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The societal cost of Huntington's disease: are we underestimating the burden?
BACKGROUND AND PURPOSE: Approximately 9000 people in the UK are affected by Huntington's disease (HD). People with HD require ongoing health and social care support. There is a knowledge gap about costs of health and social care use associated with HD in the UK. This paper estimates the economi...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5096063/ https://www.ncbi.nlm.nih.gov/pubmed/27461550 http://dx.doi.org/10.1111/ene.13107 |
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author | Jones, C. Busse, M. Quinn, L. Dawes, H. Drew, C. Kelson, M. Hood, K. Rosser, A. Edwards, R. T. |
author_facet | Jones, C. Busse, M. Quinn, L. Dawes, H. Drew, C. Kelson, M. Hood, K. Rosser, A. Edwards, R. T. |
author_sort | Jones, C. |
collection | PubMed |
description | BACKGROUND AND PURPOSE: Approximately 9000 people in the UK are affected by Huntington's disease (HD). People with HD require ongoing health and social care support. There is a knowledge gap about costs of health and social care use associated with HD in the UK. This paper estimates the economic cost in the UK. METHODS: Data on UK patients for the year 2013 were extracted from the European Huntington's Disease Network REGISTRY study, a full clinical dataset, including the full medical history and medication history for patients with HD. National unit costs for the price year 2013 were applied to health and social care services. RESULTS: Data were available for 131 people. The mean annual cost per person with HD was £21 605. The largest proportion of this cost (65%) was due to informal care (£14 085). CONCLUSIONS: Informal care was the largest driver of costs across all stages of HD; thus there is a need to also consider the needs of carers when planning services for people with HD. |
format | Online Article Text |
id | pubmed-5096063 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-50960632016-11-09 The societal cost of Huntington's disease: are we underestimating the burden? Jones, C. Busse, M. Quinn, L. Dawes, H. Drew, C. Kelson, M. Hood, K. Rosser, A. Edwards, R. T. Eur J Neurol Short Communication BACKGROUND AND PURPOSE: Approximately 9000 people in the UK are affected by Huntington's disease (HD). People with HD require ongoing health and social care support. There is a knowledge gap about costs of health and social care use associated with HD in the UK. This paper estimates the economic cost in the UK. METHODS: Data on UK patients for the year 2013 were extracted from the European Huntington's Disease Network REGISTRY study, a full clinical dataset, including the full medical history and medication history for patients with HD. National unit costs for the price year 2013 were applied to health and social care services. RESULTS: Data were available for 131 people. The mean annual cost per person with HD was £21 605. The largest proportion of this cost (65%) was due to informal care (£14 085). CONCLUSIONS: Informal care was the largest driver of costs across all stages of HD; thus there is a need to also consider the needs of carers when planning services for people with HD. John Wiley and Sons Inc. 2016-07-27 2016-10 /pmc/articles/PMC5096063/ /pubmed/27461550 http://dx.doi.org/10.1111/ene.13107 Text en © 2016 The Authors. European Journal of Neurology published by John Wiley & Sons Ltd on behalf of European Academy of Neurology. This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial (http://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | Short Communication Jones, C. Busse, M. Quinn, L. Dawes, H. Drew, C. Kelson, M. Hood, K. Rosser, A. Edwards, R. T. The societal cost of Huntington's disease: are we underestimating the burden? |
title | The societal cost of Huntington's disease: are we underestimating the burden? |
title_full | The societal cost of Huntington's disease: are we underestimating the burden? |
title_fullStr | The societal cost of Huntington's disease: are we underestimating the burden? |
title_full_unstemmed | The societal cost of Huntington's disease: are we underestimating the burden? |
title_short | The societal cost of Huntington's disease: are we underestimating the burden? |
title_sort | societal cost of huntington's disease: are we underestimating the burden? |
topic | Short Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5096063/ https://www.ncbi.nlm.nih.gov/pubmed/27461550 http://dx.doi.org/10.1111/ene.13107 |
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