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急性缺血性中风患者的关键早期溶栓和血管内再灌注治疗:呼吁辅助神经保护。

Critical early thrombolytic and endovascular reperfusion therapy for acute ischemic stroke victims: a call for adjunct neuroprotection.

作者信息

Lapchak Paul A

机构信息

Department of Neurology & Neurosurgery, Cedars-Sinai Medical Center Advanced Healthcare Science Pavilion, 127 S. San Vicente Blvd., Suite 8305, Los Angeles, CA, 90048, USA,

出版信息

Transl Stroke Res. 2015 Oct;6(5):345-54. doi: 10.1007/s12975-015-0419-5. Epub 2015 Aug 29.

Abstract

Today, there is an enormous amount of excitement in the field of stroke victim care due to the recent success of MR. CLEAN, SWIFT PRIME, ESCAPE, EXTEND-IA, and REVASCAT endovascular trials. Successful intravenous (IV) recombinant tissue plasminogen activator (rt-PA) clinical trials [i.e., National Institute of Neurological Disorders and Stroke (NINDS) rt-PA trial, Third European Cooperative Acute Stroke Study (ECASSIII), and Third International Stroke study (IST-3)] also need to be emphasized. In the recent endovascular and thrombolytic trials, there is statistically significant improvement using both the National Institutes of Health Stroke Scale (NIHSS) and the modified Rankin Score (mRS) scale, but neither approach promotes complete recovery in patients enrolled within any particular NIHSS or mRS score tier. Absolute improvement (mRS 0-2 at 90 days) with endovascular therapy is 13.5-31 %, whereas thrombolytics alone also significantly improve patient functional independence, but to a lesser degree (NINDS rt-PA trial 13 %). This article has 3 main goals: (1) first to emphasize the utility and cost-effectiveness of rt-PA to treat stroke; (2) second to review the recent endovascular trials with respect to efficacy, safety, and cost-effectiveness as a stroke treatment; and (3) to further consider and evaluate strategies to develop novel neuroprotective drugs. A thesis will be put forth so that future stroke trials and therapy development can optimally promote recovery so that stroke victims can return to "normal" life.

摘要

如今,由于MR. CLEAN、SWIFT PRIME、ESCAPE、EXTEND - IA和REVASCAT血管内治疗试验最近取得的成功,中风患者护理领域出现了极大的兴奋之情。成功的静脉注射重组组织型纤溶酶原激活剂(rt - PA)临床试验[即美国国立神经疾病与中风研究所(NINDS)rt - PA试验、第三次欧洲急性中风协作研究(ECASSIII)以及第三次国际中风研究(IST - 3)]也需要被强调。在最近的血管内治疗和溶栓试验中,使用美国国立卫生研究院卒中量表(NIHSS)和改良Rankin量表(mRS)均有统计学上的显著改善,但两种方法都无法促使任何特定NIHSS或mRS评分层级内的患者完全康复。血管内治疗的绝对改善率(90天时mRS为0 - 2)为13.5% - 31%,而单纯溶栓也能显著提高患者的功能独立性,但程度较小(NINDS rt - PA试验为13%)。本文有3个主要目标:(1)首先强调rt - PA治疗中风的效用和成本效益;(2)其次回顾最近血管内治疗试验在作为中风治疗方法方面的疗效、安全性和成本效益;(3)进一步考虑和评估开发新型神经保护药物的策略。将提出一个论点,以便未来的中风试验和治疗开发能够最佳地促进康复,使中风患者能够回归“正常”生活。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/41f9/4568436/c58b5c54fe5e/nihms719374f1.jpg

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