Muscle impairment in neuromuscular disease using an expiratory/inspiratory pressure ratio

Detalhes bibliográficos
Autor(a) principal: Dourado Junior, Mário Emílio Teixeira
Data de Publicação: 2015
Outros Autores: Fregonezi, Guilherme, Azevedo, Ingrid G, Resqueti, Vanessa R, Andrade, Arme`le D De, Gualdi, Lucien P, Aliverti, Andrea, Parreira, Veronica F
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UFRN
Texto Completo: https://repositorio.ufrn.br/handle/123456789/54254
https://doi.org/10.4187/respcare.03367
Resumo: Neuromuscular diseases (NMDs) lead to different weakness patterns, and most patients with NMDs develop respiratory failure. Inspiratory and expiratory muscle strength can be measured by maximum static inspiratory pressure (PImax) and maximum static expiratory pressure (PEmax), and the relationship between them has not been well described in healthy subjects and subjects with NMDs. Our aim was to assess expiratory/inspiratory muscle strength in NMDs and healthy subjects and calculate PEmax/PImax ratio for these groups. METHODS: Seventy (35 males) subjects with NMDs (amyotrophic lateral sclerosis, myasthenia gravis, and myotonic dystrophy), and 93 (47 males) healthy individuals 20 – 80 y of age were evaluated for anthropometry, pulmonary function, PImax, and PEmax, respectively. RESULTS: Healthy individuals showed greater values for PImax and PEmax when compared with subjects with NMDs. PEmax/PImax ratio for healthy subjects was 1.31 0.26, and PEmax%/PImax% was 1.04 0.05; for subjects with NMDs, PEmax/PImax ratio was 1.45 0.65, and PEmax%/PImax% ratio was 1.42 0.67. We found that PEmax%/PImax% for myotonic dystrophy was 0.93 0.24, for myasthenia gravis 1.94 0.6, and for amyotrophic lateral sclerosis 1.33 0.62 when we analyzed them separately. All healthy individuals showed higher PEmax compared with PImax. For subjects with NMDs, the impairment of PEmax and PImax is different among the 3 pathologies studied (P < .001). CONCLUSIONS: Healthy individuals and subjects with NMDs showed higher PEmax in comparison to PImax regarding the PEmax/PImax ratio. Based on the ratio, it is possible to state that NMDs show different patterns of respiratory muscle strength loss. PEmax/PImax ratio is a useful parameter to assess the impairment of respiratory muscles in a patient and to customize rehabilitation and treatment.
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spelling Dourado Junior, Mário Emílio TeixeiraFregonezi, GuilhermeAzevedo, Ingrid GResqueti, Vanessa RAndrade, Arme`le D DeGualdi, Lucien PAliverti, AndreaParreira, Veronica Fhttps://orcid.org/0000-0002-9462-22942023-07-28T12:54:35Z2023-07-28T12:54:35Z2015FREGONEZI, Guilherme; AZEVEDO, Ingrid G; RESQUETI, Vanessa R; ANDRADE, Armèle D de; GUALDI, Lucien P; ALIVERTI, Andrea; DOURADO JUNIOR, Mário Emílio Teixeira; PARREIRA, Verônica F. Muscle Impairment in Neuromuscular Disease Using an Expiratory/Inspiratory Pressure Ratio. Respiratory Care, [S.L.], v. 60, n. 4, p. 533-539, 13 jan. 2015. Daedalus Enterprises. http://dx.doi.org/10.4187/respcare.03367. Disponível em: https://rc.rcjournal.com/content/60/4/533. Acesso em: 21 jul. 2023.https://repositorio.ufrn.br/handle/123456789/54254https://doi.org/10.4187/respcare.03367Respiratory Carerespiratory muscle strengthrespiratory muscle imbalanceneuromuscular diseasesrespiratory therapyMuscle impairment in neuromuscular disease using an expiratory/inspiratory pressure ratioinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleNeuromuscular diseases (NMDs) lead to different weakness patterns, and most patients with NMDs develop respiratory failure. Inspiratory and expiratory muscle strength can be measured by maximum static inspiratory pressure (PImax) and maximum static expiratory pressure (PEmax), and the relationship between them has not been well described in healthy subjects and subjects with NMDs. Our aim was to assess expiratory/inspiratory muscle strength in NMDs and healthy subjects and calculate PEmax/PImax ratio for these groups. METHODS: Seventy (35 males) subjects with NMDs (amyotrophic lateral sclerosis, myasthenia gravis, and myotonic dystrophy), and 93 (47 males) healthy individuals 20 – 80 y of age were evaluated for anthropometry, pulmonary function, PImax, and PEmax, respectively. RESULTS: Healthy individuals showed greater values for PImax and PEmax when compared with subjects with NMDs. PEmax/PImax ratio for healthy subjects was 1.31 0.26, and PEmax%/PImax% was 1.04 0.05; for subjects with NMDs, PEmax/PImax ratio was 1.45 0.65, and PEmax%/PImax% ratio was 1.42 0.67. We found that PEmax%/PImax% for myotonic dystrophy was 0.93 0.24, for myasthenia gravis 1.94 0.6, and for amyotrophic lateral sclerosis 1.33 0.62 when we analyzed them separately. All healthy individuals showed higher PEmax compared with PImax. For subjects with NMDs, the impairment of PEmax and PImax is different among the 3 pathologies studied (P < .001). CONCLUSIONS: Healthy individuals and subjects with NMDs showed higher PEmax in comparison to PImax regarding the PEmax/PImax