Evidence map›Paper›PMID 42607703›Full record

SynthesisThe lancet. HIV2026

Programmatic effectiveness of tuberculosis preventive treatment for people with HIV in six high-tuberculosis-burden countries (PROTECT): a prospective cohort study and meta-analysis.

N Sarita Shah, Fadimatu Mishara, Seth Zissette, Romaine Nephtalie Mesidor, Solomon Ssevvume, Serhii Riabokon, Blessing Mushangwe, John Motoku, Stephen Balogun, Nassir Kashmiri and 18 more

Abstract readMeta-Analysis
In one paragraph

Synthesis in The lancet. HIV, 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

28 authors.

N Sarita ShahDepartment of Epidemiology, Rollins School of Public Health, Emory University, Atlanta, GA, USA; Department of Medicine, School of Medicine, Emory University, Atlanta, GA, USA. Electronic address: sarita.shah@emory.edu.
Fadimatu MisharaNational Foundation for the Centers for Disease Control and Prevention, Atlanta, GA, USA.
Seth ZissetteDepartment of Epidemiology, Rollins School of Public Health, Emory University, Atlanta, GA, USA.
Romaine Nephtalie MesidorCatholic Medical Mission Board, Port-au-Prince, Haiti.
Solomon SsevvumeMonitoring and Evaluation Technical Support Program, Makere University School of Public Health, Kampala, Uganda.
Serhii RiabokonPublic Health Center of Ukraine, Ministry of Health, Kyiv, Ukraine.
Blessing MushangweZimbabwe Technical Assistance, Training & Education Center for Health, Harare, Zimbabwe.
John MotokuEastern Deanery AIDS Relief Program, Nairobi, Kenya.
Stephen BalogunDivision of Global HIV and Tuberculosis, US Centers for Disease Control and Prevention Nigeria, Abuja, Nigeria.
Nassir KashmiriNational Foundation for the Centers for Disease Control and Prevention, Atlanta, GA, USA.
Maryam BelloNational Foundation for the Centers for Disease Control and Prevention, Atlanta, GA, USA.
Gerry Marcel AugustinDivision of Global HIV and Tuberculosis, US Centers for Disease Control and Prevention Haiti, Port-au-Prince, Haiti.
Deus LukoyeDivision of Global HIV and Tuberculosis, US Centers for Disease Control and Prevention Uganda, Kampala, Uganda.
Ezra J BarzilayDivision of Global HIV and Tuberculosis, US Centers for Disease Control and Prevention Ukraine, Kyiv, Ukraine.
Talent MaphosaDivision of Global HIV and Tuberculosis, US Centers for Disease Control and Prevention Zimbabwe, Harare, Zimbabwe.
Herman WeyengaDivision of Global HIV and Tuberculosis, US Centers for Disease Control and Prevention Kenya, Nairobi, Kenya.
Ademola OladipoDivision of Global HIV and Tuberculosis, US Centers for Disease Control and Prevention Nigeria, Abuja, Nigeria.
Odile Ferroussier-DavisDivision of Global HIV and Tuberculosis, US Centers for Disease Control and Prevention, Atlanta, GA, USA.
Juliana da SilvaDivision of Global HIV and Tuberculosis, US Centers for Disease Control and Prevention, Atlanta, GA, USA.
Julia ErshovaDivision of Global HIV and Tuberculosis, US Centers for Disease Control and Prevention, Atlanta, GA, USA.
Aderonke S AjiboyeDivision of Global HIV and Tuberculosis, US Centers for Disease Control and Prevention, Atlanta, GA, USA.
Brigette L GleasonDivision of Global HIV and Tuberculosis, US Centers for Disease Control and Prevention, Atlanta, GA, USA.
Jean Solon VallesDivision of Global HIV and Tuberculosis, US Centers for Disease Control and Prevention Haiti, Port-au-Prince, Haiti.
Kurt Jean-CharlesSolutions, Port-au-Prince, Haiti.
Thomas AchiaDivision of Global HIV and Tuberculosis, US Centers for Disease Control and Prevention Kenya, Nairobi, Kenya.
David BenkeserDepartment of Biostatistics and Bioinformatics, Rollins School of Public Health, Emory University, Atlanta, GA, USA.
Macarthur CharlesDivision of Global HIV and Tuberculosis, US Centers for Disease Control and Prevention, Atlanta, GA, USA.
PROTECT study team

