors that increase the risk of developing ankle oedema while taking calcium channel blockers include being female, older age, having heart failure, standing upright, and being in warm environments.

Calcium channel blockers are a class of drugs commonly used to treat cardiovascular disease. These drugs target voltage-gated calcium channels found in myocardial cells, cells of the conduction system, and vascular smooth muscle. The different types of calcium channel blockers have varying effects on these areas, making it important to differentiate their uses and actions.

Verapamil is used to treat angina, hypertension, and arrhythmias. It is highly negatively inotropic and should not be given with beta-blockers as it may cause heart block. Side effects include heart failure, constipation, hypotension, bradycardia, and flushing.

Diltiazem is used to treat angina and hypertension. It is less negatively inotropic than verapamil, but caution should still be exercised when patients have heart failure or are taking beta-blockers. Side effects include hypotension, bradycardia, heart failure, and ankle swelling.

Nifedipine, amlodipine, and felodipine are dihydropyridines used to treat hypertension, angina, and Raynaud’s. They affect peripheral vascular smooth muscle more than the myocardium, which means they do not worsen heart failure but may cause ankle swelling. Shorter acting dihydropyridines like nifedipine may cause peripheral vasodilation, resulting in reflex tachycardia. Side effects include flushing, headache, and ankle swelling.

According to current NICE guidelines, the management of hypertension involves a flow chart that takes into account various factors such as age, ethnicity, and comorbidities. Calcium channel blockers may be used as part of the treatment plan depending on the individual patient’s needs.

Beta-Blockers for Heart Failure: Medications and Contraindications

Heart failure is a serious condition that requires proper management to reduce mortality. Beta-blockers are a class of medications that have been shown to be effective in treating heart failure. Despite some relative contraindications, beta-blockers can be safely initiated in general practice. However, there are still absolute contraindications that should be considered before prescribing beta-blockers, such as asthma, second or third-degree heart block, sick sinus syndrome (without pacemaker), and sinus bradycardia (<50 bpm). Bisoprolol, carvedilol, and nebivolol are all licensed for the treatment of heart failure in the United Kingdom. Among these medications, bisoprolol is the recommended choice and should be started at a low dose of 1.25 mg daily and gradually increased to the maximum tolerated dose (up to 10 mg). Other beta-blockers such as labetalol, atenolol, propranolol, and sotalol have different indications and are not licensed for the treatment of heart failure. Labetalol is mainly used for hypertension in pregnancy, while atenolol is used for arrhythmias, angina, and hypertension. Propranolol is indicated for tachycardia linked to thyrotoxicosis, anxiety, migraine prophylaxis, and benign essential tremor. Sotalol is commonly used to treat atrial and ventricular arrhythmias, particularly atrial fibrillation. In summary, beta-blockers are an important class of medications for the treatment of heart failure. However, careful consideration of contraindications and appropriate medication selection is crucial for optimal patient outcomes.

It is not enough to withhold anticoagulation solely based on the risk of falls or old age. To determine the risk of stroke or bleeding in atrial fibrillation, objective measures such as the CHA2DS2-VASc and ORBIT scores should be used. The ORBIT score, rather than HAS-BLED, is now recommended by NICE for assessing bleeding risk. A history of falls doesn’t factor into the ORBIT score, but age does. Limiting the patient’s mobility by suggesting she only mobilizes with staff is impractical. There is no rationale for switching the edoxaban to an antiplatelet agent, as antiplatelets are not typically used in atrial fibrillation management unless there is a specific indication. Stopping edoxaban without calculating the appropriate scores could leave the patient at a high risk of stroke.

Atrial fibrillation (AF) is a condition that requires careful management, including the use of anticoagulation therapy. The latest guidelines from NICE recommend assessing the need for anticoagulation in all patients with a history of AF, regardless of whether they are currently experiencing symptoms. The CHA2DS2-VASc scoring system is used to determine the most appropriate anticoagulation strategy, with a score of 2 or more indicating the need for anticoagulation. However, it is important to ensure a transthoracic echocardiogram has been done to exclude valvular heart disease, which is an absolute indication for anticoagulation.

