Key result
Fixed-dose combination of isosorbide dinitrate and hydralazine reduced the risk of first hospitalization for heart failure compared with placebo (HR 0.61; 95% CI 0.47-0.80; P<0.001).
Why the study?
Does fixed-dose combination of isosorbide dinitrate and hydralazine reduce hospitalizations in black patients with moderate to severe heart failure?
RCT (n=1,050)
Does fixed-dose combination of isosorbide dinitrate and hydralazine reduce hospitalizations in black patients with moderate to severe heart failure?
In black patients with moderate to severe heart failure, fixed-dose isosorbide dinitrate and hydralazine significantly reduces first and recurrent heart failure hospitalizations as well as total all-cause hospitalizations.
Supports use in black patients with moderate-severe HF; confirms benefit on first HF hospitalization.
BACKGROUND: Fixed-dose combination of isosorbide dinitrate and hydralazine (FDC-I/H) reduced mortality by 43% and death or first hospitalization for heart failure (HF) by 37% in the African-American Heart Failure Trial (A-HeFT). Reduction in mortality makes it difficult to determine the effect on hospitalizations unless the analysis adjusts for death as a competing risk. METHODS AND RESULTS: In A-HeFT, 1050 self-identified black patients with moderate to severe HF were randomized to FDC-I/H or placebo. The effects of FDC-I/H on first and all hospitalizations and 30-day readmission rates were analyzed. Deaths as competing risks were adjusted using Fine-Gray regression and joint models of hospitalizations and mortality. There were 558 all-cause and 251 HF hospitalizations in placebo compared with 435 and 173 hospitalizations in the FDC-I/H group. Adjusting for deaths as a competing risk, the effect of FDC-I/H on the first hospitalization for HF, expressed in hazard ratio (95% confidence interval), was 0.61 (0.47-0.80; P<0.001) and 0.88 (0.72-1.06; P=0.18) on the first all-cause hospitalization. The effect of FDC-I/H on all recurrent hospitalizations for HF was 0.66 (0.52-0.83; P=0.0005), similar to the effect on the first hospitalizations for HF, whereas the effect on all hospitalizations for any cause was 0.75 (0.63-0.91; P=0.003). The 30-day all-cause readmission rate after the first hospitalization for HF was 23.6% (29 of 123) in placebo versus 14.8% (12 of 81) in the FDC-I/H group, but the effect (0.59; 0.30-1.16; P=0.12) in this small subgroup was not significant. CONCLUSIONS: Treatment with FDC-I/H was associated with a substantial reduction in the first and recurrent HF hospitalizations, and in total all-cause hospitalizations, reducing the total burden of costly and distressing hospitalizations. CLINICAL TRIAL REGISTRATION URL: http://www.clinicaltrials.gov. Unique identifier: NCT00047775.
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Anand et al. (2014) conducted an RCT in moderate to severe heart failure (n=1,050). Fixed-dose combination of isosorbide dinitrate and hydralazine (FDC-I/H) vs. placebo was evaluated on First hospitalization for heart failure (HR 0.61, 95% CI 0.47-0.80, p=<0.001). Fixed-dose combination of isosorbide dinitrate and hydralazine reduced the risk of first hospitalization for heart failure compared with placebo (HR 0.61; 95% CI 0.47-0.80; P<0.001).
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