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  • Question 1 - A fifty eight year old male presents with a four month history of...

    Incorrect

    • A fifty eight year old male presents with a four month history of an unresolved varicocoele in his left testis. Initially he was given symptomatic advice. He has now presented with macroscopic haematuria and flank pain. He describes having no energy despite being fit for his age. The testes are palpable. No discharge is elicited from the urethral meatus. His urine dipstick demonstrates blood +++ but is negative for leucocytes. You send him for a cystoscopy as you're concerned he has presented with bladder cancer. The results are returned as normal. What is the most appropriate investigation to perform next in light of his normal cystoscopy?

      Your Answer: CA 19-9

      Correct Answer: Renal tract ultrasound

      Explanation:

      Understanding Renal Cell Cancer

      Renal cell cancer, also known as hypernephroma, is a primary renal neoplasm that accounts for 85% of cases. It typically arises from the proximal renal tubular epithelium, with the clear cell subtype being the most common. This type of cancer is more prevalent in middle-aged men and is associated with smoking, von Hippel-Lindau syndrome, and tuberous sclerosis. While renal cell cancer is only slightly increased in patients with autosomal dominant polycystic kidney disease, it can present with a classical triad of haematuria, loin pain, and abdominal mass. Other features include pyrexia of unknown origin, endocrine effects, and paraneoplastic hepatic dysfunction syndrome.

      The T category criteria for renal cell cancer are based on the size and extent of the tumour. For confined disease, a partial or total nephrectomy may be recommended depending on the tumour size. Patients with a T1 tumour are typically offered a partial nephrectomy, while those with larger tumours may require a total nephrectomy. Treatment options for renal cell cancer include alpha-interferon, interleukin-2, and receptor tyrosine kinase inhibitors such as sorafenib and sunitinib. These medications have been shown to reduce tumour size and treat patients with metastases. It is important to note that renal cell cancer can have paraneoplastic effects, such as Stauffer syndrome, which is associated with cholestasis and hepatosplenomegaly. Overall, early detection and prompt treatment are crucial for improving outcomes in patients with renal cell cancer.

    • This question is part of the following fields:

      • Surgery
      152.9
      Seconds
  • Question 2 - A 28-year-old female presents with palpitations, chest pain, and shortness of breath that...

    Correct

    • A 28-year-old female presents with palpitations, chest pain, and shortness of breath that radiates to her left arm. These symptoms began six weeks ago after she witnessed her father's death from a heart attack. Over the past decade, she has undergone various investigations for abdominal pain, headaches, joint pains, and dyspareunia, but no significant cause has been identified for these symptoms. What is the probable diagnosis?

      Your Answer: Somatisation disorder

      Explanation:

      Somatisation Disorder as the Most Likely Diagnosis

      Somatisation disorder is the most probable diagnosis for the given scenario, although it lacks sufficient criteria for a complete diagnosis. This disorder is characterised by recurring pains, gastrointestinal, sexual, and pseudo-neurologic symptoms that persist for years. To meet the diagnostic criteria, the patient’s physical complaints must not be intentionally induced and must result in medical attention or significant impairment in social, occupational, or other important areas of functioning. Typically, the first symptoms appear during adolescence, and the full criteria are met by the age of 30.

      Among the other disorders, factitious disorder is the least likely explanation. The other three disorders are possible explanations, but they are not as likely as somatisation disorder.

    • This question is part of the following fields:

      • Cardiology
      25.5
      Seconds
  • Question 3 - A 20-year-old female comes to the clinic complaining of secondary amenorrhoea for the...

    Incorrect

    • A 20-year-old female comes to the clinic complaining of secondary amenorrhoea for the past six months. She recently experienced moderate vaginal bleeding and abdominal pain. Additionally, she has gained around 14 pounds in weight during this time. What is the probable diagnosis?

      Your Answer: Polycystic ovarian syndrome

      Correct Answer: Pregnancy

      Explanation:

      Secondary Amenorrhea and Miscarriage: A Possible Sign of Pregnancy

      Secondary amenorrhea, or the absence of menstrual periods for at least three consecutive months in women who have previously had regular cycles, can be a sign of pregnancy. In cases where a patient with secondary amenorrhea experiences a miscarriage, it is important to consider the possibility of pregnancy. This information is highlighted in the book Williams Gynecology, 4th edition, authored by Barbara L. Hoffman, John O. Schorge, Lisa M. Halvorson, Cherine A. Hamid, Marlene M. Corton, and Joseph I. Schaffer.

      The authors emphasize the importance of considering pregnancy as a possible cause of secondary amenorrhea, especially in cases where a miscarriage has occurred. This highlights the need for healthcare providers to be vigilant in their assessment of patients with secondary amenorrhea and to consider pregnancy as a possible diagnosis. Early detection of pregnancy can help ensure appropriate prenatal care and management, which can improve outcomes for both the mother and the baby.

      In conclusion, secondary amenorrhea followed by a miscarriage should raise suspicion of pregnancy. Healthcare providers should be aware of this possibility and consider pregnancy as a potential diagnosis in patients with secondary amenorrhea. Early detection and appropriate management of pregnancy can improve outcomes for both the mother and the baby.

    • This question is part of the following fields:

      • Endocrinology
      59.1
      Seconds
  • Question 4 - You are the pediatric doctor on call. The nurses ask you to come...

    Correct

    • You are the pediatric doctor on call. The nurses ask you to come and review a patient, as she is acting ‘odd’. Her eyes are open spontaneously, she is withdrawing to pain and she is making incomprehensible sounds.
      What is this patient’s Glasgow Coma Score (GCS)?

      Your Answer: 11

      Explanation:

      Understanding the Glasgow Coma Scale

      The Glasgow Coma Scale (GCS) is a tool used to assess a patient’s level of consciousness. It is based on three components: motor response, verbal response, and eye opening. Each component is scored on a scale from 1 to 6, with a total possible score of 15.

      A patient with a GCS score of 11 is showing M5 (localising response to pain), E4 (incomprehensible speech), and V2 (eye opening in response to pain). This indicates that the patient is obeying commands, oriented, and has spontaneous eye opening.

      It is important to note that the GCS score is just one aspect of a patient’s overall assessment and should be used in conjunction with other clinical findings.

    • This question is part of the following fields:

      • Neurology
      49.8
      Seconds
  • Question 5 - A pharmaceutical company is currently testing a new medication, Xylozyme, for the treatment...

    Incorrect

    • A pharmaceutical company is currently testing a new medication, Xylozyme, for the treatment of Parkinson's disease. Phase 2-3 trials are being conducted to determine the drug's clearance rate. The drug is primarily cleared through the hepatic system.

      A blood sample is taken at timed intervals through an IV. One sample is taken with a blood volume of 150 ml. The drug concentration in the blood is 20 mg/L and the urine concentration at the same time is 5 mg/L.

      What is the clearance rate of the drug in liters per unit time?