When considering anticoagulation therapy, doctors must also assess the patient’s bleeding risk. NICE recommends using the ORBIT scoring system to formalize this risk assessment, taking into account factors such as haemoglobin levels, age, bleeding history, renal impairment, and treatment with antiplatelet agents. While there are no formal rules on how to act on the ORBIT score, individual patient factors should be considered. The risk of bleeding increases with a higher ORBIT score, with a score of 4-7 indicating a high risk of bleeding.

For many years, warfarin was the anticoagulant of choice for AF. However, the development of direct oral anticoagulants (DOACs) has changed this. DOACs have the advantage of not requiring regular blood tests to check the INR and are now recommended as the first-line anticoagulant for patients with AF. The recommended DOACs for reducing stroke risk in AF are apixaban, dabigatran, edoxaban, and rivaroxaban. Warfarin is now used second-line, in patients where a DOAC is contraindicated or not tolerated. Aspirin is not recommended for reducing stroke risk in patients with AF.

NICE recommends primary prevention for individuals under 84 years old who have a risk of over 10% of developing cardiovascular disease, which can be estimated using the QRISK2 assessment tool. To address modifiable risk factors, interventions such as dietary advice, smoking cessation support, alcohol moderation, and weight reduction should be offered. For lipid management, both non-pharmacological and pharmacological interventions should be utilized, with atorvastatin 20 mg being the recommended prescription for primary prevention. Lipids should be checked after 3 months, with the aim of reducing non-HDL cholesterol by over 40%. However, excessive drug usage in the elderly should be considered carefully by doctors, as cardiovascular risks exceeding 5-10% may be found in elderly men based on age and gender alone. NICE advises against routinely prescribing fibrates, bile acid sequestrants, nicotinic acid, omega-3 fatty acid compounds, or a combination of a statin and another lipid-modifying drug. First-line treatment for primary hyperlipidaemia is a statin, with other options such as bile acid sequestrants being considered if statins are contraindicated or not tolerated. For primary prevention of CVD, high-intensity statin treatment should be offered to individuals under 84 years old with an estimated 10-year risk of 10% or more using the QRISK assessment tool. Diet modification alone is not recommended for individuals with a risk score over 30%. Ezetimibe can be considered for individuals with primary hypercholesterolaemia if a statin is contraindicated or not tolerated, but it is not the first choice of drug in this scenario.

Treating Hypertension in Elderly Patients

Patients of all ages should be treated to target when it comes to hypertension. The NICE guidelines on Hypertension (NG136) recommend a clinic blood pressure (BP) of less than 150/90 mmHg for patients over the age of 80. For patients over 55, calcium channel antagonists are the most appropriate first-line therapies, unless there is evidence of oedema, heart failure, or the patient is at risk of heart failure. In such cases, a thiazide-like diuretic such as chlorthalidone or indapamide should be used instead of conventional thiazides like bendroflumethiazide and hydrochlorothiazide. If a CCB is not tolerated, a thiazide-like diuretic should be offered to treat hypertension. Indapamide is a thiazide-like diuretic that is associated with less hyponatraemia compared to bendroflumethiazide, making it an appropriate choice for first-line therapy in elderly patients. Even if the target BP is not reached on two or more agents, it is important to continue therapy.

NICE Guidance on Antibiotic Prophylaxis for High-Risk Patients

NICE has released new guidance regarding the use of antibiotic prophylaxis for high-risk patients. The guidance acknowledges that patients with pre-existing cardiac lesions are at risk of developing bacterial endocarditis (IE). However, NICE has concluded that clinical and cost-effectiveness evidence supports the recommendation that at-risk patients undergoing interventional procedures should no longer be given antibiotic prophylaxis against IE.

It is important to note that antibiotic therapy is still necessary to treat active or potential infections. The current antibiotic prophylaxis regimens may even result in a net loss of life. Therefore, it is crucial to identify patient groups who may be most at risk of developing bacterial endocarditis so that prompt investigation and treatment can be undertaken. However, offering antibiotic prophylaxis for these patients during dental procedures is not considered effective. This new guidance marks a paradigm shift from current accepted practice.

