Evidence map›Paper›PMID 41774412›Full record

ReviewPaediatric drugs2026

Oral Lamivudine for Extended HIV Postnatal Prophylaxis.

Philippe Van de Perre, Nicolas Meda, Souleymane Tassembedo, Jean Pierre Moles, Chipepo Kankasa, Anais Mennecier, Mwiya Mwiya, Nicolas Nagot, Thorkild Tylleskär

Abstract readReview
In one paragraph

Review in Paediatric drugs, 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

9 authors.

Philippe Van de Perre *UMR 1058 'Pathogenesis and Control of Chronic and Emerging Infections', INSERM-Université Montpellier, Inserm ADR Languedoc-Roussillon, 60 rue de Navacelles, 34394, Montpellier Cedex 5, France. philippe.vande-perre@umontpellier.fr.ORCID http://orcid.org/0000-0002-3912-0427
Nicolas Meda *University Joseph KI-ZERBO, Ouagadougou, Burkina Faso.
Souleymane TassembedoCentre Muraz, Bobo-Dioulasso, Burkina Faso.
Jean Pierre MolesUMR 1058 'Pathogenesis and Control of Chronic and Emerging Infections', INSERM-Université Montpellier, Inserm ADR Languedoc-Roussillon, 60 rue de Navacelles, 34394, Montpellier Cedex 5, France.
Chipepo KankasaUniversity Teaching Hospital, Lusaka, Zambia.
Anais MennecierUMR 1058 'Pathogenesis and Control of Chronic and Emerging Infections', INSERM-Université Montpellier, Inserm ADR Languedoc-Roussillon, 60 rue de Navacelles, 34394, Montpellier Cedex 5, France.
Mwiya MwiyaUniversity Teaching Hospital, Lusaka, Zambia.
Nicolas Nagot *UMR 1058 'Pathogenesis and Control of Chronic and Emerging Infections', INSERM-Université Montpellier, Inserm ADR Languedoc-Roussillon, 60 rue de Navacelles, 34394, Montpellier Cedex 5, France.
Thorkild Tylleskär *Centre for International Health, Department of Global Public Health and Primary Care, University of Bergen, Bergen, Norway.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Despite considerable progress in preventing mother-to-child transmission (PMTCT) of human immunodeficiency virus (HIV), eliminating paediatric HIV has not been achieved. Extended postnatal prophylaxis (ePNP), defined as prophylaxis administered to an HIV-exposed child after PMTCT perinatal prophylaxis ends, has been evaluated and is now proposed as an improved approach towards elimination. This approach should be urgently incorporated into international PMTCT recommendations. The antiretroviral drugs most commonly studied as ePNP, either alone or in combination, are lamivudine, nevirapine, lopinavir/ritonavir and zidovudine. In this study, we examined the efficacy, safety, pharmacology, genetic barrier to resistance and practicality of various ePNP regimens. Regimens combining multiple antiretroviral drugs are no more effective than single-drug regimens in terms of protective efficacy but they are associated with increased toxicity. On the basis of these criteria, we recommend lamivudine as the preferred ePNP drug or nevirapine as an alternative. Guided by maternal HIV viral load, ePNP may be particularly indicated, as it could ensure that the prophylaxis provides the greatest benefit/risk to children at highest risk. Long-acting injectable antiretroviral drugs and broadly neutralising antibodies (bNAbs) have yet to be fully evaluated in neonates, infants and children; however, they may offer new alternatives in the future.

Indexed as

Anti-HIV AgentsHIV InfectionsInfectious Disease Transmission, VerticalLamivudineAdministration, OralFemaleHumansInfant, NewbornPregnancyAnti-HIV AgentsLamivudine

Identifiers

PMID41774412
PMCPMC13121178

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Registered trials

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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.