Evidence map›Paper›PMID 41760044›Full record

ArticleMedicine2026

Effectiveness of ART optimization on viral load suppression in children and adolescents with HIV in Uganda: A quasi-experimental study.

Esther M Nasuuna, Lillian Babirye, Joanita Kigozi, Alex Muganzi, Jonathan Izudi

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Article in Medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Esther M NasuunaInfectious Diseases Institute, College of Health Sciences, Makerere University, Kampala, Uganda.
Lillian BabiryeInfectious Diseases Institute, College of Health Sciences, Makerere University, Kampala, Uganda.
Joanita KigoziInfectious Diseases Institute, College of Health Sciences, Makerere University, Kampala, Uganda.
Alex MuganziInfectious Diseases Institute, College of Health Sciences, Makerere University, Kampala, Uganda.
Jonathan IzudiInfectious Diseases Institute, College of Health Sciences, Makerere University, Kampala, Uganda.ORCID 0000-0001-9065-0389

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Uganda implemented the antiretroviral therapy (ART) optimization program in July 2019, based on an eligibility rule. ART optimization targeted individuals with prior viral load (VL) < 1000 copies/mL, while those with VL ≥ 1000 copies/mL continued with non-optimized regimens. We assessed the effectiveness of ART optimization on VL suppression among children and adolescents with HIV (CAWH) in Uganda. We also assessed the compliance of human immunodeficiency virus (HIV) clinics with the eligibility rule and its effect on ART optimization. Therefore, we designed a quasi-experimental study using data from 21 urban and rural HIV clinics. The exposure was ART optimization, defined as the initiation or transition of CAWH on dolutegravir or a protease inhibitor (boosted lopinavir). Children and adolescents with HIV on an optimized ART regimen formed the exposed group, while those on a non-optimized ART regimen comprised the nonexposed group. The primary outcome was VL suppression, defined by VL < 1000 copies/mL after ≥6 months of ART optimization. We assessed the effectiveness of ART optimization on VL suppression using 2-stage least squares instrumental variable regression due to imperfect compliance with the eligibility rule across the clinics. We also established the effectiveness of the eligibility rule on ART optimization for individuals just below and just above the cutoff. Sensitivity analysis was performed using a noncausal approach. We analyzed data from 2999 CAWH aged ≤19 years and found an overall VL suppression of 76.1% (2282/2999). We found that ART optimization showed a trend toward improved VL suppression (risk ratio [RR] 1.81, 95% CI: 0.79-4.14). However, compliance with the rule was only for 2.6% of the participants, and the rule did not improve ART optimization (RR 0.96, 95% CI: 0.88-1.05). Overall, ART optimization, guided by an eligibility rule, did not achieve the target of ≥95% VL suppression among CAWH across the 21 public HIV clinics in Uganda, partly due to low compliance with the rule, although it showed a trend toward improvement. Addressing context-specific biological, behavioral, social, and structural barriers is needed to optimize VL outcomes.

Indexed as

Anti-HIV AgentsHIV InfectionsViral LoadAdolescentChildChild, PreschoolDolutegravirFemaleHeterocyclic Compounds, 3-RingHumansLopinavirMaleOxazinesPiperazinesPyridonesUgandaAnti-HIV AgentsDolutegravirHeterocyclic Compounds, 3-RingLopinavirOxazinesPiperazinesPyridonesART optimizationchildren and adolescentsdolutegravirHIVUgandaviral load suppression

Identifiers

PMID41760044
PMCPMC12956220

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.