Internal Medicine Flashcards
A 23-year-old male patient who lives on the road side was admitted to a medical ward for acute febrile illness. He developed diaphoresis and palpitation hours after drug administration. On examination, his BP dropped to 80/40mmHg. What is the most appropriate next step in the management of this patient?
• a. Give IV fluid and dexamethasone
b. Reassure the patient and continue the medication
• c. Send blood culture
d. Transfuse with cross-matched blood
A
A 24-year-old man came to a hospital with complaints of cough, fever and pleuritic chest pain of three days duration. He was treated with unspecified antibiotics for URTI two weeks back. On physical examination, his vital signs were unremarkable, but chest examination showed left middle lung field bronchial breath sound. What is the best initial management option for this patient?
• a. PO Augumentin plus Azithromycin
• b. PO Clarithromycin plus Doxycycline
c. PO Doxicycline plus Ciprofloxacin
• d. PO Azithromycin
The patient’s presentation (cough, fever, pleuritic chest pain, and bronchial breath sounds in the left middle lung field) strongly suggests community-acquired pneumonia (CAP), likely with consolidation. The best initial management involves selecting an appropriate antibiotic regimen for outpatient treatment of CAP.
The most appropriate option is:
According to STG for a patient with no comorbidities we only give azithromycin we give augumentin and azitro for the once with comorbidities
a. PO Augmentin (Amoxicillin-clavulanate) plus Azithromycin.
Rationale:
1. Coverage of Common Pathogens:
• Streptococcus pneumoniae (most common bacterial cause of CAP).
• Atypical pathogens like Mycoplasma pneumoniae and Chlamydia pneumoniae (covered by Azithromycin).
• Augmentin provides beta-lactam activity, while Azithromycin covers atypical organisms.
2. Guideline Support:
• According to IDSA and ATS guidelines for outpatient management of CAP, combination therapy with a beta-lactam (e.g., Amoxicillin-clavulanate) and a macrolide (e.g., Azithromycin) is appropriate for patients with risk factors (e.g., recent antibiotic use).
Why Not the Other Options?
• b. PO Clarithromycin plus Doxycycline:
• Dual coverage of atypicals but insufficient beta-lactam activity for S. pneumoniae.
• c. PO Doxycycline plus Ciprofloxacin:
• Ciprofloxacin has poor activity against S. pneumoniae, and dual coverage of atypicals is unnecessary.
• d. PO Azithromycin:
• Monotherapy is generally sufficient for low-risk, healthy individuals with no recent antibiotic use. However, this patient has recent antibiotic exposure, increasing the likelihood of resistant pathogens.
Next Steps:
1. Monitor for clinical improvement.
2. Educate the patient on signs of worsening symptoms (e.g., dyspnea or persistent fever).
3. Consider follow-up imaging if symptoms persist beyond treatment to assess for complications like abscess or effusion.
A 25-year-old female patient came to a hospital with fatigue, shortness of breath and bilateral leg swelling of one month duration. She has no previously known chronic illness. Her blood pressure is 90/60 mmHg, pulse rate is 112/min, respiration rate is 18/min and temperature is 37.2 degree centigrade. She has right side pleural effusion, raised JVP, grade 2-3/6 holosystolic murmur at apex and bilateral leg swelling. Echocardiography showed left ventricular cavity diameter of 65 mm (normal value less than 54 mm) and left atrial diameter of 45 mm (normal value less than 38 mm) with ejection fraction of 30percent. What is the most likely underlying disease of the patient?
• a. Hypertrophic cardiomyopathy
Myocarditis
Dilated cardiomyopathy
Restrictive cardiomyopathy
A 25-year-old female patient came to a hospital with fatigue, shortness of breath and bilateral leg swelling of one month duration. She has no previously known chronic illness. Her blood pressure is 90/60 mmHg, pulse rate is 112/min, respiration rate is 18/min and temperature is 37.2 degree centigrade. She has right side pleural effusion, raised JVP, grade 2-3/6 holosystolic murmur at apex and bilateral leg swelling. Echocardiography showed left ventricular cavity diameter of 65 mm (normal value less than 54 mm) and left atrial diameter of 45 mm (normal value less than 38 mm) with ejection fraction of 30percent. What is the most likely underlying disease of the patient?
• a. Hypertrophic cardiomyopathy
Myocarditis
Dilated cardiomyopathy
Restrictive cardiomyopathy
A 24-year-old man has been on RHZE for the last three weeks for the diagnosis of pulmonary tuberculosis. In the last two week, the patient started to complain of burning and tingling sensation in his feet. What is the most appropriate step in the management of the patient’s case?
a. Reassurance and continue anti-TB
b. Start on pyridoxine and continue anti-TB
c. Discontinue only Isonazid and start on pyridoxine plus RZE
d. Start on pyridoxine and stop all anti-TB
The most appropriate step in the management of this patient’s case is:
b. Start on pyridoxine and continue anti-TB
Explanation:
1. Diagnosis:
The patient is experiencing peripheral neuropathy, which is a well-known side effect of isoniazid (INH), one of the drugs in the RHZE regimen (rifampicin, isoniazid, pyrazinamide, and ethambutol).
2. Cause:
Isoniazid-induced peripheral neuropathy occurs due to interference with vitamin B6 (pyridoxine) metabolism, leading to a functional deficiency.
3. Management:
• Pyridoxine supplementation (usually 10-50 mg/day) is effective in preventing and treating this side effect.
• It is standard practice to co-administer pyridoxine with INH, especially in individuals at higher risk (e.g., malnutrition, diabetes, alcoholism, or pregnancy).
