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麻醉神经保护:历史渊源及临床前和临床数据质量评估

Anesthetic neuroprotection: antecedents and an appraisal of preclinical and clinical data quality.

作者信息

Ishida Kazuyoshi, Berger Miles, Nadler Jacob, Warner David S

机构信息

Department of Anesthesiology, Box 3094, Duke University Medical Center, Durham, North Carolina 27710, USA.

出版信息

Curr Pharm Des. 2014;20(36):5751-65. doi: 10.2174/1381612820666140204111701.

Abstract

Anesthetics have been studied for nearly fifty years as potential neuroprotective compounds in both perioperative and resuscitation medicine. Although anesthetics present pharmacologic properties consistent with preservation of brain viability in the context of an ischemic insult, no anesthetic has been proven efficacious for neuroprotection in humans. After such effort, it could be concluded that anesthetics are simply not neuroprotective in humans. Moreover, pharmacologic neuroprotection with non-anesthetic drugs has also repeatedly failed to be demonstrated in human acute brain injury. Recent focus has been on rectification of promising preclinical neuroprotection data and subsequent failed clinical trials. This has led to consensus guidelines for the process of transferring purported therapeutics from bench to bedside. In this review we first examined the history of anesthetic neuroprotection research. Then, a systematic review was performed to identify major clinical trials of anesthetic neuroprotection. Both the preclinical neuroprotection portfolio cited to justify a clinical trial and the design and conduct of that clinical trial were evaluated using modern standards that include the Stroke Therapy Academic Industry Roundtable (STAIR) and Consolidated Standards of Reporting Trials (CONSORT) guidelines. In publications intended to define anesthetic neuroprotection, we found overall poor quality of both preclinical efficacy analysis portfolios and clinical trial designs and conduct. Hence, using current translational research standards, it was not possible to conclude from existing data whether anesthetics ameliorate perioperative ischemic brain injury. Incorporation of advances in translational neuroprotection research conduct may provide a basis for more definitive and potentially successful clinical trials of anesthetics as neuroprotectants.

摘要

在围手术期医学和复苏医学中,麻醉剂作为潜在的神经保护化合物已被研究了近50年。尽管麻醉剂具有在缺血性损伤情况下与保护脑存活能力相一致的药理特性,但尚无麻醉剂被证实在人类中具有神经保护作用。经过如此多的努力,可以得出结论,麻醉剂在人类中根本没有神经保护作用。此外,非麻醉药物的药理神经保护作用在人类急性脑损伤中也多次未能得到证实。最近的重点是纠正有前景的临床前神经保护数据以及随后失败的临床试验。这导致了将所谓的治疗方法从实验室转化到临床应用过程的共识指南。在本综述中,我们首先研究了麻醉剂神经保护研究的历史。然后,进行了系统综述以确定麻醉剂神经保护的主要临床试验。使用包括中风治疗学术产业圆桌会议(STAIR)和报告试验综合标准(CONSORT)指南在内的现代标准,对为临床试验提供依据的临床前神经保护研究组合以及该临床试验的设计和实施进行了评估。在旨在定义麻醉剂神经保护作用的出版物中,我们发现临床前疗效分析组合以及临床试验设计和实施的整体质量都很差。因此,根据目前的转化研究标准,无法从现有数据得出麻醉剂是否能改善围手术期缺血性脑损伤的结论。纳入转化神经保护研究实施方面的进展可能为麻醉剂作为神经保护剂进行更明确且可能成功的临床试验提供基础。

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