Empagliflozin and health-related quality of life outcomes in patients with heart failure with reduced ejection fraction: the EMPEROR-Reduced trial.


Journal

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

Informations de publication

Date de publication:
31 03 2021
Historique:
received: 12 10 2020
revised: 17 11 2020
accepted: 26 11 2020
pubmed: 10 1 2021
medline: 29 5 2021
entrez: 9 1 2021
Statut: ppublish

Résumé

In this secondary analysis of the EMPEROR-Reduced trial, we sought to evaluate whether the benefits of empagliflozin varied by baseline health status and how empagliflozin impacted patient-reported outcomes in patients with heart failure with reduced ejection fraction. Health status was assessed by the Kansas City Cardiomyopathy Questionnaires-clinical summary score (KCCQ-CSS). The influence of baseline KCCQ-CSS (analyzed by tertiles) on the effect of empagliflozin on major outcomes was examined using Cox proportional hazards models. Responder analyses were performed to assess the odds of improvement and deterioration in KCCQ scores related to treatment with empagliflozin. Empagliflozin reduced the primary outcome of cardiovascular death or heart failure hospitalization regardless of baseline KCCQ-CSS tertiles [hazard ratio (HR) 0.83 (0.68-1.02), HR 0.74 (0.58-0.94), and HR 0.61 (0.46-0.82) for <62.5, 62.6-85.4, and ≥85.4 score tertiles, respectively; P-trend = 0.10]. Empagliflozin improved KCCQ-CSS, total symptom score, and overall summary score at 3, 8, and 12 months. More patients on empagliflozin had ≥5-point [odds ratio (OR) 1.20 (1.05-1.37)], 10-point [OR 1.26 (1.10-1.44)], and 15-point [OR 1.29 (1.12-1.48)] improvement and fewer had ≥5-point [OR 0.75 (0.64-0.87)] deterioration in KCCQ-CSS at 3 months. These benefits were sustained at 8 and 12 months and were similar for other KCCQ domains. Empagliflozin improved cardiovascular death or heart failure hospitalization risk across the range of baseline health status. Empagliflozin improved health status across various domains, and this benefit was sustained during long-term follow-up. URL: https://www.clinicaltrials.gov. Unique identifier: NCT03057977.

Identifiants

pubmed: 33420498
pii: 6072066
doi: 10.1093/eurheartj/ehaa1007
pmc: PMC8014525
doi:

Substances chimiques

Benzhydryl Compounds 0
Glucosides 0
empagliflozin HDC1R2M35U

Banques de données

ClinicalTrials.gov
['NCT03057977']

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

1203-1212

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.

Stefan D Anker (SD)

Department of Cardiology (CVK); and Berlin Institute of Health Center for Regenerative Therapies (BCRT); German Centre for Cardiovascular Research (DZHK) partner site Berlin; Charité Universitätsmedizin Berlin, Augustenburger Platz 1, D-13353 Berlin, Germany.

Gerasimos Filippatos (G)

Heart Failure Unit, National and Kapodistrian University of Athens School of Medicine, Athens University Hospital Attikon, 2 Thivon Street, Athens 157 72, Greece.

Muhammad Shahzeb Khan (MS)

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

João Pedro Ferreira (JP)

Department of Cardiothoracic Physiology and Surgery, Cardiovascular R&D Unit, Institut Lorrain du Coeur et des Vaisseaux, 5 Rue du Morvan, 54500 Vandeuvre-lès-Nancy, France.

Stuart J Pocock (SJ)

Department of Medical Statistics, London School of Hygiene & Tropical Medicine, Keppel Street, London WCIE 7HT, UK.

Nadia Giannetti (N)

Division of Cardiology, McGill University Health Center, 1001 Decarie Blvd.Royal Victoria Hospital, D05.5115 Montreal, Quebec H4A 3J1, Canada.

James L Januzzi (JL)

Cardiology Division, Harvard Medical School, Massachusetts General Hospital, 25 Shattuck St, Boston, MA 02115, USA.

Ileana L Piña (IL)

Department of Medicine, Wayne State and Central Michigan Universities, 540 E. Canfield Ave, Detroit, MI 48201, USA.

Carolyn S P Lam (CSP)

National Heart Centre Singapore & Duke-National University of Singapore, 8 College Rd, Singapore 169857, Singapore.

Piotr Ponikowski (P)

Centre for Heart Diseases, Wroclaw Medical University, Borowska 213, 50-556 Wroclaw, Poland.

Naveed Sattar (N)

Institute of Cardiovascular and Medical Sciences, University of Glasgow, BHF Glasgow Cardiovascular Research Centre (GCRC), 126 University Place, Glasgow G12 8TA, UK.

Subodh Verma (S)

Division of Cardiac Surgery, St Michael's Hospital, University of Toronto, 30 Bond Street, Toronto, ON, M5B 1W8, Canada.

Martina Brueckmann (M)

Boehringer Ingelheim International GmbH, Binger Strasse 173 Ingelheim am Rhein, 55216, Germany.
Faculty of Medicine Mannheim, University of Heidelberg, Ludolf-Krehl-Straße 13-17, 68167 Mannheim, Germany.

Waheed Jamal (W)

Boehringer Ingelheim International GmbH, Binger Strasse 173 Ingelheim am Rhein, 55216, Germany.

Ola Vedin (O)

Boehringer Ingelheim AB, Hammarby allé 29, 120 32 Stockholm, Sweden.

Barbara Peil (B)

Boehringer Ingelheim Pharma GmbH & Co. KG, Binger Strasse 173 Ingelheim am Rhein, 55216, Germany.

Cordula Zeller (C)

Boehringer Ingelheim Pharma GmbH & Co. KG, Birkendorfer Str. 65, 88397 Biberach an der Riß, Germany.

Faiez Zannad (F)

Department of Cardiothoracic Physiology and Surgery, Cardiovascular R&D Unit, Institut Lorrain du Coeur et des Vaisseaux, 5 Rue du Morvan, 54500 Vandeuvre-lès-Nancy, France.

Milton Packer (M)

Cardiovascular Science, Baylor Heart and Vascular Institute, Baylor University Medical Center, 621 N. Hall Street, Dallas, TX 75226, USA.
Faculty of Medicine, National Heart and Lung Institute, Imperial College, Guy Scadding Building, Cale Street, SW3 6LY London, UK.

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