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Question 1
Incorrect
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A 30-year-old male patient comes to you with a rash that has spread all over his body. He has multiple erythematous lesions less than 1 cm in diameter on his torso and limbs, some of which are covered by a fine scale. Two weeks ago, he had exudative tonsillitis when he was seen with a sore throat. Apart from asthma, he has no other medical history. What is the probable diagnosis?
Your Answer: Pityriasis rosea
Correct Answer: Guttate psoriasis
Explanation:Tear-drop scaly papules suddenly appearing on the trunk and limbs may indicate guttate psoriasis.
Guttate psoriasis is a type of psoriasis that is more commonly seen in children and adolescents. It is often triggered by a streptococcal infection that occurred 2-4 weeks prior to the appearance of the lesions. The name guttate comes from the Latin word for drop, as the lesions appear as small, tear-shaped papules on the trunk and limbs. These papules are pink and scaly, and the onset of the condition is usually acute, occurring over a few days.
In most cases, guttate psoriasis will resolve on its own within 2-3 months. There is no clear evidence to support the use of antibiotics to treat the underlying streptococcal infection. Treatment options for guttate psoriasis include topical agents commonly used for psoriasis and UVB phototherapy. In cases where the condition recurs, a tonsillectomy may be necessary.
It is important to differentiate guttate psoriasis from pityriasis rosea, another skin condition that can present with similar symptoms. Guttate psoriasis is often preceded by a streptococcal sore throat, while pityriasis rosea may be preceded by a respiratory tract infection. The appearance of guttate psoriasis is characterized by tear-shaped papules on the trunk and limbs, while pityriasis rosea presents with a herald patch followed by multiple oval lesions with a fine scale. While guttate psoriasis resolves within a few months, pityriasis rosea typically resolves after around 6 weeks.
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This question is part of the following fields:
- Dermatology
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Question 2
Incorrect
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How frequently is the Depo Provera (medroxyprogesterone acetate) injectable birth control administered?
Your Answer: Every 4 weeks
Correct Answer: Every 12 weeks
Explanation:Injectable Contraceptives: Depo Provera
Injectable contraceptives are a popular form of birth control in the UK, with Depo Provera being the main option available. This contraceptive contains 150mg of medroxyprogesterone acetate and is administered via intramuscular injection every 12 weeks. It can be given up to 14 weeks after the last dose without the need for extra precautions. The primary method of action is by inhibiting ovulation, while secondary effects include cervical mucus thickening and endometrial thinning.
However, there are some disadvantages to using Depo Provera. Once the injection is given, it cannot be reversed, and there may be a delayed return to fertility of up to 12 months. Adverse effects may include irregular bleeding and weight gain, and there is a potential increased risk of osteoporosis. It should only be used in adolescents if no other method of contraception is suitable.
It is important to note that there are contraindications to using Depo Provera, such as current breast cancer (UKMEC 4) or past breast cancer (UKMEC 3). While Noristerat is another injectable contraceptive licensed in the UK, it is rarely used in clinical practice and is given every 8 weeks. Overall, injectable contraceptives can be an effective form of birth control, but it is important to weigh the potential risks and benefits before deciding on this method.
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This question is part of the following fields:
- Reproductive Medicine
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Question 3
Correct
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A 25-year-old G2P1 woman presents to her midwife at 12 weeks gestation. She has a history of well-controlled type 1 diabetes mellitus and a family history of pre-eclampsia. Her urine dipstick and blood pressure are both normal. Based on this information, what advice should be given regarding her risk of developing pre-eclampsia?
Your Answer: She should take aspirin from 12 weeks gestation until delivery
Explanation:A woman with a moderate or high risk of pre-eclampsia, such as this patient who has a family history of pre-eclampsia and type 1 diabetes mellitus, should take aspirin 75-150mg daily from 12 weeks gestation until delivery to reduce the risk of developing pre-eclampsia.
Pre-eclampsia is a condition that occurs during pregnancy and is characterized by high blood pressure, proteinuria, and edema. It can lead to complications such as eclampsia, neurological issues, fetal growth problems, liver involvement, and cardiac failure. Severe pre-eclampsia is marked by hypertension, proteinuria, headache, visual disturbances, and other symptoms. Risk factors for pre-eclampsia include hypertension in a previous pregnancy, chronic kidney disease, autoimmune disease, diabetes, chronic hypertension, first pregnancy, and age over 40. Aspirin may be recommended for women with high or moderate risk factors. Treatment involves emergency assessment, admission for observation, and medication such as labetalol, nifedipine, or hydralazine. Delivery of the baby is the most important step in management, with timing depending on the individual case.
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This question is part of the following fields:
- Reproductive Medicine
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Question 4
Correct
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A 68-year-old man presents with complaints of weight loss and fatigue that have been ongoing for several months. Upon examination, the only notable finding is pallor. A blood film reveals the presence of immature blasts, and genetic testing shows the presence of a chromosomal translocation t(9;22) - the Philadelphia chromosome. Further investigations reveal the following results: Hb of 95 g/l (normal range: 135-175 g/l), leukocytes of 62 × 109/l (normal range: 4.0-11.0 × 109/l), and PLT of 101 × 109/l (normal range: 150-400 × 109/l). What is the most likely diagnosis?
Your Answer: Chronic myeloid leukaemia (CML)
Explanation:Chronic myeloid leukaemia (CML) is a rare form of cancer that occurs due to the abnormal growth of myeloid precursors or blasts. This leads to an increase in white blood cells and a decrease in the normal functions of the bone marrow, resulting in anaemia and thrombocytopenia. CML is most commonly seen in people between the ages of 60 and 70 and has a slow onset that can last for months or even years. The majority of cases are caused by a genetic mutation called the Philadelphia chromosome, which produces a protein that promotes the growth of cancer cells. Symptoms of CML include fatigue, weight loss, night sweats, abdominal distension, and left upper quadrant pain. Treatment for CML involves inhibiting the genetic mutation with a drug called imatinib.
