Evidence map›Paper›PMID 40791690›Full record

ArticlemedRxiv : the preprint server for health sciences2025

Cumulative TB disease burden following sputum Xpert Ultra 'Trace' results in clinical settings: Results from a multi-site observational clinical study.

Ronit R Dalmat, Caitlin Visek, Elvira Budiawan, Gabrielle Stein, Annet Nalutaaya, James Mukiibi, Mariam Nantale, Patrick Biché, Joowhan Sung, Zanele Magcaba and 12 more

Abstract readPreprint
In one paragraph

Article in medRxiv : the preprint server for health sciences, 2025. 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

22 authors.

Ronit R DalmatDepartment of Global Health, University of Washington, Seattle, Washington, USA.ORCID 0000-0002-6959-0817
Caitlin VisekDivision of Infectious Diseases, Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
Elvira BudiawanDepartment of Global Health, University of Washington, Seattle, Washington, USA.
Gabrielle SteinDepartment of Global Health, University of Washington, Seattle, Washington, USA.
Annet NalutaayaUganda Tuberculosis Implementation Research Consortium, Walimu, Kampala, Uganda.
James MukiibiUganda Tuberculosis Implementation Research Consortium, Walimu, Kampala, Uganda.
Mariam NantaleUganda Tuberculosis Implementation Research Consortium, Walimu, Kampala, Uganda.
Patrick BichéDepartment of Epidemiology, Johns Hopkins Bloomberg School of Public Health, Baltimore, Maryland, USA.
Joowhan SungDivision of Infectious Diseases, Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.ORCID 0000-0002-4726-9651
Zanele MagcabaUmkhuseli Innovation and Research Management, Pietermaritzburg, South Africa.
Nompumelelo NgcoboUmkhuseli Innovation and Research Management, Pietermaritzburg, South Africa.
Jennifer F MortonDepartment of Global Health, University of Washington, Seattle, Washington, USA.
Meena LennDepartment of Global Health, University of Washington, Seattle, Washington, USA.
Samantha AucockUmkhuseli Innovation and Research Management, Pietermaritzburg, South Africa.
Adrienne E ShapiroDepartment of Global Health, University of Washington, Seattle, Washington, USA.ORCID 0000-0002-3106-1258
Amy SteadmanGlobal Health Labs, Inc., Bellevue, WA USA.ORCID 0000-0002-5605-1240
Robin DraperUmkhuseli Innovation and Research Management, Pietermaritzburg, South Africa.
Amanda GangulooUmkhuseli Innovation and Research Management, Pietermaritzburg, South Africa.
Douglas WilsonUmkhuseli Innovation and Research Management, Pietermaritzburg, South Africa.
Achilles KatambaUganda Tuberculosis Implementation Research Consortium, Walimu, Kampala, Uganda.
Emily A KendallDivision of Infectious Diseases, Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
Paul K DrainDepartment of Global Health, University of Washington, Seattle, Washington, USA.

Funding

Who are the Ultra-positive, culture-negative? Understanding the trajectories of individuals in Uganda with trace M. tuberculosis nucleic acid in sputumR01HL153611 · NHLBI · JOHNS HOPKINS UNIVERSITY · PI KENDALL, EMILY A · 2020 to 2024
$3.2M
Optimizing Implementation of Digital X-ray with Computer-Aided Detection for Community-Based Tuberculosis ScreeningK23AI185268 · NIAID · JOHNS HOPKINS UNIVERSITY · PI Joowhan Sung · 2024 to 2026
$591k
NHLBI NIH HHS R01 HL153611NIAID NIH HHS K23 AI185268
6 · The paper itself

Abstract

Background: Highly sensitive molecular tests, like Xpert Ultra, are reshaping TB diagnosis-detecting paucibacillary TB but sometimes creating uncertainty when they detect DNA in extremely low quantities that may not signal disease. This ambiguity also complicates the evaluation of novel diagnostic strategies. We sought to monitor adults with a 'Trace' result on an Xpert Ultra test to estimate the risk of tuberculosis disease up to 24 months later. Methods: We conducted a multi-site clinical observational study in South Africa and Uganda, where we enrolled ambulatory participants aged >=15 years with a sputum Xpert Ultra Trace result who had not yet initiated TB treatment. All participants underwent comprehensive clinical evaluation and repeated, standard sputum TB testing. Clinicians deferred treatment recommendations if TB status remained uncertain after evaluation. Untreated participants were followed regularly until TB diagnosis and/or treatment initiation. We estimated cumulative incidence of TB disease, defined by three reference standards. Results: Of 311 participants with Trace results (50% male, 57% PLHIV, 37% treated for TB within the last 5 years), 24% were positive for TB within 12 months by culture, 37% by sputum Xpert or culture, and 54% by culture or clinical diagnosis. After excluding those diagnosed with TB at baseline, patients identified at baseline as having recent TB history, abnormal chest x-ray, or positive tongue swab, had higher risk of TB diagnosis (hazard ratios: 2.6, 2.4, 4.5, respectively) during follow-up. This hazard was highest in the first three months after the negative baseline evaluation (0.22 [95% CI: 0.19-0.26] per person-month) and decreased to 0.01 [95% CI: 0-0.02] per person-month in both the 3-6 and 6-12-month intervals. Conclusion: Approximately half of adults and adolescents with a sputum Trace result were diagnosed with TB disease within twelve months. Although most TB diagnoses were made within 3 months, risk remained higher than estimated population incidence rates through the follow-up period. Individuals with sputum Trace results should receive close clinical monitoring, despite initial clinical treatment decision.

Indexed as

diagnosticsGeneXpertpaucibacillaryTraceTuberculosis

Identifiers

PMID40791690
PMCPMC12338891

What Socratic holds

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LicenceCC BY-NC-ND
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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 Socratic graph.