dc.contributor.author | Atwine, Daniel | |
dc.contributor.author | Orikiriza, Patrick | |
dc.contributor.author | Taremwa, Ivan | |
dc.contributor.author | Ayebare, Arnold | |
dc.contributor.author | Logoose, Suzan | |
dc.contributor.author | Mwanga-Amumpaire, Juliet | |
dc.contributor.author | Jindani, Amina | |
dc.contributor.author | Bonnet, Maryline | |
dc.date.accessioned | 2024-06-04T10:18:02Z | |
dc.date.available | 2024-06-04T10:18:02Z | |
dc.date.issued | 2017 | |
dc.identifier.citation | Atwine, 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.uri | http://ir.must.ac.ug/xmlui/handle/123456789/3702 | |
dc.description.abstract | Background: 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.iso | en_US | en_US |
dc.publisher | BMC infectious diseases | en_US |
dc.subject | Delayed culture conversion | en_US |
dc.subject | Efficacy | en_US |
dc.subject | HIV-negative TB patients | en_US |
dc.subject | Time-to-detection | en_US |
dc.subject | Treatment failure | en_US |
dc.title | Predictors of delayed culture conversion among Ugandan patients | en_US |
dc.type | Article | en_US |