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Question 1
Incorrect
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A 67-year-old male is admitted to the emergency department after his daughter found him unconscious next to a bottle of pills. She suspects he may have overdosed on his medication for Parkinson's disease.
Upon assessment, he is observed to be sweating profusely, excessively drooling, his pupils are constricted, and he seems disoriented.
What is the appropriate antidote for this situation?Your Answer: Haemodialysis
Correct Answer: Atropine
Explanation:Atropine, an anticholinergic, is used to treat overdose of acetylcholinesterase inhibitors which are commonly used in the treatment of myasthenia gravis. Overdosing on these inhibitors can cause an abnormal increase in acetylcholine concentration in the synaptic cleft, leading to stimulation of the parasympathetic nervous system and potentially resulting in bradycardia and respiratory arrest. Atropine works by reducing parasympathetic nervous system firing, thereby increasing heart rate. However, it cannot reverse respiratory arrest as the brain communicates with the diaphragm using nicotinic acetylcholine receptors. In cases of respiratory arrest, intubation and mechanical ventilation are necessary.
In cases of acidaemia caused by overdoses of salicylates and tricyclic antidepressants, IV bicarbonate is administered.
Varenicline, an agonist for nicotinic acetylcholine receptors, would worsen symptoms in cases of acetylcholinesterase inhibitor overdose. It is typically used for smoking cessation.
N-acetyl cysteine is used to treat paracetamol overdose by replenishing glutathione stores, which aids in the conjugation of the toxic metabolite N-acetyl-p-benzoquinone imine and facilitates excretion.
The management of overdoses and poisonings involves specific treatments for each toxin. For example, in cases of paracetamol overdose, activated charcoal may be given if ingested within an hour, and N-acetylcysteine or liver transplantation may be necessary. Salicylate overdose may require urinary alkalinization with IV bicarbonate or haemodialysis. Opioid/opiate overdose can be treated with naloxone, while benzodiazepine overdose may require flumazenil, although this is only used in severe cases due to the risk of seizures. Tricyclic antidepressant overdose may require IV bicarbonate to reduce the risk of seizures and arrhythmias, while lithium toxicity may respond to volume resuscitation with normal saline or haemodialysis. Warfarin overdose can be treated with vitamin K or prothrombin complex, while heparin overdose may require protamine sulphate. Beta-blocker overdose may require atropine or glucagon. Ethylene glycol poisoning can be treated with fomepizole or ethanol, while methanol poisoning may require the same treatment or haemodialysis. Organophosphate insecticide poisoning can be treated with atropine, and digoxin overdose may require digoxin-specific antibody fragments. Iron overdose may require desferrioxamine, and lead poisoning may require dimercaprol or calcium edetate. Carbon monoxide poisoning can be treated with 100% oxygen or hyperbaric oxygen, while cyanide poisoning may require hydroxocobalamin or a combination of amyl nitrite, sodium nitrite, and sodium thiosulfate.
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This question is part of the following fields:
- General Principles
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Question 2
Incorrect
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A 38-year-old woman comes to see her GP complaining of increasing fatigue, especially towards the end of the day. During the consultation, she mentions having difficulty swallowing and experiencing two instances of almost choking on her dinner. Her husband has also noticed that her speech becomes quieter in the evenings, almost like a whisper.
Upon examination in the morning, there are no significant findings except for some bilateral eyelid twitching after looking at the floor briefly.
What is the likely diagnosis, and what is the mechanism of action of the first-line treatment?Your Answer: Increases the breakdown of acetylcholine at the neuromuscular junction
Correct Answer: Increases the amount of acetylcholine reaching the postsynaptic receptors
Explanation:Pyridostigmine is a medication that inhibits the breakdown of acetylcholine in the neuromuscular junction, leading to an increase in the amount of acetylcholine that reaches the postsynaptic receptors. This temporary improvement in symptoms is particularly beneficial for individuals with myasthenia gravis, who experience increased fatigue following exercise, quiet speech, and difficulty swallowing. Pyridostigmine is considered a first-line treatment for MG, as it directly affects the acetylcholinesterase inhibitors and not the postsynaptic receptors.
Myasthenia gravis is an autoimmune disorder that results in muscle weakness and fatigue, particularly in the eyes, face, neck, and limbs. It is more common in women and is associated with thymomas and other autoimmune disorders. Diagnosis is made through electromyography and testing for antibodies to acetylcholine receptors. Treatment includes acetylcholinesterase inhibitors and immunosuppression, and in severe cases, plasmapheresis or intravenous immunoglobulins may be necessary.
