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Question 1
Incorrect
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Which factors affect water excretion in the kidneys?
Your Answer: Integrity of collecting ducts
Correct Answer: Vasopressin
Explanation:The Renal Tubules: Functions and Regulation
The kidneys play a crucial role in maintaining the body’s fluid and electrolyte balance. This is achieved through the intricate workings of the renal tubules, which are responsible for filtering and reabsorbing various substances from the blood.
Vasopressin, also known as antidiuretic hormone, regulates water excretion in the distal convoluted tubule and collecting ducts. Its receptor, vasopressin 2, triggers the insertion of aquaporin-2 channels, allowing water to be reabsorbed down an osmotic gradient.
The distal convoluted tubule regulates pH by absorbing bicarbonate and secreting protons, as well as controlling sodium and potassium levels through aldosterone-mediated ion transport. It also participates in calcium regulation by reabsorbing it in response to parathyroid hormone.
The proximal convoluted tubule reabsorbs the majority of ions and water in the urinary space back into the body.
The ascending limb of the loop of Henle is impermeable to water, but actively reabsorbs sodium, potassium, and chloride ions. This generates a positive electrochemical potential difference in the lumen, driving more paracellular reabsorption of sodium and other cations.
The collecting ducts continue the work of water reabsorption and electrolyte balance initiated in the collecting tubules. Progenitor cells within the collecting duct epithelium respond to tubular injury by proliferating and expanding the principal cell population to maintain epithelial integrity, or by committing to a myofibroblastic phenotype and forming peritubular collars in response to increased intraluminal pressure.
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This question is part of the following fields:
- Renal Medicine/Urology
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Question 2
Correct
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A 20 year-old female patient visits her GP to request a refill of her COCP prescription. She reports experiencing intense headaches on the left side of her head, accompanied by visual disturbances prior to the onset of the headache. Upon examination, no abnormalities are detected. What is the best course of action for managing her symptoms?
Your Answer: Stop the COCP and start treatment on a progesterone only contraceptive pill.
Explanation:The woman is experiencing migraines with aura, a condition that can be exacerbated by the use of COCP. If a woman has migraine with aura, it is recommended that she discontinue the use of the pill immediately. This is because the oestrogen component of COCP can increase the risk of ischaemic stroke. The only alternative contraceptive medication that can be prescribed is a progesterone-only contraceptive pill, as other options contain oestrogen.
Counselling for Women Considering the Combined Oral Contraceptive Pill
Women who are considering taking the combined oral contraceptive pill (COC) should receive counselling on the potential harms and benefits of the pill. The COC is highly effective if taken correctly, with a success rate of over 99%. However, there is a small risk of blood clots, heart attacks, and strokes, as well as an increased risk of breast and cervical cancer.
In addition to discussing the potential risks and benefits, women should also receive advice on how to take the pill. If the COC is started within the first 5 days of the menstrual cycle, there is no need for additional contraception. However, if it is started at any other point in the cycle, alternative contraception should be used for the first 7 days. Women should take the pill at the same time every day and should be aware that intercourse during the pill-free period is only safe if the next pack is started on time.
There have been recent changes to the guidelines for taking the COC. While it was previously recommended to take the pill for 21 days and then stop for 7 days to mimic menstruation, it is now recommended to discuss tailored regimes with women. This is because there is no medical benefit to having a withdrawal bleed, and options include never having a pill-free interval or taking three 21-day packs back-to-back before having a 4 or 7 day break.
Women should also be informed of situations where the efficacy of the pill may be reduced, such as vomiting within 2 hours of taking the pill, medication that induces diarrhoea or vomiting, or taking liver enzyme-inducing drugs. It is also important to discuss sexually transmitted infections and precautions that should be taken with enzyme-inducing antibiotics such as rifampicin.
Overall, counselling for women considering the COC should cover a range of topics to ensure that they are fully informed and able to make an informed decision about their contraceptive options.
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This question is part of the following fields:
- Neurology
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Question 3
Correct
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A characteristic clinical finding of opioid overdose is:
Your Answer: Bradycardia
Explanation:Understanding the Symptoms of Opioid Overdose: The Opioid Overdose Triad
Opioid overdose is a serious and potentially life-threatening condition that can result from the misuse or abuse of opioids. It is important to recognize the symptoms of opioid overdose in order to provide prompt and effective treatment. The opioid overdose triad is a set of three hallmark symptoms that are commonly seen in opioid overdose: decreased level of consciousness, pinpoint pupils, and respiratory depression.