4. Why Not Other Options?:
• a. Reassurance and continue anti-TB: This would not address the underlying issue and may worsen the neuropathy.
• c. Discontinue only Isoniazid and start on pyridoxine plus RZE: Discontinuing INH is unnecessary because the neuropathy can be managed with pyridoxine.
• d. Start on pyridoxine and stop all anti-TB: Stopping the entire regimen would risk treatment failure and drug resistance.
Conclusion:
The correct approach is to start pyridoxine and continue the full RHZE regimen.
A 25-year-old male patient came to a neurology clinic for his regular epilepsy follow-up. He has been taking the maximum dose of valproic acid, but he had six episodes of seizure in the last two months.
He claimed that he is adherent to his medication.
What is the most appropriate next step in the management of this patient?
•a. Taper Valproic acid and start regular doses of diazepam
b. Add other anti-epileptic drug with different mechanism of action
• c. Add two drugs with similar mechanisms of action
• d. Discontinue Valproic acid and start other anti-epileptic drug
The most appropriate next step in the management of this patient is:
b. Add another anti-epileptic drug with a different mechanism of action
Explanation:
1. Diagnosis:
The patient is experiencing drug-resistant epilepsy, defined as the failure of adequate trials of two appropriately chosen and tolerated anti-epileptic drugs (AEDs) to achieve sustained seizure freedom.
2. Current Situation:
• The patient is on the maximum dose of valproic acid but continues to have frequent seizures.
• He claims adherence, so treatment failure is likely due to insufficient seizure control with valproic acid alone.
3. Management:
• Adding a second AED with a different mechanism of action is the next step. This combination may increase the likelihood of seizure control. Examples include levetiracetam, lamotrigine, or topiramate, depending on the type of epilepsy.
• A different mechanism minimizes the risk of additive side effects while maximizing efficacy.
4. Why Not Other Options?
• a. Taper Valproic acid and start regular doses of diazepam: Diazepam is used for acute seizure management, not long-term control. Tapering valproic acid without another long-term AED risks worsening seizure control.
• c. Add two drugs with similar mechanisms of action: Using drugs with similar mechanisms increases the risk of additive side effects without significant therapeutic benefit.
• d. Discontinue Valproic acid and start another AED: Abruptly discontinuing valproic acid could provoke withdrawal seizures. Changing the AED is only considered after the failure of multiple combination strategies.
Conclusion:
The best course of action is to add a second AED with a different mechanism of action to optimize seizure control.
A 23-year-old male patient who lives on the road side was admitted to a medical ward for acute febrile illness. He developed diaphoresis and palpitation hours after drug administration. On examination, his BP dropped to 80/40mmHg. What is the most appropriate next step in the management of this patient?
• a. Give IV fluid and dexamethasone
b. Reassure the patient and continue the medication
• c. Send blood culture
• d. Transfuse with cross-matched blood
The most appropriate next step in the management of this patient is:
a. Give IV fluid and dexamethasone.
Reasoning:
• The patient has hypotension (BP 80/40 mmHg) and symptoms of diaphoresis and palpitation, which could indicate an adverse drug reaction or an episode of anaphylaxis.
• Immediate management of hypotension involves IV fluid resuscitation to restore intravascular volume.
• Dexamethasone, a corticosteroid, is used to address potential hypersensitivity or allergic reactions.
Why not the other options?
• b. Reassure the patient and continue the medication: This is inappropriate in a potentially life-threatening situation like hypotension and signs of shock.
• c. Send blood culture: Blood cultures may be part of the diagnostic workup for febrile illness but are not immediately life-saving in the presence of hypotension.
• d. Transfuse with cross-matched blood: This is not indicated unless the patient has signs of severe blood loss or anemia, which is not mentioned in this scenario.
Priority: Stabilize the patient’s hemodynamics first, then investigate the underlying cause.
A 25-year-old young man came to an emergency
OPD after having dry cough, running nose fever and headache of three days duration. He did not have history of chronic lung problems and he is not smoker. His vital signs were within the normal range except temperature of 38.4 degree centigrade, he has clear chest and normal mental status. What is the most appropriate next step in the management of this patient?
a. Do not give any medications
•b. Prescribe antibiotics
• c. Prescribe antiviral
• d. Prescribe antipyretics
The most appropriate next step in the management of this patient is:
d. Prescribe antipyretics.
Reasoning:
• The patient presents with symptoms of a likely viral upper respiratory tract infection (URTI): dry cough, runny nose, fever, and headache.
• His vital signs are stable, with no evidence of bacterial infection (e.g., purulent sputum, localized chest findings, or severe systemic symptoms).
• Antipyretics like paracetamol (acetaminophen) or ibuprofen can be given to manage fever and associated discomfort.
Why not the other options?
• a. Do not give any medications: While most viral URTIs are self-limiting, symptomatic management (e.g., with antipyretics) improves patient comfort.
• b. Prescribe antibiotics: Antibiotics are not indicated for viral infections and their unnecessary use can lead to antibiotic resistance.
• c. Prescribe antiviral: Antivirals are not indicated unless there is suspicion of specific viral infections (e.g., influenza in high-risk patients) that require targeted therapy.
Additional Advice:
• Encourage adequate hydration, rest, and monitoring of symptoms.
• Advise the patient to return if symptoms worsen or new concerning signs develop (e.g., high fever, difficulty breathing).
