Effect of Empagliflozin on Heart Failure Outcomes After Acute Myocardial Infarction: Insights from the EMPACT-MI Trial

恩帕吉菲 医学 心力衰竭 射血分数 心肌梗塞 内科学 心脏病学 安慰剂 随机对照试验 糖尿病 2型糖尿病 内分泌学 替代医学 病理
作者
Adrian F. Hernandez,Jacob A. Udell,W. Schuyler Jones,Stefan D. Anker,Mark C Petrie,Josephine Harrington,Michaela Mattheus,Svenja Seide,Isabella Zwiener,Offer Amir,Marıa Cecilia Bahit,Johann Bauersachs,Antoni Bayés‐Genís,Yundai Chen,Vijay Chopra,Gemma A. Figtree,Junbo Ge,Shaun G. Goodman,Nina Gotcheva,Shinya Goto,Tomasz Gąsior,Waheed Jamal,James L. Januzzi,Myung Ho Jeong,Yuri Lopatin,Renato D. Lópes,Béla Merkely,Puja B. Parikh,Alexander Parkhomenko,Piotr Ponikowski,Xavier Rosselló,Morten Schou,Dragan Šimić,Philippe Gabriel Steg,Joanna Szachniewicz,Peter van der Meer,Dragoş Vinereanu,Shelley Zieroth,Martina Brueckmann,Mikhail Sumin,Deepak L. Bhatt,Javed Butler
出处
期刊:Circulation [Ovid Technologies (Wolters Kluwer)]
标识
DOI:10.1161/circulationaha.124.069217
摘要

Empagliflozin reduces the risk of heart failure events in patients with type 2 diabetes at high cardiovascular risk, chronic kidney disease, and in those with prevalent heart failure irrespective of ejection fraction. While EMPACT-MI showed empagliflozin does not reduce the risk of the composite of hospitalization of heart failure and all-cause mortality, the impact of empagliflozin on first and recurrent heart failure events in patients after myocardial infarction is unknown.EMPACT-MI was a double-blind, randomized, placebo-controlled, event-driven trial that randomized 6522 patients hospitalized for acute myocardial infarction at risk for heart failure based on newly developed left ventricular ejection fraction of <45% and/or signs or symptoms of congestion to receive empagliflozin 10 mg daily or placebo within 14 days of admission. In prespecified secondary analyses, treatment groups were analyzed for heart failure outcomes.Over a median of follow-up of 17.9 months, the risk for first heart failure hospitalization and total heart failure hospitalizations was significantly lower in the empagliflozin compared with the placebo group (118 (3.6%) vs. 153 (4.7%) patients with events, HR 0.77 [95% CI 0.60, 0.98], P=0.031 for first heart failure hospitalization and 148 vs. 207 events, RR 0.67 [95% CI 0.51, 0.89], P=0.006 for total heart failure hospitalizations). Subgroup analysis showed consistency of empagliflozin benefit across clinically relevant patient subgroups for first and total heart failure hospitalizations. Post-discharge need for new use of diuretics, renin-angiotensin modulators, and mineralocorticoid receptor antagonists were less in patients randomized to empagliflozin than placebo (all p<0.05).In patients after acute myocardial infarction with left ventricular dysfunction or congestion, empagliflozin reduced the risk of heart failure.
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