中国循证儿科杂志 ›› 2016, Vol. 11 ›› Issue (2): 113-117.

• 论著 • 上一篇    下一篇

早产儿支气管肺发育不良危险因素及2岁时随访结局

尹燕丹1 祁媛媛2 洪达2 王传凯2 张晓波2 钱莉玲2   

  1. 浙江省台州市立医院 台州,318000;2 复旦大学附属儿科医院呼吸科 上海,201102
  • 收稿日期:2016-03-01 修回日期:2016-04-21 出版日期:2016-04-25 发布日期:2016-04-21
  • 通讯作者: 钱莉玲,张晓波

Study on risk factors and follow-up outcome at 2 years in preterm infants with bronchopulmonary dysplasia

YIN Yan-dan1, QI Yuan-yuan2, HONG Da2, WANG Chuan-kai2, ZHANG Xiao-bo2, QIAN Li-ling2   

  1. 1 Taizhou Municipal Hospital, Zhejiang Province, Taizhou 318000; 2 Department of Pneumology, Children′s Hospital of Fudan University, Shanghai 201102, China
  • Received:2016-03-01 Revised:2016-04-21 Online:2016-04-25 Published:2016-04-21
  • Contact: QIAN Li-ling, QIAN Li-ling

摘要:

目的探讨早产儿发生支气管肺发育不良(BPD)的危险因素及远期随访结局。方法 以2012年1月至2013年12月在复旦大学附属儿科医院新生儿科病房住院的胎龄≤32周、出生体重≤1 500 g及生后7 d内入院的BPD早产儿为BPD组,同期入住我院的非BPD早产儿中选取与BPD组等同样本量的病例为对照组。采集与BPD发生的母亲和新生儿因素行单因素分析和多因素分析。同时统计BPD早产儿生后1岁内和~2岁的支气管炎、肺炎、喘息发作次数和住院次数等指标。结果 BPD组和对照组均纳入了156例早产儿。单因素分析显示,BPD组母亲年龄(P=0.046)、先兆子(P=0.025)和阴道产(P<0.001)比例显著高于对照组;BPD组出生胎龄、出生体重显著低于对照组 (P均<0.001 )。BPD组1 和5 min Apgar 评分,败血症 ≥72 h、动脉导管未闭(PDA)、早产儿视网膜病变、应用肺表面活性物质、呼吸机相关性肺炎、机械通气≥7 d的比例均与对照组差异有统计学意义。多因素Logistic回归分析显示胎龄(OR= 0.46,95%CI:0.37~0.58)、机械通气≥7 d(OR=9.47,95%CI:3.70~24.27)、PDA(OR=2.21,95%CI:1.18~4.12)、先兆子(OR=4.91,95%CI:1.26~19.15 )是发生BPD的危险因素。BPD组1岁以内支气管炎、喘息的发生率高于对照组,再入院率两组差异无统计学意义;BPD组生后~2岁较生后1岁以内肺炎的发生率显著下降,支气管炎、喘息的发生率及再入院率差异无统计学意义。结论 低出生胎龄、机械通气≥7 d、PDA、先兆子是发生BPD的危险因素;BPD早产儿在生后1年以内下呼吸道感染的发生率增高。

Abstract:

Objective To investigate the main risk factors and long term outcome of preterm infants with bronchopulmonary dysplasia (BPD). Methods Children with BPD were collected from neonatal intensive care units (NICU) in Children′s Hospital Fudan University, from January 1, 2012 to December 31, 2013. All babies with gestational age ≤ 32 weeks, birth weight ≤1 500 g, and admission within 7 days after birth were included in this study. In the same period,according to the inclusion criteria, the same sample size of non BPD was collected as control group. Univariate and multiple logistic regression analyses were used to determine factors associated with the risk of BPD. At the same time ,the incidence of bronchitis,pneumonia,wheezing and rehospitalization were analyzed during the first two years of life. Results There were 156 cases in BPD group and matched 156 infants without BPD in control group. Mother′s information including age, the proportion of preeclampsia and vaginal delivery was significantly higher in BPD group than that in control group(P=0.046,0.025 and <0.001). Birth gestational age and birth weight of BPD group were significantly lower than those of control grouop ( P <0.001 ).Infant information including 1 min Apgar score, 5 min Apgar score, sepsis ≥72 h , patent ductus arteriosus ( PDA ), retinopathy of prematurity ( ROP ) , ventilator associated pneumonia ( VAP ) , the application of PS and mechanical ventilation ≥7 d was significantly higher in BPD group than that in control group. The factors increasing the risk of BPD determined by multivariate logistic analysis were: gestational age (OR=0.46,95%CI:0.37-0.58), mechanical ventilation ≥7 d(OR= 9.47,95%CI:3.70-24.27), PDA (OR= 2.21,95%CI:1.18-4.12 ) and preeclampsia( OR= 4.91,95%CI:1.26-19.15). In the first year of life, the incidence of bronchitis and wheezing in preterm-born children with a history of BPD was significantly higher than that in preterm-born children without BPD, but there was no significant difference in rehospitalization between the two groups. The incidence of pneumonia of BPD group was significantly decreased in the second year of life, while there was no significant difference in bronchitis, wheezing and rehospitalization compared to the first year of life. Conclusion Low gestational age, mechanical ventilation ≥7 d, patent ductus arteriosus, preeclampsia were highest risk factors for BPD. Among premature infants, BPD substantially increased the risk of lower respiratory tract infection during the first year of life.

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