Health utilities and costs for neuromyelitis optica spectrum disorder

Allbwn ymchwil: Cyfraniad at gyfnodolynErthygladolygiad gan gymheiriaid

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Health utilities and costs for neuromyelitis optica spectrum disorder. / Hughes, Dyfrig; Bourke, Siobhan; Jones, Angela et al.
Yn: Orphanet Journal of Rare Diseases, Cyfrol 17, 159, 2022.

Allbwn ymchwil: Cyfraniad at gyfnodolynErthygladolygiad gan gymheiriaid

HarvardHarvard

Hughes, D, Bourke, S, Jones, A, Bhatt, R, Huda, S, Mutch, K & Jacob, A 2022, 'Health utilities and costs for neuromyelitis optica spectrum disorder', Orphanet Journal of Rare Diseases, cyfrol. 17, 159.

APA

Hughes, D., Bourke, S., Jones, A., Bhatt, R., Huda, S., Mutch, K., & Jacob, A. (2022). Health utilities and costs for neuromyelitis optica spectrum disorder. Orphanet Journal of Rare Diseases, 17, Erthygl 159.

CBE

Hughes D, Bourke S, Jones A, Bhatt R, Huda S, Mutch K, Jacob A. 2022. Health utilities and costs for neuromyelitis optica spectrum disorder. Orphanet Journal of Rare Diseases. 17:Article 159.

MLA

VancouverVancouver

Hughes D, Bourke S, Jones A, Bhatt R, Huda S, Mutch K et al. Health utilities and costs for neuromyelitis optica spectrum disorder. Orphanet Journal of Rare Diseases. 2022;17:159. Epub 2022 Ebr 7.

Author

Hughes, Dyfrig ; Bourke, Siobhan ; Jones, Angela et al. / Health utilities and costs for neuromyelitis optica spectrum disorder. Yn: Orphanet Journal of Rare Diseases. 2022 ; Cyfrol 17.

RIS

TY - JOUR

T1 - Health utilities and costs for neuromyelitis optica spectrum disorder

AU - Hughes, Dyfrig

AU - Bourke, Siobhan

AU - Jones, Angela

AU - Bhatt, Rikesh

AU - Huda, Saif

AU - Mutch, Kerry

AU - Jacob, Anu

PY - 2022

Y1 - 2022

N2 - Background: Neuromyelitis optica spectrum disorder (NMOSD) is a rare, neurological disease that places a significant burden on patients, their carers, and healthcare systems.Objectives: To estimate patient and carer health utilities and costs of NMOSD within the UK setting.Methods: Patients with NMOSD and their carers, recruited via a regional specialist treatment centre, completed a postal questionnaire that included a resource use measure, the EuroQoL (EQ)-5D-5L, EQ-5D-VAS, Vision and Quality of Life Index (VisQoL), Carer Experience Survey (CES) and the Expanded Disability Status Scale (EDSS). The questionnaire asked about respondents’ use of health and community care services, non-medical costs, informal care and work capacity. Data were analysed descriptively. Uncertainties in costs and utilities were assessed using bootstrap analysis.Results: 117 patients and 74 informal carers responded to the survey. Patients’ mean EQ-5D-5L and VisQoL health utilities (95% central range) were 0.54 (-0.29, 1.00) and 0.79 (0.11, 0.99), respectively. EQ-5D-5L utility decreased with increasing EDSS score bandings, from 0.80 (0.75, 0.85) for EDSS ≤ 4.0, to 0.20 (-0.29, 0.56) for EDSS 8.0 to 9.5. Mean, 3-month total costs were £5,623 (£2,096, £12,156), but ranged from £562 (£381, £812) to £32,717 (£2,888, £98,568) for these EDSS bandings. Carer-reported EQ-5D-5L utility and CES index scores were 0.85 (0.82, 0.89) and 57.67 (52.69, 62.66). Mean, 3-month costs of informal care were £13,150 to £24,560.Conclusions: NMOSD has significant impacts on health utilities and NHS and carer costs. These data can be used as inputs to cost-effectiveness analyses of new medicines for NMOSD.

AB - Background: Neuromyelitis optica spectrum disorder (NMOSD) is a rare, neurological disease that places a significant burden on patients, their carers, and healthcare systems.Objectives: To estimate patient and carer health utilities and costs of NMOSD within the UK setting.Methods: Patients with NMOSD and their carers, recruited via a regional specialist treatment centre, completed a postal questionnaire that included a resource use measure, the EuroQoL (EQ)-5D-5L, EQ-5D-VAS, Vision and Quality of Life Index (VisQoL), Carer Experience Survey (CES) and the Expanded Disability Status Scale (EDSS). The questionnaire asked about respondents’ use of health and community care services, non-medical costs, informal care and work capacity. Data were analysed descriptively. Uncertainties in costs and utilities were assessed using bootstrap analysis.Results: 117 patients and 74 informal carers responded to the survey. Patients’ mean EQ-5D-5L and VisQoL health utilities (95% central range) were 0.54 (-0.29, 1.00) and 0.79 (0.11, 0.99), respectively. EQ-5D-5L utility decreased with increasing EDSS score bandings, from 0.80 (0.75, 0.85) for EDSS ≤ 4.0, to 0.20 (-0.29, 0.56) for EDSS 8.0 to 9.5. Mean, 3-month total costs were £5,623 (£2,096, £12,156), but ranged from £562 (£381, £812) to £32,717 (£2,888, £98,568) for these EDSS bandings. Carer-reported EQ-5D-5L utility and CES index scores were 0.85 (0.82, 0.89) and 57.67 (52.69, 62.66). Mean, 3-month costs of informal care were £13,150 to £24,560.Conclusions: NMOSD has significant impacts on health utilities and NHS and carer costs. These data can be used as inputs to cost-effectiveness analyses of new medicines for NMOSD.

KW - Neuromyelitis optica spectrum disorder

KW - Carers

KW - Cost of illness

KW - EQ-5D

KW - Utility

M3 - Article

VL - 17

JO - Orphanet Journal of Rare Diseases

JF - Orphanet Journal of Rare Diseases

SN - 1750-1172

M1 - 159

ER -