J 2021

Empagliflozin in Heart Failure with a Preserved Ejection Fraction

ANKER, S.D., J. BUTLER, G. FILIPPATOS, J. P. FERREIRA, E. BOCCHI et. al.

Basic information

Original name

Empagliflozin in Heart Failure with a Preserved Ejection Fraction

Authors

ANKER, S.D. (guarantor), J. BUTLER, G. FILIPPATOS, J. P. FERREIRA, E. BOCCHI, M. BOHM, Rocca H. P. BRUNNER-LA, D. J. CHOI, V. CHOPRA, E. CHUQUIURE-VALENZUELA, N. GIANNETTI, J. E. GOMEZ-MESA, S. JANSSENS, J. L. JANUZZI, J. R. GONZALEZ-JUANATEY, B. MERKELY, S. J. NICHOLLS, S. V. PERRONE, I. L. PINA, P. PONIKOWSKI, M. SENNI, D. SIM, Jindřich ŠPINAR (203 Czech Republic, belonging to the institution), I. SQUIRE, S. TADDEI, H. TSUTSUI, S. VERMA, D. VINEREANU, J. ZHANG, P. CARSON, C. S. P. LAM, N. MARX, C. ZELLER, N. SATTAR, W. JAMAL, S. SCHNAIDT, J. M. SCHNEE, M. BRUECKMANN, S. J. POCOCK, F. ZANNAD and M. PACKER

Edition

New England Journal of Medicine, Waltham, Massachussetts Medical Society, 2021, 0028-4793

Other information

Language

English

Type of outcome

Článek v odborném periodiku

Field of Study

30218 General and internal medicine

Country of publisher

Slovenia

Confidentiality degree

není předmětem státního či obchodního tajemství

References:

Impact factor

Impact factor: 176.079

RIV identification code

RIV/00216224:14110/21:00122279

Organization unit

Faculty of Medicine

UT WoS

000691622000001

Keywords in English

Heart Failure; Empagliflozin; Preserved Ejection Fraction

Tags

Tags

International impact, Reviewed
Změněno: 7/12/2021 10:49, Mgr. Tereza Miškechová

Abstract

V originále

BACKGROUND Sodium-glucose cotransporter 2 inhibitors reduce the risk of hospitalization for heart failure in patients with heart failure and a reduced ejection fraction, but their effects in patients with heart failure and a preserved ejection fraction are uncertain. METHODS In this double-blind trial, we randomly assigned 5988 patients with class II-IV heart failure and an ejection fraction of more than 40% to receive empagliflozin (10 mg once daily) or placebo, in addition to usual therapy. The primary outcome was a composite of cardiovascular death or hospitalization for heart failure. RESULTS Over a median of 26.2 months, a primary outcome event occurred in 415 of 2997 patients (13.8%) in the empagliflozin group and in 511 of 2991 patients (17.1%) in the placebo group (hazard ratio, 0.79; 95% confidence interval [CI], 0.69 to 0.90; P<0.001). This effect was mainly related to a lower risk of hospitalization for heart failure in the empagliflozin group. The effects of empagliflozin appeared consistent in patients with or without diabetes. The total number of hospitalizations for heart failure was lower in the empagliflozin group than in the placebo group (407 with empagliflozin and 541 with placebo; hazard ratio, 0.73; 95% CI, 0.61 to 0.88; P<0.001). Uncomplicated genital and urinary tract infections and hypotension were reported more frequently with empagliflozin. CONCLUSIONS Empagliflozin reduced the combined risk of cardiovascular death or hospitalization for heart failure in patients with heart failure and a preserved ejection fraction, regardless of the presence or absence of diabetes.