Detailed Information on Publication Record
2022
Empagliflozin benefits in patients with heart failure and preserved ejection fraction
ANKER, Stefan D, Javed BUTLER, Muhammad Shariq USMAN, Gerasimos FILIPPATOS, João Pedro FERREIRA et. al.Basic information
Original name
Empagliflozin benefits in patients with heart failure and preserved ejection fraction
Authors
ANKER, Stefan D (guarantor), Javed BUTLER, Muhammad Shariq USMAN, Gerasimos FILIPPATOS, João Pedro FERREIRA, Edimar BOCCHI, Michael BÖHM, Hans Pieter Brunner-La ROCCA, Choi DONG-JU, Vijay CHOPRA, Eduardo CHUQUIURE, Nadia GIANNETTI, Juan Esteban GOMEZ-MESA, Stefan JANSSENS, James L JANUZZI, José R GONZÁLEZ-JUANATEY, Bela MERKELY, Stephen J NICHOLLS, Sergio V PERRONE, Ileana L PIÑA, Piotr PONIKOWSKI, Michele SENNI, David SIM, Jindřich ŠPINAR (203 Czech Republic, belonging to the institution), Iain SQUIRE, Stefano TADDEI, Hiroyuki TSUTSUI, Subodh VERMA, Dragos VINEREANU, Jian ZHANG, Tomoko IWATA, Janet M SCHNEE, Martina BRUECKMANN, Stuart J POCOCK and Faiez ZANNAD
Edition
NATURE MEDICINE, BERLIN, NATURE PORTFOLIO, 2022, 1078-8956
Other information
Language
English
Type of outcome
Článek v odborném periodiku
Field of Study
30201 Cardiac and Cardiovascular systems
Country of publisher
Germany
Confidentiality degree
není předmětem státního či obchodního tajemství
References:
Impact factor
Impact factor: 82.900
RIV identification code
RIV/00216224:14110/22:00128843
Organization unit
Faculty of Medicine
UT WoS
000896466000001
Keywords in English
empagliflozin in heart failure; versus mid-range ejection fraction
Tags
International impact, Reviewed
Změněno: 19/2/2024 09:38, Mgr. Tereza Miškechová
Abstract
V originále
The EMPEROR-Preserved trial showed that the sodium–glucose co-transporter 2 inhibitor empagliflozin significantly reduces the risk of cardiovascular death or hospitalization for heart failure (HHF) in heart failure patients with left ventricular ejection fraction (LVEF) > 40%. Here, we report the results of a pre-specified analysis that separately evaluates these patients stratified by LVEF: preserved (≥ 50%) (n = 4,005; 66.9%) or mid-range (41–49%). In patients with LVEF ≥ 50%, empagliflozin reduced the risk of cardiovascular death or HHF (the primary endpoint) by 17% versus placebo (hazard ratio (HR) 0.83; 95% confidence interval (CI): 0.71–0.98, P = 0.024). For the key secondary endpoint, the HR for total HHF was 0.83 (95%CI: 0.66–1.04, P = 0.11). For patients with an LVEF of 41–49%, the HR for empagliflozin versus placebo was 0.71 (95%CI: 0.57–0.88, P = 0.002) for the primary outcome (Pinteraction = 0.27), and 0.57 (95%CI: 0.42–0.79, P < 0.001) for total HHF (Pinteraction = 0.06). These results, together with those from the EMPEROR-Reduced trial in patients with LVEF < 40%, support the use of empagliflozin across the full spectrum of LVEF in heart failure.