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Question 1
Incorrect
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A 55-year-old man is found to have an irregularly, irregular pulse during a routine check-up. An ECG reveals absent P waves and irregular R-R intervals. The patient has moderate renal impairment. What is the most appropriate treatment option?
Your Answer: Dipyridamole
Correct Answer: No treatment
Explanation:Understanding Anticoagulation Treatment for Atrial Fibrillation: A CHADS-VASc Scoring System Overview
Atrial fibrillation (AF) is a common rhythm disturbance that can increase the risk of stroke. To determine the appropriate treatment for primary prevention of stroke, healthcare professionals use the CHADS-VASc scoring system. This system assigns points based on various risk factors, including age, sex, hypertension, diabetes, previous stroke or transient ischemic attack, and vascular disease.
This score is based on a point system in which 2 points are assigned for a history of stroke or transient ischemic attack or age 75 years or more and 1 point each is assigned for age 65 to 74 years; a history of hypertension, diabetes, recent cardiac failure, vascular disease (myocardial infarction, complex aortic plaque, and peripheral arterial disease (PAD), including prior revascularization, amputation due to PAD, or angiographic evidence of PAD, etc.); and female gender, resulting in a maximum score of 9 points.
Score Risk Anticoagulation Therapy 0 (male) or 1 (female) Low No anticoagulant therapy 1 (male) Moderate Oral anticoagulant should be considered 2 or greater High Oral anticoagulant is recommended Aspirin is not recommended for primary prevention of stroke in patients with AF, but may be used for secondary prevention after a stroke. Clexane, a low-molecular-weight heparin, is not used for long-term treatment of AF. Dipyridamole may be used in combination with clopidogrel or aspirin for stroke treatment, but not for prevention in AF patients.
It is important to accurately identify AF and assess the patient’s risk using the CHADS-VASc scoring system to determine the appropriate anticoagulation treatment. NOACs are only licensed for non-valvular AF, so patients with valvular AF should be treated with warfarin or seek advice from a specialist.
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This question is part of the following fields:
- Cardiovascular
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Question 2
Incorrect
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A 67-year-old man with worsening dyspnea is suspected to have idiopathic pulmonary fibrosis. What is the preferred diagnostic test to confirm the diagnosis?
Your Answer: Serum ACE level
Correct Answer: High-resolution CT scan
Explanation:Understanding Idiopathic Pulmonary Fibrosis
Idiopathic pulmonary fibrosis (IPF) is a chronic lung condition that causes progressive fibrosis of the interstitium of the lungs. Unlike other causes of lung fibrosis, IPF has no underlying cause. It is typically seen in patients aged 50-70 years and is more common in men.
The symptoms of IPF include progressive exertional dyspnoea, dry cough, clubbing, and bibasal fine end-inspiratory crepitations on auscultation. Diagnosis is made through spirometry, impaired gas exchange tests, and imaging such as chest x-rays and high-resolution CT scans.
Management of IPF includes pulmonary rehabilitation, but very few medications have been shown to be effective. Some evidence suggests that pirfenidone, an antifibrotic agent, may be useful in selected patients. Many patients will eventually require supplementary oxygen and a lung transplant.
The prognosis for IPF is poor, with an average life expectancy of around 3-4 years. CT scans can show advanced pulmonary fibrosis, including honeycombing. While there is no cure for IPF, early diagnosis and management can help improve quality of life and potentially prolong survival.
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This question is part of the following fields:
- Respiratory Medicine
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Question 3
Correct
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A 32-year-old woman presents with worries about hair loss. She reports experiencing hair loss in small patches on her scalp. During examination, you observe distinct patches of hair loss with some ‘broken exclamation mark’ hairs at the edges.
What is the most probable diagnosis?Your Answer: Alopecia areata
Explanation:Understanding Hair Loss: Causes and Symptoms
Hair loss is a common concern for many individuals, causing anxiety and worry. There are various causes of hair loss, each with their own unique symptoms. Alopecia areata is a chronic inflammatory disease that affects the hair follicles, resulting in patchy, non-scarring hair loss on the scalp. Androgenic alopecia, on the other hand, is more common in men and causes a receding hairline and loss of hair from the top and front of the head. Fungal infections, such as tinea capitis, can also cause hair loss accompanied by scaling, itching, and pain. Scalp psoriasis can range from mild scaling to severe crusted plaques covering the entire scalp, while erosive pustular dermatosis of the scalp affects elderly individuals with scarring and yellow-brown crusts. It is important to understand the various causes and symptoms of hair loss in order to properly diagnose and treat the condition.
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This question is part of the following fields:
- Dermatology
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Question 4
Incorrect
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Which of the following conditions is most likely to result in secondary dysmenorrhoea?
Your Answer: Hypothyroidism
Correct Answer: Adenomyosis
Explanation:Adenomyosis is the condition where the tissue lining the uterus (endometrium) grows into the muscular wall of the uterus (myometrium).
Dysmenorrhoea is a condition where women experience excessive pain during their menstrual period. There are two types of dysmenorrhoea: primary and secondary. Primary dysmenorrhoea affects up to 50% of menstruating women and is not caused by any underlying pelvic pathology. It usually appears within 1-2 years of the menarche and is thought to be partially caused by excessive endometrial prostaglandin production. Symptoms include suprapubic cramping pains that may radiate to the back or down the thigh, and pain typically starts just before or within a few hours of the period starting. NSAIDs such as mefenamic acid and ibuprofen are effective in up to 80% of women, and combined oral contraceptive pills are used second line for management.
Secondary dysmenorrhoea, on the other hand, typically develops many years after the menarche and is caused by an underlying pathology. The pain usually starts 3-4 days before the onset of the period. Causes of secondary dysmenorrhoea include endometriosis, adenomyosis, pelvic inflammatory disease, intrauterine devices, and fibroids. Clinical Knowledge Summaries recommend referring all patients with secondary dysmenorrhoea to gynaecology for investigation. It is important to note that the intrauterine system (Mirena) may help dysmenorrhoea, but this only applies to normal copper coils.
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This question is part of the following fields:
- Reproductive Medicine
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Question 5
Correct
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What is the most appropriate statement regarding GI bleeding caused by NSAID therapy? Choose only one option from the list.
Your Answer: It is due to depletion of mucosal prostaglandin E (PGE) levels
Explanation:Misconceptions about Non-Steroidal Anti-Inflammatory Drugs (NSAIDs)
Non-steroidal anti-inflammatory drugs (NSAIDs) are commonly used to relieve pain and inflammation. However, there are several misconceptions about their side effects. Here are some clarifications:
Clarifying Misconceptions about NSAIDs
Misconception 1: NSAIDs cause gastrointestinal (GI) bleeding by depleting mucosal prostaglandin E (PGE) levels.
