Evidence map›Paper›PMID 40826403›Full record

ArticleBMC public health2025

Parents' perspectives of the new neonatal BCG vaccination pathway in England: a qualitative study.

Kate Bisset, Georgia Chisnall, Colin N J Campbell, Vanessa Saliba, Sandra Mounier-Jack, Tracey Chantler

Abstract read
In one paragraph

Article in BMC public health, 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

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2 · The registry

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Kate BissetLondon School of Hygiene and Tropical Medicine, London, UK. kate.bisset2@nhs.net.
Georgia ChisnallLondon School of Hygiene and Tropical Medicine, London, UK.
Colin N J CampbellUK Health Security Agency, London, UK.
Vanessa SalibaUK Health Security Agency, London, UK.
Sandra Mounier-JackLondon School of Hygiene and Tropical Medicine, London, UK.
Tracey ChantlerLondon School of Hygiene and Tropical Medicine, London, UK. Tracey.Chantler@lshtm.ac.uk.

Funding

National Institute for Health and Care Research NIHR200929
6 · The paper itself

Abstract

backgroundThe neonatal Bacillus Calmette-Guérin (BCG) selective vaccination pathway in England was revised in September 2021 due to the introduction of a national evaluation of newborn screening for Severe Combined Immunodeficiency (SCID). BCG is a live attenuated vaccine that is contraindicated in infants with SCID, hence BCG vaccination was moved from soon after birth to after SCID results were available, typically at 14-17 days. The transition also shifted vaccination delivery from maternity units to community clinics, raising concerns about potential barriers to access and lower vaccine uptake. This study explored parents' experiences of navigating the new neonatal BCG vaccination pathway and identified access barriers and enablers.

methodsA qualitative study was conducted involving semi-structured interviews with 30 parents of infants eligible (or invited) for BCG vaccination in two urban areas where SCID screening was implemented. Participants were recruited through vaccine providers and community centres. Thematic analysis of interview transcripts was conducted using the 'Framework Method', incorporating an inductive approach.

resultsParents were unaware of SCID screening and the changes to the neonatal BCG vaccination schedule and encountered diverse challenges in accessing the vaccine. Assessment errors led to eligibility confusion, with some ineligible infants receiving vaccine invitations. Many parents first learned about BCG vaccination on the postnatal ward, describing it as a "surprise vaccine," with limited antenatal discussion diminishing informed decision-making. Appointment notification systems were inconsistent, with some parents receiving short-notice invitations or no notification at all. Physical access barriers included unfamiliar and distant clinic locations, transport, and the physical challenges of traveling soon after birth with a newborn. Parents with limited social support or financial constraints faced additional difficulties.

conclusionParents were generally accepting of the need to amend the BCG timeline on account of SCID screening; however, we identified distinct accessibility concerns that varied from those associated with the routine immunisation programme. These barriers, and the separateness of the BCG programme from routine services, impacted parental experiences and vaccine uptake. Addressing these challenges is important to meet neonatal BCG uptake targets and support tuberculosis prevention efforts in England.

Indexed as

BCG VaccineParentsVaccinationAdultEnglandFemaleHumansInfant, NewbornInterviews as TopicMaleNeonatal ScreeningQualitative ResearchBCG VaccineEnglandNeonatal BCGParental experiencesSCID screeningTuberculosisVaccine uptake

Identifiers

PMID40826403
PMCPMC12359992

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