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华法林预防心房颤动中的血栓栓塞:“真实世界”密歇根抗凝质量改进计划(MAQI)注册研究与 RE-LY、ROCKET-AF 和 ARISTOTLE 试验中患者特征和结局的比较。

Warfarin for prevention of thromboembolism in atrial fibrillation: comparison of patient characteristics and outcomes of the "Real-World" Michigan Anticoagulation Quality Improvement Initiative (MAQI) registry to the RE-LY, ROCKET-AF, and ARISTOTLE trials.

机构信息

Frankel Cardiovascular Center, University of Michigan Health System, 1500 E. Medical Center Drive, 2386-B CVC SPC 5853, Ann Arbor, MI, 48109, USA.

Michigan Heart Group, William Beaumont Hospital, Royal Oak, MI, USA.

出版信息

J Thromb Thrombolysis. 2018 Oct;46(3):316-324. doi: 10.1007/s11239-018-1698-y.

Abstract

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), a regional network of six community- and academic-based anticoagulation clinics. Of the 1446 non-valvular AF patients in the MAQI 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 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 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.

摘要

随机对照试验(RCT)研究华法林用于预防心房颤动(AF)中的卒中可能无法准确反映真实世界人群。我们旨在确定 RCT 人群与真实世界患者的代表性,并描述真实世界环境中试验人群与符合试验条件的患者之间特征的差异。我们假设,相当一部分真实世界的患者不符合 RE-LY、ROCKET-AF 和 ARISTOTLE 试验的入选标准,而符合研究标准的真实世界患者可能会有更多的卒中及出血事件。我们将 RE-LY、ROCKET-AF 和 ARISTOTLE 的纳入和排除标准、患者特征及临床结局与密歇根抗凝质量改进倡议(MAQI)的数据进行了比较,后者是一个由六个社区和学术抗凝诊所组成的区域网络。在 MAQI 注册处接受华法林治疗的 1446 例非瓣膜性 AF 患者中,约有 40-60%符合 RE-LY(788 例,54.5%)、ROCKET-AF(566 例,39.1%)和 ARISTOTLE(866 例,59.9%)的入选标准。在一项或多项试验中被排除的最常见原因是贫血(15.1%)、其他同时使用的药物(11.2%)和慢性肾病(9.4%)。MAQI 中符合试验入选标准的患者年龄较大,女性更常见,阵发性 AF 发生率更高,充血性心力衰竭、既往卒中及既往心肌梗死的发生率更低。与试验人群相比,符合每个试验入选标准的 MAQI 患者的卒中发生率更低,大出血发生率相似。在抗凝诊所接受治疗的真实世界 AF 患者中,相当一部分不符合 RE-LY、ROCKET-AF 和 ARISOTLE 试验的入选标准。真实世界 AF 患者使用华法林的预期卒中风险降低和出血风险可能与已发表的临床试验数据不一致。

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