      Your Answer: 0.2

      Correct Answer: 0.02

      Explanation:

      Drug Clearance

      Drug clearance refers to the rate at which active drugs are removed from the circulation. This process involves both renal excretion and hepatic metabolism, but in practice, clearance is mostly measured by the renal excretion of a drug. The glomerular filtration rate can affect drug clearance, but other factors such as the drug’s plasma concentration, structure, and distribution can also play a significant role. Clearance can be calculated by multiplying urine concentration and urine volume, and it can follow either zero order or first order kinetics.

      In zero order kinetics, the clearance of a drug remains constant regardless of its plasma concentration. On the other hand, first order kinetics means that the clearance of a drug is dependent on its plasma concentration. High plasma concentrations result in faster clearance, while low concentrations lead to slower clearance. A graph of drug concentration over time following a single dose will show an exponential decay. Under normal physiological conditions, most drugs are cleared by first order kinetics.

    • This question is part of the following fields:

      • Pharmacology
      73.9
      Seconds
  • Question 6 - A 5-day-old infant presents with feeding difficulties for the past day. The baby...

    Incorrect

    • A 5-day-old infant presents with feeding difficulties for the past day. The baby was born at 38 weeks, induced 48 hours after pre-labor spontaneous rupture of membranes. Following observation, there were no concerns and the baby was discharged. The infant is breastfed every 1-2 hours, but over the past 24 hours, has been less interested in feeding, occurring every 3-4 hours, sometimes being woken to feed. The baby appears uncomfortable during feeding and frequently pulls away. The mother also reports an unusual grunting sound after the baby exhales. Based on this information, what is the most likely diagnosis?

      Your Answer: Gastro-oesophageal reflux disease

      Correct Answer: Neonatal sepsis

      Explanation:

      Neonatal Sepsis: Causes, Risk Factors, and Management

      Neonatal sepsis is a serious bacterial or viral infection in the blood that affects babies within the first 28 days of life. It is categorized into early-onset (EOS) and late-onset (LOS) sepsis, with each category having distinct causes and common presentations. The most common causes of neonatal sepsis are group B streptococcus (GBS) and Escherichia coli, accounting for approximately two-thirds of cases. Premature and low birth weight babies are at higher risk, as well as those born to mothers with GBS colonization or infection during pregnancy. Symptoms can vary from subtle signs of illness to clear septic shock, and diagnosis is usually established through blood culture. Treatment involves early identification and use of intravenous antibiotics, with duration depending on ongoing investigations and clinical picture. Other important management factors include maintaining adequate oxygenation and fluid and electrolyte status.

      Neonatal Sepsis: Causes, Risk Factors, and Management

      Neonatal sepsis is a serious infection that affects newborn babies within the first 28 days of life. It can be caused by a variety of bacteria and viruses, with GBS and E. coli being the most common. Premature and low birth weight babies, as well as those born to mothers with GBS colonization or infection during pregnancy, are at higher risk. Symptoms can range from subtle signs of illness to clear septic shock, and diagnosis is usually established through blood culture. Treatment involves early identification and use of intravenous antibiotics, with duration depending on ongoing investigations and clinical picture. Other important management factors include maintaining adequate oxygenation and fluid and electrolyte status.

    • This question is part of the following fields:

      • Paediatrics
      26.5
      Seconds
  • Question 7 - A 32-year-old man is referred to the Respiratory Outpatient clinic due to a...

    Correct

    • A 32-year-old man is referred to the Respiratory Outpatient clinic due to a chronic non-productive cough. He is a non-smoker and reports no other symptoms. Initial tests show a normal full blood count and C-reactive protein, normal chest X-ray, and normal spirometry. What is the next most suitable test to perform?

      Your Answer: Bronchial provocation testing

      Explanation:

      Investigating Chronic Cough: Recommended Tests and Procedures

      Chronic cough with normal chest X-ray and spirometry, and no ‘red flag’ symptoms in a non-smoker can be caused by cough-variant asthma, gastro-oesophageal reflux, and post-nasal drip. To investigate for bronchial hyper-reactivity, bronchial provocation testing is recommended using methacholine or histamine. A CT thorax may eventually be required to look for underlying structural lung disease, but in the first instance, investigating for cough-variant asthma is appropriate. Bronchoscopy is not a first-line investigation but may be used in specialist centres to investigate chronic cough. Sputum culture is unlikely to be useful in a patient with a dry cough. Maximal inspiratory and expiratory pressures are used to investigate respiratory muscle weakness.

    • This question is part of the following fields:

      • Respiratory
      70.7
      Seconds
  • Question 8 - A 6-year-old girl is brought to the emergency department by her parents after...

    Incorrect

    • A 6-year-old girl is brought to the emergency department by her parents after she was woken up from sleep at night with unilateral jerking movements of the left face and upper limb lasting for 2 minutes. During the episode, she did not lose consciousness. This has only happened once before a few nights ago.

      A neurological examination is unremarkable, and her temperature is 37.5ºC and her heart rate is 90 bpm. She is slightly drowsy. Another episode occurs and an EEG is performed, which shows centrotemporal spikes.

      She has no past medical history.

      What is the most likely diagnosis?

      Your Answer: Juvenile myoclonic epilepsy

      Correct Answer: Benign rolandic epilepsy

      Explanation:

      The child’s symptoms and medical history suggest that they have benign rolandic epilepsy, which is characterized by partial seizures occurring at night. This type of epilepsy typically affects children between the ages of 4 and 12 and is confirmed by an EEG showing centrotemporal spikes. The seizures originate from the central sulcus of the brain in a region called the Rolandic fissure. Although the child is drowsy, postictal states can occur in benign rolandic epilepsy as well. The prognosis for this condition is usually excellent, with most children outgrowing it. Febrile convulsions, generalised tonic-clonic epilepsy, and infantile spasms are not applicable to this case.

      Benign rolandic epilepsy is a type of epilepsy that usually affects children between the ages of 4 and 12 years. This condition is characterized by seizures that typically occur at night and are often partial, causing sensations in the face. However, these seizures may also progress to involve the entire body. Despite these symptoms, children with benign rolandic epilepsy are otherwise healthy and normal.

      Diagnosis of benign rolandic epilepsy is typically confirmed through an electroencephalogram (EEG), which shows characteristic centrotemporal spikes. Fortunately, the prognosis for this condition is excellent, with seizures typically ceasing by adolescence. While the symptoms of benign rolandic epilepsy can be concerning for parents and caregivers, it is important to remember that this condition is generally not associated with any long-term complications or developmental delays.

    • This question is part of the following fields:

      • Paediatrics
      135.2
      Seconds
  • Question 9 - A 28-year-old woman has just had her 34 week check. The patient reported...

    Correct

    • A 28-year-old woman has just had her 34 week check. The patient reported reduced fetal movements 3 days ago, but they are now back to normal. An ultrasound was performed to investigate any potential issues. The obstetrician informs her that a defect in the abdominal wall has been detected and the baby's intestines are outside the body but enclosed in a membrane. Despite this, the baby is healthy. What is the best course of action for this patient?

