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Absolute and Relative Contraindications to IV rt-PA for Acute Ischemic Stroke

机译:急性缺血性卒中IV rt-PA的绝对禁忌症和相对禁忌症

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摘要

Most of the contraindications to the administration of intravenous (IV) recombinant tissue plasminogen activator (rtPA) originated as exclusion criteria in major stroke trials. These were derived from expert consensus for the National Institute of Neurological Disorders and Stroke (NINDS) trial. Despite the fact that the safety and efficacy of IV rtPA has been repeatedly confirmed in large international observational studies over the past 20 years, most patients with acute ischemic stroke disappointingly still do not receive thrombolytic treatment. Some of the original exclusion criteria have proven to be unnecessarily restrictive in real-world clinical practice. It has been suggested that application of relaxed exclusion criteria might increase the IV thrombolysis rate up to 20% with comparable outcomes to thrombolysis with more conventional criteria. We review the absolute and relative contraindications to IV rtPA for acute ischemic stroke, discussing the underlying rationale and evidence supporting these exclusion criteria.
机译:静脉注射(IV)重组组织纤溶酶原激活剂(rtPA)的大多数禁忌症是作为主要卒中试验中的排除标准提出的。这些来自国家神经疾病和中风研究所(NINDS)试验的专家共识。尽管在过去的20年中,大型国际观察研究已经反复证实IV rtPA的安全性和有效性,但令人失望的是,大多数患有急性缺血性中风的患者仍未接受溶栓治疗。一些原始的排除标准已被证明在现实世界的临床实践中是不必要的限制。有人提出,采用宽松的排除标准可以使静脉溶栓率提高至20%,其结果与常规溶栓方法相当。我们回顾了针对急性缺血性卒中的IV rtPA的绝对和相对禁忌症,讨论了支持这些排除标准的基本原理和证据。

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