Department of Neurosurgery, School of Medicine and Biomedical Sciences, University at Buffalo, State University of New York, Buffalo, New York 14209, USA.
J Neurosurg. 2011 Apr;114(4):1008-13. doi: 10.3171/2010.8.JNS10318. Epub 2010 Sep 24.
Experience with the use of platelet glycoprotein (GP) IIb-IIIa inhibitor eptifibatide in patients with ischemic stroke is limited. The authors report the off-label use of intraarterial eptifibatide during endovascular ischemic stroke revascularization procedures for reocclusion after documented recanalization or formed fresh thrombi in distal vessels that were inaccessible to endovascular devices.
Patients who received intraarterial eptifibatide were identified from a prospectively collected database of patients in whom endovascular revascularization for acute ischemic stroke was attempted between 2005 and 2008. Data were analyzed retrospectively. The intraarterial eptifibatide dose was a single-bolus dose of 180 μg/kg body weight. Primary outcome measures were angiographic recanalization (Thrombolysis in Myocardial Infarction Grade 2 or 3), symptomatic intracranial hemorrhage rate, overall mortality rate, and favorable 3-month modified Rankin Scale score (≤ 2).
The study included 35 patients (mean age 62 years, range 18-85 years). The median presenting National Institutes of Health Stroke Scale score was 13. Two patients received intravenous tissue plasminogen activator before endovascular therapy. The median time from symptom onset to therapy initiation was 230 minutes (range 90-1370 minutes). Twelve patients (34%) received intraarterial tissue plasminogen activator without mechanical measures. Mechanical revascularization measures used were Merci retriever in 19 (54%), Penumbra device in 1 (3%), balloon angioplasty in 15 (43%), and stent placement in 22 (63%) patients. The mean dose of intraarterial eptifibatide was 11.6 mg (range 5-16.6 mg). Partial-to-complete recanalization (Thrombolysis in Myocardial Infarction Grade 2 or 3) was achieved in 27 patients (77%). Postprocedure intracranial hemorrhage occurred in 13 patients (37%), causing symptoms in 5 (14%). In the 5 symptomatic intracranial hemorrhage cases, all patients but one presented more than 8 hours after symptom onset and all received intraarterial recombinant tissue plasminogen activator. The median discharge National Institutes of Health Stroke Scale score was 7 (range 0-17). At 3 months postprocedure, 21 patients (60%) had a modified Rankin Scale score ≤ 2, and 8 patients (23%) had died.
Adjunctive intraarterial eptifibatide is a feasible option for salvage of reocclusion and thrombolysis of distal inaccessible thrombi during endovascular stroke revascularization. Its safety and efficacy need to be studied further in larger, multicenter, controlled studies.
在缺血性脑卒中患者中使用血小板糖蛋白(GP)IIb-IIIa 抑制剂依替巴肽的经验有限。作者报告了在血管内缺血性脑卒中再通后或远端血管内无法使用血管内装置的新形成的新鲜血栓形成的情况下,经血管内再通过程中使用动脉内依替巴肽的经验,这些患者的再闭塞。
从 2005 年至 2008 年间尝试进行急性缺血性脑卒中血管内再通的患者前瞻性收集的数据库中确定接受动脉内依替巴肽的患者。数据进行回顾性分析。动脉内依替巴肽的剂量为 180μg/kg 体重的单次推注剂量。主要终点为血管造影再通(血栓溶解心肌梗死分级 2 或 3)、症状性颅内出血率、总死亡率和 3 个月时改良 Rankin 量表评分(≤2)。
该研究纳入了 35 例患者(平均年龄 62 岁,范围 18-85 岁)。发病 NIHSS 评分中位数为 13 分。2 例患者在血管内治疗前接受了静脉注射组织型纤溶酶原激活剂。从症状发作到开始治疗的中位时间为 230 分钟(范围 90-1370 分钟)。12 例患者(34%)接受了单纯动脉内组织型纤溶酶原激活剂治疗而未采用机械措施。机械再通措施分别为 Merci 取栓器 19 例(54%)、Penumbra 装置 1 例(3%)、球囊血管成形术 15 例(43%)和支架置入术 22 例(63%)。动脉内依替巴肽的平均剂量为 11.6mg(范围 5-16.6mg)。27 例患者(77%)达到了部分至完全再通(血栓溶解心肌梗死分级 2 或 3)。13 例患者(37%)发生了术后颅内出血,其中 5 例(14%)有症状。在 5 例有症状的颅内出血病例中,所有患者均在症状发作后 8 小时以上出现,且均接受了动脉内重组组织型纤溶酶原激活剂治疗。出院时 NIHSS 评分中位数为 7 分(范围 0-17 分)。术后 3 个月,21 例患者(60%)改良 Rankin 量表评分≤2,8 例患者(23%)死亡。
在血管内脑卒中再通过程中,辅助性动脉内依替巴肽是挽救再闭塞和溶栓治疗远端无法到达的血栓的可行选择。其安全性和有效性需要在更大的多中心对照研究中进一步研究。