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  • Question 1 - A murmur is incidentally discovered by a GP in a 9-year-old girl. The...

    Incorrect

    • A murmur is incidentally discovered by a GP in a 9-year-old girl. The murmur is described as a 'continuous blowing noise' heard below both clavicles. What type of murmur is most likely to be diagnosed?

      Your Answer: Still's murmur

      Correct Answer: Venous hum

      Explanation:

      A venous hum is a harmless murmur commonly found in children. It is characterized by a constant blowing sound that can be heard beneath the collarbones. In contrast, a Still’s murmur is also benign but produces a low-pitched noise on the lower left side of the sternum. A pulmonary flow murmur is another harmless murmur, but it is heard on the upper left side of the sternum. The remaining murmurs are considered pathological.

      Innocent murmurs are common in children and are usually harmless. There are different types of innocent murmurs, including ejection murmurs, venous hums, and Still’s murmur. Ejection murmurs are caused by turbulent blood flow at the outflow tract of the heart, while venous hums are due to turbulent blood flow in the great veins returning to the heart. Still’s murmur is a low-pitched sound heard at the lower left sternal edge.

      An innocent ejection murmur is characterized by a soft-blowing murmur in the pulmonary area or a short buzzing murmur in the aortic area. It may vary with posture and is localized without radiation. There is no diastolic component, no thrill, and no added sounds such as clicks. The child is usually asymptomatic, and there are no other abnormalities.

      Overall, innocent murmurs are not a cause for concern and do not require treatment. However, if a child has symptoms such as chest pain, shortness of breath, or fainting, further evaluation may be necessary to rule out any underlying heart conditions.

    • This question is part of the following fields:

      • Paediatrics
      13.6
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  • Question 2 - A 25-year-old woman has experienced difficulty with lactation during the first week after...

    Incorrect

    • A 25-year-old woman has experienced difficulty with lactation during the first week after giving birth to her second child. She successfully breastfed her first child for nine months. She delivered at full term and suffered from a significant postpartum hemorrhage six hours after delivery. She received an IV oxytocin infusion and a blood transfusion. What is the most probable location of the lesion?

      Your Answer: Posterior pituitary

      Correct Answer: Anterior pituitary

      Explanation:

      Understanding Pituitary Lesions and their Symptoms

      The pituitary gland is a small gland located at the base of the brain that produces and releases hormones that regulate various bodily functions. Lesions in different parts of the pituitary gland can cause a range of symptoms.

      Anterior Pituitary: Ischaemic necrosis of the anterior pituitary can occur following post-partum haemorrhage, leading to varying symptoms of hypopituitarism. The most common initial symptom is low or absent prolactin, resulting in failure to commence lactation. Other symptoms may include amenorrhoea, hypothyroidism, glucocorticoid deficiency, and loss of genital and axillary hair. Treatment requires hormone supplementation and involvement of an endocrinologist.

      Hypothalamus: Lesions in the hypothalamus can cause hyperthermia/hypothermia, aggressive behaviour, somnolence, and Horner syndrome.

      Cerebral Cortex: Lesions in the cerebral cortex are associated with stroke or multiple sclerosis and affect different functions such as speech, movement, hearing, and sight.

      Posterior Pituitary: Lesions in the posterior pituitary are associated with central diabetes insipidus.

      Pituitary Stalk: Lesions in the pituitary stalk are associated with diabetes insipidus, hypopituitarism, and hyperprolactinaemia. The patient presents with galactorrhoea, irregular menstrual periods, and other symptoms related to hyperprolactinaemia due to the lifting of dopamine neurotransmitter release inhibition.

    • This question is part of the following fields:

      • Obstetrics
      25.7
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  • Question 3 - A 25-year-old woman who is a law student has severe anxiety about public...

    Correct

    • A 25-year-old woman who is a law student has severe anxiety about public speaking and in informal social settings. She avoids situations where she might have to enter into conversations with strangers. She reports that she thinks others are frustrated by her inability in casual social interactions and that she ‘feels stupid and awkward’. Her social problems are also affecting her academic performance. She is considering leaving university for a less stressful environment.
      Which is the most appropriate form of psychotherapy for this woman?

      Your Answer: Cognitive behavioural therapy

      Explanation:

      Choosing the Right Treatment for Social Phobia: Cognitive Behavioural Therapy

      Social phobia is a type of anxiety disorder that can cause panic and avoidance of social situations. For patients with this condition, cognitive behavioural therapy (CBT) is often the best treatment option. CBT can help patients identify and change negative thought patterns that contribute to their anxiety, and it often includes exposure therapy as a component.

      Other treatment options, such as vocational counselling or psychoanalytic psychotherapy, may not be as effective for social phobia. Suggesting these options could reinforce the patient’s belief that their symptoms cannot be treated therapeutically. Network therapy is designed for substance abusers, and self-help groups may be helpful for some patients, but only if they can manage their anxiety enough to participate effectively.

      In summary, for patients with social phobia, cognitive behavioural therapy is the most effective treatment option. It can help patients overcome their anxiety and improve their quality of life.

    • This question is part of the following fields:

      • Psychiatry
      36.7
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  • Question 4 - A 59-year-old woman was recently diagnosed with essential hypertension and prescribed medication to...

    Incorrect

    • A 59-year-old woman was recently diagnosed with essential hypertension and prescribed medication to lower her blood pressure. However, she stopped taking the medication due to reported dizziness. Her blood pressure readings usually run at 150/100 mmHg. She denies any chest pain, shortness of breath, leg swelling, or visual problems. She has a history of occasional migraines but no other medical conditions. She has no known drug allergies. Her vital signs are within normal limits, other than high blood pressure. The S1 and S2 sounds are normal. There is no S3 or S4 sound, murmur, rub, or gallop. The peripheral pulses are normal and symmetric. The serum electrolytes (sodium, potassium, calcium, and chloride), creatinine, and urea nitrogen are within normal range. What is the most appropriate antihypertensive medication for this patient?

      Your Answer: Propranolol

      Correct Answer: Indapamide

      Explanation:

      The best medication for the patient in the scenario would be indapamide, a thiazide diuretic that blocks the Na+/Cl− cotransporter in the distal convoluted tubules, increasing calcium reabsorption and reducing the risk of osteoporotic fractures. Common side-effects include hyponatraemia, hypokalaemia, hypercalcaemia, hyperglycaemia, hyperuricaemia, gout, postural hypotension and hypochloraemic alkalosis.

      Prazosin is used for benign prostatic hyperplasia.

      Enalapril is not preferred for patients over 55 years old and can increase osteoporosis risk.

      Propranolol is not a preferred initial treatment for hypertension, and amlodipine can cause ankle swelling and should be avoided in patients with myocardial infarction and symptomatic heart failure.

    • This question is part of the following fields:

      • Cardiology
      19.2
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  • Question 5 - A 72-year-old male is brought to the emergency department by his daughter. His...

    Incorrect

    • A 72-year-old male is brought to the emergency department by his daughter. His daughter reports that 3 days ago, he fell down the stairs and hit his head. Initially, he seemed fine and did not want to go to the hospital. However, his daughter is now concerned as he has been acting confused on and off, which is unusual for him.

      The patient has a medical history of atrial fibrillation, which is managed with warfarin. He also has well-controlled high blood pressure and diabetes. He does not consume alcohol.

