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Question 1
Incorrect
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A 68-year-old man presents with intermittent dull abdominal pain for the past few weeks. He reports no weight loss but has had one episode of dark, foul-smelling stool in the past week. On examination, he appears well and all vital signs are within normal limits. A rectal exam is unremarkable. Laboratory tests reveal a hemoglobin level of 112 g/L (normal range for males: 135-180 g/L), a hematocrit of 0.38 L/L (normal range: 0.37-0.49 L/L), a mean cell volume of 70 fL (normal range: 80-101 fL), a mean cell hemoglobin of 28 pg (normal range: 27-34 pg), a platelet count of 165 * 109/L (normal range: 150-400 * 109/L), and a white blood cell count of 6.4 * 109/L (normal range: 4.0-11.0 * 109/L). What is the most appropriate next step in management?
Your Answer: Admit to hospital
Correct Answer: Refer on 2 week wait pathway
Explanation:Microcytic Anaemia: Causes and Considerations
Microcytic anaemia is a condition characterized by small red blood cells and low haemoglobin levels. There are several possible causes of microcytic anaemia, including iron-deficiency anaemia, thalassaemia, congenital sideroblastic anaemia, and lead poisoning. It is important to note that while anaemia of chronic disease can also present with microcytosis, it typically appears as a normocytic, normochromic picture.
In some cases, a normal haemoglobin level may be observed alongside microcytosis. This can be a red flag for polycythaemia rubra vera, which can cause iron-deficiency secondary to bleeding. Additionally, new onset microcytic anaemia in elderly patients should be investigated promptly to rule out underlying malignancy. It is worth noting that in beta-thalassaemia minor, the microcytosis may be disproportionate to the anaemia.
Overall, understanding the potential causes and considerations of microcytic anaemia is crucial for proper diagnosis and treatment.
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This question is part of the following fields:
- Gastroenterology/Nutrition
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Question 2
Correct
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What is an accurate statement about alcoholic liver disease (ALD)?
Your Answer: In alcoholic hepatitis the AST : ALT ratio is at least 2 : 1
Explanation:Alcoholic Liver Disease: Facts and Myths
Alcoholic liver disease (ALD) is a common liver disease caused by overconsumption of alcohol. Here are some facts and myths about ALD:
Myth: In alcoholic hepatitis, the AST:ALT ratio is less than 2:1.
Fact: Unlike most other liver diseases, including viral hepatitis, alcoholic hepatitis exhibits at least a 2:1 AST:ALT ratio.Myth: Hepatic iron overload is not indicative of concomitant heterozygote haemochromatosis.
Fact: Evidence of iron overload, such as elevated levels of transferrin saturation and serum ferritin, is common in ALD and may indicate concomitant heterozygote haemochromatosis.Myth: Women are less susceptible to ALD than men.
Fact: Women are actually twice as susceptible to ALD than men, even when consumption is corrected for body weight, and may develop ALD with shorter durations and doses of chronic consumption.Myth: Alcoholic fatty infiltration is irreversible once established.
Fact: Although steatosis (fatty infiltration) will develop in any individual who consumes a large quantity of alcohol over a long period of time, this process is usually transient and reversible. Alcoholic hepatitis and alcoholic fatty infiltration are reversible with abstinence and adequate nutrition.Myth: Alcoholic cirrhosis does not progress to hepatocellular carcinoma.
Fact: Like other causes of liver cirrhosis, alcoholic cirrhosis can also progress to hepatocellular carcinoma.In conclusion, ALD is a serious liver disease that can have irreversible consequences if not addressed in a timely manner. It is important to understand the facts and myths surrounding this disease to ensure proper diagnosis and treatment.