Clarification: While it is true that NSAIDs can irritate the GI tract and reduce the levels of protective prostaglandins, not all NSAIDs have the same risk of causing GI bleeding. High-risk NSAIDs such as piroxicam have a higher prevalence of gastric side effects, while ibuprofen and diclofenac have lower rates. Additionally, GI bleeding can occur in patients without pre-existing peptic ulcers. Therefore, NSAIDs should be used at the lowest effective dose and for the shortest period possible.
Misconception 2: NSAIDs cause GI bleeding only in patients with pre-existing gastric and/or duodenal ulcers.
Clarification: While patients with pre-existing peptic ulcer disease are at higher risk of GI bleeding, NSAIDs can also cause GI bleeding in patients without ulcers. Therefore, caution should be exercised when prescribing NSAIDs to all patients.
Misconception 3: Severe dyspepsia is the only symptom of GI bleeding caused by NSAIDs.
Clarification: While dyspepsia is a common symptom of NSAID use, endoscopic evidence of peptic ulceration can be seen in up to 20% of asymptomatic patients taking NSAIDs. Therefore, regular monitoring and endoscopic evaluation may be necessary in patients taking NSAIDs.
Misconception 4: NSAIDs increase platelet adhesiveness.
Clarification: NSAIDs actually reduce platelet aggregation and adhesiveness, except for aspirin, which irreversibly inhibits COX-1 and is indicated for inhibition of platelet aggregation. However, aspirin use increases the risk of bleeding.
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This question is part of the following fields:
- Pharmacology/Therapeutics
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Question 6
Incorrect
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An 80-year-old woman comes in for a routine eye exam and is found to have a reproducible peripheral vision defect in her left eye. She reports no noticeable changes in her vision. Tonometry shows intraocular pressure of 17 mmHg in the left eye and 19 mmHg in the right eye (normal range is 10-21 mmHg). Direct ophthalmoscopy reveals a cup-to-disc ratio of 0.8 (increased) in the left eye. Gonioscopy is normal and she has no significant medical history. What is the most likely diagnosis?
Your Answer:
Correct Answer: Chronic open-angle glaucoma
Explanation:The correct diagnosis for this patient is chronic open-angle glaucoma, which can sometimes occur even with normal intraocular pressure. The patient’s symptoms, such as gradual peripheral vision loss, and the increased cup-to-disc ratio seen on investigations point towards this diagnosis. Gonioscopy also revealed a normal drainage angle, confirming that this is open-angle glaucoma.
Dry age-related macular degeneration is an incorrect diagnosis in this case, as it typically presents with central vision loss and drusen on ophthalmoscopy, not changes in the cup-to-disc ratio.
Hypertensive retinopathy is also an unlikely diagnosis, as it is often asymptomatic and associated with a medical history of hypertension. Additionally, it has a characteristic appearance on ophthalmoscopy that does not include changes in the cup-to-disc ratio.
Optic neuritis is another incorrect diagnosis, as it typically presents with painful vision loss and other symptoms such as loss of color vision or acuity. It is also often associated with multiple sclerosis, which would present with additional symptoms such as sensory or motor deficits or other cranial nerve palsies.
Glaucoma is a condition where the optic nerve is damaged due to increased pressure in the eye. Primary open-angle glaucoma (POAG) is a type of glaucoma where the peripheral iris is clear of the trabecular meshwork, which is important in draining aqueous humour from the eye. POAG is more common in older individuals and those with a family history of the condition. It may present insidiously with symptoms such as peripheral visual field loss, decreased visual acuity, and optic disc cupping. Diagnosis is made through a series of investigations including automated perimetry, slit lamp examination, applanation tonometry, central corneal thickness measurement, and gonioscopy. It is important to assess the risk of future visual impairment based on factors such as IOP, CCT, family history, and life expectancy. Referral to an ophthalmologist is typically done through a GP.
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This question is part of the following fields:
- Ophthalmology
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Question 7
Incorrect
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A 57-year-old woman presents for follow-up. She developed a blistering rash under her left breast that spread to her back about 4 weeks ago, and was diagnosed with shingles. However, she has been experiencing intense shooting pains and tenderness in the affected area since then, despite trying both paracetamol and ibuprofen. What would be the most suitable course of action for managing her symptoms?
Your Answer:
Correct Answer: Amitriptyline
Explanation:The woman is suffering from post-herpetic neuralgia and NICE suggests starting treatment with amitriptyline, duloxetine, gabapentin, or pregabalin.
Understanding Neuropathic Pain and its Management
Neuropathic pain is a type of pain that occurs due to damage or disruption of the nervous system. It is a complex condition that is often difficult to treat and does not respond well to standard painkillers. Examples of neuropathic pain include diabetic neuropathy, post-herpetic neuralgia, trigeminal neuralgia, and prolapsed intervertebral disc.
To manage neuropathic pain, the National Institute for Health and Care Excellence (NICE) updated their guidance in 2013. The first-line treatment options include amitriptyline, duloxetine, gabapentin, or pregabalin. If the first-line drug treatment does not work, patients may try one of the other three drugs. Unlike standard painkillers, drugs for neuropathic pain are typically used as monotherapy, meaning that if they do not work, patients should switch to a different drug rather than adding another one.
Tramadol may be used as rescue therapy for exacerbations of neuropathic pain, while topical capsaicin may be used for localized neuropathic pain, such as post-herpetic neuralgia. Pain management clinics may also be useful for patients with resistant problems. However, it is important to note that for some specific conditions, such as trigeminal neuralgia, the guidance may vary, and carbamazepine may be used as a first-line treatment. Overall, understanding neuropathic pain and its management is crucial for improving the quality of life for patients suffering from this condition.
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This question is part of the following fields:
- Neurology
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Question 8
Incorrect
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A 70-year-old man presents with sudden onset right-sided weakness and difficulty understanding speech at 9:30 am. It is now 12:15 pm. He has a medical history of hypertension, type 2 diabetes, and hyperlipidemia, and takes lisinopril, metformin, and atorvastatin.