A 27-year-old patient came to an emergency unit complaining about nausea, vomiting, thirst, abdominal pain and shortness of breath for the last two days. On evaluation, temperature was 36.7 degree centigrade, respirations were 28/min, pulse rate was 116/min and blood pressure was 80/60mmHg. He is lethargic; however, he has no remarkable finding in other systems. His laboratory results reveal; WBC count of 4.8x103/microlitre, platelet count of 156x103/microlitre, hemoglobin level of 11.4g/dl, liver and kidney functions were normal, serum K+ 4.5mmol/L (NR; 3.5-5.5mmol/L), serum Na2+ 140mmol/L (NR; 136-146mmol/L), RBS
560mg/dl and urine analysis shows ketone +3. What is the most appropriate initial step in the management of this patient?
a. Metformin 1gm
• b. Start feeding by nasogastric tube
c. 0.9percent saline 10 ml/kg/hr
The most appropriate initial step in the management of this patient is:
c. 0.9% saline 10 ml/kg/hr.
Reasoning:
The patient presents with signs and symptoms consistent with diabetic ketoacidosis (DKA):
• Symptoms: Nausea, vomiting, abdominal pain, and shortness of breath (Kussmaul respirations).
• Signs: Hypotension (BP 80/60 mmHg), tachycardia (pulse 116/min), and lethargy, indicating dehydration and metabolic acidosis.
• Laboratory findings: Hyperglycemia (RBS 560 mg/dl), ketonuria (+3 ketones in urine), and normal potassium (serum K+ 4.5 mmol/L).
Initial Management:
1. Fluid Resuscitation:
• Start 0.9% normal saline at 10 ml/kg/hr to correct dehydration and improve perfusion.
• Fluids are critical to stabilize hemodynamics and dilute circulating glucose and ketones.
2. Potassium Monitoring:
• Potassium levels should be closely monitored because insulin therapy (given later) can cause hypokalemia.
3. Insulin Therapy:
• After initial fluid resuscitation, start a low-dose IV insulin infusion to address hyperglycemia and ketosis.
4. Correct Acidosis:
• Fluids and insulin are typically sufficient to resolve acidosis; bicarbonate is rarely needed.
Why not the other options?
• a. Metformin 1 gm: This is inappropriate for acute management of DKA. Metformin is used for chronic glucose control in type 2 diabetes and does not address the acute metabolic derangements of DKA.
• b. Start feeding by nasogastric tube: Feeding is not indicated in the acute phase of DKA and could exacerbate nausea and vomiting.
• d. Insulin infusion: While insulin is essential for DKA management, fluids must be administered first to avoid worsening hypotension and hypovolemia.
Key Priorities:
1. Fluid resuscitation.
2. Electrolyte monitoring and management.
3. Insulin therapy.
4. Address the underlying cause of DKA (e.g., infection, missed insulin doses).
10 of 37 8-year-old male patient came to a health center arter noticing skin discoloration on his back for unknown duration. Five hypo-pigmented skin lesions with loss of sensation on the lesion and enlarged ulnar nerves were found during examination. What is the most likely diagnosis?
a. Leprosy
• b. Ulnar nerve neuropathy
C. Tinea corporis
• d. Pityriasis alba
The most likely diagnosis is:
a. Leprosy
Explanation:
• Hypopigmented lesions with loss of sensation are characteristic of leprosy (Hansen’s disease), caused by Mycobacterium leprae.
• Enlarged peripheral nerves (such as the ulnar nerve) are another hallmark feature of leprosy, as the disease primarily affects the skin and peripheral nerves.
• Tinea corporis and pityriasis alba can cause hypopigmented lesions, but they are not associated with nerve enlargement or loss of sensation.
• Ulnar nerve neuropathy could explain the enlarged ulnar nerve but would not cause the characteristic skin lesions.
Further diagnostic confirmation with a skin biopsy or slit-skin smear would be necessary.
Clinical evaluation
Physical examination — The diagnosis of leprosy should be considered in patients with skin lesions and/or enlarged nerve(s) accompanied by sensory loss. Leprosy should be suspected in the setting of the following clinical manifestations:
●Diminished sensation or loss of sensation within skin lesions
●Paresthesias (tingling or numbness in the hands or feet)
●Painless wounds or burns on the hands or feet
●Tender, enlarged peripheral nerves
27-year-old male patient came to a medical OPD with a complaint of retrosternal chest pain of two days duration. On evaluation, his temperature is 36.5 degree centigrade, respiratory rate is 25/min, pulse rate is 92/min, and blood pressure is 100/60mmHg.
There are no remarkable findings in other systems.
Laboratory results show hemoglobin level of 12g/dl, WBC count of 5 x 103/microlitre, and platelet count of 250,000/microlitre. Cardiac biomarkers are in the normal range. Chest X-ray findings are normal. ECG shows diffuse ST-segment elevations with upward concavity in leads I, II, AVF, and v2 to v6. What is the most likely diagnosis of this patient?
• a. Acute coronary syndrome.
b. Pericarditis
• c. Pulmonary thromboembolism
d. Pneumonia
The most likely diagnosis is:
b. Pericarditis
Explanation:
• Diffuse ST-segment elevations with upward concavity on ECG are a hallmark of acute pericarditis. This pattern is typically seen in multiple leads and helps differentiate it from acute coronary syndrome (which usually shows localized ST elevations).
• Normal cardiac biomarkers argue against myocardial infarction (part of acute coronary syndrome).
• The absence of fever, elevated WBC, or focal findings on chest X-ray makes pneumonia less likely.
• Pulmonary thromboembolism typically presents with signs of right heart strain on ECG, hypoxia, and possible hemodynamic instability, none of which are seen here.
