Original Research

Viral suppression in adults on efavirenz- or dolutegravir-based antiretroviral therapy in Mopani District, South Africa

Christine Njuguna, Christina Maluleke, Natasha Davies, Lucia Hans, Barry Mutasa, Kate Rees
Southern African Journal of HIV Medicine | Vol 26, No 1 | a1718 | DOI: https://doi.org/10.4102/sajhivmed.v26i1.1718 | © 2025 Christine Njuguna, Christina Maluleke, Natasha Davies, Lucia Hans, Barry Mutasa, Kate Rees | This work is licensed under CC Attribution 4.0
Submitted: 11 March 2025 | Published: 29 August 2025

About the author(s)

Christine Njuguna, Anova Health Institute, Johannesburg, South Africa
Christina Maluleke, Anova Health Institute, Johannesburg, South Africa
Natasha Davies, Anova Health Institute, Johannesburg, South Africa
Lucia Hans, National Priority Programme, National Health Laboratory Service, Johannesburg, South Africa; and Department of Molecular Medicine and Haemotology, Faculty of Health Sciences, University of the Witwatersrand, Johannesburg, South Africa
Barry Mutasa, Anova Health Institute, Johannesburg, South Africa
Kate Rees, Anova Health Institute, Johannesburg, South Africa; and Department of Community Health, Faculty of Health Sciences, University of the Witwatersrand, Johannesburg, South Africa

Abstract

Background: Dolutegravir- has superior viral suppression compared to efavirenz-based antiretroviral therapy (ART). However, there are limited programmatic data on suppression in rural areas of South Africa.
Objectives: We aimed to compare 6- and 12-month viral suppression of dolutegravir and efavirenz regimens and determine factors available in TIER.Net (the national electronic database for HIV and tuberculosis care) associated with suppression.
Method: We conducted a retrospective cohort study using Mopani District programme data from TIER.Net. Clients aged ≥ 15 years initiated on tenofovir-lamivudine-dolutegravir (TLD) or tenofovir-emtricitabine-efavirenz (TEE) between 01 October 2021 and 31 March 2023, with ≥ 150 days in care, were included. We analysed 6- and 12-month suppression proportions and factors associated with suppression using logistic regression.
Results: A total of 472 clients on TEE and 944 on TLD were included. Six-month viral loads were available for 47.7% (225/472) of TEE and 57.4% (542/944) of TLD clients. Six-month suppression (< 50 copies/mL) was 65.5% (355/542) for TLD and 53.8% (121/225) for TEE (P = 0.002). TLD was associated with increased odds of suppression at 6 months (adjusted odds ratio [aOR] 1.6; 95% CI: 1.1–2.2). At 12 months, viral loads were available for 60.7% (573/944) of TLD and 56.1% (265/472) of TEE clients. Twelve-month suppression (< 50 copies/mL) was 70.0% (401/573) for TLD and 68.3% (181/265) for TEE with no statistically significant differences between TEE and TLD clients. Low-level viraemia (50 copies/mL – 999 copies/mL) at 12 months was 25.0% for TLD and 20.8% for TEE.
Conclusion: TLD showed improved suppression compared to TEE at 6 but not 12 months. The high proportion of clients with low-level viraemia is concerning. All clients, regardless of regimen, need evaluation for adherence support.


Keywords

dolutegravir; viral suppression; low-level viremia; TLD; rural health

Sustainable Development Goal

Goal 3: Good health and well-being

Metrics

Total abstract views: 1579
Total article views: 3174


Crossref Citations

No related citations found.