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Question 1
Correct
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A 35-year-old male presents to the emergency department complaining of gradual onset sharp chest pain over the past 24 hours. The patient reports that the pain worsens with deep inspiration and feels more comfortable when sitting leaning forward. When asked about pain radiation, the patient confirms that the pain extends to the left side of the neck and points to the ridge of the trapezius. Physical examination reveals clear lung fields, regular rhythm with quiet heart sounds, and no murmurs. The patient's vital signs are as follows:
Blood pressure: 108/66 mmHg
Pulse rate: 94 bpm
Respiratory rate: 18 rpm
Temperature: 37.3ºC
Oxygen saturations: 97% on room air
What is the most likely diagnosis?Your Answer: Acute pericarditis
Explanation:Radiation to the trapezius ridge is a distinct symptom of acute pericarditis. The patient in question exhibits characteristics that align with a diagnosis of pericarditis. Pericarditis is a common condition affecting the pericardium, and it is often considered as a potential cause for chest pain. It is worth noting that the specific radiation of pain to the trapezius ridge is highly indicative of pericarditis, as it occurs when the phrenic nerve, which also innervates the trapezius muscle, becomes irritated while passing through the pericardium.
Further Reading:
Pericarditis is an inflammation of the pericardium, which is the protective sac around the heart. It can be acute, lasting less than 6 weeks, and may present with chest pain, cough, dyspnea, flu-like symptoms, and a pericardial rub. The most common causes of pericarditis include viral infections, tuberculosis, bacterial infections, uremia, trauma, and autoimmune diseases. However, in many cases, the cause remains unknown. Diagnosis is based on clinical features, such as chest pain, pericardial friction rub, and electrocardiographic changes. Treatment involves symptom relief with nonsteroidal anti-inflammatory drugs (NSAIDs), and patients should avoid strenuous activity until symptoms improve. Complicated cases may require treatment for the underlying cause, and large pericardial effusions may need urgent drainage. In cases of purulent effusions, antibiotic therapy is necessary, and steroid therapy may be considered for pericarditis related to autoimmune disorders or if NSAIDs alone are ineffective.
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This question is part of the following fields:
- Cardiology
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Question 2
Incorrect
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A 72 year old male comes to the emergency department with complaints of vertigo. What signs would indicate a central cause?
Your Answer: Positive Romberg's test
Correct Answer: Negative head impulse test
Explanation:A patient with central vertigo would typically show a normal head impulse test result, indicating a normal vestibulo-ocular reflex. However, they would likely have an abnormal alternate cover test result, with a slight vertical correction, suggesting a central lesion like a stroke. A positive Romberg’s test can identify instability related to vertigo but cannot differentiate between peripheral and central causes. On the other hand, a positive Unterberger’s test indicates labyrinth dysfunction but does not indicate a central cause.
Further Reading:
Vertigo is a symptom characterized by a false sensation of movement, such as spinning or rotation, in the absence of any actual physical movement. It is not a diagnosis itself, but rather a description of the sensation experienced by the individual. Dizziness, on the other hand, refers to a perception of disturbed or impaired spatial orientation without a false sense of motion.
Vertigo can be classified as either peripheral or central. Peripheral vertigo is more common and is caused by problems in the inner ear that affect the labyrinth or vestibular nerve. Examples of peripheral vertigo include BPPV, vestibular neuritis, labyrinthitis, and Meniere’s disease. Central vertigo, on the other hand, is caused by pathology in the brain, such as in the brainstem or cerebellum. Examples of central vertigo include migraine, TIA and stroke, cerebellar tumor, acoustic neuroma, and multiple sclerosis.
There are certain features that can help differentiate between peripheral and central vertigo. Peripheral vertigo is often associated with severe nausea and vomiting, hearing loss or tinnitus, and a positive head impulse test. Central vertigo may be characterized by prolonged and severe vertigo, new-onset headache, recent trauma, cardiovascular risk factors, inability to stand or walk with eyes open, focal neurological deficit, and a negative head impulse test.
Nystagmus, an involuntary eye movement, can also provide clues about the underlying cause of vertigo. Central causes of vertigo often have nystagmus that is direction-changing on lateral gaze, purely vertical or torsional, not suppressed by visual fixation, non-fatigable, and commonly large amplitude. Peripheral causes of vertigo often have horizontal nystagmus with a torsional component that does not change direction with gaze, disappears with fixation of the gaze, and may have large amplitude early in the course of Meniere’s disease or vestibular neuritis.
There are various causes of vertigo, including viral labyrinthitis, vestibular neuritis, benign paroxysmal positional vertigo, Meniere’s disease, vertebrobasilar ischemia, and acoustic neuroma. Each of these disorders has its own unique characteristics and may be associated with other symptoms such as hearing loss, tinnitus, or neurological deficits.
When assessing a patient with vertigo, it is important to perform a cardiovascular and neurological examination, including assessing cranial nerves, cerebellar signs, eye movements, gait, coordination, and evidence of peripheral neuropathy.
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This question is part of the following fields:
- Neurology
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Question 3
Correct
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A 5 year old girl is brought into the emergency room. Her mother witnessed her putting something in her mouth. She believes it was a small object, but the girl swallowed it and within 5 minutes her face began to swell. You determine that she is experiencing anaphylaxis and start administering the necessary first-line medications. After stabilizing her condition, you decide to administer cetirizine. What is the appropriate dosage of cetirizine for this patient?
Your Answer: Cetirizine 2.5–5 mg
Explanation:Antihistamines do not help in treating the life-threatening aspects of anaphylaxis and should not be used instead of adrenaline. However, they can be used to relieve symptoms such as skin reactions and itching once the patient’s condition has stabilized. The appropriate dose of cetirizine for children between the ages of 2 and 6 is 2.5-5 mg. It is important to note that chlorpheniramine is no longer recommended. The recommended doses of oral cetirizine for different age groups are as follows: less than 2 years – 250 micrograms/kg, 2-6 years – 2.5-5 mg, 6-11 years – 5-10 mg, 12 years and older – 10-20 mg.
Further Reading:
Anaphylaxis is a severe and life-threatening allergic reaction that affects the entire body. It is characterized by a rapid onset and can lead to difficulty breathing, low blood pressure, and loss of consciousness. In paediatrics, anaphylaxis is often caused by food allergies, with nuts being the most common trigger. Other causes include drugs and insect venom, such as from a wasp sting.
When treating anaphylaxis, time is of the essence and there may not be enough time to look up medication doses. Adrenaline is the most important drug in managing anaphylaxis and should be administered as soon as possible. The recommended doses of adrenaline vary based on the age of the child. For children under 6 months, the dose is 150 micrograms, while for children between 6 months and 6 years, the dose remains the same. For children between 6 and 12 years, the dose is increased to 300 micrograms, and for adults and children over 12 years, the dose is 500 micrograms. Adrenaline can be repeated every 5 minutes if necessary.
The preferred site for administering adrenaline is the anterolateral aspect of the middle third of the thigh. This ensures quick absorption and effectiveness of the medication. It is important to follow the Resuscitation Council guidelines for anaphylaxis management, as they have recently been updated.
In some cases, it can be challenging to determine if a patient had a true episode of anaphylaxis. In such cases, serum tryptase levels may be measured, as they remain elevated for up to 12 hours following an acute episode of anaphylaxis. This can help confirm the diagnosis and guide further management.
Overall, prompt recognition and administration of adrenaline are crucial in managing anaphylaxis in paediatrics. Following the recommended doses and guidelines can help ensure the best outcomes for patients experiencing this severe allergic reaction.
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This question is part of the following fields:
- Paediatric Emergencies
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Question 4
Incorrect
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You are present at a pediatric cardiac arrest. The cardiac arrest team has, unfortunately, been unable to establish IV access, and an intraosseous needle is inserted. The child weighs 20 kg.