Initial investigations reveal a capillary blood glucose of 5.2 mmol/L (4.0-6.0 mmol/L) and oxygen saturations of 97%. What is the most appropriate next step in his management?Your Answer:
Correct Answer: Immediate CT head (non-contrast)
Explanation:The Royal College of Physicians (RCP) and NICE have published guidelines on the diagnosis and management of patients following a stroke. The management of acute stroke includes maintaining normal levels of blood glucose, hydration, oxygen saturation, and temperature. Blood pressure should not be lowered in the acute phase unless there are complications. Aspirin should be given as soon as possible if a haemorrhagic stroke has been excluded. Anticoagulants should not be started until brain imaging has excluded haemorrhage. Thrombolysis with alteplase should only be given if administered within 4.5 hours of onset of stroke symptoms and haemorrhage has been definitively excluded. Mechanical thrombectomy is a new treatment option for patients with an acute ischaemic stroke. NICE recommends thrombectomy for people who have acute ischaemic stroke and confirmed occlusion of the proximal anterior circulation demonstrated by computed tomographic angiography or magnetic resonance angiography. Secondary prevention includes the use of clopidogrel and dipyridamole. Carotid artery endarterectomy should only be considered if carotid stenosis is greater than 70% according to ECST criteria or greater than 50% according to NASCET criteria.
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This question is part of the following fields:
- Neurology
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Question 9
Incorrect
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A 32-year-old female patient comes to the clinic complaining of intermittent bloating and loose stools that have been going on for 5 months. She reports no blood in her stool but has lost a few kilograms in weight. Recently, she has noticed some itchy, vesicular rashes on her knees that have been persistent. Routine blood tests were ordered and all came back normal except for one positive result. What is the name of the dermatological condition she is experiencing?
Your Answer:
Correct Answer: Dermatitis herpetiformis
Explanation:Understanding Dermatitis Herpetiformis
Dermatitis herpetiformis is a skin condition that is linked to coeliac disease and is caused by the deposition of IgA in the dermis. It is an autoimmune blistering disorder that is characterized by itchy, vesicular skin lesions that appear on the extensor surfaces of the body, such as the elbows, knees, and buttocks.
To diagnose dermatitis herpetiformis, a skin biopsy is required, which will show the deposition of IgA in a granular pattern in the upper dermis. This condition can be managed by following a gluten-free diet and taking dapsone medication.
It is important to understand the symptoms and management of dermatitis herpetiformis to ensure that proper treatment is given. By following a gluten-free diet and taking medication, individuals with this condition can manage their symptoms and improve their quality of life.
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This question is part of the following fields:
- Dermatology
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Question 10
Incorrect
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A 35-year-old woman presents to the Emergency Department with a gradual decrease in the hearing from her right ear. On further questioning, she reports that occasionally she hears a buzzing sound in this ear, but denies any episodes of dizziness or vomiting. Otoscopy of her right ear only reveals a reddish tympanic membrane. Rinne’s test is negative on the right, Weber’s test lateralises to the right. Which of the following describes the best management option for this condition?
Your Answer:
Correct Answer: Hearing aid
Explanation:The best option for managing the patient’s unilateral conductive hearing loss, tinnitus, and pinkish tympanic membrane is either a hearing aid or stapedectomy. The tuning fork tests indicate left-sided conductive hearing loss, which is consistent with otosclerosis. This condition is characterized by the replacement of normal bone with vascular spongy bone, leading to progressive conductive hearing loss due to stapes fixation at the oval window. Amoxicillin, betahistine and vestibular rehabilitation exercises, ear syringing, and prochlorperazine are not effective treatments for otosclerosis. Amoxicillin is used to manage acute otitis media, betahistine and vestibular rehabilitation exercises are used to prevent acute attacks in Ménière’s disease, ear syringing is used to remove impacted ear wax, and prochlorperazine is used to decrease dizziness in viral labyrinthitis.
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This question is part of the following fields:
- ENT
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Question 11
Incorrect
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A 35-year-old man visits his family doctor complaining of recurrent episodes of severe facial pain that have been occurring for the past 6 months. He reports experiencing sharp shooting pains in his right cheek and teeth, which worsen during the cold winter months and when he brushes his teeth. Despite visiting the dentist multiple times, no abnormality has been found. His neurological and ENT examination is normal.
What is the most suitable primary care treatment for this condition?Your Answer:
Correct Answer: Carbamazepine
Explanation:Comparing Medications for Trigeminal Neuralgia Treatment
Trigeminal neuralgia is a condition characterized by severe facial pain that occurs in one or more branches of the trigeminal nerve. To treat this condition, anticonvulsant medications are often prescribed. Here, we compare five commonly used medications for trigeminal neuralgia treatment.
Carbamazepine is the recommended first-line treatment for trigeminal neuralgia by the National Institute for Health and Care Excellence (NICE). Topiramate is not typically used for trigeminal neuralgia, as it is primarily indicated for migraine prophylaxis. Amitriptyline is recommended for neuropathic pain, but not specifically for trigeminal neuralgia. Duloxetine is also indicated for neuropathic pain, but not for trigeminal neuralgia. Gabapentin is recommended for neuropathic pain, but not for trigeminal neuralgia, as carbamazepine is the preferred first-line treatment for this condition.
In summary, carbamazepine is the recommended first-line treatment for trigeminal neuralgia, while the other medications mentioned may be more appropriate for other conditions.
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This question is part of the following fields:
- Neurology
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Question 12
Incorrect
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A 35-year-old female patient complains of indigestion for the past three months. She denies any weight loss, anorexia, dysphagia, vomiting, or alteration in bowel habits. Her abdominal examination is normal. What factor could potentially reduce the reliability of a 13C-urea breath test?
Your Answer:
Correct Answer: Course of amoxicillin stopping 3 weeks ago
Explanation:To undergo a urea breath test, one must not have taken antibiotics within the last four weeks and must not have taken any antisecretory drugs, such as PPI, within the last two weeks.
Tests for Helicobacter pylori
There are several tests available to diagnose Helicobacter pylori infection. One of the most common tests is the urea breath test, where patients consume a drink containing carbon isotope 13 (13C) enriched urea. The urea is broken down by H. pylori urease, and after 30 minutes, the patient exhales into a glass tube. Mass spectrometry analysis calculates the amount of 13C CO2, which indicates the presence of H. pylori. However, this test should not be performed within four weeks of treatment with an antibacterial or within two weeks of an antisecretory drug.
Another test is the rapid urease test, also known as the CLO test. This involves mixing a biopsy sample with urea and a pH indicator. If there is a color change, it indicates the presence of H. pylori urease activity. Serum antibody tests can also be used, but they remain positive even after eradication. Culture of gastric biopsy can provide information on antibiotic sensitivity, while histological evaluation alone can be done through gastric biopsy. Lastly, the stool antigen test has a sensitivity of 90% and specificity of 95%.
Overall, these tests have varying levels of sensitivity and specificity, and the choice of test depends on the patient’s clinical presentation and the availability of resources.
