Secondary prevention of sudden death: The Dutch Study, the AntiarrhythmicsVersus Implantable Defibrillator Trial, the Cardiac Arrest Study Hamburg, and the Canadian Implantable Defibrillator Study
R. Cappato, Secondary prevention of sudden death: The Dutch Study, the AntiarrhythmicsVersus Implantable Defibrillator Trial, the Cardiac Arrest Study Hamburg, and the Canadian Implantable Defibrillator Study, AM J CARD, 83(5B), 1999, pp. 68D-73D
Citations number
45
Categorie Soggetti
Cardiovascular & Respiratory Systems","Cardiovascular & Hematology Research
Although indisputably effective in the prevention of sudden death, use of i
mplantable cardioverter defibrillator (ICD) therapy may not necessarily aff
ect all-cause mortality, as most patients at risk also present with severel
y depressed left ventricular dysfunction. Correction of the sudden death ri
sk in these patients creates a new clinical condition in need of a careful
assessment. Should all-cause mortality be affected by the expected reductio
n in sudden death rate associated with ICD therapy, issues of critical impo
rtance such as the time extent of life prolongation and the associated qual
ity of life, still remain to established. To investigate the potential bene
fit of ICD therapy compared with antiarrhythmic drug treatment, 4 prospecti
ve studies-the Dutch trial, the Antiarrhythmics Versus Implantable Defibril
lators (AVID) study, the Cardiac Arrest Study Hamburg (CASH), and the Canad
ian Implantable Defibrillator Study (CIDS)-have been conducted in which pat
ients with documented sustained ventricular arrhythmia were randomized to 1
of these 2 treatment strategies. The enrollment criteria differed in these
4 studies: (1) in the Dutch trial, they included cardiac arrest secondary
to a ventricular arrhythmia, old (>4 weeks) myocardial infarction, and indu
cible ventricular arrhythmia; (2) in AVID and CIDS, ventricular fibrillatio
n or poorly tolerated ventricular tachycardia; and (3) in CASH, cardiac att
est secondary to a ventricular arrhythmia regardless of the underlying dise
ase. With regard to the antiarrhythmic drugs, the Dutch trial tested class
I and III agents, whereas AVID and CIDS compared ICD therapy with class III
agents (mostly amiodarone). In CASH, 3 drug subgroups were investigated: p
ropafenone, amiodarone, and metoprolol. All trials used all-cause mortality
as the primary endpoint. Data from these trials provide support for ICD as
a therapy superior to antiarrhythmic drugs in prolonging survival in patie
nts meeting the entry criteria. This review briefly summarizes the methods,
results, limitations, and clinical implications of these 4 studies. (C) 19
99 by Excerpta Medico, Inc.