What is the appropriate dose of adrenaline to administer via the IO route in this situation?Your Answer: 150 mcg
Correct Answer: 300 mcg
Explanation:When administering adrenaline to a pediatric patient experiencing cardiac arrest, the dosage given through the intraosseous (IO) route is identical to that given through the intravenous (IV) route. Both routes require a dosage of 10 mcg/kg. For instance, if the child weighs 30 kg, the appropriate dosage would be 300 mcg (0.3 mg).
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This question is part of the following fields:
- Paediatric Emergencies
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Question 5
Correct
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A 32-year-old woman comes in with a history of urgency, bloody diarrhea, and crampy abdominal pain for the past 8 weeks. She occasionally experiences pain before having a bowel movement, but it is relieved once the stool is passed. A sigmoidoscopy is conducted, and a rectal biopsy reveals the presence of inflammatory cell infiltrate and crypt abscesses.
What is the SINGLE most probable diagnosis?Your Answer: Ulcerative colitis
Explanation:In a young patient who has been experiencing bloody diarrhea for more than 6 weeks, it is important to consider inflammatory bowel disease as a possible diagnosis. The challenge lies in distinguishing between ulcerative colitis and Crohn’s disease. In this case, a biopsy was performed and the results showed the presence of inflammatory cell infiltrate and crypt abscesses, which strongly suggests a diagnosis of ulcerative colitis.
Ulcerative colitis:
– Typically affects only the rectum and colon
– The terminal ileum may be affected if backwash ileitis occurs
– Does not have skip lesions (areas of normal mucosa between affected areas)
– Decreased incidence in smokers
– Common associations include liver conditions such as primary biliary cirrhosis, chronic active hepatitis, and primary sclerosing cholangitis
– Other systemic manifestations are less common compared to Crohn’s disease
– Pathological features include primarily affecting the mucosa and submucosa, presence of mucosal ulcers, inflammatory cell infiltrate, and crypt abscesses
– Clinical features include less prominent abdominal pain, bloody diarrhea in 90% of cases, passage of mucus, and possible fever
– Barium studies may show a granular appearance, button-shaped ulcers, and loss of normal haustral markings
– Complications include a 20-fold increase in the 20-year risk of colonic carcinoma, iron deficiency anemia, and rare occurrence of fistulaeCrohn’s disease:
– Can affect any part of the gastrointestinal tract from the mouth to the anus
– May have skip lesions of normal mucosa between affected areas
– Increased incidence in smokers
– Systemic manifestations are more common compared to ulcerative colitis, including erythema nodosum, pyoderma gangrenosum, iritis/uveitis, cholelithiasis, and joint pain/arthropathy
– Pathological features include transmural inflammation, presence of lymphoid aggregates and neutrophil infiltrates, and non-caseating granulomas seen in 30% of cases
– Clinical features include more prominent abdominal pain, common occurrence of diarrhea (which can also be bloody), frequent and oral lesions, and possible fever
– Barium studies may show severe mucosal ulcers -
This question is part of the following fields:
- Gastroenterology & Hepatology
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Question 6
Incorrect
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A 75 year old man is brought into the emergency room by ambulance. He started with a cough about a week ago but now appears somewhat confused and drowsy. His vital signs are as follows:
Temperature: 37.9ºC
Blood pressure: 98/65 mmHg
Respiration rate: 22 rpm
Pulse rate: 105 bpm
Blood glucose: 6.9 mmol/l
SpO2: 91% on air rising to 96% on 2L oxygen
Which of the above parameters, if any, would be a cause for concern indicating sepsis?Your Answer: Pulse rate of 105 beats per minute
Correct Answer: SpO2 of 91% on air rising to 96% on 2L oxygen
Explanation:This individual’s condition should be closely monitored and they should be promptly placed on the Sepsis pathway due to the presence of red flags. Please refer to the notes below for a comprehensive list of red and amber flags.
Further Reading:
There are multiple definitions of sepsis, leading to confusion among healthcare professionals. The Sepsis 3 definition describes sepsis as life-threatening organ dysfunction caused by a dysregulated host response to infection. The Sepsis 2 definition includes infection plus two or more SIRS criteria. The NICE definition states that sepsis is a clinical syndrome triggered by the presence of infection in the blood, activating the body’s immune and coagulation systems. The Sepsis Trust defines sepsis as a dysregulated host response to infection mediated by the immune system, resulting in organ dysfunction, shock, and potentially death.
The confusion surrounding sepsis terminology is further compounded by the different versions of sepsis definitions, known as Sepsis 1, Sepsis 2, and Sepsis 3. The UK organizations RCEM and NICE have not fully adopted the changes introduced in Sepsis 3, causing additional confusion. While Sepsis 3 introduces the use of SOFA scores and abandons SIRS criteria, NICE and the Sepsis Trust have rejected the use of SOFA scores and continue to rely on SIRS criteria. This discrepancy creates challenges for emergency department doctors in both exams and daily clinical practice.
To provide some clarity, RCEM now recommends referring to national standards organizations such as NICE, SIGN, BTS, or others relevant to the area. The Sepsis Trust, in collaboration with RCEM and NICE, has published a toolkit that serves as a definitive reference point for sepsis management based on the sepsis 3 update.
There is a consensus internationally that the terms SIRS and severe sepsis are outdated and should be abandoned. Instead, the terms sepsis and septic shock should be used. NICE defines septic shock as a life-threatening condition characterized by low blood pressure despite adequate fluid replacement and organ dysfunction or failure. Sepsis 3 defines septic shock as persisting hypotension requiring vasopressors to maintain a mean arterial pressure of 65 mmHg or more, along with a serum lactate level greater than 2 mmol/l despite adequate volume resuscitation.
NICE encourages clinicians to adopt an approach of considering sepsis in all patients, rather than relying solely on strict definitions. Early warning or flag systems can help identify patients with possible sepsis.
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This question is part of the following fields:
- Infectious Diseases
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Question 7
Incorrect
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You assess a patient who has recently been diagnosed with chronic myeloid leukemia (CML).
Which ONE statement about CML is accurate?Your Answer: A blast crisis can be diagnosed when 20% of the blood cells in the bone marrow are immature blast cells
Correct Answer: The Philadelphia chromosome is present in over 80% of cases
Explanation:Chronic myeloid leukaemia (CML) is a type of blood disorder that arises from an abnormal pluripotent haemopoietic stem cell. The majority of CML cases, more than 80%, are caused by a cytogenetic abnormality called the Philadelphia chromosome. This abnormality occurs when there is a reciprocal translocation between the long arms of chromosomes 9 and 22.
CML typically develops slowly over a period of several years, known as the chronic stage. During this stage, patients usually do not experience any symptoms, and it is often discovered incidentally through routine blood tests. Around 90% of CML cases are diagnosed during this stage. In the bone marrow, less than 10% of the white cells are immature blasts.
Symptoms start to appear when the CML cells begin to expand, which is known as the accelerated stage. Approximately 10% of cases are diagnosed during this stage. Between 10 and 30% of the blood cells in the bone marrow are blasts at this point. Common clinical features during this stage include tiredness, fatigue, fever, night sweats, abdominal distension, left upper quadrant pain (splenic infarction), splenomegaly (enlarged spleen), hepatomegaly (enlarged liver), easy bruising, gout (due to rapid cell turnover), and hyperviscosity (which can lead to complications like stroke, priapism, etc.).
In some cases, a small number of patients may present with a blast crisis, also known as the blast stage. During this stage, more than 30% of the blood cells in the bone marrow are immature blast cells. Patients in this stage are generally very ill, experiencing severe constitutional symptoms such as fever, weight loss, and bone pain, as well as infections and bleeding tendencies.
