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发育医学电子杂志  2022, Vol. 10 Issue (5): 365-372    DOI: 10.3969/j.issn.2095-5340.2022.05.007
  围产医学   论著 |新生儿 |
母源性疾病对新生儿的影响及早产儿发生小于胎龄儿的高危因素分析
房晓祎 邹新飞 李管明 张霭润 王启闯 杨斯岚 林霓阳
(1. 中山大学附属第七医院 新生儿科,广东 深圳 518107;2. 广东省妇幼保健院 儿童重
症监护病房,广东 广州 511400;3. 汕头大学医学院第一附属医院 新生儿科,广东 汕头 515041)
Analysis of effects of maternal diseases on neonates and risk factors for small for gestationalage in preterm infants
FangG Xiaoyi, Zou Xinfei, Li uanming, et al
(1. Department of Neonatology, the Seventh Affiliated Hospital, Sun Yat-sen University, Guangdong,Shenzhen 518107, China; 2. Department of Pediatric Intensive Care Unit, Maternal and Children Hospitalof Guangdong Province, Guangdong, Guangzhou 511400, China; 3. Department of Neonatology, the FirstAffiliated Hospital, Shantou University Medical College, Guangdong, Shantou 515041, China)
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摘要 【摘要】 目的  探讨母源性疾病对新生儿的影响及早产儿发生小于胎龄儿(small for gestational age,
SGA)的高危因素。 方法 查阅2013 年1 月至2017 年12 月汕头大学医学院第一附属医院自产科转至
新生儿科的3 387 例新生儿及其母亲资料,分析母源性疾病对新生儿的影响。将其中的1 794 例早产儿
分为SGA 组(n=303)和非SGA 组(n=1 491),采用多因素Logistic 回归分析以下因素与早产儿发生SGA
的关系:胎膜早破(premature rupture of membrane,PROM)、高龄(年龄>35 岁)、妊娠期糖尿病、妊娠期高血压疾病、多胎、产次(初产/ 经产)、试管婴儿、先天性宫内感染、乙肝、阴道炎、甲状腺功能异常、产前贫血、系统性红斑狼疮(systemic lupus erythematosus,SLE)、胆汁淤积、HELLP(hemolysis, elevated liverfunction and low platelet count) 综合征、胎盘早剥、前置胎盘,并评价其预测效能。统计学方法采用t 检验、χ2 检验、受试者操作特征曲线下面积(area under the curve,AUC)。 结果  ①产科来源新生儿主要疾病:早产儿52.97% (1 794/3 387)、低出生体质量儿(low birth weight,LBW)48.15%(1 631/3 387)、病理性黄疸34.72% (1 176/3 387)、肺炎32.97%(1 117/3 387)、SGA18.01%(610/3 387)。② PROM 组新生儿胎龄小、体质量低,SGA 发生率低,肺炎、颅内出血(intracranial hemorrhage,ICH)发生率高(P<0.05);与非高龄组比较,产妇高龄组新生儿胎龄小,其中,高龄初产组新生儿低血糖症发生率高于高龄经产妇组[(26/147(17.69%)与47/426(11.03%),P<0.05];产妇妊娠期糖尿病组新生儿体质量大、低血糖症发生率高,SGA、缺氧缺血性脑病(hypoxic ischemic encephalopathy,HIE)发生率低(P<0.05);产妇妊娠期高血压疾病组新生儿胎龄小、体质量低,SGA、新生儿呼吸窘迫综合征(neonatal respiratory distress syndrome,NRDS)、窒息、低血糖症发生率高,病理性黄疸发生率低(P<0.05);产妇多胎组新生儿胎龄小、体质量低,SGA、NRDS、低血糖症发生率高,病理性黄疸、HIE 发生率低(P<0.05)。③多因素Logistic 回归分析显示,母亲初产(OR=1.382,95%CI:1.061~1.801)、妊娠期高血压疾病(OR=4.270,95%CI:3.155~5.779)和多胎[双胎OR=1.561,95%CI :1.155~2.110 ;三胎:OR=2.690,95%CI :1.180~6.133]是影响早产儿发生SGA 的独立因素(P 值均<0.05)。 结论 母亲存在PROM、多胎、高龄、妊娠期糖尿病、妊娠期高血压疾病等是引起新生儿疾病的主要原因;初产、妊娠期高血压疾病和多胎是早产儿发生SGA 的独立危险因素。
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关键词:  母源性疾病  早产儿  小于胎龄儿  围产期管理  预防    
Abstract: 【Abstract】 Objective To explore the effects of maternal diseases on neonates and risk factors for smallfor gestational age (SGA) in premature infants. Method Data of the 3 387 newborns and their maternalstransferred from the Department of Obstetrics to Neonatology, the First Affiliated Hospital, ShantouUniversity Medical College, from January 2013 to December 2017 were collected and the effects of thematernal origins diseases on newborn were analyzed. The 1 794 premature infants were divided into the SGAgroup (n=303) and non-SGA group (n=1 491). The risk factors from mother, including premature rupture ofthe membrane (PROM), advanced maternal age (AMA, >35 years old), gestational diabetes mellites (GDM),gestational hypertension, multiple pregnancy, parity, in-vitro fertilization, intrauterine