      Your Answer: Plan a caesarean section at 37 weeks

      Explanation:

      If the unborn baby has exomphalos, it is recommended to opt for a caesarean section to minimize the chances of sac rupture. The presence of a membrane containing the abdominal content suggests that the baby is likely to have exomphalos. While vaginal delivery is possible, a caesarean section is the safest delivery option. There is no need for an emergency caesarean section as the baby is not experiencing any distress. Inducing labor for vaginal delivery is not advisable, and a caesarean section is a better option. Additionally, IM corticosteroids are not necessary as there is no risk of premature delivery at present. These steroids are typically used when women are at risk of or experience premature labor.

      Gastroschisis and exomphalos are both types of congenital visceral malformations. Gastroschisis refers to a defect in the anterior abdominal wall located just beside the umbilical cord. In contrast, exomphalos, also known as omphalocoele, involves the protrusion of abdominal contents through the anterior abdominal wall, which are covered by an amniotic sac formed by amniotic membrane and peritoneum.

      When it comes to managing gastroschisis, vaginal delivery may be attempted, but newborns should be taken to the operating theatre as soon as possible after delivery, ideally within four hours. As for exomphalos, a caesarean section is recommended to reduce the risk of sac rupture. In cases where primary closure is difficult due to lack of space or high intra-abdominal pressure, a staged repair may be undertaken. This involves allowing the sac to granulate and epithelialise over several weeks or months, forming a shell. As the infant grows, the sac contents will eventually fit within the abdominal cavity, at which point the shell can be removed and the abdomen closed.

      Overall, both gastroschisis and exomphalos require careful management to ensure the best possible outcome for the newborn. By understanding the differences between these two conditions and the appropriate steps to take, healthcare professionals can provide effective care and support to both the infant and their family.

    • This question is part of the following fields:

      • Paediatrics
      28.1
      Seconds
  • Question 10 - You are seeing a 6-year-old boy that has been brought in by his...

    Incorrect

    • You are seeing a 6-year-old boy that has been brought in by his mother with a sudden onset of fever and a sore throat this morning. His mother informs you that he is prone to tonsillitis and would like some antibiotics as they had worked well previously.

      On examination he is alert, sitting upright and unaided with a slight forward lean. He has a temperature of 38.5 ºC, heart rate of 130/min, respiratory rate is normal. There is no cyanosis or use of accessory muscles, but you do note a mild inspiratory fine-pitched stridor.

      What would be the most appropriate next course of action?

      Your Answer: Examine her throat, calculate her CENTOR score and, if appropriate, prescribe antibiotics

      Correct Answer: Arrange an urgent admission to hospital

      Explanation:

      If acute epiglottitis is suspected, do not attempt to examine the throat. Instead, contact the paediatrician on call and arrange for the child to be reviewed and admitted to the hospital on the same day. This condition can be life-threatening and requires urgent assessment and treatment in secondary care. Hospital transfer should be done by a blue light ambulance. Treatment usually involves intravenous antibiotics after securing the airway, which may require intubation. Nebulised adrenaline may also be used to stabilise the airway, and intravenous steroids are often given. It would be clinically unsafe to advise expectant management or prescribe immediate or delayed antibiotics for this condition.

      Acute epiglottitis is a rare but serious infection caused by Haemophilus influenzae type B. It is important to recognize and treat it promptly as it can lead to airway obstruction. Although it was once considered a disease of childhood, it is now more common in adults in the UK due to the immunization program. The incidence of epiglottitis has decreased since the introduction of the Hib vaccine. Symptoms include a rapid onset, high temperature, stridor, drooling of saliva, and a tripod position where the patient leans forward and extends their neck to breathe easier. Diagnosis is made by direct visualization, but x-rays may be done to rule out a foreign body.

      Immediate senior involvement is necessary, including those who can provide emergency airway support such as anaesthetics or ENT. Endotracheal intubation may be necessary to protect the airway. It is important not to examine the throat if epiglottitis is suspected due to the risk of acute airway obstruction. The diagnosis is made by direct visualization, but only senior staff who are able to intubate if necessary should perform this. Treatment includes oxygen and intravenous antibiotics.

    • This question is part of the following fields:

      • Paediatrics
      116.4
      Seconds
  • Question 11 - A 10-year-old boy falls off his bike and lands on his right arm....

    Correct

    • A 10-year-old boy falls off his bike and lands on his right arm. He is taken to the Emergency Department where an X-ray reveals a mid-humeral shaft fracture. There is no sign of a growing haematoma, and the patient has a strong radial pulse with good perfusion. Doppler studies of the arm show no evidence of bleeding.
      What is the most probable condition that this patient is experiencing?

      Your Answer: Loss of sensation to the dorsum of the right hand

      Explanation:

      Common Nerve Injuries Associated with Mid-Humeral Shaft Fractures

      Mid-humeral shaft fractures can result in nerve damage, leading to various symptoms. Here are some common nerve injuries associated with this type of fracture:

      1. Loss of sensation to the dorsum of the right hand: This is likely due to damage to the radial nerve, which provides sensation to the dorsum of the hand and innervates the extensor compartment of the forearm.

      2. Atrophy of the deltoid muscle: This may occur in shoulder dislocation or compression of the axilla, leading to weakness of adduction and loss of sensation over a small patch of the lateral upper arm.

      3. Inability to flex the wrist: This is controlled by the median nerve, which is more likely to be damaged in a supracondylar fracture.

      4. Loss of sensation to the right fifth finger: This is innervated by the ulnar nerve, which can be compressed at the medial epicondyle of the humerus, causing ulnar entrapment.

      While compartment syndrome can also occur with mid-humeral shaft fractures, it is unlikely if no major bleeding was observed. It is important to be aware of these potential nerve injuries and seek medical attention if any symptoms arise.

    • This question is part of the following fields:

      • Orthopaedics
      144
      Seconds
  • Question 12 - A twenty-five-year-old male with Crohn's disease is admitted to the gastroenterology ward. Despite...

    Incorrect

    • A twenty-five-year-old male with Crohn's disease is admitted to the gastroenterology ward. Despite infliximab therapy, the patient's symptoms persist, and he complains of abdominal pain and high output through his stoma. On examination, he appears pale and cachectic, with a heart rate of 74/minute, regular respiratory rate of 14/minute, oxygen saturations of 99%, temperature of 38.2 ºC, and blood pressure of 122/74 mmHg. The stoma bag is situated in the left iliac fossa, and the stoma site is pink and spouted without evidence of infarction or parastomal hernias. What type of stoma does this patient have?

      Your Answer: Colostomy

      Correct Answer: Ileostomy

      Explanation:

      An ileostomy is a type of stoma that is created to prevent the skin from being exposed to the enzymes in the small intestine. This is commonly seen in patients with Crohn’s disease, which affects the entire gastrointestinal tract. While the location of the stoma may vary, it is the structure of the stoma itself that determines whether it is an ileostomy or a colostomy. In contrast, a tracheostomy is an opening in the trachea, while a nephrostomy is an opening in the kidneys that is used to drain urine into a bag. A urostomy is another type of stoma that is used to divert urine from the urinary system into a bag, but it differs from an ileostomy in that it involves the use of an ileal conduit.

