Mineralocorticoid receptor antagonist use and the effects of empagliflozin on clinical outcomes in patients admitted for acute heart failure: Findings from EMPULSE

恩帕吉菲 医学 心力衰竭 危险系数 内科学 射血分数 安慰剂 盐皮质激素受体 心脏病学 置信区间 MRAS公司 糖尿病 醛固酮 2型糖尿病 内分泌学 物理 替代医学 病媒控制 病理 量子力学 电压 感应电动机
作者
João Pedro Ferreira,Jon Blatchford,John R. Teerlink,Mikhail Kosiborod,Christiane E. Angermann,Jan Biegus,Sean P. Collins,Jasper Tromp,Michael E. Nassif,Mitchell A. Psotka,Josep Comín‐Colet,Robert J. Mentz,Martina Brueckmann,Matias Nordaby,Piotr Ponikowski,Adriaan A. Voors
出处
期刊:European Journal of Heart Failure [Wiley]
卷期号:25 (10): 1797-1805 被引量:3
标识
DOI:10.1002/ejhf.2982
摘要

In patients hospitalized for acute heart failure (AHF) empagliflozin produced greater clinical benefit than placebo. Many patients with AHF are treated with mineralocorticoid receptor antagonists (MRAs). The interplay between empagliflozin and MRAs in AHF is yet to be explored. This study aimed to evaluate the efficacy and safety of empagliflozin versus placebo according to MRA use at baseline in the EMPULSE trial (NCT04157751).In this analysis all comparisons were performed between empagliflozin and placebo, stratified by baseline MRA use. The primary outcome included all-cause death, heart failure events, and a ≥5 point difference in Kansas City Cardiomyopathy Questionnaire (KCCQ) total symptom score at 90 days, assessed using the win ratio (WR). First heart failure hospitalization or cardiovascular death was a secondary outcome. From the 530 patients randomized, 276 (52%) were receiving MRAs at baseline. MRA users were younger, had lower ejection fraction, better renal function, and higher KCCQ scores. The primary outcome showed benefit of empagliflozin irrespective of baseline MRA use (WR 1.46, 95% confidence interval [CI] 1.08-1.97 and WR 1.27, 95% CI 0.93-1.73 in MRA users and non-users, respectively; interaction p = 0.52). The effect of empagliflozin on first heart failure hospitalization or cardiovascular death was not modified by MRA use (hazard ratio [HR] 0.58, 95% CI 0.30-1.11 and HR 0.85, 95% CI 0.47-1.52 in MRA users and non-users, respectively; interaction p = 0.39). Investigator-reported and severe hyperkalaemia events were infrequent (<6%) irrespective of MRA use.In patients admitted for AHF, initiation of empagliflozin produced clinical benefit and was well tolerated irrespective of background MRA use. These findings support the early use of empagliflozin on top of MRA therapy in patients admitted for AHF.
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