Cardiac Arrhythmia Suppression Trial

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The Cardiac Arrhythmia Suppression Trial (CAST) was a double-blind, randomized controlled study designed to test the hypothesis that suppression of premature ventricular complexes (PVC) with class I antiarrhythmic agents after a myocardial infarction (MI) would reduce mortality. It was conducted between 1986 and 1998 and included over 1700 patients in 27 centres.[1] The study found that the tested drugs increased mortality instead of lowering it, as was expected.[2] The publication of these results in 1991/92, in combination with large follow-up studies for drugs that had not been tested in CAST, led to a paradigm shift in the treatment of MI patients. Class I and III antiarrhythmics are now only used with extreme caution after MI, or they are contraindicated completely.[3] Heart Rhythm Society Distinguished Scientist D. George Wyse was a member of the CAST trial's steering and executive committees.

Background[edit]

The study was prompted by the fact that patients who suffer from myocardial infarctions have a high risk of sudden death, presumably due to arrhythmia. Around the time of the study onset (1986), it was estimated that 8 to 15 percent of patients would die in the subsequent year following an MI, with about half of those deaths resulting from arrhythmia. This warranted the investigation as to whether PVC suppression could improve outcomes in post-MI patients. The trial was conducted by the National Heart, Lung, and Blood Institute.

Study design[edit]

CAST was a multicenter, double-blind, randomized controlled trial. Patients were randomized to drug therapy or placebo if they met the following criteria: 1) They had a myocardial infarction occurring six days to two years prior to the onset of the study, and 2) they had asymptomatic ventricular premature beats, detected by Holter monitor, which could be suppressed by either encainide, flecainide, and moracizine in an open-label design. A total of 1727 subjects that responded were randomized, 1455 to encainide, flecainide, or placebo, and 272 to moracizine or placebo. The primary endpoint was sudden cardiac death, and the secondary endpoint was all-cause mortality.

The second Cardiac Arrhythmia Suppression Trial (CAST II) modified the enrollment criteria to include patients at higher risk for serious arrhythmia.[4] This included 1) patients enrolled within 4 to 90 days of a previous MI, 2) a left ventricular ejection fraction lower than 40%, 3) prior to enrollment, suppression of PVCs had occurred with the drugs (vs. placebo) using a double-blinded design, and 4) patients having more serious arrhythmias would also be included.

Results[edit]

The drugs used (encainide, flecainide, and moracizine) successfully reduced the amount of PVCs, but consequently led to more arrhythmia-related deaths. Total mortality was significantly higher with both encainide and flecainide at a mean follow-up period of ten months. Within about two years after enrollment, encainide and flecainide were discontinued because of increased mortality and sudden cardiac death. CAST II compared moracizine to placebo but was also stopped because of early (within two weeks) cardiac death in the moracizine group, and long-term survival seemed highly unlikely. The excess mortality was attributed to proarrhythmic effects of the agents.

References[edit]

  1. ^ "Preliminary Report: Effect of Encainide and Flecainide on Mortality in a Randomized Trial of Arrhythmia Suppression after Myocardial Infarction". New England Journal of Medicine 321 (6): 406–412. 1989. doi:10.1056/NEJM198908103210629. PMID 2473403.  edit
  2. ^ Echt, D. S.; Liebson, P. R.; Mitchell, L. B.; Peters, R. W.; Obias-Manno, D.; Barker, A. H.; Arensberg, D.; Baker, A.; Friedman, L.; Greene, H. L.; Huther, M. L.; Richardson, D. W. (1991). "Mortality and Morbidity in Patients Receiving Encainide, Flecainide, or Placebo". New England Journal of Medicine 324 (12): 781–788. doi:10.1056/NEJM199103213241201. PMID 1900101.  edit
  3. ^ Mutschler, Ernst; Schäfer-Korting, Monika (2001). Arzneimittelwirkungen (in German) (8 ed.). Stuttgart: Wissenschaftliche Verlagsgesellschaft. p. 544. ISBN 3-8047-1763-2. 
  4. ^ Brooks, M. M.; Gorkin, L.; Schron, E. B.; Wiklund, I.; Campion, J.; Ledingham, R. B. (1994). "Moricizine and quality of life in the Cardiac Arrhythmia Suppression Trial II (CAST II)". Controlled clinical trials 15 (6): 437–449. PMID 7851106.  edit

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