Bradycardia, or a slow heart rate, is a common side effect of opioid overdose. However, hypothermia is not typically seen in opioid overdose and is more commonly associated with barbiturate overdose. Tachypnoea, or rapid respiration, is not a symptom of opioid overdose; instead, respiratory depression, or slow and shallow breathing, is a key feature. Prolonged hypoxia from respiratory depression can lead to permanent damage to the central nervous system or even death, even if treatment with naloxone is given. It is important to note that alcohol can also cause respiratory depression and increase the risk of overdose when taken with opioids.
Sweating and lacrimation, or excessive sweating and tearing, are frequently seen in early opioid withdrawal but are not symptoms of overdose. Pupillary constriction, or pinpoint pupils, is a hallmark feature of opioid overdose, while pupillary dilatation is not.
Recognizing the symptoms of opioid overdose, including the opioid overdose triad, is crucial for prompt and effective treatment. If you suspect someone is experiencing an opioid overdose, call for emergency medical assistance immediately.
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This question is part of the following fields:
- Pharmacology/Therapeutics
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Question 4
Incorrect
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A 36-year-old patient arrives at the emergency department experiencing confusion and vomiting. Upon further inquiry, she reports six months of weight loss, fatigue, and dizziness upon standing. Blood tests reveal the following results: Na+ 126 mmol/L (135 - 145), K+ 5.6 mmol/L (3.5 - 5.0), Urea 6.8 mmol/L (2.0 - 7.0), and Creatinine 95 µmol/L (55 - 120). After stabilization, she undergoes additional testing and is prescribed a daily maintenance regimen of 20 mg hydrocortisone and 100mcg fludrocortisone. In the event of an acute illness, such as an infection, what dosage of medication should she take?
Your Answer: 40mg hydrocortisone, 200mcg fludrocortisone
Correct Answer: 40mg hydrocortisone, 100mcg fludrocortisone
Explanation:To manage this patient with Addison’s disease who is experiencing an intercurrent illness, it is recommended to increase the glucocorticoid dose by double while keeping the fludrocortisone dose the same. The patient’s symptoms, including vomiting, confusion, fatigue, weight loss, and postural hypotension, suggest adrenal insufficiency. Blood tests reveal hyponatremia and hyperkalemia due to aldosterone deficiency. Aldosterone normally regulates sodium and potassium levels in the body, and its absence leads to sodium loss and potassium elevation. The prescribed steroid replacement regimen is appropriate for intercurrent illness, as it mimics the body’s natural response by increasing glucocorticoid secretion while maintaining mineralocorticoid secretion. The patient’s hydrocortisone dose has been doubled from 20mg to 40mg, while the fludrocortisone dose remains at 100mcg.
Addison’s disease is a condition that requires patients to undergo both glucocorticoid and mineralocorticoid replacement therapy. This treatment usually involves taking a combination of hydrocortisone and fludrocortisone. Hydrocortisone is typically given in 2 or 3 divided doses, with patients requiring 20-30 mg per day, mostly in the first half of the day. Patient education is crucial, and it is essential to emphasize the importance of not missing glucocorticoid doses. Additionally, patients should consider wearing MedicAlert bracelets and steroid cards, and they should be provided with hydrocortisone for injection with needles and syringes to treat an adrenal crisis.
During an intercurrent illness, it is crucial to manage the glucocorticoid dose properly. In simple terms, the glucocorticoid dose should be doubled, while the fludrocortisone dose should remain the same. The Addison’s Clinical Advisory Panel has produced guidelines that detail specific scenarios, and patients should refer to these guidelines for more information. It is essential to discuss how to adjust the glucocorticoid dose during an intercurrent illness with a healthcare professional. Proper management of Addison’s disease is crucial to ensure that patients can lead healthy and fulfilling lives.
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This question is part of the following fields:
- Endocrinology/Metabolic Disease
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Question 5
Correct
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A 5-year-old boy presents to the emergency department with generalised facial swelling. He recently recovered from viral pharyngitis. He is otherwise healthy and meeting developmental milestones.
Upon examination, he is alert and not experiencing any respiratory distress. There is pitting edema in his face and legs.
Urinalysis reveals 4+ protein and no hematuria. Blood tests show a hemoglobin level of 180 g/L (normal range for males: 135-180, females: 115-160), platelets at 450 * 109/L (normal range: 150-400), WBC at 8.0 * 109/L (normal range: 4.0-11.0), bilirubin at 12 µmol/L (normal range: 3-17), ALP at 60 u/L (normal range: 30-100), ALT at 35 u/L (normal range: 3-40), γGT at 32 u/L (normal range: 8-60), and albumin at 10 g/L (normal range: 35-50).
