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Upper Limb Strength and Function Changes during a One-Year Follow-Up in Non-Ambulant Patients with Duchenne Muscular Dystrophy: An Observational Multicenter Trial

INTRODUCTION: 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 dat...

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Autores principales: Seferian, Andreea Mihaela, Moraux, Amélie, Annoussamy, Mélanie, Canal, Aurélie, Decostre, Valérie, Diebate, Oumar, Le Moing, Anne-Gaëlle, Gidaro, Teresa, Deconinck, Nicolas, Van Parys, Frauke, Vereecke, Wendy, Wittevrongel, Sylvia, Mayer, Michèle, Maincent, Kim, Desguerre, Isabelle, Thémar-Noël, Christine, Cuisset, Jean-Marie, Tiffreau, Vincent, Denis, Severine, Jousten, Virginie, Quijano-Roy, Susana, Voit, Thomas, Hogrel, Jean-Yves, Servais, Laurent
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4314080/
https://www.ncbi.nlm.nih.gov/pubmed/25643053
http://dx.doi.org/10.1371/journal.pone.0113999
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author Seferian, Andreea Mihaela
Moraux, Amélie
Annoussamy, Mélanie
Canal, Aurélie
Decostre, Valérie
Diebate, Oumar
Le Moing, Anne-Gaëlle
Gidaro, Teresa
Deconinck, Nicolas
Van Parys, Frauke
Vereecke, Wendy
Wittevrongel, Sylvia
Mayer, Michèle
Maincent, Kim
Desguerre, Isabelle
Thémar-Noël, Christine
Cuisset, Jean-Marie
Tiffreau, Vincent
Denis, Severine
Jousten, Virginie
Quijano-Roy, Susana
Voit, Thomas
Hogrel, Jean-Yves
Servais, Laurent
author_facet Seferian, Andreea Mihaela
Moraux, Amélie
Annoussamy, Mélanie
Canal, Aurélie
Decostre, Valérie
Diebate, Oumar
Le Moing, Anne-Gaëlle
Gidaro, Teresa
Deconinck, Nicolas
Van Parys, Frauke
Vereecke, Wendy
Wittevrongel, Sylvia
Mayer, Michèle
Maincent, Kim
Desguerre, Isabelle
Thémar-Noël, Christine
Cuisset, Jean-Marie
Tiffreau, Vincent
Denis, Severine
Jousten, Virginie
Quijano-Roy, Susana
Voit, Thomas
Hogrel, Jean-Yves
Servais, Laurent
author_sort Seferian, Andreea Mihaela
collection PubMed
description INTRODUCTION: 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. PATIENTS AND METHODS: 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). RESULTS: 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. TRIAL REGISTRATION: ClinicalTrials.gov NCT00993161 NCT00993161
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spelling pubmed-43140802015-02-13 Upper Limb Strength and Function Changes during a One-Year Follow-Up in Non-Ambulant Patients with Duchenne Muscular Dystrophy: An Observational Multicenter Trial Seferian, Andreea Mihaela Moraux, Amélie Annoussamy, Mélanie Canal, Aurélie Decostre, Valérie Diebate, Oumar Le Moing, Anne-Gaëlle Gidaro, Teresa Deconinck, Nicolas Van Parys, Frauke Vereecke, Wendy Wittevrongel, Sylvia Mayer, Michèle Maincent, Kim Desguerre, Isabelle Thémar-Noël, Christine Cuisset, Jean-Marie Tiffreau, Vincent Denis, Severine Jousten, Virginie Quijano-Roy, Susana Voit, Thomas Hogrel, Jean-Yves Servais, Laurent PLoS One Research Article INTRODUCTION: 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. PATIENTS AND METHODS: 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). RESULTS: 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. TRIAL REGISTRATION: ClinicalTrials.gov NCT00993161 NCT00993161 Public Library of Science 2015-02-02 /pmc/articles/PMC4314080/ /pubmed/25643053 http://dx.doi.org/10.1371/journal.pone.0113999 Text en © 2015 Seferian et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Seferian, Andreea Mihaela
Moraux, Amélie
Annoussamy, Mélanie
Canal, Aurélie
Decostre, Valérie
Diebate, Oumar
Le Moing, Anne-Gaëlle
Gidaro, Teresa
Deconinck, Nicolas
Van Parys, Frauke
Vereecke, Wendy
Wittevrongel, Sylvia
Mayer, Michèle
Maincent, Kim
Desguerre, Isabelle
Thémar-Noël, Christine
Cuisset, Jean-Marie
Tiffreau, Vincent
Denis, Severine
Jousten, Virginie
Quijano-Roy, Susana
Voit, Thomas
Hogrel, Jean-Yves
Servais, Laurent
Upper Limb Strength and Function Changes during a One-Year Follow-Up in Non-Ambulant Patients with Duchenne Muscular Dystrophy: An Observational Multicenter Trial
title Upper Limb Strength and Function Changes during a One-Year Follow-Up in Non-Ambulant Patients with Duchenne Muscular Dystrophy: An Observational Multicenter Trial
title_full Upper Limb Strength and Function Changes during a One-Year Follow-Up in Non-Ambulant Patients with Duchenne Muscular Dystrophy: An Observational Multicenter Trial
title_fullStr Upper Limb Strength and Function Changes during a One-Year Follow-Up in Non-Ambulant Patients with Duchenne Muscular Dystrophy: An Observational Multicenter Trial
title_full_unstemmed Upper Limb Strength and Function Changes during a One-Year Follow-Up in Non-Ambulant Patients with Duchenne Muscular Dystrophy: An Observational Multicenter Trial
title_short Upper Limb Strength and Function Changes during a One-Year Follow-Up in Non-Ambulant Patients with Duchenne Muscular Dystrophy: An Observational Multicenter Trial
title_sort upper limb strength and function changes during a one-year follow-up in non-ambulant patients with duchenne muscular dystrophy: an observational multicenter trial
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4314080/
https://www.ncbi.nlm.nih.gov/pubmed/25643053
http://dx.doi.org/10.1371/journal.pone.0113999
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