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卒中治疗学术产业圆桌会议(STAIR)关于延长窗口期急性卒中治疗试验的建议。

Stroke Therapy Academic Industry Roundtable (STAIR) recommendations for extended window acute stroke therapy trials.

作者信息

Saver Jeffrey L, Albers Gregory W, Dunn Billy, Johnston Karen C, Fisher Marc

机构信息

Department of Neurology, Geffen School of Medicine, UCLA, Los Angeles, CA, USA.

出版信息

Stroke. 2009 Jul;40(7):2594-600. doi: 10.1161/STROKEAHA.109.552554. Epub 2009 May 28.

Abstract

The Stroke Therapy Academic Industry Roundtable (STAIR) meetings focus on helping to advance the development of acute stroke therapies. Further extending the time window for acute stroke therapies is an important endeavor for increasing the number of stroke patients who might benefit from treatment. The STAIR group recommends that future extended time window trials initially should focus on selected patient groups most likely to respond to investigational therapies and that penumbral imaging is one tool that may identify such patients. The control group in these trials should receive best locally available medical care; if regulatory approval for intravenous (i.v.) tPA is extended to 4.5 hours, then tPA will become the most appropriate comparator in trials conducted within this time window. In future well-designed extended window clinical trials randomization is appropriate and should not be precluded by using unproven treatment with intraarterial (i.a.) thrombolysis or mechanical devices. For proof of concept, extended time window, phase II trials of i.v. thrombolysis, or mechanical devices in which early recanalization/reperfusion is the primary end point, rescue therapy/bailout treatment with i.a. thrombolysis or devices may be acceptable. Statistical considerations and definitions of successful recanalization/reperfusion are suggested for these trials.

摘要

中风治疗学术产业圆桌会议(STAIR)聚焦于助力急性中风治疗的发展。进一步延长急性中风治疗的时间窗,对于增加可能从治疗中获益的中风患者数量而言是一项重要工作。STAIR小组建议,未来的延长时间窗试验最初应聚焦于最有可能对研究性治疗产生反应的特定患者群体,而半暗带成像则是一种可能识别此类患者的工具。这些试验中的对照组应接受当地可得的最佳医疗护理;如果静脉注射(i.v.)组织型纤溶酶原激活剂(tPA)的监管批准延长至4.5小时,那么tPA将成为在此时间窗内开展的试验中最合适的对照物。在未来设计良好的延长时间窗临床试验中,随机分组是合适的,不应因使用未经证实的动脉内(i.a.)溶栓或机械装置治疗而被排除。为了进行概念验证,对于以早期再通/再灌注为主要终点的静脉溶栓或机械装置的延长时间窗II期试验,采用动脉内溶栓或装置进行挽救治疗/补救治疗可能是可接受的。针对这些试验,提出了关于成功再通/再灌注的统计考量和定义。

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