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This question is part of the following fields:
- Gastroenterology/Nutrition
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Question 3
Incorrect
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A 14-year-old girl presents to a gastroenterology clinic with a history of diarrhoea, bloating, and severe abdominal pain for the past 8 months. Her full blood count results are as follows:
Hb 118 g/L Male: (135-180)
Female: (115 - 160)
Platelets 190 * 109/L (150 - 400)
WBC 7.5 * 109/L (4.0 - 11.0)
What would be the most appropriate next investigation?Your Answer: Faecal calprotectin
Correct Answer: Serum immunoglobulin IgA tissue transglutaminase antibody (tTGA) and total IgA
Explanation:Investigating Coeliac Disease
Coeliac disease is a condition caused by sensitivity to gluten, which can lead to villous atrophy and malabsorption. It is often associated with other conditions such as dermatitis herpetiformis and autoimmune disorders. Diagnosis of coeliac disease is made through a combination of serology and endoscopic intestinal biopsy. The gold standard for diagnosis is the biopsy, which should be performed in all patients with suspected coeliac disease to confirm or exclude the diagnosis. The biopsy traditionally takes place in the duodenum, but jejunal biopsies are also sometimes performed. Findings supportive of coeliac disease include villous atrophy, crypt hyperplasia, an increase in intraepithelial lymphocytes, and lamina propria infiltration with lymphocytes. Serology tests for coeliac disease include tissue transglutaminase antibodies and endomyseal antibodies, while anti-gliadin antibodies are not recommended. Patients who are already on a gluten-free diet should reintroduce gluten for at least six weeks prior to testing. Rectal gluten challenge is not widely used. A gluten-free diet can reverse villous atrophy and immunology in patients with coeliac disease.
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This question is part of the following fields:
- Gastroenterology/Nutrition
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Question 4
Correct
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A 60-year-old man who was recently diagnosed with chronic pancreatitis presents to his General Practitioner due to persistent central abdominal pain. This has been present ever since he was admitted to the hospital and diagnosed with chronic pancreatitis; however, he feels that the medication he was prescribed is losing its effects.
The patient is currently on amlodipine, amitriptyline, perindopril and pancreatic enzyme replacement.
Which of the following management options is the best next step to control the patient’s pain?
Select the SINGLE best management plan from the list below.
Select ONE option only.Your Answer: Stop amitriptyline, start duloxetine
Explanation:Managing Neuropathic Pain: Choosing the Right Medication
Neuropathic pain can be a challenging condition to manage, especially when standard analgesia such as non-steroidal anti-inflammatory drugs and paracetamol prove ineffective. According to the National Institute for Health and Care Excellence (NICE) guidelines, the first-line management of neuropathic pain involves starting the patient on amitriptyline, duloxetine, gabapentin or pregabalin. However, if the first-line drug treatment does not work, one of the other drugs can be tried.
It is important to note that drugs for neuropathic pain are typically used as monotherapy rather than in combinations. Therefore, if a drug does not achieve the desired clinical effect, it should be replaced by another drug rather than adding a new drug to it. Duloxetine is a good next option, but it should replace the amitriptyline rather than be added to it.
Further management of neuropathic pain includes pain management clinics and tramadol as rescue therapy for exacerbations of neuropathic pain. By choosing the right medication and following appropriate management strategies, patients with neuropathic pain can achieve better pain control and improved quality of life.
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This question is part of the following fields:
- Gastroenterology/Nutrition
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Question 5
Incorrect
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A 38-year-old man complains of dyspepsia without any alarm symptoms. He has no significant medical history and this is his first episode. The plan is to use a test-and-treat approach. What is the most suitable test to detect Helicobacter pylori?
Your Answer: CLO test (rapid urease test)
Correct Answer: 13C-urea breath test
Explanation:The urea breath test is a non-invasive, highly specific and sensitive method. Therefore, there is no need for an endoscopy. Instead, an alternative option is to use stool antigen instead of culture.
Tests for Helicobacter pylori
There are several tests available to diagnose Helicobacter pylori infection. One of the most common tests is the urea breath test, where patients consume a drink containing carbon isotope 13 (13C) enriched urea. The urea is broken down by H. pylori urease, and after 30 minutes, the patient exhales into a glass tube. Mass spectrometry analysis calculates the amount of 13C CO2, which indicates the presence of H. pylori. However, this test should not be performed within four weeks of treatment with an antibacterial or within two weeks of an antisecretory drug.
Another test is the rapid urease test, also known as the CLO test. This involves mixing a biopsy sample with urea and a pH indicator. If there is a color change, it indicates the presence of H. pylori urease activity. Serum antibody tests can also be used, but they remain positive even after eradication. Culture of gastric biopsy can provide information on antibiotic sensitivity, while histological evaluation alone can be done through gastric biopsy. Lastly, the stool antigen test has a sensitivity of 90% and specificity of 95%.
Overall, these tests have varying levels of sensitivity and specificity, and the choice of test depends on the patient’s clinical presentation and the availability of resources.
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This question is part of the following fields:
- Gastroenterology/Nutrition
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Question 6
Incorrect
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A 75-year-old man presents to the emergency department with acute upper gastrointestinal bleeding due to alcoholic liver cirrhosis. The medical team performs an ABCDE assessment and administers terlipressin. An urgent endoscopy is requested. What medication should be administered to the patient prior to the endoscopy?
