Tireli Derya, He Jun, Nordling Mette Maria, Wienecke Troels
Neurovascular Center, Department of Neurology, Zealand University Hospital, Roskilde, Denmark.
Neurovascular Center, Department of Neurology, Zealand University Hospital, Roskilde, Denmark.
J Stroke Cerebrovasc Dis. 2017 Jul;26(7):e123-e125. doi: 10.1016/j.jstrokecerebrovasdis.2017.03.039. Epub 2017 May 4.
Idarucizumab is a reversal agent for dabigatran etexilate. By reversing the anticoagulating effect of dabigatran etexilate with idarucizumab (Praxbind), patients presenting with an acute ischemic stroke can now be eligible for thrombolysis.
We describe our experience with idarucizumab in a 71-year-old male patient pretreated with dabigatran etexilate. The patient arrived with a hemiparesis, central facial palsy, and dysarthria.
Dabigatran etexilate was antagonized with idarucizumab, approximately 2.5 hours after the patient's last dose. Immediately after the infusion of idarucizumab, the patient received thrombolytic therapy.
The hemiparesis and the central facial palsy were fully remitted 3 days after the onset of symptoms, and the dysarthria was remitted 2 days afterwards.
Non-vitamin K oral anticoagulants (NOACs) are widely used for the prevention of embolic stroke in patients with atrial fibrillation. Dabigatran etexilate is an oral thrombin inhibitor that can be reversed by idarucizumab. Idarucizumab, a monoclonal antibody fragment, directly binds dabigatran etexilate and neutralizes its activity.
Reversal of dabigatran etexilate using idarucizumab was safe and successful with no recombinant tissue plasminogen activator interactions.
依达赛珠单抗是达比加群酯的逆转剂。通过使用依达赛珠单抗(Praxbind)逆转达比加群酯的抗凝作用,急性缺血性卒中患者现在有资格接受溶栓治疗。
我们描述了依达赛珠单抗在一名接受达比加群酯预处理的71岁男性患者中的应用经验。该患者入院时出现偏瘫、中枢性面瘫和构音障碍。
在患者最后一次服药约2.5小时后,使用依达赛珠单抗拮抗达比加群酯。输注依达赛珠单抗后,患者立即接受溶栓治疗。
偏瘫和中枢性面瘫在症状出现后3天完全缓解,构音障碍在2天后缓解。
非维生素K口服抗凝剂(NOACs)广泛用于预防房颤患者的栓塞性卒中。达比加群酯是一种口服凝血酶抑制剂,可被依达赛珠单抗逆转。依达赛珠单抗是一种单克隆抗体片段,直接结合达比加群酯并中和其活性。
使用依达赛珠单抗逆转达比加群酯是安全且成功的,未出现与重组组织型纤溶酶原激活剂的相互作用。