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

Author:

Ssemwanga Deogratius12ORCID,Asio Juliet2,Watera Christine2,Nannyonjo Maria1,Nassolo Faridah1,Lunkuse Sandra1,Salazar-Gonzalez Jesus F1,Salazar Maria G1,Sanyu Grace2,Lutalo Tom2,Kabuga Usher2,Ssewanyana Isaac3,Namatovu Faridah3,Namayanja Grace4,Namale Alice4,Raizes Elliot5ORCID,Kaggwa Mugagga6,Namuwenge Norah7,Kirungi Wilford7,Katongole-Mbidde Edward2,Kaleebu Pontiano12,Kaleebu Pontiano,Kirungi Wilford,Munderi Paula,Ssali Francis,Lutalo Tom,Etukoit Bernard,Namayanja Grace,Watera Christine,Byomire Helen,Kambugu Andrew,Kityo Cissy,Namuwenge Norah,Namagala Elizabeth,

Affiliation:

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

2. Uganda Virus Research Institute, Entebbe, Uganda

3. Central Public Health Laboratories, Kampala, Uganda

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

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

6. World Health Organization, Kampala, Uganda

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

Abstract

Abstract Objectives 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. Methods 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. Results 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). Conclusions 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.

Funder

President’s Emergency Plan for AIDS Relief (PEPFAR) through the CDC

MRC and the UK Department for International Development

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,Pharmacology (medical),Pharmacology,Microbiology (medical)

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