Other supportive findings for pericarditis could include pleuritic chest pain (worsened by lying flat and relieved by sitting up) or a pericardial rub on auscultation, though these are not mentioned in this case.
A 30-year-old female patient comes to a medical
referral clinic complaining of bilateral recurrent pain
and swelling of her hand joints for two years. She
has no skin rash or photosensitivity. Her vital signs
are in the normal range. Musculoskeletal
examinations reveal swan neck like deformity of her
hands. What is the most likely diagnosis of the
patient?
a. Osteoarthritis
b. Reactive arthritis
C.
Gout
• d. Rheumatoid arthritis
The most likely diagnosis is:
d. Rheumatoid arthritis
Explanation:
• Bilateral recurrent pain and swelling of hand joints over two years strongly suggest a chronic inflammatory arthritis, which is typical of rheumatoid arthritis (RA).
• Swan neck deformity (hyperextension of the proximal interphalangeal joint and flexion of the distal interphalangeal joint) is a classic deformity associated with long-standing RA.
• Osteoarthritis typically involves the distal interphalangeal joints (Heberden’s nodes) and lacks significant inflammatory signs or deformities like swan neck.
• Reactive arthritis is usually associated with a preceding infection and often involves larger joints asymmetrically.
• Gout is characterized by acute monoarticular arthritis and does not usually cause chronic deformities like swan neck.
Further diagnostic confirmation can be made by testing for rheumatoid factor (RF) and anti-cyclic citrullinated peptide (anti-CCP) antibodies.
A 32-year-old male patient came to a hospital with
the complaints of cough and severe left side chest
pain while breathing for the last one week. His blood
pressure is 110/60 mmHg, pulse rate is 100/min,
respirations are 32/min and temperature is 38.4
degree centigrade. Respiratory system examination
showed dullness and absent air entry over the left
lower half of the lung fields. What is the most
appropriate initial investigation for the patient?
• a. Echocardiography
• b. Chest x-ray
• c. Thoracentesis
• d. Complete blood count
The most appropriate initial investigation is:
b. Chest X-ray
Explanation:
• The patient’s symptoms (pleuritic chest pain, fever, cough, and tachypnea) and examination findings (dullness and absent air entry) suggest a possible pleural effusion or consolidation, such as pneumonia with a parapneumonic effusion or empyema.
• A chest X-ray is the initial investigation of choice to confirm the presence of pleural effusion, determine its extent, and assess for other abnormalities like consolidation or pneumothorax.
• Thoracentesis would be the next step if pleural effusion is confirmed to determine its nature (e.g., transudate vs. exudate) and possibly guide treatment.
• Complete blood count can provide supportive information (e.g., leukocytosis suggesting infection), but it is not the primary diagnostic test.
• Echocardiography is useful if a cardiac cause (e.g., pericardial effusion) is suspected, but the clinical presentation here is more consistent with a pulmonary/pleural condition.
P Flag question
A 33-year-old woman came to a clinic with
complaints of decreased urine output and foamy
urine of one week duration. On physical examination,
a blood pressure of 150/90 mmg, peri orbital
edema and malar rash were noted. Investigation
results show a urine analysis blood of +2, protein of
+3 and many RBC cast, 24-hour urine protein of 2.5g
and serum creatinine of 1.3mg/dl. What is the most
likely cause of the patient’s condition?
• a. Lupus nephritis
• b. Post streptococcus glomerulonephritis
c. IgA nephropathy
• d. Focal segmental glomerulosclerosis
Previous page
The most likely cause of the patient’s condition is:
a. Lupus nephritis
Explanation:
• The patient’s malar rash, peri-orbital edema, and hypertension suggest an underlying systemic autoimmune condition, most likely systemic lupus erythematosus (SLE).
• Urinalysis findings of proteinuria (+3), hematuria (RBC casts), and a 24-hour urine protein of 2.5 g indicate significant renal involvement, consistent with lupus nephritis.
• Serum creatinine elevation further supports renal dysfunction.
Why not the other options?
• Post-streptococcal glomerulonephritis (PSGN): Typically occurs after a streptococcal infection and is more common in children. It usually presents with low complement levels (especially C3). No history of recent infection is noted here.
• IgA nephropathy: Usually presents with episodic gross hematuria, often following an upper respiratory infection, but it lacks systemic symptoms like malar rash.
• Focal segmental glomerulosclerosis (FSGS): Characterized by nephrotic syndrome (heavy proteinuria >3.5 g/day) without significant hematuria or systemic symptoms like rash.
Next Steps:
• Confirm the diagnosis with ANA, anti-dsDNA, and complement levels (C3, C4).
• A renal biopsy may be necessary to classify the lupus nephritis and guide treatment.
A 35-year-old female patient came to a hospital with
anterior neck swelling of five years duration. Since
the last three month, she has started to experience
palpitation and has a history of hot intolerance with
no history of bone pain, cough or yellowish
discoloration of the eye. On examination, her pulse
rate is 110/min, blood pressure is 120/70mmHg,
and there is lid lag and lid retraction. On thyroid
examination, there is diffusely enlarged thyroid
measuring of 4*3cm,the lower border is reachable.
She is investigated with thyroid function test and the
results show that TSH is 0.3micro unit/mL(Normal;
0.5-5 micro unit/mL), Total T4 is 180
nmol/L(Normal; 55-150 nmol/L), Total T3 is 5
nmol/L(Normal; 1.5-3.5 nmol/L). What is the most
likely diagnosis of the patient?