Laboratory findings in CML include a significantly elevated white cell count (often greater than 100 x 109/l), a left shift with an increased number of immature leukocytes, mild to moderate normochromic, normocytic anaemia, variable platelet counts (low, normal, or elevated), presence of the Philadelphia chromosome in more than 80% of cases, and elevated levels of serum uric acid and alkaline phosphatase.
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This question is part of the following fields:
- Haematology
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Question 8
Correct
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A 45-year-old man presents with severe nausea and recurrent vomiting. The vomiting episodes occur every few weeks and are accompanied by colicky abdominal pain. However, his bowel movements are normal. He reports that the only relief he gets during these episodes is by taking hot baths. He has no significant medical history but admits to being a heavy and regular cannabis user. A complete set of blood tests and an abdominal X-ray are performed, both of which come back normal.
What is the most probable diagnosis in this case?Your Answer: Cannabinoid hyperemesis syndrome
Explanation:Cannabinoid hyperemesis syndrome (CHS) is an extremely rare form of cannabinoid toxicity that occurs in chronic smokers. It is characterized by recurring episodes of severe nausea and vomiting. One distinctive feature of this syndrome is that individuals who suffer from it often find relief from their symptoms by taking hot baths or showers, and they may compulsively bathe during episodes of nausea and vomiting.
CHS typically develops in heavy, long-term cannabis users who consume the drug multiple times a day for many years. On average, symptoms appear after about 16 years of cannabis use, although some patients may experience symptoms after as little as three years.
In 2009, Sontineni and colleagues established criteria for diagnosing cannabinoid hyperemesis syndrome. These criteria include essential factors such as long-term cannabis use, major factors like severe nausea and vomiting that occur in a cyclic pattern over months, and resolution of symptoms after discontinuing cannabis use. Supportive criteria include compulsive hot baths with symptom relief, colicky abdominal pain, and no evidence of inflammation in the gallbladder or pancreas.
The exact cause of CHS is not fully understood, but there are two main theories. One theory suggests that the syndrome is a result of a build-up of cannabinoids in the body, which leads to toxicity. Another theory proposes that the functionality of cannabinoid receptors in the brain, particularly in the hypothalamus, is affected, resulting in CHS.
Most conventional anti-emetic drugs are effective in treating the vomiting phase of CHS. During acute episodes, it is important to monitor the patient’s hydration status as the combination of hot baths and prolonged vomiting can lead to cannabinoid hyperemesis acute renal failure (CHARF). This can be easily prevented and treated with intravenous fluids.
Once the acute episode of vomiting and dehydration has been addressed, the condition can be easily cured by discontinuing cannabis consumption.
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This question is part of the following fields:
- Gastroenterology & Hepatology
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Question 9
Correct
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A 35-year-old woman comes in with complaints of painful urination and frequent urination. A urine dipstick test is conducted, which shows the presence of blood, protein, white blood cells, and nitrites. Based on these findings, you diagnose her with a urinary tract infection and prescribe antibiotics.
Which antibiotic has the highest resistance rate against E.coli in the UK?Your Answer: Trimethoprim
Explanation:Nitrofurantoin is currently the preferred antibiotic for treating uncomplicated urinary tract infections in non-pregnant women. However, antibiotic resistance is becoming a significant concern in the management of urinary tract infections and pyelonephritis in the UK. In England, the resistance of E. coli (the main bacteria causing these infections) to certain antibiotics is as follows:
Trimethoprim: 30.3% (varies between areas from 27.1% to 33.4%)
Co-amoxiclav: 19.8% (varies between areas from 10.8% to 30.7%)
Ciprofloxacin: 10.6% (varies between areas from 7.8% to 13.7%)
Cefalexin: 9.9% (varies between areas from 8.1% to 11.4%) -
This question is part of the following fields:
- Urology
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Question 10
Incorrect
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A 2-week-old baby comes in with vomiting, decreased weight, and an electrolyte imbalance. After being referred to the pediatricians, they are diagnosed with congenital adrenal hyperplasia (CAH).
Which ONE statement is correct about this condition?Your Answer: The commonest cause is 11-beta-hydroxylase deficiency
Correct Answer: Diagnosis can be made by finding elevated 17-hydroxyprogesterone levels
Explanation:Congenital adrenal hyperplasia (CAH) is a group of inherited disorders that are caused by autosomal recessive genes. The majority of affected patients, over 90%, have a deficiency of the enzyme 21-hydroxylase. This enzyme is encoded by the 21-hydroxylase gene, which is located on chromosome 6p21 within the HLA histocompatibility complex. The second most common cause of CAH is a deficiency of the enzyme 11-beta-hydroxylase. The condition is rare, with an incidence of approximately 1 in 500 births in the UK. It is more prevalent in the offspring of consanguineous marriages.
The deficiency of 21-hydroxylase leads to a deficiency of cortisol and/or aldosterone, as well as an excess of precursor steroids. As a result, there is an increased secretion of ACTH from the anterior pituitary, leading to adrenocortical hyperplasia.
The severity of CAH varies depending on the degree of 21-hydroxylase deficiency. Female infants often exhibit ambiguous genitalia, such as clitoral hypertrophy and labial fusion. Male infants may have an enlarged scrotum and/or scrotal pigmentation. Hirsutism, or excessive hair growth, occurs in 10% of cases.
Boys with CAH often experience a salt-losing adrenal crisis at around 1-3 weeks of age. This crisis is characterized by symptoms such as vomiting, weight loss, floppiness, and circulatory collapse.
The diagnosis of CAH can be made by detecting markedly elevated levels of the metabolic precursor 17-hydroxyprogesterone. Neonatal screening is possible, primarily through the identification of persistently elevated 17-hydroxyprogesterone levels.
In infants presenting with a salt-losing crisis, the following biochemical abnormalities are observed: hyponatremia (low sodium levels), hyperkalemia (high potassium levels), metabolic acidosis, and hypoglycemia.
Boys experiencing a salt-losing crisis will require fluid resuscitation, intravenous dextrose, and intravenous hydrocortisone.
Affected females will require corrective surgery for their external genitalia. However, they have an intact uterus and ovaries and are capable of having children.
The long-term management of both sexes involves lifelong replacement of hydrocortisone (to suppress ACTH levels).
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This question is part of the following fields:
- Endocrinology
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Question 11
Incorrect
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A 35 year old patient is brought into the resuscitation bay by paramedics after being rescued from a lake. The patient has a core temperature of 29.5ºC. CPR is in progress. What modifications, if any, would you make to the administration of adrenaline in a patient with a core temperature below 30ºC?
Your Answer: No change to dose
Correct Answer: Withhold adrenaline
Explanation:The administration of IV drugs (adrenaline and amiodarone) should be delayed until the core body temperature of patients with severe hypothermia reaches above 30°C, as recommended by the resus council.
Further Reading:
Cardiopulmonary arrest is a serious event with low survival rates. In non-traumatic cardiac arrest, only about 20% of patients who arrest as an in-patient survive to hospital discharge, while the survival rate for out-of-hospital cardiac arrest is approximately 8%. The Resus Council BLS/AED Algorithm for 2015 recommends chest compressions at a rate of 100-120 per minute with a compression depth of 5-6 cm. The ratio of chest compressions to rescue breaths is 30:2.
After a cardiac arrest, the goal of patient care is to minimize the impact of post cardiac arrest syndrome, which includes brain injury, myocardial dysfunction, the ischaemic/reperfusion response, and the underlying pathology that caused the arrest. The ABCDE approach is used for clinical assessment and general management. Intubation may be necessary if the airway cannot be maintained by simple measures or if it is immediately threatened. Controlled ventilation is aimed at maintaining oxygen saturation levels between 94-98% and normocarbia. Fluid status may be difficult to judge, but a target mean arterial pressure (MAP) between 65 and 100 mmHg is recommended. Inotropes may be administered to maintain blood pressure. Sedation should be adequate to gain control of ventilation, and short-acting sedating agents like propofol are preferred. Blood glucose levels should be maintained below 8 mmol/l. Pyrexia should be avoided, and there is some evidence for controlled mild hypothermia but no consensus on this.
