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组织型纤溶酶原激活剂再灌注治疗缺血性卒中后的出血性转化:机制、模型与生物标志物

Hemorrhagic Transformation after Tissue Plasminogen Activator Reperfusion Therapy for Ischemic Stroke: Mechanisms, Models, and Biomarkers.

作者信息

Wang Wei, Li Mingchang, Chen Qianxue, Wang Jian

机构信息

Department of Neurosurgery, Renmin Hospital of Wuhan University, Wuhan, 430060, People's Republic of China.

Department of Anesthesiology and Critical Care Medicine, The Johns Hopkins University School of Medicine, 720 Rutland Ave, Ross Bldg 370B, Baltimore, MD, 21205, USA.

出版信息

Mol Neurobiol. 2015 Dec;52(3):1572-1579. doi: 10.1007/s12035-014-8952-x. Epub 2014 Nov 4.

Abstract

Intracerebral hemorrhagic transformation (HT) is well recognized as a common cause of hemorrhage in patients with ischemic stroke. HT after acute ischemic stroke contributes to early mortality and adversely affects functional recovery. The risk of HT is especially high when patients receive thrombolytic reperfusion therapy with tissue plasminogen activator, the only available treatment for ischemic stroke. Although many important publications address preclinical models of ischemic stroke, there are no current recommendations regarding the conduct of research aimed at understanding the mechanisms and prediction of HT. In this review, we discuss the underlying mechanisms for HT after ischemic stroke, provide an overview of the models commonly used for the study of HT, and discuss biomarkers that might be used for the early detection of this challenging clinical problem.

摘要

脑内出血转化(HT)是缺血性脑卒中患者出血的常见原因,这一点已得到广泛认可。急性缺血性脑卒中后的HT会导致早期死亡,并对功能恢复产生不利影响。当患者接受组织纤溶酶原激活剂溶栓再灌注治疗(缺血性脑卒中唯一可用的治疗方法)时,HT的风险尤其高。尽管许多重要出版物涉及缺血性脑卒中的临床前模型,但目前尚无关于旨在了解HT机制和预测的研究开展的建议。在本综述中,我们讨论了缺血性脑卒中后HT的潜在机制,概述了常用于研究HT的模型,并讨论了可能用于早期检测这一具有挑战性的临床问题的生物标志物。

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