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静脉注射重组组织型纤溶酶原激活剂治疗急性缺血性卒中的真实世界结局

Real-World Outcomes of Acute Ischemic Stroke Treatment with Intravenous Recombinant Tissue Plasminogen Activator.

作者信息

Betts Keith A, Hurley Dana, Song Jinlin, Sajeev Gautam, Guo Jenny, Du Ella Xiaoyan, Paschoalin Marco, Wu Eric Q

机构信息

Analysis Group, Inc., Los Angeles, California.

HUTH Global, LLC, Seattle, Washington.

出版信息

J Stroke Cerebrovasc Dis. 2017 Sep;26(9):1996-2003. doi: 10.1016/j.jstrokecerebrovasdis.2017.06.010. Epub 2017 Jul 6.

Abstract

BACKGROUND AND PURPOSE

In clinical trials, intravenous (IV) recombinant tissue-type plasminogen activator (rt-PA) reduces the likelihood of disability if given within 3 hours of acute ischemic stroke. This study compared real-world outcomes between patients treated and patients not treated with IV rt-PA.

METHODS

In this retrospective study, United States-based neurologists randomly selected eligible acute ischemic stroke patients from their charts who were and were not treated with IV rt-PA. Mortality, hospital readmission, and independence were compared between patients treated and patients not treated with IV rt-PA using Kaplan-Meier curves, log-rank tests, and Cox proportional hazards models.

RESULTS

A total of 1026 charts were reviewed with a median follow-up time of 15.5 months. Pretreatment stroke severity, as measured by the National Institutes of Health Stroke Scale, was comparable between cohorts (IV rt-PA =11.7; non-rt-PA = 11.3; P = .165). IV rt-PA patients experienced significantly longer survival (P = .013), delayed hospital readmission (P = .012), and shorter time to independence (P < .001) compared with patients not treated with rt-PA. After adjusting for baseline characteristics, IV rt-PA patients had significantly lower mortality (hazard ratio [95% confidence interval] = .52 [.30, .90]) and greater rates of independence (hazard ratio [95% confidence interval] = 1.42 [1.17, 1.71]) than patients not treated with rt-PA.

CONCLUSIONS

This real-world study indicated that acute ischemic stroke patients treated with IV rt-PA experience long-term clinical benefits in survival and functional status.

摘要

背景与目的

在临床试验中,静脉注射重组组织型纤溶酶原激活剂(rt-PA)若在急性缺血性卒中发作3小时内给药,可降低致残可能性。本研究比较了接受和未接受静脉rt-PA治疗的患者的实际治疗效果。

方法

在这项回顾性研究中,美国的神经科医生从其病历中随机选取符合条件的急性缺血性卒中患者,这些患者接受或未接受静脉rt-PA治疗。采用Kaplan-Meier曲线、对数秩检验和Cox比例风险模型,比较接受和未接受静脉rt-PA治疗的患者的死亡率、再次入院率和独立情况。

结果

共审查了1026份病历,中位随访时间为15.5个月。根据美国国立卫生研究院卒中量表测量,治疗前卒中严重程度在两组之间具有可比性(静脉rt-PA组=11.7;非rt-PA组=11.3;P=0.165)。与未接受rt-PA治疗的患者相比,静脉rt-PA治疗的患者生存时间显著更长(P=0.013),再次入院延迟(P=0.012),达到独立的时间更短(P<0.001)。在对基线特征进行调整后,与未接受rt-PA治疗的患者相比,静脉rt-PA治疗的患者死亡率显著更低(风险比[95%置信区间]=0.52[0.30,0.90]),独立率更高(风险比[95%置信区间]=1.42[1.17,1.71])。

结论

这项实际研究表明,接受静脉rt-PA治疗的急性缺血性卒中患者在生存和功能状态方面具有长期临床益处。

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