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Anaesthesia · Intravenous and inhalational agents: myotonic dystrophy and suxamethonium
Sample itemA 32-year-old man with myotonic dystrophy and a cardiac conduction defect needs general anaesthesia. Why is suxamethonium best avoided?
Original practice item, not a recalled exam question. Nothing here is recorded.
The answer and the reasoning
C. It can provoke a sustained generalised myotonic contracture that makes ventilation and intubation difficult
Depolarisation in myotonic muscle can cause prolonged contracture that is not reliably relieved by non-depolarising agents, and it may impair ventilation. Short-acting non-depolarisers with sugammadex reversal are preferred, with attention to the cardiac conduction defect and sensitivity to sedatives.
Option by option
A. It causes life-threatening hyperkalaemia in all patients with a myopathy
Hyperkalaemia is a concern in denervation and muscular dystrophies such as Duchenne, not the principal issue here.
B. It is cleared slowly because plasma cholinesterase is usually absent
Cholinesterase activity is not characteristically absent in myotonic dystrophy.
C. It can provoke a sustained generalised myotonic contracture that makes ventilation and intubation difficult (correct)
Correct. Myotonic contracture after suxamethonium is the specific hazard.
D. It triggers malignant hyperthermia in every patient with myotonia
Myotonia is not an established trigger state for malignant hyperthermia in every patient.
Source note: Original NextPrep sample item — pending expert review. This item is original practice material awaiting independent expert review, so confirm important facts in a standard textbook.
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