Prevalence of viral load suppression, predictors of virological failure and patterns of HIV drug resistance after 12 and 48 months on first-line antiretroviral therapy: a national cross-sectional survey in Uganda.


Journal

The Journal of antimicrobial chemotherapy
ISSN: 1460-2091
Titre abrégé: J Antimicrob Chemother
Pays: England
ID NLM: 7513617

Informations de publication

Date de publication:
01 05 2020
Historique:
received: 19 08 2019
revised: 03 12 2019
accepted: 11 12 2019
pubmed: 7 2 2020
medline: 25 6 2021
entrez: 7 2 2020
Statut: ppublish

Résumé

We implemented the WHO cross-sectional survey protocol to determine rates of HIV viral load (VL) suppression (VLS), and weighted prevalence, predictors and patterns of acquired drug resistance (ADR) in individuals with virological failure (VF) defined as VL ≥1000 copies/mL. We enrolled 547 and 1064 adult participants on first-line ART for 12 (±3) months (ADR12) and ≥48 months (ADR48), respectively. Dried blood spots and plasma specimens were collected for VL testing and genotyping among the VFs. VLS was 95.0% (95% CI 93.4%-96.5%) in the ADR12 group and 87.9% (95% CI 85.0%-90.9%) in the ADR48 group. The weighted prevalence of ADR was 96.1% (95% CI 72.9%-99.6%) in the ADR12 and 90.4% (95% CI 73.6-96.8%) in the ADR48 group, out of the 30 and 95 successful genotypes in the respective groups. Initiation on a zidovudine-based regimen compared with a tenofovir-based regimen was significantly associated with VF in the ADR48 group; adjusted OR (AOR) 1.96 (95% CI 1.13-3.39). Independent predictors of ADR in the ADR48 group were initiation on a zidovudine-based regimen compared with tenofovir-based regimens, AOR 3.16 (95% CI 1.34-7.46) and ART duration of ≥82 months compared with <82 months, AOR 1.92 (95% CI 1.03-3.59). While good VLS was observed, the high prevalence of ADR among the VFs before they underwent the recommended three intensive adherence counselling (IAC) sessions followed by repeat VL testing implies that IAC prior to treatment switching may be of limited benefit in improving VLS.

Identifiants

pubmed: 32025714
pii: 5727896
doi: 10.1093/jac/dkz561
pmc: PMC7177494
doi:

Substances chimiques

Anti-HIV Agents 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Langues

eng

Sous-ensembles de citation

IM

Pagination

1280-1289

Subventions

Organisme : World Health Organization
ID : 001
Pays : International
Organisme : Medical Research Council
ID : MC_UU_00027/1
Pays : United Kingdom
Organisme : CGH CDC HHS
ID : U2G GH000785
Pays : United States
Organisme : PEPFAR
Pays : United States

Investigateurs

Pontiano Kaleebu (P)
Wilford Kirungi (W)
Paula Munderi (P)
Francis Ssali (F)
Tom Lutalo (T)
Bernard Etukoit (B)
Grace Namayanja (G)
Christine Watera (C)
Helen Byomire (H)
Andrew Kambugu (A)
Cissy Kityo (C)
Norah Namuwenge (N)
Elizabeth Namagala (E)

Informations de copyright

© The Author(s) 2020. Published by Oxford University Press on behalf of the British Society for Antimicrobial Chemotherapy.

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Auteurs

Deogratius Ssemwanga (D)

Medical Research Council/Uganda Virus Research Institute (UVRI), and London School of Hygiene and Tropical Medicine (LSHTM) Uganda Research Unit, Entebbe, Uganda.
Uganda Virus Research Institute, Entebbe, Uganda.

Juliet Asio (J)

Uganda Virus Research Institute, Entebbe, Uganda.

Christine Watera (C)

Uganda Virus Research Institute, Entebbe, Uganda.

Maria Nannyonjo (M)

Medical Research Council/Uganda Virus Research Institute (UVRI), and London School of Hygiene and Tropical Medicine (LSHTM) Uganda Research Unit, Entebbe, Uganda.

Faridah Nassolo (F)

Medical Research Council/Uganda Virus Research Institute (UVRI), and London School of Hygiene and Tropical Medicine (LSHTM) Uganda Research Unit, Entebbe, Uganda.

Sandra Lunkuse (S)

Medical Research Council/Uganda Virus Research Institute (UVRI), and London School of Hygiene and Tropical Medicine (LSHTM) Uganda Research Unit, Entebbe, Uganda.

Jesus F Salazar-Gonzalez (JF)

Medical Research Council/Uganda Virus Research Institute (UVRI), and London School of Hygiene and Tropical Medicine (LSHTM) Uganda Research Unit, Entebbe, Uganda.

Maria G Salazar (MG)

Medical Research Council/Uganda Virus Research Institute (UVRI), and London School of Hygiene and Tropical Medicine (LSHTM) Uganda Research Unit, Entebbe, Uganda.

Grace Sanyu (G)

Uganda Virus Research Institute, Entebbe, Uganda.

Tom Lutalo (T)

Uganda Virus Research Institute, Entebbe, Uganda.

Usher Kabuga (U)

Uganda Virus Research Institute, Entebbe, Uganda.

Isaac Ssewanyana (I)

Central Public Health Laboratories, Kampala, Uganda.

Faridah Namatovu (F)

Central Public Health Laboratories, Kampala, Uganda.

Grace Namayanja (G)

United States Centers for Disease Control and Prevention, Kampala, Uganda.

Alice Namale (A)

United States Centers for Disease Control and Prevention, Kampala, Uganda.

Elliot Raizes (E)

United States Centers for Disease Control and Prevention, Atlanta, GA, USA.

Mugagga Kaggwa (M)

World Health Organization, Kampala, Uganda.

Norah Namuwenge (N)

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

Wilford Kirungi (W)

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

Edward Katongole-Mbidde (E)

Uganda Virus Research Institute, Entebbe, Uganda.

Pontiano Kaleebu (P)

Medical Research Council/Uganda Virus Research Institute (UVRI), and London School of Hygiene and Tropical Medicine (LSHTM) Uganda Research Unit, Entebbe, Uganda.
Uganda Virus Research Institute, Entebbe, Uganda.

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