Xu Huan, Xu Ping
Department of Neonatal Intensive Care Unit, Liaocheng People's Hospital, Liaocheng 252000, Shandong, China.
Key Laboratory for Pediatrics of Integrated Traditional and Western Medicine, Liaocheng People's Hospital, Liaocheng 252000, Shandong, China. Corresponding author: Xu Ping, Email:
Zhonghua Wei Zhong Bing Ji Jiu Yi Xue. 2021 Feb;33(2):174-179. doi: 10.3760/cma.j.cn121430-20201009-00660.
To explore high-risk factors of respiratory distress syndrome (RDS) and to compare the clinical efficacy of calf pulmonary surfactant (PS) combined with budesonide suspension and poractant alfa injection in the treatment of RDS in premature infants.
A retrospective analysis was conducted. Preterm infants who were born in the obstetrics department of Liaocheng People's Hospital and admitted to the neonatal intensive care unit (NICU) within 24 hours from July 2016 to July 2020 were enrolled. The clinical data of these patients including perinatal conditions, clinical features, therapeutic regimens of PS and outcomes were collected and analyzed. According to the diagnostic criteria of neonatal respiratory distress syndrome (NRDS), premature infants were divided into NRDS group and non-NRDS group. First, the clinical data of the two groups were compared to analyze the related factors of NRDS. Then the related factors of NRDS were confirmed by Logistic regression analysis. In addition, according to the trapeutic regimens of PS, the children were divided into calf PS combined with budesonide suspension group and poractant alfa injection group, and the efficacy of the two PS was compared.
(1) A total of 1 690 preterm infants were included, including 297 preterm infants were diagnosed with NRDS which accounted for 17.6% of live preterm infants. There were significant differences in gender, gestational age (GA), birth parity, birth weight (BW), asphyxia of newborn, caesarean section, premature rupture of membrane, placental abruption, gestational diabetes and father's smoking addiction (maternal exposure to smoke during pregnancy) between NRDS group and non-NRDS group (male: 71.0% vs. 59.0%; GA: < 28 weeks was 4.1% vs. 0.1%, 28 weeks ≤ GA < 34 weeks was 70.0% vs. 29.9%, 34 weeks ≤ GA < 37 weeks was 25.9% vs.70.0%; birth parity: 2 (1, 3) vs. 2 (1, 3); BW: < 1 000 g was 4.1% vs. 0.4%, 1 000 g ≤ BW < 1 500 g was 31.3% vs. 6.5%, 1 500 g ≤ BW < 2 500 g was 51.5% vs. 58.9%, 2 500 g ≤ BW < 4 000 g was 12.8% vs. 33.1%, BW ≥ 4 000 g was 0.3% vs. 1.1%; asphyxia of newborn: 50.8% vs. 14.6%; caesarean section: 71.7% vs. 65.0%; premature rupture of membrane: 66.7% vs. 42.2%; premature rupture of fetal membranes: 11.4% vs. 5.2%; gestational diabetes: 12.1% vs. 7.0%; father's smoking addiction: 80.8% vs. 71.5%, all P < 0.05), but there was no significant difference in prenatal use of dexamethasone (DEX) between NRDS group and non-NRDS group (80.1% vs. 84.1%, P > 0.05). Binary multivariate Logistic regression analysis showed that GA, gender, cesarean section, premature rupture of membranes, gestational diabetes, father's smoking addiction and neonatal asphyxia were the risk factors of RDS [odds ratio (OR) and 95% confidence interval (95%CI) were 0.621 (0.557-0.693), 2.043 (1.478-2.825), 1.365 (1.036-1.797), 0.697 (0.506-0.961), 3.223 (1.906-5.449), 1.836 (1.261-2.673), 3.596 (2.622-4.933), all P < 0.05]. (2) A total of 160 patients diagnosed with grade III/IV NRDS were included to analyze the efficacy of PS. Among them, 42 cases were treated with calf PS combined with budesonide suspension, and 118 cases were treated with poractant alfa injection. Compared with the poractant alfa injection group, the total oxygen consumption time of the calf PS group was shorter [days: 9.0 (5.0, 19.0) vs. 13.0 (6.0, 26.0)], the hospitalization expenses were lower [ten thousand Yuan: 3.46 (2.88, 5.18) vs. 4.58 (3.08, 6.06)], and the incidence of bronchopulmonary dysplasia (BPD) was lower (11.9% vs. 28.8%), with statistically significant differences (all P < 0.05).
