From the Department of Neurosurgery (A.P.J.), Barrow Neurological Institute, Phoenix, AZ; HonorHealth Research Institute (S.M.D.), Scottsdale, AZ; and Cooper Neurologic Institute (T.G.J.), Camden, NJ.
Neurology. 2021 Nov 16;97(20 Suppl 2):S126-S136. doi: 10.1212/WNL.0000000000012801.
This article reviews recent breakthroughs in the treatment of acute ischemic stroke, mainly focusing on the evolution of endovascular thrombectomy, its impact on guidelines, and the need for and implications of next-generation randomized controlled trials.
Endovascular thrombectomy is a powerful tool to treat large vessel occlusion strokes and multiple trials over the past 5 years have established its safety and efficacy in the treatment of anterior circulation large vessel occlusion strokes up to 24 hours from stroke onset.
In 2015, multiple landmark trials (MR CLEAN, ESCAPE, SWIFT PRIME, REVASCAT, and EXTEND IA) established the superiority of endovascular thrombectomy over medical management for the treatment of anterior circulation large vessel occlusion strokes. Endovascular thrombectomy has a strong treatment effect with a number needed to treat ranging from 3 to 10. These trials selected patients based on occlusion location (proximal anterior occlusion: internal carotid or middle cerebral artery), time from stroke onset (early window: up to 6-12 hours), and acceptable infarct burden (Alberta Stroke Program Early CT Score [ASPECTS] ≥6 or infarct volume <50 mL). In 2017, the DAWN and DEFUSE-3 trials successfully extended the time window up to 24 hours in appropriately selected patients. Societal and national thrombectomy guidelines have incorporated these findings and offer Class 1A recommendation to a subset of well-selected patients. Thrombectomy ineligible stroke subpopulations are being studied in ongoing randomized controlled trials. These trials, built on encouraging data from pooled analysis of early trials (HERMES collaboration) and emerging retrospective data, are studying large vessel occlusion strokes with mild deficits (National Institutes of Health Stroke Scale <6) and large infarct burden (core volume >70 mL).
本文主要综述急性缺血性脑卒中治疗领域的最新进展,重点关注血管内取栓治疗的演变、对指南的影响,以及新一代随机对照试验的必要性和意义。
血管内取栓是治疗大血管闭塞性脑卒中的有力手段,过去 5 年的多项临床试验证实了血管内取栓在治疗发病 24 小时内的前循环大血管闭塞性脑卒中的安全性和有效性。
2015 年,多项里程碑式试验(MR CLEAN、ESCAPE、SWIFT PRIME、REVASCAT、EXTEND IA)证实血管内取栓治疗在前循环大血管闭塞性脑卒中治疗方面优于单纯药物治疗。血管内取栓治疗效果显著,其治疗效果数(NNT)为 3-10。这些试验根据闭塞部位(近端前循环:颈内动脉或大脑中动脉)、发病时间(早期窗口:6-12 小时)和可接受的梗死负担(Alberta 卒中项目早期 CT 评分[ASPECTS]≥6 或梗死体积<50 mL)选择患者。2017 年,DAWN 和 DEFUSE-3 试验成功地将时间窗扩展至适合的患者 24 小时内。社会和国家的取栓指南纳入了这些发现,并为部分精选患者提供了 1A 类推荐。正在进行的随机对照试验正在研究不适合取栓的卒中亚组。这些试验基于早期试验(HERMES 合作)汇总分析和新兴回顾性数据的令人鼓舞的结果,研究了轻度神经功能缺损(NIHSS<6)和大梗死负担(核心体积>70 mL)的大血管闭塞性脑卒中患者。