Funding

Virology and Molecular Biomarkers CoreP30AI050409 · NIAID · EMORY UNIVERSITY · PI Ann M Chahroudi, Colleen F Kelley · 2002 to 2026
$74.0M
Emory/Georgia TB Research Advancement Center (TRAC)P30AI168386 · NIAID · EMORY UNIVERSITY · PI Jeffrey M Collins · 2022 to 2026
$5.8M
Mentoring of multidisciplinary global health research in tuberculosis and HIVK24AI155045 · NIAID · ALBERT EINSTEIN COLLEGE OF MEDICINE · PI BRUST, JAMES C M · 2020 to 2025
$889k
Bill & Melinda Gates Foundation INV-004550NIAID NIH HHS K24 AI155045NIAID NIH HHS P30 AI050409NIAID NIH HHS P30 AI168386
6 · The paper itself

Abstract

backgroundIn randomised clinical trials (RCTs), tuberculosis preventive treatment (TPT) reduced tuberculosis incidence and mortality among people with HIV; however, real-world impact has not been evaluated since antiretroviral therapy (ART) was expanded to all people with HIV regardless of CD4 cell count. This study aimed to determine the programmatic effectiveness of TPT on reducing tuberculosis incidence and all-cause mortality among people with HIV initiating ART.

methodsThis prospective cohort study emulated six RCTs using individual-level data from electronic health records in Haiti, Kenya, Nigeria, Uganda, Ukraine, and Zimbabwe to estimate TPT effectiveness among people with HIV initiating ART between Jan 1, 2018, and Dec 31, 2021 (Haiti, Kenya, Nigeria, and Ukraine) or Dec 31, 2022 (Uganda and Zimbabwe). In each country, we created cohorts of newly enrolled people with HIV initiating ART, regardless of age. We excluded people diagnosed with tuberculosis 6 months before to 30 days after ART start. De-identified extracted data for each patient included visit-level data for selected study variables between the date of enrolment into HIV care and Dec 31, 2023 (Haiti, Kenya, Nigeria, and Ukraine) or Dec 31, 2024 (Uganda and Zimbabwe). Target trial emulation was used to define a hypothetical randomised trial of TPT initiation during an 8-week grace period compared with no TPT initiation. TPT effectiveness was summarised using adjusted hazard ratios (HRs) for tuberculosis and all-cause mortality estimated using an inverse propensity weighting approach, with weights adjusted for confounders including age and sex (time-fixed) and CD4 cell count, viral load, clinical stage, ART initiation, and ART adherence (time-varying). The six countries were pooled in a meta-analysis using inverse-variance weighting with effect heterogeneity assessed using I

findingsWe included 235 424 people with HIV: 69 936 people from Haiti, 65 936 from Uganda, 57 851 from Ukraine, 24 099 from Zimbabwe, 9549 from Kenya, and 8053 from Nigeria. In 235 424 people, 147 667 (62·7%) were aged 25-44 years, 133 582 (56·7%) were female, 101 842 (43·3%) were male, 104  277 (44·3%) had clinical stage 1, and 138 914 (59·0%) were on dolutegravir-based regimens. The adjusted HR for tuberculosis ranged from 0·35 (95% CI 0·28-0·43) in Haiti to 0·60 (0·36-0·91) in Kenya. The pooled HR for tuberculosis was 0·39 (0·34-0·43) with minimal variation across countries (I

interpretationTPT was effective in reducing tuberculosis incidence and mortality in people with HIV across various epidemiological contexts and risk groups. In an era of universal test-and-treat and new ART regimens, these data reinforce support for TPT as essential in HIV care.

fundingGates Foundation. TRANSLATIONS: For the French and Ukrainian translations of the abstract see Supplementary Materials section.

Indexed as

Antitubercular AgentsHIV InfectionsTuberculosisAdultAnti-HIV AgentsCD4 Lymphocyte CountFemaleHaitiHumansIncidenceKenyaMaleMiddle AgedNigeriaProspective StudiesTreatment OutcomeAnti-HIV AgentsAntitubercular Agents

Identifiers

PMID42607703
PMCPMC13626977

What Socratic holds

Textmetadata
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 Socratic graph.