Department of Neurology, Neurosurgery and Radiology, University of Iowa Hospitals and Clinics, Iowa City, Iowa, USA.
Department of Neurology, University of Iowa Hospitals and Clinics, Iowa City, Iowa, USA.
Stroke Vasc Neurol. 2019 Feb 3;4(1):36-42. doi: 10.1136/svn-2018-000192. eCollection 2019 Mar.
Endovascular treatment of intracranial aneurysms usually involves stent-assisted coiling (SAC) and flow diverters. Glycoprotein IIb/IIIa inhibitors such as tirofiban and dual antiplatelet therapy (DAPT) are required to prevent thromboembolic complications afterwards. We sought to determine the safety of tirofiban and DAPT in these cases.
We conducted a retrospective analysis of our database for patients with intracranial aneurysms who underwent SAC or flow diversion. The tirofiban-DAPT protocol used is described. Data regarding duration of infusion, placement of external ventricular devices (EVDs), complications, haemoglobin levels and platelet count before and 24 hours after antiplatelet therapy were collected and analysed.
One-hundred and forty-one patients with 148 aneurysms/procedures were included. 110 aneurysms were treated acutely and 38 electively. Minor and major haemorrhagic events were recognised in 20% (30/148) aneurysms. Only 5 (3.4%) intracerebral haemorrhages were symptomatic: 3 cortical/SAH and 2 EVD-related. The average blood volume in symptomatic haemorrhages was 24.8 cc versus 5.42 cc in asymptomatic haemorrhages (p=0.002). The rate of EVD-related haemorrhages was 15.7% (19/121) and only 2 (1.7%) were symptomatic. Most haemorrhagic events occurred in ruptured aneurysms (90.1%, p=0.01). No significant change in platelet count or haemoglobin levels before and 24 hours after administration of tirofiban and DAPT was documented. Concomitant administration of heparin did not increase haemorrhagic events.
The use of the GP IIb/IIIa inhibitors tirofiban and DAPT in this series was safe. Tirofiban and DAPT did not affect platelet count or haemoglobin levels and did not increase rate of symptomatic haemorrhages or thromboembolic complications.
颅内动脉瘤的血管内治疗通常涉及支架辅助弹簧圈栓塞(SAC)和血流导向装置。需要使用糖蛋白 IIb/IIIa 抑制剂(如替罗非班)和双联抗血小板治疗(DAPT)来预防血栓栓塞并发症。我们旨在确定这些情况下替罗非班和 DAPT 的安全性。
我们对接受 SAC 或血流导向装置治疗的颅内动脉瘤患者的数据库进行了回顾性分析。描述了替罗非班-DAPT 方案。收集并分析了输注时间、外部脑室引流装置(EVD)放置、并发症、抗血小板治疗前后血红蛋白和血小板计数等数据。
共纳入 141 例患者的 148 个动脉瘤/手术。110 个动脉瘤为急性治疗,38 个为择期治疗。148 个动脉瘤中有 20%(30/148)出现轻微和严重出血事件。仅 5 例(3.4%)颅内出血有症状:3 例皮质/蛛网膜下腔出血,2 例与 EVD 相关。有症状出血的平均出血量为 24.8cc,无症状出血为 5.42cc(p=0.002)。EVD 相关出血的发生率为 15.7%(19/121),仅 2 例(1.7%)有症状。大多数出血事件发生在破裂动脉瘤中(90.1%,p=0.01)。替罗非班和 DAPT 给药前后血小板计数和血红蛋白水平无明显变化。同时使用肝素并未增加出血事件的发生。
本系列中使用糖蛋白 IIb/IIIa 抑制剂替罗非班和 DAPT 是安全的。替罗非班和 DAPT 不影响血小板计数或血红蛋白水平,也不会增加症状性出血或血栓栓塞并发症的发生率。