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This question is part of the following fields:
- Neurological System
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Question 3
Correct
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How can we describe the structure of the cell membrane? This vital component is present in all mammalian cells and is composed of lipids, proteins, carbohydrates, and other structures. The arrangement of these components is often referred to as the fluid mosaic model.
Your Answer: A phospholipid bilayer with hydrophobic tails directly apposed with the hydrophilic heads facing the cytosolic and extracellular environments
Explanation:The Fluid Mosaic Model of the Cell Membrane
The cell membrane is composed of a bilayer of phospholipids with hydrophilic heads and hydrophobic tails. This arrangement allows for the passive diffusion of hydrophobic molecules while preventing the transfer of polar solutes. Cholesterol is also present in the membrane, with higher concentrations leading to greater insulation. The cell membrane is supported by a complex network of microtubules and microfilaments, which can assist in modulating the cell’s shape and allow for endocytosis and exocytosis. These processes involve the invagination of the substrate and formation of a vesicle before expelling it into the intracellular or extracellular compartment. The cytoskeleton also plays a role in internal scaffolding, cilia, filopodia, and microvilli. The fluid mosaic model of the cell membrane describes the arrangement of these components as a floating sandwich with the heads facing the cytosolic and extracellular compartments.
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This question is part of the following fields:
- Clinical Sciences
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Question 4
Incorrect
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Which section of the digestive system is primarily involved in the enterohepatic circulation?
Your Answer: Pancreas
Correct Answer: Terminal ileum
Explanation:The Enterohepatic Circulation and Bile Recycling
The enterohepatic circulation is a process that allows for the recycling of certain waste materials that are excreted in the bile. This process occurs at the terminal ileum, where bile salts and some bilirubin derivatives are reabsorbed and returned to the liver through the portal circulation. The regulation of this process involves transporter proteins in both the liver canaliculi and the ileum.
Bacterial flora in the colon also play a role in the enterohepatic circulation of bilirubin derivatives. Some bacteria contain an enzyme called beta-glucuronidase, which converts conjugated bilirubin to unconjugated bilirubin. This unconjugated form is more lipid-soluble and can be more easily reabsorbed.
Overall, the enterohepatic circulation is an important mechanism for bile recycling and waste management in the body.
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This question is part of the following fields:
- Clinical Sciences
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Question 5
Incorrect
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A 42-year-old female arrives at the emergency department with sudden onset of drooping on the right side of her mouth. She is unable to smile on the right-hand side but can frown and lift her eyebrows. The patient has a medical history of asthma and has experienced four miscarriages in the past. She does not smoke and drinks alcohol moderately on weekends. Based on this information, what is the probable diagnosis?
Your Answer: Bell's palsy
Correct Answer: Stroke
Explanation:If a facial palsy only affects the lower face and spares the forehead, it is likely caused by an upper motor neuron (UMN) lesion. In this case, stroke is the most probable cause of the UMN lesion. However, the patient’s young age and social history make stroke less likely. The patient’s history of multiple miscarriages suggests antiphospholipid syndrome, which is a significant risk factor for stroke. Bell’s palsy, HIV, diabetes mellitus, and acoustic neuroma would all cause lower motor neuron (LMN) lesions, resulting in LMN signs that involve the forehead.
The facial nerve is responsible for supplying the muscles of facial expression, the digastric muscle, and various glandular structures. It also contains a few afferent fibers that originate in the genicular ganglion and are involved in taste. Bilateral facial nerve palsy can be caused by conditions such as sarcoidosis, Guillain-Barre syndrome, Lyme disease, and bilateral acoustic neuromas. Unilateral facial nerve palsy can be caused by these conditions as well as lower motor neuron disease like Bell’s palsy and upper motor neuron disease like stroke.
The upper motor neuron lesion typically spares the upper face, specifically the forehead, while a lower motor neuron lesion affects all facial muscles. The facial nerve path includes the subarachnoid path, where it originates in the pons and passes through the petrous temporal bone into the internal auditory meatus with the vestibulocochlear nerve. The facial canal path passes superior to the vestibule of the inner ear and contains the geniculate ganglion at the medial aspect of the middle ear. The stylomastoid foramen is where the nerve passes through the tympanic cavity anteriorly and the mastoid antrum posteriorly, and it also includes the posterior auricular nerve and branch to the posterior belly of the digastric and stylohyoid muscle.
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This question is part of the following fields:
- Neurological System
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Question 6
Incorrect
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In the Vaughan Williams classification of antihypertensives, lisinopril is an example of a:
Your Answer: Class III agent
Correct Answer: Class IV agent
Explanation:The Vaughan Williams Classification of Antiarrhythmics
The Vaughan Williams classification is a widely used system for categorizing antiarrhythmic drugs based on their mechanism of action. The classification system is divided into four classes, each with a different mechanism of action. Class I drugs block sodium channels, Class II drugs are beta-adrenoceptor antagonists, Class III drugs block potassium channels, and Class IV drugs are calcium channel blockers.