• a. Toxic multinodular goiter
• b. Toxic Adenoma
• c. Graves’ disease
• d. Follicular neoplasm
7 : 3 9 巴
Doctor of Medicine Model
The most likely diagnosis is:
c. Graves’ disease
Explanation:
• Thyroid findings: Diffusely enlarged thyroid with no nodules suggests a condition involving the entire gland, such as Graves’ disease.
• Symptoms: Palpitations, heat intolerance, and lid lag/lid retraction are classic features of hyperthyroidism, which is most commonly caused by Graves’ disease.
• Thyroid function test results: Suppressed TSH (0.3 µU/mL) with elevated T4 and T3 confirms primary hyperthyroidism.
• Examination findings: Lid lag and lid retraction are often seen in Graves’ disease due to orbital inflammation (thyroid eye disease).
Why not the other options?
• Toxic multinodular goiter (TMNG): Typically presents with an irregularly enlarged thyroid with multiple nodules, which is not described here.
• Toxic adenoma: Characterized by a single hyperfunctioning nodule, which is not consistent with a diffusely enlarged thyroid.
• Follicular neoplasm: Usually presents as a solitary thyroid nodule and does not cause hyperthyroidism or systemic symptoms.
Next Steps:
• Confirm the diagnosis with thyroid-stimulating immunoglobulins (TSI) or TRAb (TSH receptor antibodies).
• Consider a thyroid ultrasound and radioactive iodine uptake (RAIU) test to differentiate Graves’ disease from other causes of hyperthyroidism.
A 35-year-old woman presented with complaints of
foul smelling greasy diarrhea, fatigability and weight
loss. On examination, she is emaciated and has pale
conjunctiva. Laboratory is notable for hemoglobin
level of 8.5g/dl with MCV of 105fL. What is the most
likely nutrient deficiency the patient has?
• a. Iron
• b. Cobalamin
• c. Copper
• d. Phosphorus
The most likely nutrient deficiency is:
b. Cobalamin (Vitamin B12)
Explanation:
• Foul-smelling, greasy diarrhea and weight loss suggest malabsorption, likely due to a condition such as celiac disease or small intestinal bacterial overgrowth (SIBO), which can impair the absorption of vitamin B12.
• Macrocytic anemia (MCV of 105 fL) is characteristic of vitamin B12 or folate deficiency. Given the malabsorption symptoms, vitamin B12 deficiency is more likely.
• Fatigability and emaciation further support a nutrient deficiency, with vitamin B12 deficiency commonly leading to neurological symptoms over time if untreated.
Why not the other options?
• Iron: Iron deficiency causes microcytic anemia (low MCV), which is not seen here.
• Copper: Copper deficiency typically causes anemia and neutropenia but is much rarer and does not typically present with diarrhea.
• Phosphorus: Phosphorus deficiency is not associated with anemia or the symptoms described.
Next Steps:
• Confirm with serum vitamin B12 levels.
• Test for underlying causes of malabsorption, such as anti-tissue transglutaminase antibodies for celiac disease or a stool test for fat malabsorption.
A 35-year-old male patient came to an emergency
OPD complaining of high grade fever, headache and
neck pain of three days duration. He has been
admitted to a private hospital for three days taking
unidentified medications but had no improvement.
His temperature is 38.2 degree centigrade, pulse
rate is 100/min and respirations are 24/min. On
neurologic evaluation, he has neck stiffness and
kerning sign is positive. Laboratory studies show;
WBC count of 16.3x103/mm3, platelet count of
480x103/mm3, hemoglobin level of 14g/dl, there are
450 cells in CSF of which 75percent are neutrophils
and he is positive for HIV. What is the most
appropriate empiric management for the patient?
a. Ceftazidime and Metronidazole
• b. Ceftriaxone, Prednisolone and
Chloramphenicol
• c. Ceftriaxone, Vancomycin and Ampicillin
• d. Cefipime and Dexamethasone
The most appropriate empiric management is:
c. Ceftriaxone, Vancomycin, and Ampicillin
Explanation:
This patient has acute bacterial meningitis, likely due to his immunocompromised status (HIV-positive) and clinical findings of fever, headache, neck stiffness, positive Kernig’s sign, and CSF analysis showing neutrophilic pleocytosis (450 cells, 75% neutrophils).
• Ceftriaxone: Covers Streptococcus pneumoniae and Neisseria meningitidis, the most common causes of bacterial meningitis in adults.
• Vancomycin: Added to cover drug-resistant S. pneumoniae.
• Ampicillin: Included due to the patient’s HIV status, which places him at higher risk for Listeria monocytogenes.
Why not the other options?
• a. Ceftazidime and Metronidazole: These are not first-line agents for bacterial meningitis. Ceftazidime primarily covers Pseudomonas, and metronidazole targets anaerobes, which are uncommon in meningitis.
• b. Ceftriaxone, Prednisolone, and Chloramphenicol: Chloramphenicol is used in resource-limited settings but is not preferred due to resistance concerns. Prednisolone is not recommended; dexamethasone is the steroid of choice.
• d. Cefepime and Dexamethasone: Cefepime is used for broad-spectrum Gram-negative coverage (e.g., in nosocomial meningitis) but is not optimal for community-acquired bacterial meningitis.
Additional Considerations:
• Dexamethasone: Should be administered before or with the first dose of antibiotics to reduce inflammation in pneumococcal meningitis.
• Blood cultures and CSF cultures should be obtained before starting antibiotics, if possible.