Post ROSC investigations may include a chest X-ray, ECG monitoring, serial potassium and lactate measurements, and other imaging modalities like ultrasonography, echocardiography, CTPA, and CT head, depending on availability and skills in the local department. Treatment should be directed towards the underlying cause, and PCI or thrombolysis may be considered for acute coronary syndrome or suspected pulmonary embolism, respectively.
Patients who are comatose after ROSC without significant pre-arrest comorbidities should be transferred to the ICU for supportive care. Neurological outcome at 72 hours is the best prognostic indicator of outcome.
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This question is part of the following fields:
- Environmental Emergencies
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Question 12
Incorrect
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You are present for the unexpected delivery of a baby in one of the cubicles in the Emergency Department. Your consultant evaluates the newborn one minute after birth and informs you that:
The hands and feet appear bluish in color
The heart rate is 110 beats per minute
There is no response to stimulation
There is slight bending of the limbs
The cry is feeble, and the baby is gasping for breath
What is the Apgar score of the newborn at one minute?Your Answer: 2
Correct Answer: 5
Explanation:The Apgar score is a straightforward way to evaluate the well-being of a newborn baby right after birth. It consists of five criteria, each assigned a score ranging from zero to two. Typically, the assessment is conducted at one and five minutes after delivery, with the possibility of repeating it later if the score remains low. A score of 7 or higher is considered normal, while a score of 4-6 is considered fairly low, and a score of 3 or below is regarded as critically low. To remember the five criteria, you can use the acronym APGAR:
Appearance
Pulse rate
Grimace
Activity
Respiratory effortThe Apgar score criteria are as follows:
Score of 0:
Appearance (skin color): Blue or pale all over
Pulse rate: Absent
Reflex irritability (grimace): No response to stimulation
Activity: None
Respiratory effort: AbsentScore of 1:
Appearance (skin color): Blue at extremities (acrocyanosis)
Pulse rate: Less than 100 per minute
Reflex irritability (grimace): Grimace on suction or aggressive stimulation
Activity: Some flexion
Respiratory effort: Weak, irregular, gaspingScore of 2:
Appearance (skin color): No cyanosis, body and extremities pink
Pulse rate: More than 100 per minute
Reflex irritability (grimace): Cry on stimulation
Activity: Flexed arms and legs that resist extension
Respiratory effort: Strong, robust cry -
This question is part of the following fields:
- Neonatal Emergencies
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Question 13
Correct
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A 65 year old female is brought into the emergency department by her husband following a fall. The patient seems unsure about how the fall occurred. The patient's husband takes you aside to express his growing concern about the patient's memory and overall functioning in the past year. He has previously suggested visiting the doctor about it, but the patient has consistently refused, claiming to be perfectly fine. The patient's husband is worried that the patient might be suffering from dementia. What is the leading cause of dementia?
Your Answer: Alzheimer's disease
Explanation:Dementia is a condition characterized by a decline in cognitive abilities, such as memory, thinking, and reasoning, that is severe enough to interfere with daily functioning. There are several different causes of dementia, but the leading cause is Alzheimer’s disease. Alzheimer’s disease is a progressive brain disorder that affects memory, thinking, and behavior. It is the most common cause of dementia, accounting for approximately 60-80% of cases.
Further Reading:
Dementia is a progressive and irreversible clinical syndrome characterized by cognitive and behavioral symptoms. These symptoms include memory loss, impaired reasoning and communication, personality changes, and reduced ability to carry out daily activities. The decline in cognition affects multiple domains of intellectual functioning and is not solely due to normal aging.
To diagnose dementia, a person must have impairment in at least two cognitive domains that significantly impact their daily activities. This impairment cannot be explained by delirium or other major psychiatric disorders. Early-onset dementia refers to dementia that develops before the age of 65.
The most common cause of dementia is Alzheimer’s disease, accounting for 50-75% of cases. Other causes include vascular dementia, dementia with Lewy bodies, and frontotemporal dementia. Less common causes include Parkinson’s disease dementia, Huntington’s disease, prion disease, and metabolic and endocrine disorders.
There are several risk factors for dementia, including age, mild cognitive impairment, genetic predisposition, excess alcohol intake, head injury, depression, learning difficulties, diabetes, obesity, hypertension, smoking, Parkinson’s disease, low social engagement, low physical activity, low educational attainment, hearing impairment, and air pollution.
Assessment of dementia involves taking a history from the patient and ideally a family member or close friend. The person’s current level of cognition and functional capabilities should be compared to their baseline level. Physical examination, blood tests, and cognitive assessment tools can also aid in the diagnosis.
Differential diagnosis for dementia includes normal age-related memory changes, mild cognitive impairment, depression, delirium, vitamin deficiencies, hypothyroidism, adverse drug effects, normal pressure hydrocephalus, and sensory deficits.
Management of dementia involves a multi-disciplinary approach that includes non-pharmacological and pharmacological measures. Non-pharmacological interventions may include driving assessment, modifiable risk factor management, and non-pharmacological therapies to promote cognition and independence. Drug treatments for dementia should be initiated by specialists and may include acetylcholinesterase inhibitors, memantine, and antipsychotics in certain cases.
In summary, dementia is a progressive and irreversible syndrome characterized by cognitive and behavioral symptoms. It has various causes and risk factors, and its management involves a multi-disciplinary approach.
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This question is part of the following fields:
- Neurology
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Question 14
Correct
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A fit and healthy 40-year-old woman presents with a sudden onset of facial palsy that began 48 hours ago. After conducting a thorough history and examination, a diagnosis of Bell's palsy is determined.
Which of the following statements about Bell's palsy is NOT true?Your Answer: It typically spares the upper facial muscles
Explanation:Bell’s palsy is a condition characterized by a facial paralysis that affects the lower motor neurons. It can be distinguished from an upper motor neuron lesion by the individual’s inability to raise their eyebrow and the involvement of the upper facial muscles.
One notable feature of Bell’s palsy is the occurrence of Bell’s phenomenon, which refers to the upward and outward rolling of the eye on the affected side when attempting to close the eye and bare the teeth.
Approximately 80% of sudden onset lower motor neuron facial palsies are attributed to Bell’s palsy. It is believed that this condition is caused by swelling of the facial nerve within the petrous temporal bone, which is thought to be a result of a latent herpesvirus, specifically HSV-1 and HZV.
Treatment for Bell’s palsy often involves the use of steroids and acyclovir. These medications can help alleviate symptoms and promote recovery.
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This question is part of the following fields:
- Ear, Nose & Throat
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Question 15
Correct
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You are called to a VF cardiac arrest in the resus area of your Pediatric Emergency Department.
Epinephrine should be administered at which of the following points during a pediatric VF arrest?Your Answer: After the 3rd shock once chest compressions have been resumed
Explanation:Adrenaline is recommended to be administered after the third shock in a shockable cardiac arrest (Vf/pVT) once chest compressions have been resumed. The recommended dose is 1 mg, which can be administered as either 10 mL of a 1:10,000 solution or 1 mL of a 1:1000 solution.
Subsequently, adrenaline should be given every 3-5 minutes, alternating with chest compressions. It is important to administer adrenaline without interrupting chest compressions to ensure continuous circulation and maximize the chances of successful resuscitation.
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This question is part of the following fields:
- Cardiology
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Question 16
Correct
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A 35 year old male is brought into the emergency department after being found disoriented and lethargic by a family member. The family member informs you that the patient has a history of depression and that there were multiple empty bottles of aspirin at the patient's residence. Initial tests are conducted, including a salicylate level. Upon reviewing the salicylate result, you commence the urinary alkalinisation protocol. What is the desired treatment range?
