脑溶素在预防急性缺血性脑卒中后出血性转化中的可能作用

N. Elsaid, A. Saied
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摘要

出血性转化(HT)是急性缺血性中风(AIS)治疗中最令人担忧的挑战之一,它影响治疗计划和临床预后。HT的风险不是单一的,几乎不可能定义一个单一的预防HT的靶点。因此,我们认为有必要研究和回顾脑溶素作为一种多模式、多效性神经保护和神经营养剂在预防HT中的可能作用。脑溶素一直是多种动物和体外研究的主题,其中大多数在多效性和多模式神经保护和神经恢复活性方面产生了令人鼓舞的结果。脑溶素已在多项临床试验中进行了研究。在过去的10年里,在研究脑溶素在急性缺血性中风中的作用的研究中,有5项研究报告了出血转化的程度作为结果的一部分。在所有研究中,脑活素治疗患者的HT发生率均低于对照组。因此,报告的结果在所有研究中都是一致的,然而,除了一项研究外,差异没有达到统计学显著性的水平。对这些结果的解释受到几个因素的限制。尽管存在这些限制,但鉴于脑溶素在功能恢复方面的明显积极临床结果及其良好的安全性,可以给予30毫升/天的剂量,持续10-21天,以降低HT的风险。这一观察结果应通过进一步的HT定义标准化的大型随机对照临床试验来证实。
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The Possible Role of Cerebrolysin in Prevention of Hemorrhagic Transformation after Acute Ischemic Stroke
Hemorrhagic transformation (HT) is one of the most feared challenges in management of acute ischemic stroke (AIS) that affects both the treatment plan and the clinical prognosis.  The risk for HT is not monocausal and it is almost impossible to define a single target for prevention of HT. Thus, we consider that it is worthwhile to investigate and review the possible role of Cerebrolysin as a multimodal, pleiotropic neuroprotective and neurotrophic agent in the prevention of HT. Cerebrolysin has been the subject of multiple animal and in vitro studies, the majority of which have yielded encouraging results in terms of pleiotropic and multimodal neuroprotective and neurorestorative activity. Cerebrolysin has been investigated in multiple clinical trials. Over the past 10 years, among the studies investigating the effect of Cerebrolysin in acute ischemic stroke, 5 studies have reported the extent of hemorrhagic transformation as a part of the outcome. Lower HT rates were reported for Cerebrolysin treated patients versus controls across all studies. Thus, the reported results are consistent across all studies, however, the differences did not reach the level of statistical significance except for one study. The interpretation of these results is limited by several considerations. Despite these limitations, in the light of the clearly positive clinical results of Cerebrolysin on functional recovery and its favorable safety profile, a dose of 30 ml/day for 10-21 days may be given to reduce the risk of HT. This observation should be confirmed by further large randomized controlled clinical trials with standardization of the HT definition.
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