Mazumdar Avi, Derdeyn Colin P
Mallinckrodt Institute of Radiology, Washington University School of Medicine, St. Louis, MO 63110, USA.
Expert Opin Pharmacother. 2006 Feb;7(3):287-96. doi: 10.1517/14656566.7.3.287.
Ischaemic stroke is a leading cause of death and disability in the US. At present, intravenous administration of tissue plasminogen activator within 3 h of symptom onset is the only proven effective treatment for patients with acute ischaemic stroke. Unfortunately, most treated patients do not make a functional recovery and very few patients presenting with acute stroke qualify for intravenous tissue plasminogen activator therapy. The focus of current research is to extend the therapeutic window for intervention beyond 3 h, and to improve the outcome of treated patients. The purpose of the present paper is to describe the current state of affairs for intravenous plasminogen activators, and to review recently published research. Agents and strategies under investigation include the intra-arterial delivery of plasminogen activators or antiplatelet agents, as well as combined intravenous/intra-arterial protocols.
缺血性中风是美国死亡和残疾的主要原因。目前,症状发作后3小时内静脉注射组织纤溶酶原激活剂是急性缺血性中风患者唯一经证实有效的治疗方法。不幸的是,大多数接受治疗的患者并未实现功能恢复,而且很少有急性中风患者符合静脉注射组织纤溶酶原激活剂治疗的条件。当前研究的重点是将干预的治疗窗口延长至3小时以上,并改善接受治疗患者的预后。本文的目的是描述静脉纤溶酶原激活剂的现状,并综述最近发表的研究。正在研究的药物和策略包括纤溶酶原激活剂或抗血小板药物的动脉内给药,以及静脉/动脉联合方案。