1 Department of Neurology, Nordwestkrankenhaus Sanderbusch, Sande, Germany.
2 Medical Affairs Germany, Boehringer Ingelheim Pharma GmbH & Co KG, Ingelheim am Rhein, Germany.
Int J Stroke. 2017 Jun;12(4):383-391. doi: 10.1177/1747493017701944. Epub 2017 Mar 24.
Background Idarucizumab is a monoclonal antibody fragment with high affinity for dabigatran that reverses its anticoagulant effects within minutes. It may exhibit the potential for patients under dabigatran therapy suffering ischemic stroke to regain eligibility for thrombolysis with rt-PA and may inhibit lesion growth in patients with intracerebral hemorrhage on dabigatran. Aims To provide insights into the clinical use of idarucizumab in patients under effective dabigatran anticoagulation presenting with signs of ischemic stroke or intracranial hemorrhage. Methods Retrospective data collected from German neurological/neurosurgical departments administering idarucizumab following product launch from January to August 2016 were used. Results Thirty-one patients presenting with signs of stroke received idarucizumab in 22 stroke centers. Nineteen patients treated with dabigatran presented with ischemic stroke and 12 patients suffered from intracranial bleeding. In patients receiving rt-PA thrombolysis following idarucizumab, 79% benefitted from i.v. thrombolysis with a median improvement of five points in NIHSS. No bleeding complications occurred. Hematoma growth was observed in 2 out of 12 patients with intracranial hemorrhage. The outcome was favorable with a median NIHSS improvement of 5.5 points and mRS 0-3 in 67%. Overall, mortality was low with 6.5% (one patient in each group). Conclusion Administration of rt-PA after reversing dabigatran activity with idarucizumab in case of ischemic stroke is feasible, easy to manage, effective, and appears to be safe. In dabigatran-associated intracranial hemorrhage, idarucizumab has the potential to prevent hematoma growth and improve outcome. Idarucizumab represents a new therapeutic option for patients under dabigatran treatment presenting with ischemic stroke or intracranial hemorrhage.
依达鲁单抗是一种对达比加群具有高亲和力的单克隆抗体片段,可在数分钟内逆转其抗凝作用。它可能为正在接受达比加群治疗的缺血性卒中患者恢复接受 rt-PA 溶栓的资格,并可能抑制正在接受达比加群治疗的脑出血患者的病灶生长。目的:提供达比加群抗凝有效患者出现缺血性卒中和/或颅内出血时使用依达鲁单抗的临床应用相关信息。方法:回顾性收集了德国神经科/神经外科部门自 2016 年 1 月至 8 月依达鲁单抗上市后使用该药的数据。结果:22 家卒中中心共 31 例有卒中表现的患者接受了依达鲁单抗治疗。19 例接受达比加群治疗的患者表现为缺血性卒中,12 例患者发生颅内出血。在接受依达鲁单抗治疗后接受 rt-PA 溶栓的患者中,79%接受静脉溶栓获益,NIHSS 中位数改善 5 分。未发生出血并发症。12 例颅内出血患者中观察到血肿增大。2 例患者的结局良好,NIHSS 中位数改善 5.5 分,mRS 0-3 占 67%。总体而言,死亡率较低,两组均为 6.5%(各 1 例)。结论:在缺血性卒中的情况下,用依达鲁单抗逆转达比加群的作用后使用 rt-PA 是可行的,易于管理,有效且似乎安全。在达比加群相关的颅内出血中,依达鲁单抗有潜力预防血肿增大并改善结局。依达鲁单抗为正在接受达比加群治疗的缺血性卒中和/或颅内出血患者提供了一种新的治疗选择。