Cardiovascular and Renal Outcomes with Empagliflozin in Heart Failure

Milton Packer(Imperial Valley College), Stefan D. Anker(British Heart Foundation), Javed Butler(British Heart Foundation), Gerasimos Filippatos(National and Kapodistrian University of Athens), Stuart Pocock(University of London), Peter E. Carson(British Heart Foundation), James L. Januzzi(Harvard University), Subodh Verma(St. Michael's Hospital), Hiroyuki Tsutsui(Kyushu University), Martina Brueckmann(University of Mannheim), Waheed Jamal(British Heart Foundation), Karen Kimura(British Heart Foundation), Janet Schnee(British Heart Foundation), Cordula Zeller(Boehringer Ingelheim (Germany)), Daniel Cotton(British Heart Foundation), Edimar Alcides Bocchi(Universidade de São Paulo), Michael Böhm(British Heart Foundation), Dong‐Ju Choi(Seoul National University), Vijay Chopra(Max Super Speciality Hospital), Eduardo Chuquiure‐Valenzuela(British Heart Foundation), Nadia Giannetti(McGill University Health Centre), Stefan Janssens(British Heart Foundation), Jian Zhang(Chinese Academy of Medical Sciences & Peking Union Medical College), José Ramón González‐Juanatey(Universidade de Santiago de Compostela), Sanjay Kaul(Cedars-Sinai Medical Center), Hans‐Peter Brunner‐La Rocca(Maastricht University Medical Centre), Béla Merkely(Semmelweis University), Stephen J. Nicholls(British Heart Foundation), Sergio V. Perrone(British Heart Foundation), Ileana L. Piña(British Heart Foundation), Piotr Ponikowski(British Heart Foundation), Naveed Sattar(British Heart Foundation), Michele Senni(British Heart Foundation), Marie‐France Seronde(British Heart Foundation), Jindřich Špinar(British Heart Foundation), Iain Squire(University of Leicester), Stefano Taddei(University of Pisa), Christoph Wanner(British Heart Foundation), Faı̈ez Zannad(British Heart Foundation)
New England Journal of Medicine
August 28, 2020
Cited by 4,971Open Access
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Abstract

BACKGROUND: Sodium-glucose cotransporter 2 (SGLT2) inhibitors reduce the risk of hospitalization for heart failure in patients regardless of the presence or absence of diabetes. More evidence is needed regarding the effects of these drugs in patients across the broad spectrum of heart failure, including those with a markedly reduced ejection fraction. METHODS: In this double-blind trial, we randomly assigned 3730 patients with class II, III, or IV heart failure and an ejection fraction of 40% or less to receive empagliflozin (10 mg once daily) or placebo, in addition to recommended therapy. The primary outcome was a composite of cardiovascular death or hospitalization for worsening heart failure. RESULTS: of body-surface area per year, P<0.001), and empagliflozin-treated patients had a lower risk of serious renal outcomes. Uncomplicated genital tract infection was reported more frequently with empagliflozin. CONCLUSIONS: Among patients receiving recommended therapy for heart failure, those in the empagliflozin group had a lower risk of cardiovascular death or hospitalization for heart failure than those in the placebo group, regardless of the presence or absence of diabetes. (Funded by Boehringer Ingelheim and Eli Lilly; EMPEROR-Reduced ClinicalTrials.gov number, NCT03057977.).


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