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更快的急性缺血性脑卒中患者门到溶栓时间及相关结局

Even Faster Door-to-Alteplase Times and Associated Outcomes in Acute Ischemic Stroke.

机构信息

Emory Healthcare, Atlanta, Georgia.

Christiana Care Health System, Newark, Delaware.

出版信息

J Stroke Cerebrovasc Dis. 2019 Dec;28(12):104329. doi: 10.1016/j.jstrokecerebrovasdis.2019.104329. Epub 2019 Oct 10.

Abstract

BACKGROUND AND PURPOSE

The timely administration of thrombolytic therapy for acute ischemic stroke has been associated with good functional outcomes. Current guidelines recommend alteplase administration within 60 minutes in 75% of eligible patients and within 45 minutes in 50% of patients. There is limited evidence guiding these measures and their effect on outcomes. We report a single-center, retrospective assessment of the safety and efficacy of alteplase treatment within 45 minutes.

METHODS

Five hundred and eighty-six patients were treated with alteplase in our emergency departments (EDs) between January 2014 and October 2016; 368 patients were included for analysis. Multivariate regression analysis was used to assess the association between door-to-alteplase (DTA) times and 90-day modified Rankin scale (mRS) scores. Incidence of intracerebral hemorrhage (ICH) was also documented.

RESULTS

The median DTA time was 29 minutes versus 64 minutes in the DTA less than or equal to 45 minutes arm and more than 45 minutes arm, respectively. The primary outcome of 90-day mRS 0-1 was achieved in 56% of patients in the less than or equal to 45 minutes group versus 58% in more than 45 minutes group (P = .67). Odds of achieving mRS 0-1 were not significantly impacted by DTA times. In the multivariate regression analysis, patient characteristics associated with achieving mRS 0-1 were: younger age, male sex, not requiring intubation in the ED, and without prior history of hypertension, atrial fibrillation, or stroke. There was no significant difference in rates of ICH for patients less than or equal to 45 minutes versus more than 45 minutes.

CONCLUSIONS

Rapid administration of alteplase was not associated with significantly better outcomes nor increased risk of ICH. Conclusions about efficacy are limited due to the retrospective nature of the study, small sample size, and incomplete data points.

摘要

背景与目的

急性缺血性脑卒中患者及时接受溶栓治疗与良好的功能预后相关。目前的指南建议在 75%的适宜患者中在 60 分钟内给予阿替普酶,在 50%的患者中在 45 分钟内给予阿替普酶。目前仅有有限的证据指导这些措施及其对结局的影响。我们报告了一项单中心、回顾性评估阿替普酶在 45 分钟内治疗的安全性和疗效。

方法

2014 年 1 月至 2016 年 10 月期间,我们的急诊部有 586 例患者接受了阿替普酶治疗;其中 368 例患者被纳入分析。多变量回归分析用于评估门到阿替普酶(DTA)时间与 90 天改良 Rankin 量表(mRS)评分之间的关联。还记录了颅内出血(ICH)的发生率。

结果

中位数 DTA 时间为 29 分钟,DTA 小于或等于 45 分钟组与大于 45 分钟组分别为 64 分钟。DTA 小于或等于 45 分钟组的主要结局为 90 天 mRS 0-1 的患者占 56%,大于 45 分钟组为 58%(P=0.67)。DTA 时间对实现 mRS 0-1 的可能性没有显著影响。多变量回归分析显示,与实现 mRS 0-1 相关的患者特征为:年龄较小、男性、在急诊部无需插管、且无高血压、心房颤动或中风既往史。DTA 小于或等于 45 分钟组与大于 45 分钟组的 ICH 发生率无显著差异。

结论

快速给予阿替普酶与显著更好的结局或增加的 ICH 风险无关。由于研究的回顾性性质、样本量小和数据点不完整,关于疗效的结论是有限的。

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