Circulation, Vol 54, 885-889, Copyright © 1976 by American Heart Association
RA Winkle, PJ Meffin, JW Fitzgerald and DC Harrison
Tocainide, a new oral antiarrhythmic agent, was studied in man in a
short-term protocol designed to evaluate the efficacy, kinetics, and
toxicity of this compound. Premature ventricular contractions (PVCs) were
suppressed by less than 70% in 11 of 15 patients compared with pre- drug
placebo controls. For these 11 responders, there was an average PVC
reduction of 91% +/- 10 (range 70 to 100%) at tocainide doses not
associated with side effects. Mild transient central nervous system
toxicity was observed in some patients near the time of peak concentrations
during the highest dose administered. The drug was found to have linear
kinetics over the dose range studied and a plasma half- life of 13.5 +/- 2
hours. Plasma concentration-response curves indicate antiarrhythmic
activity over all plasma concentrations, with 70% PVC reduction above 6.0
mug/ml. This study suggests that tocainide is a safe and effective
antiarrhythmic agent during short-term administration and is worthy of
further clinical trials.
ARTICLES
Clinical efficacy and pharmacokinetics of a new orally effective antiarrhythmic, tocainide
This article has been cited by other articles:
![]() |
S. P. KUTALEK, J. MORGANROTH, and L. N. HOROWITZ Tocainide: A New Oral Antiarrhythmic Agent Ann Intern Med, September 1, 1985; 103(3): 387 - 391. [Abstract] [PDF] |
||||
|
Circulation Home | Subscriptions | Archives | Feedback | Authors | Help | AHA Journals Home | Search Copyright © 1976 American Heart Association, Inc. All rights reserved. Unauthorized use prohibited. |