Irbesartan in Patients with Heart Failure and Preserved Ejection Fraction.

被引:1536
作者
Massie, Barry M. [1 ]
Carson, Peter E. [2 ,3 ]
McMurray, John J. [4 ]
Komajda, Michel [5 ,6 ]
McKelvie, Robert [7 ]
Zile, Michael R. [8 ,9 ]
Anderson, Susan [10 ]
Donovan, Mark [11 ]
Iverson, Erik [10 ]
Staiger, Christoph [12 ]
Ptaszynska, Agata [11 ]
机构
[1] Vet Affairs Med Ctr, San Francisco, CA 94121 USA
[2] Georgetown Univ, Washington, DC USA
[3] Vet Affairs Med Ctr, Washington, DC 20422 USA
[4] Univ Glasgow, British Heart Fdn Glasgow Cardiovasc Res Ctr, Glasgow, Lanark, Scotland
[5] Univ Paris 06, Paris, France
[6] Grp Hosp Pitie Salpetriere, F-75634 Paris, France
[7] McMaster Univ, Hamilton, ON, Canada
[8] Ralph H Johnson Vet Affairs Med Ctr, Charleston, SC USA
[9] Med Univ S Carolina, Charleston, SC 29425 USA
[10] Univ Wisconsin, Madison, WI USA
[11] Bristol Myers Squibb Co, Princeton, NJ USA
[12] Sanofi Aventis, Bridgewater, NJ USA
关键词
D O I
10.1056/NEJMoa0805450
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Approximately 50% of patients with heart failure have a left ventricular ejection fraction of at least 45%, but no therapies have been shown to improve the outcome of these patients. Therefore, we studied the effects of irbesartan in patients with this syndrome. Methods: We enrolled 4128 patients who were at least 60 years of age and had New York Heart Association class II, III, or IV heart failure and an ejection fraction of at least 45% and randomly assigned them to receive 300 mg of irbesartan or placebo per day. The primary composite outcome was death from any cause or hospitalization for a cardiovascular cause (heart failure, myocardial infarction, unstable angina, arrhythmia, or stroke). Secondary outcomes included death from heart failure or hospitalization for heart failure, death from any cause and from cardiovascular causes, and quality of life. Results: During a mean follow-up of 49.5 months, the primary outcome occurred in 742 patients in the irbesartan group and 763 in the placebo group. Primary event rates in the irbesartan and placebo groups were 100.4 and 105.4 per 1000 patient-years, respectively (hazard ratio, 0.95; 95% confidence interval [CI], 0.86 to 1.05; P=0.35). Overall rates of death were 52.6 and 52.3 per 1000 patient-years, respectively (hazard ratio, 1.00; 95% CI, 0.88 to 1.14; P=0.98). Rates of hospitalization for cardiovascular causes that contributed to the primary outcome were 70.6 and 74.3 per 1000 patient-years, respectively (hazard ratio, 0.95; 95% CI, 0.85 to 1.08; P=0.44). There were no significant differences in the other prespecified outcomes. Conclusions: Irbesartan did not improve the outcomes of patients with heart failure and a preserved left ventricular ejection fraction. (ClinicalTrials.gov number, NCT00095238.).
引用
收藏
页码:2456 / 2467
页数:12
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