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This question is part of the following fields:
- Gastroenterology/Nutrition
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Question 13
Incorrect
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A 40-year-old man comes to the emergency department after experiencing syncope. Upon conducting an ECG, it is found that he has sinus rhythm with a rate of 85 bpm. The QRS duration is 110 ms, PR interval is 180 ms, and corrected QT interval is 500ms. What is the reason for the abnormality observed on the ECG?
Your Answer:
Correct Answer: Hypokalaemia
Explanation:Long QT syndrome can be caused by hypokalaemia, which is an electrolyte imbalance that leads to a prolonged corrected QT interval on an ECG. This condition is often seen in young people and can present as cardiac syncope, tachyarrhythmias, palpitations, or cardiac arrest. Long QT syndrome can be inherited or acquired, with hypokalaemia being one of the acquired causes. Other causes include medications, CNS lesions, malnutrition, and hypothermia. It’s important to note that hypercalcaemia is associated with a shortened QT interval, not a prolonged one.
Understanding Long QT Syndrome
Long QT syndrome (LQTS) is a genetic condition that causes delayed repolarization of the ventricles, which can lead to ventricular tachycardia and sudden death. The most common types of LQTS are caused by defects in the alpha subunit of the slow delayed rectifier potassium channel. A normal corrected QT interval is less than 430 ms in males and 450 ms in females.
There are various causes of a prolonged QT interval, including congenital factors, drugs, and other medical conditions. Some drugs that can prolong the QT interval include amiodarone, tricyclic antidepressants, and selective serotonin reuptake inhibitors. Electrolyte imbalances, acute myocardial infarction, and subarachnoid hemorrhage can also cause a prolonged QT interval.
LQTS may be picked up on routine ECG or following family screening. The symptoms and events associated with LQTS can vary depending on the type of LQTS. Long QT1 is usually associated with exertional syncope, while Long QT2 is often associated with syncope following emotional stress or exercise. Long QT3 events often occur at night or at rest.
Management of LQTS involves avoiding drugs that prolong the QT interval and other precipitants if appropriate. Beta-blockers may be used, and in high-risk cases, implantable cardioverter defibrillators may be necessary. It is important to recognize and manage LQTS to prevent sudden cardiac death.
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This question is part of the following fields:
- Cardiovascular
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Question 14
Incorrect
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Which of the following is most commonly linked to elevated levels of CA 19-9?
Your Answer:
Correct Answer: Pancreatic cancer
Explanation:CA 19-9 and Pancreatic Cancer
Understanding Tumour Markers
Tumour markers are substances that can be found in the blood, urine, or tissues of people with cancer. They are often used to help diagnose and monitor cancer, as well as to determine the effectiveness of treatment. Tumour markers can be divided into different categories, including monoclonal antibodies against carbohydrate or glycoprotein tumour antigens, tumour antigens, enzymes, and hormones.
Monoclonal antibodies are used to target specific tumour antigens, which are proteins or other molecules that are found on the surface of cancer cells. Some common tumour markers include CA 125 for ovarian cancer, CA 19-9 for pancreatic cancer, and CA 15-3 for breast cancer. However, it is important to note that tumour markers usually have a low specificity, meaning that they can also be found in people without cancer.
Tumour antigens are proteins that are produced by cancer cells and can be detected in the blood or tissues of people with cancer. Some examples of tumour antigens include prostate specific antigen (PSA) for prostatic carcinoma, alpha-feto protein (AFP) for hepatocellular carcinoma and teratoma, and carcinoembryonic antigen (CEA) for colorectal cancer.
Enzymes and hormones can also be used as tumour markers. For example, alkaline phosphatase and neurone specific enolase are enzymes that can be elevated in people with cancer, while hormones such as calcitonin and ADH can be used to detect certain types of cancer.
In summary, tumour markers are an important tool in the diagnosis and monitoring of cancer. However, they should be used in conjunction with other diagnostic tests and imaging studies, as they are not always specific to cancer and can also be elevated in people without cancer.
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This question is part of the following fields:
- Gastroenterology/Nutrition
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Question 15
Incorrect
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A 68-year-old man comes to the Emergency Department complaining of left-sided chest pain that has been ongoing for 2 hours. He mentions experiencing similar pains that occur during exercise and subside when he rests. The patient appears to be in distress, sweating, and having difficulty breathing. An ECG is conducted, revealing new T-wave inversion in V3-V6. His troponin and d-dimer levels are as follows:
Troponin 223 ng/L (<5)
D-Dimer 932 ng/mL (< 400)
What is the most probable diagnosis?Your Answer:
Correct Answer: Non-ST-elevation myocardial infarction (NSTEMI)
Explanation:Acute coronary syndrome (ACS) is a term that covers various acute presentations of ischaemic heart disease, including ST elevation myocardial infarction (STEMI), non-ST elevation myocardial infarction (NSTEMI), and unstable angina. ACS develops in patients with ischaemic heart disease, which is the gradual build-up of fatty plaques in the coronary arteries. ACS can cause chest pain, dyspnoea, sweating, and nausea and vomiting. The two most important investigations for ACS are an ECG and cardiac markers. Treatment for ACS includes preventing worsening of presentation, revascularising the vessel is occluded, and treating pain. Patients who have had an ACS require lifelong drug therapy to reduce the risk of a further event.
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This question is part of the following fields:
- Cardiovascular
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Question 16
Incorrect
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A 28-year-old female patient arrives at the Emergency Department at 37 weeks gestation with blurred vision and severe headache. She reports upper abdominal pain for the last few hours. Upon examination, her blood pressure is 160/110 mmHg and urinalysis shows proteinuria. While taking her medical history, she experiences a tonic-clonic seizure. What is the appropriate pharmacological treatment to stop this seizure?
Your Answer:
Correct Answer: Intravenous magnesium sulfate
Explanation:When a seizure is suspected to be caused by eclampsia, the recommended first-line treatment is intravenous magnesium sulfate, given as a loading dose followed by an infusion. In the case of convulsive status epilepticus, intravenous lorazepam is the preferred in-hospital treatment, with phenytoin as an alternative if lorazepam is ineffective. Glucose may be administered if hypoglycemia is a contributing factor. It is not appropriate to administer oral medications to a patient with a decreased level of consciousness. (Adapted from BMJ Best Practice – Pre-eclampsia)
Understanding Eclampsia and its Treatment
Eclampsia is a condition that occurs when seizures develop in association with pre-eclampsia, a pregnancy-induced hypertension that is characterized by proteinuria and occurs after 20 weeks of gestation. To prevent seizures in patients with severe pre-eclampsia and treat seizures once they develop, magnesium sulphate is commonly used. However, it is important to note that this medication should only be given once a decision to deliver has been made. In cases of eclampsia, an IV bolus of 4g over 5-10 minutes should be given, followed by an infusion of 1g/hour. During treatment, it is crucial to monitor urine output, reflexes, respiratory rate, and oxygen saturations. Respiratory depression can occur, and calcium gluconate is the first-line treatment for magnesium sulphate-induced respiratory depression. Treatment should continue for 24 hours after the last seizure or delivery, as around 40% of seizures occur post-partum. Additionally, fluid restriction is necessary to avoid the potentially serious consequences of fluid overload.
