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Question 1
Correct
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A 45-year-old man has been referred by his GP due to a history of uncontrolled hypertension. He has come in today to undergo an aldosterone: renin ratio test. The results indicate high levels of aldosterone and low levels of renin. Additionally, a CT scan has revealed bilateral adrenal gland hyperplasia.
What is the recommended management plan for this patient?Your Answer: Spironolactone
Explanation:The patient is suffering from primary hyperaldosteronism, which is caused by bilateral adrenal gland hyperplasia. This condition leads to elevated aldosterone levels, resulting in increased sodium retention and negative feedback to renin release. The most common cause of primary hyperaldosteronism is bilateral adrenal hyperplasia, which can be treated with spironolactone, an aldosterone receptor antagonist, for four weeks. Adrenalectomy is only recommended for unilateral adrenal adenoma, which is not the case for this patient. Fludrocortisone and hydrocortisone are not appropriate treatments for hyperaldosteronism as they act on mineralocorticoid receptors, exacerbating the condition. Reassurance and discharge are not recommended as untreated primary hyperaldosteronism can lead to chronic elevation of blood pressure, increasing the risk of cardiovascular disease, stroke, and kidney damage.
Understanding Primary Hyperaldosteronism
Primary hyperaldosteronism is a medical condition that was previously believed to be caused by an adrenal adenoma, also known as Conn’s syndrome. However, recent studies have shown that bilateral idiopathic adrenal hyperplasia is the cause in up to 70% of cases. It is important to differentiate between the two as this determines the appropriate treatment. Adrenal carcinoma is an extremely rare cause of primary hyperaldosteronism.
The common features of primary hyperaldosteronism include hypertension, hypokalaemia, and alkalosis. Hypokalaemia can cause muscle weakness, but this is seen in only 10-40% of patients. To diagnose primary hyperaldosteronism, the 2016 Endocrine Society recommends a plasma aldosterone/renin ratio as the first-line investigation. This should show high aldosterone levels alongside low renin levels due to negative feedback from sodium retention caused by aldosterone.
If the plasma aldosterone/renin ratio is high, a high-resolution CT abdomen and adrenal vein sampling are used to differentiate between unilateral and bilateral sources of aldosterone excess. If the CT is normal, adrenal venous sampling (AVS) can be used to distinguish between unilateral adenoma and bilateral hyperplasia. The management of primary hyperaldosteronism depends on the underlying cause. Adrenal adenoma is treated with surgery, while bilateral adrenocortical hyperplasia is treated with an aldosterone antagonist such as spironolactone.
In summary, primary hyperaldosteronism is a medical condition that can be caused by adrenal adenoma, bilateral idiopathic adrenal hyperplasia, or adrenal carcinoma. It is characterized by hypertension, hypokalaemia, and alkalosis. Diagnosis involves a plasma aldosterone/renin ratio, high-resolution CT abdomen, and adrenal vein sampling. Treatment depends on the underlying cause and may involve surgery or medication.
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This question is part of the following fields:
- Endocrinology/Metabolic Disease
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Question 2
Incorrect
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A 59 year old man with a history of aortic stenosis presents to his cardiology clinic with complaints of worsening shortness of breath and fainting episodes. His recent ECHO reveals a mean gradient of 45 mmHg and mild aortic regurgitation, while his ECG shows left ventricular hypertrophy, left bundle branch block, and a prolonged PR interval. What factor is most indicative of the need for valve replacement surgery?
Your Answer: 1st degree atrioventricular block
Correct Answer: Presence of symptoms
Explanation:Aortic valve replacement is typically recommended for patients with severe aortic stenosis who are experiencing symptoms such as dyspnea, chest pain, and syncope. Without treatment, these symptoms can lead to a mortality rate of 2-3 years. However, the decision to perform valve replacement on asymptomatic patients is a topic of debate.
Aortic Stenosis: Symptoms, Causes, and Management
Aortic stenosis is a condition characterized by the narrowing of the aortic valve, which can lead to various symptoms. These symptoms include chest pain, dyspnea, syncope, and a characteristic ejection systolic murmur that radiates to the carotids. Severe aortic stenosis can also cause a narrow pulse pressure, slow rising pulse, delayed ESM, soft/absent S2, S4, thrill, and left ventricular hypertrophy or failure. The most common causes of aortic stenosis are degenerative calcification in older patients and bicuspid aortic valve in younger patients.
If a patient is asymptomatic, observation is usually recommended. However, if the patient is symptomatic or has a valvular gradient greater than 40 mmHg with features such as left ventricular systolic dysfunction, valve replacement is necessary. Surgical AVR is the preferred treatment for young, low/medium operative risk patients, while TAVR is used for those with a high operative risk. Balloon valvuloplasty may be used in children without aortic valve calcification and in adults with critical aortic stenosis who are not fit for valve replacement.
