Recommended INR Levels for Anticoagulation Therapy

Anticoagulation therapy is used to prevent blood clots in individuals with certain medical conditions. The target level for the majority of indications is an INR (international normalized ratio) of 2.5. However, for individuals who are already receiving warfarin and have recurrent deep vein thrombosis or pulmonary embolism, a higher INR of 3.5 is recommended. Additionally, for patients with mechanical prosthetic heart valves, the recommended INR level ranges from 3.0 to 3.5 depending on the type of valve. It is important to closely monitor INR levels and adjust the dosage of anticoagulation therapy as needed to prevent complications.

It is recommended that patients diagnosed with heart failure receive an annual influenza vaccine and a single pneumococcal vaccine.

The Department of Health recommends that people over the age of 65 and those with certain medical conditions receive an annual influenza vaccination. These medical conditions include chronic respiratory disease, chronic heart disease, chronic kidney disease, chronic liver disease, chronic neurological disease, diabetes mellitus, immunosuppression, asplenia or splenic dysfunction, and pregnancy. Additionally, health and social care staff, those living in long-stay residential care homes, and carers of the elderly or disabled may also be considered for vaccination at the discretion of their GP.

The pneumococcal polysaccharide vaccine is recommended for all adults over the age of 65 and those with certain medical conditions. These medical conditions include asplenia or splenic dysfunction, chronic respiratory disease, chronic heart disease, chronic kidney disease, chronic liver disease, diabetes mellitus, immunosuppression, cochlear implants, and patients with cerebrospinal fluid leaks. Asthma is only included if it requires the use of oral steroids at a dose sufficient to act as a significant immunosuppressant. Controlled hypertension is not an indication for vaccination.

Travel Restrictions After Myocardial Infarction

After experiencing a myocardial infarction (MI), also known as a heart attack, patients may wonder when it is safe to travel by air. The minimum time for flying after an uncomplicated MI is generally accepted to be seven days, although some authorities suggest waiting up to three weeks. It is important to note that this question specifically asks for the minimum time after an uncomplicated MI that would be safe for air travel.

Consensus national guidance in the UK, including advice from the Civil Aviation Authority and British Airways, supports the seven-day minimum for uncomplicated MI. Patients who have had a complicated MI should wait four to six weeks before flying. Patients with severe angina may require oxygen during the flight and should pre-book a supply with the airline. Patients who have undergone coronary artery bypass graft (CABG) or suffered a stroke should not travel for ten days. Decompensated heart failure or uncontrolled hypertension are contraindications to flying.

In summary, patients who have experienced an uncomplicated MI may fly after seven days without requiring an exercise test. It is important to follow national guidance and consult with a healthcare provider before making any travel plans after a heart attack.

Patients with rheumatoid arthritis may have an increased risk of developing accelerated atherosclerosis, which is believed to be linked to the inflammatory process. The QRisk2 calculator, used to predict the 10-year risk of developing cardiovascular disease, includes rheumatoid arthritis as a risk factor. However, a blood pressure reading of 130/80 mmHg and a BMI of 24 kg/m2 are within the normal range and not a cause for concern. Additionally, the HbA1c level of 41 mmol/mol is normal and doesn’t indicate an increased risk of diabetes. While a family history of myocardial infarction is significant, it is only considered a risk factor if the relative was diagnosed before the age of 60, not at 65.

Understanding Symptoms of Aortic Stenosis

Aortic stenosis is a condition where the aortic valve becomes narrowed, leading to restricted blood flow from the heart. One of the most common symptoms of aortic stenosis is a murmur heard in the aortic area. This is often due to calcification of the valve. However, symptoms usually only appear when the stenosis becomes severe.

Patients with aortic stenosis may experience dyspnea on exertion, which is difficulty breathing during physical activity. More concerning symptoms include angina, syncope, or symptoms of heart failure. Angina is caused by left ventricular hypertrophy, while syncope is thought to be due to a failure to increase cardiac output during times of peripheral vasodilation and subsequent hypotension. It’s important to note that drugs that cause peripheral vasodilation, such as nitrates or ACE inhibitors, can increase the risk of syncope.

Dysphagia is a rare complication of left atrial hypertrophy due to mitral valve disease. Palpitations and transient ischemic attacks are not symptoms that are typically associated with aortic stenosis. The most common source of emboli with transient ischemic attacks is the carotids. Vertigo is not caused by aortic stenosis.

In summary, understanding the symptoms of aortic stenosis is crucial for early detection and treatment. If you experience any concerning symptoms, it’s important to speak with your healthcare provider.