Your Answer: Tranexamic acid
Correct Answer: Antibiotic therapy
Explanation:Antibiotic therapy is the appropriate course of action to reduce mortality in cirrhotic patients experiencing gastrointestinal bleeding. Prophylactic antibiotics, particularly quinolones, should be administered alongside terlipressin for individuals suspected of having variceal bleeding. The use of cimetidine is not recommended for acute treatment before endoscopy, but it may be used as a preventative measure for mild acid reflux symptoms. Octreotide is sometimes used as an alternative to terlipressin, but studies indicate that it is less effective in reducing mortality. Propranolol is utilized as a prophylactic measure to decrease the incidence of variceal bleeding.
Variceal haemorrhage is a serious condition that requires prompt management. The initial treatment involves resuscitation of the patient before endoscopy. Correcting clotting with FFP and vitamin K is important, as is the use of vasoactive agents such as terlipressin or octreotide. Prophylactic IV antibiotics are also recommended to reduce mortality in patients with liver cirrhosis. Endoscopic variceal band ligation is the preferred method of treatment, and the use of a Sengstaken-Blakemore tube or Transjugular Intrahepatic Portosystemic Shunt (TIPSS) may be necessary if bleeding cannot be controlled. Propranolol and EVL are effective in preventing rebleeding and mortality, and are recommended by NICE guidelines. Proton pump inhibitor cover is given to prevent EVL-induced ulceration.
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This question is part of the following fields:
- Gastroenterology/Nutrition
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Question 7
Incorrect
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A 65-year-old man is admitted to the hospital with severe abdominal pain that is typically worst shortly after eating a meal. He admits to regularly drinking at least 30 units of alcohol per week for the last 35 years and has recently been diagnosed with type 2 diabetes mellitus by his GP. An abdominal CT scan shows calcification of his pancreas.
What tests can be used to assess the exocrine function of the pancreas, given the likely diagnosis?Your Answer: Serum lipase
Correct Answer: Faecal elastase
Explanation:The most appropriate test to assess exocrine function in chronic pancreatitis is faecal elastase. This is particularly relevant for a patient who has a history of long-term alcohol consumption and has recently been diagnosed with diabetes, which are both common complications of chronic pancreatitis. Faecal calprotectin is not relevant in this context as it is used to diagnose inflammatory bowel diseases. Serum amylase may not be useful in chronic pancreatitis as patients may have normal levels despite loss of pancreatic function. Serum calcium is not used to assess pancreatic function in chronic pancreatitis, but is part of the Glasgow score for acute pancreatitis. Lipase is not typically used to assess exocrine function, but deficiency in this enzyme can lead to steatorrhoea in patients with chronic pancreatitis.
Understanding Chronic Pancreatitis
Chronic pancreatitis is a condition characterized by inflammation that can affect both the exocrine and endocrine functions of the pancreas. While alcohol excess is the leading cause of this condition, up to 20% of cases are unexplained. Other causes include genetic factors such as cystic fibrosis and haemochromatosis, as well as ductal obstruction due to tumors, stones, and structural abnormalities like pancreas divisum and annular pancreas.
Symptoms of chronic pancreatitis include pain that worsens 15 to 30 minutes after a meal, steatorrhoea, and diabetes mellitus. Abdominal x-rays can show pancreatic calcification in 30% of cases, while CT scans are more sensitive at detecting calcification with a sensitivity of 80% and specificity of 85%. Functional tests like faecal elastase may be used to assess exocrine function if imaging is inconclusive.
Management of chronic pancreatitis involves pancreatic enzyme supplements, analgesia, and antioxidants, although the evidence base for the latter is limited. It is important to understand the causes, symptoms, and management of chronic pancreatitis to effectively manage this condition.
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This question is part of the following fields:
- Gastroenterology/Nutrition
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Question 8
Correct
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A 50-year-old man visits the Gastroenterology Clinic with concerns about his tongue. He has noticed unusual patterns on his tongue that have been present for a while, but he is worried about tongue cancer as he has been a heavy smoker for the past 20 years. What is the most suitable initial management option for this patient?
Your Answer: None
Explanation:Geographic Tongue: A Benign Condition Requiring No Medical Intervention
Geographic tongue, also known as benign migratory glossitis, is a common condition that affects up to 3% of the general population. While some patients may experience a burning sensation when consuming hot or spicy foods, most are asymptomatic. The diagnosis of geographic tongue can usually be confirmed from history and physical examination alone, and no medical intervention is required.
