Prevalence of nonsuppressed viral load and associated factors among HIV-positive adults receiving antiretroviral therapy in Eswatini, Lesotho, Malawi, Zambia and Zimbabwe (2015 to 2017): results from population-based nationally representative surveys.


Journal

Journal of the International AIDS Society
ISSN: 1758-2652
Titre abrégé: J Int AIDS Soc
Pays: Switzerland
ID NLM: 101478566

Informations de publication

Date de publication:
11 2020
Historique:
received: 08 05 2020
revised: 28 09 2020
accepted: 02 10 2020
entrez: 23 11 2020
pubmed: 24 11 2020
medline: 23 4 2021
Statut: ppublish

Résumé

The global target for 2020 is that ≥90% of people living with HIV (PLHIV) receiving antiretroviral therapy (ART) will achieve viral load suppression (VLS). We examined VLS and its determinants among adults receiving ART for at least four months. We analysed data from the population-based HIV impact assessment (PHIA) surveys in Eswatini, Lesotho, Malawi, Zambia and Zimbabwe (2015 to 2017). PHIA surveys are nationally representative, cross-sectional household surveys. Data collection included structured interviews, home-based HIV testing and laboratory testing. Blood samples from PLHIV were analysed for HIV RNA, CD4 counts and recent exposure to antiretroviral drugs (ARVs). We calculated representative estimates for the prevalence of VLS (viral load <1000 copies/mL), nonsuppressed viral load (NVL; viral load ≥1000 copies/mL), virologic failure (VF; ARVs present and viral load ≥1000 copies/mL), interrupted ART (ARVs absent and viral load ≥1000 copies/mL) and rates of switching to second-line ART (protease inhibitors present) among PLHIV aged 15 to 59 years who participated in the PHIA surveys in Eswatini, Lesotho, Malawi, Zambia and Zimbabwe, initiated ART at least four months before the survey and were receiving ART at the time of the survey (according to self-report or ARV testing). We calculated odds ratios and incidence rate ratios for factors associated with NVL, VF, interrupted ART, and switching to second-line ART. We included 9200 adults receiving ART of whom 88.8% had VLS and 11.2% had NVL including 8.2% who experienced VF and 3.0% who interrupted ART. Younger age, male sex, less education, suboptimal adherence, receiving nevirapine, HIV non-disclosure, never having married and residing in Zimbabwe, Lesotho or Zambia were associated with higher odds of NVL. Among people with NVL, marriage, female sex, shorter ART duration, higher CD4 count and alcohol use were associated with lower odds for VF and higher odds for interrupted ART. Many people with VF (44.8%) had CD4 counts <200 cells/µL, but few (0.31% per year) switched to second-line ART. Countries are approaching global VLS targets for adults. Treatment support, in particular for younger adults, and people with higher CD4 counts, and switching of people to protease inhibitor- or integrase inhibitor-based regimens may further reduce NVL prevalence.

Identifiants

pubmed: 33225559
doi: 10.1002/jia2.25631
pmc: PMC7680921
doi:

Substances chimiques

Anti-HIV Agents 0
Nevirapine 99DK7FVK1H

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

e25631

Subventions

Organisme : CGH CDC HHS
ID : U2G GH001226
Pays : United States
Organisme : Swiss National Science Foundation
ID : P2BEP3_178602
Pays : Switzerland
Organisme : CDC HHS
ID : U2GGH001226
Pays : United States
Organisme : PEPFAR
Pays : United States
Organisme : CGH CDC HHS
ID : U2G GH001271
Pays : United States
Organisme : CGH CDC HHS
ID : U2G GH000994
Pays : United States

Informations de copyright

© 2020 The Authors. Journal of the International AIDS Society published by John Wiley & Sons Ltd on behalf of the International AIDS Society.

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Auteurs

Andreas D Haas (AD)

ICAP at Columbia University, Mailman School of Public Health, Columbia University, New York, NY, USA.
Institute of Social and Preventive Medicine (ISPM), University of Bern, Bern, Switzerland.

Elizabeth Radin (E)

ICAP at Columbia University, Mailman School of Public Health, Columbia University, New York, NY, USA.

Avi J Hakim (AJ)

Division of Global HIV and TB, Center for Global Health, CDC, Atlanta, GA, USA.

Andreas Jahn (A)

Ministry of Health Malawi, Lilongwe, Malawi.

Neena M Philip (NM)

ICAP at Columbia University, Mailman School of Public Health, Columbia University, New York, NY, USA.

Sasi Jonnalagadda (S)

Division of Global HIV and TB, Center for Global Health, CDC, Atlanta, GA, USA.

Suzue Saito (S)

ICAP at Columbia University, Mailman School of Public Health, Columbia University, New York, NY, USA.

Andrea Low (A)

ICAP at Columbia University, Mailman School of Public Health, Columbia University, New York, NY, USA.

Hetal Patel (H)

Division of Global HIV and TB, Center for Global Health, CDC, Atlanta, GA, USA.

Amee M Schwitters (AM)

Division of Global HIV and TB, Center for Global Health, CDC Lesotho, Maseru, Lesotho.

John H Rogers (JH)

Division of Global HIV and TB, Center for Global Health, CDC Zimbabwe, Harare, Zimbabwe.

Koen Frederix (K)

ICAP at Columbia University, Mailman School of Public Health, Columbia University, New York, NY, USA.

Evelyn Kim (E)

Division of Global HIV and TB, Center for Global Health, CDC Malawi, Lilongwe, Malawi.

George Bello (G)

Ministry of Health Malawi, Lilongwe, Malawi.

Daniel B Williams (DB)

Division of Global HIV and TB, Center for Global Health, CDC, Atlanta, GA, USA.

Bharat Parekh (B)

Division of Global HIV and TB, Center for Global Health, CDC, Atlanta, GA, USA.

Karampreet Sachathep (K)

ICAP at Columbia University, Mailman School of Public Health, Columbia University, New York, NY, USA.

Danielle T Barradas (DT)

Division of Global HIV and TB, Center for Global Health, CDC Zambia, Lusaka, Zambia.

Thokozani Kalua (T)

Ministry of Health Malawi, Lilongwe, Malawi.

Sehin Birhanu (S)

Division of Global HIV and TB, Center for Global Health, CDC, Atlanta, GA, USA.

Godfrey Musuka (G)

ICAP at Columbia University, Mailman School of Public Health, Columbia University, New York, NY, USA.

Owen Mugurungi (O)

Ministry of Health & Child Welfare, Harare, Zimbabwe.

Beth A Tippett Barr (BA)

Division of Global HIV and TB, Center for Global Health, CDC Zimbabwe, Harare, Zimbabwe.

Katrina Sleeman (K)

Division of Global HIV and TB, Center for Global Health, CDC, Atlanta, GA, USA.

Lloyd B Mulenga (LB)

Ministry of Health, Lusaka, Zambia.

Kyaw Thin (K)

Research Coordination Unit, Ministry of Health, Maseru, Lesotho.

Trong T Ao (TT)

Division of Global HIV and TB, Center for Global Health, CDC Eswatini, Mbabane, Swaziland.

Kristin Brown (K)

Division of Global HIV and TB, Center for Global Health, CDC, Atlanta, GA, USA.

Andrew C Voetsch (AC)

Division of Global HIV and TB, Center for Global Health, CDC, Atlanta, GA, USA.

Jessica E Justman (JE)

ICAP at Columbia University, Mailman School of Public Health, Columbia University, New York, NY, USA.

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