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

Author:

Butler Javed1ORCID,Packer Milton2,Filippatos Gerasimos3ORCID,Ferreira Joao Pedro4ORCID,Zeller Cordula5ORCID,Schnee Janet6ORCID,Brueckmann Martina7ORCID,Pocock Stuart J8,Zannad Faiez4,Anker Stefan D9

Affiliation:

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

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

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

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

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

6. Boehringer Ingelheim Pharmaceuticals, Ridgefield, CT, USA

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

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

9. 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

Abstract

Abstract Aims 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. Methods and results 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. Conclusion 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%. Key Question How does ejection fraction influence the effects of empagliflozin in patients with heart failure and either a reduced or a preserved ejection fraction? Key Finding 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%. Take Home Message 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.

Funder

Boehringer Ingelheim and Eli Lilly and Company

Publisher

Oxford University Press (OUP)

Subject

Cardiology and Cardiovascular Medicine

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