Evidence map›Paper›PMID 40526733›Full record

ArticlePloS one2025

Obstetric and newborn outcomes of mothers with and without HIV infection in Anaka general hospital in Northern Uganda.

Jolly Joe Lapat, Jimmyy Opee, James Okello, Nixson Oyoo, Christopher Wanican, Gloria Becky Labong, Daniel S Ebbs, Felix Bongomin

Abstract read
In one paragraph

Article in PloS one, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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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

The trial behind it

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

8 authors.

Jolly Joe LapatDepartment of Public Health, Faculty of Medicine, Gulu, Uganda.ORCID 0000-0001-9868-7565
Jimmyy OpeeDepartment of Public Health, Faculty of Medicine, Gulu, Uganda.
James OkelloAnaka General Hospital, Nwoya District Local Government, Gulu, Uganda.
Nixson OyooDepartment of Public Health, Faculty of Medicine, Gulu, Uganda.
Christopher WanicanAnaka General Hospital, Nwoya District Local Government, Gulu, Uganda.
Gloria Becky LabongAnaka General Hospital, Nwoya District Local Government, Gulu, Uganda.
Daniel S EbbsSection of Critical Care Medicine, Department of Paediatrics, Yale University, New Haven, Connecticut, United States of America.
Felix BongominDepartment of Public Health, Faculty of Medicine, Gulu, Uganda.

Funding

Minnesota-Makerere-Mbarara Neuro-Infectious Disease Research Training ConsortiumD43TW012266 · FIC · UNIVERSITY OF MINNESOTA · PI David R Boulware, David Bisagaya Meya · 2024 to 2026
$747k
FIC NIH HHS D43 TW012266
6 · The paper itself

Abstract

backgroundWomen of reproductive age constitute a significant proportion of the global HIV burden, with millions becoming pregnant while on lifelong antiretroviral therapy (ART). Although ART has dramatically improved maternal and child health outcomes, concerns persist regarding its safety in pregnancy. This study compares obstetric and neonatal outcomes between women with and without HIV infection at Anaka General Hospital, a rural hospital in northern Uganda.

methodsA hospital-based retrospective cross-sectional study at Anaka General Hospital in northern Uganda was conducted from July 2020 to June 2023. A total of 914 delivery records were included, sampled using systematic random sampling from the hospital maternity register. Data were extracted from maternity and neonatal records using a structured tool. Associations between HIV status and obstetric or neonatal outcomes were assessed using Chi-square or Fisher's exact tests for categorical variables and independent sample t-tests for continuous variables. Multivariable logistic regression was used to adjust for potential confounders and a p < 0.05 was considered statistically significant.

resultsOf the 914 participants included in the study 38 (4.2%) were HIV-positive. The odds of congenital anomalies were significantly higher among infants born to HIV-positive women compared with HIV-negative women (adjusted odds ratio = 9.76, 95% confidence interval: 1.72-55.48, p < 0.01). No significant differences were observed in maternal or neonatal outcomes between the two groups.

conclusionHIV infection was significantly associated with an increased risk of congenital anomalies, while other obstetric and neonatal outcomes were similar between HIV-positive and HIV-negative women. We recommend enhanced prenatal monitoring and early fetal screening among HIV-positive pregnant women on dolutegravir-based ART. Additionally, prospective studies are needed to better understand the contribution of dolutegravir and maternal factors to congenital anomalies in HIV-exposed pregnancies.

Indexed as

HIV InfectionsPregnancy Complications, InfectiousAdultAnti-HIV AgentsCross-Sectional StudiesFemaleHospitals, GeneralHumansInfant, NewbornInfectious Disease Transmission, VerticalPregnancyPregnancy OutcomeRetrospective StudiesUgandaYoung AdultAnti-HIV Agents

Identifiers

PMID40526733
PMCPMC12173179

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