TY - JOUR
T1 - Clinical benefits of eplerenone in patients with systolic heart failure and mild symptoms when initiated shortly after hospital discharge: analysis from the EMPHASIS-HF trial
AU - Girerd, Nicolas
AU - Collier, Timothy
AU - Pocock, Stuart J
AU - Krum, Henry
AU - McMurray, John J V
AU - Swedberg, Karl
AU - van Veldhuisen, Dirk Jan
AU - Vincent, John
AU - Pitt, Bertram
AU - Zannad, Faiez
PY - 2015
Y1 - 2015
N2 - Aims Cardiovascular hospitalization (CVH) in patients with heart failure (HF) is associated with a high post-discharge rate of early re-admission and CV death. Eplerenone might be effective in reducing the incidence of these adverse clinical outcomes during this period. Methods and results The EMPHASIS-HF trial compared eplerenone with placebo added to standard therapy in 2737 patients with New York Heart Association class II HF and left ventricular ejection fraction =35 . We conducted a post hoc analysis in the 2338 patients randomized within 180 days of a CVH. The interaction between the time from the qualifying CVH to randomization and the primary outcome of CV death or hospitalization for HF (HHF), as well as other secondary outcomes, was assessed in Cox survival models. Most of the qualifying CVHs were HHF (N = 1496, 64.0 ), acute coronary syndromes (N = 390, 16.7 ), and arrhythmias (N = 197, 7.2 ). The median time of study drug initiation from qualifying CVH was 42 days. The relative rate reductions in CV death/HHF, HHF, and all-cause mortality were similar (P for interaction = 0.65, 0.44, and 0.40, respectively) whether the treatment was initiated
AB - Aims Cardiovascular hospitalization (CVH) in patients with heart failure (HF) is associated with a high post-discharge rate of early re-admission and CV death. Eplerenone might be effective in reducing the incidence of these adverse clinical outcomes during this period. Methods and results The EMPHASIS-HF trial compared eplerenone with placebo added to standard therapy in 2737 patients with New York Heart Association class II HF and left ventricular ejection fraction =35 . We conducted a post hoc analysis in the 2338 patients randomized within 180 days of a CVH. The interaction between the time from the qualifying CVH to randomization and the primary outcome of CV death or hospitalization for HF (HHF), as well as other secondary outcomes, was assessed in Cox survival models. Most of the qualifying CVHs were HHF (N = 1496, 64.0 ), acute coronary syndromes (N = 390, 16.7 ), and arrhythmias (N = 197, 7.2 ). The median time of study drug initiation from qualifying CVH was 42 days. The relative rate reductions in CV death/HHF, HHF, and all-cause mortality were similar (P for interaction = 0.65, 0.44, and 0.40, respectively) whether the treatment was initiated
UR - http://eurheartj.oxfordjournals.org/content/ehj/36/34/2310.full.pdf
U2 - 10.1093/eurheartj/ehv273
DO - 10.1093/eurheartj/ehv273
M3 - Article
VL - 36
SP - 2310
EP - 2317
JO - European Heart Journal
JF - European Heart Journal
SN - 0195-668X
IS - 34
ER -