I have enough information from the library and my knowledge to provide comprehensive answers to all questions. Here are the detailed answers:
Q.No 2 - Anaphylactic Shock Treatment
Correct Answer: Intramuscular adrenaline hydrochloride ✅ (already marked green)
Explanation: Adrenaline (epinephrine) is the only life-saving drug for anaphylactic shock. The intramuscular (IM) route - specifically into the anterolateral thigh - is the standard first-line route because:
- IM delivers faster and more reliable absorption than subcutaneous
- IV adrenaline is reserved for cardiac arrest or refractory cases under close monitoring, as it carries risk of fatal arrhythmias
- Hydrocortisone and antihistamines are adjuncts, NOT life-saving agents
- IV glucose saline has no role as primary treatment
Dermatology 5e: "Epinephrine (adrenaline) by subcutaneous or intramuscular injection is the treatment of choice for anaphylactic shock."
Q.No 3 - Prolonged Paralysis After Succinylcholine
Correct Answer: Deficiency of plasma pseudocholinesterase leading to delayed drug metabolism ✅ (already marked green)
Explanation: Succinylcholine is a depolarizing neuromuscular blocker whose action is terminated almost entirely by plasma pseudocholinesterase (butyrylcholinesterase). In this patient:
- Repeated doses were given throughout a long procedure
- Atypical or deficient pseudocholinesterase = failure to hydrolyze succinylcholine rapidly
- Result: persistent depolarizing block that mimics a non-depolarizing pattern on monitoring (Phase II block can develop with repeated doses, but the PRIMARY mechanism here is enzyme deficiency)
- The NMB monitor showing a "non-depolarizing pattern" is consistent with Phase II block from repeated succinylcholine, but the root cause is pseudocholinesterase deficiency
Barash Clinical Anesthesia 9e: "There is genetic variation in this enzyme [pseudocholinesterase] that can result in the duration of paralysis being significantly prolonged."
Note on option "Development of Phase II block": This is also plausible - repeated succinylcholine can cause Phase II block. However, the question asks for the mechanism responsible for prolonged paralysis in a patient who fails to recover - pseudocholinesterase deficiency is the more fundamental explanation and the classic pharmacology answer.
Q.No 4 - Nocturnal Enuresis Treatment with Tricyclic Antidepressant
Correct Answer: Imipramine ✅ (already marked green)
Explanation: Among tricyclic antidepressants, imipramine is the only one with FDA approval specifically for nocturnal enuresis in children. Mechanism:
- Anticholinergic effect on bladder (reduces detrusor overactivity)
- Possible central effect on sleep arousal
- Alpha-adrenergic effect increasing bladder outlet resistance
- Dose: 25-50 mg at bedtime
Kaplan & Sadock's Comprehensive Textbook of Psychiatry: "Imipramine has been used with FDA approval for the treatment of nocturnal enuresis in children. Usual doses are 25 to 50 mg at bedtime."
Other TCAs (amitriptyline, desipramine, clomipramine) are NOT approved for this indication.
Q.No 5 - Drug Holiday in Parkinson's Disease
Correct Answer: It involves abrupt withdrawal of levodopa to restore drug responsiveness but carries serious risks ✅ (already marked green)
Explanation: A "drug holiday" in Parkinson's disease refers to the deliberate, complete withdrawal of levodopa (usually for 1-3 weeks) with the goal of resensitizing dopamine receptors and restoring drug responsiveness after prolonged use leads to wearing-off and dyskinesias.
- Serious risks include: neuroleptic malignant-like syndrome, aspiration pneumonia, deep vein thrombosis, severe immobility, and even death
- It is NOT routinely recommended, is NOT the first-line for wearing-off (dose adjustments, adjuncts like MAO-B inhibitors are preferred), and does NOT safely prevent dyskinesia without hospitalization
- Requires hospitalization and close monitoring when performed
Q.No 6 - Anaemia in Chronic Kidney Disease
Correct Answer: Erythropoietin ✅ (already marked green)
Explanation: The anaemia of chronic kidney disease (CKD) is classically normocytic, normochromic and caused by decreased production of erythropoietin (EPO) by the peritubular fibroblasts of the kidney.
- EPO is the primary hormone driving red cell production in the bone marrow
- As GFR falls, EPO production drops progressively
- Iron deficiency can co-exist but causes microcytic anaemia
- Intrinsic factor deficiency causes megaloblastic (macrocytic) anaemia (B12/folate)
- Vitamin B12 deficiency also causes macrocytic anaemia
The normocytic pattern here specifically points to EPO deficiency as the primary mechanism.
Q.No 7 - Antiarrhythmic for Acute AV Nodal Tachycardia
Correct Answer: Adenosine (the marked answer "Quinidine" is INCORRECT)
⚠️ The image shows Quinidine highlighted green, but this is the wrong answer.
Correct answer is Adenosine.
Explanation:
- Adenosine is the drug of choice for acute paroxysmal supraventricular tachycardia (PSVT) including AV nodal reentrant tachycardia (AVNRT) - the most common cause of paroxysmal rapid heart rate in a 16-year-old girl
- Adenosine transiently blocks AV nodal conduction, interrupting the reentrant circuit
- Onset within seconds, half-life ~10 seconds - extremely safe
- Tintinalli's Emergency Medicine: Adenosine for AV nodal-dependent SVT is standard therapy
Why not Quinidine?
- Quinidine is a Class IA antiarrhythmic used for atrial flutter/fibrillation, not first-line for acute AVNRT
- It has serious toxicity (cinchonism, QT prolongation, torsades de pointes)
Why not others?
- Amiodarone: reserved for refractory/complex arrhythmias
- Propranolol: can be used for chronic prevention, not first-line acute termination
Summary Table
| Q# | Correct Answer | Status |
|---|
| Q2 | Intramuscular adrenaline hydrochloride | ✅ Correct |
| Q3 | Deficiency of plasma pseudocholinesterase | ✅ Correct |
| Q4 | Imipramine | ✅ Correct |
| Q5 | Abrupt withdrawal of levodopa to restore responsiveness (with serious risks) | ✅ Correct |
| Q6 | Erythropoietin | ✅ Correct |
| Q7 | Adenosine (NOT Quinidine - the marked answer is wrong) | ❌ Marked incorrectly |