      Abdominal stomas are created during various abdominal procedures to bring the lumen or contents of organs onto the skin. Typically, this involves the bowel, but other organs may also be diverted if necessary. The type and method of construction of the stoma will depend on the contents of the bowel. Small bowel stomas should be sprouted to prevent irritant contents from coming into contact with the skin, while colonic stomas do not require spouting. Proper siting of the stoma is crucial to reduce the risk of leakage and subsequent maceration of the surrounding skin. The type and location of the stoma will vary depending on the purpose, such as defunctioning the colon or providing feeding access. Overall, abdominal stomas are a necessary medical intervention that requires careful consideration and planning.

    • This question is part of the following fields:

      • Surgery
      58892.3
      Seconds
  • Question 13 - Which patient has a creatinine level indicating CKD3?

    Patient A:
    Adjusted calcium -...

    Incorrect

    • Which patient has a creatinine level indicating CKD3?

      Patient A:
      Adjusted calcium - 2.3 mmol/L
      Phosphate - 0.9 mmol/L
      PTH - 8.09 pmol/L
      Urea - 7.8 mmol/L
      Creatinine - 145 μmol/L
      Albumin - 36 g/L

      Patient B:
      Adjusted calcium - 2.9 mmol/L
      Phosphate - 2.0 mmol/L
      PTH - 4.2 pmol/L
      Urea - 50 mmol/L
      Creatinine - 280 μmol/L
      Albumin - 38 g/L

      Patient C:
      Adjusted calcium - 2.0 mmol/L
      Phosphate - 2.8 mmol/L
      PTH - 12.53 pmol/L
      Urea - 32.8 mmol/L
      Creatinine - 540 μmol/L
      Albumin - 28 g/L

      Patient D:
      Adjusted calcium - 2.5 mmol/L
      Phosphate - 1.6 mmol/L
      PTH - 2.05 pmol/L
      Urea - 32.8 mmol/L
      Creatinine - 367 μmol/L
      Albumin - 40 g/L

      Patient E:
      Adjusted calcium - 2.2 mmol/L
      Phosphate - 0.7 mmol/L
      PTH - 5.88 pmol/L
      Urea - 4.6 mmol/L
      Creatinine - 81 μmol/L
      Albumin - 18 g/L

      Your Answer: Patient D

      Correct Answer: Patient A

      Explanation:

      Renal Impairment and Calcium Homeostasis

      Although interpreting creatinine levels can be challenging without information about body habitus and muscle mass, Patient A likely has CKD3 based on their creatinine level of 145. It is important to have a general of the severity of renal impairment based on creatinine levels. Patients with an eGFR of 30-59 ml/min/1.73m2 are classified as having CKD3. This classification applies to men and women between the ages of 20 and 80 years old.

      Patients B, C, and D have more advanced renal disease, and depending on the clinical context, patients B and D may have acute renal failure. Patient E, on the other hand, does not have any renal impairment.

      Patients with kidney disease often experience multiple abnormalities in calcium homeostasis. At the CKD3 stage, most patients have normal plasma concentrations of calcium and phosphate. However, as CKD3 progresses towards CKD 4, more subtle abnormalities may arise, such as a slight increase in PTH due to reduced hydroxylation of vitamin D by the kidney enzyme 1-alpha hydroxylase.

      Although Patient A has suboptimal levels of vitamin D, this is not uncommon. Risk factors for vitamin D insufficiency include old age, immobility, institutionalization, and darker skin color.

    • This question is part of the following fields:

      • Nephrology
      22.3
      Seconds
  • Question 14 - A 56-year-old homeless man is discovered unresponsive on the pavement. Upon arrival at...

    Correct

    • A 56-year-old homeless man is discovered unresponsive on the pavement. Upon arrival at the emergency department, blood tests are conducted, revealing an abnormality - Amylase 1100 U/l. An ultrasound is performed, indicating no biliary tree dilatation. What is the probable reason for this man's condition?

      Your Answer: Hypothermia

      Explanation:

      Acute pancreatitis is a condition that is mainly caused by gallstones and alcohol in the UK. A popular mnemonic to remember the causes is GET SMASHED, which stands for gallstones, ethanol, trauma, steroids, mumps, autoimmune diseases, scorpion venom, hypertriglyceridaemia, hyperchylomicronaemia, hypercalcaemia, hypothermia, ERCP, and certain drugs. CT scans of patients with acute pancreatitis show diffuse parenchymal enlargement with oedema and indistinct margins. It is important to note that pancreatitis is seven times more common in patients taking mesalazine than sulfasalazine.

    • This question is part of the following fields:

      • Surgery
      71.2
      Seconds
  • Question 15 - A 35-year-old woman comes to the Emergency Department following a fall while decorating...

    Correct

    • A 35-year-old woman comes to the Emergency Department following a fall while decorating on a chair. She experienced intense pain in her hip immediately after the fall. X-rays show a fracture in the left neck of her femur. She has a history of seizures and takes topiramate. Her menstrual cycle is regular, and she is a non-smoker and non-vegetarian. She works as a landscaper. What is the probable cause of her fracture?

      Your Answer: Chronic acidosis

      Explanation:

      Differential Diagnosis for Chronic Acidosis and Pathological Fracture

      Chronic acidosis can lead to defective bone mineralization and an osteomalacia-like state, which can cause pathological fractures. Topiramate, an antiepileptic and migraine prophylaxis drug, has been found to cause chronic metabolic acidosis through renal tubular acidosis. The type of RTA induced by topiramate is debated, but it is considered a mixed RTA with features of both types 1 and 2. Topiramate-induced osteopathy is a differential diagnosis for vitamin D deficiency, hereditary hypophosphatasia, and chronic bisphosphonate use.

      In the case of a 36-year-old woman with a minor trauma resulting in a serious fracture, osteoporosis is unlikely, especially since there is no mention of drug intake like heparin, bisphosphonates, or steroids. Vitamin D deficiency is a common condition, but there is no mention of other features like bone pain or weakness, and her profession as an architect suggests substantial sunlight exposure. Multiple myeloma is also unlikely at this age, and there is no mention of other symptoms like renal failure or anemia. Therefore, the most likely cause of the pathological fracture is the chronic acidosis induced by topiramate.

    • This question is part of the following fields:

      • Orthopaedics
      66.3
      Seconds
  • Question 16 - A 62-year-old practising solicitor attends the Neurology Clinic with his wife. She is...

    Incorrect

    • A 62-year-old practising solicitor attends the Neurology Clinic with his wife. She is deeply concerned regarding his worsening memory. Over the past three months, he has become increasingly forgetful, to the point where he has had to take sick leave from work. He has had two recent presentations to the Emergency Department following falls, though a computed tomography (CT) head scan did not demonstrate any abnormality. On examination, there is an ataxic gait and you notice fasciculations and involuntary jerking movements of the upper limbs. He has had no family history of neurological disease and was previously fit and well.
      What is the most likely underlying cause of this presentation?

      Your Answer: Lewy body dementia

      Correct Answer: Creutzfeldt–Jakob disease (CJD)

      Explanation:

      Distinguishing Neurodegenerative Diseases: A Case Study

      A patient presents with rapidly progressive dementia, imbalance leading to falls, and myoclonus. The most likely diagnosis is Creutzfeldt–Jakob disease (CJD), a devastating prion disease without cure. Magnetic resonance imaging (MRI) is preferred for diagnosis, as CT head is ineffective.

