Intensity of Guideline-Directed Medical Therapy for Coronary Heart Disease and Ischemic Heart Failure Outcomes.


Journal

The American journal of medicine
ISSN: 1555-7162
Titre abrégé: Am J Med
Pays: United States
ID NLM: 0267200

Informations de publication

Date de publication:
05 2021
Historique:
received: 11 09 2020
revised: 11 10 2020
accepted: 12 10 2020
pubmed: 13 11 2020
medline: 23 6 2021
entrez: 12 11 2020
Statut: ppublish

Résumé

The impact of guideline-directed medical therapy for coronary heart disease in those hospitalized with acute heart failure is unknown. We studied guideline-directed medical therapies for coronary disease: angiotensin-converting enzyme (ACE) inhibitors or angiotensin II receptor blockers (ARBs), beta-adrenoreceptor antagonists, antiplatelet agents or anticoagulants, and statins. Using inverse probability of treatment weighting the propensity score, we examined associations of guideline-directed medical therapy intensity (categorized as low [0-1], high [2-3], or very high [4] number of drugs) with mortality in 1873 patients with angina, troponin elevation, or prior myocardial infarction. At discharge, 0-1, 2-3, and 4 medications were prescribed in 467 (25%), 705 (38%), and 701 (37%) patients, respectively. Relative to those prescribed 0-1 drugs (reference), all-cause mortality was lower with 2-3 (hazard ratio [HR] 0.48, 95% confidence interval [CI] 0.28-0.84, P = 0.009) or all 4 drug classes (HR 0.56, 95% CI 0.33-0.96, P = 0.034) over 181-365 days, with similar reductions present from 0-180 days. In those with heart failure with preserved ejection fraction, mortality trended lower with 2-3 drug classes (HR 0.43, 95% CI 0.18-1.02, P = 0.054) and was significantly reduced with 4 drugs (HR 0.32, 95%CI 0.12-0.84, P = 0.021) during 0-180 day follow-up. In heart failure with reduced ejection fraction, all-cause mortality was reduced during both 0-180 and 181-365 days when discharged on 2-3 (HR 0.30 for 181-365 days, 95%CI 0.14-0.64, P = 0.002) or all 4 drug classes (HR 0.43, 95%CI 0.19-0.95, P = 0.038). Increasing guideline-directed medical therapy intensity for coronary heart disease resulted in lower mortality in patients with acute ischemic heart failure with both preserved and reduced ejection fractions.

Identifiants

pubmed: 33181105
pii: S0002-9343(20)30957-8
doi: 10.1016/j.amjmed.2020.10.017
pii:
doi:

Substances chimiques

Adrenergic beta-Antagonists 0
Angiotensin Receptor Antagonists 0
Angiotensin-Converting Enzyme Inhibitors 0
Anticoagulants 0
Hydroxymethylglutaryl-CoA Reductase Inhibitors 0
Platelet Aggregation Inhibitors 0

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

672-681.e4

Subventions

Organisme : CIHR
ID : FDN 148446
Pays : Canada

Informations de copyright

Copyright © 2020 The Authors. Published by Elsevier Inc. All rights reserved.

Auteurs

Rebecca Crosier (R)

Department of Medicine, University of Toronto, Toronto, Ontario.

Peter C Austin (PC)

ICES, Toronto, Ontario; Institute for Health Policy, Management and Evaluation Toronto, Ontario.

Dennis T Ko (DT)

Department of Medicine, University of Toronto, Toronto, Ontario; ICES, Toronto, Ontario; Institute for Health Policy, Management and Evaluation Toronto, Ontario; Sunnybrook Health Sciences Centre, Toronto, Ontario.

Patrick R Lawler (PR)

Department of Medicine, University of Toronto, Toronto, Ontario; Peter Munk Cardiac Centre of University Health Network, Toronto, Ontario; Ted Rogers Centre for Heart Research, Toronto, Ontario.

Therese A Stukel (TA)

ICES, Toronto, Ontario; Institute for Health Policy, Management and Evaluation Toronto, Ontario.

Michael E Farkouh (ME)

Department of Medicine, University of Toronto, Toronto, Ontario; Peter Munk Cardiac Centre of University Health Network, Toronto, Ontario.

Xuesong Wang (X)

ICES, Toronto, Ontario.

John A Spertus (JA)

Saint Luke's Mid America Heart Institute/UMKC, Kansas City, Missouri.

Heather J Ross (HJ)

Department of Medicine, University of Toronto, Toronto, Ontario; Peter Munk Cardiac Centre of University Health Network, Toronto, Ontario; Ted Rogers Centre for Heart Research, Toronto, Ontario.

Douglas S Lee (DS)

Department of Medicine, University of Toronto, Toronto, Ontario; ICES, Toronto, Ontario; Institute for Health Policy, Management and Evaluation Toronto, Ontario; Peter Munk Cardiac Centre of University Health Network, Toronto, Ontario; Ted Rogers Centre for Heart Research, Toronto, Ontario. Electronic address: dlee@ices.on.ca.

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Classifications MeSH