Raynaud’s phenomenon is a condition where the arteries in the fingers and toes constrict excessively in response to cold or emotional stress. It can be classified as primary (Raynaud’s disease) or secondary (Raynaud’s phenomenon) depending on the underlying cause. Raynaud’s disease is more common in young women and typically affects both sides of the body. Secondary Raynaud’s phenomenon is often associated with connective tissue disorders such as scleroderma, rheumatoid arthritis, or systemic lupus erythematosus. Other causes include leukaemia, cryoglobulinaemia, use of vibrating tools, and certain medications.

If there is suspicion of secondary Raynaud’s phenomenon, patients should be referred to a specialist for further evaluation. Treatment options include calcium channel blockers such as nifedipine as a first-line therapy. In severe cases, intravenous prostacyclin (epoprostenol) infusions may be used, which can provide relief for several weeks or months. It is important to identify and treat any underlying conditions that may be contributing to the development of Raynaud’s phenomenon. Factors that suggest an underlying connective tissue disease include onset after 40 years, unilateral symptoms, rashes, presence of autoantibodies, and digital ulcers or calcinosis. In rare cases, chilblains may also be present.

Seeking Expert Advice for Resistant Blood Pressure

As per NICE guidelines, if a patient is already taking four antihypertensive medications and their blood pressure remains resistant, it is recommended to seek expert advice. This is because if the blood pressure remains uncontrolled even after taking the optimal or maximum tolerated doses of four drugs, it may indicate a need for further evaluation and management. Seeking expert advice can help in identifying any underlying causes of resistant hypertension and developing an effective treatment plan. Therefore, it is important to consult with a specialist if the blood pressure remains uncontrolled despite taking four antihypertensive medications.

Understanding the Number Needed to Treat (NNT)

When evaluating the efficacy of a treatment, it’s important to look beyond statistical significance and consider the practical impact on patients. The Number Needed to Treat (NNT) is a statistical figure that provides valuable information about the effectiveness of a treatment. For example, if 1000 patients are treated with a new statin for five years and 50 MIs are prevented, the NNT to prevent one MI is 20 (1000/50). This means that by treating just 20 patients, one MI can be prevented over a five-year period.

The NNT can also be used to calculate cost economic data by factoring in the cost of the drug against the costs of treating and rehabilitating a patient with an MI. By understanding the NNT, healthcare professionals can make informed decisions about the most effective and cost-efficient treatments for their patients.

Treatment Options for Erectile Dysfunction: Alprostadil, Tadalafil, Penile Prosthesis, and Psychosexual Counselling

Erectile dysfunction affects a significant percentage of men, with prevalence increasing with age. The condition shares the same risk factors as cardiovascular disease. The usual first-line treatment with a phosphodiesterase-5 (PDE5) inhibitor is contraindicated in patients taking nitrates, as concurrent use can lead to severe hypotension or even death. Therefore, alternative treatment options are available.

Alprostadil is an effective treatment for erectile dysfunction, either topically or in the form of an intracavernosal injection. It is the most appropriate treatment to offer where PDE5 inhibitors are ineffective or for people who find PDE5 inhibitors ineffective.

Tadalafil, a PDE5 inhibitor, is a first-line treatment for erectile dysfunction. It lasts longer than sildenafil, which can help improve spontaneity. However, it is contraindicated in patients taking nitrates, and a second-line treatment, such as alprostadil, should be used.

A penile prosthesis is a rare third-line option if both PDE5 inhibitors and alprostadil are either ineffective or inappropriate. It involves the insertion of a fluid-filled reservoir under the abdominal wall, with a pump and a release valve in the scrotum, that are used to inflate two implanted cylinders in the penis.

Psychosexual counselling is recommended for treatment of psychogenic erectile dysfunction or in those men with severe psychological distress. It is not recommended for routine treatment, but studies have shown that psychotherapy is just as effective as vacuum devices and penile prosthesis.

In summary, treatment options for erectile dysfunction include alprostadil, tadalafil, penile prosthesis, and psychosexual counselling, depending on the individual’s needs and contraindications.

For patients with prosthetic heart valves, antithrombotic therapy varies depending on the type of valve. Bioprosthetic valves typically require aspirin, while mechanical valves require a combination of warfarin and aspirin.

