Upper Limb Strength and Function Changes during a One-Year Follow-Up in Non-Ambulant Patients with Duchenne Muscular Dystrophy: An Observational Multicenter Trial
Male
info:eu-repo/classification/mesh/Young Adult
[SDV]Life Sciences [q-bio]
Mesh:Muscular Dystrophy
Mesh:Adult
Mesh:Adolescent
0302 clinical medicine
info:eu-repo/classification/mesh/Female
Mesh:Duchenne/drug therapy
Muscular Dystrophy
Mesh:Muscle Strength*/drug effects
info:eu-repo/classification/mesh/Child
Child
Mesh:Duchenne/physiopathology*
info:eu-repo/classification/mesh/Adult
info:eu-repo/classification/mesh/Follow-Up Studies
info:eu-repo/classification/mesh/Muscle Strength*/drug effects
Q
R
Mesh:Recovery of Function*/drug effects
Sciences bio-médicales et agricoles
3. Good health
[SDV] Life Sciences [q-bio]
info:eu-repo/classification/mesh/Muscular Dystrophy
Medicine
Female
info:eu-repo/classification/mesh/Male
Research Article
Mesh:Follow-Up Studies
Mesh:Female
Adult
info:eu-repo/classification/mesh/Duchenne/drug therapy
Mesh:Child
Adolescent
Science
610
Mesh:Male
Mesh:Young Adult
Upper Extremity
Young Adult
03 medical and health sciences
Upper Extremity -- physiopathology
Muscular Dystrophy, Duchenne -- drug therapy -- physiopathology
617
Humans
Muscle Strength
Recovery of Function -- drug effects
info:eu-repo/classification/mesh/Adolescent
Recovery of Function
Muscular Dystrophy, Duchenne
Mesh:Humans
info:eu-repo/classification/mesh/Duchenne/physiopathology*
Muscle Strength -- drug effects
Mesh:Upper Extremity/physiopathology*
Duchenne -- drug therapy -- physiopathology
info:eu-repo/classification/mesh/Recovery of Function*/drug effects
info:eu-repo/classification/mesh/Humans
info:eu-repo/classification/mesh/Upper Extremity/physiopathology*
Follow-Up Studies
DOI:
10.1371/journal.pone.0113999
Publication Date:
2015-02-02T20:14:09Z
AUTHORS (24)
ABSTRACT
Upper limb evaluation of patients with Duchenne Muscular Dystrophy is crucially important to evaluations of efficacy of new treatments in non-ambulant patients. In patients who have lost ambulation, there are few validated and informative outcome measures. In addition, longitudinal data demonstrating sensitivity to clinical evolution of outcome measures over short-term periods are lacking.We report here the results of a one-year multicenter study using specifically designed tools to assess grip, pinch strength, and hand function in wheelchair-bound patients. Our study assessed 53 non-ambulant patients with Duchenne muscular dystrophy aged 17.1 ± 4.8 years (range: 9 - 28.1 years). The average Brooke functional score of these patients was 4.6 ± 1.1. The average forced vital capacity was 44.5% predicted and 19 patients used non-invasive ventilation. Patients were assessed at baseline, 6 months, and one year using the Motor Function Measure and innovative devices (namely the MyoSet composed of MyoGrip, MyoPinch, and MoviPlate).Our study confirmed preliminary data previously reported regarding feasibility of use and of reliability of the MyoSet and the correlation at baseline between distal strength and clinical outcomes such as FVC, Brooke score, age, and duration since loss of ambulation. A significant correlation was observed between the distal upper limb strength and clinical variables. The sensitive dynamometers (MyoGrip and MyoPinch) and MoviPlate captured a 12-month change in non-ambulant Duchenne muscular dystrophy patients of all ages.ClinicalTrials.gov NCT00993161 NCT00993161.
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