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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

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机构: [1]Leiden Univ, Med Ctr, Dept Thrombosis & Hemostasis, NL-2333 ZA Leiden, Netherlands; [2]Univ Birmingham, City Hosp, Ctr Cardiovasc Sci, Birmingham, W Midlands, England; [3]Univ Hosp Essen, Dept Neurol, Essen, Germany; [4]Univ Hosp Essen, Stroke Ctr, Essen, Germany; [5]Clin & Maternidad Suizo Argentina, Arrhythmias & Electrophysiol Serv, Buenos Aires, DF, Argentina; [6]Mt Sinai Med Ctr, Cardiovasc Inst, New York, NY 10029 USA; [7]Beijing An Zhen Hosp, Atrial Fibrillat Ctr, Dept Cardiol, Beijing, Peoples R China; [8]Res Triangle Inst, RTI Hlth Solut, Res Triangle Pk, NC 27709 USA; [9]Boston Univ, Sch Publ Hlth, Dept Epidemiol, Boston, MA USA; [10]Boehringer Ingelheim GmbH & Co KG, TA Cardiovasc, Corporate Div Med, Ingelheim, Germany; [11]Boehringer Ingelheim GmbH & Co KG, Corporate Dept Global Epidemiol, Ingelheim, Germany; [12]Hannover Med Sch, Hannover, Germany; [13]Leiden Univ, Med Ctr, Dept Thrombosis & Hemostasis, Albinusdreef 2, NL-2333 ZA Leiden, Netherlands
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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.

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出版当年[2013]版:
大类 | 2 区 医学
小类 | 2 区 心脏和心血管系统
最新[2025]版:
大类 | 2 区 医学
小类 | 3 区 心脏和心血管系统
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出版当年[2012]版:
Q1 CARDIAC & CARDIOVASCULAR SYSTEMS
最新[2023]版:
Q1 CARDIAC & CARDIOVASCULAR SYSTEMS

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第一作者机构: [1]Leiden Univ, Med Ctr, Dept Thrombosis & Hemostasis, NL-2333 ZA Leiden, Netherlands;
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通讯机构: [1]Leiden Univ, Med Ctr, Dept Thrombosis & Hemostasis, NL-2333 ZA Leiden, Netherlands; [13]Leiden Univ, Med Ctr, Dept Thrombosis & Hemostasis, Albinusdreef 2, NL-2333 ZA Leiden, Netherlands
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