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Anaesthesia · Muscle relaxants: volatile agents potentiate block
Sample itemDuring a long laparotomy under 1.5 MAC sevoflurane, the interval between rocuronium top-ups is much longer than it was in an earlier case under propofol infusion. What is the best explanation?
Original practice item, not a recalled exam question. Nothing here is recorded.
The answer and the reasoning
B. Volatile agents potentiate non-depolarising block
Inhalational agents, especially sevoflurane, desflurane and isoflurane, enhance non-depolarising block in a dose-dependent way, so less relaxant is needed than under intravenous anaesthesia. The effect is partly central and partly at the postjunctional membrane. The anaesthetist must therefore adjust relaxant doses to the technique.
Option by option
A. Sevoflurane inhibits plasma cholinesterase
Rocuronium is cleared by liver and kidney and does not depend on plasma cholinesterase.
B. Volatile agents potentiate non-depolarising block (correct)
Correct. Volatile agents add to the block, lengthening the effect of each dose.
C. Sevoflurane displaces rocuronium from plasma proteins into muscle
Protein-binding displacement is not a recognised action of sevoflurane on relaxants.
D. Sevoflurane increases the number of junctional receptors
More receptors would make the patient resistant, the opposite of what was seen.
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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