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Estimated costs for Duchenne muscular dystrophy care in Brazil
BACKGROUND: The economic burden of rare diseases on health systems is still not widely measured, with the generation of accurate information about the costs with medical care for subjects with rare diseases being crucial when defining health policies. Duchenne Muscular Dystrophy (DMD) is the most co...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10288739/ https://www.ncbi.nlm.nih.gov/pubmed/37349725 http://dx.doi.org/10.1186/s13023-023-02767-6 |
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author | Schneider, Nayê Balzan Roos, Erica Caetano Staub, Ana Lúcia Portella Bevilacqua, Isabela Possebon de Almeida, Ana Carolina de Camargo Martins, Tamiê Ramos, Natalia Bergamelli Loze, Priscilla Saute, Jonas Alex Morales Etges, Ana Paula Beck da Silva Polanczyk, Carisi Anne |
author_facet | Schneider, Nayê Balzan Roos, Erica Caetano Staub, Ana Lúcia Portella Bevilacqua, Isabela Possebon de Almeida, Ana Carolina de Camargo Martins, Tamiê Ramos, Natalia Bergamelli Loze, Priscilla Saute, Jonas Alex Morales Etges, Ana Paula Beck da Silva Polanczyk, Carisi Anne |
author_sort | Schneider, Nayê Balzan |
collection | PubMed |
description | BACKGROUND: The economic burden of rare diseases on health systems is still not widely measured, with the generation of accurate information about the costs with medical care for subjects with rare diseases being crucial when defining health policies. Duchenne Muscular Dystrophy (DMD) is the most common form of muscular dystrophy, with new technologies recently being studied for its management. Information about the costs related to the disease in Latin America is scarce, and the objective of this study is to evaluate the annual hospital, home care and transportation costs per patient with DMD treatment in Brazil. RESULTS: Data from 27 patients were included, the median annual cost per patient was R$ 17,121 (IQR R$ 6,786; 25,621). Home care expenditures accounted for 92% of the total costs, followed by hospital costs (6%) and transportation costs (2%). Medications and loss of family, and patient’s productivity are among the most representative consumption items. When disease worsening due to loss of the ability to walk was incorporated to the analysis, it was shown that wheelchair users account for an incremental cost of 23% compared with non-wheelchair users. CONCLUSIONS: This is an original study in Latin America to measure DMD costs using the micro-costing technique. Generating accurate information about costs is crucial to provide health managers with information that could help establish more sustainable policies when deciding upon rare diseases in emerging countries. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13023-023-02767-6. |
format | Online Article Text |
id | pubmed-10288739 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-102887392023-06-24 Estimated costs for Duchenne muscular dystrophy care in Brazil Schneider, Nayê Balzan Roos, Erica Caetano Staub, Ana Lúcia Portella Bevilacqua, Isabela Possebon de Almeida, Ana Carolina de Camargo Martins, Tamiê Ramos, Natalia Bergamelli Loze, Priscilla Saute, Jonas Alex Morales Etges, Ana Paula Beck da Silva Polanczyk, Carisi Anne Orphanet J Rare Dis Research BACKGROUND: The economic burden of rare diseases on health systems is still not widely measured, with the generation of accurate information about the costs with medical care for subjects with rare diseases being crucial when defining health policies. Duchenne Muscular Dystrophy (DMD) is the most common form of muscular dystrophy, with new technologies recently being studied for its management. Information about the costs related to the disease in Latin America is scarce, and the objective of this study is to evaluate the annual hospital, home care and transportation costs per patient with DMD treatment in Brazil. RESULTS: Data from 27 patients were included, the median annual cost per patient was R$ 17,121 (IQR R$ 6,786; 25,621). Home care expenditures accounted for 92% of the total costs, followed by hospital costs (6%) and transportation costs (2%). Medications and loss of family, and patient’s productivity are among the most representative consumption items. When disease worsening due to loss of the ability to walk was incorporated to the analysis, it was shown that wheelchair users account for an incremental cost of 23% compared with non-wheelchair users. CONCLUSIONS: This is an original study in Latin America to measure DMD costs using the micro-costing technique. Generating accurate information about costs is crucial to provide health managers with information that could help establish more sustainable policies when deciding upon rare diseases in emerging countries. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13023-023-02767-6. BioMed Central 2023-06-22 /pmc/articles/PMC10288739/ /pubmed/37349725 http://dx.doi.org/10.1186/s13023-023-02767-6 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Schneider, Nayê Balzan Roos, Erica Caetano Staub, Ana Lúcia Portella Bevilacqua, Isabela Possebon de Almeida, Ana Carolina de Camargo Martins, Tamiê Ramos, Natalia Bergamelli Loze, Priscilla Saute, Jonas Alex Morales Etges, Ana Paula Beck da Silva Polanczyk, Carisi Anne Estimated costs for Duchenne muscular dystrophy care in Brazil |
title | Estimated costs for Duchenne muscular dystrophy care in Brazil |
title_full | Estimated costs for Duchenne muscular dystrophy care in Brazil |
title_fullStr | Estimated costs for Duchenne muscular dystrophy care in Brazil |
title_full_unstemmed | Estimated costs for Duchenne muscular dystrophy care in Brazil |
title_short | Estimated costs for Duchenne muscular dystrophy care in Brazil |
title_sort | estimated costs for duchenne muscular dystrophy care in brazil |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10288739/ https://www.ncbi.nlm.nih.gov/pubmed/37349725 http://dx.doi.org/10.1186/s13023-023-02767-6 |
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