Angina pectoris can be managed through lifestyle changes, medication, percutaneous coronary intervention, and surgery. In 2011, NICE released guidelines for the management of stable angina. Medication is an important aspect of treatment, and all patients should receive aspirin and a statin unless there are contraindications. Sublingual glyceryl trinitrate can be used to abort angina attacks. NICE recommends using either a beta-blocker or a calcium channel blocker as first-line treatment, depending on the patient’s comorbidities, contraindications, and preferences. If a calcium channel blocker is used as monotherapy, a rate-limiting one such as verapamil or diltiazem should be used. If used in combination with a beta-blocker, a longer-acting dihydropyridine calcium channel blocker like amlodipine or modified-release nifedipine should be used. Beta-blockers should not be prescribed concurrently with verapamil due to the risk of complete heart block. If initial treatment is ineffective, medication should be increased to the maximum tolerated dose. If a patient is still symptomatic after monotherapy with a beta-blocker, a calcium channel blocker can be added, and vice versa. If a patient cannot tolerate the addition of a calcium channel blocker or a beta-blocker, long-acting nitrate, ivabradine, nicorandil, or ranolazine can be considered. If a patient is taking both a beta-blocker and a calcium-channel blocker, a third drug should only be added while awaiting assessment for PCI or CABG.

Nitrate tolerance is a common issue for patients who take nitrates, leading to reduced efficacy. NICE advises patients who take standard-release isosorbide mononitrate to use an asymmetric dosing interval to maintain a daily nitrate-free time of 10-14 hours to minimize the development of nitrate tolerance. However, this effect is not seen in patients who take once-daily modified-release isosorbide mononitrate.

Certain medications and substances can cause an increase in blood pressure, known as drug-induced hypertension. Non-steroidal anti-inflammatory drugs (NSAIDs) and COX-2 selective agents cause sodium and water retention, leading to elevated blood pressure. Sympathomimetic amines, such as amphetamines and pseudoephedrine, can also have this effect. Corticosteroids, particularly those with strong mineralocorticoid effects, can cause fluid retention and hypertension. Oral contraceptives may slightly raise blood pressure in some women. Venlafaxine increases levels of norepinephrine, contributing to hypertension. Cyclosporine and tacrolimus, used in transplant and autoimmune patients, can also have a significant effect on blood pressure. Caffeine and certain dietary supplements, such as ginseng, natural liquorice, and yohimbine, can also cause drug-induced hypertension.

For provoked cases of venous thromboembolism, such as those following recent surgery, warfarin treatment is typically recommended for a duration of three months. However, for unprovoked cases, where the cause is unknown, a longer duration of six months is typically recommended.

Deep vein thrombosis (DVT) is a serious condition that requires prompt diagnosis and management. The National Institute for Health and Care Excellence (NICE) updated their guidelines in 2020, recommending the use of direct oral anticoagulants (DOACs) as first-line treatment for most people with VTE, including as interim anticoagulants before a definite diagnosis is made. They also recommend the use of DOACs in patients with active cancer, as opposed to low-molecular weight heparin as was previously recommended. Routine cancer screening is no longer recommended following a VTE diagnosis.

If a patient is suspected of having a DVT, a two-level DVT Wells score should be performed to assess the likelihood of the condition. If a DVT is ‘likely’ (2 points or more), a proximal leg vein ultrasound scan should be carried out within 4 hours. If the result is positive, then a diagnosis of DVT is made and anticoagulant treatment should start. If the result is negative, a D-dimer test should be arranged. If a proximal leg vein ultrasound scan cannot be carried out within 4 hours, a D-dimer test should be performed and interim therapeutic anticoagulation administered whilst waiting for the proximal leg vein ultrasound scan (which should be performed within 24 hours).