      The patient is unresponsive and unable to provide a history. During the neurological examination, there is no weakness in the face or limbs.

      What is the most likely diagnosis based on this information?

      Your Answer: Intracerebral haematoma

      Correct Answer: Subdural haematoma

      Explanation:

      The patient’s age, history of trauma, and fluctuating confusion and decreased consciousness suggest that she may have a subdural haematoma, especially since she is taking warfarin which increases the risk of intracranial bleeds. Diffuse axonal injury is another possibility, but this type of brain injury is usually caused by shearing forces from rapid acceleration-deceleration, such as in road traffic accidents. Extradural haematomas are more common in younger people and typically occur as a result of acceleration-deceleration trauma or a blow to the side of the head. Although intracerebral haemorrhage is a possibility due to the patient’s risk factors, such as atrial fibrillation, anticoagulant use, hypertension, and older age, this condition usually presents with stroke symptoms such as facial weakness, arm/leg weakness, and slurred speech, which the patient does not have. Subarachnoid haemorrhages, on the other hand, usually present with a sudden-onset ‘thunderclap’ headache in the occipital area.

      Types of Traumatic Brain Injury

      Traumatic brain injury can result in primary and secondary brain injury. Primary brain injury can be focal or diffuse. Diffuse axonal injury occurs due to mechanical shearing, which causes disruption and tearing of axons. intracranial haematomas can be extradural, subdural, or intracerebral, while contusions may occur adjacent to or contralateral to the side of impact. Secondary brain injury occurs when cerebral oedema, ischaemia, infection, tonsillar or tentorial herniation exacerbates the original injury. The normal cerebral auto regulatory processes are disrupted following trauma rendering the brain more susceptible to blood flow changes and hypoxia. The Cushings reflex often occurs late and is usually a pre-terminal event.

      Extradural haematoma is bleeding into the space between the dura mater and the skull. It often results from acceleration-deceleration trauma or a blow to the side of the head. The majority of epidural haematomas occur in the temporal region where skull fractures cause a rupture of the middle meningeal artery. Subdural haematoma is bleeding into the outermost meningeal layer. It most commonly occurs around the frontal and parietal lobes. Risk factors include old age, alcoholism, and anticoagulation. Subarachnoid haemorrhage classically causes a sudden occipital headache. It usually occurs spontaneously in the context of a ruptured cerebral aneurysm but may be seen in association with other injuries when a patient has sustained a traumatic brain injury. Intracerebral haematoma is a collection of blood within the substance of the brain. Causes/risk factors include hypertension, vascular lesion, cerebral amyloid angiopathy, trauma, brain tumour, or infarct. Patients will present similarly to an ischaemic stroke or with a decrease in consciousness. CT imaging will show a hyperdensity within the substance of the brain. Treatment is often conservative under the care of stroke physicians, but large clots in patients with impaired consciousness may warrant surgical evacuation.

    • This question is part of the following fields:

      • Surgery
      38.3
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  • Question 6 - A 28-year-old woman visits her GP complaining of abdominal pain and bleeding that...

    Incorrect

    • A 28-year-old woman visits her GP complaining of abdominal pain and bleeding that has persisted for three days. Upon conducting a pregnancy test, it is discovered that she is pregnant. She is immediately referred to the emergency department where an ultrasound scan confirms a right-sided tubal ectopic pregnancy with a visible heartbeat.

      The patient has previously had an ectopic pregnancy that was managed with a left-sided salpingectomy. Although she has no children, she hopes to have a family in the future. There is no history of any sexually transmitted infections.

      What is the most appropriate course of action for management?

      Your Answer: Methotrexate

      Correct Answer: salpingostomy

      Explanation:

      Surgical intervention is necessary for the management of ectopic pregnancy.

      Ectopic pregnancy is a serious condition that requires prompt investigation and management. Women who are stable are typically investigated and managed in an early pregnancy assessment unit, while those who are unstable should be referred to the emergency department. The investigation of choice for ectopic pregnancy is a transvaginal ultrasound, which will confirm the presence of a positive pregnancy test.

      There are three ways to manage ectopic pregnancies: expectant management, medical management, and surgical management. The choice of management will depend on various criteria, such as the size of the ectopic pregnancy, whether it is ruptured or not, and the patient’s symptoms and hCG levels. Expectant management involves closely monitoring the patient over 48 hours, while medical management involves giving the patient methotrexate and requires follow-up. Surgical management can involve salpingectomy or salpingostomy, depending on the patient’s risk factors for infertility.

      Salpingectomy is the first-line treatment for women without other risk factors for infertility, while salpingostomy should be considered for women with contralateral tube damage. However, around 1 in 5 women who undergo a salpingostomy require further treatment, such as methotrexate and/or a salpingectomy. It is important to carefully consider the patient’s individual circumstances and make a decision that will provide the best possible outcome.

    • This question is part of the following fields:

      • Gynaecology
      34.7
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  • Question 7 - A 54-year-old patient is evaluated in the Pre-Assessment Clinic before undergoing elective surgery...

    Incorrect

    • A 54-year-old patient is evaluated in the Pre-Assessment Clinic before undergoing elective surgery for varicose veins. The patient is in good health, with the only significant medical history being well-controlled hypertension with lisinopril. During the examination, the clinician hears an early opening snap in diastole when listening to the patient's heart. What is the most probable cause of this finding?

      Your Answer:

      Correct Answer: Mitral stenosis

      Explanation:

      Common Heart Murmurs and Their Characteristics

      Heart murmurs are abnormal sounds heard during a heartbeat and can indicate underlying heart conditions. Here are some common heart murmurs and their characteristics:

      Mitral Stenosis: This condition causes a mid-diastolic murmur that is best heard with the bell of the stethoscope over the apex while the patient is lying in the left lateral position. Severe mitral stenosis can also cause a quiet first heart sound and an early opening snap.

      Pulmonary Stenosis: Pulmonary stenosis causes an ejection systolic murmur.

      Ventricular Septal Defect: This condition causes a pan-systolic murmur.

      Mitral Valve Prolapse: Mitral valve prolapse may cause a mid-systolic click, followed by a late systolic murmur.

      Right Bundle Branch Block: This condition is a cause of wide splitting of the second heart sound.

    • This question is part of the following fields:

      • Cardiology
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  • Question 8 - A 50-year-old woman arrives at the emergency department with symptoms of sweating, confusion,...

    Incorrect

    • A 50-year-old woman arrives at the emergency department with symptoms of sweating, confusion, and agitation that have developed over the past hour. She has a history of schizophrenia, hay fever, and lower back pain and is currently taking sertraline, cetirizine, and olanzapine. The patient admits to occasional recreational use of cannabis and diazepam and also uses her partner's tramadol. Upon examination, the patient has a temperature of 39.0ºC, a heart rate of 105 bpm, and a blood pressure of 143/75 mmHg. The doctor notes hyperreflexia, rigidity, bilateral mydriasis, and bilateral ankle clonus. What is the most likely cause of her presentation?

      Your Answer:

      Correct Answer: Tramadol use

      Explanation:

      Serotonin syndrome is often caused by co-prescription of tramadol and SSRIs, and the patient in the vignette exhibits symptoms such as neuromuscular excitation, fever, agitation, and confusion.

