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J Stroke Cerebrovasc Dis · Sep 2017
Observational StudyReal-World Outcomes of Acute Ischemic Stroke Treatment with Intravenous Recombinant Tissue Plasminogen Activator.
- Keith A Betts, Dana Hurley, Jinlin Song, Gautam Sajeev, Jenny Guo, Ella Xiaoyan Du, Marco Paschoalin, and Eric Q Wu.
- Analysis Group, Inc., Los Angeles, California. Electronic address: Keith.Betts@analysisgroup.com.
- J Stroke Cerebrovasc Dis. 2017 Sep 1; 26 (9): 1996-2003.
Background And PurposeIn 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.MethodsIn 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.ResultsA 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.ConclusionsThis real-world study indicated that acute ischemic stroke patients treated with IV rt-PA experience long-term clinical benefits in survival and functional status.Copyright © 2017 The Authors. Published by Elsevier Inc. All rights reserved.
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