The cornerstone of VTE management is anticoagulant therapy. The big change in the 2020 guidelines was the increased use of DOACs. Apixaban or rivaroxaban (both DOACs) should be offered first-line following the diagnosis of a DVT. Instead of using low-molecular weight heparin (LMWH) until the diagnosis is confirmed, NICE now advocate using a DOAC once a diagnosis is suspected, with this continued if the diagnosis is confirmed. If neither apixaban or rivaroxaban are suitable, then either LMWH followed by dabigatran or edoxaban OR LMWH followed by a vitamin K antagonist (VKA, i.e. warfarin) can be used.

All patients should have anticoagulation for at least 3 months. Continuing anticoagulation after this period is partly determined by whether the VTE was provoked or unprovoked. If the VTE was provoked, the treatment is typically stopped after the initial 3 months (3 to 6 months for people with active cancer). If the VTE was

Understanding NICE Guidelines on Hypertension

Managing hypertension is a crucial aspect of a general practitioner’s role, and it is essential to have a good understanding of the latest NICE guidelines on hypertension (NG136). Step 4 of the guidelines recommends seeking expert advice or adding low-dose spironolactone if the blood potassium level is ≤4.5 mmol/l, and an alpha-blocker or beta-blocker if the blood potassium level is >4.5 mmol/l. If blood pressure remains uncontrolled on optimal tolerated doses of four drugs, expert advice should be sought.

It is important to note that hypertension management is a topic that may be tested in various areas of the MRCGP exam, including the AKT. Therefore, it is crucial to have a good understanding of the NICE guidelines on hypertension to perform well in the exam. By following the guidelines, general practitioners can provide optimal care to their patients with hypertension.

Managing Warfarin Patients on Antibiotics

When a patient on warfarin requires antibiotics, it is a common clinical scenario that requires careful management. While there is no need to stop warfarin or switch to aspirin, it is important to monitor the patient’s INR levels closely. Typically, extra INR monitoring should be performed three to five days after starting the antibiotics to check for any potential impact on the INR. If necessary, a dosing change for warfarin may be needed.

According to the British Committee for Standards in Haematology Guidelines for oral anticoagulation with warfarin (2011), it is important to follow specific recommendations for INR testing when a potential drug interaction occurs. By carefully monitoring INR levels and adjusting warfarin dosing as needed, healthcare providers can help ensure the safety and efficacy of treatment for patients on warfarin who require antibiotics.

Hypertension, or high blood pressure, is a common condition that can lead to serious health problems if left untreated. The National Institute for Health and Care Excellence (NICE) has published updated guidelines for the management of hypertension in 2019. Some of the key changes include lowering the threshold for treating stage 1 hypertension in patients under 80 years old, allowing the use of angiotensin receptor blockers instead of ACE inhibitors, and recommending the use of calcium channel blockers or thiazide-like diuretics in addition to ACE inhibitors or angiotensin receptor blockers.

Lifestyle changes are also important in managing hypertension. Patients should aim for a low salt diet, reduce caffeine intake, stop smoking, drink less alcohol, eat a balanced diet rich in fruits and vegetables, exercise more, and lose weight.

Treatment for hypertension depends on the patient’s blood pressure classification. For stage 1 hypertension with ABPM/HBPM readings of 135/85 mmHg or higher, treatment is recommended for patients under 80 years old with target organ damage, established cardiovascular disease, renal disease, diabetes, or a 10-year cardiovascular risk equivalent to 10% or greater. For stage 2 hypertension with ABPM/HBPM readings of 150/95 mmHg or higher, drug treatment is recommended regardless of age.

The first-line treatment for patients under 55 years old or with a background of type 2 diabetes mellitus is an ACE inhibitor or angiotensin receptor blocker. Calcium channel blockers are recommended for patients over 55 years old or of black African or African-Caribbean origin. If a patient is already taking an ACE inhibitor or angiotensin receptor blocker, a calcium channel blocker or thiazide-like diuretic can be added.

If blood pressure remains uncontrolled with the optimal or maximum tolerated doses of four drugs, NICE recommends seeking expert advice or adding a fourth drug. Blood pressure targets vary depending on age, with a target of 140/90 mmHg for patients under 80 years old and 150/90 mmHg for patients over 80 years old. Direct renin inhibitors, such as Aliskiren, may be used in patients who are intolerant of other antihypertensive drugs, but their role is currently limited.

