Change in ejection fraction and long-term mortality in adults referred for echocardiography.


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:
04 2021
Historique:
revised: 18 03 2021
received: 24 12 2020
accepted: 22 03 2021
pubmed: 27 3 2021
medline: 6 7 2021
entrez: 26 3 2021
Statut: ppublish

Résumé

We investigated long-term mortality associated with changes in left ventricular ejection fraction (LVEF) in a large, real-world patient cohort. A total of 117 275 adults (63 ± 16 years, 46% women) had LVEF quantified by the same method ≥6 months apart. This included 17 343 cases (66 ± 15 years, 48% women) being initially investigated for heart failure (HF). During 3.3 [interquartile range (IQR) 1.7-6.0] years from first to last echocardiogram, median change in LVEF was -1 (IQR -8 to +5) units from a baseline of 62% (IQR 54-69%). During subsequent 7.6 (IQR 4.3-10.1) years of follow-up, 11 397 (9.7%) and 34 101 (29.1%) cases died from cardiovascular disease and all causes, respectively. Actual 5-year, all-cause mortality increased from 12% to 29% among those with the smallest to the largest decrease in LVEF (from <5 units to >30 units); the adjusted risk of cardiovascular-related mortality increased two- to eightfold beyond a >10-unit decline in LVEF (vs. minimal change; P < 0.001 for all comparisons). Among those initially investigated for HF (32% with initial LVEF <50%), the adjusted hazard ratio for cardiovascular-related mortality ranged from 0.35 [95% confidence interval (CI) 0.28-0.49] to 4.21 (95% CI 3.30-5.22) for a >30-unit increase to >30-unit decline in LVEF (vs. minimal change; P < 0.001 for both comparisons). A distinctive, bi-directional plateau of improved vs. worsening mortality was evident around a final LVEF of 50% to 55%. These data, derived from a large, heterogeneous cohort of adults being followed up with echocardiography, suggest that modest LVEF changes (particularly around an LVEF of 50-55%) may be of clinical significance.

Identifiants

pubmed: 33768605
doi: 10.1002/ejhf.2161
doi:

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

555-563

Subventions

Organisme : NHMRC
ID : GNT1135894

Commentaires et corrections

Type : CommentIn

Informations de copyright

© 2021 European Society of Cardiology.

Références

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Auteurs

Geoff Strange (G)

The University of Notre Dame, Fremantle, Australia.
University of Sydney, Sydney, Australia.

David Playford (D)

The University of Notre Dame, Fremantle, Australia.

Gregory M Scalia (GM)

The Prince Charles Hospital, Brisbane, 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.

Yih-Kai Chan (YK)

Australian Catholic University, Melbourne, Australia.

Max K Bulsara (MK)

The University of Notre Dame, Fremantle, Australia.

Simon Stewart (S)

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

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