首页> 外文期刊>The American heart journal >Design and rationale of Global Registry on Long-Term Oral Antithrombotic Treatment in Patients with Atrial Fibrillation: A global registry program on long-term oral antithrombotic treatment in patients with atrial fibrillation
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Design and rationale of Global Registry on Long-Term Oral Antithrombotic Treatment in Patients with Atrial Fibrillation: A global registry program on long-term oral antithrombotic treatment in patients with atrial fibrillation

机译:心房颤动患者长期口服抗血栓治疗的全球注册管理系统的设计和原理:房颤患者长期口服抗血栓治疗的全球注册管理系统

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Background Atrial fibrillation (AF) is the most common cardiac arrhythmia, affecting 1% to 2% of the population and raising the risk of stroke 5-fold. Until recently, the only treatment choices for stroke prevention in patients with AF have been vitamin K antagonists (VKA) or antiplatelet drugs. With approval of novel oral anticoagulants (NOACs) antithrombotic treatment, patterns are changing. The Global Registry on Long-Term Oral Antithrombotic Treatment in Patients with Atrial Fibrillation is designed to investigate patient characteristics influencing choice of antithrombotic treatment of stroke prevention in patients with nonvalvular AF and to collect data on outcomes of antithrombotic therapy in clinical practice. Methods The GLORIA-AF is a large, international, observational registry involving patients with newly diagnosed nonvalvular AF at risk for stroke, enrolling up to 56,000 patients in nearly 50 countries. We will collect and analyze data from routine care using an inception cohort design. Phase I includes patients before approval of NOACs. Phase II, beginning early after approval of dabigatran, monitors dabigatran safety and addresses potential channeling across treatment options based on propensity scoring to assess comparability of baseline characteristics of patients treated with dabigatran or VKA. Phase III entails analysis of large treatment groups, adjusting for differences in propensity score, to provide information about the relative effectiveness and safety of NOACs and VKA in routine clinical care. Conclusions Novel features of this registry program will add data from clinical practice to those from randomized trials to expand knowledge of antithrombotic treatment in patients with AF.
机译:背景心房颤动(AF)是最常见的心律不齐,影响1%至2%的人群,并使中风的风险增加5倍。直到最近,用于房颤患者中风预防的唯一治疗选择是维生素K拮抗剂(VKA)或抗血小板药物。随着新型口服抗凝剂(NOAC)抗血栓治疗的批准,模式正在改变。心房纤颤患者长期口服抗血栓治疗全球注册表旨在调查影响非瓣膜性AF患者中风预防的抗血栓治疗选择的患者特征,并在临床实践中收集抗血栓治疗结果的数据。方法GLORIA-AF是一个大型的国际性观察性注册机构,涉及新诊断为中风风险的非瓣膜性房颤患者,在近50个国家/地区招募了56,000名患者。我们将使用初始队列设计来收集和分析来自常规护理的数据。第一阶段包括未批准NOAC的患者。第二阶段从达比加群批准后开始,开始监测达比加群的安全性,并根据倾向评分评估达比加群或VKA治疗患者基线特征的可比性,探讨跨治疗方案的潜在渠道。第三阶段需要对大型治疗组进行分析,并调整倾向评分的差异,以提供有关NOAC和VKA在常规临床护理中的相对有效性和安全性的信息。结论该注册程序的新功能将把临床实践中的数据添加到随机试验中,以扩大房颤患者抗栓治疗的知识。

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