Department of Women and Newborns, Intermountain Healthcare, Salt Lake City, UT, USA.
1] Department of Women and Newborns, Intermountain Healthcare, Salt Lake City, UT, USA [2] Department of Obstetrics and Gynecology, University of Utah School of Medicine, Salt Lake City, UT, USA.
J Perinatol. 2014 Feb;34(2):116-9. doi: 10.1038/jp.2013.113. Epub 2013 Sep 12.
The time between onset of fetal hypoxia and first appearance of nucleated red blood cells (NRBCs) in the blood can conceptually be divided into two periods; (1) the 'erythropoietin (EPO) generation time', which previous fetal studies suggest is 4 to 5 h, and (2) the 'NRBC emergence time'. In this study, we estimated the latter as the time required for NRBC to appear in the blood after administering a dose of recombinant EPO.
This was a retrospective analysis of data from a multihospital healthcare system (Intermountain Healthcare). Data were included only for neonates born ≥34 weeks gestation between the dates 1 January 2005 and 31 October 2012 and only if they received a dose of darbepoetin during their neonatal intensive care unit stay and had one or more complete blood cell counts (CBCs) obtained during the 3-day period before the dose was given and one or more CBCs in the 7-day period after the dose.
The study involved 31 neonates who received 34 doses of darbepoetin. Seven doses were 4 μg kg(-1) and twenty-seven doses were 10 μg kg(-1). Twenty-six CBCs were obtained during the 24-h period following the darbepoetin dose and none had NRBC identified. NRBC first appeared in the blood between 24 and 36 h after the dose. Recipients of the higher dose generally had a higher peak NRBC count but the NRBC 'emergence time' did not appear to depend on dose.
Following fetal hypoxia, transcription and translation of the EPO gene result in an elevation in plasma EPO concentration. Previous fetal studies suggest this process requires 4 to 5 h. The present studies suggest that, following the increase in plasma EPO, NRBC emerge into the circulation in ≥24 h. If this model serves as a reasonable estimate, it suggests that neonates with an elevated NRBC count at birth had the onset of hypoxia at least 28 to 29 h before birth.
胎儿缺氧发作与血中出现有核红细胞(NRBC)之间的时间概念上可分为两个时期;(1)“促红细胞生成素(EPO)生成时间”,先前的胎儿研究表明该时间为 4 至 5 小时,以及(2)“NRBC 出现时间”。在这项研究中,我们将后者估计为给予重组 EPO 剂量后 NRBC 出现在血液中的时间。
这是对来自多医院医疗保健系统(Intermountain Healthcare)的数据的回顾性分析。仅包括在 2005 年 1 月 1 日至 2012 年 10 月 31 日期间出生且胎龄≥34 周的新生儿的数据,并且仅在新生儿重症监护病房期间接受达贝泊汀剂量治疗且在给予剂量前 3 天内获得了一份或多份完整的血细胞计数(CBC)并且在剂量给予后的 7 天内获得了一份或多份 CBC。
该研究涉及 31 名接受 34 次达贝泊汀剂量的新生儿。7 次剂量为 4μg·kg-1,27 次剂量为 10μg·kg-1。在给予达贝泊汀剂量后的 24 小时内获得了 26 次 CBC,均未发现 NRBC。NRBC 最早在剂量后 24 至 36 小时出现在血液中。较高剂量的接受者通常具有较高的 NRBC 计数峰值,但 NRBC“出现时间”似乎与剂量无关。
胎儿缺氧后,EPO 基因的转录和翻译导致血浆 EPO 浓度升高。先前的胎儿研究表明,这一过程需要 4 至 5 小时。本研究表明,在血浆 EPO 增加后,NRBC 在≥24 小时内进入循环。如果该模型可作为合理的估计,那么出生时 NRBC 计数升高的新生儿在出生前至少 28 至 29 小时就已经发生了缺氧。