Amy Zheng, Matthew P Fox, Ross Greener, Emma M Kileel, Jacob Bor, Willem Df Venter, Pedro T Pisa, Alana T Brennan, Mhairi Maskew
{"title":"Initiation of Dolutegravir vs Efavirenz on Viral Suppression and Retention at 6-months: A Regression Discontinuity Design.","authors":"Amy Zheng, Matthew P Fox, Ross Greener, Emma M Kileel, Jacob Bor, Willem Df Venter, Pedro T Pisa, Alana T Brennan, Mhairi Maskew","doi":"10.1097/QAI.0000000000003642","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>In 2019, South Africa's Antiretroviral Therapy (ART) Treatment Guidelines replaced efavirenz with dolutegravir in first-line ART.</p><p><strong>Setting: </strong>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.</p><p><strong>Methods: </strong>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 endpoint. Viral suppression was defined as having a viral load < 1000 copies/mL 3-months prior to and up to 6-months after the 6-month endpoint.</p><p><strong>Results: </strong>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, 38.6). We saw a small increase in viral suppression (Risk Difference (RD): 7.4 percentage points; 95% CI: -1.6, 16.5) and no change in retention (RD: -1.7 percentage points; 95% CI: -13.9, 10.5) at 6 months, though our findings were imprecise.</p><p><strong>Conclusion: </strong>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.</p>","PeriodicalId":14588,"journal":{"name":"JAIDS Journal of Acquired Immune Deficiency Syndromes","volume":" ","pages":""},"PeriodicalIF":2.9000,"publicationDate":"2025-02-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"JAIDS Journal of Acquired Immune Deficiency Syndromes","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1097/QAI.0000000000003642","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"IMMUNOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Background: 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 endpoint. Viral suppression was defined as having a viral load < 1000 copies/mL 3-months prior to and up to 6-months after the 6-month endpoint.
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, 38.6). We saw a small increase in viral suppression (Risk Difference (RD): 7.4 percentage points; 95% CI: -1.6, 16.5) and no change in retention (RD: -1.7 percentage points; 95% CI: -13.9, 10.5) at 6 months, though our findings were imprecise.
Conclusion: 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.
期刊介绍:
JAIDS: Journal of Acquired Immune Deficiency Syndromes seeks to end the HIV epidemic by presenting important new science across all disciplines that advance our understanding of the biology, treatment and prevention of HIV infection worldwide.
JAIDS: Journal of Acquired Immune Deficiency Syndromes is the trusted, interdisciplinary resource for HIV- and AIDS-related information with a strong focus on basic and translational science, clinical science, and epidemiology and prevention. Co-edited by the foremost leaders in clinical virology, molecular biology, and epidemiology, JAIDS publishes vital information on the advances in diagnosis and treatment of HIV infections, as well as the latest research in the development of therapeutics and vaccine approaches. This ground-breaking journal brings together rigorously peer-reviewed articles, reviews of current research, results of clinical trials, and epidemiologic reports from around the world.