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Safety of Dabigatran in Acute Ischemic Stroke Patients with Microbleeds: Post Hoc Analysis of DATAS-II Randomized Trial.

The Canadian journal of neurological sciences Le journal canadien des sciences neurologiques(2025)

University of South Wales | University of Pennsylvania

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Abstract
BACKGROUND:Cerebral microbleeds are associated with an increased risk of hemorrhagic transformation (HT) following acute ischemic stroke. We investigated whether the effect of dabigatran (vs. aspirin) in patients with acute minor non-cardioembolic ischemic stroke/transient ischemic attack (TIA) is modified by baseline microbleeds on MRI. METHODS:The Dabigatran Treatment of Acute Stroke II trial randomized 305 patients with acute minor non-cardioembolic ischemic stroke/TIA to dabigatran (150/110 mg twice daily) or aspirin (81 mg daily) for 30 days. Microbleeds were centrally adjudicated in patients with an interpretable blood-sensitive sequence on baseline MRI. In this post hoc analysis, we used multivariable regression models to determine the association between microbleeds and any incident HT on day-30 MRI and excellent functional outcome (modified Rankin scale = 0-1) at 90 days. RESULTS:A total of 251 (82.3%) participants (mean age = 66 ± 13 years, 36% women, median [IQR] onset-to-randomization time = 40[27-55] hours; median [IQR] NIHSS = 1 [0-2]) were included, of whom 82 (33%) had microbleeds. On day-30 MRI, 6% (n = 14) developed HT, and 80% (n = 191) achieved 90-day mRS of 0-1. We found no association between microbleed presence and HT (adjusted OR = 0.84; 95%CI:0.21-3.25) or excellent functional outcome (adjusted RR = 1.09; 95%CI:0.94-1.26). The rate of HT in patients with microbleeds was 3% with dabigatran and 4% with aspirin (OR = 0.85; 95%CI:0.11-6.75). Excellent functional outcome occurred in 74% and 84% of dabigatran and aspirin-treated patients, respectively (RR = 0.88; 95%CI:0.69-1.12). The presence, severity or location of microbleeds did not modify the effect of dabigatran on these outcomes (p-interaction > 0.05). CONCLUSIONS:Early dabigatran treatment appears safe in patients with acute minor non-cardioembolic ischemic stroke/TIA and hemorrhage-prone cerebral small vessel disease marked by microbleeds on MRI.
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要点】:本研究通过事后分析DATAS-II随机试验的数据,探讨了在急性缺血性脑卒中并伴有脑微出血的患者中使用达比加群(与阿司匹林相比)的安全性。

方法】:利用多变量回归模型确定微出血与第30天MRI上的任何新发出血转化及90天时功能良好结局(改良Rankin量表评分为0-1)之间的关联。

实验】:305例急性非心源性轻微缺血性脑卒中/短暂性脑缺血发作(TIA)的患者被随机分配到达比加群(150/110毫克,每日两次)或阿司匹林(81毫克,每日一次)治疗30天,其中251名患者(平均年龄66±13岁,女性占36%)的基线MRI上进行了微出血的判定,通过30天MRI和90天的功能结局评估达比加群的安全性。结果显示,微出血的存在与出血转化或良好功能结局无显著相关性,且微出血的存在、严重程度或位置并未改变达比加群对这些结局的影响。