Garcia Maria G, Hutson Alan D, Christensen Robert D
The National Institute of Perinatology, Mexico City, Mexico.
J Perinatol. 2002 Mar;22(2):108-11. doi: 10.1038/sj.jp.7210677.
Using the approach of a meta-analysis, we sought to determine whether the administration of recombinant erythropoietin (rEpo) to very low birth weight (VLBW) infants, after the first week of life, results in fewer "late" transfusions.
The guidelines set forth by the Cochrane Neonatal Review Group were used to identify all relevant studies. Medline was searched from January 1990 to November of 2000. Studies that used a randomized, placebo-controlled, and double-masked design were deemed acceptable.
Eight studies meet the inclusion criteria. These involved 357 VLBW neonates: 183 rEpo and 174 placebo recipients. The neonates in the rEpo group received fewer erythrocyte transfusions during the study period than did those in the placebo group; the common odds ratio (OR)=0.33; 95% confidence interval (CI) 0.21-0.51. Furthermore, the rEpo effect size was a function of the dose of rEpo administered (p=0.0001).
A meta-analysis of the most scientifically rigorous studies on this topic indicates that administration of rEpo to VLBW infants reduces "late" erythrocyte transfusions in a dose-dependent manner.
采用荟萃分析方法,我们试图确定出生后第一周后对极低出生体重(VLBW)婴儿给予重组促红细胞生成素(rEpo)是否会减少“晚期”输血。
采用Cochrane新生儿综述小组制定的指南来识别所有相关研究。检索了1990年1月至2000年11月的Medline。采用随机、安慰剂对照和双盲设计的研究被认为是可接受的。
八项研究符合纳入标准。这些研究涉及357例极低出生体重儿:183例接受rEpo治疗,174例接受安慰剂治疗。在研究期间,rEpo组的新生儿接受的红细胞输血比安慰剂组少;共同优势比(OR)=0.33;95%置信区间(CI)为0.21 - 0.51。此外,rEpo的效应大小是所给予rEpo剂量的函数(p = 0.0001)。
对该主题最科学严谨的研究进行的荟萃分析表明,对极低出生体重儿给予rEpo可剂量依赖性地减少“晚期”红细胞输血。