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First-line antiretroviral drug discontinuations in children
INTRODUCTION: There are a limited number of paediatric antiretroviral drug options. Characterising the long term safety and durability of different antiretrovirals in children is important to optimise management of HIV infected children and to determine the estimated need for alternative drugs in pa...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5305232/ https://www.ncbi.nlm.nih.gov/pubmed/28192529 http://dx.doi.org/10.1371/journal.pone.0169762 |
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author | Fortuin-de Smidt, Melony de Waal, Reneé Cohen, Karen Technau, Karl-Günter Stinson, Kathryn Maartens, Gary Boulle, Andrew Igumbor, Ehimario U. Davies, Mary-Ann |
author_facet | Fortuin-de Smidt, Melony de Waal, Reneé Cohen, Karen Technau, Karl-Günter Stinson, Kathryn Maartens, Gary Boulle, Andrew Igumbor, Ehimario U. Davies, Mary-Ann |
author_sort | Fortuin-de Smidt, Melony |
collection | PubMed |
description | INTRODUCTION: There are a limited number of paediatric antiretroviral drug options. Characterising the long term safety and durability of different antiretrovirals in children is important to optimise management of HIV infected children and to determine the estimated need for alternative drugs in paediatric regimens. We describe first-line antiretroviral therapy (ART) durability and reasons for discontinuations in children at two South African ART programmes, where lopinavir/ritonavir has been recommended for children <3 years old since 2004, and abacavir replaced stavudine as the preferred nucleoside reverse transcriptase inhibitor in 2010. METHODS: We included children (<16 years at ART initiation) who initiated ≥3 antiretrovirals between 2004–2014 with ≥1 follow-up visit on ART. We estimated the incidence of first antiretroviral discontinuation using Kaplan-Meier analysis. We determined the reasons for antiretroviral discontinuations using competing risks analysis. We used Cox regression to identify factors associated with treatment-limiting toxicity. RESULTS: We included 3579 children with median follow-up duration of 41 months (IQR 14–72). At ART initiation, median age was 44 months (IQR 13–89) and median CD4 percent was 15% (IQR 9–21%). At three and five years on ART, 72% and 26% of children respectively remained on their initial regimen. By five years on ART, the most common reasons for discontinuations were toxicity (32%), treatment failure (18%), treatment simplification (5%), drug interactions (3%), and other or unspecified reasons (18%). The incidences of treatment limiting toxicity were 50.6 (95% CI 46.2–55.4), 1.6 (0.5–4.8), 2.0 (1.2–3.3), and 1.3 (0.6–2.8) per 1000 patient years for stavudine, abacavir, efavirenz and lopinavir/ritonavir respectively. CONCLUSIONS: While stavudine was associated with a high risk of treatment-limiting toxicity, abacavir, lopinavir/ritonavir and efavirenz were well-tolerated. This supports the World Health Organization recommendation to replace stavudine with abacavir or zidovudine in paediatric first-line ART regimens in order to improve paediatric first-line ART durability. |
format | Online Article Text |
id | pubmed-5305232 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-53052322017-02-28 First-line antiretroviral drug discontinuations in children Fortuin-de Smidt, Melony de Waal, Reneé Cohen, Karen Technau, Karl-Günter Stinson, Kathryn Maartens, Gary Boulle, Andrew Igumbor, Ehimario U. Davies, Mary-Ann PLoS One Research Article INTRODUCTION: There are a limited number of paediatric antiretroviral drug options. Characterising the long term safety and durability of different antiretrovirals in children is important to optimise management of HIV infected children and to determine the estimated need for alternative drugs in paediatric regimens. We describe first-line antiretroviral therapy (ART) durability and reasons for discontinuations in children at two South African ART programmes, where lopinavir/ritonavir has been recommended for children <3 years old since 2004, and abacavir replaced stavudine as the preferred nucleoside reverse transcriptase inhibitor in 2010. METHODS: We included children (<16 years at ART initiation) who initiated ≥3 antiretrovirals between 2004–2014 with ≥1 follow-up visit on ART. We estimated the incidence of first antiretroviral discontinuation using Kaplan-Meier analysis. We determined the reasons for antiretroviral discontinuations using competing risks analysis. We used Cox regression to identify factors associated with treatment-limiting toxicity. RESULTS: We included 3579 children with median follow-up duration of 41 months (IQR 14–72). At ART initiation, median age was 44 months (IQR 13–89) and median CD4 percent was 15% (IQR 9–21%). At three and five years on ART, 72% and 26% of children respectively remained on their initial regimen. By five years on ART, the most common reasons for discontinuations were toxicity (32%), treatment failure (18%), treatment simplification (5%), drug interactions (3%), and other or unspecified reasons (18%). The incidences of treatment limiting toxicity were 50.6 (95% CI 46.2–55.4), 1.6 (0.5–4.8), 2.0 (1.2–3.3), and 1.3 (0.6–2.8) per 1000 patient years for stavudine, abacavir, efavirenz and lopinavir/ritonavir respectively. CONCLUSIONS: While stavudine was associated with a high risk of treatment-limiting toxicity, abacavir, lopinavir/ritonavir and efavirenz were well-tolerated. This supports the World Health Organization recommendation to replace stavudine with abacavir or zidovudine in paediatric first-line ART regimens in order to improve paediatric first-line ART durability. Public Library of Science 2017-02-13 /pmc/articles/PMC5305232/ /pubmed/28192529 http://dx.doi.org/10.1371/journal.pone.0169762 Text en https://creativecommons.org/publicdomain/zero/1.0/ This is an open access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. The work is made available under the Creative Commons CC0 (https://creativecommons.org/publicdomain/zero/1.0/) public domain dedication. |
spellingShingle | Research Article Fortuin-de Smidt, Melony de Waal, Reneé Cohen, Karen Technau, Karl-Günter Stinson, Kathryn Maartens, Gary Boulle, Andrew Igumbor, Ehimario U. Davies, Mary-Ann First-line antiretroviral drug discontinuations in children |
title | First-line antiretroviral drug discontinuations in children |
title_full | First-line antiretroviral drug discontinuations in children |
title_fullStr | First-line antiretroviral drug discontinuations in children |
title_full_unstemmed | First-line antiretroviral drug discontinuations in children |
title_short | First-line antiretroviral drug discontinuations in children |
title_sort | first-line antiretroviral drug discontinuations in children |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5305232/ https://www.ncbi.nlm.nih.gov/pubmed/28192529 http://dx.doi.org/10.1371/journal.pone.0169762 |
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