Circulation, Vol 79, 783-790, Copyright © 1989 by American Heart Association
F Morady, WH Kou, AH Kadish, LK Toivonen, JA Kushner and S Schmaltz
The purpose of our study was to determine whether an infusion of
epinephrine reverses the electrophysiologic effects of verapamil and
whether reversal of verapamil's effects on the induction of paroxysmal
supraventricular tachycardia (PSVT) by epinephrine during
electropharmacologic testing is predictive of stress-related recurrences of
PSVT during long-term treatment with verapamil. The infusion rates of
epinephrine used in this study were 25 and 50 ng/kg/min, which previously
have been demonstrated to result in plasma epinephrine concentrations in
the range that occurs during a variety of stresses in humans. The subjects
of this study were 17 patients with recurrent PSVT who underwent an
electrophysiologic study in the control state and after at least 2 days of
treatment with 240-480 mg/day verapamil. After assessing the response to
verapamil, epinephrine was infused and testing was repeated. Verapamil
significantly slowed atrioventricular conduction and prolonged
refractoriness in the atrium and atrioventricular node. The effects of the
two infusion rates of epinephrine were generally similar in magnitude and,
therefore, the results were pooled. Epinephrine partially or completely
reversed all of verapamil's electrophysiologic effects. Verapamil
suppressed the induction of sustained PSVT in 15 patients. Epinephrine
facilitated the induction of PSVT in seven of these 15 patients. All 15
patients were treated on a long-term basis with verapamil. The eight
patients in whom epinephrine did not facilitate the induction of PSVT had
no recurrences of PSVT during 9-18 months of follow-up.(ABSTRACT TRUNCATED
AT 250 WORDS)
ARTICLES
Epinephrine-induced reversal of verapamil's electrophysiologic and therapeutic effects in patients with paroxysmal supraventricular tachycardia
Division of Cardiology, University of Michigan Medical Center, Ann Arbor.
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