In summary, understanding the development of eclampsia and its treatment is crucial in managing this potentially life-threatening condition. Magnesium sulphate is the primary medication used to prevent and treat seizures, but it should only be given once a decision to deliver has been made. Monitoring vital signs and urine output is essential during treatment, and calcium gluconate should be readily available in case of respiratory depression. Finally, fluid restriction is necessary to avoid complications associated with fluid overload.
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This question is part of the following fields:
- Neurology
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Question 17
Incorrect
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A 55-year-old man presents with right-sided hemianopia and is currently undergoing investigations for a possible stroke. The stroke specialist has clinically diagnosed him with a POCI, indicating a posterior circulation infarct. Which specific area of the brain is affected by this type of stroke?
Your Answer:
Correct Answer: The vertebrobasilar arteries
Explanation:A POCI (posterior circulation infarct) typically affects the vertebrobasilar arteries. In contrast, a TACI involves the middle and anterior cerebral arteries, a PACI affects the smaller arteries of anterior circulation, and a LACI involves the perforating arteries around the internal capsule, thalamus, and basal ganglia.
Stroke can be classified based on the initial symptoms using the Oxford Stroke Classification, also known as the Bamford Classification. The criteria assessed include unilateral hemiparesis and/or hemisensory loss of the face, arm, and leg, homonymous hemianopia, and higher cognitive dysfunction such as dysphasia.
Total anterior circulation infarcts (TACI) involve the middle and anterior cerebral arteries and present with all three criteria mentioned above. Partial anterior circulation infarcts (PACI) involve smaller arteries of the anterior circulation and present with two of the criteria. Lacunar infarcts (LACI) involve perforating arteries around the internal capsule, thalamus, and basal ganglia and present with one of three symptoms: unilateral weakness (and/or sensory deficit) of face and arm, arm and leg, or all three; pure sensory stroke; or ataxic hemiparesis.
Posterior circulation infarcts (POCI) involve vertebrobasilar arteries and present with one of three symptoms: cerebellar or brainstem syndromes, loss of consciousness, or isolated homonymous hemianopia. Other recognized patterns of stroke include lateral medullary syndrome (posterior inferior cerebellar artery), also known as Wallenberg’s syndrome, which presents with ipsilateral ataxia, nystagmus, dysphagia, facial numbness, cranial nerve palsy (e.g., Horner’s), and contralateral limb sensory loss. Weber’s syndrome presents with ipsilateral III palsy and contralateral weakness.
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This question is part of the following fields:
- Neurology
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Question 18
Incorrect
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A 25-year-old man presents to the emergency department with abdominal pain and lethargy. He has areas of skin hyperpigmentation and hypopigmentation consistent with vitiligo. His blood pressure is 96/58 mmHg. Laboratory tests reveal the following results, and treatment is initiated.
Hemoglobin: 138 g/L (Male: 135-180, Female: 115-160)
Platelets: 210 * 109/L (150-400)
White blood cells: 11.5 * 109/L (4.0-11.0)
Sodium: 133 mmol/L (135-145)
Potassium: 5.8 mmol/L (3.5-5.0)
Urea: 6.5 mmol/L (2.0-7.0)
Creatinine: 95 µmol/L (55-120)
C-reactive protein: 4 mg/L (<5)
Fasting blood sugar: 4.4 mmol/L (4-7)
What is the most appropriate diagnostic test for the likely diagnosis?Your Answer:
Correct Answer: Short synacthen test
Explanation:The most likely diagnosis for this patient is Addison’s disease based on their clinical presentation of hypotension, hyperpigmentation, vitiligo, and electrolyte abnormalities. Immediate treatment with intravenous fluids and glucocorticoids is necessary. The best test to confirm the diagnosis is the short synacthen test, which measures cortisol levels after administering a stimulating hormone. The aldosterone renin ratio and overnight dexamethasone suppression test are not useful in this scenario. While the serum ACTH level can aid in the diagnosis, dynamic testing with suppression/stimulation is more accurate in endocrine conditions.
Investigating Addison’s Disease: ACTH Stimulation Test and Serum Cortisol Levels
When a patient is suspected of having Addison’s disease, the definitive investigation is an ACTH stimulation test, also known as a short Synacthen test. This involves measuring plasma cortisol levels before and 30 minutes after administering Synacthen 250ug IM. Adrenal autoantibodies, such as anti-21-hydroxylase, may also be demonstrated.
However, if an ACTH stimulation test is not readily available, a 9 am serum cortisol level can be useful. A level of over 500 nmol/l makes Addison’s disease very unlikely, while a level of less than 100 nmol/l is definitely abnormal. A level between 100-500 nmol/l should prompt an ACTH stimulation test to be performed.
It is important to note that around one-third of undiagnosed patients with Addison’s disease may also have associated electrolyte abnormalities, such as hyperkalaemia, hyponatraemia, hypoglycaemia, and metabolic acidosis. Therefore, it is crucial to investigate these patients thoroughly to ensure a proper diagnosis and appropriate treatment.
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This question is part of the following fields:
- Endocrinology/Metabolic Disease
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Question 19
Incorrect
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You are a foundation year 2 Doctor on your GP placement. Your first appointment is 6-year-old Jack. His mother has brought him to see you as he has had a cold over the past 6 days and now has developed a productive cough with green sputum. On examination you hear bilateral crackles at the base of his lungs and there is dullness to percussion at the left base. All basic observations are within normal limits. You diagnose a lower respiratory tract infection and decide to prescribe some antibiotics. Jack has no allergies.
What is the first line antibiotic you would prescribe for Jack?Your Answer:
Correct Answer: Amoxicillin
Explanation:For children without a penicillin allergy, amoxicillin is the primary treatment for pneumonia according to the 2011 guidelines from the British Thoracic Society. If the initial treatment is ineffective, macrolides may be added. Macrolides are recommended if Mycoplasma or Chlamydia is suspected. Co-amoxiclav is suggested for pneumonia associated with influenza.