Your Answer: Urinary pH is 7.5-8.5
Explanation:Urinary alkalinisation aims to achieve a urinary pH of 7.5-8.5. This process helps enhance the elimination of salicylates. It is important to regularly monitor urinary pH, ideally on an hourly basis.
Further Reading:
Salicylate poisoning, particularly from aspirin overdose, is a common cause of poisoning in the UK. One important concept to understand is that salicylate overdose leads to a combination of respiratory alkalosis and metabolic acidosis. Initially, the overdose stimulates the respiratory center, leading to hyperventilation and respiratory alkalosis. However, as the effects of salicylate on lactic acid production, breakdown into acidic metabolites, and acute renal injury occur, it can result in high anion gap metabolic acidosis.
The clinical features of salicylate poisoning include hyperventilation, tinnitus, lethargy, sweating, pyrexia (fever), nausea/vomiting, hyperglycemia and hypoglycemia, seizures, and coma.
When investigating salicylate poisoning, it is important to measure salicylate levels in the blood. The sample should be taken at least 2 hours after ingestion for symptomatic patients or 4 hours for asymptomatic patients. The measurement should be repeated every 2-3 hours until the levels start to decrease. Other investigations include arterial blood gas analysis, electrolyte levels (U&Es), complete blood count (FBC), coagulation studies (raised INR/PTR), urinary pH, and blood glucose levels.
To manage salicylate poisoning, an ABC approach should be followed to ensure a patent airway and adequate ventilation. Activated charcoal can be administered if the patient presents within 1 hour of ingestion. Oral or intravenous fluids should be given to optimize intravascular volume. Hypokalemia and hypoglycemia should be corrected. Urinary alkalinization with intravenous sodium bicarbonate can enhance the elimination of aspirin in the urine. In severe cases, hemodialysis may be necessary.
Urinary alkalinization involves targeting a urinary pH of 7.5-8.5 and checking it hourly. It is important to monitor for hypokalemia as alkalinization can cause potassium to shift from plasma into cells. Potassium levels should be checked every 1-2 hours.
In cases where the salicylate concentration is high (above 500 mg/L in adults or 350 mg/L in children), sodium bicarbonate can be administered intravenously. Hemodialysis is the treatment of choice for severe poisoning and may be indicated in cases of high salicylate levels, resistant metabolic acidosis, acute kidney injury, pulmonary edema, seizures and coma.
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This question is part of the following fields:
- Pharmacology & Poisoning
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Question 17
Incorrect
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A 14 year old boy is brought into the emergency department after being bitten on the leg while playing in the woods near his neighborhood. The patient claims that the bite was from a snake that he saw quickly disappear into the bushes after biting him. You present the patient with pictures of native snake species in the area, and the patient identifies the common Eastern garter snake as the culprit. Which of the following statements is accurate regarding the treatment of bites from this particular snake species?
Your Answer: The patient should receive heparin as the snake venom causes a hypercoagulable state
Correct Answer: The affected limb should immobilised in a sling
Explanation:The key components of first aid for snake bites in the UK involve immobilizing the patient and the affected limb, as well as administering paracetamol for pain relief. When it comes to venomous snake bites, it is important to immobilize the limb using a splint or sling, but not to use a tourniquet or pressure bandage for adder bites. In certain areas, such as NSW, Australia, where venomous snakes can cause rapidly progressing and life-threatening paralysis, pressure bandage immobilization is recommended. However, this is not the case in the UK. Anti-venom is not always necessary for adder bites, and its administration should be based on a thorough assessment of the patient’s condition and the presence of appropriate indications. Paracetamol is the preferred choice for pain relief in UK snake bites, as aspirin and ibuprofen can worsen bleeding tendencies that may result from adder bites. Similarly, heparin should be avoided for the same reason.
Further Reading:
Snake bites in the UK are primarily caused by the adder, which is the only venomous snake species native to the country. While most adder bites result in minor symptoms such as pain, swelling, and inflammation, there have been cases of life-threatening illness and fatalities. Additionally, there are instances where venomous snakes that are kept legally or illegally also cause bites in the UK.
Adder bites typically occur from early spring to late autumn, with the hand being the most common site of the bite. Symptoms can be local or systemic, with local symptoms including sharp pain, tingling or numbness, and swelling that spreads proximally. Systemic symptoms may include spreading pain, tenderness, inflammation, regional lymph node enlargement, and bruising. In severe cases, anaphylaxis can occur, leading to symptoms such as nausea, vomiting, abdominal pain, diarrhea, and shock.
It is important for clinicians to be aware of the potential complications and complications associated with adder bites. These can include acute renal failure, pulmonary and cerebral edema, acute gastric dilatation, paralytic ileus, acute pancreatitis, and coma and seizures. Anaphylaxis symptoms can appear within minutes or be delayed for hours, and hypotension is a critical sign to monitor.
Initial investigations for adder bites include blood tests, ECG, and vital sign monitoring. Further investigations such as chest X-ray may be necessary based on clinical signs. Blood tests may reveal abnormalities such as leukocytosis, raised hematocrit, anemia, thrombocytopenia, and abnormal clotting profile. ECG changes may include tachyarrhythmias, bradyarrhythmias, atrial fibrillation, and ST segment changes.
First aid measures at the scene include immobilizing the patient and the bitten limb, avoiding aspirin and ibuprofen, and cleaning the wound site in the hospital. Tetanus prophylaxis should be considered. In cases of anaphylaxis, prompt administration of IM adrenaline is necessary. In the hospital, rapid assessment and appropriate resuscitation with intravenous fluids are required.
Antivenom may be indicated in cases of hypotension, systemic envenoming, ECG abnormalities, peripheral neutrophil leucocytosis, elevated serum creatine kinase or metabolic acidosis, and extensive or rapidly spreading local swelling. Zagreb antivenom is commonly used in the UK, with an initial dose of 8 mL.
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This question is part of the following fields:
- Pharmacology & Poisoning
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Question 18
Correct
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A 3-year-old toddler comes in with a high temperature, trouble swallowing, and drooling. Speaking is also challenging for the child. The medical team calls in a senior anesthesiologist and an ENT specialist, who diagnose the child with acute epiglottitis.
What is the preferred investigation method considered the most reliable in this case?Your Answer: Fibre-optic laryngoscopy
Explanation:Acute epiglottitis is inflammation of the epiglottis, which can be life-threatening if not treated promptly. When the soft tissues surrounding the epiglottis are also affected, it is called acute supraglottitis. This condition is most commonly seen in children between the ages of 3 and 5, but it can occur at any age, with adults typically presenting in their 40s and 50s.
In the past, Haemophilus influenzae type B was the main cause of acute epiglottitis, but with the introduction of the Hib vaccination, it has become rare in children. Streptococcus spp. is now the most common causative organism. Other potential culprits include Staphylococcus aureus, Pseudomonas spp., Moraxella catarrhalis, Mycobacterium tuberculosis, and the herpes simplex virus. In immunocompromised patients, Candida spp. and Aspergillus spp. infections can occur.
The typical symptoms of acute epiglottitis include fever, sore throat, painful swallowing, difficulty swallowing secretions (especially in children who may drool), muffled voice, stridor, respiratory distress, rapid heartbeat, tenderness in the front of the neck over the hyoid bone, ear pain, and swollen lymph nodes in the neck. Some patients may also exhibit the tripod sign, where they lean forward on outstretched arms to relieve upper airway obstruction.
To diagnose acute epiglottitis, fibre-optic laryngoscopy is considered the gold standard investigation. However, this procedure should only be performed by an anaesthetist in a setting prepared for intubation or tracheostomy in case of airway obstruction. Other useful tests include a lateral neck X-ray to look for the thumbprint sign, throat swabs, blood cultures, and a CT scan of the neck if an abscess is suspected.
