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静脉注射组织型纤溶酶原激活剂适用范围超出美国国立神经疾病与中风研究所及欧洲急性中风协作研究III标准。

Expansion of Intravenous Tissue Plasminogen Activator Eligibility Beyond National Institute of Neurological Disorders and Stroke and European Cooperative Acute Stroke Study III Criteria.

作者信息

Marchidann Adrian, Balucani Clotilde, Levine Steven R

机构信息

Department of Neurology, SUNY Downstate Medical Center & Stroke Center, 450 Clarkson Avenue, Brooklyn, NY 11203, USA; Department of Neurology, The Kings County Hospital Center, 451 Clarkson Avenue, Brooklyn, NY 11203, USA.

Department of Neurology, SUNY Downstate Medical Center & Stroke Center, 450 Clarkson Avenue, Brooklyn, NY 11203, USA.

出版信息

Neurol Clin. 2015 May;33(2):381-400. doi: 10.1016/j.ncl.2015.01.004. Epub 2015 Feb 28.

Abstract

Intravenous tPA is the standard treatment for acute ischemic stroke. Multiple contraindications for thrombolysis developed during the design of the clinical trials may be overly cautious and limit the number of patients who may be eligible and potentially benefit from treatment. As clinicians have become more comfortable with off-label use of tPA, new data on the safety of thrombolysis have become available and shaped the current guidelines. This article updates our knowledge on the evidence available for these contraindications to help guide the clinician in choosing the optimal approach to some of the most commonly encountered clinical scenarios.

摘要

静脉注射组织型纤溶酶原激活剂(tPA)是急性缺血性卒中的标准治疗方法。在临床试验设计过程中出现的多种溶栓禁忌症可能过于谨慎,限制了可能符合条件并有可能从治疗中获益的患者数量。随着临床医生对tPA的超说明书使用越来越得心应手,关于溶栓安全性的新数据已经出现并形成了当前的指南。本文更新了我们对这些禁忌症现有证据的认识,以帮助指导临床医生在一些最常见的临床场景中选择最佳治疗方法。

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