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The societal cost of Huntington’s disease: are we underestimating the burden?

Jones, C., Busse, Monica, Quinn, Lori, Dawes, H., Drew, Cheney, Kelson, Mark, Hood, Kerenza, Rosser, Anne Elizabeth and Tudor-Edwards, R. 2016. The societal cost of Huntington’s disease: are we underestimating the burden? European Journal of Neurology 23 (10) , pp. 1588-1590. 10.1111/ene.13107

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Abstract

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.

Item Type: Article
Date Type: Publication
Status: Published
Schools: Biosciences
Cardiff University Brain Research Imaging Centre (CUBRIC)
Healthcare Sciences
Medicine
Neuroscience and Mental Health Research Institute (NMHRI)
Subjects: R Medicine > RC Internal medicine > RC0321 Neuroscience. Biological psychiatry. Neuropsychiatry
Uncontrolled Keywords: cost; health economics; Huntington's disease
Publisher: Wiley-Blackwell
ISSN: 1351-5101
Funders: Health and Care Research Wales
Date of First Compliant Deposit: 13 June 2016
Date of Acceptance: 9 June 2016
Last Modified: 22 Feb 2019 22:37
URI: http://orca.cf.ac.uk/id/eprint/91776

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