When dealing with a case of acute epiglottitis, it is crucial not to panic or distress the patient, especially in pediatric cases. Avoid attempting to examine the throat with a tongue depressor, as this can trigger spasm and worsen airway obstruction. Instead, keep the patient as calm as possible and immediately call a senior anaesthetist, a senior paediatrician, and an ENT surgeon. Nebulized adrenaline can be used as a temporary measure if there is critical airway obstruction.
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This question is part of the following fields:
- Ear, Nose & Throat
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Question 19
Correct
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A 25 year old female is brought to the emergency department with a gunshot wound to the abdomen. You observe that the patient is breathing rapidly and her neck veins are distended. The trachea is centrally located. Her vital signs are as follows:
Blood pressure: 88/56 mmHg
Heart rate: 127 bpm
Respiration rate: 28 rpm
SpO2: 99% on 15L oxygen
What is the probable diagnosis?Your Answer: Cardiac tamponade
Explanation:Cardiac tamponade is characterized by several classical signs, including distended neck veins, muffled heart sounds, and hypotension. When neck veins are distended, it suggests that the right ventricle is not filling properly. In cases of trauma, this is often caused by the compression of air (tension pneumothorax) or fluid (blood in the pericardial space). One important distinguishing feature is the deviation of the trachea.
Further Reading:
Cardiac tamponade, also known as pericardial tamponade, occurs when fluid accumulates in the pericardial sac and compresses the heart, leading to compromised blood flow. Classic clinical signs of cardiac tamponade include distended neck veins, hypotension, muffled heart sounds, and pulseless electrical activity (PEA). Diagnosis is typically done through a FAST scan or an echocardiogram.
Management of cardiac tamponade involves assessing for other injuries, administering IV fluids to reduce preload, performing pericardiocentesis (inserting a needle into the pericardial cavity to drain fluid), and potentially performing a thoracotomy. It is important to note that untreated expanding cardiac tamponade can progress to PEA cardiac arrest.
Pericardiocentesis can be done using the subxiphoid approach or by inserting a needle between the 5th and 6th intercostal spaces at the left sternal border. Echo guidance is the gold standard for pericardiocentesis, but it may not be available in a resuscitation situation. Complications of pericardiocentesis include ST elevation or ventricular ectopics, myocardial perforation, bleeding, pneumothorax, arrhythmia, acute pulmonary edema, and acute ventricular dilatation.
It is important to note that pericardiocentesis is typically used as a temporary measure until a thoracotomy can be performed. Recent articles published on the RCEM learning platform suggest that pericardiocentesis has a low success rate and may delay thoracotomy, so it is advised against unless there are no other options available.
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This question is part of the following fields:
- Cardiology
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Question 20
Correct
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A 68-year-old man suffers a fractured neck of femur. He is later diagnosed with osteoporosis and is prescribed medication for the secondary prevention of osteoporotic fragility fractures.
What is the recommended initial treatment for the secondary prevention of osteoporotic fragility fractures?Your Answer: Oral bisphosphonate
Explanation:Oral bisphosphonates are the primary choice for treating osteoporotic fragility fractures in individuals who have already experienced such fractures. After a fragility fracture, it is advised to start taking a bisphosphonate, typically alendronic acid, and consider supplementing with calcium and vitamin D.
There are other treatment options available for preventing fragility fractures after an initial occurrence. These include raloxifene, teriparatide, and denosumab.
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This question is part of the following fields:
- Elderly Care / Frailty
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Question 21
Correct
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You are evaluating a 25-year-old male with a puncture wound to the stomach. Which of the following is NOT a reason for immediate laparotomy in cases of penetrating abdominal injury?
Your Answer: Negative diagnostic peritoneal lavage
Explanation:Urgent laparotomy is necessary in cases of penetrating abdominal trauma when certain indications are present. These indications include peritonism, the presence of free air under the diaphragm on an upright chest X-ray, evisceration, hypotension or signs of unstable blood flow, a gunshot wound that has penetrated the peritoneum or retroperitoneum, gastrointestinal bleeding following penetrating trauma, genitourinary bleeding following penetrating trauma, the presence of a penetrating object that is still in place (as removal may result in significant bleeding), and the identification of free fluid on a focused assessment with sonography for trauma (FAST) or a positive diagnostic peritoneal lavage (DPL).
Further Reading:
Abdominal trauma can be classified into two categories: blunt trauma and penetrating trauma. Blunt trauma occurs when compressive or deceleration forces are applied to the abdomen, often resulting from road traffic accidents or direct blows during sports. The spleen and liver are the organs most commonly injured in blunt abdominal trauma. On the other hand, penetrating trauma involves injuries that pierce the skin and enter the abdominal cavity, such as stabbings, gunshot wounds, or industrial accidents. The bowel and liver are the organs most commonly affected in penetrating injuries.
When it comes to imaging in blunt abdominal trauma, there are three main modalities that are commonly used: focused assessment with sonography in trauma (FAST), diagnostic peritoneal lavage (DPL), and computed tomography (CT). FAST is a non-invasive and quick method used to detect free intraperitoneal fluid, aiding in the decision on whether a laparotomy is needed. DPL is also used to detect intraperitoneal blood and can be used in both unstable blunt abdominal trauma and penetrating abdominal trauma. However, it is more invasive and time-consuming compared to FAST and has largely been replaced by it. CT, on the other hand, is the gold standard for diagnosing intra-abdominal pathology and is used in stable abdominal trauma patients. It offers high sensitivity and specificity but requires a stable and cooperative patient. It also involves radiation and may have delays in availability.
In the case of penetrating trauma, it is important to assess these injuries with the help of a surgical team. Penetrating objects should not be removed in the emergency department as they may be tamponading underlying vessels. Ideally, these injuries should be explored in the operating theater.
In summary, abdominal trauma can be classified into blunt trauma and penetrating trauma. Blunt trauma is caused by compressive or deceleration forces and commonly affects the spleen and liver. Penetrating trauma involves injuries that pierce the skin and commonly affect the bowel and liver. Imaging modalities such as FAST, DPL, and CT are used to assess and diagnose abdominal trauma, with CT being the gold standard. Penetrating injuries should be assessed by a surgical team and should ideally be explored in the operating theater.
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This question is part of the following fields:
- Trauma
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Question 22
Correct
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A 4-year-old girl presents accompanied by her Mom. She suffers from asthma for which she takes a salbutamol inhaler as needed. She has had a runny nose for the past few days and has developed wheezing this evening.
Which ONE characteristic indicates acute severe asthma in this age range?Your Answer: Use of accessory muscles
Explanation:The presence of certain clinical features can indicate the possibility of acute severe asthma in children over the age of 5. These features include oxygen saturations below 92%, peak flow measurements below 50% of what is expected, a heart rate exceeding 120 beats per minute, a respiratory rate exceeding 30 breaths per minute, and the use of accessory muscles.
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This question is part of the following fields:
- Respiratory
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Question 23
Incorrect
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A 25-year-old type 1 diabetic arrives at the emergency department complaining of a worsening sore throat, fever, and overall feeling of illness. The patient reports that the symptoms began a week ago. During the examination, the patient's temperature is measured at 38.3ºC, bilateral posterior cervical lymphadenopathy is observed, and there is exudate on both tonsils. Additionally, tenderness is noted in the right upper quadrant. Glandular fever is suspected.
What would be the most suitable approach for conducting further investigations?Your Answer: Arrange blood test for monospot heterophile antibodies in 7 -10 days
Correct Answer: Send blood for Epstein-Barr virus (EBV) viral serology
Explanation:Glandular fever, also known as infectious mononucleosis or mono, is a clinical syndrome characterized by symptoms such as sore throat, fever, and swollen lymph nodes. It is primarily caused by the Epstein-Barr virus (EBV), with other viruses and infections accounting for the remaining cases. Glandular fever is transmitted through infected saliva and primarily affects adolescents and young adults. The incubation period is 4-8 weeks.