Acute lymphocytic leukaemia (ALL) is a type of cancer that occurs due to the abnormal growth of immature lymphocytes, which replace the normal cells of the bone marrow and lead to a decrease in blood cell production. ALL is most commonly seen in children and presents with symptoms such as anaemia, fever, and abdominal pain. Diagnosis is made through bone marrow biopsy and genetic analysis, which can reveal chromosomal abnormalities associated with the disease.
Hodgkin’s lymphoma (HL) is a type of cancer that typically presents with enlarged lymph nodes and is associated with the presence of Reed-Sternberg cells, which are abnormal B cells. Multiple myeloma (MM) is a cancer that affects plasma cells in the bone marrow, leading to a decrease in blood cell production and other symptoms such as hypercalcemia and kidney dysfunction. Non-Hodgkin’s lymphoma (NHL) is a type of cancer that arises from the abnormal growth of B cells, T cells, or natural killer cells and can be caused by genetic mutations, infections, or chronic inflammation. Symptoms of NHL include enlarged lymph nodes throughout the body.
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This question is part of the following fields:
- Haematology/Oncology
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Question 5
Incorrect
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A 35-year-old woman experiences weekly migraines despite making lifestyle changes and avoiding triggers. Her doctor has agreed to prescribe medication for migraine prevention. She is in good health and does not take any regular medications. Her blood pressure measures 130/83 mmHg.
Which medication would be the most appropriate for this patient?Your Answer: Verapamil
Correct Answer: Propranolol
Explanation:For migraine treatment, the recommended acute options are a combination of triptan with NSAID or paracetamol. For prophylaxis, the recommended options are topiramate or propranolol. In a woman of childbearing age with no asthma history and requiring migraine prophylaxis, propranolol is the most appropriate option. Although it should be avoided during pregnancy, it does not carry the high risk of birth defects associated with topiramate. Carbamazepine is not recommended for migraine treatment but is licensed for trigeminal neuralgia. Gabapentin is not effective for migraine prophylaxis and is not recommended by NICE guidelines. Topiramate is an option for migraine prophylaxis, but it is not the most appropriate first-line option for a woman of childbearing age due to its teratogenic effects. Highly effective contraception is required if topiramate is used. The recommended safe options for contraception are the copper intrauterine device, levonorgestrel intrauterine system (Mirena), or Depo-Provera injections plus condoms, as per guidelines from the Faculty of Reproductive and Sexual Health (FSRH).
Managing Migraines: Guidelines and Treatment Options
Migraines can be debilitating and affect a significant portion of the population. To manage migraines, it is important to understand the different treatment options available. According to the National Institute for Health and Care Excellence (NICE) guidelines, acute treatment for migraines involves a combination of an oral triptan and an NSAID or paracetamol. For young people aged 12-17 years, a nasal triptan may be preferred. If these measures are not effective, non-oral preparations of metoclopramide or prochlorperazine may be considered, along with a non-oral NSAID or triptan.
Prophylaxis should be given if patients are experiencing two or more attacks per month. NICE recommends topiramate or propranolol, depending on the patient’s preference, comorbidities, and risk of adverse events. Propranolol is preferred in women of childbearing age as topiramate may be teratogenic and reduce the effectiveness of hormonal contraceptives. Acupuncture and riboflavin may also be effective in reducing migraine frequency and intensity for some people. For women with predictable menstrual migraines, frovatriptan or zolmitriptan may be recommended as a type of mini-prophylaxis.
Specialists may consider other treatment options, such as candesartan or monoclonal antibodies directed against the calcitonin gene-related peptide (CGRP) receptor, like erenumab. However, pizotifen is no longer recommended due to common adverse effects like weight gain and drowsiness. It is important to exercise caution with young patients as acute dystonic reactions may develop. By following these guidelines and considering various treatment options, migraines can be effectively managed.
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This question is part of the following fields:
- Neurology
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Question 6
Correct
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A young librarian seeks therapy as he is lonely and unhappy. He describes a solitary life cataloguing books all day and then remaining alone all night and on weekends. He declines invitations for dinners, as he feels anxious when other people are around.
Which of the following is the most likely diagnosis?
Your Answer: Social phobia
Explanation:Differentiating Anxiety Disorders: A Vignette Analysis
The following vignette describes a patient with symptoms of anxiety in a social situation. To properly diagnose the patient, it is important to differentiate between various anxiety disorders.
Social Phobia: This disorder is characterized by anxiety in public, particularly when feeling scrutinized. It typically starts in adolescence and is equally prevalent in men and women. Some patients have a specific social phobia, while others have a more diffuse type. Treatment is mainly with psychological interventions.
Generalized Anxiety Disorder (GAD): GAD is characterized by non-specific and persistent anxiety. Patients feel anxious most days for periods of at least several weeks, and may experience a variety of worries that are not objectively warranted by their circumstances. Autonomic and motor overactivity are also common.
Panic Disorder: Panic attacks are recurrent episodes of severe anxiety that occur unpredictably and under unrestricted circumstances. A diagnosis of panic disorder can be given only if several panic attacks have occurred in about 1 month in situations that do not pose an objective danger, in unrestricted circumstances and with relative freedom from symptoms of anxiety between attacks.
Separation Anxiety Disorder: This disorder is mainly diagnosed in children, although an adult form has been increasingly recognized. Symptoms include anxiety and fear when separated from emotionally attached individuals, and avoidance of being alone.
Conduct Disorder: This disorder is a precursor to dissocial personality disorder and presents as a persistent and repetitive pattern of dissocial behavior beyond the expected mischief and rebelliousness of childhood and adolescence.
In the vignette, the patient’s anxiety is specific to certain situations and therefore predictable, which excludes the diagnosis of panic disorder. The patient’s symptoms do not fit the criteria for GAD or separation anxiety disorder. The most likely diagnosis is social phobia, which is characterized by anxiety in public situations.
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This question is part of the following fields:
- Psychiatry
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Question 7
Incorrect
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A 45-year-old woman has noticed progressive enlargement of her hands and feet over the past two years, resulting in increasing glove and shoe size. Six months ago, a deepening of her voice was noted. Her family has observed that she snores most of the time and she reports occasional episodes of daytime sleepiness. For three months, she has had progressive blurring of vision with associated headache and dizziness. Visual acuity examination shows 20/20-2. Visual field testing shows bitemporal hemianopias.
Which of the following is the most appropriate first line investigation to confirm a diagnosis in this woman?Your Answer: Serum prolactin
Correct Answer: Insulin-like growth factor 1 (IGF-1) measurement
Explanation:The measurement of insulin-like growth factor 1 (IGF-1) is now the preferred method for screening and monitoring suspected cases of acromegaly, replacing the oral glucose tolerance test (OGTT). IGF-1, also known as somatomedin C, is produced by the liver and plays a crucial role in childhood growth and has anabolic effects in adults. OGTT with growth hormone assay is no longer the first-line investigation for acromegaly diagnosis, but can be used as a second-line test to confirm the diagnosis if IGF-1 levels are elevated. The insulin tolerance test is used to assess pituitary and adrenal function, as well as insulin sensitivity, and is not useful for diagnosing acromegaly. Random growth hormone assay is also not helpful in diagnosing acromegaly due to the pulsatile nature of GH secretion. Elevated serum prolactin levels may also be present in up to 20% of GH-secreting pituitary adenomas, but this is not diagnostic.
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This question is part of the following fields:
- Endocrinology/Metabolic Disease
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Question 8
Incorrect
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In which of the following respiratory diseases is clubbing not a feature?
Your Answer: Asbestosis
Correct Answer: Bronchitis
Explanation:The Significance of Finger Clubbing in Respiratory and Non-Respiratory Diseases
Finger clubbing, the loss of the natural angle between the nail and the nailbed, is a significant clinical sign that can indicate underlying respiratory and non-respiratory diseases. Suppurative lung diseases such as long-standing bronchiectasis, acute lung abscesses, and empyema are commonly associated with finger clubbing. However, uncomplicated bronchitis and chronic obstructive pulmonary disease (COPD) do not typically cause clubbing, and patients with COPD who develop clubbing should be promptly investigated for other causes, particularly lung cancer.
Finger clubbing is also commonly found in fibrosing alveolitis (idiopathic pulmonary fibrosis), asbestosis, and malignant diseases such as bronchial carcinoma and mesothelioma. In cases where finger clubbing is associated with hypertrophic pulmonary osteoarthropathy, a painful osteitis of the distal ends of the long bones of the lower arms and legs, it is designated grade IV.
Overall, finger clubbing is an important clinical sign that should prompt further investigation to identify underlying respiratory and non-respiratory diseases.
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This question is part of the following fields:
- Respiratory Medicine
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Question 9
Incorrect
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Helicobacter pylori infection is most commonly associated with which disorder?
Your Answer: Achalasia of the cardia
Correct Answer: Gastric lymphoma
Explanation:Understanding the Association between H. pylori Infection and Gastric Diseases
H. pylori infection is a common bacterial infection that affects approximately 50% of the global population. While it is primarily associated with peptic ulcer disease, it can also lead to other gastric diseases. Gastric malignancies, for instance, are often caused by chronic inflammation of MALT from H. pylori infection. MALTomas, which are extranodal marginal zone B-cell lymphomas, are the most common type of gastric lymphoma and are associated with H. pylori infection in over 90% of cases.
However, not all gastric diseases are associated with H. pylori infection. Coeliac disease, for example, is an autoimmune disorder related to gluten sensitivity. Non-ulcer dyspepsia, a group of upper gastrointestinal symptoms, is not generally associated with H. pylori infection. Reflux oesophagitis, a condition caused by the failure of relaxation of the lower end of the oesophagus, is also not associated with H. pylori infection.
It is important to note that the development of gastric malignancies from H. pylori infection is a slow process that may stop at any step. The disease process starts with chronic gastritis, followed by atrophic gastritis, intestinal metaplasia, dysplasia, and eventually gastric malignancy (Correa’s cascade). However, other factors are also required for gastric cancers to develop, not just H. pylori infection.
In conclusion, understanding the association between H. pylori infection and gastric diseases is crucial in the diagnosis and treatment of these conditions. While H. pylori infection is a common cause of gastric malignancies, it is not associated with all gastric diseases.
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This question is part of the following fields:
- Gastroenterology/Nutrition
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Question 10
Incorrect
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A 45-year-old woman has been using diphenhydramine (Benadryl) for allergy relief. She reports using it frequently and her doctor suspects she may be experiencing symptoms of the anticholinergic syndrome (ACS).
Which of the following statements accurately describes the anticholinergic syndrome?Your Answer: Constricted pupils occur
Correct Answer: Hot, dry skin occurs
Explanation:Understanding Anticholinergic Syndrome: Symptoms and Treatment
Anticholinergic syndrome is a condition that occurs when there is an inhibition of cholinergic neurotransmission at muscarinic receptor sites. It can be caused by the ingestion of various medications, intentional overdose, inadvertent ingestion, medical non-compliance, or geriatric polypharmacy. The syndrome produces central nervous system effects, peripheral nervous system effects, or both, resulting in a range of symptoms.
Symptoms of anticholinergic syndrome include flushing, dry skin and mucous membranes, mydriasis with loss of accommodation, altered mental status, fever, sinus tachycardia, decreased bowel sounds, functional ileus, urinary retention, hypertension, tremulousness, and myoclonic jerking. Hot, dry skin and constricted pupils are also common manifestations.
Treatment for anticholinergic syndrome involves stabilizing the patient in A&E and removing the toxin from the gastrointestinal tract. This can be done with a single dose of activated charcoal by mouth or nasogastric tube. Gastric lavage, followed by activated charcoal administration, is acceptable for patients presenting with altered mental state and within 1 hour of ingestion.
Physostigmine salicylate is the classic antidote for anticholinergic toxicity. While most patients can be safely treated without it, it is recommended when tachydysrhythmia is present. However, physostigmine is contraindicated in patients with cardiac conduction disturbances on ECG.
In conclusion, understanding the symptoms and treatment of anticholinergic syndrome is crucial for healthcare professionals to provide appropriate care for patients who may present with this condition.
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This question is part of the following fields:
- Pharmacology/Therapeutics
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Question 11
Incorrect
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A 70 year-old male patient complains of leg weakness and exhibits purple plaques on the dorsum of the hands. You suspect dermatomyositis. What underlying condition should be considered, as it is associated with dermatomyositis?
