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Erythropoietin improves long-term neurological outcome in acute ischemic stroke patients: a randomized, prospective, placebo-controlled clinical trial

INTRODUCTION: 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 e...

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Autores principales: Tsai, Tzu-Hsien, Lu, Cheng-Hsien, Wallace, Christopher Glenn, Chang, Wen-Neng, Chen, Shu-Feng, Huang, Chi-Ren, Tsai, Nai-Wen, Lan, Min-Yu, Sung, Pei-Hsun, Liu, Chu-Feng, Yip, Hon-Kan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4349661/
https://www.ncbi.nlm.nih.gov/pubmed/25888250
http://dx.doi.org/10.1186/s13054-015-0761-8
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author Tsai, Tzu-Hsien
Lu, Cheng-Hsien
Wallace, Christopher Glenn
Chang, Wen-Neng
Chen, Shu-Feng
Huang, Chi-Ren
Tsai, Nai-Wen
Lan, Min-Yu
Sung, Pei-Hsun
Liu, Chu-Feng
Yip, Hon-Kan
author_facet Tsai, Tzu-Hsien
Lu, Cheng-Hsien
Wallace, Christopher Glenn
Chang, Wen-Neng
Chen, Shu-Feng
Huang, Chi-Ren
Tsai, Nai-Wen
Lan, Min-Yu
Sung, Pei-Hsun
Liu, Chu-Feng
Yip, Hon-Kan
author_sort Tsai, Tzu-Hsien
collection PubMed
description INTRODUCTION: 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. METHODS: This was a prospective, randomized, placebo-controlled trial that was conducted between October 2008 and March 2010 in a tertiary referral center. IS stroke patients who were eligible for EPO therapy were enrolled into the study. RESULTS: The results showed that long-term recurrent stroke and mortality did not differ between group 1 (placebo-control; n = 71) and group 2 (EPO-treated; n = 71). Long-term Barthel index of <35 (defining a severe neurological deficit) was lower in group 2 than group 1 (P = 0.007). Multiple-stepwise logistic-regression analysis showed that EPO therapy was significantly and independently predictive of freedom from a Barthel index of <35 (P = 0.029). Long-term major adverse neurological event (MANE; defined as: death, recurrent stroke, or long-term Barthel index < 35) was lower in group 2 than group 1 (P = 0.04). Log-Rank test showed that MANE-free rate was higher in group 2 than group 1 (P = 0.031). Multiple-stepwise Cox-regression analysis showed that EPO therapy and higher Barthel Index at day 90 were independently predictive of freedom from long-term MANE (all P <0.04). CONCLUSION: EPO therapy significantly improved long-term neurological outcomes in patients after IS. TRIAL REGISTRATION: ISRCTN71371114. Registered 10 October 2008.
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spelling pubmed-43496612015-03-05 Erythropoietin improves long-term neurological outcome in acute ischemic stroke patients: a randomized, prospective, placebo-controlled clinical trial Tsai, Tzu-Hsien Lu, Cheng-Hsien Wallace, Christopher Glenn Chang, Wen-Neng Chen, Shu-Feng Huang, Chi-Ren Tsai, Nai-Wen Lan, Min-Yu Sung, Pei-Hsun Liu, Chu-Feng Yip, Hon-Kan Crit Care Research INTRODUCTION: 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. METHODS: This was a prospective, randomized, placebo-controlled trial that was conducted between October 2008 and March 2010 in a tertiary referral center. IS stroke patients who were eligible for EPO therapy were enrolled into the study. RESULTS: The results showed that long-term recurrent stroke and mortality did not differ between group 1 (placebo-control; n = 71) and group 2 (EPO-treated; n = 71). Long-term Barthel index of <35 (defining a severe neurological deficit) was lower in group 2 than group 1 (P = 0.007). Multiple-stepwise logistic-regression analysis showed that EPO therapy was significantly and independently predictive of freedom from a Barthel index of <35 (P = 0.029). Long-term major adverse neurological event (MANE; defined as: death, recurrent stroke, or long-term Barthel index < 35) was lower in group 2 than group 1 (P = 0.04). Log-Rank test showed that MANE-free rate was higher in group 2 than group 1 (P = 0.031). Multiple-stepwise Cox-regression analysis showed that EPO therapy and higher Barthel Index at day 90 were independently predictive of freedom from long-term MANE (all P <0.04). CONCLUSION: EPO therapy significantly improved long-term neurological outcomes in patients after IS. TRIAL REGISTRATION: ISRCTN71371114. Registered 10 October 2008. BioMed Central 2015-02-25 2015 /pmc/articles/PMC4349661/ /pubmed/25888250 http://dx.doi.org/10.1186/s13054-015-0761-8 Text en © Tsai et al.; licensee BioMed Central. 2015 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.
spellingShingle Research
Tsai, Tzu-Hsien
Lu, Cheng-Hsien
Wallace, Christopher Glenn
Chang, Wen-Neng
Chen, Shu-Feng
Huang, Chi-Ren
Tsai, Nai-Wen
Lan, Min-Yu
Sung, Pei-Hsun
Liu, Chu-Feng
Yip, Hon-Kan
Erythropoietin improves long-term neurological outcome in acute ischemic stroke patients: a randomized, prospective, placebo-controlled clinical trial
title Erythropoietin improves long-term neurological outcome in acute ischemic stroke patients: a randomized, prospective, placebo-controlled clinical trial
title_full Erythropoietin improves long-term neurological outcome in acute ischemic stroke patients: a randomized, prospective, placebo-controlled clinical trial
title_fullStr Erythropoietin improves long-term neurological outcome in acute ischemic stroke patients: a randomized, prospective, placebo-controlled clinical trial
title_full_unstemmed Erythropoietin improves long-term neurological outcome in acute ischemic stroke patients: a randomized, prospective, placebo-controlled clinical trial
title_short Erythropoietin improves long-term neurological outcome in acute ischemic stroke patients: a randomized, prospective, placebo-controlled clinical trial
title_sort erythropoietin improves long-term neurological outcome in acute ischemic stroke patients: a randomized, prospective, placebo-controlled clinical trial
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4349661/
https://www.ncbi.nlm.nih.gov/pubmed/25888250
http://dx.doi.org/10.1186/s13054-015-0761-8
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