In summary, aortic stenosis is a condition that can cause various symptoms and requires prompt management to prevent complications. The causes of aortic stenosis vary, and treatment options depend on the patient’s age, operative risk, and overall health.
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This question is part of the following fields:
- Cardiovascular
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Question 3
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A 6-year-old girl is brought to the clinic by her mother due to complaints of itching around her vulva and anus for the past 3 days. Upon examination, the area appears red and the skin on her vulva is broken from excessive scratching. Her mother has been applying sudocrem but it has not provided relief. There are no other individuals at home with similar symptoms. Based on the probable diagnosis, what is the most suitable course of action?
Your Answer: Prescribe a single dose of mebendazole for the household and give hygiene advice
Explanation:The recommended first line treatment for threadworm is mebendazole. In this case, as the patient is showing symptoms of threadworm, it is important to treat all members of the household with a single dose of mebendazole and provide hygiene advice. While a ‘Scotch tape test’ can be used to confirm the presence of eggs or worms, treatment is often based on symptoms. It is not appropriate to only treat the daughter and provide hygiene advice, as other members of the household may also be infected. Additionally, prescribing 7 days of mebendazole for the daughter alone is incorrect, as a single dose is recommended and a second dose should be taken 14 days later. Piperazine is only recommended for children under 2 years old, so it is not appropriate to prescribe 14 days of piperazine for the daughter in this case.
Threadworm Infestation in Children
Threadworm infestation, caused by Enterobius vermicularis or pinworms, is a common occurrence among children in the UK. The infestation happens when eggs present in the environment are ingested. In most cases, threadworm infestation is asymptomatic, but some possible symptoms include perianal itching, especially at night, and vulval symptoms in girls. Diagnosis can be made by applying Sellotape to the perianal area and sending it to the laboratory for microscopy to see the eggs. However, most patients are treated empirically, and this approach is supported in the CKS guidelines.
The CKS recommends a combination of anthelmintic with hygiene measures for all members of the household. Mebendazole is the first-line treatment for children over six months old, and a single dose is given unless the infestation persists. It is essential to treat all members of the household to prevent re-infection. Proper hygiene measures, such as washing hands regularly, keeping fingernails short, and washing clothes and bedding at high temperatures, can also help prevent the spread of threadworm infestation.
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This question is part of the following fields:
- Paediatrics
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Question 4
Incorrect
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During a routine check-up, a 7 week-old baby boy is seen. His mother has a history of asthma and used inhaled steroids while pregnant. He was delivered via planned Caesarian at 39 weeks due to breech presentation and weighed 3.1kg at birth. What condition is he at a higher risk for?
Your Answer: Congenital cataract
Correct Answer: Developmental dysplasia of the hip
Explanation:If a baby was in a breech presentation, it is important to ensure that they have been referred for screening for developmental dysplasia of the hip (DDH) as it is a risk factor for this condition. The Department of Health recommends that all babies who were breech at any point from 36 weeks (even if not breech at birth), babies born before 36 weeks who were in a breech presentation, and all babies with a first degree relative who had a hip problem in early life, should undergo ultrasound screening for hip dysplasia. If one twin was breech, both should be screened. Some hospitals also refer babies with other conditions such as oligohydramnios, high birth weight, torticollis, congenital talipes calcaneovalgus, and metatarsus adductus for screening. For more information on screening for DDH, please refer to the link provided.
Developmental dysplasia of the hip (DDH) is a condition that affects 1-3% of newborns and is more common in females, firstborn children, and those with a positive family history or breech presentation. It used to be called congenital dislocation of the hip (CDH). DDH is more often found in the left hip and can be bilateral in 20% of cases. Screening for DDH is recommended for infants with certain risk factors, and all infants are screened using the Barlow and Ortolani tests at the newborn and six-week baby check. Clinical examination includes testing for leg length symmetry, restricted hip abduction, and knee level when hips and knees are flexed. Ultrasound is used to confirm the diagnosis if clinically suspected, but x-ray is the first line investigation for infants over 4.5 months. Management includes the use of a Pavlik harness for children under 4-5 months and surgery for older children with unstable hips.
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This question is part of the following fields:
- Paediatrics
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Question 5
Correct
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A 32-year-old woman presents with flank pain and a 48-hour history of dysuria. Her past medical history includes polycystic ovary syndrome. She is not sexually active at present. There is haematuria on urine dipstick testing. Examination reveals a pyrexia of 38.1 °C and flank pain.
