Association of heart failure and its comorbidities with loss of life expectancy.
heart failure
heart failure with reduced ejection fraction
Journal
Heart (British Cardiac Society)
ISSN: 1468-201X
Titre abrégé: Heart
Pays: England
ID NLM: 9602087
Informations de publication
Date de publication:
09 2021
09 2021
Historique:
received:
16
07
2020
revised:
13
10
2020
accepted:
16
10
2020
pubmed:
7
11
2020
medline:
15
12
2021
entrez:
6
11
2020
Statut:
ppublish
Résumé
Estimating survival can aid care planning, but the use of absolute survival projections can be challenging for patients and clinicians to contextualise. We aimed to define how heart failure and its major comorbidities contribute to loss of actuarially predicted life expectancy. We conducted an observational cohort study of 1794 adults with stable chronic heart failure and reduced left ventricular ejection fraction, recruited from cardiology outpatient departments of four UK hospitals. Data from an 11-year maximum (5-year median) follow-up period (999 deaths) were used to define how heart failure and its major comorbidities impact on survival, relative to an age-sex matched control UK population, using a relative survival framework. After 10 years, mortality in the reference control population was 29%. In people with heart failure, this increased by an additional 37% (95% CI 34% to 40%), equating to an additional 2.2 years of lost life or a 2.4-fold (2.2-2.5) excess loss of life. This excess was greater in men than women (2.4 years (2.2-2.7) vs 1.6 years (1.2-2.0); p<0.001). In patients without major comorbidity, men still experienced excess loss of life, while women experienced less and were non-significantly different from the reference population (1 year (0.6-1.5) vs 0.4 years (-0.3 to 1); p<0.001). Accrual of comorbidity was associated with substantial increases in excess lost life, particularly for diabetes, chronic kidney and lung disease. Comorbidity accounts for the majority of lost life expectancy in people with heart failure. Women, but not men, without comorbidity experience survival close to reference controls.
Identifiants
pubmed: 33153996
pii: heartjnl-2020-317833
doi: 10.1136/heartjnl-2020-317833
pmc: PMC8372397
doi:
Types de publication
Journal Article
Observational Study
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
1417-1421Subventions
Organisme : British Heart Foundation
ID : CH/13/1/30086
Pays : United Kingdom
Organisme : Department of Health
ID : NIHR-CS-012-032
Pays : United Kingdom
Organisme : British Heart Foundation
ID : FS/14/10/30472
Pays : United Kingdom
Organisme : British Heart Foundation
ID : FS/18/44/33792
Pays : United Kingdom
Organisme : British Heart Foundation
ID : PG/08/020/24617
Pays : United Kingdom
Organisme : British Heart Foundation
ID : FS/CRTF/20/24071
Pays : United Kingdom
Organisme : British Heart Foundation
ID : RG/09/010/28087
Pays : United Kingdom
Organisme : British Heart Foundation
ID : FS/12/80/29821
Pays : United Kingdom
Informations de copyright
© Author(s) (or their employer(s)) 2021. Re-use permitted under CC BY. Published by BMJ.
Déclaration de conflit d'intérêts
Competing interests: JG has received a research grant from Medtronic. KKW has received speaker fees from Medtronic, Livanova, St. Jude Medical, Pfizer, Bayer and BMS. MTK has received speaker fees from Merck, Novo Nordisk and unrestricted research awards from Medtronic. ADS has received speaker fees from Abbott, BMS, AstraZeneca, Bayer, Novartis, Boehringer Ingelheim and Servier. VKG has received speaker fees from Abbott and Novartis.
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