Early and sustained benefit on event-free survival and heart failure hospitalization from fixed-dose combination of isosorbide dinitrate/hydralazine - Consistency across subgroups in the African-American Heart Failure Trial

被引:62
作者
Taylor, Anne L.
Ziesche, Susan
Yancy, Clyde W.
Carson, Peter
Ferdinand, Keith
Taylor, Malcolm
Adams, Kirkwood
Olukotun, Adeoye Y.
Ofili, Elizabeth
Tam, S. William
Sabolinski, Michael L.
Worcel, Manuel
Cohn, Jay N.
机构
[1] Univ Minnesota, Dept Med, Minneapolis, MN 55455 USA
[2] Minneapolis Vet Affairs Med Ctr, Minneapolis, MN USA
[3] Baylor Univ, Med Ctr, Dallas, TX USA
[4] Vet Affairs Med Ctr, Washington, DC 20422 USA
[5] Xavier Univ Louisiana, New Orleans, LA USA
[6] Assoc Black Cardiologists, Jackson, MS USA
[7] Univ N Carolina, Chapel Hill, NC USA
[8] Clin & Regulatory Strategies, Princeton, NJ USA
[9] Moorehouse Sch Med, Atlanta, GA USA
[10] NitroMed Inc, Lexington, MA USA
关键词
heart failure; cardiovascular diseases; nitric oxide; African Americans; trials;
D O I
10.1161/CIRCULATIONAHA.106.644013
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background-We previously reported that the fixed-dose combination of isosorbide dinitrate and hydralazine hydrochloride (FDC I/H) significantly decreased the risk of all-cause death and first hospitalization for heart failure (HF) and improved quality of life in patients with New York Heart Association class III or IV heart failure in the African-American Heart Failure Trial (A-HeFT). The current analyses further define the effect of FDC I/H on the timing of event-free survival (mortality or first hospitalization for HF) and time to first hospitalization for HF, as well as effects by subgroups and effects on cause-specific mortality. Methods and Results-Kaplan-Meier analyses of the 1050 A-HeFT patients on standard neurohormonal blockade demonstrated that FDC I/H produced a 37% improvement in event-free survival (P < 0.001) and a 39% reduction in the risk for first hospitalization for HF (P < 0.001). These benefits appeared to emerge early (at approximate to 50 days of treatment) and were sustained through the duration of the trial. Subgroup analyses of treatment effect by age, sex, baseline blood pressure, history of chronic renal insufficiency, presence of diabetes mellitus, cause of HF, and baseline medication usage demonstrated consistent beneficial effect of FDC I/H on the primary composite score and event-free survival across all subgroups. Mortality from pump failure was reduced by 75% (P = 0.012). Conclusions-FDC I/H treatment of black patients with moderate to severe HF who were taking neurohormonal blockers produced early and sustained significant improvement in event-free survival and hospitalization for HF in the A-HeFT cohort, with significant reduction in mortality from cardiovascular and pump failure deaths. The treatment effects on the primary composite end point and event-free survival were consistent across subgroups.
引用
收藏
页码:1747 / 1753
页数:7
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