Background Patients who survive life-threatening ventriculararrhythmias are at risk for recurrent arrhythmias. They canbe treated with either an implantable cardioverterdefibrillatoror antiarrhythmic drugs, but the relative efficacy of thesetwo treatment strategies is unknown.
Methods To address this issue, we conducted a randomized comparisonof these two treatment strategies in patients who had been resuscitatedfrom near-fatal ventricular fibrillation or who had undergonecardioversion from sustained ventricular tachycardia. Patientswith ventricular tachycardia also had either syncope or otherserious cardiac symptoms, along with a left ventricular ejectionfraction of 0.40 or less. One group of patients was treatedwith implantation of a cardioverterdefibrillator; theother received class III antiarrhythmic drugs, primarily amiodaroneat empirically determined doses. Fifty-six clinical centersscreened all patients who presented with ventricular tachycardiaor ventricular fibrillation during a period of nearly four years.Of 1016 patients (45 percent of whom had ventricular fibrillation,and 55 percent ventricular tachycardia), 507 were randomly assignedto treatment with implantable cardioverterdefibrillatorsand 509 to antiarrhythmic-drug therapy. The primary end pointwas overall mortality.
Results Follow-up was complete for 1013 patients (99.7 percent).Overall survival was greater with the implantable defibrillator,with unadjusted estimates of 89.3 percent, as compared with82.3 percent in the antiarrhythmic-drug group at one year, 81.6percent versus 74.7 percent at two years, and 75.4 percent versus64.1 percent at three years (P<0.02). The corresponding reductionsin mortality (with 95 percent confidence limits) with the implantabledefibrillator were 39±20 percent, 27±21 percent,and 31±21 percent.
Conclusions Among survivors of ventricular fibrillation or sustainedventricular tachycardia causing severe symptoms, the implantablecardioverterdefibrillator is superior to antiarrhythmicdrugs for increasing overall survival.
Source Information
From the AVID Clinical Trial Center, University of Washington, Seattle. The manuscript was prepared by members of the AVID Executive Committee, who accept responsibility for its scientific content: Douglas P. Zipes, M.D. (chairman), Indiana University, Indianapolis; D. George Wyse, M.D., Ph.D., University of Calgary, Calgary, Alta., Canada; Peter L. Friedman, M.D., Ph.D., Brigham and Women's Hospital, Boston; Andrew E. Epstein, M.D., University of Alabama, Birmingham; Alfred P. Hallstrom, Ph.D., and H. Leon Greene, M.D., University of Washington, Seattle; and Eleanor B. Schron, M.S., R.N., and Michael Domanski, M.D., National Heart, Lung, and Blood Institute, Bethesda, Md.
Address reprint requests to the AVID Clinical Trial Center, 1107 N.E. 45th St., Rm. 505, Seattle, WA 98105.
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