The majority of EBV infections are asymptomatic, with over 95% of adults worldwide having evidence of prior infection. Clinical features of glandular fever include fever, sore throat, exudative tonsillitis, lymphadenopathy, and prodromal symptoms such as fatigue and headache. Splenomegaly (enlarged spleen) and hepatomegaly (enlarged liver) may also be present, and a non-pruritic macular rash can sometimes occur.
Glandular fever can lead to complications such as splenic rupture, which increases the risk of rupture in the spleen. Approximately 50% of splenic ruptures associated with glandular fever are spontaneous, while the other 50% follow trauma. Diagnosis of glandular fever involves various investigations, including viral serology for EBV, monospot test, and liver function tests. Additional serology tests may be conducted if EBV testing is negative.
Management of glandular fever involves supportive care and symptomatic relief with simple analgesia. Antiviral medication has not been shown to be beneficial. It is important to identify patients at risk of serious complications, such as airway obstruction, splenic rupture, and dehydration, and provide appropriate management. Patients can be advised to return to normal activities as soon as possible, avoiding heavy lifting and contact sports for the first month to reduce the risk of splenic rupture.
Rare but serious complications associated with glandular fever include hepatitis, upper airway obstruction, cardiac complications, renal complications, neurological complications, haematological complications, chronic fatigue, and an increased risk of lymphoproliferative cancers and multiple sclerosis.
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This question is part of the following fields:
- Infectious Diseases
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Question 24
Incorrect
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A 14-year-old girl was cycling down a hill when a car backed up in front of her, resulting in a collision. She visits the emergency department, reporting upper abdominal pain caused by the handlebars. You determine that a FAST scan is necessary. What is the main objective of performing a FAST scan for blunt abdominal trauma?
Your Answer: Identify shear injuries in solid abdominal organs
Correct Answer: Detect the presence of intraperitoneal fluid
Explanation:The primary goal of performing a FAST scan in cases of blunt abdominal trauma is to identify the existence of intraperitoneal fluid. According to the Royal College of Emergency Medicine (RCEM), the purpose of using ultrasound in the initial evaluation of abdominal trauma is specifically to confirm the presence of fluid within the peritoneal cavity, with the assumption that it is blood. However, it is important to note that ultrasound is not reliable for diagnosing injuries to solid organs or hollow viscus.
Further Reading:
Abdominal trauma can be classified into two categories: blunt trauma and penetrating trauma. Blunt trauma occurs when compressive or deceleration forces are applied to the abdomen, often resulting from road traffic accidents or direct blows during sports. The spleen and liver are the organs most commonly injured in blunt abdominal trauma. On the other hand, penetrating trauma involves injuries that pierce the skin and enter the abdominal cavity, such as stabbings, gunshot wounds, or industrial accidents. The bowel and liver are the organs most commonly affected in penetrating injuries.
When it comes to imaging in blunt abdominal trauma, there are three main modalities that are commonly used: focused assessment with sonography in trauma (FAST), diagnostic peritoneal lavage (DPL), and computed tomography (CT). FAST is a non-invasive and quick method used to detect free intraperitoneal fluid, aiding in the decision on whether a laparotomy is needed. DPL is also used to detect intraperitoneal blood and can be used in both unstable blunt abdominal trauma and penetrating abdominal trauma. However, it is more invasive and time-consuming compared to FAST and has largely been replaced by it. CT, on the other hand, is the gold standard for diagnosing intra-abdominal pathology and is used in stable abdominal trauma patients. It offers high sensitivity and specificity but requires a stable and cooperative patient. It also involves radiation and may have delays in availability.
In the case of penetrating trauma, it is important to assess these injuries with the help of a surgical team. Penetrating objects should not be removed in the emergency department as they may be tamponading underlying vessels. Ideally, these injuries should be explored in the operating theater.
In summary, abdominal trauma can be classified into blunt trauma and penetrating trauma. Blunt trauma is caused by compressive or deceleration forces and commonly affects the spleen and liver. Penetrating trauma involves injuries that pierce the skin and commonly affect the bowel and liver. Imaging modalities such as FAST, DPL, and CT are used to assess and diagnose abdominal trauma, with CT being the gold standard. Penetrating injuries should be assessed by a surgical team and should ideally be explored in the operating theater.
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This question is part of the following fields:
- Trauma
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Question 25
Correct
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A 55-year-old woman presents with fevers and severe pain in the left hypochondrium that radiates to her back. The pain has been present for 24 hours. On examination, she is tender in the left upper quadrant, and Murphy’s sign is positive. Her temperature is 38°C.
Her blood results are as follows:
CRP: 94 mg/l (< 5 mg/l)
Hb: 12.4 g/dl (11.5-16 g/dl)
WCC: 14.4 x 109/l (4-11 x 109/l)
Neut: 11.6 x 109/l (2.5-7.5 x 109/l)
Bilirubin 18 mmol (3-20)
ALT 34 IU/L (5-40)
ALP: 103 IU/L (20-140)
What is the SINGLE most likely diagnosis?Your Answer: Acute cholecystitis
Explanation:The patient’s symptoms strongly suggest a diagnosis of acute cholecystitis. This condition occurs when a gallstone becomes stuck in the outlet of the gallbladder, causing irritation and inflammation of the gallbladder wall. As a result, the gallbladder fills with pus, which is initially sterile but can become infected with bacteria such as Escherichia coli and Klebsiella spp.
The clinical features of acute cholecystitis include severe pain in the upper right quadrant or epigastric, which can radiate to the back and lasts for more than 12 hours. Fevers and rigors are also commonly present, along with nausea and vomiting. Murphy’s sign, a physical examination finding, is highly sensitive and has a high positive predictive value for acute cholecystitis. However, its specificity is lower, as it can also be positive in biliary colic and ascending cholangitis.
In acute cholecystitis, the white cell count and C-reactive protein (CRP) levels are usually elevated. Liver function tests, such as AST, ALT, and ALP, may also be elevated but can often be within the normal range. Bilirubin levels may be mildly elevated, but they can also be normal. If there is a significant elevation in AST, ALT, ALP, or bilirubin, it may indicate other biliary tract conditions, such as ascending cholangitis or choledocholithiasis.
It is important to differentiate acute cholecystitis from other conditions with similar presentations. Renal colic, for example, presents with pain in the loin area and tenderness in the renal angle, which is different from the symptoms seen in acute cholecystitis. Cholangiocarcinoma, a rare type of cancer originating from the biliary epithelium, typically presents with painless jaundice and itching.
To help distinguish between biliary colic, acute cholecystitis, and ascending cholangitis, the following summarizes their key differences:
Biliary colic:
– Pain duration: Less than 12 hours
– Fever: Absent
– Murphy’s sign: Negative
– WCC & CRP: Normal
– AST, ALT & ALP: Normal
– Bilirubin: NormalAcute cholecystitis:
– Pain duration: More than 12 hours
– Fever: Present
– Murphy’s sign: Positive
– WCC & -
This question is part of the following fields:
- Surgical Emergencies
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Question 26
Incorrect
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You are present at a trauma call for an elderly pedestrian who has been hit by a car. She has bruising on the right side of her chest. The primary survey has been completed and you have been asked to perform a secondary survey.
According to the ATLS guidelines, which of the following indicates a potentially life-threatening chest injury that should be identified and treated during the SECONDARY survey?Your Answer: Cardiac tamponade
Correct Answer: Blunt oesophageal rupture
Explanation:The ATLS guidelines categorize chest injuries in trauma into two groups: life-threatening injuries that require immediate identification and treatment in the primary survey, and potentially life-threatening injuries that should be identified and treated in the secondary survey.
