医学
心房颤动
四分位间距
内科学
危险系数
冲程(发动机)
入射(几何)
队列研究
急性冠脉综合征
前瞻性队列研究
冠状动脉疾病
队列
置信区间
心肌梗塞
物理
光学
工程类
机械工程
作者
Keith A Fox,Priscilla Velentgas,A. John Camm,Jean‐Pierre Bassand,David Fitzmaurice,Bernard J. Gersh,Samuel Z. Goldhaber,Shinya Goto,Sylvia Haas,Frank Misselwitz,Karen S. Pieper,Alexander G. G. Turpie,Freek W.A. Verheugt,Elizabeth Dabrowski,Kaiyi Luo,Liza Gibbs,Ajay K. Kakkar
出处
期刊:JAMA network open
[American Medical Association]
日期:2020-02-26
卷期号:3 (2): e200107-e200107
被引量:22
标识
DOI:10.1001/jamanetworkopen.2020.0107
摘要
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.
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