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阿哌沙班治疗来源不明的栓塞性卒中(ATTICUS 随机试验):原理和研究设计。

Apixaban for treatment of embolic stroke of undetermined source (ATTICUS randomized trial): Rationale and study design.

机构信息

1 Department of Cardiology, German Heart Competence Centre, Tübingen, Germany.

2 Department of Neurology and Stroke, Tübingen Center of Neurovascular Diseases, Tübingen, Germany.

出版信息

Int J Stroke. 2017 Dec;12(9):985-990. doi: 10.1177/1747493016681019. Epub 2016 Nov 23.

Abstract

Rationale Optimal secondary prevention of embolic stroke of undetermined source is not established. The current standard in these patients is acetylsalicylic acid, despite high prevalence of yet undetected paroxysmal atrial fibrillation. Aim The ATTICUS randomized trial is designed to determine whether the factor Xa inhibitor apixaban administered within 7 days after embolic stroke of undetermined source, is superior to acetylsalicylic acid for prevention of new ischemic lesions documented by brain magnetic resonance imaging within 12 months after index stroke. Design Prospective, randomized, blinded, parallel-group, open-label, German multicenter phase III trial in approximately 500 patients with embolic stroke of undetermined source. A key inclusion criterion is the presence or the planned implantation of an insertable cardiac monitor. Patients are 1:1 randomized to apixaban or acetylsalicylic acid and treated for a 12-month period. It is an event-driven trial aiming for core-lab adjudicated primary outcome events. Study outcomes The primary outcome is the occurrence of at least one new ischemic lesion identified by axial T2-weighted FLAIR magnetic resonance imaging and/or axial DWI magnetic resonance imaging at 12 months when compared with the baseline magnetic resonance imaging. Key secondary outcomes are the combination of recurrent ischemic strokes, hemorrhagic strokes, systemic embolism; combination of MACE including recurrent stroke, myocardial infarction, and cardiovascular death and combination of major and clinically relevant non-major bleeding defined according to ISTH, and change of cognitive function and quality of life (EQ-5D, Stroke Impact Scale). Discussion Embolic stroke of undetermined source is caused by embolic disease and associated with a high risk of recurrent ischemic strokes and clinically silent cerebral ischemic lesions. ATTICUS will investigate the impact of atrial fibrillation detected by insertable cardiac monitor and the effects of early anticoagulation with apixaban compared with antiplatelet therapy with acetylsalicylic acid on the incidence of new ischemic lesion after embolic stroke of undetermined source.

摘要

背景

不明来源栓塞性卒中的最佳二级预防措施尚未确定。目前这些患者的标准治疗方法是使用乙酰水杨酸,尽管阵发性心房颤动尚未被检测到的情况很常见。

目的

ATTICUS 随机试验旨在确定在不明来源栓塞性卒中发生后 7 天内使用因子 Xa 抑制剂阿哌沙班与乙酰水杨酸相比,是否能更有效地预防索引性卒中后 12 个月内通过脑磁共振成像(MRI)记录的新缺血性病变。

设计

这是一项在大约 500 例不明来源栓塞性卒中患者中进行的前瞻性、随机、双盲、平行组、开放性标签、德国多中心 III 期试验。主要纳入标准是存在或计划植入可植入式心脏监测仪。患者以 1:1 的比例随机分为阿哌沙班组和乙酰水杨酸组,并接受为期 12 个月的治疗。这是一项事件驱动的试验,旨在确定经核心实验室裁定的主要结局事件。

研究结果

主要结局是与基线 MRI 相比,12 个月时通过轴向 T2 加权 FLAIR MRI 和/或轴向 DWI MRI 确定至少存在一处新的缺血性病变。次要结局主要包括复发性缺血性卒中和出血性卒中和系统性栓塞的复合终点;包括复发性卒中和心血管死亡的 MACE 复合终点以及根据 ISTH 定义的主要和临床相关非主要出血的复合终点,以及认知功能和生活质量(EQ-5D、卒中影响量表)的变化。

讨论

不明来源的栓塞性卒中由栓塞性疾病引起,与复发性缺血性卒中和临床上无症状的脑缺血性病变的风险增加相关。ATTICUS 将研究通过可植入式心脏监测仪发现的心房颤动以及与抗血小板治疗乙酰水杨酸相比,早期抗凝治疗阿哌沙班对不明来源栓塞性卒中后新缺血性病变的发生率的影响。

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