Pneumonia is a common illness in children, with S. pneumoniae being the most likely cause of bacterial pneumonia. The British Thoracic Society has published guidelines for the management of community acquired pneumonia in children. According to these guidelines, amoxicillin is the first-line treatment for all children with pneumonia. Macrolides may be added if there is no response to first-line therapy, or if mycoplasma or chlamydia is suspected. In cases of pneumonia associated with influenza, co-amoxiclav is recommended. It is important to follow these guidelines to ensure effective treatment and management of pneumonia in children.
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This question is part of the following fields:
- Paediatrics
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Question 20
Incorrect
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A 21-year-old man visits his GP with complaints of increased thirst throughout the day and difficulty performing everyday tasks. He was recently treated for a UTI with ciprofloxacin. His father has a history of diabetes, but is unsure of the type. He drinks about 8 units of alcohol per week. Fasting plasma glucose is 17.1 mmol/L (3.9-5.6), ketone bodies are 0.4 mmol/L (< 0.6 mmol/L), and C-peptide level is 2.87 ng/mL (0.51-2.72). What is the most likely diagnosis based on the patient's presentation?
Your Answer:
Correct Answer: Type 2 diabetes
Explanation:Distinguishing between type 1 and type 2 diabetes can be achieved through the measurement of C-peptide levels and diabetes-specific autoantibodies.
Diagnosis of Type 1 Diabetes Mellitus
Type 1 diabetes mellitus (T1DM) is typically diagnosed through symptoms and signs that are similar to those seen in diabetic ketoacidosis (DKA), although the diagnosis may take longer. Symptoms of DKA include abdominal pain, polyuria, polydipsia, dehydration, Kussmaul respiration, and an acetone-smelling breath. To confirm a diagnosis, urine should be dipped for glucose and ketones, and fasting glucose and random glucose levels should be measured. C-peptide levels are typically low in patients with T1DM, and diabetes-specific autoantibodies can be useful in distinguishing between type 1 and type 2 diabetes. Antibodies to glutamic acid decarboxylase (anti-GAD), islet cell antibodies (ICA), insulin autoantibodies (IAA), and insulinoma-associated-2 autoantibodies (IA-2A) are commonly used.
The diagnostic criteria for T1DM include a fasting glucose level greater than or equal to 7.0 mmol/l or a random glucose level greater than or equal to 11.1 mmol/l if the patient is symptomatic. If the patient is asymptomatic, the criteria must be demonstrated on two separate occasions. To distinguish between type 1 and type 2 diabetes, age of onset, speed of onset, weight of the patient, and symptoms should be considered. NICE recommends further investigation for adults suspected of having T1DM if the clinical presentation includes atypical features. Conversely, for patients suspected of having type 2 diabetes, if they respond well to oral hypoglycaemic agents and are over the age of 40 years, further testing for T1DM may not be necessary.
Example scenarios include a 15-year-old with weight loss and lethargy, a 38-year-old obese man with polyuria, a 52-year-old woman with polyuria and polydipsia, and a 59-year-old obese man with polyuria. The appropriate diagnostic tests should be conducted based on the patient’s symptoms and risk factors.
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This question is part of the following fields:
- Endocrinology/Metabolic Disease
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Question 21
Incorrect
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A 50-year-old woman is admitted to the Surgical Ward with severe loin-to-groin abdominal pain. A computed tomography scan of the kidney, ureter and bladder (CT-KUB) reveals a right-sided renal calculus. During the morning ward round she admits that for the previous few weeks she has been having trouble with increased urinary frequency, thirst, constipation and altered mood.
A diagnosis of primary hyperparathyroidism is suspected. Some blood tests are taken which show:
Investigation Result Normal value
Estimated glomerular filtration rate > 60 ml/min
Adjusted calcium 3.0 mmol/l 2.1–2.6 mmol/l
Phosphate 0.6 mmol/l 0.8–1.4 mmol/l
Parathyroid hormone (PTH) 5.3 pmol/l 1.2–5.8 pmol/l
Which of the following is the definitive management option?
Select ONE option only.Your Answer:
Correct Answer: Refer for parathyroid surgery
Explanation:Referral for Parathyroid Surgery in Primary Hyperparathyroidism
Primary hyperparathyroidism is a condition where the parathyroid glands produce too much parathyroid hormone (PTH), leading to high levels of calcium in the blood. The National Institute for Health and Care Excellence (NICE) recommends parathyroidectomy as the preferred treatment for most patients with diagnosed primary hyperparathyroidism due to its high cure rates and reduced risk of drug side effects.
Referral for parathyroid surgery is indicated for patients with confirmed hyperparathyroidism who have symptoms of hypercalcaemia, end-organ disease, or an albumin-adjusted serum calcium level of 2.85 mmol/l or above. This patient fits all three criteria and should be referred for parathyroid surgery.
Bisphosphonates and cinacalcet are only indicated when parathyroid surgery is not acceptable, patients are unfit for surgery, or have mild hypercalcaemia and symptoms. Laxatives and watchful waiting are not appropriate management options for hyperparathyroidism.
In conclusion, referral for parathyroid surgery is the most appropriate management option for patients with primary hyperparathyroidism who meet the criteria for surgery.
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This question is part of the following fields:
- Endocrinology/Metabolic Disease
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Question 22
Incorrect
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Which of the following statements best describes bladder cancer?
Your Answer:
Correct Answer: Survival correlates well with TNM staging at diagnosis.
Explanation:Bladder Cancer: Prognostic Factors, Staging, and Treatment Options
Bladder cancer is a common malignancy that affects the urinary system. Survival rates are closely linked to the TNM staging at diagnosis, with non-muscle invasive bladder cancer having a good prognosis and decreasing survival rates with increasing stage. The most significant prognostic factors for bladder cancer are grade, depth of invasion, and the presence of carcinoma in situ. Chemotherapy for metastatic disease is seldom used and has limited effectiveness. Cisplatin-based chemotherapy regimens are the standard treatment for metastatic bladder cancer, with a median overall patient survival of 13-15 months and a 2-year survival rate of 15-20%. Careful follow-up is necessary for non-muscle invasive bladder cancer due to the high rate of disease recurrence and progression.
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This question is part of the following fields:
- Renal Medicine/Urology
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Question 23
Incorrect
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A mother who refused regular prenatal check-ups delivers a male infant. During delivery, a defect is observed on the side of the belly button, revealing the intestines.
What could be the possible diagnosis?Your Answer:
Correct Answer: Gastroschisis
Explanation:Gastroschisis is a bowel condition where the intestines are exposed and not encased by a sac. It is not associated with cardiac and kidney diseases, unlike exomphalos. It can be diagnosed through routine ultrasound, but may be missed if the mother does not engage in antenatal care. It is not a normal variant and is not necessarily associated with prematurity.
