Erythropoietin improves long-term neurological outcome in acute ischemic stroke patients: a randomized, prospective, placebo-controlled clinical trial.
Author
Tsai, T-H
Lu, C-H
Wallace, Christopher G
Chang, W-N
Chen, S-F
Huang, C-R
Tsai, N-W
Lan, M-Y
Sung, P-H
Liu, C-F
Yip, H-K
Date
2015-02-25Journal
Critical care (London, England)Type
Journal ArticleRandomized Controlled Trial
Research Support, Non-U.S. Gov't
Publisher
BioMed CentralDOI
10.1186/s13054-015-0761-8Rights
Archived with thanks to Critical care (London, England). This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.Metadata
Show full item recordAbstract
Mortality and disability following ischemic stroke (IS) remains unacceptably high with respect to the conventional therapies. This study tested the effect of erythropoietin (EPO) on long-term neurological outcome in patients after acute IS. This study aimed to evaluate the safety and efficacy of two consecutive doses of EPO (5,000 IU/dose, subcutaneously administered at 48 hours and 72 hours after acute IS) on improving the 90-day combined endpoint of recurrent stroke or death that has been previously reported. A secondary objective was to evaluate the long-term (that is, five years) outcome of patients who received EPO.