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Correlation between the Gait Deviation Index and gross motor function (GMFCS level) in children with cerebral palsy
AIM: The Gait Deviation Index (GDI) is a score derived from three-dimensional gait analysis (3DGA). The GDI provides a numerical value that expresses overall gait pathology (ranging from 0 to 100, where 100 indicates the absence of gait pathology). The aim of this study was to investigate the associ...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4909653/ https://www.ncbi.nlm.nih.gov/pubmed/27177476 http://dx.doi.org/10.1007/s11832-016-0738-4 |
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author | Malt, Merete A. Aarli, Ånen Bogen, Bård Fevang, Jonas M. |
author_facet | Malt, Merete A. Aarli, Ånen Bogen, Bård Fevang, Jonas M. |
author_sort | Malt, Merete A. |
collection | PubMed |
description | AIM: The Gait Deviation Index (GDI) is a score derived from three-dimensional gait analysis (3DGA). The GDI provides a numerical value that expresses overall gait pathology (ranging from 0 to 100, where 100 indicates the absence of gait pathology). The aim of this study was to investigate the association between the GDI and different levels of gross motor function [defined as the Gross Motor Function Classification System (GMFCS)] and to explore if age, height, weight, gender and cerebral palsy (CP) subclass (bilateral and unilateral CP) exert any influence on the GDI in children with unilateral and bilateral spastic CP. METHODS: We calculated the GDI of 109 children [73 % boys, mean age 9.7 years (standard deviation, SD 3.5)] with spastic CP, classified at GMFCS levels I, II and III. Twenty-three normally developing children were used as controls [61 % boys, mean age 9.9 years (SD 2.6)]. Multiple linear regression analysis was performed. RESULTS: The mean GDI in the control group was 100 (SD 7.5). The mean GDI in the GMFCS level I group was 81 (SD 11), in the GMFCS level II group 71 (SD 11) and in the GMFCS level III group 60 (SD 9). Multiple linear regression analysis showed that gender, age and CP subclass had no significant correlation with the GDI, whereas height and weight had a slight impact. CONCLUSION: This study showed a strong correlation between the GDI and GMFCS levels. The present data indicate that calculation of the GDI is a useful tool to characterise walking difficulties in children with spastic CP. |
format | Online Article Text |
id | pubmed-4909653 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-49096532016-07-01 Correlation between the Gait Deviation Index and gross motor function (GMFCS level) in children with cerebral palsy Malt, Merete A. Aarli, Ånen Bogen, Bård Fevang, Jonas M. J Child Orthop Original Clinical Article AIM: The Gait Deviation Index (GDI) is a score derived from three-dimensional gait analysis (3DGA). The GDI provides a numerical value that expresses overall gait pathology (ranging from 0 to 100, where 100 indicates the absence of gait pathology). The aim of this study was to investigate the association between the GDI and different levels of gross motor function [defined as the Gross Motor Function Classification System (GMFCS)] and to explore if age, height, weight, gender and cerebral palsy (CP) subclass (bilateral and unilateral CP) exert any influence on the GDI in children with unilateral and bilateral spastic CP. METHODS: We calculated the GDI of 109 children [73 % boys, mean age 9.7 years (standard deviation, SD 3.5)] with spastic CP, classified at GMFCS levels I, II and III. Twenty-three normally developing children were used as controls [61 % boys, mean age 9.9 years (SD 2.6)]. Multiple linear regression analysis was performed. RESULTS: The mean GDI in the control group was 100 (SD 7.5). The mean GDI in the GMFCS level I group was 81 (SD 11), in the GMFCS level II group 71 (SD 11) and in the GMFCS level III group 60 (SD 9). Multiple linear regression analysis showed that gender, age and CP subclass had no significant correlation with the GDI, whereas height and weight had a slight impact. CONCLUSION: This study showed a strong correlation between the GDI and GMFCS levels. The present data indicate that calculation of the GDI is a useful tool to characterise walking difficulties in children with spastic CP. Springer Berlin Heidelberg 2016-05-13 2016-06 /pmc/articles/PMC4909653/ /pubmed/27177476 http://dx.doi.org/10.1007/s11832-016-0738-4 Text en © The Author(s) 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. |
spellingShingle | Original Clinical Article Malt, Merete A. Aarli, Ånen Bogen, Bård Fevang, Jonas M. Correlation between the Gait Deviation Index and gross motor function (GMFCS level) in children with cerebral palsy |
title | Correlation between the Gait Deviation Index and gross motor function (GMFCS level) in children with cerebral palsy |
title_full | Correlation between the Gait Deviation Index and gross motor function (GMFCS level) in children with cerebral palsy |
title_fullStr | Correlation between the Gait Deviation Index and gross motor function (GMFCS level) in children with cerebral palsy |
title_full_unstemmed | Correlation between the Gait Deviation Index and gross motor function (GMFCS level) in children with cerebral palsy |
title_short | Correlation between the Gait Deviation Index and gross motor function (GMFCS level) in children with cerebral palsy |
title_sort | correlation between the gait deviation index and gross motor function (gmfcs level) in children with cerebral palsy |
topic | Original Clinical Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4909653/ https://www.ncbi.nlm.nih.gov/pubmed/27177476 http://dx.doi.org/10.1007/s11832-016-0738-4 |
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