Related Experiment Video
Updated: May 23, 2025

Assessment and Evaluation of the High Risk Neonate: The NICU Network Neurobehavioral Scale
Published on: August 25, 2014
Timing of Antenatal Corticosteroid Administration and Neonatal Outcomes
Nir Melamed1, Kellie E Murphy2, Christy Pylypjuk3
1Division of Maternal-Fetal Medicine, Department of Obstetrics and Gynaecology, Sunnybrook Health Sciences Centre, Temerty Faculty of Medicine, University of Toronto, Toronto, Ontario, Canada.
Insights
Antenatal corticosteroids (ACS) reduce neonatal mortality when given 12 hours to 14 days before birth, a wider window than previously thought. This finding impacts timing for imminent preterm births and repeat ACS courses.
Area of Science:
- Neonatal Medicine
- Obstetrics
- Pharmacology
Background:
- Antenatal corticosteroids (ACS) are crucial for reducing neonatal mortality and morbidity associated with preterm birth.
- The optimal timing for ACS administration to maximize benefits remains incompletely defined, with current guidelines suggesting 1-7 days prior to delivery.
Purpose of the Study:
- To investigate the association between the interval from antenatal corticosteroid (ACS) administration to birth and neonatal outcomes in preterm neonates.
- To determine if the established optimal timing of 1-7 days for ACS administration is accurate.
Main Methods:
- A national retrospective cohort study analyzed data from 7950 preterm neonates (23-31 weeks gestation) born between 2018-2021.
- Restricted cubic splines modeled the association between the ACS-to-birth interval and neonatal mortality, as well as a composite of mortality or severe neurologic injury.
Main Results:
- ACS administration was linked to reduced neonatal mortality starting as early as 2 hours post-dose.
- The greatest mortality reduction was observed with intervals between 12 hours and 14 days.
- This benefit persisted for two weeks and was not affected by gestational age or plurality.
Conclusions:
- ACS administration is associated with reduced neonatal mortality from 2 hours up to 14 days after the first dose.
- The optimal interval for ACS benefit is wider than the traditional 1-7 days, extending up to 14 days.
- These findings support ACS administration even with imminent preterm birth and inform timing for repeat doses.
Importance:
Antenatal corticosteroids (ACS) are accepted to be most effective in reducing prematurity-related neonatal mortality and morbidity when administered 1 to 7 days before birth. However, precise data on the optimal timing of administration are scarce.
Objective:
To investigate the association between ACS administration to birth interval as a continuous variable and neonatal outcomes among preterm neonates.
Design, Setting, And Participants:
This national retrospective cohort study was conducted from 2018 to 2021 at level III neonatal intensive care units participating in the Canadian Neonatal Network. Participants included singleton and twin neonates born from 23 weeks 0 days' to 31 weeks 6 days' gestation. Data were analyzed from November 29, 2023, to March 8, 2024.
Exposure:
ACS administration to birth interval.
Main Outcomes And Measures:
The primary outcome was neonatal mortality. The secondary outcome was a composite of mortality or severe neurologic injury. Associations of the ACS administration to birth interval with the study outcomes were modeled using restricted cubic splines with 5 knots.
Results:
A total of 7950 neonates met the study criteria, from 7124 pregnancies (mean [SD] maternal age, 31.1 [5.7] years). Compared with individuals who received ACS, those who did not were younger and had lower rates of nulliparity, twin pregnancy, hypertension, and gestational diabetes. The overall rates of neonatal mortality and the composite outcome were 8% (670 of 7950) and 14% (1132 of 7950), respectively. ACS exposure was associated with reduced neonatal mortality as early as 2 hours after administration (adjusted risk ratio [ARR], 0.83 [95% CI, 0.70-1.00]). The reduction in mortality risk increased to a plateau 12 hours following exposure (ARR, 0.56 [95% CI, 0.40-0.78]), remained stable for the first 2 weeks following exposure, and gradually decreased after that. The association with reduced mortality was no longer observed at 4 weeks after administration (ARR, 0.82 [95% CI, 0.56-1.20]), and the ARR approached the null 5 weeks after administration (ARR, 0.99 [95% CI, 0.56-1.73]). This pattern was not affected by gestational age at birth or the number of fetuses.
Conclusions And Relevance:
In this cohort of neonates born from 23 weeks 0 days' gestation to 31 weeks 6 days' gestation, ACS administration was associated with a reduction in neonatal mortality as early as 2 hours after the administration of the first dose. The interval associated with the greatest reduction in neonatal mortality was between 12 hours and 14 days before birth, which was wider than the currently accepted optimal interval of 1 to 7 days. These findings may have important clinical implications for the management of pregnancies at risk of preterm birth, particularly regarding the administration of ACS even in cases in which preterm birth is imminent, and the timing of repeat courses of ACS.
More Related Videos
Related Concept Videos
Antiasthma Drugs: Inhaled Corticosteroids and Glucocorticoids
ICS work through a multifaceted mechanism of action. They suppress the inflammatory response caused by the proliferation of TH cells. They also reduce the transcription of the IL-2 gene, which is involved in the...
Factors Affecting Drug Response: Overview
Upper Respiratory Drugs: Antitussives, Expectorants, and Mucolytics
Antitussives include codeine, dextromethorphan (Robitussin), and benzonatate (Tessalon). Codeine and dextromethorphan exert their effects centrally by suppressing the cough reflex center in the medulla. Benzonatate operates peripherally within the respiratory tract by...
Teratogenicity
Drugs for Treatment of Crohn's Disease in IBD Using Glucocorticoids
Chronopharmacokinetics: Circadian Rhythms and Influence on Drug Response
The time of drug administration is an important factor to consider, as it can influence the toxic dose of a drug. For example, a study conducted by Prins et al. in 1997 examined the effects of the timing of...