Your Answer: Pulmonary fibrosis
Correct Answer: Internal malignancy
Explanation:Dermatomyositis primarily results from an autoimmune disorder and is prevalent among women aged 50-70. Nevertheless, it can also be a paraneoplastic ailment, with ovarian, breast, and lung cancers being the most frequent underlying malignancies. It is crucial to contemplate the likelihood of an underlying tumor, particularly in elderly patients.
Dermatomyositis is a condition that causes inflammation and muscle weakness, as well as distinct skin lesions. It can occur on its own or be associated with other connective tissue disorders or underlying cancers, particularly ovarian, breast, and lung cancer. Screening for cancer is often done after a diagnosis of dermatomyositis. Polymyositis is a variant of the disease that does not have prominent skin manifestations.
The skin features of dermatomyositis include a photosensitive macular rash on the back and shoulders, a heliotrope rash around the eyes, roughened red papules on the fingers’ extensor surfaces (known as Gottron’s papules), extremely dry and scaly hands with linear cracks on the fingers’ palmar and lateral aspects (known as mechanic’s hands), and nail fold capillary dilatation. Other symptoms may include proximal muscle weakness with tenderness, Raynaud’s phenomenon, respiratory muscle weakness, interstitial lung disease (such as fibrosing alveolitis or organizing pneumonia), dysphagia, and dysphonia.
Investigations for dermatomyositis typically involve testing for ANA antibodies, which are positive in around 80% of patients. Approximately 30% of patients have antibodies to aminoacyl-tRNA synthetases, including antibodies against histidine-tRNA ligase (also called Jo-1), antibodies to signal recognition particle (SRP), and anti-Mi-2 antibodies.
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This question is part of the following fields:
- Musculoskeletal
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Question 12
Incorrect
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A mother is referred to a paediatric gynaecologist with her 12-year-old daughter. Her daughter is extremely short for her age, is deaf in both ears and has shown no signs of pubertal development. On examination, the clinician notes neck webbing, a high arched palate and low-set ears. He suspects that the child may have Turner syndrome.
Which of the following chromosomal abnormalities best describes Turner syndrome?Your Answer: 46,XY
Correct Answer: 45,XO
Explanation:Understanding Turner Syndrome: Causes, Symptoms, and Treatment
Turner Syndrome is a genetic disorder that affects females and is caused by the absence of an entire sex chromosome or a partial deletion of the X chromosome. The normal female karyotype is 46XX, but in Turner Syndrome, it is 45X or 46XdelXp. This condition affects 1 in 2500 female births and is associated with various clinical features such as dwarfism, sexual infantilism, neck webbing, and streak gonads. Other associated stigmata include shield chest, high arched palate, low-set ears, lymphoedema, deafness, coarctation of the aorta, and pigmented moles.
Mosaicism is common in Turner Syndrome, which means that the severity of the condition can vary from person to person. Girls with Turner Syndrome are infertile and require hormone replacement therapy until menopause. Treatment aims to achieve normal pubertal progression through estradiol replacement therapy.
In conclusion, understanding Turner Syndrome is crucial for early diagnosis and management of the condition. With proper treatment and support, individuals with Turner Syndrome can lead healthy and fulfilling lives.
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This question is part of the following fields:
- Genetics
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Question 13
Incorrect
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A 32-year-old woman has come in for her 6-week baby check with no postnatal issues. She is currently breastfeeding and has a history of frequent migraines. She is seeking treatment for a migraine today. Which of the following medications should be avoided?
Your Answer: Paracetamol
Correct Answer: Aspirin
Explanation:Breastfeeding mothers should avoid taking aspirin as it may increase the risk of Reye’s syndrome. High doses of aspirin can also affect platelet function and cause hypoprothrombinaemia in infants with low vitamin K stores. However, paracetamol is safe to use for pain relief during breastfeeding. Anti-emetics such as cyclizine and prochlorperazine are also safe to use while breastfeeding and are unlikely to cause any harm.
Breastfeeding has some contraindications that are important to know, especially when it comes to drugs. Antibiotics like penicillins, cephalosporins, and trimethoprim are safe for breastfeeding mothers, as are endocrine drugs like glucocorticoids (in low doses) and levothyroxine. Epilepsy drugs like sodium valproate and carbamazepine, asthma drugs like salbutamol and theophyllines, and hypertension drugs like beta-blockers and hydralazine are also safe. Anticoagulants like warfarin and heparin, as well as digoxin, are also safe. However, some drugs should be avoided, such as antibiotics like ciprofloxacin, tetracycline, chloramphenicol, and sulphonamides, psychiatric drugs like lithium and benzodiazepines, aspirin, carbimazole, methotrexate, sulfonylureas, cytotoxic drugs, and amiodarone. Other contraindications include galactosaemia and viral infections, although the latter is controversial in the developing world due to the increased risk of infant mortality and morbidity associated with bottle feeding.
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This question is part of the following fields:
- Neurology
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Question 14
Incorrect
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Which one of the following statements regarding endometriosis is false?
Your Answer: Around 10% of women have a degree of endometriosis
Correct Answer: Laparoscopic findings correlate well with the severity of symptoms and can guide treatment
Explanation:Understanding Endometriosis
Endometriosis is a common condition where endometrial tissue grows outside of the uterus. It affects around 10% of women of reproductive age and can cause chronic pelvic pain, painful periods, painful intercourse, and subfertility. Other symptoms may include urinary problems and painful bowel movements. Diagnosis is typically made through laparoscopy, and treatment options depend on the severity of symptoms.
First-line treatments for symptomatic relief include NSAIDs and/or paracetamol. If these do not help, hormonal treatments such as the combined oral contraceptive pill or progestogens may be tried. If symptoms persist or fertility is a priority, referral to secondary care may be necessary. Secondary treatments may include GnRH analogues or surgery. For women trying to conceive, laparoscopic excision or ablation of endometriosis plus adhesiolysis is recommended, as well as ovarian cystectomy for endometriomas.
It is important to note that there is poor correlation between laparoscopic findings and severity of symptoms, and that there is little role for investigation in primary care. If symptoms are significant, referral for a definitive diagnosis is recommended.
