Evidence map›Paper›PMID 42607088›Full record

SynthesisPloS one2026

Artificial Intelligence and Machine Learning-based prediction of tuberculosis treatment failure: A systematic review and meta-analysis.

Rogers Kamulegeya, Rose Nabatanzi, Derrick Semugenze, Faridah Mugala, Mercy Takuwa, Emmanuel Nasinghe, Denis Musinguzi, Sharon Namiiro, Andrew Katumba, Willy Ssengooba and 3 more

Abstract readSystematic ReviewMeta-Analysis
In one paragraph

Synthesis in PloS one, 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

5 · Who and what money

Authors and funding

13 authors.

Rogers KamulegeyaDepartment of Immunology and Molecular Biology, Makerere University College of Health Sciences (MakCHS), Kampala, Uganda.
Rose NabatanziDepartment of Immunology and Molecular Biology, Makerere University College of Health Sciences (MakCHS), Kampala, Uganda.
Derrick SemugenzeDepartment of Immunology and Molecular Biology, Makerere University College of Health Sciences (MakCHS), Kampala, Uganda.
Faridah MugalaDepartment of Immunology and Molecular Biology, Makerere University College of Health Sciences (MakCHS), Kampala, Uganda.
Mercy TakuwaDepartment of Immunology and Molecular Biology, Makerere University College of Health Sciences (MakCHS), Kampala, Uganda.
Emmanuel NasingheDepartment of Immunology and Molecular Biology, Makerere University College of Health Sciences (MakCHS), Kampala, Uganda.
Denis MusinguziDepartment of Computer Science, College of Computing and Information Sciences, Makerere University (CoCIS), Kampala, Uganda.
Sharon NamiiroMasaka Regional Referral Hospital, Masaka, Uganda.
Andrew KatumbaDepartment of Electrical and Computer Engineering, College of Engineering, Art and Design, Makerere University (CEDAT), Kampala, Uganda.
Willy SsengoobaDepartment of Immunology and Molecular Biology, Makerere University College of Health Sciences (MakCHS), Kampala, Uganda.ORCID https://orcid.org/0000-0002-1643-110X
Joyce Nakatumba-NabendeDepartment of Computer Science, College of Computing and Information Sciences, Makerere University (CoCIS), Kampala, Uganda.
Florence Nameere KivunikeDepartment of Information Technology, College of Computing and Information Sciences, Makerere University (CoCIS), Kampala, Uganda.ORCID https://orcid.org/0000-0001-6305-5242
David Patrick KateeteDepartment of Immunology and Molecular Biology, Makerere University College of Health Sciences (MakCHS), Kampala, Uganda.ORCID https://orcid.org/0000-0001-8075-3069

Funding

Makerere University Data Science Research Training to Strengthen Evidence-Based Health Innovation, Intervention and Policy (MakDARTA)U2RTW012116 · FIC · MAKERERE UNIVERSITY COLLEGE OF HEALTH SCIENCES · PI William Checkley, Moses Lutaakome Joloba · 2021 to 2026
$2.0M
Tuberculosis in households with infectious cases in Kampala city: Harnessing health data science for new insights on TB transmission and treatment response (DS-IAFRICA-TB)U01TW012534 · FIC · MAKERERE UNIVERSITY COLLEGE OF HEALTH SCIENCES · PI KATEETE, DAVID PATRICK, NAKATUMBA, JOYCE NABENDE · 2023 to 2025
$750k
FIC NIH HHS U01 TW012534FIC NIH HHS U2R TW012116
6 · The paper itself

Abstract

backgroundTuberculosis (TB) remains a leading cause of infectious disease mortality worldwide, and treatment failure contributes to ongoing transmission, drug resistance, and poor clinical outcomes. Artificial intelligence (AI) and machine learning (ML) approaches have attracted growing interest in predicting TB treatment outcomes, but the literature is heterogeneous and lacks a comprehensive synthesis.

methodsWe systematically searched PubMed/MEDLINE and Embase (January 2000-October 2025) for studies developing or validating AI/ML models to predict TB treatment failure. Two reviewers independently screened records and extracted data on study characteristics, predictor modalities, algorithms, validation strategies, and performance metrics, i.e., area under the curve (AUC), sensitivity, specificity, and confidence intervals. Studies reporting AUC with confidence intervals or sufficient data for calculation were included in random-effects meta-analysis. Missing standard errors were estimated from sample sizes and event rates using established methods. Risk of bias was assessed using PROBAST. Subgroup analyses and meta-regression explored heterogeneity, and publication bias was assessed using funnel plots, Egger's test, and trim-and-fill analysis. The study is registered with PROSPERO (CRD420251101443).

resultsThirty-four studies met the inclusion criteria. Publications increased markedly from 2019 onwards (91% of studies). Tree-based methods predominated (52.9%), and multimodal models (≥3 data types) were used in 41.2% of the studies. Nineteen studies (100,790 participants) contributed to the meta-analysis. The pooled AUC was 0.836 (95% CI 0.799-0.868), with substantial heterogeneity (I² = 97.9%). In subgroup analyses, studies including HIV-positive participants showed lower discrimination (AUC 0.748) than those excluding them (0.924). Only eight studies (23.5%) performed external validation, and only one study (2.9%) was rated low risk of bias overall (PROBAST), primarily due to analytical domain deficiencies. Egger's test suggested publication bias (p = 0.024). Major evidence gaps included underrepresentation of high-burden countries, HIV-affected populations, social determinants, pediatric TB, and extrapulmonary disease.

conclusionsAI/ML models for predicting TB treatment failure show promising discrimination but are not yet ready for routine clinical implementation. Performance varies substantially across populations and settings, and methodological limitations, including inadequate validation, poor calibration assessment, and high risk of bias, limit confidence in current estimates. Future research should prioritize rigorous external validation, calibration assessment, and development in underrepresented populations, particularly HIV-affected and high TB burden settings.

Indexed as

Antitubercular AgentsArtificial IntelligenceMachine LearningTuberculosisHumansPredictive Learning ModelsTreatment FailureAntitubercular Agents

Identifiers

PMID42607088
PMCPMC13480653

What OpenQuestion 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 OpenQuestion graph.