Respiratory function and the mechanism of cough in Duchenne Muscular Dystrophy - doi:10.5020/18061230.2009.p113

Detalhes bibliográficos
Autor(a) principal: Faria, Ingrid de Castro Bolina
Data de Publicação: 2012
Outros Autores: Dalmonch, Renata Menezes
Tipo de documento: Artigo
Idioma: por
Título da fonte: Revista Brasileira em Promoção da Saúde
Texto Completo: https://ojs.unifor.br/RBPS/article/view/355
Resumo: bjective: To describe the relationship between the inefficiency of the mechanism of cough and the degradation of respiratory function in patients with Duchenne Muscular Dystrophy (DMD). Methods: A documentary study carried out from the following databases: Pubmed, Cochrane and Scielo. The terms “Duchenne muscular Dystrophy”, “Respiratory Function” and “Peak Cough Flow” were used as descriptors, individually or in association. Articles that addressed other types of muscular dystrophy or were not suitable for the aim of the study were excluded. Results: The search resulted in 294 articles and of these, 40 were selected. The findings were divided into four categories: “Normal mechanism of cough”; “Mechanism and peak cough flow in DMD”; “Pulmonary complications” and “Physiotherapy approach and treatment”. In patients with DMD, the efficiency of cough occur secondary to progressive muscle weakness, making them susceptible to respiratory tract infection. The production of effective cough is a predictor of pulmonary function in these patients. The goals of treatment should include the increase of both maximum insufflation capacity as the peak cough flow and the correction of hypopnea and hypercapnia. Conclusion: The efficiency of the mechanism of cough is associated with both vital capacity and maximum insufflation capacity as with the strength of respiratory muscles to produce peak cough flow. These are issues to be addressed in treatment of patients with DMD and constant evaluation during the course of illness should guide the intervention.
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spelling Respiratory function and the mechanism of cough in Duchenne Muscular Dystrophy - doi:10.5020/18061230.2009.p113Função respiratória e mecanismo da tosse na Distrofia Muscular de Duchenne - doi:10.5020/18061230.2009.p113Distrofia Muscular de DuchenneTestes de Função RespiratóriaPico do FluxoExpiratórioTosse.bjective: To describe the relationship between the inefficiency of the mechanism of cough and the degradation of respiratory function in patients with Duchenne Muscular Dystrophy (DMD). Methods: A documentary study carried out from the following databases: Pubmed, Cochrane and Scielo. The terms “Duchenne muscular Dystrophy”, “Respiratory Function” and “Peak Cough Flow” were used as descriptors, individually or in association. Articles that addressed other types of muscular dystrophy or were not suitable for the aim of the study were excluded. Results: The search resulted in 294 articles and of these, 40 were selected. The findings were divided into four categories: “Normal mechanism of cough”; “Mechanism and peak cough flow in DMD”; “Pulmonary complications” and “Physiotherapy approach and treatment”. In patients with DMD, the efficiency of cough occur secondary to progressive muscle weakness, making them susceptible to respiratory tract infection. The production of effective cough is a predictor of pulmonary function in these patients. The goals of treatment should include the increase of both maximum insufflation capacity as the peak cough flow and the correction of hypopnea and hypercapnia. Conclusion: The efficiency of the mechanism of cough is associated with both vital capacity and maximum insufflation capacity as with the strength of respiratory muscles to produce peak cough flow. These are issues to be addressed in treatment of patients with DMD and constant evaluation during the course of illness should guide the intervention.Objetivo: Descrever a relação entre a ineficiência do mecanismo da tosse e a degradação da função respiratória em pacientes com Distrofia Muscular de Duchenne (DMD). Métodos: Estudo documental realizado a partir das bases de dados Pubmed, Scielo e Cochrane. Os descritores utilizados foram “DMD”, “Função Respiratória” e “Pico de Fluxo da Tosse” individualmente ou em associação. Os artigos que abordavam outros tipos de distrofia muscular ou não se adequavam ao objetivo do estudo foram excluídos. Resultados: A busca resultou em 294 artigos, e dentre estes 40 foram selecionados. Os achados foram divididos em quatro categorias: “Mecanismo normal da tosse”; “Mecanismo e pico de fluxo da tosse na DMD”; “Complicações pulmonares” e “Abordagem e tratamento fisioterapeutico”. Evidenciou-se que no paciente com DMD ocorre redução da eficiência da tosse, secundária à fraqueza muscular progressiva, tornando-os susceptíveis à infecção do trato respiratório. A produção de tosse efetiva é um preditor da função pulmonar nesses pacientes. Os objetivos de tratamento devem incluir o aumento da capacidade de insuflação máxima, do pico de fluxo da tosse, e correção da hipopnéia e da hipercapnia. Conclusão: A eficiência do mecanismo da tosse está relacionada tanto com a capacidade vital e capacidade de insuflação máxima quanto com a força da musculatura respiratória para a produção de pico de fluxo da tosse. Esses são aspectos a serem abordados no tratamento do paciente com DMD e a avaliação constante durante todo o curso da doença deve nortear a intervenção.Universidade de Fortaleza2012-01-04info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersion"Peer-reviewed Article""Avaliado pelos pares""Avaliado pelos pares"application/pdfhttps://ojs.unifor.br/RBPS/article/view/35510.5020/355Brazilian Journal in Health Promotion; Vol. 22 No. 2 (2009); 113-119Revista Brasileña en Promoción de la Salud; Vol. 22 Núm. 2 (2009); 113-119Revista Brasileira em Promoção da Saúde; v. 22 n. 2 (2009); 113-1191806-1230reponame:Revista Brasileira em Promoção da Saúdeinstname:Universidade de Fortaleza (Unifor)instacron:UFORporhttps://ojs.unifor.br/RBPS/article/view/355/2260Faria, Ingrid de Castro BolinaDalmonch, Renata Menezesinfo:eu-repo/semantics/openAccess2012-01-10T12:19:46Zoai:ojs.ojs.unifor.br:article/355Revistahttps://periodicos.unifor.br/RBPS/oai1806-12301806-1222opendoar:2012-01-10T12:19:46Revista Brasileira em Promoção da Saúde - Universidade de Fortaleza (Unifor)false
dc.title.none.fl_str_mv Respiratory function and the mechanism of cough in Duchenne Muscular Dystrophy - doi:10.5020/18061230.2009.p113
Função respiratória e mecanismo da tosse na Distrofia Muscular de Duchenne - doi:10.5020/18061230.2009.p113
title Respiratory function and the mechanism of cough in Duchenne Muscular Dystrophy - doi:10.5020/18061230.2009.p113
spellingShingle Respiratory function and the mechanism of cough in Duchenne Muscular Dystrophy - doi:10.5020/18061230.2009.p113
Faria, Ingrid de Castro Bolina
Distrofia Muscular de Duchenne
Testes de Função Respiratória
Pico do FluxoExpiratório
Tosse.