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This question is part of the following fields:
- Reproductive Medicine
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Question 15
Incorrect
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A 50-year-old woman presents to the GP clinic with complaints of heavy vaginal bleeding. She reports having regular menstrual cycles and denies any intermenstrual or postcoital bleeding. The patient has no significant gynaecological history and is not on any regular medications. She is not in a committed relationship and uses condoms for contraception. Additionally, she has no desire to have children. What is the recommended initial treatment option?
Your Answer: Intrauterine device
Correct Answer: Intrauterine system
Explanation:For the treatment of menorrhagia, the first-line option would be the intrauterine system. Specifically, the Mirena, which contains levonorgestrel, is highly effective in treating menorrhagia and also serves as a long-acting reversible contraceptive. While the combined oral contraceptive pill, tranexamic acid, and mefenamic acid may provide relief from symptoms, they are not the preferred initial treatment. On the other hand, the intrauterine device would not be suitable for addressing this patient’s menorrhagia.
Managing Heavy Menstrual Bleeding
Heavy menstrual bleeding, also known as menorrhagia, is a condition where a woman experiences excessive blood loss during her menstrual cycle. While it was previously defined as total blood loss of over 80 ml per cycle, the management of menorrhagia now depends on the woman’s perception of what is excessive. In the past, hysterectomy was a common treatment for heavy periods, but the approach has changed significantly since the 1990s.
To manage menorrhagia, a full blood count should be performed in all women. If symptoms suggest a structural or histological abnormality, a routine transvaginal ultrasound scan should be arranged. For women who do not require contraception, mefenamic acid or tranexamic acid can be used. If there is no improvement, other drugs can be tried while awaiting referral.
For women who require contraception, options include the intrauterine system (Mirena), combined oral contraceptive pill, and long-acting progestogens. Norethisterone can also be used as a short-term option to rapidly stop heavy menstrual bleeding. The flowchart below shows the management of menorrhagia.
[Insert flowchart here]
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This question is part of the following fields:
- Reproductive Medicine
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Question 16
Incorrect
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A 50-year-old woman presents to you with a 3-week history of shoulder pain in both shoulders. A shoulder X-ray taken 2 weeks ago did not reveal any signs of osteoarthritis. Her blood tests show an elevated ESR of 50mm/hour. What is the most appropriate course of action for this probable diagnosis?
Your Answer: Refer for an MRI shoulder
Correct Answer: Prescribe a trial of oral prednisolone 15mg daily and arrange follow up after 1 week to assess clinical response
Explanation:The symptoms exhibited by this patient strongly indicate the presence of polymyalgia rheumatica, and thus, a one-week course of steroids should be administered to produce a significant improvement. Prescribing paracetamol for a month is unlikely to yield any noticeable relief. An MRI scan is not likely to aid in the diagnosis. Administering a prolonged course of steroids without periodic review is not recommended.
Polymyalgia Rheumatica: A Condition of Muscle Stiffness in Older People
Polymyalgia rheumatica (PMR) is a common condition that affects older people. It is characterized by muscle stiffness and elevated inflammatory markers. Although it is closely related to temporal arteritis, the underlying cause is not fully understood, and it does not appear to be a vasculitic process. PMR typically affects patients over the age of 60 and has a rapid onset, usually within a month. Patients experience aching and morning stiffness in proximal limb muscles, along with mild polyarthralgia, lethargy, depression, low-grade fever, anorexia, and night sweats.
To diagnose PMR, doctors look for raised inflammatory markers, such as an ESR of over 40 mm/hr. Creatine kinase and EMG are normal. Treatment for PMR involves prednisolone, usually at a dose of 15mg/od. Patients typically respond dramatically to steroids, and failure to do so should prompt consideration of an alternative diagnosis.
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This question is part of the following fields:
- Musculoskeletal
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Question 17
Incorrect
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A 6-week-old baby is brought in by his first-time mother concerned about a flaky/scaly rash on his scalp.
Which of the following is the diagnosis?Your Answer: Erythema toxicum neonatorum (ETN)
Correct Answer: Seborrhoeic dermatitis
Explanation:Understanding Infantile Seborrhoeic Dermatitis (Cradle Cap)
Infantile seborrhoeic dermatitis, commonly known as cradle cap, is a condition that typically affects infants between the second week of life and the sixth month. It presents as a yellow scaly/flaky rash on the scalp, but can also affect other areas such as the ears, neck, face, and napkin area. While the condition is not harmful, it can be unsightly and uncomfortable for the infant.
Management of cradle cap involves simple measures such as regular washing of the scalp with baby shampoo, softening of scales with baby oil or soaking the crusts overnight with white petroleum jelly, then shampooing in the morning. If these measures are not effective, topical imidazole cream can be used.
It is important to note that cradle cap is not a fungal infection, eczema, erythema toxicum neonatorum (ETN), or scalp psoriasis. These conditions have different presentations and require different management strategies. Understanding the differences between these conditions can help parents and caregivers provide appropriate care for their infants.
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This question is part of the following fields:
- Paediatrics
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Question 18
Incorrect
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Which one of the following statements regarding listeria infection is accurate?
Your Answer: Infection is spread via the air droplet route
Correct Answer: Pregnant women are 20 times more likely to develop listeriosis compared with the rest of the population
Explanation:Listeria monocytogenes is a type of bacteria that can cause serious illness in certain populations. This Gram-positive bacillus has the unique ability to multiply at low temperatures, making it a common contaminant in unpasteurized dairy products. The infection is particularly dangerous for pregnant women, as it can lead to miscarriage and other complications. Other at-risk populations include the elderly, neonates, and those with weakened immune systems.
Listeria infections can present in a variety of ways, including gastroenteritis, diarrhoea, bacteraemia, and flu-like illness. In severe cases, it can lead to central nervous system infections such as meningoencephalitis, ataxia, and seizures. Diagnosis is typically made through blood cultures or cerebrospinal fluid findings.
Treatment for Listeria infections typically involves antibiotics such as amoxicillin or ampicillin. In cases of Listeria meningitis, gentamicin may also be used. Pregnant women are at a particularly high risk for Listeria infection, and diagnosis can only be made through blood cultures. Treatment with amoxicillin is recommended to prevent complications such as miscarriage, premature labor, stillbirth, and chorioamnionitis.