Prosthetic Heart Valves: Options and Considerations

Prosthetic heart valves are commonly used to replace damaged or diseased valves in the heart. The two main options for replacement are biological (bioprosthetic) or mechanical valves. Bioprosthetic valves are usually derived from bovine or porcine sources and are preferred for 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 location. Aspirin is only given in addition if there is an additional indication, such as ischaemic heart disease.

It is important to consider the patient’s age, medical history, and lifestyle when choosing a prosthetic heart valve. While bioprosthetic valves may not require long-term anticoagulation, they may need to be replaced sooner than mechanical valves. Mechanical valves, on the other hand, may require lifelong anticoagulation, which can be challenging for some patients. Additionally, following the 2008 NICE guidelines, antibiotics are no longer recommended for common procedures such as dental work for prophylaxis of endocarditis. Therefore, it is crucial to weigh the benefits and risks of each option and make an informed decision with the patient.

Management of Hypertriglyceridaemia

Hypertriglyceridaemia is a condition that increases the risk of pancreatitis, making prompt management crucial. The National Institute for Health and Care Excellence (NICE) has provided specific guidance on how to manage this condition.

If the triglyceride level is above 20 mmol/L and not due to alcohol excess or poor glycaemic control, urgent referral to a lipid clinic is necessary. For levels between 10 mmol/L and 20 mmol/L, a fasting sample should be repeated no sooner than 5 days and no longer than 2 weeks later. If the level remains above 10 mmol/L, secondary causes of hypertriglyceridaemia should be considered, and specialist advice should be sought.

For those with a triglyceride level between 4.5 and 9.9 mmol/L, clinicians should consider that cardiovascular disease (CVD) risk may be underestimated using risk assessment tools such as QRISK. They should optimize the management of other CVD risk factors, and specialist advice should be sought if the non-HDL cholesterol level is above 7.5 mmol/L.

In summary, the management of hypertriglyceridaemia requires careful consideration of the triglyceride level and other risk factors. Early referral to a lipid clinic and specialist advice can help prevent complications such as pancreatitis and reduce the risk of CVD.

DVLA guidance after angioplasty – refrain from driving for a period of 7 days.

DVLA Guidelines for Cardiovascular Disorders and Driving

The DVLA has specific guidelines for individuals with cardiovascular disorders who wish to drive a car or motorcycle. For those with hypertension, driving is permitted unless the treatment causes unacceptable side effects, and there is no need to notify the DVLA. However, if the individual has Group 2 Entitlement, they will be disqualified from driving if their resting blood pressure consistently measures 180 mmHg systolic or more and/or 100 mm Hg diastolic or more.

Individuals who have undergone elective angioplasty must refrain from driving for one week, while those who have undergone CABG or acute coronary syndrome must wait four weeks before driving. If an individual experiences angina symptoms at rest or while driving, they must cease driving altogether. Pacemaker insertion requires a one-week break from driving, while implantable cardioverter-defibrillator (ICD) implantation results in a six-month driving ban if implanted for sustained ventricular arrhythmia. If implanted prophylactically, the individual must cease driving for one month, and Group 2 drivers are permanently barred from driving with an ICD.

Successful catheter ablation for an arrhythmia requires a two-day break from driving, while an aortic aneurysm of 6 cm or more must be reported to the DVLA. Licensing will be permitted subject to annual review, but an aortic diameter of 6.5 cm or more disqualifies patients from driving. Finally, individuals who have undergone a heart transplant must refrain from driving for six weeks, but there is no need to notify the DVLA.

The current prescription of Atorvastatin alone is not sufficient for this patient. In addition to lipid-lowering therapy, he should also be offered an antihypertensive agent. However, it is important to note that due to his age and ethnicity, he should first be offered an ACE and/or angiotensin-II receptor antagonist. If he doesn’t have type 2 diabetes and is aged 55 years or over, or if he is of black African or African-Caribbean family origin and doesn’t have type 2 diabetes (of any age), calcium-channel blockers may be considered as the first-line antihypertensive agent. It is not appropriate to suggest that no treatment is required.

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.

Understanding Hypertension

Ninety five percent of patients diagnosed with hypertension have essential or primary hypertension, while the remaining five percent have secondary hypertension. Essential hypertension is caused by a combination of genetic and environmental factors, resulting in high blood pressure. On the other hand, secondary hypertension is caused by a specific abnormality in one of the organs or systems of the body.

It is important to understand the type of hypertension a patient has in order to determine the appropriate treatment plan. While essential hypertension may be managed through lifestyle changes and medication, secondary hypertension requires addressing the underlying cause. Regular blood pressure monitoring and consultation with a healthcare professional can help manage hypertension and reduce the risk of complications.