Guidelines for Measuring Blood Pressure

When measuring blood pressure, it is important to follow certain guidelines to ensure accurate readings. The patient should be seated for at least five minutes, in a relaxed state without moving or speaking. Blood pressure should be recorded three times, initially testing in both arms. If there is a sustained difference of more than 20 mmHg, use the arm with the higher reading for subsequent measurements. The arm must be supported at the level of the heart.

If the blood pressure is 140/90 mmHg or higher, up to three readings should be taken, and the lower of the last two recorded as the blood pressure. It is important to note that automated devices may not measure blood pressure accurately if there is pulse irregularity, such as atrial fibrillation. In such cases, blood pressure should be measured manually using direct auscultation over the brachial artery. By following these guidelines, healthcare professionals can ensure accurate blood pressure readings for their patients.

Optimum Treatments for Post-Myocardial Infarction Patients

After a myocardial infarction, it is crucial for patients to receive the appropriate medications to prevent further complications. The following are some of the optimum treatments for post-MI patients:

1. Aspirin, clopidogrel, bisoprolol, ramipril, and a statin: Beta-blockers like bisoprolol are essential for patients with left ventricular dysfunction. ACE inhibitors like ramipril are also recommended for post-MI and asymptomatic left ventricular dysfunction. Aspirin, another antiplatelet drug, and a statin are also widely used.

2. Aspirin, ticagrelor, losartan, and a statin: Ticagrelor can be used instead of clopidogrel for certain patients. Losartan, an angiotensin 2 receptor blocker, can replace an ACE inhibitor if the latter is not tolerated.

3. Aspirin, bisoprolol, ramipril, amlodipine, and a statin: Amlodipine can be added for hypertensive control if needed. However, other calcium blockers can increase mortality in patients with poor left ventricular function post-MI.

4. Aspirin, bisoprolol, ramipril, furosemide, and a statin: Furosemide is only added for the treatment of symptomatic congestive cardiac failure.

5. Aspirin, isosorbide mononitrate, ramipril, and a statin: Isosorbide mononitrate may be used for symptomatic relief of angina symptoms but is not routinely prescribed after an MI. The absence of a beta-blocker and second antiplatelet also makes this choice suboptimal.

In conclusion, post-MI patients should receive a combination of medications tailored to their individual needs to prevent further complications and improve their quality of life.

Cardioversion for Atrial Fibrillation: NICE Guidelines and Considerations

The National Institute for Health and Care Excellence (NICE) recommends referral to a cardiologist for rhythm-control treatment (cardioversion) in certain cases of atrial fibrillation. These include atrial fibrillation with a reversible cause, heart failure primarily caused or worsened by atrial fibrillation, and new-onset atrial fibrillation. If onset is known to be within 48 hours, referral to an acute medical unit is recommended for immediate cardioversion without anticoagulation treatment. Pharmacological cardioversion is often used as a first-line therapy, with electrical cardioversion reserved for non-responders. However, cardioversion may be less successful or not recommended in cases of long-standing atrial fibrillation, significant valve problems, cardiomegaly, or multiple recurrences of atrial fibrillation.

Given his background, he is a suitable candidate for a formal evaluation of his risk for cardiovascular disease through a lipid profile, which can provide additional information to enhance the QRISK2 score.

Management of Hyperlipidaemia: NICE Guidelines

Hyperlipidaemia, or high levels of lipids in the blood, is a major risk factor for cardiovascular disease (CVD). In 2014, the National Institute for Health and Care Excellence (NICE) updated their guidelines on lipid modification, which caused controversy due to the recommendation of statins for a significant proportion of the population over the age of 60. The guidelines suggest a systematic strategy to identify people over 40 years who are at high risk of CVD, using the QRISK2 CVD risk assessment tool. A full lipid profile should be checked before starting a statin, and patients with very high cholesterol levels should be investigated for familial hyperlipidaemia. The new guidelines recommend offering a statin to people with a QRISK2 10-year risk of 10% or greater, with atorvastatin 20 mg offered first-line. Special situations, such as type 1 diabetes mellitus and chronic kidney disease, are also addressed. Lifestyle modifications, including a cardioprotective diet, physical activity, weight management, alcohol intake, and smoking cessation, are important in managing hyperlipidaemia.

