Evidence map›Paper›PMID 41557852›Full record

ArticleThe Pediatric infectious disease journal2026

Linking Children and Adolescents With TB Disease to HIV Services in 16 PEPFAR-supported High TB/HIV-Burden Countries in Sub-Saharan Africa, October 2018-September 2022.

Nickolas T Agathis, Kimi Sato, Stephanie O'Connor, Rebeca I Briceño Robaugh, Cleophas D'Auvergne, Maletsatsi Motebang, Mamorapeli Ts'oeu, Matela Mpe, Talent Maphosa, Immaculate Mutisya and 23 more

Abstract read
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Article in The Pediatric infectious disease journal, 2026. 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

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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

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5 · Who and what money

Authors and funding

33 authors.

Nickolas T AgathisFrom the Division of Global HIV and TB, U.S. Centers of Disease Control and Prevention, Atlanta, Georgia.ORCID 0000-0003-2641-4888
Kimi SatoFrom the Division of Global HIV and TB, U.S. Centers of Disease Control and Prevention, Atlanta, Georgia.ORCID 0000-0001-7970-6193
Stephanie O'ConnorFrom the Division of Global HIV and TB, U.S. Centers of Disease Control and Prevention, Atlanta, Georgia.
Rebeca I Briceño RobaughTB Division, Office of Infectious Disease, Global Health Bureau, U.S. Agency for International Development, Washington, District of Columbia.
Cleophas D'AuvergneTB Division, Office of Infectious Disease, Global Health Bureau, U.S. Agency for International Development, Washington, District of Columbia.
Maletsatsi MotebangDivision of Global HIV and TB, U.S. Centers of Disease Control and Prevention, Maseru, Lesotho.
Mamorapeli Ts'oeuDivision of Global HIV and TB, U.S. Centers of Disease Control and Prevention, Maseru, Lesotho.
Matela MpeDivision of Global HIV and TB, U.S. Centers of Disease Control and Prevention, Maseru, Lesotho.
Talent MaphosaDivision of Global HIV and TB, U.S. Centers of Disease Control and Prevention, Harare, Zimbabwe.
Immaculate MutisyaDivision of Global HIV and TB, U.S. Centers of Disease Control and Prevention, Nairobi, Kenya.
Lennah NyabiageDivision of Global HIV and TB, U.S. Centers of Disease Control and Prevention, Nairobi, Kenya.
Wondimu TeferiDivision of Global HIV and TB, U.S. Centers of Disease Control and Prevention, Addis Ababa, Ethiopia.
Beniam FelekeDivision of Global HIV and TB, U.S. Centers of Disease Control and Prevention, Addis Ababa, Ethiopia.
Flora NwagagboDivision of Global HIV and TB, U.S. Centers of Disease Control and Prevention, Abuja, Nigeria.
Eyitayo FolorunshoDivision of Global HIV and TB, U.S. Centers of Disease Control and Prevention, Abuja, Nigeria.
Yagna VarajidasDivision of Global HIV and TB, U.S. Centers of Disease Control and Prevention, Maputo, Mozambique.
Criménia Mbate-MutembaMinistry of Health, Maputo, Mozambique.
Deus LukoyeDivision of Global HIV and TB, U.S. Centers of Disease Control and Prevention, Kampala, Uganda.
Sophie NantumeDivision of Global HIV and TB, U.S. Centers of Disease Control and Prevention, Kampala, Uganda.
Madina ApolotDivision of Global HIV and TB, U.S. Centers of Disease Control and Prevention, Kampala, Uganda.
Steven BaveewoDivision of Global HIV and TB, U.S. Centers of Disease Control and Prevention, Kampala, Uganda.
Tuduetso MolefiMinistry of Health, Gaborone, Botswana.
Mothusi B KeatlhotsweDivision of Global HIV and TB, U.S. Centers of Disease Control and Prevention, Gaborone, Botswana.
Ramadhani GongoDivision of Global HIV and TB, U.S. Centers of Disease Control and Prevention, Dar es Salaam, Tanzania.
Jaiving C KazitangaDivision of Global HIV and TB, U.S. Centers of Disease Control and Prevention, Dar es Salaam, Tanzania.
Kgomotso Vilakazi NhlapoNational Department of Health, Pretoria, South Africa.
Katlego MotlhaolengDivision of Global HIV and TB, U.S. Centers of Disease Control and Prevention, Pretoria, South Africa.
Heather PaulinDivision of Global HIV and TB, U.S. Centers of Disease Control and Prevention, Pretoria, South Africa.
Gurpreet KindraDivision of Global HIV and TB, U.S. Centers of Disease Control and Prevention, Pretoria, South Africa.
Neha ShahDepartment of International HIV Prevention and Treatment, U.S. Military HIV Research Program, Walter Reed Army Institute of Research, Department of Defense, Bethesda, Maryland.
HilaryT WolfGlobal Health Security and Diplomacy Bureau, U.S. Department of State, Washington, District of Columbia.
Paul PierreGlobal Health Security and Diplomacy Bureau, U.S. Department of State, Washington, District of Columbia.
Brittany MooreFrom the Division of Global HIV and TB, U.S. Centers of Disease Control and Prevention, Atlanta, Georgia.