      Vascular dementia, another common cause of cognitive impairment, typically has a slower and stepwise onset in patients with a significant vascular history. A CT head would likely identify existing small vessel disease in the brain of a patient with vascular dementia.

      Huntington’s disease, characterized by abnormal movements and cognitive impairment, is not the most likely diagnosis due to the rapid progression and lack of family history.

      Lewy body dementia, which features visual hallucinations and Parkinsonian symptoms, usually presents over a longer period of time.

      Motor neuron disease, which includes weakness and fasciculations, is unlikely due to the absence of weakness in this presentation. Frontotemporal dementia may rarely develop in motor neuron disease, but it is a slowly progressive phenomenon, unlike the rapid deterioration in this case.

    • This question is part of the following fields:

      • Infectious Diseases
      29.3
      Seconds
  • Question 17 - A 67-year-old man presents to secondary care for a routine follow-up. He is...

    Incorrect

    • A 67-year-old man presents to secondary care for a routine follow-up. He is asymptomatic. Routine blood tests reveal the following:
      Calcium 3.1 mmol/L (2.1-2.6)
      Phosphate 0.3 mmol/L (0.8-1.4)
      Parathyroid hormone (PTH) 11.8 pmol/L (1.6 - 6.9)
      Magnesium 0.9 mmol/L (0.7-1.0)
      Thyroid stimulating hormone (TSH) 3.2 mU/L (0.5-5.5)
      Free thyroxine (T4) 17 pmol/L (9.0 - 18)
      What is the patient's most likely risk factor for developing a condition?

      Your Answer: Gallstones

      Correct Answer: Pseudogout

      Explanation:

      Primary hyperparathyroidism is often asymptomatic and can be detected through routine blood tests that show raised calcium, low phosphate, and raised parathyroid hormone levels. This condition is a known risk factor for the development of pseudogout or calcium pyrophosphate dihydrate deposition (CPPD) and chondrocalcinosis. However, there is no evidence to suggest an increased risk of gallstones. On the other hand, hyperparathyroidism can increase the risk of renal stones due to elevated serum and urinary calcium levels. Hypoparathyroidism, not hyperparathyroidism, is associated with ectopic soft tissue calcifications. Prolonged hypocalcaemia can increase the risk of cataracts, while hypercalcaemia can lead to corneal calcification. Primary hyperparathyroidism can also increase the risk of osteoporosis, osteitis fibrosa cystica, and pathological fractures, but it is not associated with osteopetrosis.

      Pseudogout, also known as acute calcium pyrophosphate crystal deposition disease, is a type of microcrystal synovitis that occurs when calcium pyrophosphate dihydrate crystals are deposited in the synovium. This condition is more common in older individuals, but those under 60 years of age may develop it if they have underlying risk factors such as haemochromatosis, hyperparathyroidism, low magnesium or phosphate levels, acromegaly, or Wilson’s disease. The knee, wrist, and shoulders are the most commonly affected joints, and joint aspiration may reveal weakly-positively birefringent rhomboid-shaped crystals. X-rays may show chondrocalcinosis, which appears as linear calcifications of the meniscus and articular cartilage in the knee. Treatment involves joint fluid aspiration to rule out septic arthritis, as well as the use of NSAIDs or steroids, as with gout.

    • This question is part of the following fields:

      • Musculoskeletal
      311.9
      Seconds
  • Question 18 - A 62-year-old man is recuperating in the hospital after experiencing a stroke. During...

    Incorrect

    • A 62-year-old man is recuperating in the hospital after experiencing a stroke. During the examination, it is revealed that he has a right homonymous superior quadrantanopia. What is the location of the lesion responsible for this visual field impairment?

      Your Answer: Right parietal (upper) optic radiation

      Correct Answer: Left temporal (lower) optic radiation

      Explanation:

      Understanding Optic Radiation Lesions and Visual Field Defects

      The optic radiation is a crucial pathway for visual information processing in the brain. Lesions in different parts of this pathway can result in specific visual field defects.

      Left Temporal (Lower) Optic Radiation: A lesion in this area would cause a quadrantanopia, affecting the upper quadrants of the contralateral visual field.

      Left Parietal (Upper) Optic Radiation: A lesion in this area would result in a right homonymous inferior quadrantanopia.

      Left Occipital Visual Cortex: A lesion in this area would cause a right contralateral homonymous hemianopia, with central sparing.

      Right Parietal (Upper) Optic Radiation: A lesion in this area would cause a left homonymous inferior quadrantanopia.

      Right Temporal (Lower) Optic Radiation: A lesion in this area would cause a left homonymous superior quadrantanopia.

      Understanding these specific visual field defects can aid in localizing lesions in the optic radiation and visual cortex, leading to better diagnosis and treatment of neurological conditions affecting vision.

    • This question is part of the following fields:

      • Neurology
      40.2
      Seconds
  • Question 19 - A 14-year-old female has been experiencing multiple, non-tender, erythematosus, annular lesions with a...

    Correct

    • A 14-year-old female has been experiencing multiple, non-tender, erythematosus, annular lesions with a collarette of scales at the periphery for the past two weeks. These lesions are only present on her trunk. What is the most probable diagnosis?

      Your Answer: Pityriasis rosea

      Explanation:

      Pityriasis Rosea

      Pityriasis rosea (PR) is a common skin condition that typically affects adolescents and young adults. It is often associated with upper respiratory infections and is characterized by a herald patch, which is a circular or oval-shaped lesion that appears on the trunk, neck, or extremities. The herald patch is usually about 1-2 cm in diameter and has a central, salmon-colored area surrounded by a dark red border.

      About one to two weeks after the herald patch appears, a generalized rash develops. This rash is symmetrical and consists of macules with a collarette scale that aligns with the skin’s cleavage lines. The rash can last for up to six weeks before resolving on its own.

      Overall, PR is a benign condition that does not require treatment. However, if the rash is particularly itchy or uncomfortable, topical corticosteroids or antihistamines may be prescribed to alleviate symptoms. It is important to note that PR is not contagious and does not pose any serious health risks.

    • This question is part of the following fields:

      • Dermatology
      42.3
      Seconds
  • Question 20 - A 50-year-old runner experiences chest pain and collapses while jogging. He is brought...

    Correct

    • A 50-year-old runner experiences chest pain and collapses while jogging. He is brought to the Emergency department within an hour. Upon arrival, he is conscious and given a sublingual nitrate which provides some relief. His heart rate is 90 beats per minute and his blood pressure is 120/85 mmHg. An ECG reveals 3 mm of ST segment elevation in leads II, III, AVF, V5 and V6. What is the most appropriate next step in managing this patient?

      Your Answer: Admission for cardiac catheterisation and percutaneous transluminal coronary angioplasty

      Explanation:

      Initial and Long-Term Treatment for Inferolateral ST-Elevation MI

      The patient’s history and ECG findings suggest that they are experiencing an Inferolateral ST-elevation MI. The best initial treatment for this condition would be percutaneous coronary intervention. It is likely that the patient would have already received aspirin in the ambulance.

