Health status across major subgroups of patients with heart failure and preserved ejection fraction.


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:
09 2023
Historique:
revised: 10 02 2023
received: 21 10 2022
accepted: 18 03 2023
medline: 23 10 2023
pubmed: 29 3 2023
entrez: 28 3 2023
Statut: ppublish

Résumé

There are limited data on health status and changes in it over time across major subgroups of patients with heart failure and preserved ejection fraction (HFpEF), including ejection fraction spectrum, age, sex, region, body mass index (BMI), and comorbidities including diabetes, chronic kidney disease (CKD), anaemia, and atrial fibrillation/flutter. In the EMPEROR-Preserved trial, the Kansas City Cardiomyopathy Questionnaire (KCCQ) was assessed at baseline, 12, 32 and 52 weeks. Determinants of baseline KCCQ score and change over time, and the impact of empagliflozin on KCCQ scores were studied in specified subgroups. A Cox model was used to assess the association between 5- and 10-point increase and 5-point decrease in KCCQ score from baseline to week 12 and later outcomes. Among 2979 participants in the placebo arm, mean KCCQ clinical summary score (CSS) was 70.7 (20.8). Older age, female sex, BMI, anaemia, and a history of diabetes, and CKD were associated with worse scores. KCCQ-CSS score improved during follow-up; patients with atrial fibrillation/flutter at enrollment (p trend = 0.014) and CKD (p trend < 0.001) had less improvement. A 5-point increase in KCCQ-CSS at week 12 was associated with lower risk of cardiovascular death or heart failure hospitalization (5%), cardiovascular death (8%), and first heart failure hospitalization (4%) subsequently. A similar trend was seen with KCCQ total symptom score (TSS) and overall summary score (OSS). Empagliflozin improved KCCQ-CSS, -TSS and -OSS scores similarly across subgroups studied except for greater improvement in patients with the highest BMI (p trend = 0.153, 0.08 and 0.078, respectively). Health status in patients with HFpEF is impaired, especially in elderly, women, and those with obesity and comorbidities. Empagliflozin improved health status among all key subgroups studied with a greater effect in obese patients.

Identifiants

pubmed: 36974746
doi: 10.1002/ejhf.2831
doi:

Substances chimiques

empagliflozin HDC1R2M35U

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1623-1631

Commentaires et corrections

Type : CommentIn

Informations de copyright

© 2023 The Authors. European Journal of Heart Failure published by John Wiley & Sons Ltd on behalf of European Society of Cardiology.

Références

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Auteurs

Tariq Jamal Siddiqi (TJ)

Department of Medicine, University of Mississippi Medical Center, Jackson, MS, USA.

Stefan D Anker (SD)

Department of Cardiology and Berlin Institute of Health Center for Regenerative Therapies, Berlin, Germany.
German Centre for Cardiovascular Research partner site, Berlin, Germany.
Charité Universitätsmedizin, Berlin, Germany.

Gerasimos Filippatos (G)

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

João Pedro Ferreira (JP)

UnIC@RISE, Cardiovascular Research and Development Center, Department of Surgery and Physiology, Faculty of Medicine, University of Porto, Porto, Portugal.
Heart Failure Clinic, Internal Medicine Department, Centro Hospitalar de Vila Nova de Gaia/Espinho, Portugal.
Inserm, Centre d'Investigations Cliniques - Plurithématique 14-33, Université de Lorraine, Nancy, France.
Inserm U1116, CHRU Nancy, F-CRIN INI-CRCT (Cardiovascular and Renal Clinical Trialists), Nancy, France.

Stuart J Pocock (SJ)

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

Michael Böhm (M)

Klinik für Innere Medizin III, Universitätsklinikum des Saarlandes, Saarland University, Homburg/Saar, Germany.

Martina Brueckmann (M)

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

Vijay K Chopra (VK)

Max Superspeciality Hospital, Saket, New Delhi, India.

Tomoko Iwata (T)

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

James Januzzi (J)

Massachusetts General Hospital and Baim Institute for Clinical Research, Boston, MA, USA.

Ileana L Piña (IL)

Central Michigan University, Mount Pleasant, MI, USA.

Piotr Ponikowski (P)

Wroclaw Medical University, Wroclaw, Poland.

Michele Senni (M)

Cardiology Division, Cardiovascular Department, Papa Giovanni XXIII Hospital, Bergamo, Italy.

Ola Vedin (O)

Boehringer Ingelheim AB, Stockholm, Sweden.

Subodh Verma (S)

Division of Cardiac Surgery, St. Michael's Hospital, University of Toronto, Toronto, ON, Canada.

Yuhui Zhang (Y)

Heart Failure Center, Fuwai Hospital, Chinese Academy of Medical Science and Peking Union Medical College, Beijing, China.

Faiez Zannad (F)

Centre d'Investigations Cliniques Plurithématique 1433 and Inserm U1116, CHRU, FCRIN INI-CRCT (Cardiovascular and Renal Clinical Trialists), Université de Lorraine, Nancy, France.

Milton Packer (M)

Baylor Heart and Vascular Institute, Baylor University Medical Center, Dallas, TX, USA.
Imperial College, London, UK.

Javed Butler (J)

Department of Medicine, University of Mississippi Medical Center, Jackson, MS, USA.
Baylor Scott and White Research Institute, Dallas, TX, USA.

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