Effect of empagliflozin in patients with heart failure across the spectrum of left ventricular ejection fraction.


Journal

European heart journal
ISSN: 1522-9645
Titre abrégé: Eur Heart J
Pays: England
ID NLM: 8006263

Informations de publication

Date de publication:
03 Feb 2022
Historique:
received: 18 08 2021
revised: 23 09 2021
accepted: 23 11 2021
pubmed: 9 12 2021
medline: 1 4 2022
entrez: 8 12 2021
Statut: ppublish

Résumé

No therapy has shown to reduce the risk of hospitalization for heart failure across the entire range of ejection fractions seen in clinical practice. We assessed the influence of ejection fraction on the effect of the sodium-glucose cotransporter 2 inhibitor empagliflozin on heart failure outcomes. A pooled analysis was performed on both the EMPEROR-Reduced and EMPEROR-Preserved trials (9718 patients; 4860 empagliflozin and 4858 placebo), and patients were grouped based on ejection fraction: <25% (n = 999), 25-34% (n = 2230), 35-44% (n = 1272), 45-54% (n = 2260), 55-64% (n = 2092), and ≥65% (n = 865). Outcomes assessed included (i) time to first hospitalization for heart failure or cardiovascular mortality, (ii) time to first heart failure hospitalization, (iii) total (first and recurrent) hospitalizations for heart failure, and (iv) health status assessed by the Kansas City Cardiomyopathy Questionnaire (KCCQ). The risk of cardiovascular death and hospitalization for heart failure declined progressively as ejection fraction increased from <25% to ≥65%. Empagliflozin reduced the risk of cardiovascular death or heart failure hospitalization, mainly by reducing heart failure hospitalizations. Empagliflozin reduced the risk of heart failure hospitalization by ≈30% in all ejection fraction subgroups, with an attenuated effect in patients with an ejection fraction ≥65%. Hazard ratios and 95% confidence intervals were: ejection fraction <25%: 0.73 (0.55-0.96); ejection fraction 25-34%: 0.63 (0.50-0.78); ejection fraction 35-44%: 0.72 (0.52-0.98); ejection fraction 45-54%: 0.66 (0.50-0.86); ejection fraction 55-64%: 0.70 (0.53-0.92); and ejection fraction ≥65%: 1.05 (0.70-1.58). Other heart failure outcomes and measures, including KCCQ, showed a similar response pattern. Sex did not influence the responses to empagliflozin. The magnitude of the effect of empagliflozin on heart failure outcomes was clinically meaningful and similar in patients with ejection fractions <25% to <65%, but was attenuated in patients with an ejection fraction ≥65%. How does ejection fraction influence the effects of empagliflozin in patients with heart failure and either a reduced or a preserved ejection fraction? The magnitude of the effect of empagliflozin on heart failure outcomes and health status was similar in patients with ejection fractions <25% to <65%, but it was attenuated in patients with an ejection fraction ≥65%. The consistency of the response in patients with ejection fractions of <25% to <65% distinguishes the effects of empagliflozin from other drugs that have been evaluated across the full spectrum of ejection fractions in patients with heart failure.

Identifiants

pubmed: 34878502
pii: 6455932
doi: 10.1093/eurheartj/ehab798
pmc: PMC8825259
doi:

Substances chimiques

Benzhydryl Compounds 0
Glucosides 0
empagliflozin HDC1R2M35U

Types de publication

Journal Article Meta-Analysis Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

416-426

Commentaires et corrections

Type : CommentIn

Informations de copyright

© The Author(s) 2021. Published by Oxford University Press on behalf of the European Society of Cardiology.

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Auteurs

Javed Butler (J)

Department of Medicine, University of Mississippi School of Medicine, Jackson, MS, USA.

Milton Packer (M)

Baylor Heart and Vascular Institute, 621 North Hall Street, Dallas, TX 75226, USA.

Gerasimos Filippatos (G)

National and Kapodistrian University of Athens School of Medicine, Athens University Hospital Attikon, Chaidari, Greece.

Joao Pedro Ferreira (JP)

Université de Lorraine, Inserm INI-CRCT, CHRU, Nancy, France.

Cordula Zeller (C)

Boehringer Ingelheim Pharma GmbH & Co. KG, Biberach, Germany.

Janet Schnee (J)

Boehringer Ingelheim Pharmaceuticals, Ridgefield, CT, USA.

Martina Brueckmann (M)

Boehringer Ingelheim International GmbH, Ingelheim, Germany and Faculty of Medicine Mannheim, University of Heidelberg, Mannheim, Germany.

Stuart J Pocock (SJ)

Department of Medical Statistics, London School of Hygiene & Tropical Medicine, London, UK.

Faiez Zannad (F)

Université de Lorraine, Inserm INI-CRCT, CHRU, Nancy, France.

Stefan D Anker (SD)

Department of Cardiology (CVK), Berlin Institute of Health Center for Regenerative Therapies (BCRT), German Centre for Cardiovascular Research (DZHK) partner site Berlin, Charité - Universitätsmedizin Berlin, Berlin, Germany.

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