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首页> 外文期刊>Journal of thrombosis and thrombolysis >Warfarin for prevention of thromboembolism in atrial fibrillation: comparison of patient characteristics and outcomes of the “Real-World” Michigan Anticoagulation Quality Improvement Initiative (MAQI 2 ) registry to the RE-LY, ROCKET-AF, and ARISTOTLE trials
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Warfarin for prevention of thromboembolism in atrial fibrillation: comparison of patient characteristics and outcomes of the “Real-World” Michigan Anticoagulation Quality Improvement Initiative (MAQI 2 ) registry to the RE-LY, ROCKET-AF, and ARISTOTLE trials

机译:Warfarin预防心房颤动的血栓栓塞:“真实世界”密歇根抗凝质量改善倡议(Maqi 2)登记处的患者特征和结果与Re-Ly,Rocket-AF和Aristotle试验的比较

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Randomized controlled trials (RCTs) examining warfarin use for stroke prevention in atrial fibrillation (AF) may not accurately reflect real-world populations. We aimed to determine the representativeness of the RCT populations to real-world patients and to describe differences in the characteristics of trial populations from trial eligible patients in a real-world setting. We hypothesized that a significant fraction of real-world patients would not qualify for the RE-LY, ROCKET-AF, and ARISTOTLE trials and that real-world patients qualifying for the studies may have more strokes and bleeding events. We compared the inclusion and exclusion criteria, patient characteristics, and clinical outcomes from RE-LY, ROCKET-AF, and ARISTOTLE against data from the Michigan Anticoagulation Quality Improvement Initiative (MAQI_(2)), a regional network of six community- and academic-based anticoagulation clinics. Of the 1446 non-valvular AF patients in the MAQI_(2)registry taking warfarin, approximately 40–60% would meet the selection criteria used in RE-LY (788, 54.5%), ROCKET-AF (566, 39.1%), and ARISTOTLE (866, 59.9%). The most common reasons for exclusion from one or more trial were anemia (15.1%), other concurrent medications (11.2%), and chronic kidney disease (9.4%). Trial-eligible MAQI_(2)patients were older, more frequently female, with a higher rate of paroxysmal AF, and lower rates of congestive heart failure, previous stroke, and previous myocardial infarction than the trial populations. MAQI_(2)patients eligible for each trial had a lower rate of stroke and similar rate of major bleeding than was observed in the trials. A sizable proportion of real-world AF patients managed in anticoagulation clinics would not have been eligible for the RE-LY, ROCKET-AF, and ARISOTLE trials. The expected stroke risk reduction and bleeding risk among real-world AF patients on warfarin may not be congruent with published clinical trial data.
机译:随机对照试验(RCTS)检查风暴预防在心房颤动(AF)中的卒中预防可能无法准确反映现实世界的人群。我们旨在确定RCT人群对现实世界患者的代表性,并描述在真实世界环境中审判符合验证患者的试验人口特征的差异。我们假设大部分现实世界患者不符合RE-LY,ROCKET-AF和Aristotle试验,并且鉴定所述研究的真实患者可能有更多的笔触和出血事件。我们将纳入和排除标准,患者特征和临床结果与来自密歇根抗菌质量改善倡议(Maqi_(2)),六个社区和学术的区域网络进行了比较了Re-Ly,Rocket-AF和Aristotle免受Re-Ly,Rocket-AF和Aristotle的临床结果。基于抗凝诊所。在Maqi_(2)令人携带华法林的注册表中的1446名非瓣膜AF患者中,大约40-60%会符合重新提供的选择标准(788,54.5%),Rocket-AF(566,39.1%),和亚里士多德(866,59.9%)。排除一个或多个试验的最常见原因是贫血(15.1%),其他并发药物(11.2%)和慢性肾病(9.4%)。试验符合条件的Maqi_(2)患者患者较大,更频繁的女性,具有较高的阵发性AF,较低的充血性心力衰竭率,先前的中风和先前的心肌梗死而不是试验群体。 Maqi_(2)符合每次试验条件的患者的行程率较低,主要出血的类似速度比试验在审判中观察到。在抗凝诊所管理的大量现实世界AF患者不符合RE-LY,ROCKET-AF和ARISOTLE试验的资格。在华法林的现实世界AF患者中预期的卒中风险降低和出血风险可能不会与公布的临床试验数据一致。

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