High levels of pretreatment and acquired HIV drug resistance in Nicaragua: results from the first nationally representative survey, 2016.


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:
12 2019
Historique:
received: 22 02 2019
revised: 04 11 2019
accepted: 20 11 2019
entrez: 21 12 2019
pubmed: 21 12 2019
medline: 5 6 2020
Statut: ppublish

Résumé

A nationally representative HIV drug resistance (HIVDR) survey in Nicaragua was conducted to estimate the prevalence of pretreatment HIVDR (PDR) among antiretroviral therapy (ART) initiators and acquired HIVDR among people living with HIV (PLHIV) who had received ART for 12 ± 3 months (ADR12) and ≥48 months (ADR48). A nationwide cross-sectional survey with a two-stage cluster sampling was conducted from March to November 2016. Nineteen of 45 total ART clinics representing >90% of the national cohort of adults on ART were included. ART initiators were defined as PLHIV initiating or reinitiating first-line ART. HIVDR was assessed for protease, reverse transcriptase and integrase Sanger sequences using the Stanford HIVdb algorithm. Viral load (VL) suppression was defined as <1000 copies/mL. Results were weighted according to the survey design. A total of 638 participants were enrolled (PDR: 171; ADR12: 114; ADR48: 353). The proportion of ART initiators with prior exposure to antiretrovirals (ARVs) was 12.3% (95% CI: 5.8% to 24.3%). PDR prevalence to any drug was 23.4% (95% CI: 14.4% to 35.6%), and 19.3% (95% CI: 12.2% to 29.1%) to non-nucleoside reverse transcriptase inhibitors (NNRTI). NNRTI PDR was higher in ART initiators with previous ARV exposure compared with those with no exposure (76.2% vs. 11.0%, p < 0.001). Protease inhibitors (PI) and integrase strand transfer inhibitors PDR was not observed. VL suppression rate was 77.8% (95% CI: 67.1% to 85.8%) in ADR12 and 70.3% (95% CI: 66.7% to 73.8%) in ADR48. ADR12 prevalence to any drug among PLHIV without VL suppression was 85.1% (95% CI: 66.1% to 94.4%), 82.4% to NNRTI and 70.2% to nucleoside reverse transcriptase inhibitors (NRTI). ADR48 prevalence to any drug among PLHIV without VL suppression was 75.5% (95% CI: 63.5% to 84.5 %), 70.7% to NNRTI, 59.4% to NRTI and 4.6% to PI. Despite implementation challenges yielding low-precision HIVDR estimates, high rates of NNRTI PDR were observed in Nicaragua, suggesting consideration of non-NNRTI-based first-line regimens for ART initiators. Strengthened HIVDR monitoring, systematic VL testing, and improved ART adherence support are also warranted.

Identifiants

pubmed: 31860167
doi: 10.1002/jia2.25429
pmc: PMC6924533
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

e25429

Subventions

Organisme : PEPFAR
Pays : United States

Informations de copyright

© 2019 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

Amalia Girón-Callejas (A)

Universidad del Valle de Guatemala, Guatemala City, Guatemala.

Claudia García-Morales (C)

Centre for Research in Infectious Diseases, National Institute of Respiratory Diseases, Mexico City, Mexico.

Ricardo Mendizabal-Burastero (R)

Universidad del Valle de Guatemala, Guatemala City, Guatemala.

Matilde Román (M)

Ministry of Health of Nicaragua, Managua, Nicaragua.

Daniela Tapia-Trejo (D)

Centre for Research in Infectious Diseases, National Institute of Respiratory Diseases, Mexico City, Mexico.

Marissa Pérez-García (M)

Centre for Research in Infectious Diseases, National Institute of Respiratory Diseases, Mexico City, Mexico.

Verónica S Quiroz-Morales (VS)

Centre for Research in Infectious Diseases, National Institute of Respiratory Diseases, Mexico City, Mexico.

Sandra I Juárez (SI)

U.S. Centers for Disease Control and Prevention, Guatemala City, Guatemala.

Giovanni Ravasi (G)

Pan-American Health Organization, Washington, DC, USA.

Carlos Vargas (C)

Universidad del Valle de Guatemala, Guatemala City, Guatemala.

René Gutiérrez (R)

Universidad del Valle de Guatemala, Managua, Nicaragua.

Luz Romero (L)

Universidad del Valle de Guatemala, Managua, Nicaragua.

Aleyda Solórzano (A)

Universidad del Valle de Guatemala, Managua, Nicaragua.

Edgar Sajquim (E)

Universidad del Valle de Guatemala, Guatemala City, Guatemala.

Sanny Northbrook (S)

U.S. Centers for Disease Control and Prevention, Guatemala City, Guatemala.

Santiago Ávila-Ríos (S)

Centre for Research in Infectious Diseases, National Institute of Respiratory Diseases, Mexico City, Mexico.

Gustavo Reyes-Terán (G)

Centre for Research in Infectious Diseases, National Institute of Respiratory Diseases, Mexico City, Mexico.

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