In addition to GA, gender, cesarean section, premature rupture of membranes, gestational diabetes, and neonatal asphyxia, the father's smoking addiction (maternal smoke exposure during pregnancy) is an important risk factor of RDS in premature infants. The efficacy of prenatal use of DEX for prevention of RDS in preterm infants is affected by many factors, such as prenatal smoke exposure, timing of use, multiple fetuses, etc. Calf PS combined with budesonide suspension is better than poractant alfa injection in reducing the incidence of BPD.
探讨呼吸窘迫综合征(RDS)的高危因素,并比较牛肺表面活性物质(PS)联合布地奈德混悬液与固尔苏注射液治疗早产儿RDS的临床疗效。
进行回顾性分析。纳入2016年7月至2020年7月在聊城市人民医院产科出生且在24小时内入住新生儿重症监护病房(NICU)的早产儿。收集并分析这些患者的围产期情况、临床特征、PS治疗方案及结局等临床资料。根据新生儿呼吸窘迫综合征(NRDS)的诊断标准,将早产儿分为NRDS组和非NRDS组。首先,比较两组的临床资料以分析NRDS的相关因素。然后通过Logistic回归分析确定NRDS的相关因素。此外,根据PS治疗方案,将患儿分为牛PS联合布地奈德混悬液组和固尔苏注射液组,比较两种PS的疗效。
(1)共纳入1690例早产儿,其中297例早产儿被诊断为NRDS,占存活早产儿的17.6%。NRDS组与非NRDS组在性别、胎龄(GA)、出生胎次、出生体重(BW)、新生儿窒息、剖宫产、胎膜早破、胎盘早剥、妊娠期糖尿病及父亲吸烟(孕期母亲暴露于烟雾)方面存在显著差异(男性:71.0%对59.0%;GA:<28周为4.1%对0.1%,28周≤GA<34周为70.0%对29.9%,34周≤GA<37周为25.9%对70.0%;出生胎次:2(1,3)对2(1,3);BW:<1000g为4.1%对0.4%,1000g≤BW<1500g为3⼗分位间距1.3%对6.5%,1500g≤BW<2500g为51.5%对58.9%,2500g≤BW<4000g为12.8%对33.1%,BW≥4000g为0.3%对1.1%;新生儿窒息:50.8%对14.6%;剖宫产:71.7%对65.0%;胎膜早破:66.7%对42.2%;胎膜早破:11.4%对5.2%;妊娠期糖尿病:12.1%对7.0%;父亲吸烟:80.8%对71.5%,均P<0.05),但NRDS组与非NRDS组产前使用地塞米松(DEX)情况无显著差异(80.1%对84.1%,P>0.05)。二元多因素Logistic回归分析显示,GA、性别、剖宫产、胎膜早破、妊娠期糖尿病、父亲吸烟及新生儿窒息是RDS的危险因素[比值比(OR)及95%置信区间(95%CI)分别为0.621(0.557 - 0.693)、2.043(1.478 - 2.825)、1.365(1.036 - 1.797)、0.697(0.506 - 0.961)、3.223(1.906 - 5.449)、1.836(1.261 - 2.673)、3.596(2.622 - 4.933),均P<0.05]。(2)共纳入160例诊断为Ⅲ/Ⅳ级NRDS的患者分析PS的疗效。其中,42例采用牛PS联合布地奈德混悬液治疗,118例采用固尔苏注射液治疗。与固尔苏注射液组相比,牛PS组的总吸氧时间更短[天:9.0(5.0,19.0)对13.0(6.0,26.0)],住院费用更低[万元:3.46(2.88,5.18)对4.58(3.08,6.06)],支气管肺发育不良(BPD)发生率更低(11.9%对28.8%),差异均有统计学意义(均P<0.05)。
除GA、性别、剖宫产、胎膜早破、妊娠期糖尿病及新生儿窒息外,父亲吸烟(孕期母亲暴露于烟雾)是早产儿RDS的重要危险因素。产前使用DEX预防早产儿RDS的疗效受多种因素影响,如产前烟雾暴露、使用时机、多胎妊娠等。牛PS联合布地奈德混悬液在降低BPD发生率方面优于固尔苏注射液。