      Understanding Serotonin Syndrome

      Serotonin syndrome is a potentially life-threatening condition caused by an excess of serotonin in the body. It can be triggered by a variety of medications and substances, including monoamine oxidase inhibitors, SSRIs, St John’s Wort, tramadol, ecstasy, and amphetamines. The condition is characterized by neuromuscular excitation, hyperreflexia, myoclonus, rigidity, autonomic nervous system excitation, hyperthermia, sweating, and altered mental state, including confusion.

      Management of serotonin syndrome is primarily supportive, with IV fluids and benzodiazepines used to manage symptoms. In more severe cases, serotonin antagonists such as cyproheptadine and chlorpromazine may be used. It is important to note that serotonin syndrome can be easily confused with neuroleptic malignant syndrome, which has similar symptoms but is caused by a different mechanism. Both conditions can cause a raised creatine kinase (CK), but it tends to be more associated with NMS. Understanding the causes, features, and management of serotonin syndrome is crucial for healthcare professionals to ensure prompt and effective treatment.

    • This question is part of the following fields:

      • Pharmacology
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  • Question 9 - A 5-year-old boy comes to his pediatrician with a complaint of daily nosebleeds...

    Incorrect

    • A 5-year-old boy comes to his pediatrician with a complaint of daily nosebleeds for the past week. During the examination, the doctor notices petechiae and bruises on the child's legs. Apart from these symptoms, the child appears to be healthy and does not report any other issues. Blood tests reveal low platelet count, but no other abnormalities are detected. The child's symptoms disappear entirely after four months. What is the likely precursor to these symptoms?

      Your Answer:

      Correct Answer: Glandular fever

      Explanation:

      ITP, a condition characterized by low platelet count and symptoms such as epistaxis and unexplained bruising/petechiae, may be preceded by a viral infection that is self-limiting and can resolve within a year. The correct answer to the question is glandular fever, as constipation, epileptic fits, asthma attacks, and stress have not been linked to triggering ITP.

      Understanding Immune Thrombocytopenia (ITP) in Children

      Immune thrombocytopenic purpura (ITP) is a condition where the immune system attacks the platelets, leading to a decrease in their count. This condition is more common in children and is usually acute, often following an infection or vaccination. The antibodies produced by the immune system target the glycoprotein IIb/IIIa or Ib-V-IX complex, causing a type II hypersensitivity reaction.

      The symptoms of ITP in children include bruising, a petechial or purpuric rash, and less commonly, bleeding from the nose or gums. A full blood count is usually sufficient to diagnose ITP, and a bone marrow examination is only necessary if there are atypical features.

      In most cases, ITP resolves on its own within six months, without any treatment. However, if the platelet count is very low or there is significant bleeding, treatment options such as oral or IV corticosteroids, IV immunoglobulins, or platelet transfusions may be necessary. It is also advisable to avoid activities that may result in trauma, such as team sports. Understanding ITP in children is crucial for prompt diagnosis and management of this condition.

    • This question is part of the following fields:

      • Paediatrics
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  • Question 10 - A mother presents with her 3-month-old baby boy to ask advice about his...

    Incorrect

    • A mother presents with her 3-month-old baby boy to ask advice about his failed newborn hearing screening. Further tests were normal; however, she has been advised to seek medical advice if she has any concerns about his hearing in the future. Which one of the following would warrant referral for a further hearing test?

      Your Answer:

      Correct Answer: Not babbling or imitating sounds by the age of nine months old

      Explanation:

      Developmental Milestones for Language Acquisition in Children

      Language acquisition is an important developmental milestone in children. Here are some key markers to look out for:

      – Not babbling or imitating sounds by the age of nine months old: If a baby is not babbling or imitating sounds by this age, it could be a sign of a social, cognitive, speech, or hearing problem. A full developmental assessment would be necessary to ensure there are no other areas of delay.

      – Putting two words together by the age of 18 months old: By this age, a child should be using 50+ words and be able to put two words together. If not, a full developmental assessment would be necessary to ensure there are no other areas of delay.

      – More than 200 spoken words by the age of two years: A 30-month-old child should be using 200+ words. If not, a full developmental assessment would be necessary to ensure there are no other areas of delay.

      – Not responding to his own name by the age of six months old: By the age of one year, a child should respond to their own name. If not, a full developmental assessment would be necessary to ensure there are no other areas of delay.

      – Speaking 6-20 words by the age of one year: By the age of one, a child should be using 6-20 words. If not, a full developmental assessment would be necessary to ensure there are no other areas of delay.

      It is important to monitor a child’s language development and seek professional help if there are any concerns. Early intervention can make a significant difference in a child’s language acquisition and overall development.

    • This question is part of the following fields:

      • Paediatrics
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  • Question 11 - A paediatrician is called to assess a 3-day-old neonate born at 37+2 weeks...

    Incorrect

    • A paediatrician is called to assess a 3-day-old neonate born at 37+2 weeks gestation due to concerns in the newborn physical examination. The neonate has absent fundal reflexes bilaterally and a loud machinery murmur is heard on auscultation. Automated otoacoustic emission suggests sensorineural deafness. The mother recently arrived from overseas where she was unable to access antenatal care. In the first trimester, she had an exanthematous rash on her trunk, but the pregnancy was otherwise unremarkable. What is the likely diagnosis for this neonate?

      Your Answer:

      Correct Answer: Congenital rubella syndrome

      Explanation:

      Congenital rubella syndrome is the correct answer, as it is known to cause both sensorineural deafness and congenital cataracts. Although rubella has been eliminated in many Western countries due to vaccination, it is still prevalent in some African, Middle Eastern, and Southeast Asian countries. Rubella may present with a non-specific viral rash, similar to the one described in this patient. Congenital rubella syndrome is also associated with a patent ductus arteriosus, which can cause a machinery murmur.

      Alport syndrome is not the correct answer, as it is associated with congenital sensorineural hearing loss but not with congenital cataracts. Alport syndrome is also linked to renal impairment and nephritic syndrome.

      Congenital cytomegalovirus infection is not the correct answer, as it is associated with congenital sensorineural deafness but not typically with congenital cataracts. Congenital CMV infection may also cause cerebral palsy, anemia, and jaundice.

      Congenital toxoplasmosis infection is not the correct answer, as it would not typically present with sensorineural deafness, congenital cataracts, or a patent ductus arteriosus. Congenital toxoplasmosis infection is known to cause cerebral calcification, chorioretinitis, and hydrocephalus.

      Congenital Infections: Rubella, Toxoplasmosis, and Cytomegalovirus

      Congenital infections are infections that are present at birth and can cause various health problems for the newborn. The three major congenital infections that are commonly encountered in medical examinations are rubella, toxoplasmosis, and cytomegalovirus. Cytomegalovirus is the most common congenital infection in the UK, and maternal infection is usually asymptomatic.

      Each of these infections has characteristic features that can help with diagnosis. Rubella can cause congenital cataracts, sensorineural deafness, and congenital heart disease, among other things. Toxoplasmosis can cause growth retardation, cerebral palsy, and visual impairment, among other things. Cytomegalovirus can cause microcephaly, cerebral calcification, and chorioretinitis, among other things.

