Department of Women and Newborns, Intermountain Healthcare, Salt Lake City, UT, USA.
J Perinatol. 2012 Nov;32(11):874-9. doi: 10.1038/jp.2011.163. Epub 2011 Nov 10.
We hypothesized that neonates with bloody stools and concomitant eosinophilia are likely to have atopic enteropathy rather than necrotizing enterocolitis (NEC).
This was a retrospective cross-sectional study using electronic medical records and paper charts. Records of neonates admitted to any Intermountain Healthcare NICU between 1 January 2005 and 30 June 2010 were eligible if 'bloody stools' were listed in any archive. Qualifying records were divided into two groups depending on whether or not within 72 h of passing bloody stool eosinophil counts were above the 95th percentile reference range limit for age.
Bloody stools were identified in 275 predominantly Caucasian neonates. Fifty-four of these had eosinophilia and 221 had normal eosinophil counts. Those with eosinophilia were born at a slightly younger gestational age (31.3 ± 4.6 vs 32.6 ± 4.0 weeks, mean ± s.d., P=0.032). Contrary to our hypothesis, those with eosinophilia did not have a lower rate of pneumatosis or bowel resection, or death ascribed to NEC. Eosinophilia was more common among those who had a red blood cell (RBC) transfusion within 48 h before passing bloody stools (P<0.001). Those with a recent RBC transfusion were the only neonates to have NEC surgery or to die from NEC. Preceding the bloody stools, those with no antecedent transfusion had been fed a larger volume (P=0.014), and had trends toward receiving calorically enriched feedings (P=0.055) and recent addition of human milk fortifier (P=0.060). Eosinophil counts following RBC transfusion tended to increase for 3-6 days, but when bloody stools were not preceded by transfusion the eosinophil counts were more static over that period.
In this predominantly Caucasian group of neonates with bloody stools, the presence of eosinophilia did not identify a benign condition distinct from NEC. A total of 44% of these neonates had transfusion-associated NEC. Eosinophils could have a previously unrecognized role in the pathogenesis of this NEC subtype.
我们假设伴有血便和嗜酸性粒细胞增多的新生儿更有可能患有特应性肠炎,而不是坏死性小肠结肠炎(NEC)。
这是一项使用电子病历和纸质图表的回顾性横断面研究。如果在任何 Intermountain Healthcare NICU 住院的新生儿的记录中在任何存档中都列出了“血便”,则符合条件。合格的记录根据在出现血便后 72 小时内嗜酸性粒细胞计数是否超过年龄的 95 百分位参考范围限值分为两组。
在 275 名主要为白种人的新生儿中发现了血便。其中 54 名有嗜酸性粒细胞增多症,221 名嗜酸性粒细胞计数正常。嗜酸性粒细胞增多症的新生儿胎龄稍小(31.3±4.6 与 32.6±4.0 周,均值±标准差,P=0.032)。与我们的假设相反,嗜酸性粒细胞增多症的新生儿的肠气肿或肠切除术发生率或归因于 NEC 的死亡率没有更低。在出现血便前 48 小时内接受过红细胞(RBC)输血的患者中嗜酸性粒细胞增多症更为常见(P<0.001)。只有接受过 RBC 输血的新生儿需要进行 NEC 手术或死于 NEC。在出现血便之前,没有输血史的患者的喂养量更大(P=0.014),并且有接受热量丰富的喂养(P=0.055)和近期添加人乳强化剂(P=0.060)的趋势。在接受 RBC 输血后,嗜酸性粒细胞计数往往会增加 3-6 天,但当血便不是由输血引起时,嗜酸性粒细胞计数在这段时间内更加稳定。
在这个以白种人为主的伴有血便的新生儿群体中,嗜酸性粒细胞增多并不能确定与 NEC 不同的良性疾病。这些新生儿中有 44%患有与输血相关的 NEC。嗜酸性粒细胞可能在这种 NEC 亚型的发病机制中具有以前未被认识到的作用。