Overall, Listeria is a dangerous bacterial infection that requires prompt diagnosis and treatment, particularly in at-risk populations.
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This question is part of the following fields:
- Infectious Diseases
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Question 19
Incorrect
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Which one of the following statements regarding scabies is untrue?
Your Answer: Malathion is suitable for the eradication of scabies
Correct Answer: Patients who complain of pruritus 4 weeks following treatment should be retreated
Explanation:It is typical for itching to continue for a period of 4-6 weeks after elimination.
Scabies: Causes, Symptoms, and Treatment
Scabies is a skin condition caused by the Sarcoptes scabiei mite, which is spread through prolonged skin contact. It is most commonly seen in children and young adults. The mite burrows into the skin and lays its eggs in the stratum corneum, leading to intense itching. This itching is caused by a delayed-type IV hypersensitivity reaction to the mites/eggs, which occurs about 30 days after the initial infection. Symptoms of scabies include widespread itching, linear burrows on the fingers, interdigital webs, and flexor aspects of the wrist. In infants, the face and scalp may also be affected. Scratching can lead to secondary features such as excoriation and infection.
The first-line treatment for scabies is permethrin 5%, while malathion 0.5% is second-line. Patients should be advised to avoid close physical contact with others until treatment is complete. All household and close physical contacts should be treated at the same time, even if asymptomatic. Clothing, bedding, and towels should be laundered, ironed, or tumble-dried on the first day of treatment to kill off mites. The insecticide should be applied to all areas, including the face and scalp, contrary to the manufacturer’s recommendation. Patients should apply the insecticide cream or liquid to cool, dry skin, paying close attention to areas between fingers and toes, under nails, armpit area, and creases of the skin such as at the wrist and elbow. The insecticide should be left on the skin for 8-12 hours for permethrin or 24 hours for malathion before washing off. Treatment should be repeated 7 days later.
Crusted scabies, also known as Norwegian scabies, is seen in patients with suppressed immunity, especially HIV. The crusted skin will be teeming with hundreds of thousands of organisms. Isolation is essential, and ivermectin is the treatment of choice.
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This question is part of the following fields:
- Dermatology
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Question 20
Incorrect
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Legionnaires' disease has several statements associated with it, but which one is true?
Your Answer: The infection is generally confined to immunocompromised patients
Correct Answer: Hyponatremia occurs significantly more often in Legionnaires’ disease than in other pneumonias
Explanation:Understanding Legionnaires’ Disease: Causes, Symptoms, and Treatment
Legionnaires’ disease is a type of pneumonia that is caused by the Legionella bacteria. This disease is often overlooked as a possible cause of community-acquired pneumonia, but it is consistently ranked among the top three or four most common causes. The bacteria are found in water sources, and most patients contract the disease through aspiration.
One of the key symptoms of Legionnaires’ disease is hyponatremia, which is a low level of sodium in the blood. This symptom is more commonly associated with Legionnaires’ disease than with other types of pneumonia. The disease is also more likely to occur in patients who are immunocompromised, as cell-mediated immunity appears to be the primary host defense mechanism against Legionella infection.
The urinary antigen test is the preferred initial test for Legionnaires’ disease, but it has low sensitivity and is not particularly specific. The test detects only L. pneumophila serogroup 1, which causes most cases of the disease. Specific therapy includes antibiotics that can achieve high intracellular concentrations, such as macrolides, quinolones, or ketolides.
Predisposing factors for Legionnaires’ disease include age over 50, cigarette smoking, excessive alcohol intake, chronic lung disease, and immunosuppression. High fever and gastrointestinal symptoms are clinical clues to this disease. It is important for healthcare providers to consider Legionnaires’ disease as a possible cause of pneumonia, especially in patients with these risk factors.
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This question is part of the following fields:
- Infectious Diseases
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Question 21
Incorrect
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Which of the following may be linked to a higher risk of venous thromboembolism?
Your Answer: Penicillin
Correct Answer: Behcet's syndrome
Explanation:Venous Thromboembolism: Common Risk Factors
Venous thromboembolism (VTE) is a condition where blood clots form in the veins, which can lead to serious complications such as pulmonary embolism (PE). While there are many factors that can increase the risk of VTE, some are more common than others. These include malignancy, pregnancy, and the period following an operation. Other general risk factors include advancing age, obesity, family history of VTE, immobility, hospitalization, anaesthesia, and the use of central venous catheters. Underlying conditions such as heart failure, thrombophilia, and antiphospholipid syndrome can also increase the risk of VTE. Additionally, certain medications like the combined oral contraceptive pill, hormone replacement therapy, raloxifene, tamoxifen, and antipsychotics have been shown to be risk factors.
It is important to note that while these factors can increase the risk of VTE, around 40% of patients diagnosed with a PE have no major risk factors.
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This question is part of the following fields:
- Haematology/Oncology
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Question 22
Correct
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A 65-year-old man is prescribed amitriptyline for his neuropathic pain. After ten days, he reports experiencing frequent urinary leakage. Which type of urinary incontinence is most commonly associated with amitriptyline use?
Your Answer: Overflow incontinence
Explanation:Overflow incontinence can be caused by tricyclic antidepressants due to their anticholinergic effects.
The drug class of tricyclic antidepressants, which includes Amitriptyline, can lead to urinary retention and frequent leaking due to their anticholinergic effects. Antimuscarinic drugs can be used to treat urge incontinence, which is caused by detrusor over-activity, while stress incontinence, which occurs when the bladder is under pressure, can result in urine leakage when coughing or laughing.
Tricyclic Antidepressants for Neuropathic Pain
Tricyclic antidepressants (TCAs) were once commonly used for depression, but their side-effects and toxicity in overdose have led to a decrease in their use. However, they are still widely used in the treatment of neuropathic pain, where smaller doses are typically required. TCAs such as low-dose amitriptyline are commonly used for the management of neuropathic pain and the prophylaxis of headache, while lofepramine has a lower incidence of toxicity in overdose. It is important to note that some TCAs, such as amitriptyline and dosulepin, are considered more dangerous in overdose than others.