title_short Respiratory function and the mechanism of cough in Duchenne Muscular Dystrophy - doi:10.5020/18061230.2009.p113
title_full Respiratory function and the mechanism of cough in Duchenne Muscular Dystrophy - doi:10.5020/18061230.2009.p113
title_fullStr Respiratory function and the mechanism of cough in Duchenne Muscular Dystrophy - doi:10.5020/18061230.2009.p113
title_full_unstemmed Respiratory function and the mechanism of cough in Duchenne Muscular Dystrophy - doi:10.5020/18061230.2009.p113
title_sort Respiratory function and the mechanism of cough in Duchenne Muscular Dystrophy - doi:10.5020/18061230.2009.p113
author Faria, Ingrid de Castro Bolina
author_facet Faria, Ingrid de Castro Bolina
Dalmonch, Renata Menezes
author_role author
author2 Dalmonch, Renata Menezes
author2_role author
dc.contributor.author.fl_str_mv Faria, Ingrid de Castro Bolina
Dalmonch, Renata Menezes
dc.subject.por.fl_str_mv Distrofia Muscular de Duchenne
Testes de Função Respiratória
Pico do FluxoExpiratório
Tosse.
topic Distrofia Muscular de Duchenne
Testes de Função Respiratória
Pico do FluxoExpiratório
Tosse.
description bjective: To describe the relationship between the inefficiency of the mechanism of cough and the degradation of respiratory function in patients with Duchenne Muscular Dystrophy (DMD). Methods: A documentary study carried out from the following databases: Pubmed, Cochrane and Scielo. The terms “Duchenne muscular Dystrophy”, “Respiratory Function” and “Peak Cough Flow” were used as descriptors, individually or in association. Articles that addressed other types of muscular dystrophy or were not suitable for the aim of the study were excluded. Results: The search resulted in 294 articles and of these, 40 were selected. The findings were divided into four categories: “Normal mechanism of cough”; “Mechanism and peak cough flow in DMD”; “Pulmonary complications” and “Physiotherapy approach and treatment”. In patients with DMD, the efficiency of cough occur secondary to progressive muscle weakness, making them susceptible to respiratory tract infection. The production of effective cough is a predictor of pulmonary function in these patients. The goals of treatment should include the increase of both maximum insufflation capacity as the peak cough flow and the correction of hypopnea and hypercapnia. Conclusion: The efficiency of the mechanism of cough is associated with both vital capacity and maximum insufflation capacity as with the strength of respiratory muscles to produce peak cough flow. These are issues to be addressed in treatment of patients with DMD and constant evaluation during the course of illness should guide the intervention.
publishDate 2012
dc.date.none.fl_str_mv 2012-01-04
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
"Peer-reviewed Article"
"Avaliado pelos pares"
"Avaliado pelos pares"
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv https://ojs.unifor.br/RBPS/article/view/355
10.5020/355
url https://ojs.unifor.br/RBPS/article/view/355
identifier_str_mv 10.5020/355
dc.language.iso.fl_str_mv por
language por
dc.relation.none.fl_str_mv https://ojs.unifor.br/RBPS/article/view/355/2260
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv Universidade de Fortaleza
publisher.none.fl_str_mv Universidade de Fortaleza
dc.source.none.fl_str_mv Brazilian Journal in Health Promotion; Vol. 22 No. 2 (2009); 113-119
Revista Brasileña en Promoción de la Salud; Vol. 22 Núm. 2 (2009); 113-119
Revista Brasileira em Promoção da Saúde; v. 22 n. 2 (2009); 113-119
1806-1230
reponame:Revista Brasileira em Promoção da Saúde
instname:Universidade de Fortaleza (Unifor)
instacron:UFOR
instname_str Universidade de Fortaleza (Unifor)
instacron_str UFOR
institution UFOR
reponame_str Revista Brasileira em Promoção da Saúde
collection Revista Brasileira em Promoção da Saúde
repository.name.fl_str_mv Revista Brasileira em Promoção da Saúde - Universidade de Fortaleza (Unifor)
repository.mail.fl_str_mv
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