Class Ia drugs, such as quinidine and procainamide, increase the duration of the action potential by blocking sodium channels. However, quinidine toxicity can cause cinchonism, which is characterized by symptoms such as headache, tinnitus, and thrombocytopenia. Procainamide may also cause drug-induced lupus.
Class Ib drugs, such as lidocaine and mexiletine, decrease the duration of the action potential by blocking sodium channels. Class Ic drugs, such as flecainide and propafenone, have no effect on the duration of the action potential but still block sodium channels.
Class II drugs, such as propranolol and metoprolol, are beta-adrenoceptor antagonists that decrease the heart rate and contractility of the heart.
Class III drugs, such as amiodarone and sotalol, block potassium channels, which prolongs the duration of the action potential.
Class IV drugs, such as verapamil and diltiazem, are calcium channel blockers that decrease the influx of calcium ions into the heart, which slows down the heart rate and reduces contractility.
It should be noted that some common antiarrhythmic drugs, such as adenosine, atropine, digoxin, and magnesium, are not included in the Vaughan Williams classification.
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This question is part of the following fields:
- General Principles
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Question 7
Correct
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A 70-year-old man presents with haemoptysis and undergoes a bronchoscopy. The carina is noted to be widened. Where does the trachea bifurcate?
Your Answer: T5
Explanation:The trachea divides into two branches at the fifth thoracic vertebrae, or sometimes the sixth in individuals who are tall.
Anatomy of the Trachea
The trachea, also known as the windpipe, is a tube-like structure that extends from the C6 vertebrae to the upper border of the T5 vertebrae where it bifurcates into the left and right bronchi. It is supplied by the inferior thyroid arteries and the thyroid venous plexus, and innervated by branches of the vagus, sympathetic, and recurrent nerves.
In the neck, the trachea is anterior to the isthmus of the thyroid gland, inferior thyroid veins, and anastomosing branches between the anterior jugular veins. It is also surrounded by the sternothyroid, sternohyoid, and cervical fascia. Posteriorly, it is related to the esophagus, while laterally, it is in close proximity to the common carotid arteries, right and left lobes of the thyroid gland, inferior thyroid arteries, and recurrent laryngeal nerves.
In the thorax, the trachea is anterior to the manubrium, the remains of the thymus, the aortic arch, left common carotid arteries, and the deep cardiac plexus. Laterally, it is related to the pleura and right vagus on the right side, and the left recurrent nerve, aortic arch, and left common carotid and subclavian arteries on the left side.
Overall, understanding the anatomy of the trachea is important for various medical procedures and interventions, such as intubation and tracheostomy.
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This question is part of the following fields:
- Respiratory System
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Question 8
Incorrect
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A 31-year-old arrives at the Emergency Department by ambulance after being involved in a car accident. During the ABCDE assessment, it is discovered that the patient has suffered a penetrating injury at the T9 level.
Following an MRI of the spine and consultation with a neurologist, the patient is diagnosed with Brown-Sequard syndrome on the left side.
What symptoms can be expected from this patient's condition?Your Answer: Bilateral loss of motor, with some loss of vibration and proprioception
Correct Answer: Left-sided loss of motor, vibration and proprioception, with right-sided loss of pain and temperature sensation
Explanation:The spinothalamic tract crosses over at the same level where the nerve root enters the spinal cord, while the corticospinal tract, dorsal column medial lemniscus, and spinocerebellar tracts cross over at the medulla.
Brown-Sequard syndrome affects one entire side of the spinal cord, resulting in the loss of motor function, vibration, and proprioception on the left side, and loss of pain and temperature sensation on the right side.
In Brown-Sequard syndrome, the loss of motor function, vibration, and proprioception occurs on the same side due to the corticospinal tract and dorsal column medial meniscus crossing over at the medulla. The loss of pain and temperature sensation occurs on the opposite side due to the crossing over of the tract at the nerve root.
Anterior cord syndrome affects the descending corticospinal tract and ascending spinothalamic tract, leading to the loss of motor function, pain, and temperature sensation below the injury site. However, proprioception and vibration sensation remain unaffected as the dorsal columns are spared.
Central cord syndrome results in the loss of motor function on both sides, as well as some loss of vibration and proprioception.
Posterior cord syndrome affects the dorsal column medial lemniscus, leading to the loss of proprioception and vibration sensation on the same side. This condition can be caused by neck hyperflexion, disc compression, ischaemia, vitamin B12 deficiency, or multiple sclerosis.
