Antidysrhythmic drug therapy for the termination of stable, monomorphic ventricular tachycardia: a systematic review

Emerg Med J. 2015 Feb;32(2):161-7. doi: 10.1136/emermed-2013-202973. Epub 2013 Sep 16.

Abstract

Objective: We performed a systematic review of the literature to compare the efficacy of different drug therapies for the termination of stable, monomorphic ventricular tachycardia (VT).

Methods: We searched EMBASE, MEDLINE and Cochrane for trials from 1965 through July 2013 using a search strategy derived from the following clinical question in PICO format:

Patients: Adults (≥18 years) with stable monomorphic VT;

Intervention: Intravenous antidysrhythmic drug; Comparator: Intravenous lidocaine or amiodarone;

Outcome: Termination of VT. For all drug comparisons, we calculated relative risks (RR; 95% CI) and number needed to treat (NNT, 95% CI) between drugs. We also evaluated the methodological quality of the studies.

Results: Our search yielded 219 articles by PubMed and 390 articles by EMBASE. 3 prospective studies (n=93 patients) and 2 retrospective studies (n=173 patients) met our inclusion and exclusion criteria. From the prospective studies, RR of VT termination of procainamide versus lidocaine was 3.7 (1.3-10.5); ajmaline versus lidocaine, RR=5.3 (1.4-20.5); and sotalol versus lidocaine, RR=3.9 (1.3-11.5). From the retrospective studies: procainamide versus lidocaine, RR=2.2 (1.2-4.0); and procainamide versus amiodarone RR=4.3 (0.8-23.6). All 5 reviewed studies had quality issues, including potential bias for randomisation and concealment.

Conclusions: Based on limited available evidence from small heterogeneous human studies, for the treatment of stable, monomorphic VT, procainamide, ajmaline and sotalol were all superior to lidocaine; amiodarone was not more effective than procainamide.

Keywords: cardiac care, arrythmia; emergency department management; resuscitation, clinical care.

Publication types

  • Review
  • Systematic Review

MeSH terms

  • Administration, Intravenous
  • Anti-Arrhythmia Agents / therapeutic use*
  • Humans
  • Prospective Studies
  • Retrospective Studies
  • Tachycardia, Ventricular / drug therapy*

Substances

  • Anti-Arrhythmia Agents