Evidence map›Paper›PMID 42872138›Full record

ArticleOpen forum infectious diseases2026

High Initiation but Suboptimal Completion of Tuberculosis-Preventive Treatment Among People Living With HIV on Antiretroviral Therapy, Persistent Tuberculosis Incidence, and Programmatic Implications: Findings From a 2-Year Multicountry Cohort Study.

L Chimoyi, S Ginindza, B A S Nonyane, C Mulder, A Bedru, N Kawaza, J E Golub, K Shearer, A Kennar, L Mvusi and 17 more

Abstract read
In one paragraph

Article in Open forum 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

27 authors.

L ChimoyiImplementation Research Division, The Aurum Institute, Isando, South Africa.ORCID https://orcid.org/0000-0002-0083-8319
S GinindzaImplementation Research Division, The Aurum Institute, Isando, South Africa.
B A S NonyaneCenter for Tuberculosis Research, Johns Hopkins University, Baltimore, Maryland, USA.ORCID https://orcid.org/0000-0001-5633-7487
C MulderDepartment of TB Elimination and Health System Innovations, KNCV Tuberculosis Plus, The Hague, the Netherlands.ORCID https://orcid.org/0000-0003-2628-7460
A BedruKNCV Tuberculosis Plus, Addis Ababa, Ethiopia.
N KawazaTB/HIV Department, Clinton Health Access Initiative, Harare, Zimbabwe.
J E GolubCenter for Tuberculosis Research, Johns Hopkins University, Baltimore, Maryland, USA.ORCID https://orcid.org/0000-0003-2398-3145
K ShearerCenter for Tuberculosis Research, Johns Hopkins University, Baltimore, Maryland, USA.ORCID https://orcid.org/0000-0003-2049-4258
A KennarCenter for Tuberculosis Research, Johns Hopkins University, Baltimore, Maryland, USA.ORCID https://orcid.org/0009-0006-7148-9773
L MvusiTB Cluster, National Department of Health, Pretoria, South Africa.
K Vilakazi-NhlapoTB Cluster, National Department of Health, Pretoria, South Africa.
T ApolloNational TB and Leprosy Program, Ministry of Health and Child Care, Harare, Zimbabwe.
M NcubeNational TB and Leprosy Program, Ministry of Health and Child Care, Harare, Zimbabwe.
C GwanzuraNational TB and Leprosy Program, Ministry of Health and Child Care, Harare, Zimbabwe.
G BisaAddis Ababa Health Bureau, Addis Ababa, Ethiopia.
D GadissaKNCV Tuberculosis Plus, Addis Ababa, Ethiopia.
T MabutoImplementation Research Division, The Aurum Institute, Isando, South Africa.
L TsopeImplementation Research Division, The Aurum Institute, Isando, South Africa.
I RabothataImplementation Research Division, The Aurum Institute, Isando, South Africa.
N NtombelaImplementation Research Division, The Aurum Institute, Isando, South Africa.ORCID https://orcid.org/0000-0002-0285-5163
K SitholeTB/HIV Department, Clinton Health Access Initiative, Harare, Zimbabwe.
S SisayKNCV Tuberculosis Plus, Addis Ababa, Ethiopia.ORCID https://orcid.org/0000-0003-1965-2837
M MakgaboImplementation Research Division, The Aurum Institute, Isando, South Africa.
R E ChaissonCenter for Tuberculosis Research, Johns Hopkins University, Baltimore, Maryland, USA.ORCID https://orcid.org/0000-0003-4710-925X
G ChurchyardImplementation Research Division, The Aurum Institute, Isando, South Africa.ORCID https://orcid.org/0000-0002-4269-3699
C J HoffmannImplementation Research Division, The Aurum Institute, Isando, South Africa.ORCID https://orcid.org/0000-0002-9422-0519
V ChihotaImplementation Research Division, The Aurum Institute, Isando, South Africa.ORCID https://orcid.org/0000-0003-1444-9266

Funding

Bill & Melinda Gates Foundation INV-006096
6 · The paper itself

Abstract

Background: Tuberculosis-preventive treatment (TPT) is recommended for those at risk of tuberculosis, but despite encouraging trial data, evidence of its effectiveness from routine settings with diverse TPT regimens is limited. We describe routine TPT implementation outcomes in people living with human immunodeficiency virus (HIV; PLWH) to identify bottlenecks and opportunities for improvement along the cascade of care. Methods: From 2021-2023, we conducted a 24-month prospective cohort study of PLWH facilities in Ethiopia, South Africa and Zimbabwe. Sociodemographic and clinical data were collected at enrollment. During follow-up, we collected TPT initiation, TPT-related adverse effects, and completion data. A subgroup was allocated digital boxes as a proxy measure for assessing treatment completion. Tuberculosis diagnoses were confirmed from clinic records or symptom agnostic sputum testing using Xpert MTB/RIF assay and mycobacteria growth indicator tube (MGIT) culture at 12- and 24 months after enrollment. Results: We enrolled 2095 participants, mostly female (n = 1489 [71.1%]), with a median age of 42 years (interquartile range, 35-50 years). Approximately 60% (n = 1312) were considered eligible for TPT, and 1110 (84.6%) initiated TPT within 60 days of antiretroviral therapy initiation or refill during follow-up (rifapentine and isoniazid [3HP] in 625 and 6 or 12 months of isoniazid [6H/12H] in 487). TPT was completed in 55.4% (406 of 733). Mild symptoms compatible with TPT adverse effects were commonly reported in 3HP versus 6H/12H (190 [31.0%] vs 51 [11.0%], respectively; Conclusions: There were losses along the cascade, particularly at completion. In programmatic settings, we observed more potential mild symptoms from 3HP compared to 6H/12H use. Interventions to support TPT completion are needed.

Indexed as

cascade of caredigital toolspeople living with HIV (PLWH)routine settingstuberculosis preventive treatment

Identifiers

PMID42872138
PMCPMC13660676

What OpenQuestion holds

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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.