Understanding Cardiomyopathy: Causes, Symptoms, and Diagnosis

Cardiomyopathy is a chronic disease that affects the heart muscle, causing it to become enlarged, thickened, or stiffened. This condition can range from being asymptomatic to causing heart failure, arrhythmia, thromboembolism, and sudden death. In this article, we will discuss the causes, symptoms, and diagnosis of cardiomyopathy.

Causes of Cardiomyopathy
Cardiomyopathy can be caused by a variety of factors, including coronary heart disease, hypertension, valvular disease, and congenital heart disease. It can also be caused by secondary factors such as ischaemia, alcohol abuse, toxins, infections, thyroid disorders, and valvular disease. In some cases, cardiomyopathy may be familial or genetic.

Symptoms of Cardiomyopathy
Most cases of cardiomyopathy present as congestive heart failure with symptoms such as dyspnoea, weakness, fatigue, oedema, raised JVP, pulmonary congestion, cardiomegaly, and a loud 3rd and/or 4th heart sound. However, some cases may remain asymptomatic for a long time.

Diagnosis of Cardiomyopathy
Diagnosis of cardiomyopathy usually involves an electrocardiogram (ECG) which may show sinus tachycardia, intraventricular conduction delay, left bundle branch block, or nonspecific changes in ST and T waves. Other diagnostic tests may include echocardiography, cardiac MRI, and cardiac catheterization.

Conclusion
Cardiomyopathy is a serious condition that can lead to heart failure, arrhythmia, thromboembolism, and sudden death. It is important to understand the causes, symptoms, and diagnosis of this condition in order to manage it effectively. If you suspect that you or a loved one may have cardiomyopathy, seek medical attention immediately.

Takayasu’s arteritis is a type of vasculitis that affects the large blood vessels, often leading to blockages in the aorta. This condition is more commonly seen in young women and Asian individuals. Symptoms may include malaise, headaches, unequal blood pressure in the arms, carotid bruits, absent or weak peripheral pulses, and claudication in the limbs during physical activity. Aortic regurgitation may also occur in around 20% of cases. Renal artery stenosis is a common association with this condition. To diagnose Takayasu’s arteritis, vascular imaging of the arterial tree is necessary, which can be done through magnetic resonance angiography or CT angiography. Treatment typically involves the use of steroids.

If a patient with hypertension is already taking an ACE inhibitor and has a history of gout, it would be more appropriate to prescribe a calcium channel blocker as the next step instead of a thiazide. This is because thiazide-type diuretics should be used with caution in individuals with gout as it may worsen the condition. Therefore, a calcium channel blocker should be considered as a second-line Antihypertensive medication.

It would be incorrect to make no changes to the patient’s medication, especially if their blood pressure readings are consistently high. In this case, a second-line Antihypertensive medication is necessary.

Stopping the patient’s current medication, ramipril, is also not recommended as it is providing some Antihypertensive effects. Instead, a second medication should be added to further manage the patient’s hypertension.

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.

Understanding the Four Types of Cardiomyopathy

Cardiomyopathy is a group of heart muscle disorders that affect the structure and function of the heart. There are four major types of cardiomyopathy: dilated, hypertrophic, restrictive, and arrhythmogenic right ventricular cardiomyopathy. Each type is characterized by specific features such as ventricular dilation, hypertrophy, restrictive filling, and fibro-fatty changes in the right ventricular myocardium.

While dilated and hypertrophic cardiomyopathies are the most common types, a familial cause has been identified in a significant percentage of patients with these conditions. On the other hand, restrictive cardiomyopathy is usually not familial.

To diagnose cardiomyopathy, a full cardiological assessment is necessary. Transthoracic Doppler echocardiography can confirm the diagnosis of hypertrophic cardiomyopathy, distinguish between restrictive cardiomyopathy and constrictive pericarditis, and assess the severity of ventricular dysfunction in dilated cardiomyopathies. Coronary angiography can help exclude coronary artery disease as the cause of dilated cardiomyopathy.

A normal ECG is uncommon in any form of cardiomyopathy, and cardiomegaly on a chest X-ray may be present in all types. Brain natriuretic peptide is a marker of ventricular dysfunction but cannot differentiate between cardiomyopathies.

In summary, understanding the different types of cardiomyopathy and their diagnostic tools is crucial in managing and treating this group of heart muscle disorders.