Surgical correction is not warranted for geographic tongue, as it is a benign condition of no clinical significance. Aspiration for cytology is also not appropriate, as the diagnosis can be made without further investigation. Excision biopsy may actually cause harm, as histological findings are identical to those seen in pustular psoriasis.
A full blood count is not necessary for the diagnosis of geographic tongue. Instead, the condition can be identified through the elongation of rete ridges, hyperparakeratosis and acanthosis at the periphery, loss of filiform papillae, and migration and clustering of neutrophils within the epithelium towards the centre of the lesions. The predominant inflammatory infiltrates in the lamina propria is neutrophils with an admixture of chronic inflammatory cells.
In summary, geographic tongue is a benign condition that requires no medical intervention. Diagnosis can be made through history and physical examination alone, and further investigation may cause harm.
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This question is part of the following fields:
- Gastroenterology/Nutrition
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Question 9
Correct
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As a foundation year two doctor on the surgical admissions unit, you encounter a thirty-year-old patient complaining of right upper abdominal pain and anorexia. Upon examination, you find an overweight Caucasian female with a soft abdomen that is tender in the right upper quadrant. Her observations indicate fever and mild tachycardia. Blood tests reveal a significantly elevated bilirubin level (87 umol/L). What is the probable diagnosis?
Your Answer: Ascending cholangitis
Explanation:The presence of fever, jaundice and right upper quadrant pain is known as Charcot’s cholangitis triad, which indicates an infection of the bile ducts. This patient is likely suffering from ascending cholangitis. Cholecystitis, which is inflammation of the gallbladder, can also cause right upper quadrant pain and may precede ascending cholangitis. While gallstones are a common cause of cholangitis, they can be asymptomatic and are not a diagnosis on their own. Pregnancy is not a likely cause of right upper quadrant pain. Gilbert’s syndrome typically causes mild jaundice only during times of stress and is usually asymptomatic.
Understanding Ascending Cholangitis
Ascending cholangitis is a bacterial infection that affects the biliary tree, with E. coli being the most common culprit. This condition is often associated with gallstones, which can predispose individuals to the infection. Patients with ascending cholangitis may present with Charcot’s triad, which includes fever, right upper quadrant pain, and jaundice. However, this triad is only present in 20-50% of cases. Other common symptoms include hypotension and confusion. In severe cases, Reynolds’ pentad may be observed, which includes the additional symptoms of hypotension and confusion.
To diagnose ascending cholangitis, ultrasound is typically used as a first-line investigation to look for bile duct dilation and stones. Raised inflammatory markers may also be observed. Treatment involves intravenous antibiotics and endoscopic retrograde cholangiopancreatography (ERCP) after 24-48 hours to relieve any obstruction.
Overall, ascending cholangitis is a serious condition that requires prompt diagnosis and treatment. Understanding the symptoms and risk factors associated with this condition can help individuals seek medical attention early and improve their chances of a successful recovery.
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This question is part of the following fields:
- Gastroenterology/Nutrition
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Question 10
Correct
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A 28-year-old female patient complains of symptoms that suggest coeliac disease. What is the primary test that should be employed for screening individuals with coeliac disease?
Your Answer: Tissue transglutaminase antibodies
Explanation:According to NICE, the initial serological test for coeliac disease should be tissue transglutaminase antibodies.
Investigating Coeliac Disease
Coeliac disease is a condition caused by sensitivity to gluten, which can lead to villous atrophy and malabsorption. It is often associated with other conditions such as dermatitis herpetiformis and autoimmune disorders. Diagnosis of coeliac disease is made through a combination of serology and endoscopic intestinal biopsy. The gold standard for diagnosis is the biopsy, which should be performed in all patients with suspected coeliac disease to confirm or exclude the diagnosis. The biopsy traditionally takes place in the duodenum, but jejunal biopsies are also sometimes performed. Findings supportive of coeliac disease include villous atrophy, crypt hyperplasia, an increase in intraepithelial lymphocytes, and lamina propria infiltration with lymphocytes. Serology tests for coeliac disease include tissue transglutaminase antibodies and endomyseal antibodies, while anti-gliadin antibodies are not recommended. Patients who are already on a gluten-free diet should reintroduce gluten for at least six weeks prior to testing. Rectal gluten challenge is not widely used. A gluten-free diet can reverse villous atrophy and immunology in patients with coeliac disease.
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This question is part of the following fields:
- Gastroenterology/Nutrition
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SESSION STATS - PERFORMANCE PER SPECIALTY
