Cardiovascular Outcomes According to Polypharmacy and Drug Adherence in Patients with Atrial Fibrillation on Long-Term Anticoagulation (from the RE-LY Trial).


Journal

The American journal of cardiology
ISSN: 1879-1913
Titre abrégé: Am J Cardiol
Pays: United States
ID NLM: 0207277

Informations de publication

Date de publication:
15 06 2021
Historique:
received: 14 01 2021
revised: 28 02 2021
accepted: 05 03 2021
pubmed: 25 3 2021
medline: 20 7 2021
entrez: 24 3 2021
Statut: ppublish

Résumé

Prevalence of atrial fibrillation (AF) increases with age, along with comorbidities and, thus, polypharmacy. Non-adherence is associated with polypharmacy. This study aimed to identify patients at risk for cardiovascular events according to their pharmacological treatment intensity and adherence. Patients (n = 18,113) with a mean age of 71.5 ± 8.7 years, at high cardiovascular risk were followed between December 2005 until December 2007 for a median time of 2 years. The association between polypharmacy and adherence and their impact on cardiovascular and bleeding events were explored. Adherence was defined as a study drug intake of ≥80%. Patients with more co-medications had a higher body mass index, higher prevalence of hypertension, coronary heart disease, heart failure, and diabetes mellitus (all p < 0.0001) compared to ≤4 or 5-8 co-medications, but no differences in history of stroke (p = 0.68) or transient ischemic attack (p = 0.065). Across all treatments, the adjusted hazard ratios (HRs) increased in patients with more co-medications (≥9 vs ≤4) for all-cause death (HR 1.30; 1.06-1.59), major bleeding (HR 1.65; 1.33-2.05), and all bleeding events (HR 1.44; 1.31-1.59). Yearly event rates were higher in non-adherent than adherent patients for stroke and systemic embolism (SSE) (3.14 vs 1.00), all-cause death (7.76 vs 2.66), major bleeding (6.21 vs 2.65), and all bleeding (28.71 vs 19.05; all p < 0.0001). After an event the patients were more likely to become non-adherent (adherence after SSE 30.3%, after major bleeding 33.4%, after all bleeding 66.7%; all p < 0.0001). The treatment effects were consistent to the overall group in the different polypharmacy groups. In conclusion, polypharmacy and non-adherence are risk indicators for increased adverse cardiovascular and bleeding events. Dabigatran is safe to use across the full spectrum of AF patients, independent of the number of co-medications and adherence. Patients with co-medications and comorbidities require special attention and encouragement to adhere to oral anticoagulation.

Identifiants

pubmed: 33757788
pii: S0002-9149(21)00267-8
doi: 10.1016/j.amjcard.2021.03.024
pii:
doi:

Substances chimiques

Anticoagulants 0
Warfarin 5Q7ZVV76EI
Dabigatran I0VM4M70GC

Banques de données

ClinicalTrials.gov
['NCT00262600']

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

27-35

Informations de copyright

Copyright © 2021 Elsevier Inc. All rights reserved.

Auteurs

Dominic Millenaar (D)

Klinik für Innere Medizin III - Kardiologie, Angiologie, Internistische Intensivmedizin. Electronic address: Dominic.Millenaar@uks.eu.

Helmut Schumacher (H)

Statistical Consultant, Ingelheim am Rhein, Rhineland-Palatinate, Germany.

Martina Brueckmann (M)

Medicine CardioMetabolism & Respiratory, Boehringer Ingelheim International GmbH, Binger Strasse 173, Ingelheim am Rhein, Rhineland-Palatinate, Germany; Medizinische Fakultät Mannheim, Universitätsklinikum Mannheim, Theodor-Kutzer Ufer 1-3, Mannheim, Baden-Württemberg, Germany.

John W Eikelboom (JW)

Population Health Research Institute, McMaster University and Hamilton Health Sciences, Hamilton, Ontario, Canada.

Michael Ezekowitz (M)

Sidney Kimmel Medical College at Jefferson University, Philadelphia, Pennsylvania; Lankenau Institute for Medical Research and The Heart Center, Wynnewood, Pennsylvania.

Jonathan Slawik (J)

Klinik für Innere Medizin III - Kardiologie, Angiologie, Internistische Intensivmedizin.

Sebastian Ewen (S)

Klinik für Innere Medizin III - Kardiologie, Angiologie, Internistische Intensivmedizin.

Christian Ukena (C)

Klinik für Innere Medizin III - Kardiologie, Angiologie, Internistische Intensivmedizin.

Lars Wallentin (L)

Uppsala Clinical Research Center and Department of Medical Sciences, Cardiology, Uppsala University, Uppsala, Sweden.

Stuart Connolly (S)

Population Health Research Institute, McMaster University and Hamilton Health Sciences, Hamilton, Ontario, Canada.

Salim Yusuf (S)

Population Health Research Institute, McMaster University and Hamilton Health Sciences, Hamilton, Ontario, Canada.

Michael Böhm (M)

Klinik für Innere Medizin III - Kardiologie, Angiologie, Internistische Intensivmedizin.

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