Hypertension Management in Type 2 Diabetes

This patient with type 2 diabetes has poorly controlled hypertension, but is currently tolerating his medication well. The recommended antihypertensive for diabetes is an ACE inhibitor, which can be combined with a calcium channel blocker like amlodipine. Beta-blockers should be avoided for routine hypertension treatment in diabetic patients. Methyldopa is used for hypertension during pregnancy, while moxonidine is used when other medications have failed. If blood pressure control is still inadequate, a thiazide diuretic can be added to the current regimen of ramipril and amlodipine. Proper management of hypertension is crucial in diabetic patients to prevent complications and improve overall health.

Acute Limb Ischaemia: Causes and Symptoms

Acute limb ischaemia is a condition characterized by a painful, paralysed, and pulseless limb that feels perishingly cold with paraesthesia. This condition is usually caused by either an embolus or thrombotic occlusion, which can occur on the background of intermittent claudication (chronic limb ischaemia). In most cases, the likely cause of acute limb ischaemia is an embolism secondary to atrial fibrillation. Other sources of emboli include defective heart valves, cardiac mural thrombi, and thrombus from within an aortic aneurysm.

If a patient presents with a painful, paralysed, and pulseless limb, an echocardiogram, abdominal ultrasound, and duplex of proximal limb vessels are indicated. These tests can help identify the underlying cause of the condition. It is important to note that acute limb ischaemia is a medical emergency that requires immediate attention. Delayed treatment can lead to irreversible tissue damage and even limb loss.

In summary, acute limb ischaemia is a serious condition that requires prompt diagnosis and treatment. Patients with this condition should seek medical attention immediately to prevent irreversible tissue damage and limb loss.

Monitoring Recommendations for Loop Diuretics

To ensure the safe and effective use of loop diuretics, the National Institute for Health and Care Excellence (NICE) recommends monitoring renal function, serum electrolytes, and blood pressure within 1-2 weeks after each dose increase. It is also important to check these parameters before starting treatment and after treatment initiation.

For patients with known chronic kidney disease (CKD), those aged 60 years or older, or those taking an ACE-I, ARB, or aldosterone antagonist, earlier monitoring (5-7 days) may be necessary. By closely monitoring these parameters, healthcare professionals can identify any potential adverse effects and adjust treatment accordingly to optimize patient outcomes.

The Role of Digoxin in Congestive Heart Failure Treatment

Digoxin, a medication commonly used in the past for congestive heart failure, has lost its popularity due to the lack of demonstrated mortality benefit in patients with this condition. However, it has shown a reduction in hospitalizations for congestive heart failure. Therefore, it is recommended to maximize the use of other therapies such as ACE inhibitors, β blockers, and spironolactone before considering digoxin. If the ACE inhibitor cannot be tolerated, an angiotensin II receptor antagonist like candesartan can be used as an alternative. Digoxin should only be considered as a third-line treatment for severe heart failure due to left ventricular systolic dysfunction after first- and second-line treatments have been exhausted.

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.

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.

For patients with type 2 diabetes who do not have chronic kidney disease, the recommended blood pressure targets are the same as for patients without diabetes. This means a clinic reading of less than 140/90 mmHg and an ambulatory or home blood pressure reading of less than 135/85 mmHg if the patient is under 80 years old. It’s important to note that even if the patient’s estimated glomerular filtration rate (eGFR) is below 90, this doesn’t necessarily mean they have CKD unless there is also evidence of microalbuminuria.

NICE has updated its guidance on the management of type 2 diabetes mellitus (T2DM) in 2022 to reflect advances in drug therapy and improved evidence regarding newer therapies such as SGLT-2 inhibitors. For the average patient taking metformin for T2DM, lifestyle changes and titrating up metformin to aim for a HbA1c of 48 mmol/mol (6.5%) is recommended. A second drug should only be added if the HbA1c rises to 58 mmol/mol (7.5%). Dietary advice includes encouraging high fiber, low glycemic index sources of carbohydrates, controlling intake of saturated fats and trans fatty acids, and initial target weight loss of 5-10% in overweight individuals.

Individual HbA1c targets should be agreed upon with patients to encourage motivation, and HbA1c should be checked every 3-6 months until stable, then 6 monthly. Targets should be relaxed on a case-by-case basis, with particular consideration for older or frail adults with type 2 diabetes. Metformin remains the first-line drug of choice, and SGLT-2 inhibitors should be given in addition to metformin if the patient has a high risk of developing cardiovascular disease (CVD), established CVD, or chronic heart failure. If metformin is contraindicated, SGLT-2 monotherapy or a DPP-4 inhibitor, pioglitazone, or sulfonylurea may be used.

