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Psychometric properties of the Friedreich Ataxia Rating Scale

OBJECTIVE: To investigate the psychometric properties of the Friedreich Ataxia Rating Scale neurologic examination (FARSn) and its subscores, as well as the influence of the modifications resulting in the now widely used modified FARS (mFARS) examination. METHODS: Based on cross-sectional FARS data...

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Autores principales: Rummey, Christian, Corben, Louise A., Delatycki, Martin B., Subramony, S.H., Bushara, Khalaf, Gomez, Christopher M., Hoyle, Joseph Chad, Yoon, Grace, Ravina, Bernard, Mathews, Katherine D., Wilmot, George, Zesiewicz, Theresa, Perlman, Susan, Farmer, Jennifer M., Lynch, David R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6927357/
https://www.ncbi.nlm.nih.gov/pubmed/32042904
http://dx.doi.org/10.1212/NXG.0000000000000371
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author Rummey, Christian
Corben, Louise A.
Delatycki, Martin B.
Subramony, S.H.
Bushara, Khalaf
Gomez, Christopher M.
Hoyle, Joseph Chad
Yoon, Grace
Ravina, Bernard
Mathews, Katherine D.
Wilmot, George
Zesiewicz, Theresa
Perlman, Susan
Farmer, Jennifer M.
Lynch, David R.
author_facet Rummey, Christian
Corben, Louise A.
Delatycki, Martin B.
Subramony, S.H.
Bushara, Khalaf
Gomez, Christopher M.
Hoyle, Joseph Chad
Yoon, Grace
Ravina, Bernard
Mathews, Katherine D.
Wilmot, George
Zesiewicz, Theresa
Perlman, Susan
Farmer, Jennifer M.
Lynch, David R.
author_sort Rummey, Christian
collection PubMed
description OBJECTIVE: To investigate the psychometric properties of the Friedreich Ataxia Rating Scale neurologic examination (FARSn) and its subscores, as well as the influence of the modifications resulting in the now widely used modified FARS (mFARS) examination. METHODS: Based on cross-sectional FARS data from the FA–Clinical Outcome Measures cohort, we conducted correlation-based psychometric analyses to investigate the interplay of items and subscores within the FARSn/mFARS constructs. RESULTS: The results provide support for both the FARSn and the mFARS constructs, as well as individually for their upper limb and lower limb coordination components. The omission of the peripheral nervous system subscore (D) and 2 items of the bulbar subscore (A) in the mFARS strengthens the overall construct compared with the complete FARS. CONCLUSIONS: A correlation-based psychometric analysis of the neurologic FARSn score justifies the overall validity of the scale. In addition, omission of items of limited functional significance as created in the mFARS improves the features of the measures. Such information is crucial to the ongoing application of the mFARS in natural history studies and clinical trials. Additional analyses of longitudinal changes will be necessary to fully ascertain its utility, especially in nonambulant patients.
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spelling pubmed-69273572020-02-10 Psychometric properties of the Friedreich Ataxia Rating Scale Rummey, Christian Corben, Louise A. Delatycki, Martin B. Subramony, S.H. Bushara, Khalaf Gomez, Christopher M. Hoyle, Joseph Chad Yoon, Grace Ravina, Bernard Mathews, Katherine D. Wilmot, George Zesiewicz, Theresa Perlman, Susan Farmer, Jennifer M. Lynch, David R. Neurol Genet Article OBJECTIVE: To investigate the psychometric properties of the Friedreich Ataxia Rating Scale neurologic examination (FARSn) and its subscores, as well as the influence of the modifications resulting in the now widely used modified FARS (mFARS) examination. METHODS: Based on cross-sectional FARS data from the FA–Clinical Outcome Measures cohort, we conducted correlation-based psychometric analyses to investigate the interplay of items and subscores within the FARSn/mFARS constructs. RESULTS: The results provide support for both the FARSn and the mFARS constructs, as well as individually for their upper limb and lower limb coordination components. The omission of the peripheral nervous system subscore (D) and 2 items of the bulbar subscore (A) in the mFARS strengthens the overall construct compared with the complete FARS. CONCLUSIONS: A correlation-based psychometric analysis of the neurologic FARSn score justifies the overall validity of the scale. In addition, omission of items of limited functional significance as created in the mFARS improves the features of the measures. Such information is crucial to the ongoing application of the mFARS in natural history studies and clinical trials. Additional analyses of longitudinal changes will be necessary to fully ascertain its utility, especially in nonambulant patients. Wolters Kluwer 2019-10-29 /pmc/articles/PMC6927357/ /pubmed/32042904 http://dx.doi.org/10.1212/NXG.0000000000000371 Text en Copyright © 2019 The Author(s). Published by Wolters Kluwer Health, Inc. on behalf of the American Academy of Neurology. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND) (http://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits downloading and sharing the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal.
spellingShingle Article
Rummey, Christian
Corben, Louise A.
Delatycki, Martin B.
Subramony, S.H.
Bushara, Khalaf
Gomez, Christopher M.
Hoyle, Joseph Chad
Yoon, Grace
Ravina, Bernard
Mathews, Katherine D.
Wilmot, George
Zesiewicz, Theresa
Perlman, Susan
Farmer, Jennifer M.
Lynch, David R.
Psychometric properties of the Friedreich Ataxia Rating Scale
title Psychometric properties of the Friedreich Ataxia Rating Scale
title_full Psychometric properties of the Friedreich Ataxia Rating Scale
title_fullStr Psychometric properties of the Friedreich Ataxia Rating Scale
title_full_unstemmed Psychometric properties of the Friedreich Ataxia Rating Scale
title_short Psychometric properties of the Friedreich Ataxia Rating Scale
title_sort psychometric properties of the friedreich ataxia rating scale
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6927357/
https://www.ncbi.nlm.nih.gov/pubmed/32042904
http://dx.doi.org/10.1212/NXG.0000000000000371
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