Evidence map›Paper›PMID 42770071›Full record

ArticleSage open chronic disease

Insights from strengthening perinatal hepatitis b prevention in healthcare facilities in Delta State, Nigeria: A prospective, pilot implementation intervention.

Prince Ochuko Okinedo, Catherine Freeland, Ehimario U Igumbor, Samuel Okwuchukwu Ilikannu, Funso Joshua Eniojukan, Ngozi Roy Maduka, Gregsonil Ogheneruemu Idibofu, Linda Peter-Enyi, Kevin Igweh, Dafe Akokotu and 11 more

Abstract read
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Article in Sage open chronic disease. 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

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.

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3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

21 authors.

Prince Ochuko OkinedoHepatitis Advocacy Foundation (HAF), Delta State, Asaba, Delta State, Nigeria.ORCID https://orcid.org/0009-0009-3961-3780
Catherine FreelandHepatitis B Foundation (HBF), Doylestown, PA, USA.ORCID https://orcid.org/0000-0002-1876-2105
Ehimario U IgumborCentre for Infectious Disease Research, Nigerian Institute of Medical Research (NIMR), Lagos, Nigeria.ORCID https://orcid.org/0000-0002-6313-6031
Samuel Okwuchukwu IlikannuDepartment of Obstetrics and Gynaecology, Federal Medical Centre, Asaba, Delta State, Nigeria.
Funso Joshua EniojukanDepartment of Clinical Pharmacy and Pharmacy Practice, Faculty of Pharmacy, Niger Delta University, Wilberforce Island, Amassoma, Bayelsa State, Nigeria.
Ngozi Roy MadukaDepartment of Obstetrics and Gynaecology, Central Hospital, Agbor, Delta State, Nigeria.ORCID https://orcid.org/0009-0007-0451-2635
Gregsonil Ogheneruemu IdibofuHepatitis Advocacy Foundation (HAF), Delta State, Asaba, Delta State, Nigeria.
Linda Peter-EnyiDepartment of Public Health, Delta State Ministry of Health, Asaba, Nigeria.
Kevin IgwehDepartment of Public Health, Delta State Ministry of Health, Asaba, Nigeria.
Dafe AkokotuDepartment of Pharmaceutical Services, Central Hospital, Agbor, Delta State, Nigeria.
Sabastine EdokpayiDepartment of Obstetrics and Gynaecology, Central Hospital, Agbor, Delta State, Nigeria.
Anita AbifadeHepatitis Advocacy Foundation (HAF), Delta State, Asaba, Delta State, Nigeria.
Sandra IgahDepartment of Public Health, Delta State Ministry of Health, Asaba, Nigeria.
Ossai Abaniwa TheresaDepartment of Nursing Services, General Hospital, Ozoro, Delta State, Nigeria.
Aki-Famous BettyDepartment of Laboratory Services, General Hospital, Ozoro and Central Hospital, Sapele, Delta State, Nigeria.
Victoria IdegbesorDepartment of Laboratory Services, Central Hospital, Warri, Delta State, Nigeria.
Ubiri ObaherhekreDepartment of Pharmaceutical Services, Central Hospital, Sapele, Delta State, Nigeria.
Idanesi O StellaDepartment of Nursing Services, Central Hospital, Warri, Delta State, Nigeria.
Kelechi OkorieDepartment of Laboratory Services, Asaba Specialist Hospital, Asaba, Delta State, Nigeria.
Kiyem Vivian WamariDepartment of Nursing Services, Central Hospital, Agbor, Delta State, Nigeria.
Christian TetsolaDepartment of Public Health, Delta State Ministry of Health, Asaba, Nigeria.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Hepatitis B virus (HBV) infection is a leading cause of chronic liver disease and cancer globally, with perinatal transmission representing the predominant route of new infections in high-burden countries such as Nigeria. Despite significant prevalence, screening, diagnosis, and timely intervention for HBV among pregnant women remain suboptimal in Nigeria, contributing to ongoing morbidity and mortality. Objectives: This analysis assessed the impact of interventions to reduce perinatal HBV transmission in five pilot health facilities in Delta State, Nigeria. It evaluated HBV and HCV prevalence among pregnant women, timing of antenatal care (ANC) booking, linkage to care for HBV-positive women, and HepB birth dose (HepB-BD) vaccination coverage and timeliness. Design: The project design was a prospective implementation research which involved a cohort of pregnant women registered for ANC in the five pilot healthcare facilities strategically located across the three senatorial districts of Delta State, Nigeria. These facilities were all high-volume public facilities located and were carefully chosen to ensure representation across different regions of Delta State, providing a diverse perspective on the project's implementation and impact. The selected facilities provide secondary and tertiary care services. Methods: All pregnant women at five health facilities were screened at their first ANC visit for HBV and HCV using rapid testing. HBV-positive women were linked to care and initiated on tenofovir disoproxil fumarate (TDF) prophylaxis. The proportion of newborns receiving timely HepB-BD vaccination (within 24 h of birth) was measured pre- and post-intervention. Statistical analysis was performed using paired Results: A total of 2844 pregnant women were screened for HBV and HCV. The pooled prevalence of HBV infection among the study population was found to be 1.86% (95% CI: 1.35%-2.37%), six times higher than HCV (0.3%). A Chi-squared test for homogeneity was conducted to determine if the proportion of HBV-reactive individuals varied significantly across the five facilities. The test revealed a statistically significant difference in HBV prevalence across facilities (χ Conclusion: Project StopHepB interventions significantly improved early identification, linkage to care, and timely HepB-BD vaccination, effectively closing gaps in HBV prevention of perinatal transmission. These findings support the scale-up of similar interventions to advance HBV elimination goals across other facilities in the state, in Nigeria, and to prevent new HBV infections in the future.

Indexed as

global public healthhepatitis Bhepatitis B birth dose (HepB-BD)implementation sciencemother-to-child transmission (MTCT)perinatal preventionprevention

Identifiers

PMID42770071
PMCPMC13592438

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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.