Fabrizio Zullo MD , Moti Gulersen MD, MSc , Daniele Di Mascio MD , Stephanie C. Roth MLIS , Teresa C. Logue MD, MPH , Giuseppe Rizzo MD , Antonella Giancotti MD , Hector Mendez Figueroa MD , Anthony C. Sciscione DO , Gabriele Saccone MD, PhD , Suneet P. Chauhan MD, Hon, DSc , Vincenzo Berghella MD
{"title":"Antenatal corticosteroids for patients at risk of late preterm birth: a systematic review and meta-analysis of randomized controlled trials","authors":"Fabrizio Zullo MD , Moti Gulersen MD, MSc , Daniele Di Mascio MD , Stephanie C. Roth MLIS , Teresa C. Logue MD, MPH , Giuseppe Rizzo MD , Antonella Giancotti MD , Hector Mendez Figueroa MD , Anthony C. Sciscione DO , Gabriele Saccone MD, PhD , Suneet P. Chauhan MD, Hon, DSc , Vincenzo Berghella MD","doi":"10.1016/j.ajogmf.2025.101709","DOIUrl":null,"url":null,"abstract":"<div><h3>Objective</h3><div>To evaluate the effectiveness of antenatal corticosteroid administration in the late preterm period (34 0/7–36 6/7 weeks of gestation).</div></div><div><h3>Data Sources</h3><div>A Medical Librarian performed a search in the following databases and grey literature sources from inception until July 15, 2024: PubMed (NLM), Embase.com (Elsevier), Scopus (Elsevier), Cochrane CENTRAL (Wiley), CINAHL Ultimate (EBSCOHost), ClinicalTrials.gov and WHO ICTRP.</div></div><div><h3>Eligibility criteria for selecting studies</h3><div>This study screened studies using 2 independent reviewers based on the predefined inclusion/exclusions criteria. This study included randomized controlled trials (RCTs) comparing antenatal corticosteroid administration with placebo or with no treatment given to individuals with singleton gestations at 34 0/7–36 6/7 weeks.</div></div><div><h3>Study appraisal and synthesis methods</h3><div>This study appraised the included randomized controlled trials using 2 independent reviewers based on the Cochrane RoB 2 tool and other assessment measures. The primary outcome was the incidence of respiratory distress syndrome (RDS) (6 trials, 5163 newborns). Secondary outcomes included hypoglycemia (as defined by each trial) (4 trials, 4750 newborns), incidence of transient tachypnea of the newborn (TTN) (4 trials, 4292 newborns), neonatal intensive care unit (NICU) admission (6 trials, 5169 newborns), continuous positive airway pressure (CPAP) use for ≥2 hours (4 trials, 4760 newborns), surfactant administration (2 trials, 3100 newborns), neonatal sepsis (4 trials, 4754 newborns), neonatal mortality (5 trials, 4920 newborns), need for resuscitation in the labor suite (4 trials, 4647 newborns), hyperbilirubinemia (2 trials, 1156 newborns), necrotizing enterocolitis (NEC) (2 trials, 3710 newborns), mechanical ventilation (5 trials, 5069 newborns) and Apgar Score at 5 minutes of life (2 trials) and maternal outcomes. The summary measures were reported as relative risk (RR) or as mean difference (MD) with 95% of confidence interval (CI) using the random effects model of DerSimonian and Laird. I-squared(Higgins I<sup>2</sup>) greater than 0% was used to identify heterogeneity.</div></div><div><h3>Results</h3><div>Six RCTs, encompassing 5143 deliveries, were included for analysis. The incidence of RDS was similar in the 2 groups (RR 0.89, 95% CI 0.68–1.16), as was the rate of transient tachypnea of the newborn (TTN) (RR 0.93, 95% CI 0.67–1.29). Antenatal corticosteroids significantly reduced the use of CPAP ≥2 hours (RR 0.78, 95% CI 0.65–0.94; <em>P=.</em>007) and surfactant (RR 0.61, 95% CI 0.38-0.99; <em>P=.</em>04) compared to the control. There were no significant differences in mechanical ventilation (RR 0.75, 95% CI 0.51–1.11), NICU admission rate (RR 0.92, 95% CI 0.82–1.03), hypoglycemia (RR 1.28 95% CI 0.93–1.74) neonatal death (RR 0.94, 95% CI 0.34–2.63), Apgar Score at 5 min (MD 0.07 95% CI 95% –0.03, 0.17) between the 2 groups. The need for resuscitation, incidence of neonatal sepsis, hyperbilirubinemia, neonatal enterocolitis, cesarean delivery, chorioamnionitis, fever and postpartum endometritis were also similar between the 2 groups.</div></div><div><h3>Conclusions</h3><div>Antenatal corticosteroids administered between 34 0/7–36 6/7 weeks of gestation in patients at risk of preterm birth do not reduce RDS but reduce the use of CPAP for more than 2 hours and surfactant.</div></div><div><h3>Systematic review registration</h3><div>CRD42024548167.</div></div>","PeriodicalId":36186,"journal":{"name":"American Journal of Obstetrics & Gynecology Mfm","volume":"7 8","pages":"Article 101709"},"PeriodicalIF":3.1000,"publicationDate":"2025-05-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"American Journal of Obstetrics & Gynecology Mfm","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2589933325001090","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"OBSTETRICS & GYNECOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Objective
To evaluate the effectiveness of antenatal corticosteroid administration in the late preterm period (34 0/7–36 6/7 weeks of gestation).
