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Opportunities for improving the efficiency of paediatric HIV treatment programmes
OBJECTIVES: To conduct two economic analyses addressing whether to: routinely monitor HIV-infected children on antiretroviral therapy (ART) clinically or with laboratory tests; continue or stop cotrimoxazole prophylaxis when children become stabilized on ART. DESIGN AND METHODS: The ARROW randomized...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Lippincott Williams & Wilkins
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4318642/ https://www.ncbi.nlm.nih.gov/pubmed/25396263 http://dx.doi.org/10.1097/QAD.0000000000000518 |
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author | Revill, Paul A. Walker, Simon Mabugu, Travor Nathoo, Kusum J. Mugyenyi, Peter Kekitinwa, Adeodata Munderi, Paula Bwakura-Dangarembizi, Mutsawashe Musiime, Victor Bakeera-Kitaka, Sabrina Nahirya-Ntege, Patricia Walker, A. Sarah Sculpher, Mark J. Gibb, Diana M. |
author_facet | Revill, Paul A. Walker, Simon Mabugu, Travor Nathoo, Kusum J. Mugyenyi, Peter Kekitinwa, Adeodata Munderi, Paula Bwakura-Dangarembizi, Mutsawashe Musiime, Victor Bakeera-Kitaka, Sabrina Nahirya-Ntege, Patricia Walker, A. Sarah Sculpher, Mark J. Gibb, Diana M. |
author_sort | Revill, Paul A. |
collection | PubMed |
description | OBJECTIVES: To conduct two economic analyses addressing whether to: routinely monitor HIV-infected children on antiretroviral therapy (ART) clinically or with laboratory tests; continue or stop cotrimoxazole prophylaxis when children become stabilized on ART. DESIGN AND METHODS: The ARROW randomized trial investigated alternative strategies to deliver paediatric ART and cotrimoxazole prophylaxis in 1206 Ugandan/Zimbabwean children. Incremental cost-effectiveness and value of implementation analyses were undertaken. Scenario analyses investigated whether laboratory monitoring (CD4(+) tests for efficacy monitoring; haematology/biochemistry for toxicity) could be tailored and targeted to be delivered cost-effectively. Cotrimoxazole use was examined in malaria-endemic and non-endemic settings. RESULTS: Using all trial data, clinical monitoring delivered similar health outcomes to routine laboratory monitoring, but at a reduced cost, so was cost-effective. Continuing cotrimoxazole improved health outcomes at reduced costs. Restricting routine CD4(+) monitoring to after 52 weeks following ART initiation and removing toxicity testing was associated with an incremental cost-effectiveness ratio of $6084 per quality-adjusted life-year (QALY) across all age groups, but was much lower for older children (12+ years at initiation; incremental cost-effectiveness ratio = $769/QALY). Committing resources to improve cotrimoxazole implementation appears cost-effective. A healthcare system that could pay $600/QALY should be willing to spend up to $12.0 per patient-year to ensure continued provision of cotrimoxazole. CONCLUSION: Clinically driven monitoring of ART is cost-effective in most circumstances. Routine laboratory monitoring is generally not cost-effective at current prices, except possibly CD4(+) testing amongst adolescents initiating ART. Committing resources to ensure continued provision of cotrimoxazole in health facilities is more likely to represent an efficient use of resources. |
format | Online Article Text |
id | pubmed-4318642 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Lippincott Williams & Wilkins |
record_format | MEDLINE/PubMed |
spelling | pubmed-43186422015-02-17 Opportunities for improving the efficiency of paediatric HIV treatment programmes Revill, Paul A. Walker, Simon Mabugu, Travor Nathoo, Kusum J. Mugyenyi, Peter Kekitinwa, Adeodata Munderi, Paula Bwakura-Dangarembizi, Mutsawashe Musiime, Victor Bakeera-Kitaka, Sabrina Nahirya-Ntege, Patricia Walker, A. Sarah Sculpher, Mark J. Gibb, Diana M. AIDS Epidemiology and Social OBJECTIVES: To conduct two economic analyses addressing whether to: routinely monitor HIV-infected children on antiretroviral therapy (ART) clinically or with laboratory tests; continue or stop cotrimoxazole prophylaxis when children become stabilized on ART. DESIGN AND METHODS: The ARROW randomized trial investigated alternative strategies to deliver paediatric ART and cotrimoxazole prophylaxis in 1206 Ugandan/Zimbabwean children. Incremental cost-effectiveness and value of implementation analyses were undertaken. Scenario analyses investigated whether laboratory monitoring (CD4(+) tests for efficacy monitoring; haematology/biochemistry for toxicity) could be tailored and targeted to be delivered cost-effectively. Cotrimoxazole use was examined in malaria-endemic and non-endemic settings. RESULTS: Using all trial data, clinical monitoring delivered similar health outcomes to routine laboratory monitoring, but at a reduced cost, so was cost-effective. Continuing cotrimoxazole improved health outcomes at reduced costs. Restricting routine CD4(+) monitoring to after 52 weeks following ART initiation and removing toxicity testing was associated with an incremental cost-effectiveness ratio of $6084 per quality-adjusted life-year (QALY) across all age groups, but was much lower for older children (12+ years at initiation; incremental cost-effectiveness ratio = $769/QALY). Committing resources to improve cotrimoxazole implementation appears cost-effective. A healthcare system that could pay $600/QALY should be willing to spend up to $12.0 per patient-year to ensure continued provision of cotrimoxazole. CONCLUSION: Clinically driven monitoring of ART is cost-effective in most circumstances. Routine laboratory monitoring is generally not cost-effective at current prices, except possibly CD4(+) testing amongst adolescents initiating ART. Committing resources to ensure continued provision of cotrimoxazole in health facilities is more likely to represent an efficient use of resources. Lippincott Williams & Wilkins 2015-01-14 2015-01-07 /pmc/articles/PMC4318642/ /pubmed/25396263 http://dx.doi.org/10.1097/QAD.0000000000000518 Text en Copyright © 2015 Wolters Kluwer Health, Inc. All rights revserved. http://creativecommons.org/licenses/by-nc-nd/3.0./ This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivitives 3.0 License, where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially. http://creativecommons.org/licenses/by-nc-nd/3.0. |
spellingShingle | Epidemiology and Social Revill, Paul A. Walker, Simon Mabugu, Travor Nathoo, Kusum J. Mugyenyi, Peter Kekitinwa, Adeodata Munderi, Paula Bwakura-Dangarembizi, Mutsawashe Musiime, Victor Bakeera-Kitaka, Sabrina Nahirya-Ntege, Patricia Walker, A. Sarah Sculpher, Mark J. Gibb, Diana M. Opportunities for improving the efficiency of paediatric HIV treatment programmes |
title | Opportunities for improving the efficiency of paediatric HIV treatment programmes |
title_full | Opportunities for improving the efficiency of paediatric HIV treatment programmes |
title_fullStr | Opportunities for improving the efficiency of paediatric HIV treatment programmes |
title_full_unstemmed | Opportunities for improving the efficiency of paediatric HIV treatment programmes |
title_short | Opportunities for improving the efficiency of paediatric HIV treatment programmes |
title_sort | opportunities for improving the efficiency of paediatric hiv treatment programmes |
topic | Epidemiology and Social |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4318642/ https://www.ncbi.nlm.nih.gov/pubmed/25396263 http://dx.doi.org/10.1097/QAD.0000000000000518 |
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