Compensatory movements during functional activities in ambulatory children with Duchenne muscular dystrophy
Autor(a) principal: | |
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Data de Publicação: | 2014 |
Outros Autores: | , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Arquivos de neuro-psiquiatria (Online) |
Texto Completo: | http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0004-282X2014000100005 |
Resumo: | Objective: During the transitional phase (ambulatory to non-ambulatory), synergies characterize the evolution of Duchenne muscular dystrophy (DMD). This study was performed to describe and quantify compensatory movements while sitting down on/rising from the floor and climbing up/down steps. Method: Eighty videos (5 children × 4 assessments × 4 tasks) were recorded quarterly in the year prior to gait loss. Compensatory movements from the videos were registered based on the Functional Evaluation Scale for DMD. Results: The most frequently observed compensatory movements were upper limb support on lower limbs/floor/handrail during all the tasks and lumbar hyperlordosis, trunk support on handrail, equinus foot, increased base of support, non-alternated descent, and pauses while climbing up/down steps. Conclusion: Climbing up/down steps showed a higher number of compensatory movements than sitting down on/rising from the floor, which seemed to be lost before climbing up/down steps in ambulatory children with DMD. |
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Arquivos de neuro-psiquiatria (Online) |
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Compensatory movements during functional activities in ambulatory children with Duchenne muscular dystrophyDuchenne muscular dystrophyevaluationscales Objective: During the transitional phase (ambulatory to non-ambulatory), synergies characterize the evolution of Duchenne muscular dystrophy (DMD). This study was performed to describe and quantify compensatory movements while sitting down on/rising from the floor and climbing up/down steps. Method: Eighty videos (5 children × 4 assessments × 4 tasks) were recorded quarterly in the year prior to gait loss. Compensatory movements from the videos were registered based on the Functional Evaluation Scale for DMD. Results: The most frequently observed compensatory movements were upper limb support on lower limbs/floor/handrail during all the tasks and lumbar hyperlordosis, trunk support on handrail, equinus foot, increased base of support, non-alternated descent, and pauses while climbing up/down steps. Conclusion: Climbing up/down steps showed a higher number of compensatory movements than sitting down on/rising from the floor, which seemed to be lost before climbing up/down steps in ambulatory children with DMD. Academia Brasileira de Neurologia - ABNEURO2014-01-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0004-282X2014000100005Arquivos de Neuro-Psiquiatria v.72 n.1 2014reponame:Arquivos de neuro-psiquiatria (Online)instname:Academia Brasileira de Neurologiainstacron:ABNEURO10.1590/0004-282X20130196info:eu-repo/semantics/openAccessMartini,JoyceVoos,Mariana CallilHukuda,Michele EmyResende,Maria Bernadete Dutra deCaromano,Fátima Aparecidaeng2014-03-28T00:00:00Zoai:scielo:S0004-282X2014000100005Revistahttp://www.scielo.br/anphttps://old.scielo.br/oai/scielo-oai.php||revista.arquivos@abneuro.org1678-42270004-282Xopendoar:2014-03-28T00:00Arquivos de neuro-psiquiatria (Online) - Academia Brasileira de Neurologiafalse |
dc.title.none.fl_str_mv |
Compensatory movements during functional activities in ambulatory children with Duchenne muscular dystrophy |
title |
Compensatory movements during functional activities in ambulatory children with Duchenne muscular dystrophy |
spellingShingle |
Compensatory movements during functional activities in ambulatory children with Duchenne muscular dystrophy Martini,Joyce Duchenne muscular dystrophy evaluation scales |
title_short |
Compensatory movements during functional activities in ambulatory children with Duchenne muscular dystrophy |
title_full |
Compensatory movements during functional activities in ambulatory children with Duchenne muscular dystrophy |
title_fullStr |
Compensatory movements during functional activities in ambulatory children with Duchenne muscular dystrophy |
title_full_unstemmed |
Compensatory movements during functional activities in ambulatory children with Duchenne muscular dystrophy |
title_sort |
Compensatory movements during functional activities in ambulatory children with Duchenne muscular dystrophy |
author |
Martini,Joyce |
author_facet |
Martini,Joyce Voos,Mariana Callil Hukuda,Michele Emy Resende,Maria Bernadete Dutra de Caromano,Fátima Aparecida |
author_role |
author |
author2 |
Voos,Mariana Callil Hukuda,Michele Emy Resende,Maria Bernadete Dutra de Caromano,Fátima Aparecida |
author2_role |
author author author author |
dc.contributor.author.fl_str_mv |
Martini,Joyce Voos,Mariana Callil Hukuda,Michele Emy Resende,Maria Bernadete Dutra de Caromano,Fátima Aparecida |
dc.subject.por.fl_str_mv |
Duchenne muscular dystrophy evaluation scales |
topic |
Duchenne muscular dystrophy evaluation scales |
description |
Objective: During the transitional phase (ambulatory to non-ambulatory), synergies characterize the evolution of Duchenne muscular dystrophy (DMD). This study was performed to describe and quantify compensatory movements while sitting down on/rising from the floor and climbing up/down steps. Method: Eighty videos (5 children × 4 assessments × 4 tasks) were recorded quarterly in the year prior to gait loss. Compensatory movements from the videos were registered based on the Functional Evaluation Scale for DMD. Results: The most frequently observed compensatory movements were upper limb support on lower limbs/floor/handrail during all the tasks and lumbar hyperlordosis, trunk support on handrail, equinus foot, increased base of support, non-alternated descent, and pauses while climbing up/down steps. Conclusion: Climbing up/down steps showed a higher number of compensatory movements than sitting down on/rising from the floor, which seemed to be lost before climbing up/down steps in ambulatory children with DMD. |
publishDate |
2014 |
dc.date.none.fl_str_mv |
2014-01-01 |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0004-282X2014000100005 |
url |
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0004-282X2014000100005 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
10.1590/0004-282X20130196 |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
text/html |
dc.publisher.none.fl_str_mv |
Academia Brasileira de Neurologia - ABNEURO |
publisher.none.fl_str_mv |
Academia Brasileira de Neurologia - ABNEURO |
dc.source.none.fl_str_mv |
Arquivos de Neuro-Psiquiatria v.72 n.1 2014 reponame:Arquivos de neuro-psiquiatria (Online) instname:Academia Brasileira de Neurologia instacron:ABNEURO |
instname_str |
Academia Brasileira de Neurologia |
instacron_str |
ABNEURO |
institution |
ABNEURO |
reponame_str |
Arquivos de neuro-psiquiatria (Online) |
collection |
Arquivos de neuro-psiquiatria (Online) |
repository.name.fl_str_mv |
Arquivos de neuro-psiquiatria (Online) - Academia Brasileira de Neurologia |
repository.mail.fl_str_mv |
||revista.arquivos@abneuro.org |
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1754212775704395776 |