Data Sources
A Medical Librarian performed a search in the following databases and grey literature sources from inception until July 15, 2024: PubMed (NLM), Embase.com (Elsevier), Scopus (Elsevier), Cochrane CENTRAL (Wiley), CINAHL Ultimate (EBSCOHost), ClinicalTrials.gov and WHO ICTRP.
Eligibility criteria for selecting studies
This study screened studies using 2 independent reviewers based on the predefined inclusion/exclusions criteria. This study included randomized controlled trials (RCTs) comparing antenatal corticosteroid administration with placebo or with no treatment given to individuals with singleton gestations at 34 0/7–36 6/7 weeks.
Study appraisal and synthesis methods
This study appraised the included randomized controlled trials using 2 independent reviewers based on the Cochrane RoB 2 tool and other assessment measures. The primary outcome was the incidence of respiratory distress syndrome (RDS) (6 trials, 5163 newborns). Secondary outcomes included hypoglycemia (as defined by each trial) (4 trials, 4750 newborns), incidence of transient tachypnea of the newborn (TTN) (4 trials, 4292 newborns), neonatal intensive care unit (NICU) admission (6 trials, 5169 newborns), continuous positive airway pressure (CPAP) use for ≥2 hours (4 trials, 4760 newborns), surfactant administration (2 trials, 3100 newborns), neonatal sepsis (4 trials, 4754 newborns), neonatal mortality (5 trials, 4920 newborns), need for resuscitation in the labor suite (4 trials, 4647 newborns), hyperbilirubinemia (2 trials, 1156 newborns), necrotizing enterocolitis (NEC) (2 trials, 3710 newborns), mechanical ventilation (5 trials, 5069 newborns) and Apgar Score at 5 minutes of life (2 trials) and maternal outcomes. The summary measures were reported as relative risk (RR) or as mean difference (MD) with 95% of confidence interval (CI) using the random effects model of DerSimonian and Laird. I-squared(Higgins I2) greater than 0% was used to identify heterogeneity.
Results
Six RCTs, encompassing 5143 deliveries, were included for analysis. The incidence of RDS was similar in the 2 groups (RR 0.89, 95% CI 0.68–1.16), as was the rate of transient tachypnea of the newborn (TTN) (RR 0.93, 95% CI 0.67–1.29). Antenatal corticosteroids significantly reduced the use of CPAP ≥2 hours (RR 0.78, 95% CI 0.65–0.94; P=.007) and surfactant (RR 0.61, 95% CI 0.38-0.99; P=.04) compared to the control. There were no significant differences in mechanical ventilation (RR 0.75, 95% CI 0.51–1.11), NICU admission rate (RR 0.92, 95% CI 0.82–1.03), hypoglycemia (RR 1.28 95% CI 0.93–1.74) neonatal death (RR 0.94, 95% CI 0.34–2.63), Apgar Score at 5 min (MD 0.07 95% CI 95% –0.03, 0.17) between the 2 groups. The need for resuscitation, incidence of neonatal sepsis, hyperbilirubinemia, neonatal enterocolitis, cesarean delivery, chorioamnionitis, fever and postpartum endometritis were also similar between the 2 groups.
Conclusions
Antenatal corticosteroids administered between 34 0/7–36 6/7 weeks of gestation in patients at risk of preterm birth do not reduce RDS but reduce the use of CPAP for more than 2 hours and surfactant.
期刊介绍:
The American Journal of Obstetrics and Gynecology (AJOG) is a highly esteemed publication with two companion titles. One of these is the American Journal of Obstetrics and Gynecology Maternal-Fetal Medicine (AJOG MFM), which is dedicated to the latest research in the field of maternal-fetal medicine, specifically concerning high-risk pregnancies. The journal encompasses a wide range of topics, including:
Maternal Complications: It addresses significant studies that have the potential to change clinical practice regarding complications faced by pregnant women.
Fetal Complications: The journal covers prenatal diagnosis, ultrasound, and genetic issues related to the fetus, providing insights into the management and care of fetal health.
Prenatal Care: It discusses the best practices in prenatal care to ensure the health and well-being of both the mother and the unborn child.
Intrapartum Care: It provides guidance on the care provided during the childbirth process, which is critical for the safety of both mother and baby.
Postpartum Issues: The journal also tackles issues that arise after childbirth, focusing on the postpartum period and its implications for maternal health. AJOG MFM serves as a reliable forum for peer-reviewed research, with a preference for randomized trials and meta-analyses. The goal is to equip researchers and clinicians with the most current information and evidence-based strategies to effectively manage high-risk pregnancies and to provide the best possible care for mothers and their unborn children.