Preferences of people living with HIV for features of tuberculosis preventive treatment regimens - a discrete choice experiment.
Preferences of people living with HIV for features of tuberculosis preventive treatment regimens - a discrete choice experiment.
复制标题
艾滋病毒感染者对结核病预防治疗方案特征的偏好——一项离散选择实验。
DOI:
10.1101/2023.09.13.23295043
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发表时间:
2023
期刊:
影响因子:
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通讯作者:
Kerkhoff,AndrewD
中科院分区:
文献类型:
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作者:
Aschmann,HélèneE;Musinguzi,Allan;Kadota,JillianL;Namale,Catherine;Kakeeto,Juliet;Nakimuli,Jane;Akello,Lydia;Welishe,Fred;Nakitende,Anne;Berger,Christopher;Dowdy,DavidW;Cattamanchi,Adithya;Semitala,FredC;Kerkhoff,AndrewD
Background 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 We conducted a discrete choice experiment among adult PLHIV engaged in care at an urban HIV clinic in Kampala, Uganda. In nine random choice tasks, participants chose between two hypothetical TPT regimens with different features (pills per dose, frequency, duration, need for adjusted antiretroviral therapy [ART] dosage and side effects). We analyzed 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 and tolerable regimens (N=63; 16%). All groups highly valued fewer pills per dose. 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, 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.