缺血性卒中患者的回顾性分析支持静脉注射阿替普酶后24小时内的早期动员是安全的,可能是有益的。

Lisa Yanase, Diane Clark, Elizabeth Baraban, Tamela Stuchiner
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引用次数: 0

摘要

摘要:背景:脑卒中护理指南建议急性缺血性脑卒中患者早期动员,但关于接受溶栓治疗的脑卒中患者的早期动员的数据很少。我们开发了普罗维登斯中风早期流动性(PEMS)方案,以在2010年中风入院后24小时内动员患者达到最高的个体耐受性,该方案已在我们的初级和综合中风中心持续使用了十多年。在这项研究中,我们评估了所有接受静脉注射阿替普酶治疗但未接受血管内治疗的患者的PEMS方案。方法:本回顾性研究包括318名接受阿替普酶治疗的急性缺血性卒中患者,他们于2013年1月至2017年12月入住2个城市卒中中心,并在接受阿替普酶治疗后24小时内通过PEMS方案动员。PEMS的安全性通过美国国立卫生研究院卒中量表在首次动员时24小时的变化进行评估。使用多变量和逻辑回归模型,我们分析了首次动员时间和90天修正的Rankin量表(mRS)。结果:首次动员的中位时间为阿替普酶给药后9小时。动员每延迟一小时,90天轻度或中度残疾(mRS,2-3)的几率增加7%(调整后的比值比,1.07;P=.004),90天重度残疾或死亡(mRS,4-6)的几率提高7%(调整的比值比:1.07;P=0.02)。此外,动员每延迟1小时,美国国立卫生研究院24小时卒中量表增加了1.8%。讨论:我们的结果支持PEMS方案对静脉注射阿替普酶治疗的急性缺血性卒中患者是安全的,可能是有益的。我们的协议与其他早期的移动协议不同,因为它没有规定活动的“剂量”。相反,只要安全,每个患者都会被动员到他/她的个人最高程度。
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A Retrospective Analysis of Ischemic Stroke Patients Supports That Very Early Mobilization Within 24 Hours After Intravenous Alteplase Is Safe and Possibly Beneficial.

Abstract: BACKGROUND: Stroke care guidelines recommend early mobilization of acute ischemic stroke patients, but there are sparse data regarding early mobilization of stroke patients receiving thrombolytic therapy. We developed the Providence Early Mobility for Stroke (PEMS) protocol to mobilize patients to their highest individual tolerance within 24 hours of stroke admission in 2010, and it has been in continuous use at our primary and comprehensive stroke centers for over a decade. In this study, we evaluated the PEMS protocol in all patients treated with intravenous alteplase without endovascular treatment. METHODS : This retrospective study includes 318 acute ischemic stroke patients treated with alteplase who were admitted to 2 urban stroke centers between January 2013 and December of 2017 and were mobilized with the PEMS protocol within 24 hours of receiving alteplase. Safety of PEMS was assessed by change in National Institutes of Health Stroke Scale at 24 hours by time first mobilized. Using multivariate and logistic regression models, we analyzed time first mobilized and 90-day modified Rankin scale (mRS). RESULTS : Median time first mobilized was 9 hours from administration of alteplase. For every hour delay in mobilization, the odds of being slightly or moderately disabled (mRS, 2-3) at 90 days increased by 7% (adjusted odds ratio, 1.07; P = .004), and the odds of being severely disabled or dead (mRS, 4-6) at 90 days increased by 7% (adjusted odds ratio, 1.07; P = .02). In addition, for every hour delay in mobilization, 24-hour National Institutes of Health Stroke Scale increased by 1.8%. DISCUSSION: Our results support that the PEMS protocol is safe, and possibly beneficial, for acute ischemic stroke patients treated with intravenous alteplase. Our protocol differs from other very early mobility protocols because it does not prescribe a "dose" of activity. Instead, each patient was mobilized to his/her individual highest degree as soon as it was safe to do so.

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