Ejection fraction and mortality: a nationwide register-based cohort study of 499 153 women and men.


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 2021
Historique:
revised: 30 10 2020
received: 27 06 2020
accepted: 01 11 2020
pubmed: 6 11 2020
medline: 6 7 2021
entrez: 5 11 2020
Statut: ppublish

Résumé

We investigated the sex-based risk of mortality across the spectrum of left ventricular ejection fraction (LVEF) in a large cohort of patients in Australia. Quantified levels of LVEF from 237 046 women (48.1%) and 256 109 men undergoing first-time, routine echocardiography (2000-2019) were linked to 119 232 deaths (median 5.6 years of follow-up). Overall, 17.6% of men vs. 8.3% of women had an LVEF <50%. An LVEF <40% was associated with the highest crude cardiovascular-related and all-cause mortality at 5 years (∼20-30% and ∼ 40-50%, respectively). Thereafter, actual cardiovascular-related and all-cause mortality at 5 years in both sexes steeply improved to a nadir LVEF of 65.0-69.9% (reference group). Below this LVEF level, the adjusted hazard ratio (HR) for cardiovascular-related mortality for a LVEF of 55.0-59.9% was 1.36 [95% confidence interval (CI) 1.16-1.59; P < 0.001] in women and 1.21 (95% CI 1.05-1.39; P = 0.008) in men. In women, an LVEF of 60.0-64.9% was also associated with a HR 1.33 (95% CI 1.16-1.52; P < 0.001) for cardiovascular-related mortality. These associations were most striking in women and men aged <65 years and were replicated in those with suspected heart failure (32 403 cases aged 65.2 ± 16.1 years, 57.0% women). For pre-existing heart failure (33 738 cases aged 67.6 ± 16.9 years, 46.5% women), the specific threshold of increased mortality was at and below 50.0-54.9%. Among patients investigated for suspected or established cardiovascular disease, we found clinically relevant sex-based differences in the distribution and mortality associated with an LVEF <65.0-69.9%. Specifically, they suggest a greater risk of mortality at higher LVEF levels among women.

Identifiants

pubmed: 33150657
doi: 10.1002/ejhf.2047
doi:

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

406-416

Subventions

Organisme : NHMRC of Australia
ID : GNT1135894
Organisme : Novartis Pharma AG

Commentaires et corrections

Type : CommentIn

Informations de copyright

© 2020 European Society of Cardiology.

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Auteurs

Simon Stewart (S)

Torrens University Australia, Adelaide, Australia/University of Glasgow, Glasgow, UK.

David Playford (D)

The University of Notre Dame, Fremantle, Australia.

Gregory M Scalia (GM)

The Prince Charles Hospital, Brisbane, Australia.

Philip Currie (P)

Cardio Vascular Services, Perth, Australia.

David S Celermajer (DS)

University of Sydney, Sydney, Australia.

David Prior (D)

St Vincent's Hospital, Melbourne, Australia.

Jim Codde (J)

The University of Notre Dame, Fremantle, Australia.

Geoff Strange (G)

The University of Notre Dame, Fremantle, Australia.

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