The spinal cord is a central structure located within the vertebral column that provides it with structural support. It extends rostrally to the medulla oblongata of the brain and tapers caudally at the L1-2 level, where it is anchored to the first coccygeal vertebrae by the filum terminale. The cord is characterised by cervico-lumbar enlargements that correspond to the brachial and lumbar plexuses. It is incompletely divided into two symmetrical halves by a dorsal median sulcus and ventral median fissure, with grey matter surrounding a central canal that is continuous with the ventricular system of the CNS. Afferent fibres entering through the dorsal roots usually terminate near their point of entry but may travel for varying distances in Lissauer’s tract. The key point to remember is that the anatomy of the cord will dictate the clinical presentation in cases of injury, which can be caused by trauma, neoplasia, inflammatory diseases, vascular issues, or infection.
One important condition to remember is Brown-Sequard syndrome, which is caused by hemisection of the cord and produces ipsilateral loss of proprioception and upper motor neuron signs, as well as contralateral loss of pain and temperature sensation. Lesions below L1 tend to present with lower motor neuron signs. It is important to keep a clinical perspective in mind when revising CNS anatomy and to understand the ways in which the spinal cord can become injured, as this will help in diagnosing and treating patients with spinal cord injuries.
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This question is part of the following fields:
- Neurological System
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Question 9
Incorrect
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A 45-year-old woman comes to the clinic complaining of polyuria. Upon further inquiry, she reports experiencing polyphagia and polydipsia as well. Her blood test reveals hyperglycaemia and low C-peptide levels.
What is the underlying mechanism causing her hyperglycaemia?Your Answer: Decreased GLUT-3 expression
Correct Answer: Decreased GLUT-4 expression
Explanation:The movement of glucose into cells requires insulin. In this case, the patient is likely suffering from type 1 diabetes mellitus or latent autoimmune diabetes in adults (LADA) with low c-peptide levels, indicating a complete lack of insulin. As a result, insulin is unable to stimulate the expression of GLUT-4, which significantly reduces the uptake of glucose into skeletal and adipose cells.
The patient’s low GLUT-1 expression is unlikely to be the cause of hyperglycemia. GLUT-1 is primarily expressed in fetal tissues and has a higher affinity for oxygen, allowing fetal cells to survive even in hypoglycemic conditions.
GLUT-2 expression is mainly found in hepatocytes and beta-cells of the pancreas. It allows for the bi-directional movement of glucose, equalizing glucose concentrations inside and outside the cell membrane, and enabling glucose-sensitive cells to measure serum glucose levels and respond accordingly.
GLUT-3 expression is mainly found in neuronal cells and has a high affinity, similar to GLUT-1. This allows for the survival of brain cells in hypoglycemic conditions.
Insulin is a hormone produced by the pancreas that plays a crucial role in regulating the metabolism of carbohydrates and fats in the body. It works by causing cells in the liver, muscles, and fat tissue to absorb glucose from the bloodstream, which is then stored as glycogen in the liver and muscles or as triglycerides in fat cells. The human insulin protein is made up of 51 amino acids and is a dimer of an A-chain and a B-chain linked together by disulfide bonds. Pro-insulin is first formed in the rough endoplasmic reticulum of pancreatic beta cells and then cleaved to form insulin and C-peptide. Insulin is stored in secretory granules and released in response to high levels of glucose in the blood. In addition to its role in glucose metabolism, insulin also inhibits lipolysis, reduces muscle protein loss, and increases cellular uptake of potassium through stimulation of the Na+/K+ ATPase pump.
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This question is part of the following fields:
- Endocrine System
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Question 10
Incorrect
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As a medical student working with a geriatric care team, we recently conducted a blood test on a patient with a history of microcytic anemia. Our goal was to determine if a blood transfusion was necessary. At what Hb level is a transfusion typically recommended for elderly patients?
Your Answer: Hb <8g/dl
Correct Answer:
Explanation:According to the NICE guidelines, patients who require red blood cell transfusions but do not have major bleeding, acute coronary syndrome, or chronic anemia requiring regular transfusions should receive transfusions with a restrictive threshold. This threshold should be set at 7g/dl, with a target hemoglobin concentration of 7-9 g/dl after transfusion. For patients with acute coronary syndrome, a threshold of 8g/dl and a target hemoglobin concentration of 8-10g/dl after transfusion should be considered. For patients with chronic anemia requiring regular transfusions, individual thresholds and hemoglobin concentration targets should be established.
