dc.contributor.author | Musaazi, J. | |
dc.contributor.author | Sekaggya-Wiltshire, C. | |
dc.contributor.author | Kiragga, K. A. | |
dc.contributor.author | Kalule, I. | |
dc.contributor.author | Reynolds, S. J. | |
dc.contributor.author | Manabe, Yukari C. | |
dc.contributor.author | Castelnuovo, B. | |
dc.date.accessioned | 2025-07-03T08:03:10Z | |
dc.date.available | 2025-07-03T08:03:10Z | |
dc.date.issued | 2019 | |
dc.identifier.citation | Musaazi, J. et al. (2019). Sustained positive impact on tuberculosis treatment outcomes of TB-HIV integrated care in Uganda, The International Journal of Tuberculosis and Lung Disease, 43(4): 514-521. | en_US |
dc.identifier.uri | https://doi.org/10.5588/ijtld.18.0306 | |
dc.identifier.uri | http://hdl.handle.net/10570/14623 | |
dc.description.abstract | OBJECTIVE: To examine tuberculosis (TB) treatment outcomes from a long-term TB-HIV (human immunodeficiency virus) integrated model of care at the Infectious Diseases Institute Clinic, Kampala, Uganda.
METHODS: We included HIV-positive adults who were new TB cases initiated on anti-tuberculosis treatment between 2009 and 2015 during TB-HIV integration. Trends in TB treatment outcomes and TB-associated deaths were analyzed using respectively the χ2 trend test and Kaplan-Meier methods.
RESULTS: The analysis involved 1318 cases: most patients were female (>50%); the median age ranged from 34 to 36 years, and >60% were late presenters (CD4 count <200 cells/μl), with a median CD4 cell count of 100–146 cells/μl at TB diagnosis. TB treatment success (cured or treatment completed) was 67–76%. Loss to follow-up (LTFU) declined systematically from 7% in 2010 to 3.4% in 2015 (P < 0.01). Antiretroviral therapy (ART) initiation during the intensive phase improved from 47% in 2009 to 97% in 2015 (P < 0.01). The mortality rate was >15% over time, and the probability of death at month 2 of anti-tuberculosis treatment was 52% higher among late presenters than in early presenters (13% vs. 6%, P < 0.01).
CONCLUSION: Significant LTFU improvement and prompt ART initiation could be due to well-implemented TB-HIV integration care; however, static TB-associated deaths may be due to late presentation. | en_US |
dc.description.sponsorship | Fogarty International Center,
National Institutes for Health (NIH; D43TW009771: ‘HIV co-infections in Uganda: TB, Cryptococcus, and viral hepatitis’),
The Division of Intramural Research, National Institute of Allergy and Infectious Diseases/NIH, Bethesda, MD, USA. | en_US |
dc.language.iso | en | en_US |
dc.publisher | The Union | en_US |
dc.subject | TB-HIV integrated care | en_US |
dc.subject | Uganda | en_US |
dc.subject | sub-Saharan Africa. | en_US |
dc.subject | Tuberculosis treatment | en_US |
dc.subject | HIV/AIDS-TB Co-infection | en_US |
dc.title | Sustained positive impact on tuberculosis treatment outcomes of TB-HIV integrated care in Uganda | en_US |
dc.type | Article | en_US |