Initiation of Dolutegravir versus Efavirenz on viral suppression and retention at 6 months : a regression discontinuity design

dc.contributor.authorZheng, Amy
dc.contributor.authorFox, Matthew P.
dc.contributor.authorGreener, Ross
dc.contributor.authorKileel, Emma M.
dc.contributor.authorBor, Jacob
dc.contributor.authorVenter, Willem Daniel Francois
dc.contributor.authorPisa, Pedro Terrence
dc.contributor.authorBrennan, Alana T.
dc.contributor.authorMaskew, Mhairi
dc.date.accessioned2026-01-22T11:56:24Z
dc.date.available2026-01-22T11:56:24Z
dc.date.issued2025-06
dc.description.abstractBACKGROUND : In 2019, South Africa's Antiretroviral Therapy (ART) Treatment Guidelines replaced efavirenz with dolutegravir in first-line ART. SETTING : We assessed the impact of this national guideline change on retention and viral suppression in the Themba Lethu Clinical Cohort, Johannesburg, South Africa. We applied a regression discontinuity design in a prospective cohort study of 1654 adults living with HIV initiating first-line ART within 12 months (±12 months) of the guideline change. METHODS : We compared outcomes in individuals presenting just before and after the guideline change and estimated intention-to-treat effects on initiating a dolutegravir- vs efavirenz-based regimen. Primary outcomes were retention and viral suppression. Participants were defined as retained in care if a visit took place within ±3 months of the 6-month end point. Viral suppression was defined as having a viral load ≤1000 copies/mL 3 months before and up to 6 months after the 6-month end point. RESULTS : The 2019 guideline change led to an increase in uptake of dolutegravir. We noted a 26.6 percentage point increase in the proportion initiating dolutegravir [95% Confidence Interval (CI): 14.1 to 38.6]. We saw a small increase in viral suppression [Risk Difference (RD): 7.4 percentage points; 95% CI: -1.6 to 16.5] and no change in retention (RD: -1.7 percentage points; 95% CI: -13.9 to 10.5) at 6 months, though our findings were imprecise. CONCLUSIONS : Our estimates suggest early uptake of the revised treatment guidelines after implementation. Despite this, there was no meaningful change in viral suppression and retention rates at 6 months.
dc.description.departmentSchool of Health Systems and Public Health (SHSPH)
dc.description.librarianam2026
dc.description.sdgSDG-03: Good health and well-being
dc.description.urihttps://journals.lww.com/jaids/pages/default.aspx
dc.identifier.citationZheng, A., Fox, M.P., Greener, R. et al. 2025, 'Initiation of Dolutegravir versus Efavirenz on viral suppression and retention at 6 months : a regression discontinuity design', JAIDS Journal of Acquired Immune Deficiency Syndromes, vol. 99, no. 2pp. 151-157. DOI: 10.1097/QAI.0000000000003642.
dc.identifier.issn1525-4135 (print)
dc.identifier.issn1077-9450 (online)
dc.identifier.other10.1097/QAI.0000000000003642
dc.identifier.urihttp://hdl.handle.net/2263/107509
dc.language.isoen
dc.publisherWolters Kluwer Health
dc.rights© 2025 The Author(s). This is an open access article distributed under the Creative Commons Attribution License 4.0 (CCBY).
dc.subjectHIV/AIDS
dc.subjectAntiretroviral therapy (ART)
dc.subjectRetention
dc.subjectSuppression
dc.subjectSouth Africa
dc.subjectHuman immunodeficiency virus (HIV)
dc.subjectAcquired immune deficiency syndrome (AIDS)
dc.subjectDolutegravir
dc.subjectEfavirenz
dc.titleInitiation of Dolutegravir versus Efavirenz on viral suppression and retention at 6 months : a regression discontinuity design
dc.typeArticle

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