Preferences of people living with HIV for features of tuberculosis preventive treatment regimens in Uganda: a discrete choice experiment
Abstract Introduction Tuberculosis (TB) preventive treatment (TPT) is recommended for people living with HIV (PLHIV) in high TB burden settings. While 6 months of daily isoniazid remains widely used, shorter regimens are now available. However, little is known about preferences of PLHIV for key features of TPT regimens. Methods From July to November 2022, we conducted a discrete choice experiment among adult PLHIV engaged in care at an urban HIV clinic in Kampala, Uganda. Participants chose between two hypothetical TPT regimens with five different features (pills per dose, frequency, duration, need for adjusted antiretroviral therapy [ART] dosage and side effects), organized across nine random choice tasks. We analysed preferences using hierarchical Bayesian estimation, latent class analysis and willingness‐to‐trade simulations. Results Of 400 PLHIV, 392 (median age 44, 72% female, 91% TPT‐experienced) had high‐quality choice task responses. Pills per dose was the most important attribute (relative importance 32.4%, 95% confidence interval [CI] 31.6–33.2), followed by frequency (20.5% [95% CI 19.7–21.3]), duration (19.5% [95% CI 18.6–20.5]) and need for ART dosage adjustment (18.2% [95% CI 17.2–19.2]). Latent class analysis identified three preference groups: one prioritized less frequent, weekly dosing ( N = 222; 57%); another was averse to ART dosage adjustment ( N = 107; 27%); and the last prioritized short regimens with fewer side effects ( N = 63; 16%). All groups highly valued fewer pills per dose. Overall, participants were willing to accept a regimen of 2.8 months’ additional duration [95% CI: 2.4–3.2] to reduce pills per dose from five to one, 3.6 [95% CI 2.4–4.8] months for weekly rather than daily dosing and 2.2 [95% CI 1.3–3.0] months to avoid ART dosage adjustment. Conclusions To align with preferences of PLHIV in Uganda, decision‐makers should prioritize the development and implementation of TPT regimens with fewer pills, less frequent dosing and no need for ART dosage adjustment, rather than focus primarily on duration of treatment.
Authors
- Lydia Akello (ORCID: https://orcid.org/0009-0009-4013-9692)
- Adithya Cattamanchi
- Anne Nakitende (ORCID: https://orcid.org/0000-0001-8198-6681)
- Jillian L. Kadota (ORCID: https://orcid.org/0000-0003-4568-8681)
- Jane Nakimuli (ORCID: https://orcid.org/0009-0001-2701-2330)
- David W. Dowdy (ORCID: https://orcid.org/0000-0003-0481-7475)
- Fred Welishe
- Christopher A. Berger (ORCID: https://orcid.org/0000-0002-0034-7544)
- Andrew D. Kerkhoff (ORCID: https://orcid.org/0000-0002-5023-6658)
- Hélène E. Aschmann (ORCID: https://orcid.org/0000-0003-1234-4321)
- Catherine Namale (ORCID: https://orcid.org/0000-0001-9830-2266)
- Fred Collins Semitala (ORCID: https://orcid.org/0000-0002-0624-7640)
- Juliet Kakeeto
Institutions
- Johns Hopkins University (US)
- University of California, San Francisco (US)
- University of California, Irvine (US)
- University of California System (US)
- Malaria Consortium (UG)
- Infectious Diseases Research Collaboration (UG)
- Equilibrium Research (GB)
- Makerere University (UG)
Publication Details
- Journal
- Journal of the International AIDS Society
- Published
- 2024-11-26
- DOI
- https://doi.org/10.1002/jia2.26390
- Citations
- 4
- Primary Topic
- Pharmaceutical studies and practices
- Type
- article
- Field-Weighted Citation Impact
- 4.44
Funders
- Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung
- National Institutes of Health
- National Institute of Allergy and Infectious Diseases