High viral suppression rates among PLHIV on dolutegravir who had an initial episode of viral non-suppression in Uganda September 2020-July 2021.


Journal

PloS one
ISSN: 1932-6203
Titre abrégé: PLoS One
Pays: United States
ID NLM: 101285081

Informations de publication

Date de publication:
2024
Historique:
received: 10 10 2023
accepted: 23 05 2024
medline: 26 6 2024
pubmed: 26 6 2024
entrez: 26 6 2024
Statut: epublish

Résumé

In 2019, WHO recommended dolutegravir (DTG) as a backbone for first- and second-line antiretroviral therapy (ART) regimens for people living with HIV (PLHIV). According to the 2018 Uganda's HIV treatment guidelines, patients with viral non-suppression (≥1,000 copies/mL) should receive intensive adherence counseling (IAC) with repeat viral load (VL) within 6 months. This analysis focused on the prevalence and factors associated with viral suppression following IAC among PLHIV on DTG-based regimens (DBRs) with an initial episode of viral non-suppression (VNS) in Uganda. We conducted a retrospective analysis for PLHIV on DBRs with an initial episode of VNS (≥1,000 copies/mL) in Uganda during October 2019-September 2020 who had a follow up VL test result during September 2020-July 2021. Data were abstracted from the Central Public Health Laboratory (CPHL) database, including patient demographics and VL results. Viral non-suppression (VNS) was defined as a VL test result of ≥1,000 copies/mL. We characterized PLHIV on DBRs and used logistic regression models to determine factors associated with VL suppression after an initial episode of VNS. A total of 564 PLHIV on DBRs with an initial episode of VNS were followed up and 43 were excluded due to missing data. Of the 521, 220 (42.2%) were children (<15 years) and 231 (44.3%) were female. Median age was 28 years (interquartile range [IQR]: 12-43 years), and median duration on DBRs was 12 months (IQR: 6-15 months). Overall, 80.8% (421/521) PLHIV had a suppressed viral load at first follow up testing (children = 74.5% [164/220]; adults = 85.4% [257/301]). Children with initial VL results ≥5,000 copies/mL were less likely to achieve viral suppression at follow up testing compared to those with <5,000 copies/mL (AOR: 0.38; 95% CI: 0.20-0.71; p = 0.002). In a programmatic setting, most adults and children suppressed following an initial episode of VNS on DBRs. High rates of suppression after VNS suggest adherence challenges, rather than drug resistance. Continuation of DBRs should be considered before regimen switch.

Sections du résumé

BACKGROUND BACKGROUND
In 2019, WHO recommended dolutegravir (DTG) as a backbone for first- and second-line antiretroviral therapy (ART) regimens for people living with HIV (PLHIV). According to the 2018 Uganda's HIV treatment guidelines, patients with viral non-suppression (≥1,000 copies/mL) should receive intensive adherence counseling (IAC) with repeat viral load (VL) within 6 months. This analysis focused on the prevalence and factors associated with viral suppression following IAC among PLHIV on DTG-based regimens (DBRs) with an initial episode of viral non-suppression (VNS) in Uganda.
METHODS METHODS
We conducted a retrospective analysis for PLHIV on DBRs with an initial episode of VNS (≥1,000 copies/mL) in Uganda during October 2019-September 2020 who had a follow up VL test result during September 2020-July 2021. Data were abstracted from the Central Public Health Laboratory (CPHL) database, including patient demographics and VL results. Viral non-suppression (VNS) was defined as a VL test result of ≥1,000 copies/mL. We characterized PLHIV on DBRs and used logistic regression models to determine factors associated with VL suppression after an initial episode of VNS.
RESULTS RESULTS
A total of 564 PLHIV on DBRs with an initial episode of VNS were followed up and 43 were excluded due to missing data. Of the 521, 220 (42.2%) were children (<15 years) and 231 (44.3%) were female. Median age was 28 years (interquartile range [IQR]: 12-43 years), and median duration on DBRs was 12 months (IQR: 6-15 months). Overall, 80.8% (421/521) PLHIV had a suppressed viral load at first follow up testing (children = 74.5% [164/220]; adults = 85.4% [257/301]). Children with initial VL results ≥5,000 copies/mL were less likely to achieve viral suppression at follow up testing compared to those with <5,000 copies/mL (AOR: 0.38; 95% CI: 0.20-0.71; p = 0.002).
CONCLUSIONS CONCLUSIONS
In a programmatic setting, most adults and children suppressed following an initial episode of VNS on DBRs. High rates of suppression after VNS suggest adherence challenges, rather than drug resistance. Continuation of DBRs should be considered before regimen switch.

