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Meta-analysis of dolutegravir-based ART and risk-stratified HIV care in Uganda

Meta-analysis of dolutegravir-based ART and risk-stratified HIV care in Uganda
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Key Takeaway
Consider the proposed risk-stratified model for integrated HIV care as an association-based approach, not a proven intervention.

This is a meta-analysis and cohort review of dolutegravir-based antiretroviral therapy (ART) and a proposed risk-stratified model for integrated HIV care. The scope includes people living with HIV in Uganda's The AIDS Support Organization (TASO) routine-care cohort and a regional systematic review and meta-analysis, with sample sizes of 54,348 and 29,829, respectively.

The authors synthesized findings on viral non-suppression (VL >= 1,000 copies/mL). In the TASO cohort, the viral non-suppression rate was 6.4% (2,145/33,384). In the regional meta-analysis, the viral non-suppression rate was 19.4%. Secondary outcomes included advanced HIV disease, tuberculosis co-occurrence, and non-communicable disease co-occurrence.

The authors propose using routine electronic health record signals to trigger rapid follow-up and integrate TB and non-communicable disease management within HIV platforms. However, the source reports associations and does not establish causation for the proposed model. Certainty of evidence is not reported, and follow-up duration was not reported.

Practice relevance is restrained; the proposed model may strengthen durable viral suppression, but it is not proven effective. Limitations were not reported in the source.

Study Details

Study typeMeta analysis
EvidenceLevel 1
PublishedMay 2026
View Original Abstract ↓
Despite widespread rollout of dolutegravir-based (DTG) antiretroviral therapy (ART) in East Africa, viral non-suppression, advanced HIV disease (AHD), and multimorbidity persist, reflecting gaps in service response rather than regimen potency alone. In Uganda’s The AIDS Support Organization (TASO) routine-care cohort (2014–2024; n = 54,348 people living with HIV), integrase inhibitor uptake is near universal, yet AHD remains common, and tuberculosis (TB) and non-communicable diseases (NCD) increasingly co-occur within HIV care. Among clients with a recorded most recent viral load, 6.4% (2,145/33,384) had viral non-suppression (VL ≥ 1,000 copies/mL). Second, our regional systematic review and meta-analysis (2016–2023; n = 29,829) estimates viral non-suppression at 19.4% and indicates that failure concentrates in predictable social and clinical risk strata. We propose that durable suppression may be strengthened by an accountable, time-bound viral load (VL) cascade, paired with targeted support for clients at elevated clinical and social risk. Building on WHO and national differentiated service delivery and AHD guidance, we outline a pragmatic, data-enabled, risk-stratified model that uses routine electronic health record (EHR) signals to trigger rapid viral non-suppression follow-up, guide delivery of a proposed time-limited adherence and socioeconomic stability bundle, and integrate TB and NCD management within HIV platforms. A minimum actionable dashboard focused on cascade timeliness, high-risk package delivery, and integrated care can translate ART scale-up into durable suppression, fewer preventable AHD complications, and faster progress toward 95–95–95.
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