Outcomes Associated With Oral Anticoagulants Plus Antiplatelets in Patients With Newly Diagnosed Atrial Fibrillation.


Journal

JAMA network open
ISSN: 2574-3805
Titre abrégé: JAMA Netw Open
Pays: United States
ID NLM: 101729235

Informations de publication

Date de publication:
05 02 2020
Historique:
entrez: 27 2 2020
pubmed: 27 2 2020
medline: 26 8 2020
Statut: epublish

Résumé

Patients with nonvalvular atrial fibrillation at risk of stroke should receive oral anticoagulants (OAC). However, approximately 1 in 8 patients in the Global Anticoagulant Registry in the Field (GARFIELD-AF) registry are treated with antiplatelet (AP) drugs in addition to OAC, with or without documented vascular disease or other indications for AP therapy. To investigate baseline characteristics and outcomes of patients who were prescribed OAC plus AP therapy vs OAC alone. Prospective cohort study of the GARFIELD-AF registry, an international, multicenter, observational study of adults aged 18 years and older with recently diagnosed nonvalvular atrial fibrillation and at least 1 risk factor for stroke enrolled between March 2010 and August 2016. Data were extracted for analysis in October 2017 and analyzed from April 2018 to June 2019. Participants received either OAC plus AP or OAC alone. Clinical outcomes were measured over 3 and 12 months. Outcomes were adjusted for 40 covariates, including baseline conditions and medications. A total of 24 436 patients (13 438 [55.0%] male; median [interquartile range] age, 71 [64-78] years) were analyzed. Among eligible patients, those receiving OAC plus AP therapy had a greater prevalence of cardiovascular indications for AP, including acute coronary syndromes (22.0% vs 4.3%), coronary artery disease (39.1% vs 9.8%), and carotid occlusive disease (4.8% vs 2.0%). Over 1 year, patients treated with OAC plus AP had significantly higher incidence rates of stroke (adjusted hazard ratio [aHR], 1.49; 95% CI, 1.01-2.20) and any bleeding event (aHR, 1.41; 95% CI, 1.17-1.70) than those treated with OAC alone. These patients did not show evidence of reduced all-cause mortality (aHR, 1.22; 95% CI, 0.98-1.51). Risk of acute coronary syndrome was not reduced in patients taking OAC plus AP compared with OAC alone (aHR, 1.16; 95% CI, 0.70-1.94). Patients treated with OAC plus AP also had higher rates of all clinical outcomes than those treated with OAC alone over the short term (3 months). This study challenges the practice of coprescribing OAC plus AP unless there is a clear indication for adding AP to OAC therapy in newly diagnosed atrial fibrillation.

Identifiants

pubmed: 32101311
pii: 2761869
doi: 10.1001/jamanetworkopen.2020.0107
pmc: PMC7137686
doi:

Substances chimiques

Anticoagulants 0
Platelet Aggregation Inhibitors 0

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

e200107

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Auteurs

Keith A A Fox (KAA)

Centre for Cardiovascular Science, University of Edinburgh, Edinburgh, United Kingdom.

Priscilla Velentgas (P)

Aetion Inc, New York, New York.

A John Camm (AJ)

Cardiology Clinical Academic Group Molecular & Clinical Sciences Research Institute, St George's University of London, London, United Kingdom.

Jean-Pierre Bassand (JP)

Thrombosis Research Institute, London, United Kingdom.
University of Besançon, Besançon, France.

David A Fitzmaurice (DA)

University of Warwick Medical School, Coventry, United Kingdom.

Bernard J Gersh (BJ)

Mayo Clinic College of Medicine, Rochester, Minnesota.

Samuel Z Goldhaber (SZ)

Brigham and Women's Hospital and Harvard Medical School, Boston, Massachusetts.

Shinya Goto (S)

Tokai University, Isehara, Japan.

Sylvia Haas (S)

Formerly Department of Medicine, Technical University of Munich, Munich, Germany.

Frank Misselwitz (F)

Bayer HealthCare Pharmaceuticals, Berlin, Germany.

Karen S Pieper (KS)

Thrombosis Research Institute, London, United Kingdom.
Duke University, Durham, North Carolina.

Alexander G G Turpie (AGG)

McMaster University, Hamilton, Ontario, Canada.

Freek W A Verheugt (FWA)

Onze Lieve Vrouwe Gasthuis (OLVG), Amsterdam, the Netherlands.

Elizabeth Dabrowski (E)

Aetion Inc, New York, New York.

Kaiyi Luo (K)

Aetion Inc, New York, New York.

Liza Gibbs (L)

Aetion Inc, New York, New York.

Ajay K Kakkar (AK)

Thrombosis Research Institute, London, United Kingdom.
University College London, London, United Kingdom.

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Classifications MeSH