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dc.contributor.authorAtwine, Daniel
dc.contributor.authorOrikiriza, Patrick
dc.contributor.authorTaremwa, Ivan
dc.contributor.authorAyebare, Arnold
dc.contributor.authorLogoose, Suzan
dc.contributor.authorMwanga-Amumpaire, Juliet
dc.contributor.authorJindani, Amina
dc.contributor.authorBonnet, Maryline
dc.date.accessioned2024-06-04T10:18:02Z
dc.date.available2024-06-04T10:18:02Z
dc.date.issued2017
dc.identifier.citationAtwine, D., Orikiriza, P., Taremwa, I., Ayebare, A., Logoose, S., Mwanga-Amumpaire, J., ... & Bonnet, M. (2017). Predictors of delayed culture conversion among Ugandan patients. BMC infectious diseases, 17, 1-8.en_US
dc.identifier.urihttp://ir.must.ac.ug/xmlui/handle/123456789/3702
dc.description.abstractBackground: Estimates of month-2 culture conversion, a proxy indicator of tuberculosis (TB) treatment efficacy in phase-2 trials can vary by culture-type and geographically with lower rates reported among African sites. The sub-study aimed at comparing TB detection rates of different culture media, within and across rifampicin-based regimens (R10, 15 and 20 mg/Kg) over a 6-month treatment follow-up period, and to establish predictors of month-2 culture non-conversion among HIV-negative TB patients enrolled at RIFATOX trial site in Uganda. Methods: Unlike in other Rifatox Trial sites, it is only in Uganda were Lowenstein-Jensen (LJ) and Mycobacteria growth indicator tube (MGIT) were used throughout 6-months for treatment monitoring. Conversion rates were compared at month-2, 4 and 6 across cultures and treatment-type. Binomial regression analysis performed for predictors of month-2 non-conversion. Results: Of the 100 enrolled patients, 45% had converted based on combined LJ and MGIT by month-2, with no significant differences across treatment arms, p = 0.721. LJ exhibited higher conversion rates than MGIT at month-2 (58.4% vs 56.0%, p = 0.0707) and month-4 (98.9% vs 88.4%, p = 0.0391) respectively, more so within the high-dose rifampicin arms. All patients had converted by month-6. Time-to-TB detection (TTD) on MGIT and social service jobs independently predict month-2 non-conversion. Conclusion: The month-2 culture conversion used in phase 2 clinical trials as surrogate marker of treatment efficacy is influenced by the culture method used for monitoring mycobacterial response to TB treatment. Therefore, multi-centric TB therapeutic trials using early efficacy endpoint should use the same culture method across sites. The Time-to-detection of MTB on MGIT prior to treatment and working in Social service jobs bear an increased risk of culture non-conversion at month-2.en_US
dc.language.isoen_USen_US
dc.publisherBMC infectious diseasesen_US
dc.subjectDelayed culture conversionen_US
dc.subjectEfficacyen_US
dc.subjectHIV-negative TB patientsen_US
dc.subjectTime-to-detectionen_US
dc.subjectTreatment failureen_US
dc.titlePredictors of delayed culture conversion among Ugandan patientsen_US
dc.typeArticleen_US


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