Identifiants

pubmed: 38923981
doi: 10.1371/journal.pone.0305129
pii: PONE-D-23-22283
doi:

Substances chimiques

Pyridones 0
dolutegravir DKO1W9H7M1
Heterocyclic Compounds, 3-Ring 0
Oxazines 0
Piperazines 0
HIV Integrase Inhibitors 0
Anti-HIV Agents 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e0305129

Informations de copyright

Copyright: This is an open access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. The work is made available under the Creative Commons CC0 public domain dedication.

Déclaration de conflit d'intérêts

The authors have declared no competing interest exist.

Auteurs

Grace A Namayanja (GA)

Division of Global HIV and TB, US Centers for Disease Control and Prevention, Kampala, Uganda.

Juliana de Fatima Da Silva (JF)

Division of Global HIV and TB, US Centers for Disease Control and Prevention, Atlanta, Georgia, United States of America.

Bill Elur (B)

Division of Global HIV and TB, US Centers for Disease Control and Prevention, Kampala, Uganda.

Pamela M Nasirumbi (PM)

Division of Global HIV and TB, US Centers for Disease Control and Prevention, Kampala, Uganda.

Elliot Raizes (E)

Division of Global HIV and TB, US Centers for Disease Control and Prevention, Atlanta, Georgia, United States of America.

Julius Ssempiira (J)

Division of Global HIV and TB, US Centers for Disease Control and Prevention, Kampala, Uganda.

Esther Nazziwa (E)

Division of Global HIV and TB, US Centers for Disease Control and Prevention, Kampala, Uganda.

Miriam Nabukenya (M)

Central Public Health Laboratories, Ministry of Health, Kampala, Uganda.

Isaac Sewanyana (I)

Central Public Health Laboratories, Ministry of Health, Kampala, Uganda.

Jennifer Balaba (J)

Monitoring and Evaluation Technical Support, Makerere University School of Public Health, Kampala, Uganda.

Jonathan Ntale (J)

Division of Global HIV and TB, US Centers for Disease Control and Prevention, Kampala, Uganda.

Jackie Calnan (J)

Office of Health and HIV, United States Agency for International Development, Kampala, Uganda.

Estella Birabwa (E)

Walter Reed Army Institute of Research, US Mission, Kampala, Uganda.

Juliet Akao (J)

United States Department of Defense, US Mission, Kampala, Uganda.

Christina Mwangi (C)

Division of Global HIV and TB, US Centers for Disease Control and Prevention, Kampala, Uganda.

Mary Naluguza (M)

Division of Global HIV and TB, US Centers for Disease Control and Prevention, Kampala, Uganda.

Arthur Ahimbisibwe (A)

AIDS Control Program, Ministry of Health, Kampala, Uganda.

Cordelia Katureebe (C)

AIDS Control Program, Ministry of Health, Kampala, Uganda.

Susan Nabadda (S)

Central Public Health Laboratories, Ministry of Health, Kampala, Uganda.

Lisa Nelson (L)

Division of Global HIV and TB, US Centers for Disease Control and Prevention, Kampala, Uganda.

Emilio Dirlikov (E)

Division of Global HIV and TB, US Centers for Disease Control and Prevention, Kampala, Uganda.

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Classifications MeSH