The Effect of Spironolactone on Morbidity and Mortality in Patients with Severe Heart Failure
Bertram Pitt, M.D., Faiez Zannad, M.D., Willem J. Remme, M.D., Robert Cody, M.D., Alain Castaigne, M.D., Alfonso Perez, M.D., Jolie Palensky, M.S., Janet Wittes, Ph.D., for The Randomized Aldactone Evaluation Study Investigators
Background and Methods Aldosterone is important in the pathophysiologyof heart failure. In a double-blind study, we enrolled 1663patients who had severe heart failure and a left ventricularejection fraction of no more than 35 percent and who were beingtreated with an angiotensin-convertingenzyme inhibitor,a loop diuretic, and in most cases digoxin. A total of 822 patientswere randomly assigned to receive 25 mg of spironolactone daily,and 841 to receive placebo. The primary end point was deathfrom all causes.
Results The trial was discontinued early, after a mean follow-upperiod of 24 months, because an interim analysis determinedthat spironolactone was efficacious. There were 386 deaths inthe placebo group (46 percent) and 284 in the spironolactonegroup (35 percent; relative risk of death, 0.70; 95 percentconfidence interval, 0.60 to 0.82; P<0.001). This 30 percentreduction in the risk of death among patients in the spironolactonegroup was attributed to a lower risk of both death from progressiveheart failure and sudden death from cardiac causes. The frequencyof hospitalization for worsening heart failure was 35 percentlower in the spironolactone group than in the placebo group(relative risk of hospitalization, 0.65; 95 percent confidenceinterval, 0.54 to 0.77; P<0.001). In addition, patients whoreceived spironolactone had a significant improvement in thesymptoms of heart failure, as assessed on the basis of the NewYork Heart Association functional class (P<0.001). Gynecomastiaor breast pain was reported in 10 percent of men who were treatedwith spironolactone, as compared with 1 percent of men in theplacebo group (P<0.001). The incidence of serious hyperkalemiawas minimal in both groups of patients.
Conclusions Blockade of aldosterone receptors by spironolactone,in addition to standard therapy, substantially reduces the riskof both morbidity and death among patients with severe heartfailure. (N Engl J Med 1999:341:709-17.)
Source Information
From the Department of Internal Medicine, Division of Cardiology, University of Michigan, Ann Arbor (B.P., R.C.); the Centre d'Investigation, Clinique de Nancy, Nancy, France (F.Z.); STICARES, Cardiovascular Research Foundation, Rotterdam, the Netherlands (W.J.R.); the Service de Cardiologie, Hôpital Henri Mondor, Creteil, France (A.C.); Global Medical Operations, Searle, Skokie, Ill. (A.P.); and the Statistics Collaborative, Washington, D.C. (J.P., J.W.). Preliminary data were presented at the American Heart Association meeting, Dallas, November 811, 1998.
Address reprint requests to Dr. Pitt at the Division of Cardiology, University of Michigan Medical Center, 3910 Taubman, 1500 E. Medical Center Dr., Ann Arbor, MI 48109-0366.
Spironolactone in Patients with Heart Failure
Fernandez H. M., Leipzig R. M., Larkin R. J., Atlas S. A., Donohue T. J., Vanpee D., Swine C., Glick G., Pitt B., Perez A., The Randomized Aldactone Evaluation Study Investigators
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Full Text
N Engl J Med 2000;
342:132-134, Jan 13, 2000.
Correspondence
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