From the Division of Neurology, University of Alberta, Edmonton, Canada (K.S.B., A.C.K., B.B., L.S., M.S.).
Prince of Wales Clinical School, University of New South Wales, Sydney, Australia (K.S.B.).
Stroke. 2020 Apr;51(4):1190-1198. doi: 10.1161/STROKEAHA.119.027569. Epub 2020 Feb 26.
Background and Purpose- Patients with transient ischemic attack (TIA) and minor ischemic stroke are at risk for early recurrent cerebral ischemia. Anticoagulants are associated with reduced recurrence but also increased hemorrhagic transformation (HT). The safety of the novel oral anticoagulant dabigatran in acute stroke has not been evaluated. Methods- DATAS II (Dabigatran Treatment of Acute Stroke II) was a phase II prospective, randomized open label, blinded end point trial. Patients with noncardioembolic stroke/transient ischemic attack (National Institutes of Health Stroke Scale score, ≤9; infarct volume, ≤25 mL) were randomized to dabigatran or aspirin. Magnetic resonance imaging was performed before randomization and repeated at day 30. Imaging end points were ascertained centrally by readers blinded to treatment. The primary end point was symptomatic HT within 37 days of randomization. Results- A total of 305 patients, mean age 66.59±13.21 years, were randomized to dabigatran or aspirin a mean of 42.00±17.31 hours after symptom onset. The qualifying event was a transient ischemic attack in 21%, and ischemic stroke in 79% of patients. Median National Institutes of Health Stroke Scale (interquartile range) was 1 (0-2), and mean infarct volume 3.2±6.5 mL. No symptomatic HT occurred. Asymptomatic petechial HT developed in 11/142 (7.8%) of dabigatran-assigned patients and 5/142 (3.5%) of aspirin-assigned patients (relative risk, 2.301 [95% CI, 0.778-6.802]). Baseline infarct volume predicted incident HT (odds ratio, 1.07 [95% CI, 1.03-1.12]; =0.0026). Incident covert infarcts on day 30 imaging occurred in 9/142 (6.3%) of dabigatran-assigned and 14/142 (9.8%) of aspirin-assigned patients (relative risk, 0.62 [95% CI, 0.26, 1.48]). Conclusions- Dabigatran was associated with a risk of HT similar to aspirin in acute minor noncardioembolic ischemic stroke/transient ischemic attack. Registration- URL: https://www.clinicaltrials.gov; Unique identifier: NCT02295826.
背景与目的-短暂性脑缺血发作(TIA)和小面积缺血性脑卒中患者存在早期复发性脑缺血的风险。抗凝剂可降低复发率,但也会增加出血性转化(HT)。新型口服抗凝剂达比加群酯在急性脑卒中中的安全性尚未得到评估。方法-DATAS II(达比加群酯治疗急性脑卒中 II)是一项 II 期前瞻性、随机、开放标签、盲终点试验。非心源性卒中和 TIA 患者(美国国立卫生研究院卒中量表评分≤9 分;梗死体积≤25mL)被随机分为达比加群酯或阿司匹林组。在随机分组前进行磁共振成像检查,在第 30 天重复检查。由对治疗不知情的中心阅片者确定影像学终点。主要终点是随机分组后 37 天内出现症状性 HT。结果-共有 305 例患者,平均年龄 66.59±13.21 岁,在症状出现后平均 42.00±17.31 小时被随机分配至达比加群酯或阿司匹林组。有 21%的患者为 TIA,79%的患者为缺血性脑卒中。美国国立卫生研究院卒中量表评分中位数(四分位数间距)为 1(0-2),平均梗死体积为 3.2±6.5mL。未发生症状性 HT。达比加群酯组有 11/142(7.8%)例患者出现无症状性微出血性 HT,阿司匹林组有 5/142(3.5%)例患者出现无症状性 HT(相对风险,2.301[95%CI,0.778-6.802])。基线梗死体积预测 HT 事件(比值比,1.07[95%CI,1.03-1.12];=0.0026)。达比加群酯组有 9/142(6.3%)例患者和阿司匹林组有 14/142(9.8%)例患者在第 30 天的影像检查中出现隐匿性脑梗死(相对风险,0.62[95%CI,0.26,1.48])。结论-达比加群酯与阿司匹林治疗急性小面积非心源性缺血性卒中和 TIA 相关的 HT 风险相似。注册-网址:https://www.clinicaltrials.gov;唯一标识符:NCT02295826。