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Pharmacology · Sedative-hypnotics: flumazenil
Sample itemA 40-year-old woman on long-term clonazepam is brought unconscious after ingesting an unknown quantity of clonazepam and amitriptyline. Respiration is shallow and the ECG shows a wide QRS. A colleague suggests flumazenil. Why is it generally avoided here?
Original practice item, not a recalled exam question. Nothing here is recorded.
The answer and the reasoning
B. It can precipitate seizures in a benzodiazepine-dependent patient with a pro-convulsant co-ingestant
Flumazenil is a competitive antagonist at the benzodiazepine site. In chronic users it precipitates withdrawal, and when tricyclic antidepressants or other pro-convulsant drugs are co-ingested it unmasks seizures, which are hard to control. It also has a short duration, so resedation can follow. Airway support is the safer approach.
Option by option
A. It potentiates tricyclic-induced sodium channel blockade into asystole
Flumazenil has no action on sodium channels; the wide QRS is from the tricyclic itself.
B. It can precipitate seizures in a benzodiazepine-dependent patient with a pro-convulsant co-ingestant (correct)
Reversal of benzodiazepine effect can unmask seizures from dependence and the tricyclic.
C. It permanently destroys benzodiazepine receptors
Competitive antagonism is reversible and does not destroy receptors.
D. It causes severe hypotension by alpha blockade
Flumazenil has no alpha-blocking effect and does not cause hypotension.
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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