During the primary survey, the focus is on identifying and treating life-threatening thoracic injuries. These include airway obstruction, tracheobronchial tree injury, tension pneumothorax, open pneumothorax, massive haemothorax, and cardiac tamponade. Prompt recognition and intervention are crucial in order to prevent further deterioration and potential fatality.
In the secondary survey, attention is given to potentially life-threatening injuries that may not be immediately apparent. These include simple pneumothorax, haemothorax, flail chest, pulmonary contusion, blunt cardiac injury, traumatic aortic disruption, traumatic diaphragmatic injury, and blunt oesophageal rupture. These injuries may not pose an immediate threat to life, but they still require identification and appropriate management to prevent complications and ensure optimal patient outcomes.
By dividing chest injuries into these two categories and addressing them in a systematic manner, healthcare providers can effectively prioritize and manage trauma patients, ultimately improving their chances of survival and recovery.
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This question is part of the following fields:
- Trauma
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Question 27
Correct
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You intend to utilize plain 1% lidocaine for a ring block on a finger that requires suturing. How much lidocaine hydrochloride is present in every 1 ml of plain 1% lidocaine solution?
Your Answer: 10 mg lidocaine hydrochloride
Explanation:Each milliliter of plain 1% lidocaine solution contains 10 milligrams of lidocaine hydrochloride.
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This question is part of the following fields:
- Pain & Sedation
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Question 28
Incorrect
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A 40-year-old man is brought to the Emergency Department by his wife after overdosing on one of his prescribed medications. He is restless, disoriented, and experiencing visual hallucinations. His heart rate is currently 110 bpm, and his pupils are dilated. It is challenging to gather information from him as he is speaking incoherently. Upon further inquiry, you learn that he has ingested an anticholinergic medication.
What is the antidote for this type of poisoning?Your Answer: Atropine
Correct Answer: Physostigmine
Explanation:Patients who present with an anticholinergic toxidrome can be difficult to manage due to the agitation and disruptive behavior that is typically present. It is important to provide meticulous supportive care to address the behavioral effects of delirium and prevent complications such as dehydration, injury, and pulmonary aspiration. Often, one-to-one nursing is necessary.
The management approach for these patients is as follows:
1. Resuscitate using a standard ABC approach.
2. Administer sedation for behavioral control. Benzodiazepines, such as IV diazepam in 5 mg-10 mg increments, are the first-line therapy. The goal is to achieve a patient who is sleepy but easily roused. It is important to avoid over-sedating the patient as this can increase the risk of aspiration.
3. Prescribe intravenous fluids as patients are typically unable to eat and drink, and may be dehydrated upon presentation.
4. Insert a urinary catheter as urinary retention is often present and needs to be managed.
5. Consider physostigmine as the specific antidote for anticholinergic delirium in carefully selected cases. Physostigmine acts as a reversible acetylcholinesterase inhibitor, temporarily blocking the breakdown of acetylcholine. This enhances its effects at muscarinic and nicotinic receptors, thereby reversing the effects of the anticholinergic agents.Physostigmine is indicated in the following situations:
1. Severe anticholinergic delirium that does not respond to benzodiazepine sedation.
2. Poisoning with a pure anticholinergic agent, such as atropine.The dosage and administration of physostigmine are as follows:
1. Administer in a monitored setting with appropriate staff and resources to manage adverse effects.
2. Perform a 12-lead ECG before administration to rule out bradycardia, AV block, or broadening of the QRS.
3. Administer IV physostigmine 0.5-1 mg as a slow push over 5 minutes. Repeat every 10 minutes up to a maximum of 4 mg.
4. The clinical end-point of therapy is the resolution of delirium.
5. Delirium may reoccur in 1-4 hours as the effects of physostigmine wear off. In such cases, the dose may be cautiously repeated. -
This question is part of the following fields:
- Pharmacology & Poisoning
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Question 29
Correct
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A 22-year-old presents to the emergency department with a nosebleed. You observe that they have blood-soaked tissue paper held against the nose, blocking the opening of the left nostril, and blood stains on the front of their shirt. What is the most appropriate initial management for this patient?
Your Answer: Advise the patient to sit forward and pinch just in front of the bony septum firmly and hold it for 15 minutes
Explanation:To control epistaxis, it is recommended to have the patient sit upright with their upper body tilted forward and their mouth open. Firmly pinch the cartilaginous part of the nose, specifically in front of the bony septum, and maintain pressure for 10-15 minutes without releasing it.
Further Reading:
Epistaxis, or nosebleed, is a common condition that can occur in both children and older adults. It is classified as either anterior or posterior, depending on the location of the bleeding. Anterior epistaxis usually occurs in younger individuals and arises from the nostril, most commonly from an area called Little’s area. These bleeds are usually not severe and account for the majority of nosebleeds seen in hospitals. Posterior nosebleeds, on the other hand, occur in older patients with conditions such as hypertension and atherosclerosis. The bleeding in posterior nosebleeds is likely to come from both nostrils and originates from the superior or posterior parts of the nasal cavity or nasopharynx.
The management of epistaxis involves assessing the patient for signs of instability and implementing measures to control the bleeding. Initial measures include sitting the patient upright with their upper body tilted forward and their mouth open. Firmly pinching the cartilaginous part of the nose for 10-15 minutes without releasing the pressure can also help stop the bleeding. If these measures are successful, a cream called Naseptin or mupirocin nasal ointment can be prescribed for further treatment.
If bleeding persists after the initial measures, nasal cautery or nasal packing may be necessary. Nasal cautery involves using a silver nitrate stick to cauterize the bleeding point, while nasal packing involves inserting nasal tampons or inflatable nasal packs to stop the bleeding. In cases of posterior bleeding, posterior nasal packing or surgery to tie off the bleeding vessel may be considered.
Complications of epistaxis can include nasal bleeding, hypovolemia, anemia, aspiration, and even death. Complications specific to nasal packing include sinusitis, septal hematoma or abscess, pressure necrosis, toxic shock syndrome, and apneic episodes. Nasal cautery can lead to complications such as septal perforation and caustic injury to the surrounding skin.
In children under the age of 2 presenting with epistaxis, it is important to refer them for further investigation as an underlying cause is more likely in this age group.
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This question is part of the following fields:
- Ear, Nose & Throat
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Question 30
Incorrect
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A middle-aged man presents with visual difficulties. Upon examination, it is discovered that he has a quadrantic visual field defect. He is subsequently taken to the hospital for a CT head scan, which confirms a diagnosis of a cerebrovascular accident.
Which of the following blood vessels is most likely to be impacted?Your Answer: Middle cerebral artery
Correct Answer: Posterior cerebral artery
Explanation:The symptoms and signs of strokes can vary depending on which blood vessel is affected. Here is a summary of the main symptoms based on the territory affected:
Anterior cerebral artery: This can cause weakness on the opposite side of the body, with the leg and shoulder being more affected than the arm, hand, and face. There may also be minimal loss of sensation on the opposite side of the body. Other symptoms can include difficulty speaking (dysarthria), language problems (aphasia), apraxia (difficulty with limb movements), urinary incontinence, and changes in behavior and personality.
Middle cerebral artery: This can lead to weakness on the opposite side of the body, with the face and arm being more affected than the leg. There may also be a loss of sensation on the opposite side of the body. Depending on the dominant hemisphere of the brain, there may be difficulties with expressive or receptive language (dysphasia). In the non-dominant hemisphere, there may be neglect of the opposite side of the body.
Posterior cerebral artery: This can cause a loss of vision on the opposite side of both eyes (homonymous hemianopia). There may also be defects in a specific quadrant of the visual field. In some cases, there may be a syndrome affecting the thalamus on the opposite side of the body.
It’s important to note that these are just general summaries and individual cases may vary. If you suspect a stroke, it’s crucial to seek immediate medical attention.
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This question is part of the following fields:
- Neurology
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