[地塞米松对双胎妊娠晚期早产儿短期和长期预后的影响:一项观察性研究]。

X D Zhang, Y Wei, T C Wu, Y Y Zhao, X D Liu, P B Yuan, Y Wang
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Short-term outcomes of preterm infants were analyzed, including the incidence of neonatal respiratory distress syndrome (NRDS), wet lung, hypoglycemia, neonatal septicemia, intraventricular hemorrhage (IVH), bronchopulmonary dysplasia (BPD) and neonatal necrotizing enterocolitis (NEC). \"Ages and Stages Questionnaire-Third Edition (ASQ-3) scale\" was used to follow up the late neurological development of preterm infants at the corrected age of 6-54 months, and the level of neurological development was compared. <b>Results:</b> (1) General conditions: the gestational age at delivery in the non-medication group [36.1 weeks (35.6, 36.6 weeks)] was later than that in the medication after 34 weeks group [36.1 weeks (35.2, 36.4 weeks)] and medication before 34 weeks group [35.2 weeks (34.2, 36.2 weeks)] groups, and the differences were statistically significant (all <i>P</i><0.05). 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引用次数: 0

摘要

研究目的研究产前地塞米松对双胎妊娠晚期早产儿短期预后和长期神经系统发育的影响。方法回顾性分析2019年1月至2022年12月在北京大学第三医院分娩的315例双胎妊娠孕妇及其早产儿。收集孕妇和早产儿的临床资料。他们被分为未用药组(93名孕妇和186名早产儿)、34周后用药组(123名孕妇和246名早产儿)和34周前用药组(99名孕妇和198名早产儿)。对早产儿的短期结果进行了分析,包括新生儿呼吸窘迫综合征(NRDS)、湿肺、低血糖、新生儿败血症、脑室内出血(IVH)、支气管肺发育不良(BPD)和新生儿坏死性小肠结肠炎(NEC)的发生率。采用 "年龄与分期问卷-第三版(ASQ-3)量表 "对早产儿6-54个月校正年龄的晚期神经系统发育情况进行随访,并比较神经系统发育水平。结果:(1)一般情况:未用药组[36.1周(35.6,36.6周)]的胎龄晚于34周后用药组[36.1周(35.2,36.4周)]和34周前用药组[35.2周(34.2,36.2周)],差异有统计学意义(均PH=3.808,P=0.149)。三组在性别和小于胎龄比例上无明显差异(均P>0.05)。(2)短期结果:非用药组、34 周后用药组和 34 周前用药组的湿肺发生率分别为 7.0%(13/186)、11.0%(27/246)和 16.2%(32/198),差异有统计学意义(P=0.018)。三组间的 NRDS、低血糖、败血症、IVH、BPD 和 NEC 发生率无明显差异(均 P>0.05)。以胎龄和新生儿出生体重为混杂因素的逻辑回归分析显示,胎龄过早(OR=0.884,95%CI:0.837-0.933,POR=2.967,95%CI:1.153-7.639,P=0.024)均可导致湿肺发生率增加。(3)长期结局:共有109名孕妇完成了随访,218名早产儿在随访结束时的矫正年龄为6-54个月,其中非用药组86例,34周后用药组66例,34周前用药组66例。三组婴儿在沟通、粗大运动、精细运动、解决问题和个人社交方面的得分无明显差异(均为 P>0.05)。结论产前服用一个疗程的地塞米松不会影响双胎晚期早产儿的新生儿出生体重和短期预后,也不会对纠正年龄为 6-54 个月的双胎晚期早产儿的神经系统发育产生不良影响。
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[Effects of dexamethasone on short-term and long-term outcomes in late preterm infants with twin pregnancy: an observational study].

Objective: To investigate the effect of prenatal dexamethasone on short-term outcomes and long-term neurological development in late preterm infants with twin pregnancy. Methods: A total of 315 pregnant women with twin pregnancy and their preterm infants who delivered in Peking University Third Hospital from January 2019 to December 2022 were retrospectively analyzed. The clinical data of pregnant women and preterm infants were collected. They were divided into non-medication group (93 pregnant women and 186 preterm infants), medication after 34 weeks group (123 pregnant women and 246 preterm infants), and medication before 34 weeks group (99 pregnant women and 198 preterm infants). Short-term outcomes of preterm infants were analyzed, including the incidence of neonatal respiratory distress syndrome (NRDS), wet lung, hypoglycemia, neonatal septicemia, intraventricular hemorrhage (IVH), bronchopulmonary dysplasia (BPD) and neonatal necrotizing enterocolitis (NEC). "Ages and Stages Questionnaire-Third Edition (ASQ-3) scale" was used to follow up the late neurological development of preterm infants at the corrected age of 6-54 months, and the level of neurological development was compared. Results: (1) General conditions: the gestational age at delivery in the non-medication group [36.1 weeks (35.6, 36.6 weeks)] was later than that in the medication after 34 weeks group [36.1 weeks (35.2, 36.4 weeks)] and medication before 34 weeks group [35.2 weeks (34.2, 36.2 weeks)] groups, and the differences were statistically significant (all P<0.05). After correcting for gestational age, there was no significant difference in birth weight among the three groups (H=3.808, P=0.149). There were no significant differences in gender and the proportion of small for gestational age among the three groups (all P>0.05). (2) Short-term outcome: the incidence of wet lung was 7.0% (13/186), 11.0% (27/246) and 16.2% (32/198) in the non-medication group, medication after 34 weeks group and medication before 34 weeks group, respectively, and the difference was statistically significant (P=0.018). There were no significant differences in the incidence rates of NRDS, hypoglycemia, sepsis, IVH, BPD, and NEC among the three groups (all P>0.05). Logistic regression analysis with gestational age and newborn birth weight as confounding factors showed that early gestational age (OR=0.884, 95%CI: 0.837-0.933, P<0.001) and increased incidence of selective intrauterine growth restriction type I (OR=2.967, 95%CI: 1.153-7.639, P=0.024) could both lead to an increased incidence of wet lung. (3) Long-term outcomes: a total of 109 pregnant women completed the follow-up, and 218 preterm infants with a corrected age of 6-54 months at the end of follow-up were enrolled, including 86 cases in the non-medication group, 66 cases in the medication after 34 weeks group, and 66 cases in the medication before 34 weeks group. There were no significant differences in the scores of communication, gross motor, fine motor, problem solving and personal-social among the three groups (all P>0.05). Conclusion: Prenatal administration of a single course of dexamethasone does not affect the neonatal birth weight and short-term outcomes of twin late preterm infants, and has no adverse effect on the neurological development of twin late preterm infants with a corrected age of 6-54 months.

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