Gastroschisis and exomphalos are both types of congenital visceral malformations. Gastroschisis refers to a defect in the anterior abdominal wall located just beside the umbilical cord. In contrast, exomphalos, also known as omphalocoele, involves the protrusion of abdominal contents through the anterior abdominal wall, which are covered by an amniotic sac formed by amniotic membrane and peritoneum.
When it comes to managing gastroschisis, vaginal delivery may be attempted, but newborns should be taken to the operating theatre as soon as possible after delivery, ideally within four hours. As for exomphalos, a caesarean section is recommended to reduce the risk of sac rupture. In cases where primary closure is difficult due to lack of space or high intra-abdominal pressure, a staged repair may be undertaken. This involves allowing the sac to granulate and epithelialise over several weeks or months, forming a shell. As the infant grows, the sac contents will eventually fit within the abdominal cavity, at which point the shell can be removed and the abdomen closed.
Overall, both gastroschisis and exomphalos require careful management to ensure the best possible outcome for the newborn. By understanding the differences between these two conditions and the appropriate steps to take, healthcare professionals can provide effective care and support to both the infant and their family.
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This question is part of the following fields:
- Paediatrics
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Question 24
Incorrect
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A 53-year-old man presents to his GP with vertigo and earache. He reports feeling that the room is spinning over the past 2 days. On examination, there is a left facial droop, the patient is unable to lift his left eyebrow, along with a vesicular rash around the left ear, the tympanic membrane looks healthy with a preserved cone of light. His heart rate is 78 bpm, blood pressure is 134/84 mmHg and temperature is 37.2ºC. He has a past medical history of type II diabetes mellitus for which he takes metformin.
What is the most appropriate treatment to commence?Your Answer:
Correct Answer: Aciclovir and prednisolone
Explanation:The recommended treatment for Ramsay Hunt syndrome, which this man is presenting with, includes both oral aciclovir and corticosteroids. This syndrome is caused by a herpes zoster infection of the facial nerve and can lead to symptoms such as ear pain, vertigo, facial palsy, and a vesicular rash around the ear. While aciclovir alone would not be sufficient, using prednisolone alone is also not recommended. Instead, NICE guidance suggests using both aciclovir and prednisolone to improve outcomes and increase the chances of recovery. Flucloxacillin, an antibiotic used to treat skin infections like cellulitis, would not be appropriate in this case as the presence of a vesicular rash makes cellulitis unlikely.
Understanding Ramsay Hunt Syndrome
Ramsay Hunt syndrome, also known as herpes zoster oticus, is a condition that occurs when the varicella zoster virus reactivates in the geniculate ganglion of the seventh cranial nerve. The first symptom of this condition is often auricular pain, followed by facial nerve palsy and a vesicular rash around the ear. Other symptoms may include vertigo and tinnitus.
To manage Ramsay Hunt syndrome, doctors typically prescribe oral aciclovir and corticosteroids. These medications can help reduce the severity of symptoms and prevent complications.
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This question is part of the following fields:
- ENT
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Question 25
Incorrect
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A 35-year-old woman who is 36 weeks pregnant arrives at the Emergency Department complaining of severe and constant abdominal pain. She experienced some vaginal bleeding an hour ago, but it has mostly subsided, leaving only a small amount of bloody discharge. Upon obstetric examination, her uterus is firm, woody, and extremely tender. She appears pale and clammy, with a pulse of 102 bpm and a blood pressure of 98/65 mmHg. What is the probable diagnosis?
Your Answer:
Correct Answer: Placental abruption
Explanation:Antepartum hemorrhage can be caused by placental abruption, which may result in vaginal bleeding, abdominal pain, and a firm or woody uterus. In some cases, the bleeding may be concealed, and the fetus may be difficult to feel or hear. It is important to note that young and healthy women may not show signs of shock until they have lost a significant amount of blood. Contractions during labor typically come in waves and do not cause a woody or tender uterus or low blood pressure. Placenta previa is another common cause of antepartum hemorrhage, but it is usually painless.
Placental Abruption: Causes, Symptoms, and Risk Factors
Placental abruption is a condition that occurs when the placenta separates from the uterine wall, leading to maternal bleeding into the space between them. Although the exact cause of this condition is unknown, certain factors have been associated with it, including proteinuric hypertension, cocaine use, multiparity, maternal trauma, and increasing maternal age. Placental abruption is not a common occurrence, affecting approximately 1 in 200 pregnancies.
The clinical features of placental abruption include shock that is disproportionate to the visible blood loss, constant pain, a tender and tense uterus, and a normal lie and presentation of the fetus. The fetal heart may be absent or distressed, and there may be coagulation problems. It is important to be aware of other conditions that may present with similar symptoms, such as pre-eclampsia, disseminated intravascular coagulation (DIC), and anuria.
In summary, placental abruption is a serious condition that can have significant consequences for both the mother and the fetus. Understanding the risk factors and symptoms of this condition is important for early detection and appropriate management.
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This question is part of the following fields:
- Reproductive Medicine
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Question 26
Incorrect
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At what age would a typical infant develop the skill of crawling?
Your Answer:
Correct Answer: 9 months
Explanation:Gross Motor Developmental Milestones
Gross motor skills refer to the ability to use large muscles in the body for activities such as crawling, walking, running, and jumping. These skills are essential for a child’s physical development and are achieved through a series of developmental milestones.
At 3 months, a baby should have little or no head lag when pulled to sit and should have good head control when lying on their abdomen. By 6 months, they should be able to lift and grasp their feet when lying on their back, pull themselves to a sitting position, and roll from front to back. At 9 months, they should be able to pull themselves to a standing position and crawl. By 12 months, they should be able to cruise and walk with one hand held. At 18 months, they should be able to walk unsupported and squat to pick up a toy. By 2 years, they should be able to run and walk up and down stairs holding onto a rail. At 3 years, they should be able to ride a tricycle using pedals and walk up stairs without holding onto a rail. By 4 years, they should be able to hop on one leg.It is important to note that while the majority of children crawl on all fours before walking, some children may bottom-shuffle, which is a normal variant that runs in families. These milestones serve as a guide for parents and healthcare professionals to monitor a child’s physical development and identify any potential delays or concerns.
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This question is part of the following fields:
- Paediatrics
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Question 27
Incorrect
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A 45-year-old man of South Asian descent presents with bilateral leg swelling. He works as a construction worker and has a history of multiple sexual partners without protection.
During examination, his body weight is 40 kg, and you observe some mouth sores.