      It is important to be aware of these congenital infections and their potential effects on newborns. Early diagnosis and treatment can help prevent or minimize health problems for the newborn.

    • This question is part of the following fields:

      • Paediatrics
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  • Question 12 - A 23-year-old asthmatic woman has been brought to the emergency department after experiencing...

    Incorrect

    • A 23-year-old asthmatic woman has been brought to the emergency department after experiencing seizures during her pregnancy. She is currently 35 weeks pregnant and has been diagnosed with gestational hypertension by her doctor. She is taking oral medication to manage her condition. Upon examination, her urine test shows proteinuria (3+) and her blood pressure is elevated at 170/115 mmHg. As a result, the baby is delivered and the patient's seizures have ceased. What is the most appropriate treatment option for her seizures after delivery, given her probable diagnosis?

      Your Answer:

      Correct Answer: Magnesium sulphate for 24 hours after delivery/last seizure

      Explanation:

      The correct answer is that magnesium sulphate treatment should continue for 24 hours after delivery or the last seizure. This treatment is used to prevent and treat seizures in mothers with eclampsia. In this case, the patient is showing signs of eclampsia due to high protein levels in her urine, pregnancy-induced hypertension, and seizures. Therefore, she needs to be admitted and continue magnesium treatment for 24 hours after delivery or the last seizure. Magnesium helps prevent seizures by relaxing smooth muscle tissues and slowing uterine contractions. Labetalol is not the correct answer as it is used for long-term treatment of hypertension, which may not be necessary for this patient after delivery. Nifedipine with hydralazine may be more suitable for her hypertension as she is asthmatic. Magnesium sulphate treatment for 12 or 48 hours after delivery or the last seizure is not recommended according to guidelines, which suggest 24 hours is the appropriate duration.

      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.

    • This question is part of the following fields:

      • Obstetrics
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  • Question 13 - An 80-year-old woman comes to the emergency department with intense pain in her...

    Incorrect

    • An 80-year-old woman comes to the emergency department with intense pain in her left iliac fossa. She reports no vomiting, diarrhea, or rectal bleeding. She is diagnosed with acute diverticulitis and given antibiotics before being sent home. However, she returns four days later with the same symptoms and is admitted. What is the best drug combination to prescribe for her?

      Your Answer:

      Correct Answer: Intravenous ceftriaxone and metronidazole

      Explanation:

      Patients experiencing a flare-up of diverticulitis can initially be treated with oral antibiotics at home. However, if their symptoms do not improve within 72 hours, they should be admitted to the hospital for intravenous ceftriaxone and metronidazole. This was the correct course of action for the patient in question, who had been sent home with antibiotics but continued to experience pain after four days. Intravenous vancomycin and metronidazole are not the recommended treatment for diverticulitis, as they are typically used for life-threatening Clostridium difficile infections. Oral ceftriaxone and metronidazole are also not appropriate for this patient, as they are only recommended for those who can manage their symptoms at home. Similarly, oral vancomycin and intravenous metronidazole are not the correct treatment for diverticulitis.

      Understanding Diverticulitis

      Diverticulitis is a condition where an outpouching of the intestinal mucosa becomes infected. This outpouching is called a diverticulum and the presence of these pouches is known as diverticulosis. Diverticula are common and are thought to be caused by increased pressure in the colon. They usually occur in the sigmoid colon and are more prevalent in Westerners over the age of 60. While only a quarter of people with diverticulosis experience symptoms, 75% of those who do will have an episode of diverticulitis.

      Risk factors for diverticulitis include age, lack of dietary fiber, obesity, and a sedentary lifestyle. Patients with diverticular disease may experience intermittent abdominal pain, bloating, and changes in bowel habits. Those with acute diverticulitis may experience severe abdominal pain, nausea, vomiting, changes in bowel habits, and urinary symptoms. Complications may include colovesical or colovaginal fistulas.

      Signs of diverticulitis include low-grade fever, tachycardia, tender lower left quadrant of the abdomen, and possibly a palpable mass. Imaging tests such as an erect CXR, AXR, and CT scans can help diagnose diverticulitis. Treatment may involve oral antibiotics, a liquid diet, and analgesia for mild cases. Severe cases may require hospitalization for IV antibiotics. Colonoscopy should be avoided initially due to the risk of perforation.

      Overall, understanding the symptoms, risk factors, and signs of diverticulitis can help with early diagnosis and treatment. Proper management can help prevent complications and improve outcomes for patients.

    • This question is part of the following fields:

      • Surgery
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  • Question 14 - A 32-year-old man presents for a general check-up. He is well in himself...

    Incorrect

    • A 32-year-old man presents for a general check-up. He is well in himself and reports no symptoms.
      On examination, he has a body mass index (BMI) of 33 kg/m2 and there are some thickened folds of skin in his axilla and the nape of his neck. His blood pressure is 140/90 mmHg. He is a non-smoker and does not drink.
      A set of blood work is ordered. He demonstrated impaired fasting glucose in addition to the results below.
      Investigation Result Normal value
      Haemoglobin (Hb) 140 g/l 135–175 g/l
      Cholesterol 5.8 mmol/l < 5.2 mmol/l
      Triglyceride 3.9 mmol/l 0–1.5 mmol/l
      Alanine aminotransferase (ALT) 60 IU/l 5–30 IU/l
      Aspartate aminotransferase (AST) 30 IU/l 10–40 IU/l
      Gamma-glutamyl transferase (GGT) 30 IU/l 5–30 IU/l
      What is the next best investigation?

      Your Answer:

      Correct Answer: Ultrasound liver

      Explanation:

      Choosing the Best Investigation: A Case Study

      In this case study, a patient presents with non-alcoholic fatty liver disease (NAFLD), raised ALT, impaired glucose regulation, acanthosis nigricans, and a high BMI. The question is, what investigation should be done next?

      Ultrasound liver is the best investigation in this case. It is quick, inexpensive, and can provide enough information to guide management at initial stages. Weight management and dietary modification can help abate symptoms.

      Screening for hereditary haemochromatosis is not appropriate in this case, as the patient does not complain of arthritis, diabetes, or changes to the skin.

      Haematinics are not necessary, as the Hb is normal.

      A CT scan of the abdomen would be useful, but it is costly and would result in the patient receiving radiation. It should not be the next best investigation.

      Serum ceruloplasmin is not necessary, as there is nothing in the history to suggest Wilson’s disease.

      In conclusion, choosing the best investigation requires careful consideration of the patient’s history and symptoms. In this case, ultrasound liver is the most appropriate next step.

    • This question is part of the following fields:

      • Gastroenterology
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  • Question 15 - A 36-year-old man complained of abdominal pain and weight loss. Upon investigation, he...

    Incorrect

    • A 36-year-old man complained of abdominal pain and weight loss. Upon investigation, he was diagnosed with coeliac disease. The biopsy of his small intestine revealed blunting of villi with crypt hyperplasia and intraepithelial lymphocytes ++. What is the stage of his disease?

      Your Answer:

      Correct Answer: III

      Explanation:

      The Marsh Criteria: A Morphological Classification of Coeliac Disease Biopsy

      Coeliac disease is a condition that affects the small intestine, causing damage to the lining and leading to malabsorption of nutrients. The Marsh criteria is a morphological classification system used to diagnose coeliac disease through intestinal biopsy.

