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Optimised paediatric antiretroviral treatment to achieve the 95-95-95 goals
While the progress towards reaching the UNAIDS 95-95-95 targets in South African adults seems promising, the progress in the paediatric population is lagging far behind; only 79% percent of children living with HIV know their status. Of these, only 47% are on treatment, and a mere 34% of those are v...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
AOSIS
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8517773/ https://www.ncbi.nlm.nih.gov/pubmed/34691769 http://dx.doi.org/10.4102/sajhivmed.v22i1.1278 |
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author | Archary, Moherndran van Zyl, Riana Sipambo, Nosisa Sorour, Gillian |
author_facet | Archary, Moherndran van Zyl, Riana Sipambo, Nosisa Sorour, Gillian |
author_sort | Archary, Moherndran |
collection | PubMed |
description | While the progress towards reaching the UNAIDS 95-95-95 targets in South African adults seems promising, the progress in the paediatric population is lagging far behind; only 79% percent of children living with HIV know their status. Of these, only 47% are on treatment, and a mere 34% of those are virally suppressed. Thus, virological suppression has been attained in only 13% of children living with HIV in South Africa. Multiple factors contribute to the high treatment failure rate, one of them being a lack of paediatric-friendly antiretroviral treatment (ART) formulations. For example, the Lopinavir/ritonavir syrup, which is the current mainstay of ART for young children, has an extremely unpleasant taste, contributing to the poor tolerability and lack of adherence by children using the formulation. Furthermore, the lack of appropriate formulations limits the optimisation of regimens, especially for young children and those who cannot swallow tablets. Switching from syrups to dispersible tablets will improve ease of administration and adherence and result in cost-saving. Despite the approval of simplified paediatric-friendly formulations internationally, including other sub-Saharan African countries, unnecessary delays are experienced in South Africa. Clinician groups and community organisations must speak up and demand that approvals be expedited to ensure the delivery of life-changing and life-saving formulations to our patients as a matter of urgency. |
format | Online Article Text |
id | pubmed-8517773 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | AOSIS |
record_format | MEDLINE/PubMed |
spelling | pubmed-85177732021-10-21 Optimised paediatric antiretroviral treatment to achieve the 95-95-95 goals Archary, Moherndran van Zyl, Riana Sipambo, Nosisa Sorour, Gillian South Afr J HIV Med Opinion Paper While the progress towards reaching the UNAIDS 95-95-95 targets in South African adults seems promising, the progress in the paediatric population is lagging far behind; only 79% percent of children living with HIV know their status. Of these, only 47% are on treatment, and a mere 34% of those are virally suppressed. Thus, virological suppression has been attained in only 13% of children living with HIV in South Africa. Multiple factors contribute to the high treatment failure rate, one of them being a lack of paediatric-friendly antiretroviral treatment (ART) formulations. For example, the Lopinavir/ritonavir syrup, which is the current mainstay of ART for young children, has an extremely unpleasant taste, contributing to the poor tolerability and lack of adherence by children using the formulation. Furthermore, the lack of appropriate formulations limits the optimisation of regimens, especially for young children and those who cannot swallow tablets. Switching from syrups to dispersible tablets will improve ease of administration and adherence and result in cost-saving. Despite the approval of simplified paediatric-friendly formulations internationally, including other sub-Saharan African countries, unnecessary delays are experienced in South Africa. Clinician groups and community organisations must speak up and demand that approvals be expedited to ensure the delivery of life-changing and life-saving formulations to our patients as a matter of urgency. AOSIS 2021-09-01 /pmc/articles/PMC8517773/ /pubmed/34691769 http://dx.doi.org/10.4102/sajhivmed.v22i1.1278 Text en © 2021. The Authors https://creativecommons.org/licenses/by/4.0/Licensee: AOSIS. This work is licensed under the Creative Commons Attribution License. |
spellingShingle | Opinion Paper Archary, Moherndran van Zyl, Riana Sipambo, Nosisa Sorour, Gillian Optimised paediatric antiretroviral treatment to achieve the 95-95-95 goals |
title | Optimised paediatric antiretroviral treatment to achieve the 95-95-95 goals |
title_full | Optimised paediatric antiretroviral treatment to achieve the 95-95-95 goals |
title_fullStr | Optimised paediatric antiretroviral treatment to achieve the 95-95-95 goals |
title_full_unstemmed | Optimised paediatric antiretroviral treatment to achieve the 95-95-95 goals |
title_short | Optimised paediatric antiretroviral treatment to achieve the 95-95-95 goals |
title_sort | optimised paediatric antiretroviral treatment to achieve the 95-95-95 goals |
topic | Opinion Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8517773/ https://www.ncbi.nlm.nih.gov/pubmed/34691769 http://dx.doi.org/10.4102/sajhivmed.v22i1.1278 |
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