Heightened long-term cardiovascular risks after exacerbation of chronic obstructive pulmonary disease.

Arrhythmias, Cardiac Heart Failure Risk Factors

Journal

Heart (British Cardiac Society)
ISSN: 1468-201X
Titre abrégé: Heart
Pays: England
ID NLM: 9602087

Informations de publication

Date de publication:
05 Jan 2024
Historique:
received: 20 09 2023
accepted: 27 11 2023
medline: 6 1 2024
pubmed: 6 1 2024
entrez: 5 1 2024
Statut: aheadofprint

Résumé

To examine the risk of adverse cardiovascular (CV) events following an exacerbation of chronic obstructive pulmonary disease (COPD). This retrospective cohort study identified patients with COPD using administrative data from Alberta, Canada from 2014 to 2019. Exposure periods were 12 months following moderate or severe exacerbations; the reference period was time preceding a first exacerbation. The primary outcome was the composite of all-cause death or a first hospitalisation for acute coronary syndrome, heart failure (HF), arrhythmia or cerebral ischaemia. Time-dependent Cox regression models estimated covariate-adjusted risks associated with six exposure subperiods following exacerbation. Among 1 42 787 patients (mean age 68.1 years and 51.7% men) 61 981 (43.4%) experienced at least one exacerbation and 34 068 (23.9%) died during median follow-up of 64 months. The primary outcome occurred in 43 564 (30.5%) patients with an incidence rate prior to exacerbation of 5.43 (95% CI 5.36 to 5.50) per 100 person-years. This increased to 95.61 per 100 person-years in the 1-7 days postexacerbation (adjusted HR 15.86, 95% CI 15.17 to 16.58) and remained increased for up to 1 year. The risk of both the composite and individual CV events was increased following either a moderate or a severe exacerbation, though greater and more prolonged following severe exacerbation. The highest magnitude of increased risk was observed for HF decompensation (1-7 days, HR 72.34, 95% CI 64.43 to 81.22). Moderate and severe COPD exacerbations are independent risk factors for adverse CV events, especially HF decompensation. The impact of optimising COPD management on CV outcomes should be evaluated.

Identifiants

pubmed: 38182279
pii: heartjnl-2023-323487
doi: 10.1136/heartjnl-2023-323487
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

© Author(s) (or their employer(s)) 2024. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.

Déclaration de conflit d'intérêts

Competing interests: SM, PE and TP are employed by Medlior Health Outcomes Research Ltd. which received funding for the study from AstraZeneca UK. NMH participated on advisory boards for Bayer, BI, and Servier. He also received honoraria for speakers bureau from AZ, Novartis, and Servier and grants/research support from AZ and Novartis and consulting fees from AZ. DDS received honoraria for speaking engagements on the topic of COPD from AZ, GSK and BI. AKR, MT, CN, KR are the employees of AstraZeneca and may hold shares/stock options.

Auteurs

Nathaniel M Hawkins (NM)

Centre for Cardiovascular Innovation, Division of Cardiology, The University of British Columbia, Vancouver, British Columbia, Canada nat.hawkins@ubc.ca.

Clementine Nordon (C)

AstraZeneca UK Limited, Cambridge, UK.

Kirsty Rhodes (K)

AstraZeneca UK Limited, Cambridge, UK.

Manisha Talukdar (M)

AstraZeneca Canada Inc, Mississauga, Ontario, Canada.

Suzanne McMullen (S)

Medlior Health Outcomes Research Ltd, Calgary, Alberta, Canada.

Paul Ekwaru (P)

Medlior Health Outcomes Research Ltd, Calgary, Alberta, Canada.

Tram Pham (T)

Medlior Health Outcomes Research Ltd, Calgary, Alberta, Canada.

Arsh K Randhawa (AK)

AstraZeneca Canada Inc, Mississauga, Ontario, Canada.

Don D Sin (DD)

UBC Centre for Heart Lung Innovation and Department of Medicine (Respirology), The University of British Columbia, Vancouver, British Columbia, Canada.

Classifications MeSH