Understanding Microcytic Anaemia
Microcytic anaemia is a condition characterized by small red blood cells that result in a decrease in the amount of oxygen carried in the blood. There are several causes of microcytic anaemia, including iron-deficiency anaemia, thalassaemia, congenital sideroblastic anaemia, and lead poisoning. In some cases, microcytosis may be associated with a normal haemoglobin level, which could indicate the possibility of polycythaemia rubra vera. It is important to note that new onset microcytic anaemia in elderly patients should be urgently investigated to exclude underlying malignancy.
Beta-thalassaemia minor is a type of microcytic anaemia where the microcytosis is often disproportionate to the anaemia. It is important to identify the underlying cause of microcytic anaemia to determine the appropriate treatment. Iron-deficiency anaemia is the most common cause of microcytic anaemia and can be treated with iron supplements. Thalassaemia may require blood transfusions or bone marrow transplantation. Congenital sideroblastic anaemia may require treatment with vitamin B6 supplements. Lead poisoning can be treated by removing the source of lead exposure and chelation therapy. Overall, early diagnosis and treatment of microcytic anaemia can improve outcomes and prevent complications.
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This question is part of the following fields:
- Haematology And Oncology
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Question 11
Correct
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A teenager comes to the clinic with an inability to flex his arm at the elbow and reduced sensation in the deltoid region after falling down the stairs. The diagnosis reveals axillary nerve palsy. What could be the probable reason for this?
Your Answer: Shoulder dislocation or fracture
Explanation:Axillary nerve palsy is most commonly caused by dislocation or fracture near the shoulder, rather than trauma to the axilla or chest wall. Medial epicondyle fractures do not typically result in axillary nerve palsy, but it is possible for trauma to the humerus to lead to this condition.
The shoulder joint is a shallow synovial ball and socket joint that is inherently unstable but capable of a wide range of movement. Stability is provided by the muscles of the rotator cuff. The glenoid labrum is a fibrocartilaginous rim attached to the free edge of the glenoid cavity. The fibrous capsule attaches to the scapula, humerus, and tendons of various muscles. Movements of the shoulder joint are controlled by different muscles. The joint is closely related to important anatomical structures such as the brachial plexus, axillary artery and vein, and various nerves and vessels.
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This question is part of the following fields:
- Musculoskeletal System And Skin
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Question 12
Correct
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What are the vitamins that are soluble in fat?
Your Answer: Vitamins A, D, E and K
Explanation:Absorption of Fat-Soluble Vitamins
Fat-soluble vitamins, namely A, D, E, and K, have a different absorption process compared to water-soluble vitamins. In the gut, these vitamins are combined with other fat-soluble substances such as monoacylglycerols and cholesterol to form micelles. These micelles are then transported to the lymphatic system and eventually enter the bloodstream through the subclavian vein.
However, any issues that affect the absorption of fats will also impact the absorption of fat-soluble vitamins. This means that individuals with conditions that affect fat absorption, such as cystic fibrosis or celiac disease, may have difficulty absorbing these vitamins. It is important to ensure adequate intake of fat-soluble vitamins through a balanced diet or supplements to prevent deficiencies and associated health problems.
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This question is part of the following fields:
- Basic Sciences
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Question 13
Correct
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A 45-year-old obese woman presents to the Emergency Department complaining of sudden lower back pain. Upon conducting a neurological examination, you observe a decrease in the left knee jerk reflex compared to the right. Which spinal level does this correspond to?
Your Answer: L3-L4
Explanation:Memory aid for common reflexes:
S1-S2, buckle my shoe (ankle)
L3-L4, kick the door (knee)
C5-C6, pick up sticks (biceps)
C7-C8, shut the gate (triceps)The reflex tested by tapping the knee is the L3-L4 reflex.
Reflexes are automatic responses that our body makes in response to certain stimuli. These responses are controlled by the nervous system and do not require conscious thought. There are several common reflexes that are associated with specific roots in the spinal cord. For example, the ankle reflex is associated with the S1-S2 root, while the knee reflex is associated with the L3-L4 root. Similarly, the biceps reflex is associated with the C5-C6 root, and the triceps reflex is associated with the C7-C8 root. Understanding these reflexes can help healthcare professionals diagnose and treat certain conditions.
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This question is part of the following fields:
- Neurological System
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Question 14
Incorrect
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A 54-year-old woman comes to her GP complaining of a gradual increase in numbness and tingling in her right hand's ring and little fingers. She works as a librarian and denies any physical strain or injury. There is no significant medical history or family history of similar symptoms.
The woman reports that her symptoms are causing her to take frequent breaks from work and is worried about losing her job.