      The classification system consists of four stages, with stage 0 indicating a normal biopsy and stage IV indicating total villous atrophy. In between, stages I-III show varying degrees of damage to the duodenal villi, intraepithelial lymphocytes, and crypts.

      Recently, the Marsh-Oberhuber classification was introduced, which subdivides stage III into three classes based on the degree of villous atrophy. Stage IV has been eliminated from this modified version.

      In coeliac disease and other inflammatory conditions, such as milk protein allergy, the pattern of intraepithelial lymphocytes may be reversed. In stage I disease, only increased intraepithelial lymphocytes would be seen on biopsy, while stage 0 would appear normal. Class II disease would show normal duodenal villi, and stage IV would be associated with crypt atrophy.

    • This question is part of the following fields:

      • Gastroenterology
      0
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  • Question 16 - A 48-year-old male presents to the urology clinic with complaints of impotence. He...

    Incorrect

    • A 48-year-old male presents to the urology clinic with complaints of impotence. He has a history of hypertension and reports the absence of morning erections. Upon further inquiry, the patient describes experiencing pain in his buttocks that intensifies with movement. Physical examination reveals muscle atrophy, while the penis and scrotum appear normal. What is the probable diagnosis?

      Your Answer:

      Correct Answer: Leriche syndrome

      Explanation:

      Leriche syndrome is a condition that typically affects men and is characterized by three main symptoms: claudication (painful cramping) in the buttocks and thighs, muscle wasting in the legs, and impotence caused by nerve paralysis in the L1 region. This condition is caused by atherosclerosis, which leads to blockages in the abdominal aorta and/or iliac arteries. Treatment involves addressing underlying risk factors such as high cholesterol and smoking cessation. Diagnosis is typically made through angiography.

      Understanding Leriche Syndrome

      Leriche syndrome is a condition that affects the iliac vessels, causing atheromatous disease that can compromise blood flow to the pelvic viscera. This can result in symptoms such as buttock claudication and impotence. To diagnose the condition, angiography is often used to identify any iliac occlusions. Treatment typically involves endovascular angioplasty and stent insertion to address the occlusions and improve blood flow.

      In summary, Leriche syndrome is a condition that can have significant impacts on a patient’s quality of life. By understanding the symptoms and diagnostic and treatment options available, healthcare providers can help patients manage this condition effectively.

    • This question is part of the following fields:

      • Musculoskeletal
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  • Question 17 - A newborn is 24 hours old and was born at term. The mother...

    Incorrect

    • A newborn is 24 hours old and was born at term. The mother had gestational diabetes during her pregnancy. The mother has chosen to exclusively formula feed the baby. The infant is currently comfortable on the postnatal ward, and the latest capillary blood glucose reading is 2.3mmol/L. The physical examination shows no abnormalities.
      What is the recommended course of action for management?

      Your Answer:

      Correct Answer: Encourage formula feeding

      Explanation:

      Dextrose intravenously or glucose gel would be necessary only if the baby remained hypoglycemic despite the standard feeding method or exhibited symptoms. Therefore, these responses are incorrect.

      Neonatal Hypoglycaemia: Causes, Symptoms, and Management

      Neonatal hypoglycaemia is a common condition in newborn babies, especially in the first 24 hours of life. While there is no agreed definition, a blood glucose level of less than 2.6 mmol/L is often used as a guideline. Transient hypoglycaemia is normal and usually resolves on its own, but persistent or severe hypoglycaemia may be caused by various factors such as preterm birth, maternal diabetes mellitus, IUGR, hypothermia, neonatal sepsis, inborn errors of metabolism, nesidioblastosis, or Beckwith-Wiedemann syndrome.

      Symptoms of neonatal hypoglycaemia can be autonomic, such as jitteriness, irritability, tachypnoea, and pallor, or neuroglycopenic, such as poor feeding/sucking, weak cry, drowsiness, hypotonia, and seizures. Other features may include apnoea and hypothermia. Management of neonatal hypoglycaemia depends on the severity of the condition and whether the newborn is symptomatic or not. Asymptomatic babies can be encouraged to feed normally and have their blood glucose monitored, while symptomatic or severely hypoglycaemic babies may need to be admitted to the neonatal unit and receive intravenous infusion of 10% dextrose.

    • This question is part of the following fields:

      • Paediatrics
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  • Question 18 - You are observing a doctor on the neonatal ward who is asked to...

    Incorrect

    • You are observing a doctor on the neonatal ward who is asked to assess a 3-hour-old baby delivered at 40+5 weeks by ventouse. The mother is concerned about the appearance of her baby's head. Upon examination, you notice a soft, puffy swelling at the back of the head with some light bruising from the ventouse cup. The swelling seems to extend across the suture lines. However, the baby appears to be in good health otherwise, and the neonatal hearing screen conducted earlier that morning was normal. What could be the probable cause of this presentation?

      Your Answer:

      Correct Answer: Caput succedaneum

      Explanation:

      Caput succedaneum is a puffy swelling that occurs over the presenting part during prolonged ventouse delivery and resolves spontaneously. It differs from bulging fontanelle, which is caused by increased intracranial pressure, and cephalohaematoma, which is a swelling caused by fluid collecting between the periosteum and skull. Hydrocephalus is a condition where there is an accumulation of cerebrospinal fluid around the brain, and subaponeurotic haemorrhage is a rare condition caused by rupturing of emissary veins.

      Understanding Caput Succedaneum

      Caput succedaneum is a condition that refers to the swelling of the scalp at the top of the head, usually at the vertex. This swelling is caused by the mechanical trauma that occurs during delivery, particularly in prolonged deliveries or those that involve the use of vacuum delivery. The condition is characterized by soft, puffy swelling due to localized edema that crosses suture lines.

      Compared to cephalohaematoma, which is a collection of blood under the scalp, caput succedaneum is caused by edema. While cephalohaematoma is limited to a specific area and does not cross suture lines, caput succedaneum can affect a larger area and cross suture lines. Fortunately, no treatment is needed for caput succedaneum, as the swelling usually resolves on its own within a few days.

    • This question is part of the following fields:

      • Paediatrics
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  • Question 19 - What is the term used to describe the elimination of a drug or...

    Incorrect

    • What is the term used to describe the elimination of a drug or its metabolite from the body?

      Your Answer:

      Correct Answer: Excretion

      Explanation:

      Pharmacokinetics: How the Body Processes Drugs

      Pharmacokinetics refers to the study of how the body processes drugs. It involves four main processes: absorption, distribution, metabolism, and excretion. Absorption refers to the uptake of drugs from the gut lumen and their entry into the circulation. Distribution involves the spread of drugs throughout the body, which can affect their ability to interact with their target. Metabolism involves the body’s processes for changing drug molecules, usually by deactivating them in the liver. Excretion involves the removal of drugs from the body.

      Metabolism and excretion are responsible for removing active drugs from the circulation. Metabolism converts drugs into inactive metabolites, while excretion removes drugs or their metabolites from the body. Renal excretion is common, but some drugs are excreted in the bile or feces.

      In summary, pharmacokinetics is the study of what the body does to drugs. these processes is important for determining the appropriate dosage and administration of drugs, as well as predicting their effects and potential side effects.

