Evidence map›Paper›PMID 40026670›Full record

ArticleBulletin of the World Health Organization2025

Hepatitis B vaccination of preterm infants and risk of bronchopulmonary dysplasia: a cohort study, Australia.

Hannah J Morgan, Marcel F Nold, Gonzalo Sepulveda Kattan, Diana Vlasenko, Atul Malhotra, James H Boyd, Hazel J Clothier, Jim P Buttery

Abstract read
In one paragraph

Article in Bulletin of the World Health Organization, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
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.

Hannah J MorganDepartment of Paediatrics, University of Melbourne, Royal Children's Hospital, 50 Flemington Road, Parkville3052, Victoria, Australia.
Marcel F NoldDepartment of Paediatrics, Monash University, Melbourne, Australia.
Gonzalo Sepulveda KattanEpidemiology Informatics, Centre for Health Analytics, Melbourne Children's Campus, Melbourne, Australia.
Diana VlasenkoEpidemiology Informatics, Centre for Health Analytics, Melbourne Children's Campus, Melbourne, Australia.
Atul MalhotraDepartment of Paediatrics, Monash University, Melbourne, Australia.
James H BoydDepartment of Public Health, La Trobe University, Melbourne, Australia.
Hazel J ClothierEpidemiology Informatics, Centre for Health Analytics, Melbourne Children's Campus, Melbourne, Australia.
Jim P ButteryDepartment of Paediatrics, University of Melbourne, Royal Children's Hospital, 50 Flemington Road, Parkville3052, Victoria, Australia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objective: To determine whether hepatitis B virus (HBV) vaccination of extremely preterm infants (defined in our study as < 29 weeks gestation) within 24 hours of birth (birth-dose) increases the risk of developing bronchopulmonary dysplasia. Methods: Using data from Australia, we conducted a population data linkage study using the Victorian Vaccine Safety Health Link. This platform links state-wide immunization and health outcomes from the Victorian Perinatal Data Collection and the Victorian Admitted Episodes Dataset. Our retrospective cohort study included all extremely preterm infants born alive during 2017-2020 (excluding data outliers). We investigated the relationship between birth-dose HBV vaccination and bronchopulmonary dysplasia diagnosis at 36 weeks postmenstrual age. We identified possible confounders using a directed acyclic graph, and included these confounders in a robust Poisson regression model. Findings: Of the 818 extremely preterm infants meeting our inclusion criteria, 306 received birth-dose HBV vaccination: 50.7% (155/306) of the vaccinated and 61.9% (317/512) of the unvaccinated infants developed bronchopulmonary dysplasia. After accounting for measured confounders, the adjusted relative risk was 0.83 (95% confidence interval, CI: 0.68-1.00), suggesting no increased risk. However, residual confounding by indication may still be present as it is not known how clinician perception of the stability of the newborn affects the decision to vaccinate or not, potentially underestimating any association between vaccination and outcome. Conclusion: Our findings support existing World Health Organization recommendations to immunize all infants against HBV within 24 hours of birth, including those born prematurely.

Indexed as

Bronchopulmonary DysplasiaHepatitis BHepatitis B VaccinesVaccinationAustraliaCohort StudiesFemaleHumansInfant, Extremely PrematureInfant, NewbornInfant, PrematureMaleRetrospective StudiesVictoriaHepatitis B Vaccines

Identifiers

PMID40026670
PMCPMC11865856

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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.