JACC
HOME SUBSCRIPTIONS CURRENT ISSUE PAST ISSUES CARDIOSOURCE SEARCH HELP FEEDBACK
 QUICK SEARCH:   [advanced]


     


J Am Coll Cardiol, 1988; 12:388-394
© 1988 by the American College of Cardiology Foundation
This Article
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Morady, F
Right arrow Articles by de Buitleir, M
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Morady, F
Right arrow Articles by de Buitleir, M

Antagonism of quinidine's electrophysiologic effects by epinephrine in patients with ventricular tachycardia

F Morady, WH Kou, AH Kadish, SD Nelson, LK Toivonen, JA Kushner, S Schmaltz, and M de Buitleir

Department of Internal Medicine, University of Michigan Medical Center, Ann Arbor.

The purpose of this study was to determine whether pharmacologically induced elevations in the plasma epinephrine concentration within reported physiologic limits alter the response to quinidine during electropharmacologic testing. Twenty-one patients with coronary artery disease and a history of unimorphic ventricular tachycardia were found to have inducible sustained unimorphic ventricular tachycardia that was suppressed by treatment with oral quinidine gluconate. Epinephrine was then infused at a rate of either 25 or 50 ng/kg per min and testing was repeated. These infusion rates of epinephrine were previously demonstrated to result in elevations of the plasma epinephrine concentration in the range of concentrations that occur during a variety of stresses. Quinidine significantly lengthened the ventricular refractory periods and the QRS duration at a ventricular pacing cycle length of 350 ms, which was used as an index of intraventricular conduction. Epinephrine partially or completely reversed the effects of quinidine on ventricular refractory periods, but had no effect on QRS duration. During electropharmacologic testing of quinidine, no ventricular tachycardia was inducible in 12 patients, and only nonsustained ventricular tachycardia, 8 to 48 beats in duration, was inducible in 9 patients. Retesting during infusion of epinephrine demonstrated inducible sustained unimorphic ventricular tachycardia in 2 of the 12 patients in whom quinidine had completely suppressed the induction of ventricular tachycardia and in 8 of the 9 patients in whom only nonsustained ventricular tachycardia had been inducible during testing of quinidine. In conclusion, physiologic elevations in the plasma epinephrine concentration may reverse quinidine-induced prolongation of ventricular refractoriness but not intraventricular conduction.(ABSTRACT TRUNCATED AT 250 WORDS)


This article has been cited by other articles:


Home page
J. Pharmacol. Exp. Ther.Home page
L. Sen, G. Cui, Y. Sakaguchi, and B. N. Singh
Electrophysiological Effects of MS-551, a New Class III Agent: Comparison with dl-Sotalol in Dogs
J. Pharmacol. Exp. Ther., May 1, 1998; 285(2): 687 - 694.
[Abstract] [Full Text]


Home page
CirculationHome page
K. T. Cragun, S. B. Johnson, and D. L. Packer
ß-Adrenergic Augmentation of Flecainide-Induced Conduction Slowing in Canine Purkinje Fibers
Circulation, October 21, 1997; 96(8): 2701 - 2708.
[Abstract] [Full Text]


Home page
CirculationHome page
A. M. Gillis, R. S. Sheldon, D. G. Wyse, J. W. Leitch, R. Yee, G. J. Klein, H. J. Duff, and L. B. Mitchell
Long-term Reproducibility of Ventricular Tachycardia Induction in Patients With Implantable Cardioverter/Defibrillators : Serial Noninvasive Studies
Circulation, May 15, 1995; 91(10): 2605 - 2613.
[Abstract] [Full Text]




HOME SUBSCRIPTIONS CURRENT ISSUE PAST ISSUES CARDIOSOURCE SEARCH HELP FEEDBACK
Copyright © 1988 by the American College of Cardiology Foundation.