    • This question is part of the following fields:

      • Pharmacology
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  • Question 20 - Liam, a 13-year-old with learning difficulties, visits his GP clinic. Following a practice...

    Incorrect

    • Liam, a 13-year-old with learning difficulties, visits his GP clinic. Following a practice meeting, it is concluded that Liam does not possess the capacity to make decisions regarding his medical treatment. What principles should be prioritized when making decisions for Liam?

      Your Answer:

      Correct Answer: Consent may be given by one parent for the treatment that is in her best interests

      Explanation:

      The GMC provides comprehensive guidance on obtaining consent from children. In cases where a child is incapable of giving consent, the agreement of one parent is adequate for treatment to be administered, provided it is in the child’s best interests. It is also crucial to involve Dawn in the decision-making process, despite her incapacity.

      Guidelines for Obtaining Consent in Children

      The General Medical Council has provided guidelines for obtaining consent in children. According to these guidelines, young people who are 16 years or older can be treated as adults and are presumed to have the capacity to make decisions. However, for children under the age of 16, their ability to understand what is involved determines whether they have the capacity to decide. If a competent child refuses treatment, a person with parental responsibility or the court may authorize investigation or treatment that is in the child’s best interests.

      When it comes to providing contraceptives to patients under 16 years of age, the Fraser Guidelines must be followed. These guidelines state that the young person must understand the professional’s advice, cannot be persuaded to inform their parents, is likely to begin or continue having sexual intercourse with or without contraceptive treatment, and will suffer physical or mental health consequences without contraceptive treatment. Additionally, the young person’s best interests require them to receive contraceptive advice or treatment with or without parental consent.

      Some doctors use the term Fraser competency when referring to contraception and Gillick competency when referring to general issues of consent in children. However, rumors that Victoria Gillick removed her permission to use her name or applied copyright have been debunked. It is important to note that in Scotland, those with parental responsibility cannot authorize procedures that a competent child has refused.

    • This question is part of the following fields:

      • Paediatrics
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  • Question 21 - A 47-year-old woman is admitted with central chest pain of 18 hours’ duration...

    Incorrect

    • A 47-year-old woman is admitted with central chest pain of 18 hours’ duration and shortness of breath. Her troponin is elevated, and her electrocardiogram (ECG) shows changes in leads V2–V6. While undergoing initial management in preparation for primary percutaneous coronary intervention (primary PCI), she deteriorates suddenly and goes into cardiac arrest. Efforts to resuscitate her are unsuccessful. At post-mortem, rupture of the left ventricular cardiac wall is evident at the apex.
      Which is the most likely blood vessel to have been involved in the infarct?

      Your Answer:

      Correct Answer: The anterior interventricular (left anterior descending) artery

      Explanation:

      Coronary Arteries and Their Blood Supply to the Heart

      The heart is supplied with blood by the coronary arteries. There are four main coronary arteries that provide blood to different parts of the heart.

      The anterior interventricular artery, also known as the left anterior descending artery, supplies blood to the apex of the heart, as well as the anterior part of the interventricular septum and adjacent anterior walls of the right and left ventricles.

      The right marginal artery supplies the anteroinferior aspect of the right ventricle.

      The posterior interventricular artery supplies the interventricular septum and adjacent right and left ventricles on the diaphragmatic surface of the heart, but does not reach the apex.

      The circumflex artery supplies the posterolateral aspect of the left ventricle.

      Finally, the conus branch of the right coronary artery supplies the outflow tract of the right ventricle.

      Understanding the blood supply to different parts of the heart is important in diagnosing and treating heart conditions.

    • This question is part of the following fields:

      • Cardiology
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  • Question 22 - A 32-year-old man presents to the emergency department with bright red rectal bleeding....

    Incorrect

    • A 32-year-old man presents to the emergency department with bright red rectal bleeding. The bleeding started several hours ago after he has been to the toilet to defecate and he states that if he had to guess he has lost around 'a mug's worth' of blood. He is normally fit and well and has no significant past medical history. His observations are BP 115/84 mmHg, heart rate 74/min, temperature 37.3ºC, respiration rate 12/min, and oxygen saturation 98% on room air.

      What is the appropriate course of action for managing this patient?

      Your Answer:

      Correct Answer: Supportive management

      Explanation:

      When a patient with acute PR bleeds is haemodynamically stable, the primary treatment approach is supportive management. In this scenario, the patient is likely suffering from haemorrhoids. Supportive management involves providing analgesia for pain relief, regular monitoring of the patient’s condition, and administering fluids and oxygen as necessary.

      If the patient shows signs of haemodynamic compromise, intravenous fluids and/or blood transfusions may be necessary. Endoscopy is a useful tool for identifying the underlying cause of the bleed. Colonoscopy is typically used in elective settings, while flexible sigmoidoscopy is effective in identifying haemorrhoids as the source of the bleed.

      Understanding Lower Gastrointestinal Bleeding

      Lower gastrointestinal bleeding, also known as colonic bleeding, is characterized by the presence of bright red or dark red blood in the rectum. Unlike upper gastrointestinal bleeding, colonic bleeding rarely presents as melaena type stool. This is because blood in the colon has a powerful laxative effect and is rarely retained long enough for transformation to occur. Additionally, the digestive enzymes present in the small bowel are not present in the colon. It is important to note that up to 15% of patients presenting with hematochezia will have an upper gastrointestinal source of haemorrhage.

      Right-sided bleeds tend to present with darker coloured blood than left-sided bleeds. Haemorrhoidal bleeding, on the other hand, typically presents as bright red rectal bleeding that occurs post defecation either onto toilet paper or into the toilet pan. However, it is very unusual for haemorrhoids alone to cause any degree of haemodynamic compromise.

      There are several causes of lower gastrointestinal bleeding, including colitis, diverticular disease, cancer, and angiodysplasia. The management of lower gastrointestinal bleeding involves prompt correction of any haemodynamic compromise. Unlike upper gastrointestinal bleeding, the first-line management is usually supportive. When haemorrhoidal bleeding is suspected, a proctosigmoidoscopy is reasonable as attempts at full colonoscopy are usually time-consuming and often futile. In the unstable patient, the usual procedure would be an angiogram, while in others who are more stable, a colonoscopy in the elective setting is the standard procedure. Surgery may be necessary in some cases, particularly in patients over 60 years, those with continued bleeding despite endoscopic intervention, and those with recurrent bleeding.

      In summary, lower gastrointestinal bleeding is a serious condition that requires prompt attention. It is important to identify the cause of the bleeding and manage it accordingly to prevent further complications.

    • This question is part of the following fields:

      • Surgery
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  • Question 23 - What is the mode of action of fibrates in the management of hyperlipidemia?...

    Incorrect

    • What is the mode of action of fibrates in the management of hyperlipidemia?

      Your Answer:

      Correct Answer: Stimulate increased action of the enzyme lipoprotein lipase

      Explanation:

      Mechanism of Action and Side Effects of Fibrates

      Fibrates are a class of drugs used to treat high levels of triglycerides and cholesterol in the blood. The exact mechanism of action is not fully understood, but it is believed to involve increased lipoprotein lipase (LPL) activity, which leads to the breakdown and removal of triglycerides from the blood and their storage in adipose and muscle cells. Fibrates also increase PPAR-alpha activity, which reduces triglyceride production by the liver, increases fatty acid oxidation, and may have anti-inflammatory and anti-atherogenic effects.

