4.5 Article

Do maternal demographics and prenatal history impact the efficacy of betamethasone therapy for threatened preterm labor?

期刊

BMC PREGNANCY AND CHILDBIRTH
卷 21, 期 1, 页码 -

出版社

BMC
DOI: 10.1186/s12884-021-03949-5

关键词

Betamethasone; Antenatal corticosteroids; Preterm birth; Respiratory distress syndrome (RDS); Cesarean

资金

  1. Indiana Clinical and Translational Sciences Institute
  2. National Institutes of Health [UL1TR002529]
  3. NICHD [R01HD088014]

向作者/读者索取更多资源

Among women receiving antenatal betamethasone therapy, cesarean delivery was the only maternal factor associated with neonatal respiratory distress syndrome (RDS). However, preterm premature rupture of membranes (PPROM) was negatively associated with RDS rates among women delivering within 14 days of betamethasone dosing. Other maternal characteristics such as age, BMI, race, and ethnicity were not significantly associated with RDS.
Background Betamethasone (BMZ) is used to accelerate fetal lung maturation in women with threatened preterm birth, but its efficacy is variable and limited by the lack of patient individualization in its dosing and administration. To determine sources of variability and potential opportunities for individualization of therapy, the objective of this study was to evaluate maternal factors associated with development of neonatal respiratory distress syndrome (RDS) in a cohort of women who received betamethasone. Methods This study prospectively enrolled women, gestational ages 23-34 weeks, who received betamethasone for threatened preterm birth. Maternal demographics, prenatal history, and neonatal outcomes were abstracted from hospital records. RDS was the primary outcome. Associations between RDS diagnosis and maternal demographics, prenatal history, and betamethasone dosing were evaluated in a case-control analysis and multivariable regression adjusted for gestational age at delivery. Secondary analyses limited the cohort to women who delivered within 1 or 2 weeks of betamethasone dosing. Results Of 209 deliveries, 90 (43 %) resulted in neonatal RDS. Within the overall cohort and controlling for gestational age at birth, RDS was only associated with cesarean births compared to vaginal births (adjusted OR 1.17 [1.06-1.29]). Route of delivery was also the only significant factor related to RDS in the 83 neonates delivered within 7 days of BMZ dosing. However, among 101 deliveries within 14 days of betamethasone dosing and controlling for gestational age at birth, women who experienced preterm premature rupture of membranes (PPROM) had lower RDS rates than those without PPROM (57.9 % vs. 80.2 %, adjusted OR 0.81 [0.67-0.99]). Maternal age, BMI, race, and ethnicity were not associated with RDS in the regression models. Conclusions Of maternal characteristics analyzed, only delivery by cesarean was associated with neonatal RDS after antenatal betamethasone use.

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