A 38-year-old daily laborer from Humera presents
with complaints of fatigue, abdominal swelling and
early satiety for the past six months. On physical
examination, he is wasted, has pale conjunctiva and
splenomegaly. His hemoglobin level is 9 g/di, WBC
count is 3000/mm3 and platelet count is
100000/mm3. His splenic aspirate microscopy
revealed amastigote. PITC non-reactive (NR;
Hemoglobin 13.3-16.2g/dl, WBC count 3.54-9.06 x
103/mm3, platelet count 165-415 × 103/mm3).
What is the first line drug for the management of
this patent?
• a. amphotercin B + paramomycin
b. miltefosine+amphotercin B
c. amphotercin B + sodiumstibulogluconate
• d. sodium stibulgluconate +paramomycin
The first-line drug for the management of this patient is:
d. Sodium stibogluconate + paromomycin
Explanation:
This patient has visceral leishmaniasis (kala-azar), as evidenced by:
• Clinical symptoms: Fatigue, abdominal swelling (splenomegaly), early satiety, and wasting.
• Laboratory findings: Pancytopenia (anemia, leukopenia, thrombocytopenia) and identification of amastigotes in splenic aspirate.
• Geographical context: Humera, a region endemic to leishmaniasis.
First-line treatment:
• Sodium stibogluconate + paromomycin is the recommended first-line therapy for visceral leishmaniasis in many endemic regions, including East Africa.
• This combination is highly effective, reduces the duration of treatment, and minimizes resistance.
Why not the other options?
• a. Amphotericin B + paromomycin: Liposomal amphotericin B is an alternative but more commonly used in regions with high resistance to antimonials or in immunocompromised patients (e.g., HIV-positive).
• b. Miltefosine + amphotericin B: Miltefosine is used in certain regions but is not the first-line therapy in East Africa due to cost and availability.
• c. Amphotericin B + sodium stibogluconate: Effective but associated with higher toxicity and not routinely used as the first-line therapy.
Next Steps:
• Monitor for side effects during treatment, such as cardiotoxicity (with sodium stibogluconate) and nephrotoxicity (with amphotericin B).
• Assess response to treatment with clinical improvement and follow-up splenic aspirate, if necessary.
A 40-year-old female patient came to an OPD with
the complaint of amenorrhea of three months
duration. She also had frequent abortion for which
she visited many private clinics and did not get cure.
She also complained hot intolerance and significant
weight loss. Her pulse rate is 120/min. On
examination, she has lid lag and exophthalmia,
diffused anterior neck swelling which moves with
respiration, and thickened skin over the dorsum of
the foot and pre-tibial region. What is the most likely
explanation for these findings?
O a. Hashimotos thyroiditis
• b. Secondary thyrotoxicosis
• c. Subacute thyroiditis
• d. Graves’ disease
The most likely explanation for these findings is:
d. Graves’ disease
Explanation:
• Symptoms: Amenorrhea, hot intolerance, significant weight loss, and tachycardia (pulse rate 120/min) are consistent with hyperthyroidism.
• Signs: Lid lag, exophthalmos, diffusely enlarged thyroid (goiter), and pre-tibial myxedema (thickened skin) are classic features of Graves’ disease, an autoimmune condition and the most common cause of hyperthyroidism.
• Frequent abortions: Hyperthyroidism can lead to menstrual irregularities and pregnancy complications, including miscarriages.
Why not the other options?
• a. Hashimoto’s thyroiditis: Typically causes hypothyroidism and is associated with features like fatigue, cold intolerance, and weight gain, not hyperthyroidism or exophthalmos.
• b. Secondary thyrotoxicosis: Caused by TSH-secreting pituitary adenomas, which are rare and usually do not cause exophthalmos or pre-tibial myxedema.
• c. Subacute thyroiditis: Causes a painful thyroid and transient hyperthyroidism but does not present with exophthalmos or pre-tibial myxedema.
Next Steps:
• Confirm diagnosis with TSH, free T4, and T3 levels.
• Check TSH receptor antibodies (TRAb) to confirm Graves’ disease.
• Consider a thyroid ultrasound or radioactive iodine uptake (RAIU) scan to evaluate gland activity.
A 41-year-old man came to a hospital with a three
weeks history of generalized body swelling that
started from the legs and progressed to the whole
body. He also has shortness of breath at rest and
orthopnea of three pillows equivalent. On
examination, his blood pressure is 130/80 mmHg,
pulse rate is 120/min, respirations are 32/min,
temperature is 35.8 degree centigrade, he has
bilateral basal fine crepitation and S3 gallop, and
TVLS is 14cm. Investigation showed Creatinine level
of 2.1 mg/dl. What is the best initial treatment for
the patient?
a. Enalapril
• b. Metoprolol
• c. Hydrochlothizide
• d. Furosemide
The best initial treatment for the patient is:
d. Furosemide
Explanation:
The patient presents with signs and symptoms of congestive heart failure (CHF), including:
• Generalized body swelling (edema) starting from the legs, which suggests fluid retention.
• Shortness of breath and orthopnea (difficulty breathing while lying down), indicating pulmonary congestion.
• Bilateral basal fine crepitation and S3 gallop, which are clinical signs of heart failure.
• Elevated creatinine level (2.1 mg/dL), indicating some degree of renal impairment, which is common in heart failure due to poor perfusion or volume overload.
Furosemide is a loop diuretic used to manage fluid overload in heart failure by promoting renal excretion of sodium and water, thus reducing edema and alleviating symptoms like shortness of breath and orthopnea.
Why not the other options?
• a. Enalapril: An ACE inhibitor that helps with long-term management of heart failure by improving symptoms and outcomes, but it’s not the initial treatment in an acute setting where fluid overload needs to be addressed first.