infection, hepatitis B,vaginitis, thyroid dysfunction, prenatal anemia, systemic lupus erythematosus (SLE), cholestasis, hemolysis,elevated liver function and low platelet count (HELLP) syndrome, placental abruption and placenta previa,which might affect the occurrence of SGA in premature infants were analyzed by multivariate Logisticregression and the predictive efficiency was evaluated. t-test, χ2 test, receiver operating characteristic (ROC)and area under the curve (AUC) were used for statistical analysis Result ①The main diseases of thenewborn infants transferred from the Department of Obstetrics were prematurity [1 794/3 387 (52.97%)], lowbirth weight [1 631/3 387(48.15%)], pathological jaundice [1 176/3 387 (34.72%)], pneumonia [1 117/3 387(32.97%)] and SGA [610/3 387 (18.01%)]. ②The infants in PROM group had a lower gestational age (GA),a lower birth weight (BW), a lower incidence of SGA, and a higher incidence of pneumonia and intracranialhemorrhage (IVH) compared with the non-PROM group (P<0.05). The newborns in AMA group had a lowerGA compared with the non-AMA group (P<0.05). The newborns of primiparity mother in AMA group hada higher incidence of hypoglycemia compared with the multiparity mother in AMA group [26/147(17.69%)vs 47/426(11.03%), P<0.05]. The infants of diabetes mother (IDM) had a higher BW, a higher incidence ofhypoglycemia, and a lower incidence of SGA and hypoxic ischemic encephalopathy (HIE) compared withthe non-IDM group (P<0.05). The infants of hypertension mother had a lower GA, a lower BW, a higherincidence of SGA, neonatal respiratory distress syndrome (NRDS), asphyxia, hypoglycemia and a lowerincidence of pathological jaundice compared with the non-hypertension group (P<0.05). The infants born bymultiple pregnancy had a lower GA, a lower BW, a higher incidence of SGA, NRDS and hypoglycemia, anda lower incidence of pathological jaundice and HIE compared with the singular pregnancy group (P<0.05).③Multivariate Logistic regression analysis showed that primipara (OR=1.382, 95%CI: 1.061-1.801),gestational hypertension (OR=4.270, 95%CI: 3.155-5.779) and multiple pregnancy (twin OR=1.561, 95%CI:1.155-2.110, triplet OR=2.690, 95%CI: 1.180-6.133) were the independent factors of SGA in prematureinfants (all P<0.05). Conclusion The main problems of the mother are PROM, AMA, GDM, gestationalhypertension, multiple pregnancy, and so on. Primipara, gestational hypertension and multiple pregnancy are the independent risk factors contributing to the SGA in premature infants.
Key words:  Diseases of maternal origins    Premature infant    Small for gestational age    Perinatalmanagement    Prevention
收稿日期:  2022-01-04                     发布日期:  2022-09-30     
基金资助: 广东省研究生教育创新计划项目(2019JGXM05);深圳市科技计划项目(JCYJ20190809145409829)
通讯作者:  林霓阳    E-mail:  linniyang2@126.com
引用本文:    
房晓祎 邹新飞 李管明 张霭润 王启闯 杨斯岚 林霓阳. 母源性疾病对新生儿的影响及早产儿发生小于胎龄儿的高危因素分析[J]. 发育医学电子杂志, 2022, 10(5): 365-372.
Fang Xiaoyi, Zou Xinfei, Li uanming, et al. Analysis of effects of maternal diseases on neonates and risk factors for small for gestationalage in preterm infants. Journal of Developmental Medicine(Electronic Version), 2022, 10(5): 365-372.
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