What is the recommended first-line treatment option for this likely diagnosis?Your Answer: Prednisolone
Explanation:The most appropriate treatment for minimal change glomerulonephritis, which is likely the cause of this patient’s facial edema, hypoalbuminemia, and proteinuria, is prednisolone. This medication is a corticosteroid and is considered the mainstay of therapy for this condition. Adrenaline, albumin infusion, and furosemide are not appropriate treatments for this patient’s condition. While albumin infusion may be used as adjunctive therapy, its effects will only be temporary. Adrenaline is used to treat anaphylaxis and would not be effective in treating minimal change disease. Furosemide may be used as adjunctive therapy, but its effects will also be temporary.
Minimal change disease is a condition that typically presents as nephrotic syndrome, with children accounting for 75% of cases and adults accounting for 25%. While most cases are idiopathic, around 10-20% have a known cause, such as certain drugs, Hodgkin’s lymphoma, thymoma, or infectious mononucleosis. The pathophysiology of the disease involves T-cell and cytokine-mediated damage to the glomerular basement membrane, resulting in polyanion loss and reduced electrostatic charge, which increases glomerular permeability to serum albumin. The disease is characterized by nephrotic syndrome, normotension (hypertension is rare), and highly selective proteinuria, with only intermediate-sized proteins such as albumin and transferrin leaking through the glomerulus. Renal biopsy shows normal glomeruli on light microscopy, but electron microscopy reveals fusion of podocytes and effacement of foot processes.
Management of minimal change disease typically involves oral corticosteroids, which are effective in 80% of cases. For steroid-resistant cases, cyclophosphamide is the next step. The prognosis for the disease is generally good, although relapse is common. Approximately one-third of patients have just one episode, one-third have infrequent relapses, and one-third have frequent relapses that stop before adulthood.
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This question is part of the following fields:
- Renal Medicine/Urology
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Question 6
Correct
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A 33-year-old woman, who is 14 weeks and 5 days into her first pregnancy, visits the clinic to inquire about Down's syndrome screening. She failed to attend her screening appointment at 12 weeks pregnant and is curious if she can still undergo the combined test.
What guidance would you provide to her?Your Answer: The combined test can still be offered
Explanation:Screening for Down’s syndrome, which involves the nuchal scan, is conducted during antenatal care at 11-13+6 weeks. The combined test, which also includes the nuchal scan, is performed during this time frame. However, if the patient prefers to undergo the screening at a later stage of pregnancy, they can opt for the triple or quadruple test between 15 and 20 weeks.
NICE guidelines recommend 10 antenatal visits for first pregnancies and 7 for subsequent pregnancies if uncomplicated. The purpose of each visit is outlined, including booking visits, scans, screening for Down’s syndrome, routine care for blood pressure and urine, and discussions about labour and birth plans. Rhesus negative women are offered anti-D prophylaxis at 28 and 34 weeks. The guidelines also recommend discussing options for prolonged pregnancy at 41 weeks.
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This question is part of the following fields:
- Reproductive Medicine
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Question 7
Incorrect
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A 25-year-old man with difficult to control epilepsy is being evaluated by a surgeon, four months after switching his antiepileptic medication. Despite being seizure-free, he has gained 5 kg in weight since his last check-up. Which antiepileptic drug is commonly linked to weight gain?
Your Answer: Lamotrigine
Correct Answer: Sodium valproate
Explanation:Weight gain can be a side effect of taking sodium valproate.
Sodium Valproate: Uses and Adverse Effects
Sodium valproate is a medication commonly used to manage epilepsy, particularly for generalised seizures. Its mechanism of action involves increasing the activity of GABA in the brain. However, the use of sodium valproate during pregnancy is strongly discouraged due to its teratogenic effects, which can lead to neural tube defects and neurodevelopmental delays in children. Women of childbearing age should only use this medication if it is absolutely necessary and under the guidance of a specialist neurological or psychiatric advisor.
Aside from its teratogenic effects, sodium valproate can also inhibit P450 enzymes, leading to gastrointestinal issues such as nausea, increased appetite, and weight gain. Other adverse effects include alopecia, ataxia, tremors, hepatotoxicity, pancreatitis, thrombocytopenia, hyponatremia, and hyperammonemic encephalopathy. In cases where hyperammonemic encephalopathy develops, L-carnitine may be used as a treatment option.
Overall, while sodium valproate can be an effective medication for managing epilepsy, its use should be carefully considered and monitored due to its potential adverse effects, particularly during pregnancy.
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This question is part of the following fields:
- Neurology
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Question 8
Correct
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A 32-year-old woman presents to her General Practitioner with a 4-week history of diarrhoea, opening her bowels up to 2–3 times per day. She also complains of intermittent bloating and abdominal pain mostly prior to opening her bowels. There is no history of fever or vomiting and she has no past medical history of note. She returned from Thailand two weeks ago.
Stool microscopy: trophozoites and cysts are seen.
Given the likely diagnosis, what is the recommended management for this patient?
