4.7 Article

Effect of high-dose erythropoietin on graft function after kidney transplantation: A meta-analysis of randomized controlled trials

期刊

BIOMEDICINE & PHARMACOTHERAPY
卷 69, 期 -, 页码 29-33

出版社

ELSEVIER FRANCE-EDITIONS SCIENTIFIQUES MEDICALES ELSEVIER
DOI: 10.1016/j.biopha.2014.10.029

关键词

Erythropoietin; Kidney transplantation; Graft function; Meta-analysis

资金

  1. National Natural Science Foundation of China [81070597, 81370853]
  2. Science and Education Development Program of the Jiangsu Province Health Board [LJ201107]
  3. Six Talent Peaks of the Jiangsu Province Health Bureau [2011-WS-093]
  4. Research and Innovation Program for Graduates of Jiangsu Province [CXZZ13_0583]

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Purpose: Current evidence suggests that preconditioning with erythropoietin (EPO) can protect against ischemia reperfusion injury in rodents. However, randomized controlled trials (RCTs) assessing the efficacy and safety of high-dose EPO in kidney transplantation have yielded inconclusive results. Herein, we performed a meta-analysis of RCTs to assess whether the administration of high-dose EPO can improve graft function and the potential adverse events. Methods: Relevant RCT studies that investigated high-dose EPO on graft function after kidney transplantation were comprehensively searched in Pubmed, Embase, and Cochrane Library until July 10, 2014. All statistical analyses were performed using Review Manager 5.0 and STATA 12.0. Results: A total of 4 RCTs involving 356 patients were identified. Comprehensively, a trend of reduction in the incidence of delayed graft function could be observed in the EPO group (EPO vs. placebo groups: RR = 0.88); however, the result did not reach the significance level (95% CI, 0.72-1.08; P = 0.21). Furthermore, no significant difference in the incidences of adverse events was observed between the two groups. Conclusions: The current meta-analysis indicates that the administration of high-dose EPO is, to some extent, prone to protect kidney function without increasing the susceptibility to adverse events. (C) 2014 Elsevier Masson SAS. All rights reserved.

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