      For long-term treatment, the patient will require dual antiplatelet therapy, such as aspirin and clopidogrel, a statin, a beta blocker, and an ACE-inhibitor. These medications will help manage the patient’s condition and prevent future cardiac events.

      It is important to follow the NICE guideline for Acute Coronary Syndrome to ensure that the patient receives the appropriate treatment and care. By following these guidelines, healthcare professionals can help improve the patient’s prognosis and quality of life.

    • This question is part of the following fields:

      • Emergency Medicine
      46.9
      Seconds
  • Question 21 - What is the life expectancy for a man in the UK? ...

    Correct

    • What is the life expectancy for a man in the UK?

      Your Answer: 80–84 years

      Explanation:

      The Remarkable Increase in Life Expectancy for Women in the UK

      At the beginning of the twentieth century, the life expectancy for a woman in the UK was only 59 years old. However, due to a combination of factors such as reduced infant mortality, improved public health, modern medical advances, and the introduction of the welfare state, women in the UK can now expect to live an average of 82.5 years. This remarkable increase in life expectancy is a testament to the progress made in healthcare and social welfare in the UK.

    • This question is part of the following fields:

      • Statistics
      4.3
      Seconds
  • Question 22 - A 4-week-old girl who previously had no issues with feeding is now experiencing...

    Incorrect

    • A 4-week-old girl who previously had no issues with feeding is now experiencing forceful, non-bilious vomiting after feeds. The following blood and blood gas results have been obtained:

      Investigation Result Normal Range
      Haemoglobin 170 g/l 130–200 g/l
      White cell count (WCC) 8 × 103/mm3 6–18 × 103/mm3
      Sodium (Na+) 142 mmol/l 135–145 mmol/l
      Potassium (K+) 3.2 mmol/l 3.5–6 mmol/l
      Chloride (Cl-) 80 mmol/l 95–105 mmol/l
      Bilirubin 12 mmol/l 3–17 mmol/l
      Urea 9 mmol/l 1–5 mmol/l
      Creatinine 55 μmol/l 20–65 μmol/l
      pH 7.4 7.35–7.45
      pO2 31 kPa 11–14 kPa
      pCO2 3.2 kPa 4.5–6 kPa
      HCO3- 28 mmol/l 18–25 mmol/l

      What is the most likely diagnosis?

      Your Answer: Biliary Atresia

      Correct Answer: Pyloric stenosis

      Explanation:

      Common Pediatric Gastrointestinal Disorders

      Pyloric Stenosis
      Pyloric stenosis is a condition that typically affects infants between 2 and 4 weeks of age, with boys being more commonly affected. The main symptom is projectile vomiting of non-bile-stained vomit, leading to a characteristic hypochloremic, hypokalemic metabolic alkalosis.

      Intussusception
      Intussusception is a condition that affects approximately 1 in 500 children, usually between 6 and 18 months of age. It is often associated with viral gastroenteritis. Unlike pyloric stenosis, vomiting is not a predominant feature, and if it occurs, it may be bile-stained. Intussusception causes small bowel obstruction, leading to engorgement of the intussuscepted bowel, rectal bleeding, and possible bowel gangrene.

      Biliary Atresia
      Biliary atresia is a rare birth defect with a prevalence of 0.5-0.8 per 10,000 births. It causes clinical jaundice with conjugated bilirubinemia. Surgical treatment, such as a Kasai portoenterostomy, is necessary, and outcomes are generally good.

      Hirschsprung’s Disease
      Hirschsprung’s disease is a condition that affects approximately 1 in 5000 live births. It may be familial and is associated with trisomy 21. It typically presents within the first few days of life with intestinal obstruction. The diagnosis is confirmed through rectal biopsy.

      Tracheo-Oesophageal Fistula
      Tracheo-oesophageal fistula is a condition that is usually associated with oesophageal atresia but can occur on its own. It tends to present with choking or coughing during feeding and recurrent lower respiratory tract infections. Projectile vomiting is not a common feature, and the diagnosis may not be made until later in childhood.

    • This question is part of the following fields:

      • Paediatrics
      89.4
      Seconds
  • Question 23 - A 25-year-old man experiences a severe motorbike injury and is rushed to the...

    Incorrect

    • A 25-year-old man experiences a severe motorbike injury and is rushed to the Resuscitation Department of the Emergency Department. Upon arrival, his vital signs are recorded as follows:
      Blood pressure – 200/120
      Heart rate – 45 bpm
      Saturation – 95% on 4 l of oxygen
      What is the most probable diagnosis?

      Your Answer: Tension pneumothorax

      Correct Answer: Extradural haematoma

      Explanation:

      Possible Traumatic Injuries and their Manifestations

      Extradural Haematoma, Tension Pneumothorax, Subdural Haematoma, Splenic Rupture, and Bronchial Rupture are possible traumatic injuries that can occur in high-velocity trauma. Each injury has its own unique manifestations that can help identify the injury.

      Extradural Haematoma is a possible injury that can cause a Cushing’s reflex, resulting in severe hypertension and bradycardia. This injury is caused by a tear in the middle meningeal artery, leading to the formation of a haematoma between the skull and dura mater.

      Tension Pneumothorax can cause tachycardia and hypotension due to restricted venous return caused by raised intrapleural pressures. A sympathetic response occurs in an attempt to increase cardiac output.

      Subdural Haematoma can also cause raised intracranial pressure and a Cushing’s reflex, but it is caused by torn bridging veins between the dura and arachnoid layers of the meninges. This injury is more common in the elderly due to cerebral atrophy and can occur with low-velocity injuries.

      Splenic Rupture can cause blood loss, resulting in a sympathetic response that manifests as hypotension and tachycardia.

      Bronchial Rupture is an uncommon injury that would not cause severe hypertension and bradycardia. Additionally, oxygen saturations of 95% would not be likely with bronchial rupture.

      In conclusion, understanding the manifestations of possible traumatic injuries can aid in identifying the injury and providing appropriate treatment.

    • This question is part of the following fields:

      • Neurosurgery
      63.4
      Seconds
  • Question 24 - A 25-year-old male contacts emergency services claiming to have ingested insecticide in a...

    Correct

    • A 25-year-old male contacts emergency services claiming to have ingested insecticide in a suicide attempt. He is a final year student studying agriculture and is experiencing mental health difficulties. During the assessment, he appears lethargic and uncommunicative. His eyes are constantly watering, and he is drooling saliva. Additionally, he seems to have experienced urinary and fecal incontinence.

      What physical signs would you anticipate discovering during the examination?

      Your Answer: Bradycardia

      Explanation:

      The patient’s symptoms suggest that they are suffering from organophosphate poisoning, which is caused by insecticide. Organophosphates can stimulate both the sympathetic and parasympathetic nervous systems, but in most cases, overstimulation of the parasympathetic system is observed. The mnemonic ‘DUMBELS’ can help identify the key symptoms associated with this type of poisoning, which include defecation, urinary incontinence, miosis (pupil constriction), bradycardia, emesis, lacrimation, and salivation. Hypertension is not typically associated with organophosphate poisoning, as it is more commonly seen in cases of stimulant overdose. Muscle rigidity is not a symptom of organophosphate poisoning, but patients may experience muscle weakness and fasciculations. Mydriasis, or pupil dilation, is not a symptom of organophosphate poisoning, as it is more commonly seen in cases of ecstasy, cocaine, and hallucinogenic overdose. In organophosphate poisoning, pupillary constriction (miosis) is observed.

