Erythropoietin improves long-term neurological outcome in acute ischemic stroke patients: a randomized, prospective, placebo-controlled clinical trial
文摘
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聽IU/dose, subcutaneously administered at 48聽hours and 72聽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鈥?鈥?1) and group 2 (EPO-treated; n鈥?鈥?1). Long-term Barthel index of P鈥?鈥?.007). Multiple-stepwise logistic-regression analysis showed that EPO therapy was significantly and independently predictive of freedom from a Barthel index of P鈥?鈥?.029). Long-term major adverse neurological event (MANE; defined as: death, recurrent stroke, or long-term Barthel index鈥?鈥?5) was lower in group 2 than group 1 (P鈥?鈥?.04). Log-Rank test showed that MANE-free rate was higher in group 2 than group 1 (P鈥?鈥?.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 Conclusion EPO therapy significantly improved long-term neurological outcomes in patients after IS. Trial registration ISRCTN71371114. Registered 10 October 2008.