(Circulation. 2001;103:e9049.)
© 2001 American Heart Association, Inc.
ß-Blocker Trials Seem to Be in Conflict
Two studies of ß-blockers in the same issue of the New England Journal of Medicine seem to have conflicting conclusions, but the differences could result from the alternate effects of the drugs studied (N Engl J Med. 2001;344:16591667 and N Engl J Med. 2001;344:16511658).
The studies were performed in patients with advanced chronic
heart failure, whereas previous ß-blocker studies concentrated on
patients with mild to moderate heart failure. The first study, the
Beta-Blocker Evaluation of Survival Trials (BEST), compared the
investigational drug bucindolol with placebo in a randomly assigned
group of 2708 patients designated as New York Heart Association
functional class III or IV who had ejection fractions
35%. The end
point of the study was death from any cause. Interim analyses
were performed, and the Data Safety and Monitoring Board recommended
ending the study at the seventh such period because no difference in
mortality had been identified.
In the second study, researchers randomly assigned 1133
patients to placebo and 1156 patients to treatment with the ß-blocker
carvedilol. In this study, 190 patients in the placebo group died
compared with 130 in the carvedilol group, a 35% decrease in the risk
of death with the ß-blocker. The researchers concluded that treatment
with carvedilol had benefit in this population, although "the
mechanisms by which carvedilol reduces mortality among patients with
heart failure remain unclear." The group, which was led by Milton
Packer, MD, of the College of Physicians and Surgeons at Columbia
University in New York, noted that
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