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Performance Of Fujilam Version 1 For The Diagnosis Of Tuberculosis In Children Under 5 Years In Uganda - A Brief Report

Nanteza, M. A.; Mukiza, N.; Bwanga, F.; Musiime, V.; Kisitu, G. P.; Mudrak, N.; Khambati, N.; Nakayita, G.; Nasinghe, E.; Mbekeka, P.; Desravines, R.; Upadhyay, R. U.; Douglass, E.; Kekitiinwa, A. R.; Ellner, J. J.; Dorman, S. E.; Penn-Nicholson, A.; Kim, S.; Alland, D.; Salgame, P.; Song, R.; Basile, F. W.; Joloba, M.; Bijker, E. M.; NOD-pedFEND consortium,

2025-10-19 infectious diseases
10.1101/2025.10.17.25338231 medRxiv
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BackgroundDiagnosing tuberculosis in children remains challenging due to the paucibacillary nature of the disease, non-specific symptoms, and difficulty collecting samples. New tests are urgently needed. We evaluated the diagnostic accuracy of FujiLAM version 1 urine test in children under 5 years with presumptive tuberculosis in Uganda. MethodsThis was a cross-sectional evaluation nested in the NOD-pedFEND diagnostic study. Children under 5 years with signs or symptoms of tuberculosis were recruited from three hospitals in Uganda. All participants underwent comprehensive baseline investigations, including culture and Xpert MTB/RIF Ultra on reference samples and chest X-ray. Culture and Xpert MTB/RIF Ultra results were used to define a microbiological reference standard. FujiLAM version 1 testing was performed on fresh urine at the baseline visit. ResultsSeventy-nine children were included in the study. Fifteen participants (19%) were classified as having microbiologically confirmed TB, 44 (56%) as unconfirmed TB, thirteen (16%) as unlikely TB, and seven participants (9%) were unclassifiable. Only one participant (with unlikely TB) had a positive FujiLAM test. Culture and Xpert MTB/RIF Ultra on reference samples were negative in this child, indicating poor diagnostic accuracy with a sensitivity of 0% (95% CI: 0 - 21.8) of FujiLAM version 1 against the microbiological reference standard. Conclusion: The poor diagnostic accuracy of FujiLAM version 1 in children under five years of age makes it unsuitable as a diagnostic test in this age group. Further evaluation with the optimized version 2 of this test is needed.

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