Šaňák Daniel, Jakubíček Stanislava, Černík David, Herzig Roman, Kunáš Zdeněk, Mikulík Robert, Ostrý Svatopluk, Reif Michal, Rohan Vladimír, Tomek Aleš, Veverka Tomáš
Comprehensive Stroke Center, Department of Neurology, Palacký University Medical School and Hospital, Olomouc, Czech Republic.
Department of Neurology, Masaryk University Faculty of Medicine and St. Anne's University Hospital, Brno, Czech Republic.
J Stroke Cerebrovasc Dis. 2018 Sep;27(9):2479-2483. doi: 10.1016/j.jstrokecerebrovasdis.2018.05.004. Epub 2018 May 25.
Intravenous thrombolysis (IVT) is contraindicated in patients with acute ischemic stroke (AIS) using oral anticoagulants. A specific human monoclonal antibody was introduced to reverse immediately the anticoagulation effect of the direct inhibitor of thrombin, dabigatran. Until now, mostly individual cases presenting with successful IVT after a reversal of dabigatran anticoagulation in patients with AIS were published. Thus, we aimed to report real-world data from clinical practice.
Patients with AIS on dabigatran treated with IVT after antidote reversal were enrolled in the retrospective nationwide study. Neurological deficit was scored using the National Institutes of Health Stroke Scale (NIHSS) and 90-day clinical outcome using modified Rankin scale (mRS) with a score 0-2 for a good outcome. Intracerebral hemorrhage (ICH) was defined as a presence of any sign of bleeding on control imaging after IVT, and symptomatic intracerebral hemorrhage (SICH) was assessed according to the Safe Implementation of Thrombolysis in Stroke-Monitoring Study (SITS-MOST) criteria.
In total, 13 patients (7 men, mean age 70.0 ± 9.1 years) with a median NIHSS admission score of 7 points were analyzed. Of these patients, 61.5% used 2 × 150 mg of dabigatran daily. Antidote was administrated 427 ± 235 minutes after the last intake of dabigatran, with a mean activated prothrombin time of 38.1 ± 27.8 seconds and a mean thrombin time of 72.2 ± 56.1 seconds. Of the 13 patients, 2 had ICH and 1 had SICH, and no other bleeding complications were observed after IVT. Of the total number of patients, 76.9% had a good 3-month clinical outcome and 3 patients (23.1%) died. Recurrent ischemic stroke occurred in 2 patients (15.4%).
The data presented in the study support the safety and efficacy of IVT after the reversal of the anticoagulation effect of dabigatran with antidote in a real-world clinical practice.
对于正在使用口服抗凝剂的急性缺血性卒中(AIS)患者,静脉溶栓(IVT)是禁忌的。一种特异性人单克隆抗体被用于立即逆转凝血酶直接抑制剂达比加群的抗凝作用。到目前为止,大多是关于AIS患者达比加群抗凝作用逆转后成功进行IVT的个别病例报道。因此,我们旨在报告来自临床实践的真实世界数据。
在这项全国性回顾性研究中,纳入了接受解毒剂逆转后接受IVT治疗的服用达比加群的AIS患者。使用美国国立卫生研究院卒中量表(NIHSS)对神经功能缺损进行评分,使用改良Rankin量表(mRS)对90天临床结局进行评分,mRS评分为0 - 2分表示预后良好。颅内出血(ICH)定义为IVT后对照影像学上出现任何出血迹象,症状性颅内出血(SICH)根据卒中溶栓安全实施监测研究(SITS - MOST)标准进行评估。
总共分析了13例患者(7例男性,平均年龄70.0 ± 9.1岁),入院时NIHSS评分中位数为7分。在这些患者中,61.5%的患者每天服用2×150mg达比加群。在最后一次服用达比加群后427 ± 235分钟给予解毒剂,活化部分凝血活酶时间平均为38.1 ± 27.8秒,凝血酶时间平均为72.2 ± 56.1秒。13例患者中,2例发生ICH,1例发生SICH,IVT后未观察到其他出血并发症。在所有患者中,76.9%的患者3个月临床结局良好,3例患者(23.1%)死亡。2例患者(15.4%)发生了缺血性卒中复发。
该研究中呈现的数据支持在真实世界临床实践中,使用解毒剂逆转达比加群抗凝作用后进行IVT的安全性和有效性。