• b. Metoprolol: A beta-blocker that is important in chronic heart failure management but should not be started in the acute setting of fluid overload without first stabilizing the patient.
• c. Hydrochlorothiazide: A thiazide diuretic, which is less potent than furosemide and typically used for mild fluid retention. In this patient with significant fluid overload and heart failure, a loop diuretic like furosemide is more appropriate.
Next Steps:
• Monitor renal function closely after initiating diuretics.
• Consider ACE inhibitors, beta-blockers, and aldosterone antagonists once the patient is stable and volume status is improved.
• Consider echocardiography to evaluate left ventricular function and determine the cause of heart failure.
A 55-year-old man came to an OPD with progressive
left side chest pain. The pain starts while performing
activities and improves during resting. He has
smoked about 20 pack years. Physical examination
showed normal system findings, but his blood
pressure is 140/90 mmHg. What is the most likely
cause of the patient’s chest pain?
• a. Subacute pericarditis
b. Atherosclerotic coronary artery disease
c. Chronic pulmonary thromboembolism
• d. Obstructive valve disease
The most likely cause of the patient’s chest pain is:
b. Atherosclerotic coronary artery disease
Explanation:
• Chest pain that is progressive, worsens with activity, and improves with rest is highly suggestive of angina, particularly stable angina related to coronary artery disease (CAD).
• The patient’s smoking history (20 pack years) is a major risk factor for atherosclerosis and CAD.
• Elevated blood pressure (140/90 mmHg) is another risk factor for cardiovascular disease.
Why not the other options?
• a. Subacute pericarditis: This condition causes chest pain that is usually sharp and worsens with inspiration or coughing, and may improve when sitting forward. It is not typically related to activity or rest.
• c. Chronic pulmonary thromboembolism: This condition can cause dyspnea and right heart failure but is less likely to present with chest pain that is activity-dependent.
• d. Obstructive valve disease: This can cause chest pain but is more likely to be associated with symptoms of heart failure (dyspnea, fatigue) or syncope, not activity-induced chest pain.
Next Steps:
• The patient should undergo ECG, stress testing, or coronary angiography to evaluate for coronary artery disease.
• Management may include lifestyle changes, antiplatelet therapy, and possibly statins, depending on the severity of the disease.
A 60-year-old female known diabetic patient on
follow-up was found to have hypertension. She is
not symptomatic, but her blood pressure was in the
hypertensive range for several months. She is taking
ant-diabetic medications properly and her glycemic
control is good. Currently, her blood pressure is
160/100 mm Hg. Laboratory investigation showed
protein +2 in the urine otherwise normal. What is the
preferred drug to start for blood pressure control?
• a. Amilodipine
• b. Hydrochrothiazide
• c. Atenolol
O d. Enalapril
The preferred drug to start for blood pressure control in this patient is:
d. Enalapril
Explanation:
This patient has hypertension and proteinuria, which is suggestive of diabetic nephropathy. The use of an ACE inhibitor like Enalapril is preferred because:
• ACE inhibitors (such as Enalapril) help lower blood pressure and provide renal protection, especially in patients with diabetes and proteinuria.
• They reduce glomerular hypertension and proteinuria, slowing the progression of kidney damage, which is particularly important in diabetic nephropathy.
• ACE inhibitors are also beneficial in patients with diabetic kidney disease (with or without hypertension), as they reduce both blood pressure and albuminuria.
Why not the other options?
• a. Amlodipine: A calcium channel blocker that is effective for blood pressure control, but it does not have the same protective effect on the kidneys as ACE inhibitors in patients with diabetes and proteinuria.
• b. Hydrochlorothiazide: A thiazide diuretic can help lower blood pressure, but it may not provide the renal protective benefits seen with ACE inhibitors. Additionally, it can worsen electrolyte imbalances and is not as protective against diabetic kidney disease.
• c. Atenolol: A beta-blocker can be used to control blood pressure but is not the preferred agent for diabetic nephropathy. It does not provide the same renal benefits as ACE inhibitors in this context.
Next Steps:
• Start Enalapril at an appropriate dose, monitor renal function (creatinine, potassium), and check for blood pressure response.
• Consider adding other agents if blood pressure control is inadequate.
• Continue monitoring proteinuria as a marker of kidney function.
A 55-year-old man came to an outpatient clinic with
a complaint of intermittent epigastric burning pain
which is worsened by taking food and awakes him
from sleep for the last two months. He has no
weight loss and any history of drug intake. Physical
examination shows mild epigastric tenderness.
Laboratory studies show hemoglobin level of
10.5g/dl, WBC count of 7500/mm3 and positive
stool helicobacter antigen. Upper Gl endoscopy
s h o w s d u o d e n a l ulcer. What is the b e s t
management for the patient?
• a. Start on H2 blocker
• b. Start on PPI +Clarithromycin
+Metronidazole
O c. Start on proton pump inhibitor
• d. Start on H2 blocker +Clarithromycin
+Metronidazole
The best management for the patient is:
b. Start on PPI + Clarithromycin + Metronidazole
Explanation:
The patient presents with symptoms suggestive of peptic ulcer disease (PUD), specifically a duodenal ulcer, which is confirmed by upper gastrointestinal endoscopy. The positive stool Helicobacter pylori antigen suggests that the ulcer is likely caused by an H. pylori infection.
The first-line treatment for H. pylori-associated peptic ulcers involves triple therapy, which typically includes:
• Proton pump inhibitor (PPI): Reduces gastric acid secretion, promoting ulcer healing and providing symptomatic relief.
• Clarithromycin: An antibiotic that targets H. pylori.
