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急性缺血性卒中的溶栓和取栓治疗:优势与协同作用

Thrombolysis and Thrombectomy for Acute Ischemic Stroke: Strengths and Synergies.

作者信息

Campbell Bruce C V

机构信息

Department of Medicine and Neurology, Melbourne Brain Centre, The Royal Melbourne Hospital, University of Melbourne, Parkville, Victoria, Australia.

出版信息

Semin Thromb Hemost. 2017 Mar;43(2):185-190. doi: 10.1055/s-0036-1585078. Epub 2016 Jul 29.

Abstract

Acute ischemic stroke is responsible for around 80% of all strokes and is a leading cause of disability and death globally. There are two potential treatment strategies: restoring blood flow (reperfusion) and preventing cellular injury (neuroprotection). As yet, all the successful trials have involved reperfusion with numerous failures of neuroprotectants. There are two proven reperfusion strategies. Intravenous thrombolysis with alteplase was first demonstrated to reduce disability with publication of the National Institute of Neurological Disorders and Stroke tissue plasminogen activator trial in 1995. Since that time further trials have solidified the evidence base and demonstrated benefit when alteplase is administered within 4.5 hours of stroke onset. Exploration of potentially more effective thrombolytics is still underway with tenecteplase but others, such as desmoteplase, have been unsuccessful in clinical trials. The second proven reperfusion strategy is endovascular clot retrieval. This has been practiced for several years but came of age with the publication of five strongly positive trials in 2015. This review discusses the evidence for intravenous and intra-arterial reperfusion strategies and the advantages, disadvantages, and synergies of the two approaches.

摘要

急性缺血性中风约占所有中风的80%,是全球致残和死亡的主要原因。有两种潜在的治疗策略:恢复血流(再灌注)和防止细胞损伤(神经保护)。到目前为止,所有成功的试验都涉及再灌注,而神经保护剂大多失败。有两种已证实的再灌注策略。1995年,美国国立神经疾病和中风研究所组织型纤溶酶原激活剂试验结果公布,首次证明静脉注射阿替普酶进行溶栓可减少残疾。自那时以来,进一步的试验巩固了证据基础,并表明在中风发作后4.5小时内给予阿替普酶有益。对潜在更有效的溶栓剂的探索仍在进行中,替奈普酶正在进行试验,但其他药物,如去氨普酶,在临床试验中未获成功。第二种已证实的再灌注策略是血管内取栓。这种方法已经应用了数年,但在2015年发表的五项强有力的阳性试验后才走向成熟。本综述讨论了静脉和动脉再灌注策略的证据以及两种方法的优缺点和协同作用。

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