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Intravenous Thrombolysis for Acute Ischemic Stroke Within 3 Hours Versus Between 3 and 4.5 Hours of Symptom Onset

机译:静脉溶栓治疗3个月内急性缺血性中风与症状发作3到4.5小时之间

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摘要

Data from randomized clinical trials have supported the safety and efficacy of intravenous tissue-type plasminogen activator (IV tPA) for acute ischemic stroke when administered within 3 hours of symptom onset, and regulatory approvals for this indication have been in place for almost 20 years. However, recent clinical trials have provided evidence that IV tPA may be safe and effective in selected patients up to 4.5 hours after symptom onset, thereby increasing the proportion of patients that may be eligible for treatment. Although professional organizations in the United States and many regulatory agencies internationally have supported this expanded time window for IV tPA, the US Food and Drug Administration has declined to approve this expanded indication and so this use of IV tPA has remained off-labe! in the United States. Here we review the current evidence for IV tPA in the standard and the expanded time windows and the data on current clinical practice in the United States as it relates to IV tPA treatment for acute stroke within 3 to 4.5 hours of symptom onset.
机译:随机临床试验的数据支持在症状发作后3小时内给予静脉组织型纤溶酶原激活剂(IV tPA)治疗急性缺血性中风的安全性和有效性,该适应症的监管批准已有20年了。但是,最近的临床试验提供了证据,表明IV tPA对症状发作后4.5小时内的部分患者可能是安全有效的,从而增加了有资格接受治疗的患者比例。尽管美国的专业组织和国际上许多监管机构都支持延长IV tPA的使用期限,但美国食品药品监督管理局拒绝批准这一扩大的适应症,因此IV tPA的使用仍然不可行!在美国。在这里,我们回顾了标准时间和扩大的时间窗中有关静脉tPA的当前证据以及美国目前临床实践的数据,因为它与症状发作的3到4.5小时内对急性卒中的静脉tPA治疗有关。

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