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Early virological failure and HIV drug resistance in Ugandan adults co-infected with tuberculosis
PURPOSE: This cross-sectional study took place in the integrated tuberculosis (TB) clinic of a large outpatient clinic for HIV-infected patients in Kampala, Uganda. The purpose of this study was to describe the proportion of TB/HIV co-infected adults with virological failure, type and frequency of H...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5237283/ https://www.ncbi.nlm.nih.gov/pubmed/28086929 http://dx.doi.org/10.1186/s12981-016-0128-5 |
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author | von Braun, Amrei Sekaggya-Wiltshire, Christine Scherrer, Alexandra U. Magambo, Brian Kambugu, Andrew Fehr, Jan Castelnuovo, Barbara |
author_facet | von Braun, Amrei Sekaggya-Wiltshire, Christine Scherrer, Alexandra U. Magambo, Brian Kambugu, Andrew Fehr, Jan Castelnuovo, Barbara |
author_sort | von Braun, Amrei |
collection | PubMed |
description | PURPOSE: This cross-sectional study took place in the integrated tuberculosis (TB) clinic of a large outpatient clinic for HIV-infected patients in Kampala, Uganda. The purpose of this study was to describe the proportion of TB/HIV co-infected adults with virological failure, type and frequency of HIV drug resistance-associated mutations, and the proportion of patients with suboptimal efavirenz levels. METHODS: HIV-1 plasma viral loads, CD4 cell count measurements, and efavirenz serum concentrations were done in TB/HIV co-infected adults. Genotypic resistance testing was performed in case of confirmed virological failure. RESULTS: After a median time on ART of 6 months, virological failure was found in 22/152 patients (14.5%). Of 147 participants with available efavirenz serum concentration, 26 (17.6%) had at least one value below the reference range, including 20/21 (95.2%) patients with confirmed virological failure. Genotypic resistance testing was available for 16/22 (72.7%) patients, of which 15 (93.8%) had at least one major mutation, most commonly M184V (81.2%) and K103NS (68.8%). CONCLUSION: We found a high proportion of TB/HIV co-infected patients with virological failure, the majority of which had developed relevant resistance-mutations after a median time on anti-retroviral treatment (ART) of 6 months. Virological monitoring should be prioritized in TB/HIV co-infected patients in resource-limited settings. |
format | Online Article Text |
id | pubmed-5237283 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-52372832017-01-18 Early virological failure and HIV drug resistance in Ugandan adults co-infected with tuberculosis von Braun, Amrei Sekaggya-Wiltshire, Christine Scherrer, Alexandra U. Magambo, Brian Kambugu, Andrew Fehr, Jan Castelnuovo, Barbara AIDS Res Ther Research PURPOSE: This cross-sectional study took place in the integrated tuberculosis (TB) clinic of a large outpatient clinic for HIV-infected patients in Kampala, Uganda. The purpose of this study was to describe the proportion of TB/HIV co-infected adults with virological failure, type and frequency of HIV drug resistance-associated mutations, and the proportion of patients with suboptimal efavirenz levels. METHODS: HIV-1 plasma viral loads, CD4 cell count measurements, and efavirenz serum concentrations were done in TB/HIV co-infected adults. Genotypic resistance testing was performed in case of confirmed virological failure. RESULTS: After a median time on ART of 6 months, virological failure was found in 22/152 patients (14.5%). Of 147 participants with available efavirenz serum concentration, 26 (17.6%) had at least one value below the reference range, including 20/21 (95.2%) patients with confirmed virological failure. Genotypic resistance testing was available for 16/22 (72.7%) patients, of which 15 (93.8%) had at least one major mutation, most commonly M184V (81.2%) and K103NS (68.8%). CONCLUSION: We found a high proportion of TB/HIV co-infected patients with virological failure, the majority of which had developed relevant resistance-mutations after a median time on anti-retroviral treatment (ART) of 6 months. Virological monitoring should be prioritized in TB/HIV co-infected patients in resource-limited settings. BioMed Central 2017-01-05 /pmc/articles/PMC5237283/ /pubmed/28086929 http://dx.doi.org/10.1186/s12981-016-0128-5 Text en © The Author(s) 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research von Braun, Amrei Sekaggya-Wiltshire, Christine Scherrer, Alexandra U. Magambo, Brian Kambugu, Andrew Fehr, Jan Castelnuovo, Barbara Early virological failure and HIV drug resistance in Ugandan adults co-infected with tuberculosis |
title | Early virological failure and HIV drug resistance in Ugandan adults co-infected with tuberculosis |
title_full | Early virological failure and HIV drug resistance in Ugandan adults co-infected with tuberculosis |
title_fullStr | Early virological failure and HIV drug resistance in Ugandan adults co-infected with tuberculosis |
title_full_unstemmed | Early virological failure and HIV drug resistance in Ugandan adults co-infected with tuberculosis |
title_short | Early virological failure and HIV drug resistance in Ugandan adults co-infected with tuberculosis |
title_sort | early virological failure and hiv drug resistance in ugandan adults co-infected with tuberculosis |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5237283/ https://www.ncbi.nlm.nih.gov/pubmed/28086929 http://dx.doi.org/10.1186/s12981-016-0128-5 |
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