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Parental reactions, distress, and sense of coherence after prenatal versus postnatal diagnosis of complex congenital heart disease.复杂先天性心脏病产前与产后诊断后父母的反应、痛苦及连贯感。
Cardiol Young. 2019 Nov;29(11):1328-1334. doi: 10.1017/S1047951119001781. Epub 2019 Sep 16.
2
Modifiable Risk Factors in Necrotizing Enterocolitis.坏死性小肠结肠炎的可改变风险因素
Clin Perinatol. 2019 Mar;46(1):129-143. doi: 10.1016/j.clp.2018.10.007. Epub 2018 Dec 21.
3
A critical analysis of risk factors for necrotizing enterocolitis.坏死性小肠结肠炎危险因素的批判性分析。
Semin Fetal Neonatal Med. 2018 Dec;23(6):374-379. doi: 10.1016/j.siny.2018.07.005. Epub 2018 Aug 1.
4
Red Blood Cell Transfusion in Preterm Infants: Current Evidence and Controversies.早产儿的红细胞输血:当前证据与争议
Neonatology. 2018;114(1):7-16. doi: 10.1159/000486584. Epub 2018 Mar 16.
5
Human milk and necrotizing enterocolitis.母乳与坏死性小肠结肠炎
Semin Pediatr Surg. 2018 Feb;27(1):34-38. doi: 10.1053/j.sempedsurg.2017.11.007. Epub 2017 Nov 6.
6
Red blood cell transfusion in premature infants leads to worse necrotizing enterocolitis outcomes.早产儿输血会导致坏死性小肠结肠炎的预后更差。
J Surg Res. 2017 Jun 1;213:158-165. doi: 10.1016/j.jss.2017.02.029. Epub 2017 Feb 28.
7
Risk factors for necrotizing enterocolitis in neonates: a systematic review of prognostic studies.新生儿坏死性小肠结肠炎的危险因素:预后研究的系统评价
BMC Pediatr. 2017 Apr 14;17(1):105. doi: 10.1186/s12887-017-0847-3.
8
Red blood cell transfusions can induce proinflammatory cytokines in preterm infants.红细胞输血可在早产儿中诱导促炎细胞因子。
Transfusion. 2017 May;57(5):1304-1310. doi: 10.1111/trf.14080. Epub 2017 Mar 11.
9
Pathogenesis of NEC: Impact of an altered intestinal microbiome.坏死性小肠结肠炎的发病机制:肠道微生物群改变的影响
Semin Perinatol. 2017 Feb;41(1):29-35. doi: 10.1053/j.semperi.2016.09.015. Epub 2016 Dec 13.
10
New Medical and Surgical Insights Into Neonatal Necrotizing Enterocolitis: A Review.新生儿坏死性小肠结肠炎的新医学和外科学见解:综述。
JAMA Pediatr. 2017 Jan 1;171(1):83-88. doi: 10.1001/jamapediatrics.2016.2708.

新生儿败血症并发坏死性小肠结肠炎的危险因素:一项回顾性病例对照研究。

Risk factors of necrotizing enterocolitis in neonates with sepsis: A retrospective case-control study.

机构信息

Neonatal Diagnosis and Treatment Center, Ministry of Education Key Laboratory of Child Development and Disorders, National Clinical Research Center for Child Health and Disorders (Chongqing), China International Science and Technology Cooperation base of Child development and Critical Disorders, Children's Hospital of Chongqing Medical University, Chongqing Key Laboratory of Pediatrics, Chongqing, P.R. China.

出版信息

Int J Immunopathol Pharmacol. 2020 Jan-Dec;34:2058738420963818. doi: 10.1177/2058738420963818.

DOI:10.1177/2058738420963818
PMID:33016797
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7543139/
Abstract

Sepsis, a severe infectious disease in the neonatal period, is considered a risk factor for necrotizing enterocolitis (NEC). To investigate the specific risk factors for NEC in septic infants, septic infants admitted to our center from January 2010 to April 2018 were included. Septic neonates with proven NEC (Bell's stage ⩾II) were enrolled in the NEC group, and those without NEC were enrolled in the control group. Demographics, clinical characteristics, and risk factors were compared between the two groups. Univariate and logistic regression analyses were used to evaluate the potential risk factors for NEC. A total of 610 septic neonates were included, of whom 78 (12.8%) had complicated NEC. The univariate analysis indicated that infants with NEC had a lower birth weight, a lower gestational age, and older age on admission than those without NEC ( < 0.05). Higher rates of anemia, prolonged rupture of membranes (PROM) (⩾18 h), pregnancy-induced hypertension, late-onset sepsis (LOS), red blood cell transfusion and hypoalbuminemia were observed in the NEC group than in the non-NEC group (P<0.05). Logistic regression analysis revealed LOS ( = 0.000), red blood cell transfusion ( = 0.001) and hypoalbuminemia ( = 0.001) were associated with the development of NEC. Among NEC infants, those who needed red blood cell transfusion had a longer hospitalization duration than those who did not need transfusion ( < 0.05). LOS, red blood cell transfusion and hypoalbuminemia were independent risk factors for the development of NEC in infants with sepsis. Taking measures to reduce the occurrence of hypoproteinemia and severe anemia may help to reduce the occurrence of NEC in septic neonates.

摘要

新生儿败血症是一种严重的感染性疾病,被认为是坏死性小肠结肠炎(NEC)的危险因素。为了探讨败血症患儿发生 NEC 的具体危险因素,我们纳入了 2010 年 1 月至 2018 年 4 月期间在我院住院的败血症患儿。将确诊为 NEC(Bell 分期 ⩾Ⅱ期)的败血症新生儿纳入 NEC 组,未发生 NEC 的患儿纳入对照组。比较两组患儿的一般资料、临床特征及危险因素。采用单因素及 Logistic 回归分析评估 NEC 的潜在危险因素。共纳入 610 例败血症新生儿,其中 78 例(12.8%)并发 NEC。单因素分析显示,与无 NEC 组相比,NEC 组患儿的出生体质量更低、胎龄更小、入院时年龄更大(均 P<0.05)。NEC 组患儿贫血、胎膜早破时间延长(⩾18 h)、妊娠高血压、晚发型败血症(LOS)、红细胞输注及低白蛋白血症的发生率均高于无 NEC 组(P<0.05)。Logistic 回归分析显示,LOS( = 0.000)、红细胞输注( = 0.001)及低白蛋白血症( = 0.001)与 NEC 的发生有关。在 NEC 患儿中,需要输血的患儿的住院时间长于无需输血的患儿(P<0.05)。LOS、红细胞输注和低白蛋白血症是败血症患儿发生 NEC 的独立危险因素。采取措施减少低蛋白血症和严重贫血的发生可能有助于降低败血症新生儿 NEC 的发生风险。