Common side-effects of TCAs include drowsiness, dry mouth, blurred vision, constipation, urinary retention, and lengthening of the QT interval. When choosing a TCA for neuropathic pain, the level of sedation may also be a consideration. Amitriptyline, clomipramine, dosulepin, and trazodone are more sedative, while imipramine, lofepramine, and nortriptyline are less sedative. It is important to work with a healthcare provider to determine the appropriate TCA and dosage for the individual’s specific needs.
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This question is part of the following fields:
- Psychiatry
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Question 23
Incorrect
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Given that PKU is an autosomal-recessive condition that can be diagnosed at birth or in adolescence and adulthood, a teenager seeks genetic counselling. His mother and brother have PKU, while his father is a carrier but does not have the disease. The teenager himself does not have PKU. What is the probability that he is a carrier of the disease?
Your Answer: 25%
Correct Answer: 100%
Explanation:Understanding Autosomal-Recessive Inheritance and Phenylketonuria (PKU)
Autosomal-recessive diseases require both parents to carry the gene, with one parent having the disease and the other being a carrier. In the case of Phenylketonuria (PKU), a specific enzyme deficiency leads to the accumulation of phenylalanine and a deficiency of tyrosine, resulting in reduced melanin and pigmented areas of the brain being affected. PKU is tested for at birth using the Guthrie test and can be treated by removing phenylalanine from the diet.
In the given scenario, the teenager’s mother has the disease and his father is a carrier. This means there is a 100% chance that the teenager has at least one abnormal copy of the gene, making him a carrier. It is important to understand the inheritance pattern of autosomal-recessive diseases to identify carriers and prevent mental retardation in affected children.
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This question is part of the following fields:
- Genetics
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Question 24
Incorrect
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A 65-year-old male is prescribed simvastatin for hyperlipidaemia. What is the most probable interaction with his medication?
Your Answer: Apple juice
Correct Answer: Grapefruit juice
Explanation:The enzyme CYP3A4, which belongs to the cytochrome P450 family, is strongly inhibited by grapefruit juice.
Statins are drugs that inhibit the action of an enzyme called HMG-CoA reductase, which is responsible for producing cholesterol in the liver. However, they can cause some adverse effects such as myopathy, which includes muscle pain, weakness, and damage, and liver impairment. Myopathy is more common in lipophilic statins than in hydrophilic ones. Statins may also increase the risk of intracerebral hemorrhage in patients who have had a stroke before. Therefore, they should be avoided in these patients. Statins should not be taken during pregnancy and should be stopped if the patient is taking macrolides.
Statins are recommended for people with established cardiovascular disease, those with a 10-year cardiovascular risk of 10% or more, and patients with type 2 diabetes mellitus. Patients with type 1 diabetes mellitus who were diagnosed more than 10 years ago, are over 40 years old, or have established nephropathy should also take statins. It is recommended to take statins at night as this is when cholesterol synthesis takes place. Atorvastatin 20mg is recommended for primary prevention, and the dose should be increased if non-HDL has not reduced for 40% or more. Atorvastatin 80 mg is recommended for secondary prevention. The graphic shows the different types of statins available.
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This question is part of the following fields:
- Pharmacology/Therapeutics
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Question 25
Incorrect
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A 43-year-old male accountant visits the clinic with a persistent hoarseness that has been bothering him for the past 4 weeks. He reports that this is affecting his work performance. He denies experiencing any sore throat, difficulty swallowing, or cough. He has been smoking 20 cigarettes daily for the last 25 years and drinks a glass of beer every day. Apart from this, he is in good health. What is the best course of action for managing his condition?
Your Answer: Routine referral to ENT specialist
Correct Answer: 2-week rule referral to ENT specialist
Explanation:If a patient aged over 45 years old has persistent and unexplained hoarseness, it is recommended by NICE to urgently refer them to an ENT specialist under the 2-week wait rule. This is because they may have laryngeal cancer. While a chest radiograph is important, it is more appropriate to prioritize the referral to ENT if cancer is suspected. It is not appropriate to delay the referral or provide false reassurance. While advice on smoking cessation and alcohol should be given, specialist referral is the most important aspect of management in this situation.
Understanding Hoarseness and its Causes
Hoarseness is a condition that can be caused by various factors. One of the most common causes is voice overuse, which can strain the vocal cords and lead to hoarseness. Smoking is another factor that can contribute to hoarseness, as it can irritate the throat and vocal cords. Viral illnesses, hypothyroidism, and gastro-oesophageal reflux are also known to cause hoarseness. In some cases, hoarseness can be a symptom of laryngeal or lung cancer.
When investigating patients with hoarseness, it is important to consider a chest x-ray to rule out any apical lung lesions. If laryngeal cancer is suspected, referral guidelines recommend a suspected cancer pathway referral to an ENT specialist for individuals aged 45 and over with persistent unexplained hoarseness or an unexplained lump in the neck. By understanding the causes of hoarseness and seeking appropriate medical attention, individuals can receive the necessary treatment and improve their vocal health.
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This question is part of the following fields:
- ENT
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Question 26
Incorrect
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A 4-year-old boy is brought to the doctor's office because of a rash on his upper arm. During the examination, the doctor observes several raised lesions that are approximately 2 mm in diameter. Upon closer inspection, a central dimple is visible in most of the lesions. What is the probable diagnosis?
Your Answer: Kawasaki disease
Correct Answer: Molluscum contagiosum
Explanation: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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Question 27
Incorrect
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Which one of the following nail changes is least likely to occur in psoriasis for a 30-year-old patient?
Your Answer: Onycholysis
Correct Answer: Yellow nail syndrome
Explanation:Psoriasis and Psoriatic Arthropathy: Nail Changes
Psoriasis is a skin condition that can also affect the nails. The changes in the nails do not necessarily indicate the severity of psoriasis, but they are often associated with psoriatic arthropathy. In fact, around 80-90% of patients with psoriatic arthropathy have nail changes.
The nail changes that may occur in psoriasis include pitting, onycholysis (separation of the nail from the nail bed), subungual hyperkeratosis, and loss of the nail. These changes can affect both the fingers and toes. It is important to note that while nail changes may not be a reliable indicator of psoriasis severity, they can be a sign of psoriatic arthropathy, which is a type of arthritis that can occur in people with psoriasis.
