Evidence map›Paper›PMID 41862836›Full record

ArticleBMC infectious diseases2026

Clinical outcomes and survival of HIV exposed children at 18 months in post-conflict region: insight from the Panzi Interdisciplinary PMTCT cohort (Panzi IPC) study.

Berckmans Mukanire Ntakwinja, Patrick D M C Katoto, Lampard Omari Mukanga, Mireille A M Kakubu, Benjamin Tshizubu, Mamadou Sakho, Aline Byabene, Jacques L Tamuzi, Parvine Bisimwa, Bihehe Masemo and 3 more

Abstract read
In one paragraph

Article in BMC infectious diseases, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

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

13 authors.

Berckmans Mukanire NtakwinjaDepartment of Gynaecology and Obstetrics Panzi General Referral Hospital and Medicine School of Evangelical University in Africa, Bukavu, Democratic Republic of Congo.
Patrick D M C KatotoDepartment of Internal Medicine and Centre for Tropical Diseases and Global Health, Catholic University of Bukavu, Bukavu, Democratic Republic of Congo.
Lampard Omari MukangaDepartement of Statistics Panzi General Referral Hospital, Bukavu, Democratic Republic of Congo. lampard.mukangaomari24@gmail.com.
Mireille A M KakubuDepartment of Internal Medicine and Centre for Tropical Diseases and Global Health, Catholic University of Bukavu, Bukavu, Democratic Republic of Congo.
Benjamin TshizubuUNAIDS Country Office and Regional Support Team, Goma, Western and Central Africa, Democratic Republic of Congo.
Mamadou SakhoUNAIDS Country Office and Regional Support Team, Goma, Western and Central Africa, Democratic Republic of Congo.
Aline ByabeneDepartment of Internal Medicine Panzi General Reference Hospital and Medicine School of Evangelical University in Africa, Bukavu, Democratic Republic of Congo.
Jacques L TamuziDivision of Epidemiology & Biostatistics, Department of Global Health, Faculty of Medicine and Health Sciences, Stellenbosch University, Cape Town, South Africa.
Parvine BisimwaDepartment of Internal Medicine Panzi General Reference Hospital and Medicine School of Evangelical University in Africa, Bukavu, Democratic Republic of Congo.
Bihehe MasemoDepartment of Internal Medicine Panzi General Reference Hospital and Medicine School of Evangelical University in Africa, Bukavu, Democratic Republic of Congo.
Mambo MwiloDepartment of Pediatrics, Panzi General Referral Hospital, and Medicine School of Evangelical University in Africa, Bukavu, Democratic Republic of Congo.
Birindwa ArchippeDepartment of Pediatrics, Panzi General Referral Hospital, and Medicine School of Evangelical University in Africa, Bukavu, Democratic Republic of Congo.
Denis MukwegeDepartment of Gynaecology and Obstetrics Panzi General Referral Hospital and Medicine School of Evangelical University in Africa, Bukavu, Democratic Republic of Congo.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundVertical transmission is the main mode of acquisition of HIV infection in the Democratic Republic of Congo (DRC). We aimed to determine the factors associated with the serological status of mothers and children born to HIV-positive mothers at 18 months, as well as the vital prognosis of infants within the prevention of mother-to-child transmission of HIV (PMTCT) service in the Department of Gynecology and Obstetrics at Panzi General Reference Hospital (GHRP) the vital prognosis of infants born to HIV-infected mothers at 18 months after birth.

methodsA matched retrospective cohort of HIV-positive women who delivered and brought their children before and at 18 months of life in the PMTCT/Panzi program during the period from July 1, 2015, to July 1, 2020. Multivariate logistic regression and a Cox proportional hazards model were performed to assess factors associated with positive HIV serology (couple mother-baby) and the risk of HIV MTCT or death at 18 months of life, respectively.

resultsThere were 6318 pregnant women identified, and four hundred were HIV positive. The study found that the prevalence of HIV-infected mothers was 6.3% (400/6318), and the prevalence of vertical HIV transmission was 6.9% (10/144). Premature rupture of the membranes was the most common maternal-foetal complication and was found in 11.1% of cases. Antiretroviral treatment was based on triple therapy (zidovudine (AZT) +lamivudine (3TC) + efavirenz (EFV) in the majority of cases (77.1%). Logistic regression analysis showed that the risk of HIV was higher in women with no education or primary education, no antenatal care, primiparity, and primigravida. Survival analysis showed that infant death at 18 months was characterized by maternal HIV positivity (HR=3.93; 95% CI: 1.39-11.10), prematurity (HR=4.66; 95% CI: 1.41-15.36), and the development of respiratory disease (HR=5.37; 95% CI: 1.65-17.47).

conclusionCompared WHO's elimination targets for MTCT rate of 2% or less, MTCT was high in our setting. This study’s findings highlight the need for intensified interventions to prevent MTCT and lead to healthier children, lessen the impact of HIV on individuals and healthcare systems, and are critical to achieving the goal of an HIV-free generation in DRC. CLINICAL TRIAL : Not applicable.

Indexed as

HIV InfectionsInfectious Disease Transmission, VerticalPregnancy Complications, InfectiousAdultAlkynesAnti-HIV AgentsBenzoxazinesCyclopropanesDemocratic Republic of the CongoDrug CombinationsFemaleHumansInfantInfant, NewbornLamivudineMaleAlkynesAnti-HIV AgentsBenzoxazinesCyclopropanesDrug CombinationsefavirenzLamivudinelamivudine, zidovudine drug combinationZidovudineHIV/AIDSHIV serologyMother-child transmissionPanzi HospitalThe children prognosis

Identifiers

PMID41862836
PMCPMC13127010

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

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.