Treatment options for Peripheral Arterial Disease (PAD)

Peripheral Arterial Disease (PAD) is a condition that causes intermittent claudication. Antiplatelet therapy is recommended for those with symptomatic disease to reduce major cardiovascular events. Clopidogrel is suggested as the drug of first choice by the National Institute for Health and Care Excellence (NICE). Angiotensin converting enzyme inhibitors have been shown to reduce cardiovascular morbidity and mortality in patients with PAD. However, they should be carefully monitored as more than 25% of patients have co-existent renal artery stenosis. Statins are also recommended as they reduce the risk of mortality, cardiovascular events and stroke in patients with PAD. Naftidrofuryl oxalate is an option for the treatment of intermittent claudication in people with PAD for whom vasodilator therapy is considered appropriate. Amlodipine, a calcium channel blocker, is not indicated for this case.

DVLA guidance following multiple TIAs: driving prohibited for a period of 3 months.

The DVLA has guidelines for individuals with neurological disorders who wish to drive cars or motorcycles. However, the rules for drivers of heavy goods vehicles are much stricter. For individuals with epilepsy or seizures, they must not drive and must inform the DVLA. If an individual has had a first unprovoked or isolated seizure, they must take six months off driving if there are no relevant structural abnormalities on brain imaging and no definite epileptiform activity on EEG. If these conditions are not met, the time off driving is increased to 12 months. Individuals with established epilepsy or those with multiple unprovoked seizures may qualify for a driving license if they have been free from any seizure for 12 months. If there have been no seizures for five years (with medication if necessary), a ’til 70 license is usually restored. Individuals should not drive while anti-epilepsy medication is being withdrawn and for six months after the last dose.

For individuals with syncope, a simple faint has no restriction on driving. A single episode that is explained and treated requires four weeks off driving. A single unexplained episode requires six months off driving, while two or more episodes require 12 months off. For individuals with other conditions such as stroke or TIA, they must take one month off driving. They may not need to inform the DVLA if there is no residual neurological deficit. If an individual has had multiple TIAs over a short period of time, they must take three months off driving and inform the DVLA. For individuals who have had a craniotomy, such as for meningioma, they must take one year off driving. If an individual has had a pituitary tumor, a craniotomy requires six months off driving, while trans-sphenoidal surgery allows driving when there is no debarring residual impairment likely to affect safe driving. Individuals with narcolepsy/cataplexy must cease driving on diagnosis but can restart once there is satisfactory control of symptoms. For individuals with chronic neurological disorders such as multiple sclerosis or motor neuron disease, they should inform the DVLA and complete the PK1 form (application for driving license holders’ state of health). If the tumor is a benign meningioma and there is no seizure history, the license can be reconsidered six months after surgery if the individual remains seizure-free.

Understanding the Athletic Heart

The athletic heart is a common occurrence in individuals who engage in prolonged periods of endurance training. It is characterized by a systolic flow murmur, LV enlargement, bradycardia, and third heart sounds. To differentiate it from cardiomyopathy, echocardiography is useful, with symmetric septal hypertrophy, normal diastolic function, and LVH <13 mm being features of athletic hearts. The BP response to exercise is normal, and LVH regresses in response to deconditioning. While persistent bradycardia and atrial arrhythmias are rare sequelae of the athletic heart picture, it is important to differentiate between a physiological S3 gallop (triple rhythm) and a pathological summation gallop. Although most GPs may struggle to differentiate third and fourth heart sounds, it is crucial to recognize that some signs can occur in 'normal' individuals as well as disease. Understanding the athletic heart is essential for healthcare professionals to provide appropriate care and treatment to their patients.