Single-tablet regimens improve adherence and persistence compared to multiple-tablet options for adult HIV patients in this meta-analysis
This systematic literature review and meta-analysis evaluated integrase strand transfer inhibitor-based single-tablet regimens versus multiple-tablet regimens for adult people with HIV. The synthesis included twenty-five publications to assess adherence, persistence, discontinuation, and virologic failure outcomes across diverse study designs. Results indicated that single-tablet regimens were associated with improved adherence in retrospective studies, showing a rate ratio of 1.64 with a 95% confidence interval of 1.46 to 1.83. Randomized controlled trials, however, demonstrated no significant difference in adherence between the two approaches.
persistence and discontinuation analyses revealed distinct advantages for single-tablet formulations. Patients on single-tablet regimens exhibited higher persistence rates compared to those on multiple-tablet regimens, with a rate ratio of 1.33. Retrospective and prospective cohort studies consistently showed that people with HIV treated with multiple-tablet regimens were more likely to discontinue therapy. Hazard ratios and rate ratios ranged from 1.62 to 4.43, highlighting a substantial risk of discontinuation with multiple-tablet options in observational data.
Virologic failure risks were comparable between single-tablet and multiple-tablet regimens across randomized trials and retrospective studies. The meta-analysis suggests that single-tablet regimens serve as a potential tool for supporting adherence and persistence in real-world clinical settings. These findings underscore the importance of regimen simplification for optimizing long-term treatment success without compromising virologic efficacy.