Literature DB >> 29260836

Responsiveness of performance-based outcome measures for mobility, balance, muscle strength and manual dexterity in adults with myotonic dystrophy type 1.

Marie Kierkegaard1, Émilie Petitclerc, Luc J Hébert, Jean Mathieu, Cynthia Gagnon.   

Abstract

OBJECTIVE: To assess changes and responsiveness in outcome measures of mobility, balance, muscle strength and manual dexterity in adults with myotonic dystrophy type 1.
DESIGN: A 9-year longitudinal study conducted with 113 patients.
METHODS: The responsiveness of the Timed Up and Go test, Berg Balance Scale, quantitative muscle testing, grip and pinch-grip strength, and Purdue Pegboard Test was assessed using criterion and construct approaches. Patient-reported perceived changes (worse/stable) in balance, walking, lower-limb weakness, stair-climbing and hand weakness were used as criteria. Predefined hypotheses about expected area under the receiver operating characteristic curves (criterion approach) and correlations between relative changes (construct approach) were explored.
RESULTS: The direction and magnitude of median changes in outcome measures corresponded with patient-reported changes. Median changes in the Timed Up and Go test, grip strength, pinch-grip strength and Purdue Pegboard Test did not, in general, exceed known measurement errors. Most criterion (72%) and construct (70%) approach hypotheses were supported. Promising responsiveness was found for outcome measures of mobility, balance and muscle strength. Grip strength and manual dexterity measures showed poorer responsiveness.
CONCLUSION: The performance-based outcome measures captured changes over the 9-year period and responsiveness was promising. Knowledge of measurement errors is needed to interpret the meaning of these longitudinal changes.

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Year:  2018        PMID: 29260836     DOI: 10.2340/16501977-2304

Source DB:  PubMed          Journal:  J Rehabil Med        ISSN: 1650-1977            Impact factor:   2.912


  3 in total

1.  A 9-year follow-up study of quantitative muscle strength changes in myotonic dystrophy type 1.

Authors:  Cynthia Gagnon; Émilie Petitclerc; Marie Kierkegaard; Jean Mathieu; Élise Duchesne; Luc J Hébert
Journal:  J Neurol       Date:  2018-05-21       Impact factor: 4.849

2.  Assessment of muscular strength and functional capacity in the juvenile and adult myotonic dystrophy type 1 population: a 3-year follow-up study.

Authors:  Marie-Pier Roussel; Marie-Michèle Fiset; Laurie Gauthier; Claudia Lavoie; Émilie McNicoll; Laurie Pouliot; Cynthia Gagnon; Elise Duchesne
Journal:  J Neurol       Date:  2021-04-27       Impact factor: 4.849

3.  Responsiveness of outcome measures in myotonic dystrophy type 1.

Authors:  Kirsten L Knak; Aisha M Sheikh; Nanna Witting; John Vissing
Journal:  Ann Clin Transl Neurol       Date:  2020-07-16       Impact factor: 4.511

  3 in total

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