Further drug therapy options depend on individual clinical circumstances and patient preference. Dual therapy options include adding a DPP-4 inhibitor, pioglitazone, sulfonylurea, or SGLT-2 inhibitor (if NICE criteria are met). If a patient doesn’t achieve control on dual therapy, triple therapy options include adding a sulfonylurea or GLP-1 mimetic. GLP-1 mimetics should only be added to insulin under specialist care. Blood pressure targets are the same as for patients without type 2 diabetes, and ACE inhibitors or ARBs are first-line for hypertension. Antiplatelets should not be offered unless a patient has existing cardiovascular disease, and only patients with a 10-year cardiovascular risk > 10% should be offered a statin.

The data used for QFracture is derived from primary care in the UK.

Assessing Risk for Osteoporosis

Osteoporosis is a concern due to the increased risk of fragility fractures. To determine which patients are at risk and require further investigation, NICE produced guidelines in 2012. They recommend assessing all women aged 65 years and above and all men aged 75 years and above. Younger patients should be assessed if they have risk factors such as previous fragility fracture, current or frequent use of oral or systemic glucocorticoid, history of falls, family history of hip fracture, other causes of secondary osteoporosis, low BMI, smoking, and alcohol intake.

NICE suggests using a clinical prediction tool such as FRAX or QFracture to assess a patient’s 10-year risk of developing a fracture. FRAX estimates the 10-year risk of fragility fracture and is valid for patients aged 40-90 years. QFracture estimates the 10-year risk of fragility fracture and includes a larger group of risk factors. BMD assessment is recommended in some situations, such as before starting treatments that may have a rapid adverse effect on bone density or in people aged under 40 years who have a major risk factor.

Interpreting the results of FRAX involves categorizing the results into low, intermediate, or high risk. If the assessment was done without a BMD measurement, an intermediate risk result will prompt a BMD test. If the assessment was done with a BMD measurement, the results will be categorized into reassurance, consider treatment, or strongly recommend treatment. QFracture doesn’t automatically categorize patients into low, intermediate, or high risk, and the raw data needs to be interpreted alongside local or national guidelines.

NICE recommends reassessing a patient’s risk if the original calculated risk was in the region of the intervention threshold for a proposed treatment and only after a minimum of 2 years or when there has been a change in the person’s risk factors.

Cardiac Abnormalities in Marfan Syndrome

Marfan syndrome is an inherited connective tissue disorder that affects various systems in the body. The most common cardiac complication is aortic root dilatation, which occurs in 70% of patients. Mitral valve prolapse is the second most common abnormality, affecting around 60% of patients. Beta-blockers can help reduce the rate of aortic dilatation and the risk of rupture. Aortic dissection, although not the most common abnormality, is a major diagnostic criterion of Marfan syndrome and can result from weakening of the aortic media due to root dilatation. Aortic regurgitation is less common than mitral regurgitation but can occur due to progressive aortic root dilatation and connective tissue abnormalities. Mitral annular calcification is more frequent in Marfan syndrome than in the general population but is not included in the diagnostic criteria.

Coarctation of the Aorta: A Narrowing of the Descending Aorta

Coarctation of the aorta is a congenital condition that affects the descending aorta, causing it to narrow. This condition is more common in males, despite its association with Turner’s syndrome. In infancy, coarctation of the aorta can lead to heart failure, while in adults, it can cause hypertension. Other features of this condition include radio-femoral delay, a mid systolic murmur that is maximal over the back, and an apical click from the aortic valve. Notching of the inferior border of the ribs, which is caused by collateral vessels, is not seen in young children. Coarctation of the aorta is often associated with other conditions, such as bicuspid aortic valve, berry aneurysms, and neurofibromatosis.

To determine the need for anticoagulation in patients with atrial fibrillation, it is necessary to conduct an assessment using both the CHA2DS2-VASc tool and the ORBIT bleeding risk tool. This applies to all patients with atrial fibrillation, according to current NICE CKS guidance. Therefore, the option to commence on apixaban and bisoprolol is not correct.

The patient’s symptoms and ECG findings indicate atrial fibrillation, but there is no indication for a 24-hour ECG. Therefore, referral for a 24-hour ECG and commencing on apixaban and bisoprolol is not necessary.

As there are no signs or symptoms of heart failure and no evidence of valvular heart disease on examination, referral for an echocardiogram and commencing on apixaban and bisoprolol is not the appropriate option.

The patient is currently haemodynamically stable.

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.