      However, fibrates are not without side effects. They may cause hypoglycemia, reduce fibrinogen levels, and increase the risk of rhabdomyolysis, especially in patients with renal impairment or those taking statins. Mild gastrointestinal symptoms and myalgia are also common.

      Despite these side effects, fibrates have been shown to markedly reduce serum triglycerides and LDL cholesterol levels, while also increasing HDL cholesterol levels. However, there is no consistent evidence linking fibrates to improved mortality rates or reduced risk of coronary heart disease.

      In conclusion, fibrates are a useful class of drugs for managing high levels of triglycerides and cholesterol in the blood. However, their mechanism of action is not fully understood, and they may cause side effects such as hypoglycemia and rhabdomyolysis. Patients taking fibrates should be monitored closely for these side effects and their effectiveness in reducing cholesterol levels should be regularly assessed.

    • This question is part of the following fields:

      • Pharmacology
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  • Question 24 - The results of a phase 3 study on a new antihypertensive is published...

    Incorrect

    • The results of a phase 3 study on a new antihypertensive is published (n = 8,000). Compared with placebo, there is a mean reduction of 6 mmHg in favour of the treatment group when added to medication in patients who have failed to achieve blood pressure control on an angiotensin-converting enzyme inhibitor (ACEi). The 95% confidence interval for the difference in blood pressure lies between 1.9 mmHg and 10.1 mmHg.
      Which of the following is most accurate regarding this medication?

      Your Answer:

      Correct Answer: The difference in blood pressure is statistically significant at the 5% significance level

      Explanation:

      Interpretation of Blood Pressure Reduction Data for a New Medication

      Interpretation of the Data:

      The data provided shows that the difference in blood pressure is statistically significant at the 5% significance level, as the 95% confidence interval does not include the value 0. However, it is unclear whether this medication offers advantages compared with other treatments, as a number of established anti-hypertensives may result in a similar magnitude of blood pressure reduction.

      It is also important to note that the difference in blood pressure of 6 mmHg may be considered clinically significant in terms of leading to measurable reduction in morbidity and mortality. Therefore, it is possible that this medication could offer benefits in terms of reducing cardiovascular events such as stroke, myocardial infarction, and heart failure.

      However, whether this medication should be licensed is not just a question of efficacy, but also a full evaluation of the benefit-risk profile of the product. Without information about the side-effect profile of this medication, it is difficult to make a definitive recommendation.

      Overall, while the data suggests that this medication may offer benefits in terms of reducing blood pressure, further evaluation is needed to determine its overall effectiveness and safety.

    • This question is part of the following fields:

      • Statistics
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  • Question 25 - A 35-year-old woman presents with a significant obstetric hemorrhage due to uterine atony....

    Incorrect

    • A 35-year-old woman presents with a significant obstetric hemorrhage due to uterine atony. What is the initial medical management after stabilization and general measures?

      Your Answer:

      Correct Answer: Syntocinon

      Explanation:

      To treat postpartum haemorrhage caused by uterine atony, medical options include oxytocin, ergometrine, carboprost, and misoprostol.

      The leading cause of primary postpartum haemorrhage is uterine atony. The RCOG has issued guidelines (Green-top Guideline No.52) for managing primary PPH due to uterine atony. The first-line treatment recommended is 5U of IV Syntocinon (oxytocin), followed by 0.5 mg of ergometrine.

      Understanding Postpartum Haemorrhage

      Postpartum haemorrhage (PPH) is a condition where a woman experiences blood loss of more than 500 ml after giving birth vaginally. It can be classified as primary or secondary. Primary PPH occurs within 24 hours after delivery and is caused by the 4 Ts: tone, trauma, tissue, and thrombin. The most common cause is uterine atony. Risk factors for primary PPH include previous PPH, prolonged labour, pre-eclampsia, increased maternal age, emergency Caesarean section, and placenta praevia.

      In managing PPH, it is important to involve senior staff immediately and follow the ABC approach. This includes two peripheral cannulae, lying the woman flat, blood tests, and commencing a warmed crystalloid infusion. Mechanical interventions such as rubbing up the fundus and catheterisation are also done. Medical interventions include IV oxytocin, ergometrine, carboprost, and misoprostol. Surgical options such as intrauterine balloon tamponade, B-Lynch suture, ligation of uterine arteries, and hysterectomy may be considered if medical options fail to control the bleeding.

      Secondary PPH occurs between 24 hours to 6 weeks after delivery and is typically due to retained placental tissue or endometritis. It is important to understand the causes and risk factors of PPH to prevent and manage this life-threatening emergency effectively.

    • This question is part of the following fields:

      • Obstetrics
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  • Question 26 - A 20-year-old woman arrives at the Emergency Department complaining of fever, headache, and...

    Incorrect

    • A 20-year-old woman arrives at the Emergency Department complaining of fever, headache, and feeling generally unwell for the past two days. She denies having a rash, neck stiffness, photophobia, or vomiting. Her vital signs are within normal limits. The medical team suspects she may have viral encephalitis and orders a computed tomography head scan and lumbar puncture for cerebrospinal fluid (CSF) analysis.

      The initial CSF results confirm the suspected diagnosis, showing a normal opening pressure and CSF glucose level, with a slightly elevated white cell count, mostly lymphocytes, and a protein level of 0.6 g/l (normal value < 0.45 g/l). While waiting for the CSF culture results, what is the most appropriate management for this 20-year-old woman?

      Your Answer:

      Correct Answer: acyclovir

      Explanation:

      Treatment Options for Suspected Encephalitis or Meningitis

      Encephalitis is a condition where the brain parenchyma is infected, while meningitis is characterized by inflammation of the meninges. A patient with symptoms of fever, headache, and altered mental state may have viral encephalitis, which is commonly caused by herpes simplex virus type I. In such cases, acyclovir should be started immediately, as it has been proven to improve morbidity and mortality. On the other hand, empirical ceftriaxone is often used for suspected bacterial meningitis, while benzylpenicillin is recommended for patients with a non-blanching rash. Dexamethasone is used to reduce inflammation in certain cases of bacterial meningitis. However, supportive management alone with analgesia is not appropriate for suspected encephalitis or meningitis. It is important to consider the patient’s symptoms and initial CSF results before deciding on the appropriate treatment option.

    • This question is part of the following fields:

      • Neurology
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  • Question 27 - A 14-year-old teenage girl comes to the clinic with concerns about delayed puberty...

    Incorrect

    • A 14-year-old teenage girl comes to the clinic with concerns about delayed puberty and not having started her menstrual cycle. She reports feeling generally well and has no significant medical history. During the examination, it is noted that she has a slender build and underdeveloped breasts. There is no pubic hair present. Upon palpation, marble-sized swellings are felt in both groins. What is the most probable cause of her presentation?

      Your Answer:

      Correct Answer: Androgen insensitivity

      Explanation:

      The classic presentation of androgen insensitivity is primary amenorrhoea, with the key symptom being groin swellings. When combined with the absence of pubic hair, this points towards a diagnosis of androgen insensitivity, also known as testicular feminisation syndrome. This condition occurs in individuals who are genetically male (46XY) but appear phenotypically female due to increased oestradiol levels, which cause breast development. The groin swellings in this case are undescended testes. While non-Hodgkin’s lymphoma could also cause groin swellings, it is less likely as it would typically present with systemic symptoms and is not a common cause of delayed puberty.