What is the primary pathology most commonly associated with her symptoms?Your Answer: Nerve arises from C5 of the brachial plexus
Correct Answer: Nerve entrapment of the medial epicondyle
Explanation:The correct answer is nerve entrapment of the medial epicondyle. The ulnar nerve provides sensory innervation to the palmar and dorsal aspects of the 4th and 5th digits, and it travels posterior to the medial epicondyle through the ulnar tunnel. Medial epicondylitis, an over-use injury of the flexor-pronator muscles, can cause ulnar nerve damage.
The other answer choices are incorrect. The radial nerve supplies dorsal sensation to the thumb and wrist extension, while the ulnar nerve arises from C8-T1 of the brachial plexus. Fracture of the humeral shaft is associated with radial nerve damage, not ulnar nerve damage.
The ulnar nerve originates from the medial cord of the brachial plexus, specifically from the C8 and T1 nerve roots. It provides motor innervation to various muscles in the hand, including the medial two lumbricals, adductor pollicis, interossei, hypothenar muscles (abductor digiti minimi, flexor digiti minimi), and flexor carpi ulnaris. Sensory innervation is also provided to the medial 1 1/2 fingers on both the palmar and dorsal aspects. The nerve travels through the posteromedial aspect of the upper arm and enters the palm of the hand via Guyon’s canal, which is located superficial to the flexor retinaculum and lateral to the pisiform bone.
The ulnar nerve has several branches that supply different muscles and areas of the hand. The muscular branch provides innervation to the flexor carpi ulnaris and the medial half of the flexor digitorum profundus. The palmar cutaneous branch arises near the middle of the forearm and supplies the skin on the medial part of the palm, while the dorsal cutaneous branch supplies the dorsal surface of the medial part of the hand. The superficial branch provides cutaneous fibers to the anterior surfaces of the medial one and one-half digits, and the deep branch supplies the hypothenar muscles, all the interosseous muscles, the third and fourth lumbricals, the adductor pollicis, and the medial head of the flexor pollicis brevis.
Damage to the ulnar nerve at the wrist can result in a claw hand deformity, where there is hyperextension of the metacarpophalangeal joints and flexion at the distal and proximal interphalangeal joints of the 4th and 5th digits. There may also be wasting and paralysis of intrinsic hand muscles (except for the lateral two lumbricals), hypothenar muscles, and sensory loss to the medial 1 1/2 fingers on both the palmar and dorsal aspects. Damage to the nerve at the elbow can result in similar symptoms, but with the addition of radial deviation of the wrist. It is important to diagnose and treat ulnar nerve damage promptly to prevent long-term complications.
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This question is part of the following fields:
- Neurological System
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Question 15
Incorrect
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A 32-year-old woman arrives at the emergency department complaining of sudden shortness of breath and a sharp pain on the right side of her chest that worsens with inspiration. Upon examination, the doctor observes hyper-resonance and reduced breath sounds on the right side of her chest.
What is a risk factor for this condition, considering the probable diagnosis?Your Answer: Female sex
Correct Answer: Cystic fibrosis
Explanation:Pneumothorax can be identified by reduced breath sounds and a hyper-resonant chest on the same side as the pain. Cystic fibrosis is a significant risk factor for pneumothorax due to the frequent chest infections, lung remodeling, and air trapping associated with the disease. While tall, male smokers are also at increased risk, Marfan’s syndrome, not Turner syndrome, is a known risk factor.
Pneumothorax: Characteristics and Risk Factors
Pneumothorax is a medical condition characterized by the presence of air in the pleural cavity, which is the space between the lungs and the chest wall. This condition can occur spontaneously or as a result of trauma or medical procedures. There are several risk factors associated with pneumothorax, including pre-existing lung diseases such as COPD, asthma, cystic fibrosis, lung cancer, and Pneumocystis pneumonia. Connective tissue diseases like Marfan’s syndrome and rheumatoid arthritis can also increase the risk of pneumothorax. Ventilation, including non-invasive ventilation, can also be a risk factor.
Symptoms of pneumothorax tend to come on suddenly and can include dyspnoea, chest pain (often pleuritic), sweating, tachypnoea, and tachycardia. In some cases, catamenial pneumothorax can be the cause of spontaneous pneumothoraces occurring in menstruating women. This type of pneumothorax is thought to be caused by endometriosis within the thorax. Early diagnosis and treatment of pneumothorax are crucial to prevent complications and improve outcomes.
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This question is part of the following fields:
- Respiratory System
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Question 16
Incorrect
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A 50-year-old woman presents to the Emergency Department with a several-hour history of excruciating pain in the left knee. Her medical history is significant for hypertension and a previous episode of gout. She takes amlodipine.
On examination, she is in severe pain and the left knee is swollen, red, warm and tender. Arthroscopic evaluation of the synovial fluid aspirate showed monosodium crystals that are negatively birefringent under polarized light. A diagnosis of recurrent gout is made and ultimately the patient is commenced on prophylaxis using allopurinol.