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This question is part of the following fields:
- Dermatology
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Question 28
Incorrect
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As a side-effect, which antidepressants cause the cheese effect (a hypertensive reaction)?
Your Answer: Presynaptic a 2-antagonists, eg mirtazapine
Correct Answer: Monoamine oxidase inhibitors (MAOIs)
Explanation:Differential Diagnosis: Jaundice and Abdominal Symptoms
Gilbert Syndrome:
Gilbert syndrome is an inherited condition that can manifest as jaundice on clinical examination. Patients may also experience non-specific symptoms such as abdominal cramps, fatigue, and malaise. Fasting, febrile illness, alcohol, or exercise can exacerbate jaundice in patients with Gilbert syndrome. Diagnosis is based on a thorough history and physical examination, as well as blood tests that show unconjugated hyperbilirubinaemia.Haemolytic Anaemia:
Haemolysis is the premature destruction of erythrocytes, which can lead to anaemia if bone marrow activity cannot compensate for erythrocyte loss. Mild haemolysis can be asymptomatic, while severe haemolysis can cause life-threatening symptoms such as angina and cardiopulmonary decompensation. Changes in lactate dehydrogenase and serum haptoglobin levels are the most sensitive general tests for haemolytic anaemia.Hepatitis A:
Hepatitis A is a viral infection that results almost exclusively from ingestion, typically through faecal-oral transmission. Symptoms include fatigue, anorexia, nausea, and vomiting. LFT abnormalities are common, and diagnosis is based on serologic testing for immunoglobulin M (IgM) antibody to HAV.Hepatitis B:
Hepatitis B is a viral infection that is transmitted haematogenously and sexually. Symptoms include fatigue, anorexia, nausea, and vomiting. LFT abnormalities are common, and diagnosis is based on serologic testing for hepatitis B surface antigen (HBsAg).Cholecystitis:
Cholecystitis is inflammation of the gall bladder that occurs most commonly because of an obstruction of the cystic duct by gallstones arising from the gall bladder. Symptoms include upper abdominal pain, nausea, vomiting, and fever. Signs of peritoneal irritation may also be present.Conclusion:
In summary, the differential diagnosis of jaundice and abdominal symptoms includes Gilbert syndrome, haemolytic anaemia, hepatitis A, hepatitis B, and cholecystitis. Diagnosis is based on a thorough history and physical examination, as well as blood tests and serologic testing as appropriate. Treatment -
This question is part of the following fields:
- Psychiatry
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Question 29
Incorrect
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Generalised myositis is a known side effect of certain drugs. Among the options listed below, which drug is most likely to cause this side effect?
Your Answer: Metoclopramide
Correct Answer: Simvastatin
Explanation:Muscle Effects of Common Medications
Many medications can have effects on muscles, including statins, metoclopramide, amitriptyline, cyclizine, and venlafaxine. Statins can increase the risk of muscle toxicity, especially in patients with a history of muscular disorders, high alcohol intake, renal impairment, or hypothyroidism. Metoclopramide is associated with extrapyramidal symptoms and acute dystonic reactions, but not generalised myositis. Amitriptyline and cyclizine are rarely associated with extrapyramidal symptoms and tremor, and amitriptyline may cause myalgia on drug withdrawal. Venlafaxine commonly causes hypertonia and tremor, and more rarely myoclonus, but not generalised myositis. It is important to be aware of these potential muscle effects when prescribing and monitoring these medications.
Muscle Effects of Commonly Prescribed Medications
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This question is part of the following fields:
- Pharmacology/Therapeutics
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Question 30
Incorrect
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A 42-year-old man is brought in by ambulance after falling off a 6-foot ladder and hitting his head. He has a deep laceration to the lateral left knee and is being kept overnight for observations. An x-ray of the left leg shows no fractures. He has a history of hypercholesterolemia.
During the night, he is using the maximum dose of prescribed PRN morphine due to pain in his left leg. The doctor is called to review the patient and on examination, there is reduced sensation on the medial aspect of the plantar left foot.
What is the most likely diagnosis?Your Answer:
Correct Answer: Compartment syndrome
Explanation:Compartment syndrome is the likely diagnosis in this case, as excessive use of breakthrough analgesia and a history of trauma followed by lower limb pain should raise suspicion. Compartment syndrome occurs when pressure builds up in a compartment due to oedema and blood, resulting in venous compression and compromised transferring nerves. In this case, the patient’s medial plantar nerve has been compromised, leading to reduced sensation in the medial aspect of the plantar foot and paresthesia. The fact that the patient is using the maximum dose of PRN morphine should raise clinical suspicion of compartment syndrome, as it can be extremely painful. Pallor is a late sign, and x-rays may not show any findings in the context of compartment syndrome.
Acute limb ischaemia is an unlikely diagnosis, as the usual presenting complaint is pain with associated pallor from reduced arterial perfusion, which is not present in this case. Common peroneal nerve injury is also unlikely, as this nerve supplies the dorsum and lateral aspects of the foot, whereas the medial plantar nerve has been compromised in this case. Posttraumatic osteomyelitis is also an unlikely diagnosis, as it typically presents more than 48 hours after the trauma, and the loss of sensation in the medial aspect of the plantar foot cannot be explained by this condition.
Compartment syndrome is a complication that can occur after fractures or vascular injuries. It is characterized by increased pressure within a closed anatomical space, which can lead to tissue death. Supracondylar fractures and tibial shaft injuries are the most common fractures associated with compartment syndrome. Symptoms include pain, numbness, paleness, and possible paralysis of the affected muscle group. Diagnosis is made by measuring intracompartmental pressure, with pressures over 20 mmHg being abnormal and over 40mmHg being diagnostic. X-rays typically do not show any pathology. Treatment involves prompt and extensive fasciotomies, with careful attention to decompressing deep muscles in the lower limb. Patients may develop myoglobinuria and require aggressive IV fluids. In severe cases, debridement and amputation may be necessary, as muscle death can occur within 4-6 hours.
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This question is part of the following fields:
- Musculoskeletal
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