      Understanding Organophosphate Insecticide Poisoning

      Organophosphate insecticide poisoning is a condition that occurs when there is an accumulation of acetylcholine in the body, leading to the inhibition of acetylcholinesterase. This, in turn, causes an upregulation of nicotinic and muscarinic cholinergic neurotransmission. In warfare, sarin gas is a highly toxic synthetic organophosphorus compound that has similar effects. The symptoms of organophosphate poisoning can be remembered using the mnemonic SLUD, which stands for salivation, lacrimation, urination, and defecation/diarrhea. Other symptoms include hypotension, bradycardia, small pupils, and muscle fasciculation.

      The management of organophosphate poisoning involves the use of atropine, which helps to counteract the effects of acetylcholine. However, the role of pralidoxime in the treatment of this condition is still unclear. Meta-analyses conducted to date have failed to show any clear benefit of pralidoxime in the management of organophosphate poisoning.

    • This question is part of the following fields:

      • Pharmacology
      11491
      Seconds
  • Question 25 - A 50-year-old male presents to his doctor with severe groin pain that has...

    Incorrect

    • A 50-year-old male presents to his doctor with severe groin pain that has been increasing for the past two days. He also reports developing a fever. He lives with his wife and has no other sexual partners. He is in good health and takes tamsulosin regularly. Upon examination, the doctor notes acute tenderness and swelling in the right testis, leading to a diagnosis of epididymo-orchitis. What is the most probable organism responsible for this patient's symptoms?

      Your Answer: Neisseria gonorrhoeae

      Correct Answer: Escherichia coli

      Explanation:

      Orchitis typically affects post-pubertal males and usually occurs 5-7 days after infection. It is important to note that the relief of pain when the testis is elevated, known as a positive Prehn’s sign, is not present in cases of testicular torsion.

      Epididymo-orchitis is a condition where the epididymis and/or testes become infected, leading to pain and swelling. It is commonly caused by infections spreading from the genital tract or bladder, with Chlamydia trachomatis and Neisseria gonorrhoeae being the usual culprits in sexually active younger adults, while E. coli is more commonly seen in older adults with a low-risk sexual history. Symptoms include unilateral testicular pain and swelling, with urethral discharge sometimes present. Testicular torsion, which can cause ischaemia of the testicle, is an important differential diagnosis and needs to be excluded urgently, especially in younger patients with severe pain and an acute onset.

      Investigations are guided by the patient’s age, with sexually transmitted infections being assessed in younger adults and a mid-stream urine (MSU) being sent for microscopy and culture in older adults with a low-risk sexual history. Management guidelines from the British Association for Sexual Health and HIV (BASHH) recommend ceftriaxone 500 mg intramuscularly as a single dose, plus doxycycline 100 mg orally twice daily for 10-14 days if the organism causing the infection is unknown. Further investigations are recommended after treatment to rule out any underlying structural abnormalities.

    • This question is part of the following fields:

      • Surgery
      45.4
      Seconds
  • Question 26 - A 38-year-old teacher and mother of two presents with back pain. This started...

    Incorrect

    • A 38-year-old teacher and mother of two presents with back pain. This started after lifting some heavy boxes during a move. The pain was initially limited to her lower back but now she has shooting pains radiating down the back of her thigh, the lateral aspect of her leg and into the lateral border of her left foot. The pain can wake her at night if she moves suddenly but does not otherwise disturb her sleep. She is well, without past medical history of note. She reports no lower limb weakness, disturbance of sphincter function, nor any saddle symptoms. Examination reveals a tender lumbar spine, numbness to the lateral border of the left foot and pain on straight leg raise at 40 degrees on the left. There is no limb weakness.
      What is the most appropriate management plan?

      Your Answer: Give analgesia and refer for physiotherapy while arranging a magnetic resonance (MR) scan of the lumbar spine

      Correct Answer: Give analgesia and refer for physiotherapy, with a review after 8 weeks to consider onward referral to a spinal surgeon or musculoskeletal medicine specialist if no better

      Explanation:

      Management of Sciatica: Analgesia and Referral for Physiotherapy

      Sciatica, also known as lumbar radiculopathy, is a common condition caused by a herniated disc, spondylolisthesis, or spinal stenosis. It is characterized by pain, tingling, and numbness that typically extends from the buttocks down to the foot. Diagnosis is made through a positive straight leg raise test. Management involves analgesia and early referral to physiotherapy. Bed rest is not recommended, and patients should continue to stay active. Symptoms usually resolve within 6-8 weeks, but if they persist, referral to a specialist may be necessary for further investigation and management with corticosteroid injections or surgery. Red flag symptoms, such as major motor weakness, urinary/faecal incontinence, saddle anaesthesia, night pain, fever, systemic symptoms, weight loss, past history of cancer, or immunosuppression, require urgent medical attention.

    • This question is part of the following fields:

      • Orthopaedics
      102
      Seconds
  • Question 27 - A 55-year-old woman presents to her primary care physician with complaints of lower...

    Incorrect

    • A 55-year-old woman presents to her primary care physician with complaints of lower abdominal pain and intermittent haematuria over the past two weeks. She has no significant medical history and is not taking any medications. An abdominal ultrasound reveals a bladder lesion, and a flexible cystoscopy is performed, which confirms the presence of carcinoma-in-situ bladder cancer. What would be an appropriate treatment plan for this patient?

      Your Answer: Radical cystectomy

      Correct Answer: Transurethral resection of the superficial lesions

      Explanation:

      Carcinoma in situ (CIS) is a type of bladder cancer that is considered high-grade and superficial. Unlike papillary carcinoma, CIS is more likely to invade surrounding structures. As a result, patients with CIS undergo transurethral removal of bladder tumour (TURBT) and receive intravesicle chemotherapy to reduce the risk of recurrence. Invasive bladder cancer is typically treated with radical cystectomy. It is not recommended to use watchful waiting or active surveillance for CIS in healthy patients due to its invasive potential. Hormone-based therapies are not effective in managing bladder cancer.

      Bladder cancer is the second most common urological cancer, with males aged between 50 and 80 years being the most commonly affected. Smoking and exposure to hydrocarbons such as 2-Naphthylamine increase the risk of the disease. Chronic bladder inflammation from Schistosomiasis infection is a common cause of squamous cell carcinomas in countries where the disease is endemic. Benign tumors of the bladder, including inverted urothelial papilloma and nephrogenic adenoma, are uncommon.

      Urothelial (transitional cell) carcinoma is the most common type of bladder malignancy, accounting for over 90% of cases. Squamous cell carcinoma and adenocarcinoma are less common. Urothelial carcinomas may be solitary or multifocal, with up to 70% having a papillary growth pattern. Superficial tumors have a better prognosis, while solid growths are more prone to local invasion and may be of higher grade, resulting in a worse prognosis. TNM staging is used to determine the extent of the tumor and the presence of nodal or distant metastasis.

