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急性缺血性卒中使用组织型纤溶酶原激活剂的法医学问题。

Medico-legal aspects of using tissue plasminogen activator in acute ischemic stroke.

作者信息

Bruce Nhu T, Neil William P, Zivin Justin A

机构信息

San Diego VA Healthcare System, Neurology Service (127), 3350 La Jolla Village Drive, San Diego, CA, 92161, USA.

出版信息

Curr Treat Options Cardiovasc Med. 2011 Jun;13(3):233-9. doi: 10.1007/s11936-011-0122-0.

DOI:10.1007/s11936-011-0122-0
PMID:21424751
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3085754/
Abstract

Intravenous alteplase or tissue plasminogen activator (tPA) has been the standard of care with proven efficacy for acute ischemic stroke for over a decade. Despite this, only a small fraction of potentially eligible stroke patients receive this medication. There seems to be a fear among practitioners of legal repercussions as a result of an increased risk of intracerebral hemorrhage due to tPA. This review of legal cases involving tPA will show that instead, physicians are often found liable as a result of not treating with tPA.

摘要

静脉注射阿替普酶或组织纤溶酶原激活剂(tPA)十多年来一直是急性缺血性卒中经证实有效的标准治疗方法。尽管如此,只有一小部分可能符合条件的卒中患者接受这种药物治疗。由于tPA导致脑出血风险增加,从业者似乎担心会有法律后果。对涉及tPA的法律案件的审查将表明,相反,医生往往因未使用tPA进行治疗而被认定有责任。

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Acad Emerg Med. 2012 Sep;19(9):E1027-34. doi: 10.1111/j.1553-2712.2012.01438.x.

本文引用的文献

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Time to treatment with intravenous alteplase and outcome in stroke: an updated pooled analysis of ECASS, ATLANTIS, NINDS, and EPITHET trials.静脉注射重组组织型纤溶酶原激活剂治疗时间与卒中转归:ECASS、ATLANTIS、NINDS 和 EPITHET 试验的更新汇总分析。
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