Reversal of flecainide-induced ventricular arrhythmia by hypertonic sodium bicarbonate in dogs

David M. Salerno, Maryann M. Murakami, Roland B. Johnston, Daniel E. Keyler, Paul R. Pentel

Research output: Contribution to journalArticlepeer-review

21 Scopus citations

Abstract

Flecainide occasionally produces incessant ventricular tachycardia that is difficult to treat. Reports of uncontrolled clinical studies have suggested a therapeutic role for hypertonic sodium bicarbonate (NaHCO3). To test this observation, spontaneous and pacing-induced arrhythmia canine models were designed. In the spontaneous model, flecainide was infused at 0.5 mg/kg/min until ventricular tachycardia occurred spontaneously. In the pacing-induced model, flecainide was infused at 1.0 mg/kg/min load (0.5 mg/kg/min maintenance) stepwise until the QRS was widened 50%, 75%, and 100%, with programmed ventricular stimulation at each step until ventricular arrhythmia was induced. Dogs who developed spontaneous arrhythmia were treated blindly with three doses of either NaHCO3 (3 mEq/kg/dose, with 1 minute between doses) or normal saline. Dogs who were induced in the second model were treated with the same three doses, 10 minutes apart, with programmed stimulation between each dose. Before unblinding in both protocols, dogs were classified as "responders" or "nonresponders" to therapy. In the spontaneous model, of 14 dogs with spontaneous ventricular tachycardia, all 7 dogs treated with NaHCO3 showed response, compared with only 1 of 7 dogs treated with saline (P < .01). Ventricular QRS complexes/min were reduced by NaHCO3 in that protocol. In the induced arrhythmia protocol, of 14 dogs with inducible arrhythmia, 6 of 7 responded to NaHCO3, and 1 of 7 responded to placebo (P < .05). In both protocols, arterial pH and the serum sodium concentration were increased by NaHCO3 but not by normal saline control treatment. QRS interval duration was shortened by NaHCO3 therapy. Thus, prolongation of the QRS interval and ventricular arrhythmia can be produced in dogs by flecainide infusion and can be treated effectively by administration of hypertonic NaHCO3. In view of the response to NaHCO3, the mechanism of arrhythmia may be slowed intraventricular conduction caused by sodium channel inhibition. These data suggest that hypertonic NaHCO3 may be useful in the treatment of ventricular arrhythmia due to flecainide overdose and, possibly, for proarrhythmia as well.

Original languageEnglish (US)
Pages (from-to)285-293
Number of pages9
JournalAmerican Journal of Emergency Medicine
Volume13
Issue number3
DOIs
StatePublished - May 1995

Bibliographical note

Funding Information:
From the Division of Cardiology and Division of Clinical Pharmacology and Toxicology, Department of Medicine, Hennepin County Medical Center, University of Minnesota, Minneapolis, MN. Manuscript received June 1, 1994; revision accepted August 22, 1994. Supported by a research grant from Hennepin Faculty Associates. Address reprint requests to Dr Pentel, Department of Medicine, Hennepin County Medical Center, 701 Park Ave, Minneapolis, MN 55415. Key Words: Flecainide, antiarrhythmic, arrhythmia, proar-rhythmia, sodium bicarbonate, Class IC drugs. Copyright © 1995 by W.B. Saunders Company 0735-6757/95/1303-000855.00/0

Keywords

  • Class IC drugs
  • Flecainide
  • antiarrhythmic
  • arrhythmia
  • proarrhythmia
  • sodium bicarbonate

Fingerprint Dive into the research topics of 'Reversal of flecainide-induced ventricular arrhythmia by hypertonic sodium bicarbonate in dogs'. Together they form a unique fingerprint.

Cite this