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Measuring disability in multiple sclerosis: the WHODAS 2.0

INTRODUCTION: Reliable measurement of disability in multiple sclerosis (MS) using a comprehensive, patient self-reported scale, such as the World Health Organization Disability Assessment Schedule (WHODAS) 2.0, would be of clinical and research benefit. METHODS: In the Trajectories of Outcome in Neu...

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Autores principales: Young, Carolyn A., Rog, David J., Sharrack, Basil, Constantinescu, Cris, Kalra, Seema, Harrower, Tim, Langdon, Dawn, Tennant, Alan, Mills, Roger J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10522513/
https://www.ncbi.nlm.nih.gov/pubmed/37589773
http://dx.doi.org/10.1007/s11136-023-03470-6
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author Young, Carolyn A.
Rog, David J.
Sharrack, Basil
Constantinescu, Cris
Kalra, Seema
Harrower, Tim
Langdon, Dawn
Tennant, Alan
Mills, Roger J.
author_facet Young, Carolyn A.
Rog, David J.
Sharrack, Basil
Constantinescu, Cris
Kalra, Seema
Harrower, Tim
Langdon, Dawn
Tennant, Alan
Mills, Roger J.
author_sort Young, Carolyn A.
collection PubMed
description INTRODUCTION: Reliable measurement of disability in multiple sclerosis (MS) using a comprehensive, patient self-reported scale, such as the World Health Organization Disability Assessment Schedule (WHODAS) 2.0, would be of clinical and research benefit. METHODS: In the Trajectories of Outcome in Neurological Conditions-MS study, WHODAS 2.0 (WHODAS-36 items for working, WHODAS-32 items if not working, WHODAS-12 items short-form) was examined using Rasch analysis in 5809 people with MS. RESULTS: The 36- and 32-item parallel forms, and the cognitive and physical domains, showed reliability consistent with individual or group use. The 12-item short-form is valid for group use only. Interval level measurement for parametric statistics can be derived from all three scales which showed medium to strong effect sizes for discrimination across characteristics such as age, subtype, and disease duration. Smallest detectable difference for each scale was < 6 on the standardised metric of 0–100 so < 6% of the total range. There was no substantial differential item functioning (DIF) by age, gender, education, working full/part-time, or disease duration; the finding of no DIF for time or sample supports the use of WHODAS 2.0 for longitudinal studies, with the 36- and 32-item versions and the physical and cognitive domains valid for individual patient follow-up. CONCLUSIONS: Disability in MS can be comprehensively measured at interval level by the WHODAS 2.0, and validly monitored over time. Routine use of this self-reported measure in clinical and research practice would give valuable information on the trajectories of disability of individuals and groups. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s11136-023-03470-6.
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spelling pubmed-105225132023-09-28 Measuring disability in multiple sclerosis: the WHODAS 2.0 Young, Carolyn A. Rog, David J. Sharrack, Basil Constantinescu, Cris Kalra, Seema Harrower, Tim Langdon, Dawn Tennant, Alan Mills, Roger J. Qual Life Res Article INTRODUCTION: Reliable measurement of disability in multiple sclerosis (MS) using a comprehensive, patient self-reported scale, such as the World Health Organization Disability Assessment Schedule (WHODAS) 2.0, would be of clinical and research benefit. METHODS: In the Trajectories of Outcome in Neurological Conditions-MS study, WHODAS 2.0 (WHODAS-36 items for working, WHODAS-32 items if not working, WHODAS-12 items short-form) was examined using Rasch analysis in 5809 people with MS. RESULTS: The 36- and 32-item parallel forms, and the cognitive and physical domains, showed reliability consistent with individual or group use. The 12-item short-form is valid for group use only. Interval level measurement for parametric statistics can be derived from all three scales which showed medium to strong effect sizes for discrimination across characteristics such as age, subtype, and disease duration. Smallest detectable difference for each scale was < 6 on the standardised metric of 0–100 so < 6% of the total range. There was no substantial differential item functioning (DIF) by age, gender, education, working full/part-time, or disease duration; the finding of no DIF for time or sample supports the use of WHODAS 2.0 for longitudinal studies, with the 36- and 32-item versions and the physical and cognitive domains valid for individual patient follow-up. CONCLUSIONS: Disability in MS can be comprehensively measured at interval level by the WHODAS 2.0, and validly monitored over time. Routine use of this self-reported measure in clinical and research practice would give valuable information on the trajectories of disability of individuals and groups. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s11136-023-03470-6. Springer International Publishing 2023-08-17 2023 /pmc/articles/PMC10522513/ /pubmed/37589773 http://dx.doi.org/10.1007/s11136-023-03470-6 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/) .
spellingShingle Article
Young, Carolyn A.
Rog, David J.
Sharrack, Basil
Constantinescu, Cris
Kalra, Seema
Harrower, Tim
Langdon, Dawn
Tennant, Alan
Mills, Roger J.
Measuring disability in multiple sclerosis: the WHODAS 2.0
title Measuring disability in multiple sclerosis: the WHODAS 2.0
title_full Measuring disability in multiple sclerosis: the WHODAS 2.0
title_fullStr Measuring disability in multiple sclerosis: the WHODAS 2.0
title_full_unstemmed Measuring disability in multiple sclerosis: the WHODAS 2.0
title_short Measuring disability in multiple sclerosis: the WHODAS 2.0
title_sort measuring disability in multiple sclerosis: the whodas 2.0
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10522513/
https://www.ncbi.nlm.nih.gov/pubmed/37589773
http://dx.doi.org/10.1007/s11136-023-03470-6
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