Evidence map›Paper›PMID 40297689›Full record

ArticleResearch square2025

Performance evaluation of alternative bacteriological measures of response to MDR-TB therapy during the initial 16 weeks of treatment.

Willy Ssengooba, Emmanuel Musisi, Derrick Semugenze, Kevin Komakech, Moses Ndema, Christine Wiltshire Sekaggya, Susan Adakun, Derek J Sloan, Achilles Katamba, Mohammed Lamorde and 2 more

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In one paragraph

Article in Research square, 2025. 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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0citing papers in PubMed
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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

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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

12 authors.

Willy SsengoobaDepartment of Medical Microbiology, and Makerere University Biomedical Research Center (MAKBRC), College of Health Sciences Makerere University.
Emmanuel MusisiDivision of Infection and Global Health, School of Medicine, University of St Andrews, KY16 9TF St Andrews.
Derrick SemugenzeDepartment of Medical Microbiology, and Makerere University Biomedical Research Center (MAKBRC), College of Health Sciences Makerere University.
Kevin KomakechDepartment of Medical Microbiology, and Makerere University Biomedical Research Center (MAKBRC), College of Health Sciences Makerere University.
Moses NdemaAdult Tuberculosis Unit, Mulago National Referral and Teaching Hospital.
Christine Wiltshire SekaggyaInfectious Diseases Institute, Makerere University College of Health Sciences.
Susan AdakunAdult Tuberculosis Unit, Mulago National Referral and Teaching Hospital.
Derek J SloanDivision of Infection and Global Health, School of Medicine, University of St Andrews, KY16 9TF St Andrews.
Achilles KatambaMakerere University Lung Institute.
Mohammed LamordeInfectious Diseases Institute, Makerere University College of Health Sciences.
Moses JolobaDepartment of Medical Microbiology, and Makerere University Biomedical Research Center (MAKBRC), College of Health Sciences Makerere University.
Wilber SabiitiDivision of Infection and Global Health, School of Medicine, University of St Andrews, KY16 9TF St Andrews.

Funding

NURTURE:Research Training and Mentoring Program for Career Development of Faculty at Makerere University College of Health SciencesD43TW010132 · FIC · MAKERERE UNIVERSITY COLLEGE OF HEALTH SCIENCES · PI SEWANKAMBO, NELSON K · 2015 to 2019
$4.3M
FIC NIH HHS D43 TW010132
6 · The paper itself

Abstract

Background: Monitoring response to Multi-Drug-Resistant Tuberculosis (MDR-TB) treatment is burdensome to TB programmes and may benefit from alternative effective tools. We evaluated the concordance of alternative bacteriological measures of response to therapy (AMRT) during the initial sixteen weeks of MDR-TB treatment. Methods: In a prospective study of MDR/RR-TB among smear positive adults, aged 18 year and above. Pooled early morning- and spot sputa were obtained before treatment initiation (95% on Bdq, Lzd, Lfx, Cfz, Cs regimen) and at weeks 2, 4, 6, 8, 12, and 16 during treatment between 14/02/2020 and 09/02/2024. Samples were tested using Concentrated Fluorescent Microscopy (CFM), Fluorescein-diacetate (FDA)-Acid Fast Bacilli (AFB) vital smear microscopy, the tuberculosis-Molecular bacterial load assay (TB-MBLA), and Middle brook 7H11 selective (MB7H11S) colony-forming units as the AMRT. Concordance of the AMRT for sputum conversion was compared to Mycobacterial Growth Indicator Tube (MGIT) culture conversion at weeks 12 and 16 of treatment. Results: A total of 101 MDR/RR-TB patients were screened of which 42 were smear negative. Fifty-nine participants were enrolled, of whom 58 (98%) provided baseline sputa and these were included in the analysis. The concordance, n/N (%) of each AMRT test with MGIT culture conversion at week 12 were: 31/35(88.6%) for CFM, 32/33 (97.0%) for FDA, and 25/26 (96.2%) for TB-MBLA, and 11/11 (100%) for MB7H11S. At week 16, concordance of eachAMRT were: 39/40 (97.5%) for CFM, 35/36 (97.2%) for FDA, 32/32 (100%) for TB-MBLA, and 15/15 (100%) for MB7H11S. Among people living with HIV,the concordances of AMRT with MGIT culture conversion varied at week 8 but was 100% for all tests at weeks 12 and 16. Baseline clinical and/or bacteriological factors did not influence the concordance of AMRT to MGIT culture conversion at weeks 12, and 16. Conclusion: Our data show that concentrated Fluorescent smear, Fluorescein-di-acetate smear microscopy, and TB-MBLA are suitable alternative measures of response to TB therapy compared to MGIT culture among MDR-TB participants. Use of these alternative rapid methods may allow timely decision making as well as rapid evaluation of alternative MDR-TB treatment regimens.

Identifiers

PMID40297689
PMCPMC12036452

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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.