Evidence map›Paper›PMID 38953228›Full record

ArticleJournal of paediatrics and child health2024

Prevention of vertical transmission of hepatitis B: A retrospective review of a 5-year maternal-infant cohort in London.

Elizabeth O'Mahony, Sophie Raghunanan, Ashley Brown, Caroline Foster

Abstract read
In one paragraph

Article in Journal of paediatrics and child health, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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0 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Elizabeth O'MahonyOxford Vaccine Group, Department of Paediatrics, University of Oxford University - Medical Sciences, Oxford, United Kingdom.ORCID 0000-0001-8168-8182
Sophie RaghunananDepartment of Paediatric Infectious Diseases, Imperial College Healthcare NHS Trust, London, United Kingdom.
Ashley BrownDepartment of Hepatology, Imperial College London, Imperial College NIHR BRC, London, United Kingdom.
Caroline FosterDepartment of Paediatric Infectious Diseases, Imperial College Healthcare NHS Trust, London, United Kingdom.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimsThe World Health Organization (WHO) estimates that 3.5% of the population live with hepatitis B virus (HBV); migrants to Europe are disproportionately affected. UK birth dose HBV vaccination is limited to infants born to those living with HBV (LWHBV). High-risk infants (high maternal infectivity, low birthweight) also receive HBV immunoglobulin (HBIG). The Family Hepatitis Clinic follows infants and those LWHBV working towards WHO goals of combating viral hepatitis by 2030.

methodsA trust-wide electronic note review of outcomes for infants born to those LWHBV (2016-2020).

resultsTwo hundred and eighty-three infants, 134 (47%) females, born to those LWHBV were referred. Two hundred and thirty-one (82%) attended follow-up with a vertical transmission rate of 0%. Twenty (7%) individuals LWHBV received tenofovir disoproxil fumerate in pregnancy; median viral load (VL) at initiation 125 416 376 DNA IU/mL, one having birth VL. Twenty-eight (10%) infants were stratified as high risk and all received HBIG and birth dose vaccination with 9 (32%) subsequently lost to follow-up, compared to 48 (19%) low-risk infants. 267/283 (94%) had birth dose vaccination documented and 206/283 (73%) received at least four vaccine doses. 215/283 (76%) infants had serology by 24 months; 17 (6%) with suboptimal vaccine responses: hepatitis B surface antibody <100 IU/mL. Serology before 18 months resulted in higher rates of maternal hepatitis B core antibody detection (15% vs. 3%).

conclusionPrevention of vertical transmission of HBV was universal in those attending, although high-risk infants were more likely lost to follow up. HBV post-vaccine serological protection was comparable with national data from 2021 (77% >4 doses, 77% HBsAb >100).

Indexed as

Hepatitis BInfectious Disease Transmission, VerticalAdultFemaleHepatitis B VaccinesHumansImmunoglobulinsInfantInfant, NewbornLondonMalePregnancyPregnancy Complications, InfectiousRetrospective StudiesHepatitis B VaccinesImmunoglobulinshepatitis Bhepatitis B birth dose vaccinationhepatitis B immunoglobulin (HBIG)tenofovir disoproxil fumerate (TDF)vertical transmission

Identifiers

PMID38953228
PMCPMC11656667

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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.