The following investigations are conducted:
Investigation Result Normal value
Haemoglobin (Hb) 120 g/l 135–175 g/l
White cell count (WCC) 5.0 × 109/l 4.0–11.0 × 109/l
Neutrophils 2.0 × 109/l 2.5–7.58 × 109/l
Lymphocytes 1.5 × 109/l 1.5–3.5 × 109/l
Eosinophils 0.8 × 109/l 0.1–0.4 × 109/l
Urine Protein 2+
Cholesterol 4.8 mmol/l < 5.2 mmol/l
What is the next recommended test for this patient?Your Answer:
Correct Answer: Human immunodeficiency virus (HIV) test
Explanation:Diagnostic Tests and Treatment for HIV-Associated Nephropathy
HIV infection is a high possibility in a patient with risk factors and presenting with emaciation, oral ulcers, and lymphopenia. HIV serological testing and a CD4 count should be done urgently to establish the diagnosis. HIV-associated nephropathy is a common complication, with focal and segmental glomerulosclerosis being the most frequent pathological diagnosis. Other variants include membranoproliferative nephropathy, diffuse proliferative glomerulonephritis, minimal change disease, and IgA nephropathy. Treatment involves angiotensin-converting enzyme inhibitors and antiretroviral therapy. Renal biopsy may be necessary, but HIV testing should be performed first. Serum complement levels and anti-nuclear factor may be useful in diagnosing SLE-associated nephropathy or other connective tissue diseases, but the lack of systemic symptoms in this case makes it less likely. Serum IgA levels may be elevated in IgA nephropathy, but it typically presents with haematuria rather than proteinuria.
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This question is part of the following fields:
- Infectious Diseases
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Question 28
Incorrect
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An 80-year-old man visits his GP complaining of arm weakness. He reports that while gardening three days ago, he suddenly experienced left arm weakness. He cannot recall any sensory changes but mentions that he was unable to lift his arm for approximately 20 minutes. The weakness has since resolved, and he has not had any further episodes. The patient's regular medications include ramipril for hypertension and paracetamol for osteoarthritis. The GP suspects a transient ischaemic attack (TIA).
What is the most appropriate course of action for the GP to take?Your Answer:
Correct Answer: Give 300mg aspirin now and refer for specialist review within 24 hours
Explanation:The patient with a suspected TIA who visits their GP within 7 days should receive an immediate 300 mg aspirin dose and be referred for specialist review within 24 hours. Emergency admission is not necessary as the patient has only had one episode. There is no need to rule out haemorrhage as the patient is not taking anticoagulant medication and a TIA is ischaemic by definition. Referring for specialist review within 7 days or giving aspirin now and referring for specialist review in 7 days are incorrect options. The patient requires urgent assessment by a stroke specialist, and medication such as aspirin may be started after the assessment.
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, and sudden transient loss of vision in one eye (amaurosis fugax).
NICE recommends immediate antithrombotic therapy with aspirin 300 mg unless the patient has a bleeding disorder or is taking an anticoagulant. If the patient has had more than one TIA or has a suspected cardioembolic source or severe carotid stenosis, specialist review is necessary. Urgent assessment is required within 24 hours for patients who have had a suspected TIA in the last 7 days. Referral for specialist assessment is necessary as soon as possible within 7 days for patients who have had a suspected TIA more than a week previously. Neuroimaging and carotid imaging are recommended, and antithrombotic therapy is necessary. Carotid artery endarterectomy should only be considered if the carotid stenosis is greater than 70% according to ECST criteria or greater than 50% according to NASCET criteria.
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This question is part of the following fields:
- Neurology
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Question 29
Incorrect
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A 55-year-old man presents with a chronic cough and is diagnosed with lung cancer. He asks if his occupation could be a contributing factor. What is the most probable occupational risk factor for developing lung cancer?
Your Answer:
Correct Answer: Passive smoking
Explanation:Risk Factors for Lung Cancer
Lung cancer is a deadly disease that can be caused by various factors. The most significant risk factor for lung cancer is smoking, which increases the risk by a factor of 10. However, other factors such as exposure to asbestos, arsenic, radon, nickel, chromate, and aromatic hydrocarbon can also increase the risk of developing lung cancer. Additionally, cryptogenic fibrosing alveolitis has been linked to an increased risk of lung cancer.
It is important to note that not all factors are related to lung cancer. For example, coal dust exposure has not been found to increase the risk of lung cancer. However, smoking and asbestos exposure are synergistic, meaning that a smoker who is also exposed to asbestos has a 50 times increased risk of developing lung cancer (10 x 5). Understanding these risk factors can help individuals make informed decisions about their health and take steps to reduce their risk of developing lung cancer.
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This question is part of the following fields:
- Respiratory Medicine
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Question 30
Incorrect
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A 25 year-old female patient visits her GP complaining of a two week history of pale and homogenous vaginal discharge that has an offensive odor but is not causing any itching or irritation. Upon examination, there is no inflammation of the cervix or vagina and the discharge has a pH of 6.3. A sample of the discharge is collected. What is the probable result of the analysis of the discharge sample?
Your Answer:
Correct Answer: Gram-positive and negative bacteria
Explanation:Bacterial vaginosis is the identified condition, primarily caused by an overgrowth of anaerobic organisms in the vagina, with Gardnerella vaginalis being the most prevalent. This results in the displacement of lactobacilli, which would not be detected in the sample. The presence of hyphae suggests the existence of Candida (thrush).
Bacterial vaginosis (BV) is a condition where there is an overgrowth of anaerobic organisms, particularly Gardnerella vaginalis, in the vagina. This leads to a decrease in the amount of lactobacilli, which produce lactic acid, resulting in an increase in vaginal pH. BV is not a sexually transmitted infection, but it is commonly seen in sexually active women. Symptoms include a fishy-smelling vaginal discharge, although some women may not experience any symptoms at all. Diagnosis is made using Amsel’s criteria, which includes the presence of thin, white discharge, clue cells on microscopy, a vaginal pH greater than 4.5, and a positive whiff test. Treatment involves oral metronidazole for 5-7 days, with a cure rate of 70-80%. However, relapse rates are high, with over 50% of women experiencing a recurrence within 3 months. Topical metronidazole or clindamycin may be used as alternatives.
Bacterial vaginosis during pregnancy can increase the risk of preterm labor, low birth weight, chorioamnionitis, and late miscarriage. It was previously recommended to avoid oral metronidazole in the first trimester and use topical clindamycin instead. However, recent guidelines suggest that oral metronidazole can be used throughout pregnancy. The British National Formulary (BNF) still advises against using high-dose metronidazole regimes. Clue cells, which are vaginal epithelial cells covered with bacteria, can be seen on microscopy in women with BV.
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This question is part of the following fields:
- Reproductive Medicine
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