Evidence map›Paper›PMID 40388165›Full record

ArticleJAMA network open2025

Timing of Antenatal Corticosteroid Administration and Neonatal Outcomes.

Nir Melamed, Kellie E Murphy, Christy Pylypjuk, Rebecca Sherlock, Guillaume Ethier, Eugene W Yoon, Prakesh S Shah, Canadian Neonatal Network (CNN) and Canadian Preterm Birth Network (CPTBN) Investigators

Abstract read
In one paragraph

Article in JAMA network open, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

  1. KCommunications medicine · 2026
    Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Nir MelamedDivision of Maternal-Fetal Medicine, Department of Obstetrics and Gynaecology, Sunnybrook Health Sciences Centre, Temerty Faculty of Medicine, University of Toronto, Toronto, Ontario, Canada.
Kellie E MurphyDivision of Maternal-Fetal Medicine, Department of Obstetrics and Gynaecology, Mount Sinai Hospital, Temerty Faculty of Medicine, University of Toronto, Toronto, Ontario, Canada.
Christy PylypjukDepartment Obstetrics, Gynecology and Reproductive Sciences, University of Manitoba, Winnipeg, Canada.
Rebecca SherlockDepartment of Pediatrics, Surrey Memorial Hospital, University of British Columbia, Vancouver, Canada.
Guillaume EthierDepartment of Neonatology, CHU Sainte-Justine, Montreal, Quebec, Canada.
Eugene W YoonMaternal-Infant Care Research Centre (MiCare), Mount Sinai Hospital, Toronto, Ontario, Canada.
Prakesh S ShahMaternal-Infant Care Research Centre (MiCare), Mount Sinai Hospital, Toronto, Ontario, Canada.
Canadian Neonatal Network (CNN) and Canadian Preterm Birth Network (CPTBN) Investigators

Funding

CIHR
6 · The paper itself

Abstract

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.

Indexed as

Adrenal Cortex HormonesInfant MortalityPrenatal CareAdultCanadaDrug Administration ScheduleFemaleGestational AgeHumansInfant, NewbornInfant, PrematureIntensive Care Units, NeonatalMalePregnancyRetrospective StudiesTime FactorsAdrenal Cortex Hormones

Identifiers

PMID40388165
PMCPMC12090034

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.