What diagnosis fits best with this clinical picture?Your Answer: Pyelonephritis
Explanation:Differential Diagnosis of Abdominal Pain: Overview of Common Conditions
Abdominal pain is a common presenting symptom in clinical practice. It can be caused by a wide range of conditions, including gastrointestinal, genitourinary, gynecological, and systemic disorders. Here, we provide an overview of some of the most common conditions that can cause abdominal pain and their characteristic features.
Pyelonephritis: This is a potentially life-threatening infection that affects the renal parenchyma. It typically presents with fever, unilateral costovertebral angle pain, and nausea/vomiting. Antibiotic therapy is essential, and empirical therapy should be tailored to the infecting pathogen.
Ovarian cyst pain: Ovarian cysts are usually asymptomatic, but severe pain can occur if there is torsion or rupture. The pain is sudden, sharp, and unilateral, and can be associated with trauma, exercise, or coitus.
Nephrolithiasis: This refers to the presence of calculi in the kidneys and/or ureters. The classic presentation is sudden onset of severe flank pain that radiates anteriorly and inferiorly, often accompanied by nausea and vomiting. Fever is not a typical feature.
Pelvic inflammatory disease: PID is an infectious and inflammatory disorder of the upper female genital tract. It typically presents with lower abdominal pain and abnormal vaginal discharge.
Acute glomerulonephritis: This is a specific set of renal diseases that can result in damage to the glomerular tissue. Acute nephritic syndrome is the most serious form, but it typically presents with haematuria, proteinuria, and red blood cell casts in the urine, often accompanied by hypertension and oedema.
In summary, the differential diagnosis of abdominal pain is broad and includes a range of conditions that can affect different organ systems. A careful history and physical examination, along with appropriate investigations, can help to narrow down the possible causes and guide management.
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This question is part of the following fields:
- Renal Medicine/Urology
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Question 6
Incorrect
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A 32-year-old woman presents with heavy menstrual bleeding and a haemoglobin level of 102 g/L. Iron studies are ordered to investigate for iron-deficiency anaemia. What result would support this diagnosis?
Your Answer: ↓ Ferritin, ↑ total iron-binding capacity, ↓ serum iron, ↑ transferrin saturation
Correct Answer: ↓ Ferritin, ↑ total iron-binding capacity, ↓ serum iron, ↓ transferrin saturation
Explanation:In cases of iron-deficiency anemia, it is common for both the total iron-binding capacity (TIBC) and transferrin levels to be elevated. However, it should be noted that the transferrin saturation level is typically decreased.
Iron deficiency anaemia is caused by a lack of iron, which is needed to make haemoglobin in red blood cells. It is the most common type of anaemia worldwide, with preschool-age children having the highest prevalence. Causes include excessive blood loss, inadequate dietary intake, poor intestinal absorption, and increased iron requirements. Symptoms include fatigue, shortness of breath, palpitations, and nail changes. Diagnosis is made through a full blood count and serum ferritin test. Treatment involves identifying and managing the underlying cause, as well as taking oral iron supplements and consuming an iron-rich diet.
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This question is part of the following fields:
- Haematology/Oncology
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Question 7
Correct
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A patient with a history of depression at the age of 50 presents for review. What indicates an elevated risk of suicide?
Your Answer: History of arm cutting
Explanation:Arm cutting may be seen as attention-seeking or a way to release pain, but studies indicate that it increases the risk of suicide for those with a history of deliberate self harm. Employment is a protective factor.
Suicide Risk Factors and Protective Factors
Suicide risk assessment is a common practice in psychiatric care, with patients being stratified into high, medium, or low risk categories. However, there is a lack of evidence on the positive predictive value of individual risk factors. A review in the BMJ concluded that such assessments may not be useful in guiding decision-making, as 50% of suicides occur in patients deemed low risk. Nevertheless, certain factors have been associated with an increased risk of suicide, including male sex, history of deliberate self-harm, alcohol or drug misuse, mental illness, depression, schizophrenia, chronic disease, advancing age, unemployment or social isolation, and being unmarried, divorced, or widowed.
If a patient has attempted suicide, there are additional risk factors to consider, such as efforts to avoid discovery, planning, leaving a written note, final acts such as sorting out finances, and using a violent method. On the other hand, there are protective factors that can reduce the risk of suicide, such as family support, having children at home, and religious belief. It is important to consider both risk and protective factors when assessing suicide risk and developing a treatment plan.
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This question is part of the following fields:
- Psychiatry
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Question 8
Correct
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Male infertility in cystic fibrosis is mostly due to which of the following?
