Dapagliflozin and quality of life measured using the EuroQol 5-dimension questionnaire in patients with heart failure with reduced and mildly reduced/preserved ejection fraction.

Dapagliflozin EQ‐5D index Heart failure Quality of life Symptoms Visual analogue scale

Journal

European journal of heart failure
ISSN: 1879-0844
Titre abrégé: Eur J Heart Fail
Pays: England
ID NLM: 100887595

Informations de publication

Date de publication:
03 May 2024
Historique:
revised: 13 03 2024
received: 29 01 2024
accepted: 13 04 2024
medline: 3 5 2024
pubmed: 3 5 2024
entrez: 3 5 2024
Statut: aheadofprint

Résumé

Although much is known about the usefulness of heart failure (HF)-specific instruments for assessing patient well-being, less is known about the value of generic instruments for the measurement of health-related quality of life (HRQL) in HF. The aim of this study was to assess the relationship between the EuroQol 5-dimension 5-level (EQ-5D-5L) visual analogue scale (VAS) and index scores, clinical characteristics, and outcomes in patients with HF and the effect of dapagliflozin on these scores. We performed a patient-level pooled analysis of the DAPA-HF and DELIVER trials, which investigated the effectiveness and safety of dapagliflozin in patients with HF and reduced ejection fraction (HFrEF) and mildly reduced/preserved ejection fraction (HFmrEF/HFpEF), respectively. Patients reporting higher (better) EQ-5D-5L VAS and index scores had a lower prevalence of comorbidities, including atrial fibrillation and hypertension, than patients with a worse score. They were also more likely to have better investigator-reported (New York Heart Association class) and patient-self-reported (Kansas City Cardiomyopathy Questionnaire) health status and lower median N-terminal pro-B-type natriuretic peptide levels. Compared to patients with the lowest scores (Q1), those with higher EQ-5D-5L VAS scores had better outcomes: the hazard ratio for the composite of cardiovascular death or worsening HF was 0.81 (95% confidence interval 0.72-0.91) in Q2, 0.74 (0.65-0.84) in Q3, and 0.62 (0.54-0.72) in Q4. The risk of each component of the composite outcome, and all-cause death, was also lower in patients with better scores. Similar findings were observed for the index score. Treatment with dapagliflozin improved both EQ-5D-5L VAS and index scores across the range of ejection fraction. Both higher (better) EQ-5D-5L VAS and index scores were associated with better outcomes. Dapagliflozin treatment improved EQ-5D-5L VAS and index scores, irrespective of ejection fraction.

Identifiants

pubmed: 38700986
doi: 10.1002/ejhf.3263
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : British Heart Foundation Centre of Research Excellence
ID : RE/18/6/34217
Organisme : Vera Melrose Heart Failure Research Fund

Informations de copyright

© 2024 The Authors. European Journal of Heart Failure published by John Wiley & Sons Ltd on behalf of European Society of Cardiology.

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Auteurs

Mingming Yang (M)

British Heart Foundation Cardiovascular Research Centre, University of Glasgow, Glasgow, UK.
Department of Cardiology, Zhongda Hospital, School of Medicine, Southeast University, Nanjing, China.

Toru Kondo (T)

British Heart Foundation Cardiovascular Research Centre, University of Glasgow, Glasgow, UK.
Department of Cardiology, Nagoya University Graduate School of Medicine, Nagoya, Japan.

Atefeh Talebi (A)

British Heart Foundation Cardiovascular Research Centre, University of Glasgow, Glasgow, UK.

Pardeep S Jhund (PS)

British Heart Foundation Cardiovascular Research Centre, University of Glasgow, Glasgow, UK.

Kieran F Docherty (KF)

British Heart Foundation Cardiovascular Research Centre, University of Glasgow, Glasgow, UK.

Brian L Claggett (BL)

Cardiovascular Division, Brigham and Women's Hospital, and Harvard Medical School, Boston, MA, USA.

Muthiah Vaduganathan (M)

Cardiovascular Division, Brigham and Women's Hospital, and Harvard Medical School, Boston, MA, USA.

Erasmus Bachus (E)

Late-Stage Development, Cardiovascular, Renal, and Metabolism, Biopharmaceuticals R&D AstraZeneca, Gothenburg, Sweden.

Adrian F Hernandez (AF)

Duke Clinical Research Institute, Duke University Medical Center, Durham, NC, USA.

Carolyn S P Lam (CSP)

National Heart Centre Singapore and Duke-National University of Singapore, Singapore.

Silvio E Inzucchi (SE)

Yale School of Medicine, New Haven, CT, USA.

Felipe A Martinez (FA)

Universidad Nacional de Córdoba, Córdoba, Argentina.

Rudolf A de Boer (RA)

Department of Cardiology, Erasmus Medical Center, Rotterdam, The Netherlands.

Mikhail N Kosiborod (MN)

Saint Luke's Mid America Heart Institute and University of Missouri-Kansas City, Kansas City, MO, USA.

Akshay S Desai (AS)

Cardiovascular Division, Brigham and Women's Hospital, and Harvard Medical School, Boston, MA, USA.

Lars Køber (L)

Department of Cardiology, Copenhagen University Hospital Rigshospitalet, Copenhagen, Denmark.

Piotr Ponikowski (P)

Medical University, Clinical Military Hospital, Wroclaw, Poland.

Marc S Sabatine (MS)

TIMI (Thrombolysis in Myocardial Infarction) Study Group, Cardiovascular Division, Brigham and Women's Hospital, and Harvard Medical School, Boston, MA, USA.

Scott D Solomon (SD)

Cardiovascular Division, Brigham and Women's Hospital, and Harvard Medical School, Boston, MA, USA.

John J V McMurray (JJV)

British Heart Foundation Cardiovascular Research Centre, University of Glasgow, Glasgow, UK.

Classifications MeSH