From the Stroke Center and Department of Neurology, David Geffen School of Medicine at the University of California, Los Angeles (J.L.S.); Department of Neurology, University of Pittsburgh Medical Center Stroke Institute, PA (T.G.J.); Department of Neurology, University of California, San Francisco (W.S.S.); and Stroke Center and Department of Neurology, Stanford University School of Medicine, CA (G.W.A.).
Stroke. 2013 Dec;44(12):3596-601. doi: 10.1161/STROKEAHA.113.002769. Epub 2013 Nov 5.
The goal of the Stroke Treatment Academic Industry Roundtable (STAIR) meetings is to advance the development of stroke therapies. At STAIR VIII, consensus recommendations were developed for clinical trial strategies to demonstrate the benefit of endovascular reperfusion therapies for acute ischemic stroke.
Prospects for success with forthcoming endovascular trials are robust, because new neurothrombectomy devices have superior reperfusion efficacy compared with earlier-generation interventions. Specific recommendations are provided for trial designs in 3 populations: (1) patients undergoing intravenous fibrinolysis, (2) early patients ineligible for or having failed intravenous fibrinolysis, and (3) wake-up and other late-presenting patients. Among intravenous fibrinolysis-eligible patients, key principles are that CT or MRI confirmation of target arterial occlusions should precede randomization; endovascular intervention should be pursued with the greatest rapidity possible; and combined intravenous and neurothrombectomy therapy is more promising than neurothrombectomy alone. Among patients ineligible for or having failed intravenous fibrinolysis, scientific equipoise was affirmed and the need to randomize all eligible patients emphasized. Vessel imaging to confirm occlusion is mandatory, and infarct core and penumbral imaging is desirable in later time windows. Additional STAIR VIII recommendations include approaches to test multiple devices in a single trial, utility weighting of disability end points, and adaptive designs to delineate time and tissue injury thresholds at which benefits from intervention no longer accrue.
Endovascular research priorities in acute ischemic stroke are to perform trials testing new, highly effective neuro thrombectomy devices rapidly deployed in patients confirmed to have target vessel occlusions.
Stroke Treatment Academic Industry Roundtable(STAIR)会议的目标是推进中风治疗的发展。在第八届 STAIR 会议上,针对急性缺血性中风血管内再灌注治疗的临床试验策略制定了共识建议。
即将进行的血管内试验取得成功的前景非常乐观,因为新型神经血栓切除术设备与早期干预措施相比具有更好的再灌注效果。为 3 个人群的试验设计提供了具体建议:(1)接受静脉溶栓治疗的患者;(2)不符合静脉溶栓条件或静脉溶栓失败的早期患者;(3)觉醒和其他迟发患者。在符合静脉溶栓条件的患者中,关键原则是 CT 或 MRI 应在随机分组前确认目标动脉闭塞;应尽快进行血管内介入治疗;静脉溶栓联合神经血栓切除术治疗比单纯神经血栓切除术更有前景。对于不符合静脉溶栓条件或静脉溶栓失败的患者,确认了科学上的均势,并强调应随机分配所有符合条件的患者。血管成像以确认闭塞是强制性的,在较晚的时间窗内进行梗死核心和半影成像也是可取的。第八届 STAIR 的其他建议包括在单一试验中测试多种设备的方法、残疾终点的效用加权以及适应性设计,以确定干预不再获益的时间和组织损伤阈值。
急性缺血性中风的血管内研究重点是快速部署新型、高效的神经血栓切除术设备,对确认存在目标血管闭塞的患者进行临床试验。