Many patients who receive electroconvulsive therapy (ECT) are benzodia
zepine dependent or are anxious and require benzodiazepine drugs. Beca
use these agents may diminish the therapeutic effectiveness of ECT, we
explored the dosing, safety, and efficacy of pre-ECT flumazenil admin
istration, a benzodiazepine-competitive antagonist, in patients receiv
ing benzodiazepine medications. We report our experience with 35 patie
nts who received both flumazenil and benzodiazepine drugs during their
ECT course. We compared seizure duration with and without flumazenil
and compared treatment efficacy to 49 patients who received ECT withou
t either of these medications. Flumazenil could be safely administered
with ECT. A few subjects taking higher chronic benzodiazepine dosages
experienced breakthrough anxiety or withdrawal symptoms, which were w
ell managed by dosing flumazenil immediately before the anesthetic age
nt and by immediate posttreatment benzodiazepine administration. A dos
e of 0.4-0.5 mg was adequate for all but those taking the highest benz
odiazepine dosages, where 0.8-1.0 mg resulted in a clinically more eff
ective reversal. No differences in efficacy or seizure duration were f
ound as a function of flumazenil administration. Flumazenil offers the
promise of safe and effective ECT in patients receiving benzodiazepin
e drugs. Follow-up outcome investigation on a random assignment basis
will be necessary for definitive assessment of the value of flumazenil
. In addition, the direct effect of benzodiazepine drugs and the fluma
zenil/benzodiazepine combination on ECT seizures remains to be determi
ned.