University Institute of Diagnostic and Interventional Neuroradiology, University Hospital Bern, Inselspital, University of Bern, Bern, Switzerland
University Institute of Diagnostic, Interventional and Pediatric Radiology, University Hospital Bern, Inselspital, University of Bern, Bern, Switzerland.
J Neurointerv Surg. 2021 Dec;13(12):1073-1080. doi: 10.1136/neurintsurg-2020-016680. Epub 2021 Jan 29.
Achieving the best possible reperfusion is a key determinant of clinical outcome after mechanical thrombectomy (MT). However, data on the safety and efficacy of intra-arterial (IA) fibrinolytics as an adjunct to MT with the intention to improve reperfusion are sparse.
We performed a PROSPERO-registered (CRD42020149124) systematic review and meta-analysis accessing MEDLINE, PubMed, and Embase from January 1, 2000 to January 1, 2020. A random-effect estimate (Mantel-Haenszel) was computed and summary OR with 95% CI were used as a measure of added IA fibrinolytics versus control on the risk of symptomatic intracranial hemorrhage (sICH) and secondary endpoints (modified Rankin Scale ≤2, mortality at 90 days).
The search identified six observational cohort studies and three observational datasets of MT randomized-controlled trial data reporting on IA fibrinolytics with MT as compared with MT alone, including 2797 patients (405 with additional IA fibrinolytics (100 urokinase (uPA), 305 tissue plasminogen activator (tPA)) and 2392 patients without IA fibrinolytics). Of 405 MT patients treated with additional IA fibrinolytics, 209 (51.6%) received prior intravenous tPA. We did not observe an increased risk of sICH after administration of IA fibrinolytics as adjunct to MT (OR 1.06, 95% CI 0.64 to 1.76), nor excess mortality (0.81, 95% CI 0.60 to 1.08). Although the mode of reporting was heterogeneous, some studies observed improved reperfusion after IA fibrinolytics.
The quality of evidence regarding peri-interventional administration of IA fibrinolytics in MT is low and limited to observational data. In highly selected patients, no increase in sICH was observed, but there is large uncertainty.
机械血栓切除术(MT)后,实现最佳再灌注是临床转归的关键决定因素。然而,关于动脉内(IA)纤溶酶原激活剂作为 MT 的辅助手段以改善再灌注的安全性和有效性的数据很少。
我们进行了一项 PROSPERO 注册(CRD42020149124)的系统评价和荟萃分析,检索了 2000 年 1 月 1 日至 2020 年 1 月 1 日的 MEDLINE、PubMed 和 Embase。采用随机效应估计(Mantel-Haenszel)计算,并使用汇总 OR 和 95%CI 作为衡量 IA 纤溶酶原激活剂与对照组相比增加 sICH 和次要终点(改良 Rankin 量表≤2、90 天死亡率)的风险。
检索确定了六项观察性队列研究和三项 MT 随机对照试验数据的观察性数据集,报告了 IA 纤溶酶原激活剂联合 MT 与单独 MT 相比的情况,共包括 2797 例患者(405 例接受额外的 IA 纤溶酶原激活剂治疗(100 例尿激酶(uPA),305 例组织型纤溶酶原激活剂(tPA))和 2392 例未接受 IA 纤溶酶原激活剂治疗的患者)。在接受额外 IA 纤溶酶原激活剂治疗的 405 例 MT 患者中,209 例(51.6%)接受了先前的静脉内 tPA 治疗。我们没有观察到在 MT 中联合使用 IA 纤溶酶原激活剂后 sICH 的风险增加(OR 1.06,95%CI 0.64 至 1.76),也没有观察到死亡率增加(0.81,95%CI 0.60 至 1.08)。尽管报告方式存在异质性,但一些研究观察到 IA 纤溶酶原激活剂后再灌注得到改善。
关于 MT 中经介入给予 IA 纤溶酶原激活剂的证据质量较低,仅限于观察性数据。在高度选择的患者中,未观察到 sICH 增加,但存在较大的不确定性。