The effects of betamethasone on clinical outcome of the late preterm neonates born between 34 and 36 weeks of gestation
- PMID: 34784898
- PMCID: PMC8594097
- DOI: 10.1186/s12884-021-04246-x
The effects of betamethasone on clinical outcome of the late preterm neonates born between 34 and 36 weeks of gestation
Abstract
Background: Prenatal corticosteroid administration in preterm labor is one of the most important treatments available to improve neonatal outcomes; however, its beneficial effects on late preterm infants (after the 34th week of gestation) remained unknown. We aimed to assess the effects of betamethasone on the clinical condition of the late preterm infants born between 34 and 36 weeks of gestation.
Methods: This retrospective cohort study was performed on 100 consecutive infants born between 34 and 36 weeks of gestation and received betamethasone before delivery as the cases and 100 neonates with the same delivery conditions but without receiving betamethasone. All neonates were followed up within hospitalization to assess the neonatal outcome.
Results: The neonates receiving betamethasone suffered more from respiratory distress syndrome (49% versus 31%, p = 0.008, RR = 1.59 95% CI (1.12-2.27)) and requiring more respiratory support (71% versus 50%, p = 0.002, RR = 1.43 95% CI (1.13-1.80)) as compared to the control group. There was no difference between the two groups in other neonatal adverse events or death.
Conclusion: the use of betamethasone in the late preterm period (after 34 weeks of gestation) has no beneficial effects on lung maturity or preventing neonatal adverse outcomes, even may lead to increase the risk for RDS and requiring respiratory support.
Keywords: Betamethasone; Late preterm; Neonatal outcome.
© 2021. The Author(s).
Conflict of interest statement
The authors declare that they have no competing interests.
Similar articles
-
Evaluation of the effect of antenatal betamethasone on neonatal respiratory morbidity in early-term elective cesarean.J Matern Fetal Neonatal Med. 2020 Jun;33(12):1994-1999. doi: 10.1080/14767058.2018.1535587. Epub 2019 Mar 5. J Matern Fetal Neonatal Med. 2020. PMID: 30836813
-
Comparison between two doses of betamethasone administration with 12 hours vs. 24 hours intervals on prevention of respiratory distress syndrome: a randomised trial.J Obstet Gynaecol. 2018 Aug;38(6):770-776. doi: 10.1080/01443615.2017.1413080. Epub 2018 Mar 12. J Obstet Gynaecol. 2018. PMID: 29526138 Clinical Trial.
-
Are newborn outcomes different for term babies who were exposed to antenatal corticosteroids?Am J Obstet Gynecol. 2021 Nov;225(5):536.e1-536.e7. doi: 10.1016/j.ajog.2021.04.251. Epub 2021 May 3. Am J Obstet Gynecol. 2021. PMID: 33957112 Free PMC article.
-
Betamethasone dosing interval at 12 or 24 h apart: A systematic review and meta-analysis.Eur J Obstet Gynecol Reprod Biol. 2025 Apr;307:164-169. doi: 10.1016/j.ejogrb.2025.02.017. Epub 2025 Feb 10. Eur J Obstet Gynecol Reprod Biol. 2025. PMID: 39938150
-
Antenatal corticosteroids beyond 34 weeks gestation: What do we do now?Am J Obstet Gynecol. 2016 Oct;215(4):423-30. doi: 10.1016/j.ajog.2016.06.023. Epub 2016 Jun 21. Am J Obstet Gynecol. 2016. PMID: 27342043 Review.
Cited by
-
Effects of Single-Course Betamethasone on the Outcomes of Late Preterm Neonates.Cureus. 2023 Oct 8;15(10):e46672. doi: 10.7759/cureus.46672. eCollection 2023 Oct. Cureus. 2023. PMID: 37942383 Free PMC article.
-
The influence of antenatal betamethasone timing on neonatal outcome in late preterm infants: a single-center cohort study.Arch Gynecol Obstet. 2025 Apr;311(4):1017-1027. doi: 10.1007/s00404-024-07714-9. Epub 2024 Sep 9. Arch Gynecol Obstet. 2025. PMID: 39249517 Free PMC article.
References
-
- Liggins GC, Howie RN. A controlled trial of antepartum glucocorticoid treatment for prevention of the respiratory distress syndrome in premature infants. Pediatrics. 1972;50(4):515–525. - PubMed
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical