Chinese Medical E-ournals Database

Chinese Journal of Obstetrics & Gynecology and Pediatrics(Electronic Edition) ›› 2024, Vol. 20 ›› Issue (02): 209 -215. doi: 10.3877/cma.j.issn.1673-5250.2024.02.012

Original Article

Risk factors and prognosis analysis of bronchopulmonary dysplasia in preterm small for gestational age infants

Lizhen Guo1, Tianqun Fan2, Xinkai Zhang1, Yunhong Jiang1, Rong Jin3, Dongyun Liu3,()   

  1. 1. Qingdao University, Qingdao 266000, Shandong Province, China; Children′s Medical Center of the Affiliated Hospital of Qingdao University, Qingdao 266000, Shandong Province, China
    2. Department of Pediatrics, Linyi People′s Hospital, Linyi 276000, Shandong Province, China
    3. Children′s Medical Center of the Affiliated Hospital of Qingdao University, Qingdao 266000, Shandong Province, China
  • Received:2024-02-01 Revised:2024-03-05 Published:2024-04-01
  • Corresponding author: Dongyun Liu
  • Supported by:
    Medical and Health Technology Development Plan of Shandong Province(2017WSB26008)
Objective

To investigate influencing factors and prognosis of bronchopulmonary dysplasia (BPD) in preterm small for gestational age (SGA) infants.

Methods

A total of 92 preterm (gestational age of 24-32 weeks) SGA infants who were hospitalized in Neonatal Intensive Care Unit (NICU) of Affiliated Hospital of Qingdao University from January 2019 to December 2021 were selected as study subjects. Using a retrospective cohort study method, they were divided into BPD group (n=38) and BPD-free group (n=54) according to whether BPD was diagnosed at 36 weeks′ corrected gestational age or not. The clinical data, treatment and BPD related complications of preterm SGA infants between two groups were statistically compared by chi-square test, independent samples t test and Mann-Whitney U test. Multivariate unconditional logistic regression analysis was used to analyze the independent influencing factors of BPD in preterm SGA infants. This study was approved by the Medical Ethics Committee of our hospital (Approval No. QYFY WZLL 28257), and the guardians of all subjects gave informed consent to diagnosis and treatment and signed an informed consent form for this clinical study.

Results

① The body weight at 1 month after birth, birth length and head circumference, Apgar score at 1 min and 5 min after birth of preterm SGA infants in BPD group were lower, shorter and smaller than those in BPD-free group, while invasive mechanical ventilation, noninvasive mechanical ventilation, oxygen inhalation and hospitalization time, and the utilization rate of pulmonary surfactant (PS) were longer, higher than those in BPD-free group, and all the differences were statistically significant (P<0.01). ② The results of multivariate unconditional logistic regression analysis showed that the long duration of non-invasive mechanical ventilation (OR=1.180, 95%CI: 1.064-1.308, P=0.002) and the long duration of oxygen inhalation after birth (OR=1.295, 95%CI: 1.126-1.488, P<0.001) were independent risk factors for BPD in preterm SGA infants. ③ The incidences of pneumonia, late-onset sepsis, hemodynamically significant patent ductus arteriosus (hsPDA) and retinopathy of prematurity (ROP) in the BPD group were higher than those in the BPD-free group, and the differences were statistically significant (P<0.05).

Conclusion

For preterm SGA infants, the timing of non-invasive mechanical ventilation and oxygen inhalation should be appropriately controlled to reduce the incidence of BPD and related complications.

表1 2组早产SGA儿临床资料比较
组别 例数 母亲
自然受孕[例数(%)] 顺产[例数(%)] 产前感染[例数(%)] 年龄(岁,±s) 妊娠期高血压疾病[例数(%)] 妊娠期糖尿病[例数(%)] 产前使用激素[例数(%)]
BPD组 38 37(97.4) 4(10.5) 13(34.2) 32.8±4.1 24(63.2) 6(15.8) 37(97.4)
无BPD组 54 53(98.1) 0(0) 18(33.3) 32.8±4.8 35(64.8) 11(20.4) 47(87.0)
统计量   a a χ2=0.01 t=0.03 χ2=0.03 χ2=0.31 a
P   >0.999 0.026 0.930 0.979 0.870 0.577 0.134
组别 例数 生后1个月体重(g,±s) 男性[例数(%)] 单胎[例数(%)] 出生身长(cm,±s) 出生头围(cm,±s) 生后1 min Apgar评分[分,M(Q1Q3)] 生后5 min Apgar评分[分,M(Q1Q3)]
BPD组 38 1 332±279 24(63.2) 26(68.4) 34.5±2.8 25.4±2.2 6.5(5.0,8.0) 8.0(7.0,9.0)
无BPD组 54 1 549±255 29(53.7) 47(87.0) 36.5±3.0 26.9±2.0 8.0(7.0,9.0) 9.0(8.0,10.0)
统计量   t=3.87 χ2=0.82 χ2=4.72 t=3.34 t=3.28 Z=4.32 Z=3.61
P   <0.001 0.366 0.030 0.001 0.001 <0.001 <0.001
组别 例数 出生时血小板计数[×109/L,M(Q1Q3)] 出生时Hb水平[g/L,M(Q1Q3)] 有创机械通气时间[d,M(Q1Q3)] 无创机械通气时间[d,M(Q1Q3)] 面罩/鼻导管/箱内吸氧时间[d,M(Q1Q3)] 开奶时间[d,M(Q1Q3)] 静脉营养时间[d,M(Q1Q3)]
BPD组 38 180(154,196) 171(160,182) 0(0,4) 35.5(18.0,52.0) 24(8,35) 1(1,2) 28.5(22.0,41.0)
无BPD组 54 189(156,218) 178(163,191) 0(0,0) 10.0(6.0,20.0) 0(0,4) 1(1,2) 25.0(18.0,32.0)
统计量   Z=0.96 Z=1.69 Z=3.94 Z=5.32 Z=6.36 Z=0.71 Z=2.03
P   0.339 0.092 <0.001 <0.001 <0.001 0.478 0.021
组别 例数 全胃肠营养时间[d,M(Q1Q3)] 输血[例数(%)] 使用PS[例数(%)] PS剂量[mg,M(Q1Q3)] 住院时间[d,M(Q1Q3)] 父亲年龄[岁,M(Q1Q3)]
BPD组 38 29.5(23.0,42.0) 32(84.2) 18(47.4) 0(0,220) 75.5(61.0,97.0) 33(30,39)
无BPD组 54 26.0(19.0,33.0) 34(63.0) 11(20.4) 0(0,0) 54.0(47.0,65.0) 33(30,37)
统计量   Z=2.19 χ2=4.97 χ2=7.53 Z=2.53 Z=4.93 Z=0.24
P   0.029 0.026 0.006 0.011 <0.001 0.814
表2 早产SGA儿发生BPD的多因素非条件logistic回归分析结果
表3 2组早产SGA儿并发症发生率比较[例数(%)]
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