Funding

Intramural CDC HHS CC999999
6 · The paper itself

Abstract

introductionPromptly identifying children and adolescents living with both tuberculosis (TB) disease and human immunodeficiency virus (HIV) and ensuring they receive antiretroviral treatment (ART) can reduce TB/HIV-associated mortality. We reviewed linkage of children and young adolescents with TB to HIV services at clinical sites in 16 high TB/HIV-burden sub-Saharan African countries supported by the U.S. President's Emergency Plan for AIDS Relief (PEPFAR).

methodsPEPFAR monitoring, evaluation and reporting data describing persons <15 years of age with TB disease during October 2018-September 2022 were reviewed. Indicators included known HIV status (proportion of clients with TB who have known HIV status), HIV positivity (proportion with TB and known HIV status who have HIV, including those newly identified and those already diagnosed with HIV) and ART linkage (proportion with TB/HIV coinfection who were receiving ART). Data were collected quarterly except for ART linkage (collected annually starting in October 2021). Trend performance of indicators during the 4-year period by quarter and annual performance, stratified by sex, age, geographic region and ART status in the final year are described.

resultsAmong children and adolescents <15 years old with TB during October 2018-September 2022, known HIV status quarterly coverage increased (90% [October-December 2018] to 91% [July-September 2022]); HIV positivity decreased (22%-14%), including newly positive (7%-4%); and ART coverage increased (90%-97%). In total, during October 2021-September 2022, among 73,183 children with TB, 93% (n = 67,968) had a known HIV status, of which 14% (9295/67,968) were positive (4% newly identified [2730/67,968] and 10% already diagnosed [6565/67,968]). Of 9295 with TB/HIV, 97% (9050/9295) were currently or newly started on ART. Known HIV status was lower among infants <1 year (74%, 4883/6605), and ART linkage was lower among children <1 (93%, 502/542) and 1-4 years of age (93%, 2791/2993).

conclusionsThese findings highlight effective PEPFAR-supported integration of HIV services into TB services; however, gaps among young children persist. While HIV positivity decreased among children and adolescents with TB, universal HIV testing of those with TB remains an important strategy to close pediatric HIV treatment gaps and reduce mortality in high-burden countries.

Indexed as

HIV InfectionsTuberculosisAdolescentAfrica South of the SaharaAnti-HIV AgentsChildChild, PreschoolCoinfectionFemaleHumansInfantMaleAnti-HIV AgentsadolescentsHIVpediatricsTBTB case findingTPT

Identifiers

PMID41557852
PMCPMC13403809

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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.