      Most patients with bladder cancer present with painless, macroscopic hematuria. Incidental microscopic hematuria may also indicate malignancy in up to 10% of females over 50 years old. Diagnosis is made through cystoscopy and biopsies or transurethral resection of bladder tumor (TURBT), with pelvic MRI and CT scanning used to determine locoregional spread and distant disease. Treatment options include TURBT, intravesical chemotherapy, radical cystectomy with ileal conduit, or radical radiotherapy, depending on the extent and grade of the tumor. Prognosis varies depending on the stage of the tumor, with T1 having a 90% survival rate and any T with N1-N2 having a 30% survival rate.

    • This question is part of the following fields:

      • Surgery
      188.7
      Seconds
  • Question 28 - A 25-year-old female patient visits her GP seeking advice after engaging in unprotected...

    Incorrect

    • A 25-year-old female patient visits her GP seeking advice after engaging in unprotected sexual intercourse the previous night. She took a dose of levonorgestrel 1.5mg (Levonelle) as emergency contraception about 12 hours after the act. Today is the 12th day of her menstrual cycle, and she is worried about the possibility of getting pregnant. She wants to start taking a combined oral contraceptive pill (COCP) to prevent similar situations in the future. When can she begin taking the COCP?

      Your Answer: 72 hours after her dose of levonorgestrel

      Correct Answer: Immediately

      Explanation:

      Levonorgestrel emergency contraception (Levonelle) does not affect the effectiveness of hormonal contraception, so it can be started immediately after use. However, ulipristal acetate emergency contraception (EllaOne) should not be used concurrently with hormonal contraception, and patients should wait 5 days after taking it before starting a COCP regimen. The COCP must be taken within a 24-hour window each day to ensure effectiveness, while levonorgestrel emergency contraception must be taken within 72 hours of unprotected sexual intercourse. The interval to wait before starting or restarting hormonal contraception after using ulipristal acetate emergency contraception is 5 days. Day 1 of the menstrual cycle is the preferred day to start a COCP regimen for immediate protection against pregnancy, but it is not the earliest option in this scenario.

      Emergency contraception is available in the UK through two methods: emergency hormonal contraception and intrauterine device (IUD). Emergency hormonal contraception includes two types of pills: levonorgestrel and ulipristal. Levonorgestrel works by stopping ovulation and inhibiting implantation, while ulipristal primarily inhibits ovulation. Levonorgestrel should be taken as soon as possible after unprotected sexual intercourse, within 72 hours, and is 84% effective when used within this time frame. The dose should be doubled for those with a BMI over 26 or weight over 70kg. Ulipristal should be taken within 120 hours of intercourse and may reduce the effectiveness of hormonal contraception. The most effective method of emergency contraception is the copper IUD, which can be inserted within 5 days of unprotected intercourse or up to 5 days after the likely ovulation date. It may inhibit fertilization or implantation and is 99% effective regardless of where it is used in the cycle. Prophylactic antibiotics may be given if the patient is at high risk of sexually transmitted infection.

    • This question is part of the following fields:

      • Gynaecology
      36.5
      Seconds
  • Question 29 - A 68-year-old rancher comes in with a small white spot on his right...

    Correct

    • A 68-year-old rancher comes in with a small white spot on his right cheek that has been gradually increasing in size over the past few months. It has now developed a central ulcer. What is the probable type of this lesion?

      Your Answer: Basal cell carcinoma

      Explanation:

      Lesion on the Face: Indications of Basal Cell Carcinoma

      A slow-growing lesion on the face with a central ulcer located above a line drawn from the angle of the mouth to the ear lobe is a possible indication of basal cell carcinoma. This type of cancer tends to develop slowly, and the presence of an ulcer in the center of the lesion is a common characteristic. In contrast, squamous cell carcinoma grows much faster than basal cell carcinoma.

      Another skin condition that may be mistaken for basal cell carcinoma is seborrhoeic keratoses. However, seborrhoeic keratoses have a papillary warty surface, which is different from the smooth surface of basal cell carcinoma.

    • This question is part of the following fields:

      • Dermatology
      13
      Seconds
  • Question 30 - A 50-year-old woman comes to the rheumatology clinic with poorly controlled rheumatoid arthritis....

    Incorrect

    • A 50-year-old woman comes to the rheumatology clinic with poorly controlled rheumatoid arthritis. Her hands and feet have been swollen and painful for the past five years, particularly her metacarpophalangeal joints. The stiffness and pain are worse in the morning but improve with use throughout the day. Despite trying methotrexate and sulfasalazine, both treatments have been unsuccessful. The doctor decides to start her on a trial of TNF-inhibitors. What should be done before beginning treatment?

      Your Answer: Liver function test

      Correct Answer: Chest x-ray

      Explanation:

      Performing a chest X-ray before starting biologics for rheumatoid arthritis is crucial to check for TB as these medications can trigger reactivation of the disease. This is the correct answer. An abdominal X-ray is not necessary in this scenario as it is typically used for suspected abdominal perforation. While full blood count and liver function tests are essential monitoring tools for DMARDs, they are not required before initiating treatment due to the risk of myelosuppression and liver cirrhosis.

      Managing Rheumatoid Arthritis with Disease-Modifying Therapies

      The management of rheumatoid arthritis (RA) has significantly improved with the introduction of disease-modifying therapies (DMARDs) in the past decade. Patients with joint inflammation should start a combination of DMARDs as soon as possible, along with analgesia, physiotherapy, and surgery. In 2018, NICE updated their guidelines for RA management, recommending DMARD monotherapy with a short course of bridging prednisolone as the initial step. Monitoring response to treatment is crucial, and NICE suggests using a combination of CRP and disease activity to assess it. Flares of RA are often managed with corticosteroids, while methotrexate is the most widely used DMARD. Other DMARDs include sulfasalazine, leflunomide, and hydroxychloroquine. TNF-inhibitors are indicated for patients with an inadequate response to at least two DMARDs, including methotrexate. Etanercept, infliximab, and adalimumab are some of the TNF-inhibitors available, each with their own risks and administration methods. Rituximab and Abatacept are other DMARDs that can be used, but the latter is not currently recommended by NICE.

    • This question is part of the following fields:

      • Musculoskeletal
      104.9
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SESSION STATS - PERFORMANCE PER SPECIALTY

Surgery (1/5) 20%
Cardiology (1/1) 100%
Endocrinology (0/1) 0%
Neurology (1/2) 50%
Pharmacology (1/2) 50%
Paediatrics (1/5) 20%
Respiratory (1/1) 100%
Orthopaedics (2/3) 67%
Nephrology (0/1) 0%
Infectious Diseases (0/1) 0%
Musculoskeletal (0/2) 0%
Dermatology (2/2) 100%
Emergency Medicine (1/1) 100%
Statistics (1/1) 100%
Neurosurgery (0/1) 0%
Gynaecology (0/1) 0%
Passmed