Meyer Dawn, Chu Frank, Derry Katrina, Hailey Lovella
School of Medicine, University of California San Diego, Department of Neurosciences, United States.
UC San Diego Health, Pharmacy Department, United States.
J Clin Neurosci. 2019 Jan;59:355-357. doi: 10.1016/j.jocn.2018.09.027. Epub 2018 Oct 9.
Intravenous thrombolysis with recombinant tissue plasminogen activator (rt-PA) for acute ischemic stroke (AIS) is contraindicated in patient taking either Factor Xa inhibitors or direct thrombin inhibitors. Idarucizumab completely reverses the biologic effect of dabigatran within minutes. Intravenous rt-PA treatment results in a significant benefit in functional outcome when administered 3-4.5 h after stroke onset or last seen normal time. There is little reported data and no large-scale studies of the reversal of dabigatran with Idarucizumab for the purpose of treating AIS with IV rt-PA. We describe the case of a 73 year old male with AIS and active dabigatran use. Idarucizumab was administered per an approved medical center protocol and the patient was subsequently treated with IV rt-PA. The patient had a severe stroke with no other contraindications to IV rt-PA other than dabigatran use. The patient was administered Idarucizumab and IV rt-PA was given. Within 24 h of treatment, the patient had minimal stroke deficits. Imaging revealed a right middle cerebral artery patchy infarct. The patient was restarted on dabigatran therapy for his atrial fibrillation and was discharged to a skilled nursing facility for rehabilitation. The patient did not experience any symptomatic or asymptomatic intracranial hemorrhage after treatment or through day 90. Though no randomized evidence exists for the risk of IV rt-PA after dabigatran reversal with Idarucizumab, the case experiences are mounting. This case of successful stroke treatment after reversal adds to the anecdotal literature and supports the study of dabigatran reversal with Idarucizumab for thrombolysis in AIS.
正在服用Xa因子抑制剂或直接凝血酶抑制剂的患者,禁用重组组织型纤溶酶原激活剂(rt-PA)进行急性缺血性卒中(AIS)的静脉溶栓治疗。依达赛珠单抗可在数分钟内完全逆转达比加群的生物学效应。静脉注射rt-PA治疗在卒中发作后3 - 4.5小时或最后一次正常时间后给药,可显著改善功能预后。关于使用依达赛珠单抗逆转达比加群以进行静脉rt-PA治疗AIS,几乎没有报告的数据,也没有大规模研究。我们描述了一例73岁男性AIS患者且正在使用达比加群的病例。按照批准的医疗中心方案给予依达赛珠单抗,随后患者接受静脉rt-PA治疗。该患者患有严重卒中,除使用达比加群外,无其他静脉rt-PA治疗的禁忌证。给予患者依达赛珠单抗并静脉注射rt-PA。治疗后24小时内,患者的卒中缺陷最小。影像学显示右大脑中动脉斑片状梗死。患者因房颤重新开始使用达比加群治疗,随后出院至专业护理机构进行康复治疗。治疗后直至第90天,患者未出现任何有症状或无症状的颅内出血。尽管尚无关于依达赛珠单抗逆转达比加群后静脉rt-PA风险的随机证据,但病例经验正在增加。这例达比加群逆转后成功治疗卒中的病例补充了轶事文献,并支持对依达赛珠单抗逆转达比加群用于AIS溶栓的研究。