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Single-tablet regimens improve adherence and persistence compared to multiple-tablet options for adult HIV patients in this meta-analysis

Single-tablet regimens improve adherence and persistence compared to multiple-tablet options for…
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Key Takeaway
Single-tablet regimens improve adherence and persistence versus multiple-tablet options for adults with HIV, though virologic failure risks remain comparable.

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.

Study Details

Study typeMeta analysis
EvidenceLevel 1
PublishedMay 2026
View Original Abstract ↓
INTRODUCTION: Antiretroviral single-tablet regimens (STRs) have several advantages over multiple-tablet regimens (MTRs), including increased adherence and improved treatment satisfaction for people with HIV (PWH). This analysis has systematically reviewed and compared STRs and MTRs in adult PWH receiving integrase strand transfer inhibitor (INSTI)-based regimens. METHODS: MEDLINE and Embase databases were searched on November 28, 2023, to identify studies published from 2013 to 2023 that evaluated INSTI-based STRs compared with ≥ 1 INSTI-based MTRs. Study quality was assessed based on the University of York Centre for Reviews and Dissemination guidelines. Pairwise meta-analyses were conducted to provide pooled relative estimates for key clinical outcomes. RESULTS: Twenty-five publications were included in the quantitative syntheses. STRs were associated with improved adherence based on 3 retrospective studies [rate ratio (RR) = 1.64 (95% confidence interval: 1.46-1.83)] but there was no difference in adherence in the 1 randomized controlled trial (RCT) that assessed adherence [RR = 1.02 (0.77-1.35)], though, due to blinding, both STR and MTR groups took multiple pills. STRs were associated with higher persistence than MTRs based on 7 retrospective studies [RR = 1.33 (1.17-1.52)]. PWH treated with MTRs versus STRs were more likely to discontinue therapy in retrospective studies [hazard ratio = 1.62 (1.52-1.72), 6 studies] and prospective cohort studies [RR = 4.43 (1.62-12.09), 3 studies], but not within RCTs where there was no difference in discontinuation [RR = 0.83 (0.55-1.26), 4 trials]. Risk of virologic failure was comparable between STRs and MTRs in RCTs [RR = 1.00 (0.35-2.84), 5 trials] and retrospective studies [odds ratio = 1.30 (0.30-5.53), 5 studies]. CONCLUSION: INSTI-based STRs were associated with improved adherence and persistence, and lower discontinuation rates compared with INSTI-based MTRs in observational, real-world studies, whereas no differences in adherence or discontinuation were seen in RCTs. Neither RCTs nor real-world studies showed any difference in virologic failure for STRs and MTRs. STRs are a potential tool for supporting adherence and persistence in real-world settings. REGISTRATION: PROSPERO number CRD42024525515.
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