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日本利伐沙班治疗的房颤患者血栓栓塞和大出血事件的临床危险因素。

Clinical Risk Factors of Thromboembolic and Major Bleeding Events for Patients with Atrial Fibrillation Treated with Rivaroxaban in Japan.

机构信息

Department of Neurosurgery, Graduate School of Medicine, Kyoto University, Kyoto, Japan.

Department of Cardiovascular Medicine, Graduate School of Medicine, Toho University, Tokyo, Japan.

出版信息

J Stroke Cerebrovasc Dis. 2020 Apr;29(4):104584. doi: 10.1016/j.jstrokecerebrovasdis.2019.104584. Epub 2020 Jan 23.

Abstract

BACKGROUND

It is important to understand the risk of thromboembolism and bleeding in patients with nonvalvular atrial fibrillation (NVAF) receiving direct oral anticoagulants; however, data on risk factors in Japanese patients are limited.

METHODS

XAPASS (Xarelto Post-Authorization Safety and Effectiveness Study in Japanese Patients with Atrial Fibrillation) is a prospective observational study examining the safety and effectiveness of rivaroxaban in Japanese real-world clinical practice. We investigated risk factors for stroke/noncentral nervous system systemic embolism (non-CNS SE)/myocardial infarction (MI) and major bleeding using 1-year follow-up data. Associations between baseline characteristics and outcomes were examined by Cox regression analysis.

RESULTS

During April 2012-June 2014, 11,308 patients newly started with rivaroxaban treatment were enrolled. Of 9578 patients with 1-year data fixed as of September 2017, 6220 patients who received appropriate dosages of rivaroxaban for their creatinine clearance were included in the present safety outcomes subanalysis, and 6198 were included in the effectiveness outcomes analysis. Stroke/non-CNS SE/MI was observed in 97 of 6198 patients (1.6%, 1.8 events/100 patient-years), and major bleeding occurred in 102 of 6220 patients (1.6%, 1.9 events/100 patient-years). Age greater than or equal to 75 years (hazard ratio [HR]: 2.27; [95% confidence interval (CI): 1.49, 3.47]), prior ischemic stroke/transient ischemic attack (2.08; [1.38, 3.13]), and antiplatelet use (3.23; [1.83, 5.70]) were associated with stroke/non-CNS SE/MI. Creatinine clearance less than 50 mL/min (HR: 1.86; [95% CI: 1.26, 2.75]), diabetes (1.55; [1.02, 2.35]), and antiplatelet use (3.04; [1.70, 5.45]) were associated with major bleeding.

CONCLUSIONS

These results would help physicians to assess risks in Japanese patients with NVAF receiving rivaroxaban.

摘要

背景

了解非瓣膜性心房颤动(NVAF)患者接受直接口服抗凝剂治疗后的血栓栓塞和出血风险非常重要;然而,日本患者的相关数据有限。

方法

XAPASS(日本房颤患者利伐沙班上市后安全性和有效性研究)是一项前瞻性观察性研究,旨在评估日本真实世界临床实践中利伐沙班的安全性和有效性。我们使用 1 年随访数据,研究了卒中/非中枢神经系统系统性栓塞(非 CNS SE)/心肌梗死(MI)和大出血的风险因素。采用 Cox 回归分析评估基线特征与结局之间的相关性。

结果

2012 年 4 月至 2014 年 6 月,共有 11308 例患者开始接受利伐沙班治疗。截至 2017 年 9 月,9578 例患者中有 1 年数据固定,其中 6220 例患者接受了适当剂量的利伐沙班,用于其肌酐清除率,6198 例患者被纳入有效性结局分析。6198 例患者中,97 例(1.6%,100 患者年 1.8 事件)发生卒中/非 CNS SE/MI,102 例(1.6%,100 患者年 1.9 事件)发生大出血。年龄≥75 岁(风险比[HR]:2.27;[95%置信区间(CI):1.49,3.47])、既往缺血性卒中和短暂性脑缺血发作(2.08;[1.38,3.13])和抗血小板治疗(3.23;[1.83,5.70])与卒中/非 CNS SE/MI 相关。肌酐清除率<50 mL/min(HR:1.86;[95%CI:1.26,2.75])、糖尿病(1.55;[1.02,2.35])和抗血小板治疗(3.04;[1.70,5.45])与大出血相关。

结论

这些结果将帮助医生评估日本 NVAF 患者接受利伐沙班治疗的风险。

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