      Disorders of sex hormones can have various effects on the body, as shown in the table below. Primary hypogonadism, also known as Klinefelter’s syndrome, is characterized by high levels of LH and low levels of testosterone. Patients with this disorder often have small, firm testes, lack secondary sexual characteristics, and are infertile. They may also experience gynaecomastia and have an increased risk of breast cancer. Diagnosis is made through chromosomal analysis.

      Hypogonadotrophic hypogonadism, or Kallmann syndrome, is another cause of delayed puberty. It is typically inherited as an X-linked recessive trait and is caused by the failure of GnRH-secreting neurons to migrate to the hypothalamus. Patients with Kallmann syndrome may have hypogonadism, cryptorchidism, and anosmia. Sex hormone levels are low, and LH and FSH levels are inappropriately low or normal. Cleft lip/palate and visual/hearing defects may also be present.

      Androgen insensitivity syndrome is an X-linked recessive condition that causes end-organ resistance to testosterone, resulting in genotypically male children (46XY) having a female phenotype. Complete androgen insensitivity syndrome is the new term for testicular feminisation syndrome. Patients with this disorder may experience primary amenorrhoea, undescended testes causing groin swellings, and breast development due to the conversion of testosterone to oestradiol. Diagnosis is made through a buccal smear or chromosomal analysis to reveal a 46XY genotype. Management includes counseling to raise the child as female, bilateral orchidectomy due to an increased risk of testicular cancer from undescended testes, and oestrogen therapy.

    • This question is part of the following fields:

      • Paediatrics
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  • Question 28 - What feature is typical of patent ductus arteriosus in children? ...

    Incorrect

    • What feature is typical of patent ductus arteriosus in children?

      Your Answer:

      Correct Answer: It causes a murmur which is typically loudest in systole

      Explanation:

      Patent Ductus Arteriosus (PDA)

      Patent ductus arteriosus (PDA) is a condition where the ductus arteriosus, which normally closes within a month after birth, remains open. This duct is responsible for transmitting blood from the pulmonary artery to the aortic arch in fetal circulation. However, after birth, the duct should close as the body’s prostaglandin levels decrease, resulting in the formation of the ligamentum arteriosum. In PDA, the duct remains open, creating a channel between the pulmonary and systemic circulations. The severity of the condition depends on the size of the duct, with larger PDAs causing increased pulmonary artery pressures that may lead to Eisenmenger syndrome.

      Most PDAs are asymptomatic or present with cardiac failure. A continuous murmur, louder in systole and best heard under the left clavicle, is a typical sign. Patients with PDA may also have a large pulse pressure, collapsing pulse, and prominent femoral pulses. Treatment options include NSAIDs to promote duct closure or IV prostaglandin for neonates with duct-dependent cardiac lesions. Antibiotic prophylaxis is recommended for dental extraction, although the risk of bacterial endocarditis is relatively low. Asymptomatic PDAs usually undergo closure via cardiac catheterization and the use of a coil within a year.

    • This question is part of the following fields:

      • Paediatrics
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  • Question 29 - A 30-year-old woman presents at 28 weeks’ gestation with a 3-day history of...

    Incorrect

    • A 30-year-old woman presents at 28 weeks’ gestation with a 3-day history of dysuria, urinary frequency and mild lower abdominal pain. A urine dipstick was performed, showing 2+ blood, and is positive for nitrites. There is no glycosuria or proteinuria. The patient has previously had an allergic reaction to trimethoprim.
      What is the most appropriate antibiotic for treating this patient's urinary tract infection?

      Your Answer:

      Correct Answer: Nitrofurantoin

      Explanation:

      Antibiotics for Urinary Tract Infections in Pregnancy: A Guide

      Urinary tract infections (UTIs) are common in pregnancy and require prompt treatment to prevent complications. When choosing an antibiotic, it is important to consider its safety for both the mother and the developing fetus. Here is a guide to some commonly used antibiotics for UTIs in pregnancy.

      Nitrofurantoin: This is the first-line antibiotic recommended by NICE guidelines for UTIs in pregnancy. It is safe to use, but should be avoided near term as it can cause neonatal haemolysis. It should also not be used during breastfeeding. Side-effects may include agranulocytosis, arthralgia, anaemia, chest pain and diarrhoea.

      Erythromycin: This antibiotic is not routinely used for UTIs in pregnancy, but is considered safe for both mother and fetus.

      cephalexin: This beta-lactam antibiotic is licensed as second-line treatment for UTIs in pregnancy. It is safe to use and has no documented fetal complications.

      Co-amoxiclav: This broad-spectrum antibiotic is not used for UTIs in pregnancy, but is safe for both mother and fetus.

      Trimethoprim: This antibiotic is no longer recommended for UTIs in pregnancy due to its interference with folate metabolism. If no other options are available, it can be given with increased folate intake.

      Remember to always consult with a healthcare professional before taking any medication during pregnancy.

    • This question is part of the following fields:

      • Obstetrics
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  • Question 30 - A 35-year-old man has been diagnosed with ankylosing spondylitis and his condition is...

    Incorrect

    • A 35-year-old man has been diagnosed with ankylosing spondylitis and his condition is not well controlled. His rheumatologist suggests starting him on a new medication. In cases of predominantly axial disease, how many non-steroidal anti-inflammatory drugs must be ineffective before anti-TNF alpha inhibitors can be considered?

      Your Answer:

      Correct Answer: 2

      Explanation:

      In cases of axial ankylosing spondylitis that have not responded to two different NSAIDs and meet the criteria for active disease on two separate occasions 12 weeks apart, the use of anti-TNF alpha inhibitors is recommended. Additionally, physiotherapy should be incorporated throughout the treatment process.

      Investigating and Managing Ankylosing Spondylitis

      Ankylosing spondylitis is a type of spondyloarthropathy that is associated with HLA-B27. It is more commonly seen in males aged 20-30 years old. Inflammatory markers such as ESR and CRP are usually elevated, but normal levels do not necessarily rule out ankylosing spondylitis. HLA-B27 is not a reliable diagnostic tool as it can also be positive in normal individuals. The most effective way to diagnose ankylosing spondylitis is through a plain x-ray of the sacroiliac joints. However, if the x-ray is negative but suspicion for AS remains high, an MRI can be obtained to confirm the diagnosis.

      Management of ankylosing spondylitis involves regular exercise, such as swimming, and the use of NSAIDs as the first-line treatment. Physiotherapy can also be helpful. Disease-modifying drugs used for rheumatoid arthritis, such as sulphasalazine, are only useful if there is peripheral joint involvement. Anti-TNF therapy, such as etanercept and adalimumab, should be given to patients with persistently high disease activity despite conventional treatments, according to the 2010 EULAR guidelines. Ongoing research is being conducted to determine whether anti-TNF therapies should be used earlier in the course of the disease. Spirometry may show a restrictive defect due to a combination of pulmonary fibrosis, kyphosis, and ankylosis of the costovertebral joints.

    • This question is part of the following fields:

      • Musculoskeletal
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