What is the mechanism of action of allopurinol?Your Answer: Inhibits dihydrofolate reductase
Correct Answer: Inhibits xanthine oxidase
Explanation:Allopurinol is a medication that inhibits xanthine oxidase, which is used for gout prophylaxis. By blocking the conversion of hypoxanthine to xanthine and xanthine to uric acid, it reduces the levels of uric acid in the blood. The other options, such as inhibition of dihydrofolate reductase, ribonucleotide reductase, and thymidylate synthase, are not related to gout prophylaxis. Rasburicase, which oxidizes urate to allantoin, is also used for gout prophylaxis, but it works differently than allopurinol.
Allopurinol can interact with other medications such as azathioprine, cyclophosphamide, and theophylline. It can lead to high levels of 6-mercaptopurine when used with azathioprine, reduced renal clearance when used with cyclophosphamide, and an increase in plasma concentration of theophylline. Patients at a high risk of severe cutaneous adverse reaction should be screened for the HLA-B *5801 allele.
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This question is part of the following fields:
- General Principles
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Question 17
Incorrect
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A 68-year-old man with a history of bladder cancer due to beta-naphthylamine exposure presents with painless haematuria and suprapubic pain. He underwent successful surgical resection for bladder cancer 5 years ago and is now retired as a chemical engineer. The urology team suspects a possible recurrence with locoregional spread. What imaging modality is most suitable for determining the extent of cancer spread in this patient?
Your Answer: Ultrasound scan of the bladder
Correct Answer: Pelvic MRI
Explanation:The most effective imaging technique for identifying the locoregional spread of bladder cancer is pelvic MRI.
Bladder cancer is a common urological cancer that primarily affects males aged 50-80 years old. Smoking and exposure to hydrocarbons increase the risk of developing the disease. Chronic bladder inflammation from Schistosomiasis infection is also a common cause of squamous cell carcinomas in countries where the disease is endemic. Benign tumors of the bladder, such as inverted urothelial papilloma and nephrogenic adenoma, are rare. The most common bladder malignancies are urothelial (transitional cell) carcinoma, squamous cell carcinoma, and adenocarcinoma. Urothelial carcinomas may be solitary or multifocal, with papillary growth patterns having a better prognosis. The remaining tumors may be of higher grade and prone to local invasion, resulting in a worse prognosis.
The TNM staging system is used to describe the extent of bladder cancer. Most patients present with painless, macroscopic hematuria, and a cystoscopy and biopsies or TURBT are used to provide a histological diagnosis and information on depth of invasion. Pelvic MRI and CT scanning are used to determine locoregional spread, and PET CT may be used to investigate nodes of uncertain significance. Treatment options include TURBT, intravesical chemotherapy, surgery (radical cystectomy and ileal conduit), and radical radiotherapy. The prognosis varies depending on the stage of the cancer, with T1 having a 90% survival rate and any T, N1-N2 having a 30% survival rate.
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This question is part of the following fields:
- Renal System
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Question 18
Incorrect
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A 67-year-old patient is being evaluated after being admitted for treatment of a persistent Clostridium difficile infection. The patient had received treatment for a previous infection three weeks ago, but the symptoms did not subside, and she continued to experience diarrhoea. The patient was hospitalized three days ago due to a life-threatening Clostridium difficile infection.
The patient has been receiving oral vancomycin and IV metronidazole for the past few days, but there has been no improvement in her symptoms. What would be the venous blood gas results in this case?Your Answer: Metabolic acidosis + hyperkalaemia
Correct Answer: Metabolic acidosis + hypokalaemia
Explanation:If a patient experiences prolonged diarrhoea, they may develop metabolic acidosis and hypokalaemia. This is likely the case for a patient with a history of prolonged Clostridium difficile infection, as the loss of bicarbonate ions from the GI tract during diarrhoea can lead to metabolic acidosis. Prolonged diarrhoea can also result in hypokalaemia due to the direct loss of potassium from the GI tract, which the body may be unable to compensate for. Therefore, metabolic acidosis and hypokalaemia are the expected outcomes in this scenario.
Understanding Metabolic Acidosis
Metabolic acidosis is a condition that can be classified based on the anion gap, which is calculated by subtracting the sum of chloride and bicarbonate from the sum of sodium and potassium. The normal range for anion gap is 10-18 mmol/L. If a question provides the chloride level, it may be an indication to calculate the anion gap.
