急性缺血性脑卒中的溶栓治疗

Abraham Akbar, Nicholas Peoples, Hangyu Xie, P. Sergot, Haitham M. Hussein, W. Peacock IV, Z. Rafique
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引用次数: 0

摘要

背景:组织型纤溶酶原激活剂(tPA)治疗急性缺血性脑卒中的疗效已得到证实,但极具时间依赖性。目前的指南建议睡眠时间为4.5小时。我们使用线性回归模型来量化因素影响,并比较tPA给药基准时间与目标基准时间(中位数+四分位数)。结果:71例缺血性脑卒中患者中,38例(54%)在≤60分钟内接受tPA治疗。女性患者从门到针的时间延迟为13.97分钟(95% CI 3.412 ~ 27.111)。与目标基准测试时间相比,中位数基准测试时间没有显示任何基准测试延迟的证据。结论:女性与从门到针的时间增加有关。对这些领域的进一步研究可以优化工作流程,减少从门到针的时间,并改善患者的治疗效果。
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Thrombolytic Administration for Acute Ischemic Stroke
Background: The therapeutic benefit of tissue plasminogen activator (tPA) for acute ischemic stroke is provenbut extremely time-dependent. Current guidelines recommend a <60 minute door-to-needle time. We identify here factors affecting door-to-needle time of tPA administration for acute ischemic stroke. Methods: We conducted a retrospective chart review of an emergency department from 2010 to 2013. Inclusion criteria were discharge diagnosis of acute ischemic stroke and tPA administration within 4.5 hours of onset. Exclusion criteria were non-ischemic strokes (transient ischemic attacks, subarachnoid hemorrhage, intracerebral hemorrhage) or those given tPA >4.5 hours. We used a linear regression model to quantify factor influence and compared tPA administration benchmark times to target benchmark times (median + quartiles). Results: Among the 71 ischemic stroke patients included, 38 (54%) received tPA within ≤ 60 minutes. Female sex was associated with a door-to-needle time delay of 13.97 minutes (95% CI 3.412 to 27.111). Median benchmark times did not show evidence of delay in any benchmark in comparison with target benchmark times. Conclusion: Female sex was associated with increased door-to-needle time. Further investigation of these areas may enable optimized workflow, decreased door-to-needle times, and improved patient outcomes.    
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12 weeks
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