恩帕吉菲
心力衰竭
医学
安慰剂
危险系数
内科学
心脏病学
糖尿病
置信区间
病理
2型糖尿病
内分泌学
替代医学
作者
Michel Galinier,Deborah Ittah
标识
DOI:10.1016/j.acvdsp.2021.09.067
摘要
In the EMPEROR-Reduced Trial, empagliflozin was demonstrated to reduce cardiorenal outcomes and improve quality of life in patients with HFrEF. We examined whether the benefit of empagliflozin was consistent across the doses and combinations of baseline heart failure therapies. The primary outcome of time to cardiovascular (CV) death or hospitalization for heart failure (HHF) was examined in patients receiving ACEi or ARB (RAASi), MRA or beta-blockers (BB) at ≥ 50% or < 50% of target dose. Furthermore, the primary outcome was examined in patients receiving baseline combination therapy: RAASi + BB; RAASi + BB + MRA; and ARNI + BB + MRA. At baseline, of the 3730 patients randomized, 26.8%, 61.5%, and 48.9% were treated with ≥50% of target doses of RAASi, MRA or BB respectively. Additionally, 66.7%, 17.5%, 48.4%, 13.8%, 84.1%, 61.1%, and 13.4% were treated with combination of either RAASi + BB, RAASi + BB (≥50%), RAASi + BB + MRA, RAASi + BB (≥ 50%) + MRA, RAASi or ARNI + BB, RAASi or ARNI + BB + MRA or ARNI + BB + MRA. Across all sub-groups, the hazard ratio for the primary outcome was consistent with the overall estimate of 0.75 (0.65 to 0.86; P < 0.001) in empagliflozin vs. placebo treated patients with no heterogeneity by subgroup interaction (Fig. 1). KCCQ-CSS improved across all subgroups. Tolerability was similar between groups. Empagliflozin's beneficial effects in HFrEF are observed consistently regardless of the doses and combinations of other foundational drugs for heart failure.
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