Select the SINGLE most appropriate management from the list below.
Your Answer: Metronidazole
Explanation:Antibiotics for Diarrhoeal Illnesses: Understanding the Appropriate Treatment
Giardiasis is a diarrhoeal illness caused by the protozoa Giardia lamblia, which is spread through contaminated food, water or faeces. The disease can last up to six weeks and presents with symptoms such as abdominal bloating, flatulence or malabsorption. Metronidazole is the preferred treatment for giardiasis due to its effectiveness and improved compliance.
Doxycycline is used to treat cholera, a severe disease that causes watery diarrhoea and dehydration. However, the chronic duration of symptoms and presence of parasitic organisms make cholera unlikely.
Ciprofloxacin is used to treat urinary-tract infections and some diarrhoeal illnesses such as cholera and Campylobacter jejuni infections. However, Campylobacter is usually self-limiting and has a much shorter duration of illness, making it an unlikely diagnosis.
Clindamycin is not classically used to treat giardiasis and should be used with caution due to the increased risk of developing antibiotic-associated colitis and opportunistic infections such as Clostridium difficile.
Co-amoxiclav may be used to treat intra-abdominal infections such as biliary sepsis, but it is not indicated for giardiasis.
In summary, understanding the appropriate use of antibiotics for diarrhoeal illnesses is crucial in providing effective treatment and avoiding unnecessary risks.
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This question is part of the following fields:
- Immunology/Allergy
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Question 9
Correct
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A 10-year-old girl has been treated in the hospital for her first acute asthma exacerbation. She was previously only taking salbutamol as needed. After 24 hours, she is stable on inhaled salbutamol six puffs four times a day via a spacer and twice-daily steroid inhaler.
What is the most suitable next step in managing this acute asthma exacerbation?Your Answer: Course of oral steroids
Explanation:Correct and Incorrect Treatment Approaches for Acute Asthma Exacerbation in Children
Acute asthma exacerbation in children requires prompt and appropriate treatment to prevent complications. Here are some correct and incorrect treatment approaches for this condition:
Course of oral steroids: Giving oral steroids early in the treatment of acute asthma attacks in children is advisable. The initial course length should be tailored to response.
Wean down salbutamol to 2 puffs twice a day before hospital discharge: Weaning down salbutamol to two puffs twice a day before hospital discharge is incorrect. Children may be discharged from hospital once stable on 3- to 4-hourly bronchodilators which can be continued at home.
Addition of salmeterol inhaler: Adding a salmeterol inhaler is incorrect. The initial next step of treatment should be inhaled corticosteroids (ICSs) for patients who have had an asthma attack in the last two years.
Continue monitoring in hospital until salbutamol is no longer required: Continuing monitoring in hospital until salbutamol is no longer required is incorrect. Children may be discharged from hospital once stable on 3- to 4-hourly bronchodilators which can be continued at home.
IV hydrocortisone: Administering IV hydrocortisone is incorrect. It is reserved for the treatment of acute life-threatening asthma.
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This question is part of the following fields:
- Respiratory Medicine
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Question 10
Correct
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A 40-year-old man comes to the clinic complaining of visual difficulties. He reports having poor vision in low light conditions for a while, but now he is concerned as he is experiencing tunnel vision. He mentions that his grandfather had a similar issue and was declared blind when he was in his 50s. What is the probable diagnosis?
Your Answer: Retinitis pigmentosa
Explanation:Understanding Retinitis Pigmentosa
Retinitis pigmentosa is a condition that primarily affects the peripheral retina, leading to tunnel vision. The initial sign of this condition is often night blindness, which can progress to a loss of peripheral vision. Fundoscopy, a diagnostic test, reveals black bone spicule-shaped pigmentation in the peripheral retina and mottling of the retinal pigment epithelium. Retinitis pigmentosa is often associated with other diseases such as Refsum disease, Usher syndrome, abetalipoproteinemia, Lawrence-Moon-Biedl syndrome, Kearns-Sayre syndrome, and Alport’s syndrome.
To better understand retinitis pigmentosa, it is important to know that it is a genetic disorder that affects the retina’s ability to respond to light. This condition can lead to the death of photoreceptor cells in the retina, which are responsible for detecting light and transmitting visual information to the brain. As a result, individuals with retinitis pigmentosa may experience difficulty seeing in low light conditions, loss of peripheral vision, and, in severe cases, complete blindness.
In summary, retinitis pigmentosa is a genetic condition that primarily affects the peripheral retina, leading to tunnel vision. It is often associated with other diseases and can cause night blindness, loss of peripheral vision, and, in severe cases, complete blindness. Early diagnosis and management are crucial in preventing further vision loss.
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This question is part of the following fields:
- Ophthalmology
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