Your Answer: Obliteration or failure of development of the vas deferens
Explanation:Understanding the Reproductive and Sexual Health Implications of Cystic Fibrosis
Cystic fibrosis (CF) is a genetic disorder that affects multiple organs, including the lungs, pancreas, and reproductive system. In over 95% of male patients with CF, infertility is caused by the congenital absence or obliteration of the vas deferens, leading to azoospermia. However, advancements in fertility treatments and surgical techniques have made it possible for some male patients to conceive. Impotence is not a symptom of CF. With significant improvements in diagnosis and treatment, the median survival age of CF patients has increased to around 40 years, with some individuals living into their 60s. Delayed puberty is a common occurrence in both male and female CF patients, but it is not a cause of infertility. Decreased spermatogenesis is not typically seen in CF. Understanding the reproductive and sexual health implications of CF is crucial for patients and healthcare providers to provide appropriate care and support.
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This question is part of the following fields:
- Genetics
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Question 9
Correct
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An 87-year-old woman presents to the Haematology Clinic to review her latest blood test results. These show that her international normalised ratio (INR) is 8.9 (normal range: 2–3). She usually takes warfarin for atrial fibrillation. The patient's General Practitioner has telephoned her to advise that she stop taking the warfarin. The patient says that she feels well and is asymptomatic.
What is the most appropriate next step in this patient's management?Your Answer: Give a dose of vitamin K immediately and re-check her INR in 24 hours
Explanation:Managing High INR Levels in Patients on Warfarin: Treatment Options
When a patient on warfarin presents with a high INR level, it is important to take immediate action to prevent spontaneous bleeding and haemorrhage. Here are some treatment options and their implications:
1. Give a dose of vitamin K immediately and re-check her INR in 24 hours: Administering vitamin K is necessary to reverse the effects of warfarin, which is a vitamin K antagonist. In this situation, it is important to act quickly to reduce the INR level and prevent haemorrhage.
2. Give intramuscular (IM) vitamin K immediately and re-check her INR in 24 hours: While IM vitamin K can be given in cases where peripheral access is difficult, it is slower acting. In a situation with a high INR level, it is important to reduce the INR as soon as possible to prevent haemorrhage.
3. Give vitamin K immediately and re-check her INR in one week: While giving vitamin K is necessary to prevent spontaneous haemorrhage, it is important to recheck the INR relatively soon to ensure it has dropped below the required range. Waiting a week would be too long, and the INR should be rechecked within 24 hours of administering vitamin K.
4. Stop warfarin for life: If the patient has no actual side-effects from warfarin, such as anaphylaxis, they can continue to use it long-term with tighter control.
5. Switch from warfarin to aspirin: Aspirin cannot be used as a substitute for warfarin as it does not prevent thrombosis.
In conclusion, managing high INR levels in patients on warfarin requires prompt action to prevent haemorrhage. Vitamin K administration is necessary, and the INR level should be rechecked within 24 hours to ensure it has dropped below the required range.
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This question is part of the following fields:
- Haematology/Oncology
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Question 10
Correct
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A 26-year-old patient comes in with lesions on their lower abdomen that have been present for six weeks. At first, there was only one lesion, but more have appeared since then. During the examination, around 10 raised lesions with an umbilicated appearance, each around 1-2 mm in diameter, are observed. What is the most probable diagnosis?
Your Answer: Molluscum contagiosum
Explanation:Molluscum contagiosum is typically observed in children, but the following is a classical depiction of the condition.
Understanding Molluscum Contagiosum
Molluscum contagiosum is a viral skin infection that is commonly seen in children, particularly those with atopic eczema. It is caused by the molluscum contagiosum virus and can be transmitted through direct contact or contaminated surfaces. The infection presents as pinkish or pearly white papules with a central umbilication, which can appear anywhere on the body except for the palms of the hands and soles of the feet. In children, lesions are commonly seen on the trunk and in flexures, while in adults, sexual contact may lead to lesions developing on the genitalia, pubis, thighs, and lower abdomen.
While molluscum contagiosum is a self-limiting condition that usually resolves within 18 months, it is important to avoid sharing towels, clothing, and baths with uninfected individuals to prevent transmission. Scratching the lesions should also be avoided, and treatment may be considered if the itch is problematic. However, treatment is not usually recommended, and if necessary, simple trauma or cryotherapy may be used. In some cases, referral may be necessary, such as for individuals who are HIV-positive with extensive lesions or those with eyelid-margin or ocular lesions and associated red eye.
Overall, understanding molluscum contagiosum and taking appropriate precautions can help prevent transmission and alleviate symptoms.
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This question is part of the following fields:
- Dermatology
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