• Metronidazole: An alternative antibiotic for H. pylori eradication, particularly in areas with high resistance to clarithromycin.
Why not the other options?
• a. Start on H2 blocker: H2 blockers can reduce stomach acid, but they are less effective than PPIs and do not address the underlying H. pylori infection.
• c. Start on proton pump inhibitor: While a PPI is appropriate for ulcer healing and symptom relief, H. pylori eradication requires antibiotic therapy as well, which is not provided by PPI alone.
• d. Start on H2 blocker + Clarithromycin + Metronidazole: This is not the preferred combination. While it includes the correct antibiotics, H2 blockers are less effective than PPIs in reducing gastric acid and promoting ulcer healing.
Next Steps:
• Confirm eradication: After completing the triple therapy (PPI, clarithromycin, metronidazole), re-test for H. pylori (preferably with a stool antigen test or urea breath test) to confirm eradication.
• Consider maintenance therapy with a PPI if the patient has complications like severe symptoms or if there is a history of ulcer recurrence., you can change metronidazole by amoxicillin
A 38-year-old female patient, who is on treatment for
Crohn’s disease for two years, came to a medical
referral clinic complaining about weakness,
palpitation, forgetfulness and headache of two
months duration. On evaluation, she has tachycardia
and absent deep tendon reflexes and position and
vibration sensation. Her blood cell count shows
WBC of 3.8x103/microlitre, platelet of
350x103/microlitre, and hemoglobin of 8.0g/dL. On
examination of peripheral blood smear, there are
three neutrophils with seven lobes. What is the most
appropriate initial management for this patient?
• a. Prednisolone
• b. Cyanocobalamine
• c. Iron sulfate
• d. Immunotherapy
The most appropriate initial management for this patient is:
b. Cyanocobalamin
Explanation:
The patient presents with symptoms that are indicative of vitamin B12 deficiency, which is commonly seen in patients with Crohn’s disease, particularly those with ileal involvement or those who have undergone intestinal resection. The key signs and symptoms include:
• Weakness, palpitations, forgetfulness, and headache, which may be attributed to anemia and neurological manifestations of B12 deficiency.
• Tachycardia and absent deep tendon reflexes and loss of position and vibration sensation suggest neurological involvement, which can occur with B12 deficiency (peripheral neuropathy).
• Blood findings: The patient has anemia (hemoglobin of 8.0g/dL) and neutrophils with hypersegmentation (7 lobes), which is a classic sign of megaloblastic anemia due to vitamin B12 deficiency.
• WBC count of 3.8 x 10^3/μL indicates mild leukopenia, which is consistent with B12 deficiency.
Vitamin B12 is essential for red blood cell production and nervous system function. In Crohn’s disease, particularly with ileal involvement or bowel resections, B12 malabsorption is common.
Why not the other options?
• a. Prednisolone: While steroids are used to manage flare-ups of Crohn’s disease, they do not address the underlying B12 deficiency and would not help resolve the patient’s current symptoms.
• c. Iron sulfate: While this is used for iron deficiency anemia, the patient’s symptoms and blood findings are more consistent with megaloblastic anemia (due to B12 deficiency) rather than iron deficiency.
• d. Immunotherapy: This is not relevant for vitamin B12 deficiency or for treating the current symptoms, which are due to a nutritional deficiency rather than active inflammation or immune-mediated disease.
Next Steps:
• Cyanocobalamin (B12) should be administered, typically through intramuscular injection or oral supplementation, depending on the severity of deficiency and the patient’s ability to absorb it.
• Follow-up with monitoring of B12 levels and neurological symptoms to assess response to treatment.
• If the patient has had intestinal surgery or malabsorption, long-term supplementation may be necessary.
A 48-year-old female patient was admitted to a
medical ICU with the diagnosis of NYHA Class-IV
Stage-C CHF secondary to chronic rheumatic
valvular heart disease. The physicians and nurses in
the ICU were unable to secure IV line. Where is the
most appropriate site for IV access in the patient?
a. Saphenous vein cut down
• b. Intraouseus route
• c. Scalp vein
• d. Jugular vein cut down
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The most appropriate site for IV access in this patient is:
d. Jugular vein cut down
Explanation:
In critically ill patients, especially those with severe heart failure (NYHA Class-IV Stage-C CHF), IV access may be difficult due to peripheral venous collapse or difficulty in securing a peripheral line. When standard IV access is not possible, more central veins or alternative access methods are considered. The jugular vein is an appropriate choice for central venous access because:
• It is a large, easily accessible vein with relatively predictable anatomy.
• The cut down technique involves making a small incision over the vein to gain direct access, which is useful when standard venous access techniques (e.g., peripheral IV or central venous catheter placement) fail.
Why not the other options?
• a. Saphenous vein cut down: The saphenous vein is typically used for lower extremity access in emergency situations, but it is not commonly the first choice for central access in critically ill patients due to the difficulty of performing a cut down and the potential for complications.
• b. Intraosseous route: The intraosseous route is used for emergency access in pediatric or adult patients when no other options are available (e.g., in cases of trauma or cardiac arrest), but it is generally considered a last resort, and not the best first-line option for this scenario.
• c. Scalp vein: Scalp veins are typically used in infants or small children for IV access. In an adult patient, the jugular vein would be a more appropriate choice for central venous access.
Next Steps:
• Once access is achieved (e.g., via the jugular vein cut down), ensure appropriate monitoring and management of the patient’s CHF symptoms, including diuretics, inotropes, and other supportive measures.
• Consider the need for longer-term access (e.g., for medications or nutrition) and choose the best approach based on the patient’s condition.