Hyperchloraemic metabolic acidosis is a type of metabolic acidosis with a normal anion gap. It can be caused by gastrointestinal bicarbonate loss, prolonged diarrhea, ureterosigmoidostomy, fistula, renal tubular acidosis, drugs like acetazolamide, ammonium chloride injection, and Addison’s disease. On the other hand, raised anion gap metabolic acidosis is caused by lactate, ketones, urate, acid poisoning, and other factors.
Lactic acidosis is a type of metabolic acidosis that is caused by high lactate levels. It can be further classified into two types: lactic acidosis type A, which is caused by sepsis, shock, hypoxia, and burns, and lactic acidosis type B, which is caused by metformin. Understanding the different types and causes of metabolic acidosis is important in diagnosing and treating the condition.
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This question is part of the following fields:
- Renal System
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Question 19
Incorrect
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Which one of the following is not part of the rectus sheath?
Your Answer: Pyramidalis
Correct Answer: Internal iliac artery
Explanation:The rectus sheath includes the inferior epigastric artery and the superior epigastric vein.
Muscles and Layers of the Abdominal Wall
The abdominal wall is composed of various muscles and layers that provide support and protection to the organs within the abdominal cavity. The two main muscles of the abdominal wall are the rectus abdominis and the quadratus lumborum. The rectus abdominis is located anteriorly, while the quadratus lumborum is located posteriorly.
The remaining abdominal wall is made up of three muscular layers, each passing from the lateral aspect of the quadratus lumborum to the lateral margin of the rectus sheath. These layers are muscular posterolaterally and aponeurotic anteriorly. The external oblique muscle lies most superficially and originates from the 5th to 12th ribs, inserting into the anterior half of the outer aspect of the iliac crest, linea alba, and pubic tubercle. The internal oblique arises from the thoracolumbar fascia, the anterior 2/3 of the iliac crest, and the lateral 2/3 of the inguinal ligament, while the transversus abdominis is the innermost muscle, arising from the inner aspect of the costal cartilages of the lower 6 ribs, the anterior 2/3 of the iliac crest, and the lateral 1/3 of the inguinal ligament.
During abdominal surgery, it is often necessary to divide either the muscles or their aponeuroses. It is desirable to divide the aponeurosis during a midline laparotomy, leaving the rectus sheath intact above the arcuate line and the muscles intact below it. Straying off the midline can lead to damage to the rectus muscles, particularly below the arcuate line where they may be in close proximity to each other. The nerve supply for these muscles is the anterior primary rami of T7-12.
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This question is part of the following fields:
- Musculoskeletal System And Skin
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Question 20
Incorrect
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A 26-year-old woman presents to the emergency department with abdominal pain and vaginal bleeding. She is currently 8 weeks pregnant and has not experienced any complications thus far. During a speculum examination, an open cervical os and a small amount of bleeding are observed. An ultrasound confirms the presence of intrauterine fetal tissue, but no heartbeat is detected. The physician diagnoses an inevitable miscarriage and discusses management options with the patient. She opts for medical management using misoprostol. What is the purpose of this medication in the treatment of miscarriage?
Your Answer: Stimulates the release of oxytocin to cause uterine contractions
Correct Answer: Prostaglandin analog that causes uterine contractions
Explanation:Misoprostol is a medication that mimics the effects of prostaglandins, leading to the contraction of the uterus and the expulsion of fetal tissue. It is commonly used in the medical treatment of miscarriage, but it does not have any pain-relieving properties. Pain during a miscarriage is typically managed with other medications like ibuprofen, paracetamol, and codeine. Misoprostol also does not have any effect on blood loss, which is usually light and does not require treatment. In contrast, methotrexate is a medication that destroys rapidly dividing cells and is used to manage ectopic pregnancies. Finally, it’s important to note that misoprostol does not stimulate the release of oxytocin.
Drugs Used in Obstetrics and Gynaecology
Syntocinon is a synthetic form of oxytocin that is utilized in the active management of the third stage of labor. It aids in the contraction of the uterus, which reduces the risk of postpartum hemorrhage. Additionally, it is used to induce labor. Ergometrine, an ergot alkaloid, is an alternative to oxytocin in the active management of the third stage of labor. It can decrease blood loss by constricting the vascular smooth muscle of the uterus. Its mechanism of action involves stimulating alpha-adrenergic, dopaminergic, and serotonergic receptors. However, it can cause coronary artery spasm as an adverse effect.
Mifepristone is used in combination with misoprostol to terminate pregnancies. Misoprostol is a prostaglandin analog that causes uterine contractions. Mifepristone is a competitive progesterone receptor antagonist. Its mechanism of action involves blocking the effects of progesterone, which is necessary for the maintenance of pregnancy. However, it can cause menorrhagia as an adverse effect.
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This question is part of the following fields:
- General Principles
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