Evidence map›Paper›PMID 41216881›Full record

ArticleMovement disorders clinical practice2026

Economic Cost of Current and Alternative Models of Multidisciplinary Care of Juvenile-Onset Huntington's Disease.

Tracey A Young, Penny A Curtis, Jill Thompson, Aileen K Ho, Helen Santini, Oliver W Quarrell

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Article in Movement disorders clinical practice, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Tracey A YoungHealth Economics and Decision Science, Sheffield Centre for Health and Related Research, School of Medicine and Population Health, University of Sheffield, Sheffield, UK.ORCID https://orcid.org/0000-0001-8467-0471
Penny A CurtisSchool of Allied Health Professions, Nursing and Midwifery, University of Sheffield, Sheffield, UK.
Jill ThompsonSchool of Allied Health Professions, Nursing and Midwifery, University of Sheffield, Sheffield, UK.ORCID https://orcid.org/0000-0001-9256-1208
Aileen K HoSchool of Psychology and Clinical Language Sciences, University of Reading, Reading, UK.
Helen SantiniAdvisory Service, Huntington's Disease Association, Liverpool Science Park IC1, Liverpool, UK.
Oliver W QuarrellSheffield Children's Hospital, Western Bank, Sheffield, UK.ORCID https://orcid.org/0000-0002-3818-9051

Funding

National Institute for Health Research (NIHR) PB-PG-112-29056
6 · The paper itself

Abstract

backgroundMultidisciplinary care has been advocated for Juvenile-onset Huntington's Disease but there has been no detailed analysis of this.

objectivesTo evaluate the current economic costs of providing health care for patients with Juvenile-onset Huntington's disease (JoHD) and to model the effects and economic costs of providing a multidisciplinary team (MDT) approach.

methodsPatients were recruited through the patients' organization, the Huntington's Disease Association, and specialist Huntington's disease clinics. Thirty-three adapted Client Service Receipt Inventories were completed following either a telephone or in-person interview. The effects of delivering two models of providing a systematic MDT approach, traditional in-person MDT and digital MDT were assessed.

resultsThe overall mean JoHD cost to the NHS per year (2020) was £126,966 which varied according to disease severity, costing just under £11,000 in mild disease, £132,419 in moderate disease, and £221,797 in advanced JoHD. The proportion of indirect costs to families and carers was 64% for mild disease and 17% for advanced disease. Assuming a 50% reduction in health care professionals seen, the alternative models saw reduction costs of £2490 and £2730, respectively.

conclusionWe document the high cost of care in JoHD, particularly as the disease progresses towards the later stages. We present estimates from modeling the effects of providing a systematic MDT approach to the care of patients and families with JoHD. These data have clear implications in the consideration of future JoHD models of care in an increasingly digital age and can be developed further as disease modifying treatments become available.

Indexed as

Cost of IllnessHealth Care CostsHuntington DiseasePatient Care TeamAdolescentAdultAge of OnsetChildFemaleHumansMaleState MedicineYoung Adulteconomic costHuntington's diseaseJuvenile‐onsetmultidisciplinary teamvirtual clinics

Identifiers

PMID41216881
PMCPMC13071353

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