ratio. Based on the ratio, it is possible to state that NMDs show different patterns of respiratory muscle strength loss. PEmax/PImax ratio is a useful parameter to assess the impairment of respiratory muscles in a patient and to customize rehabilitation and treatment.engreponame:Repositório Institucional da UFRNinstname:Universidade Federal do Rio Grande do Norte (UFRN)instacron:UFRNinfo:eu-repo/semantics/openAccessORIGINALMuscleImpairmentNeuromuscular_DouradoJr_2015.pdfMuscleImpairmentNeuromuscular_DouradoJr_2015.pdfapplication/pdf654587https://repositorio.ufrn.br/bitstream/123456789/54254/1/MuscleImpairmentNeuromuscular_DouradoJr_2015.pdfcccbf604e026aa82dcb62fddda85615aMD51LICENSElicense.txtlicense.txttext/plain; charset=utf-81484https://repositorio.ufrn.br/bitstream/123456789/54254/2/license.txte9597aa2854d128fd968be5edc8a28d9MD52123456789/542542023-07-28 09:54:35.807oai:https://repositorio.ufrn.br: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Repositório de PublicaçõesPUBhttp://repositorio.ufrn.br/oai/opendoar:2023-07-28T12:54:35Repositório Institucional da UFRN - Universidade Federal do Rio Grande do Norte (UFRN)false
dc.title.pt_BR.fl_str_mv Muscle impairment in neuromuscular disease using an expiratory/inspiratory pressure ratio
title Muscle impairment in neuromuscular disease using an expiratory/inspiratory pressure ratio
spellingShingle Muscle impairment in neuromuscular disease using an expiratory/inspiratory pressure ratio
Dourado Junior, Mário Emílio Teixeira
respiratory muscle strength
respiratory muscle imbalance
neuromuscular diseases
respiratory therapy
title_short Muscle impairment in neuromuscular disease using an expiratory/inspiratory pressure ratio
title_full Muscle impairment in neuromuscular disease using an expiratory/inspiratory pressure ratio
title_fullStr Muscle impairment in neuromuscular disease using an expiratory/inspiratory pressure ratio
title_full_unstemmed Muscle impairment in neuromuscular disease using an expiratory/inspiratory pressure ratio
title_sort Muscle impairment in neuromuscular disease using an expiratory/inspiratory pressure ratio
author Dourado Junior, Mário Emílio Teixeira
author_facet Dourado Junior, Mário Emílio Teixeira
Fregonezi, Guilherme
Azevedo, Ingrid G
Resqueti, Vanessa R
Andrade, Arme`le D De
Gualdi, Lucien P
Aliverti, Andrea
Parreira, Veronica F
author_role author
author2 Fregonezi, Guilherme
Azevedo, Ingrid G
Resqueti, Vanessa R
Andrade, Arme`le D De
Gualdi, Lucien P
Aliverti, Andrea
Parreira, Veronica F
author2_role author
author
author
author
author
author
author
dc.contributor.authorID.pt_BR.fl_str_mv https://orcid.org/0000-0002-9462-2294
dc.contributor.author.fl_str_mv Dourado Junior, Mário Emílio Teixeira
Fregonezi, Guilherme
Azevedo, Ingrid G
Resqueti, Vanessa R
Andrade, Arme`le D De
Gualdi, Lucien P
Aliverti, Andrea
Parreira, Veronica F
dc.subject.por.fl_str_mv respiratory muscle strength
respiratory muscle imbalance
neuromuscular diseases
respiratory therapy
topic respiratory muscle strength
respiratory muscle imbalance
neuromuscular diseases
respiratory therapy
description Neuromuscular diseases (NMDs) lead to different weakness patterns, and most patients with NMDs develop respiratory failure. Inspiratory and expiratory muscle strength can be measured by maximum static inspiratory pressure (PImax) and maximum static expiratory pressure (PEmax), and the relationship between them has not been well described in healthy subjects and subjects with NMDs. Our aim was to assess expiratory/inspiratory muscle strength in NMDs and healthy subjects and calculate PEmax/PImax ratio for these groups. METHODS: Seventy (35 males) subjects with NMDs (amyotrophic lateral sclerosis, myasthenia gravis, and myotonic dystrophy), and 93 (47 males) healthy individuals 20 – 80 y of age were evaluated for anthropometry, pulmonary function, PImax, and PEmax, respectively. RESULTS: Healthy individuals showed greater values for PImax and PEmax when compared with subjects with NMDs. PEmax/PImax ratio for healthy subjects was 1.31 0.26, and PEmax%/PImax% was 1.04 0.05; for subjects with NMDs, PEmax/PImax ratio was 1.45 0.65, and PEmax%/PImax% ratio was 1.42 0.67. We found that PEmax%/PImax% for myotonic dystrophy was 0.93 0.24, for myasthenia gravis 1.94 0.6, and for amyotrophic lateral sclerosis 1.33 0.62 when we analyzed them separately. All healthy individuals showed higher PEmax compared with PImax. For subjects with NMDs, the impairment of PEmax and PImax is different among the 3 pathologies studied (P < .001). CONCLUSIONS: Healthy individuals and subjects with NMDs showed higher PEmax in comparison to PImax regarding the PEmax/PImax ratio. Based on the ratio, it is possible to state that NMDs show different patterns of respiratory muscle strength loss. PEmax/PImax ratio is a useful parameter to assess the impairment of respiratory muscles in a patient and to customize rehabilitation and treatment.
publishDate 2015
dc.date.issued.fl_str_mv 2015
dc.date.accessioned.fl_str_mv 2023-07-28T12:54:35Z
dc.date.available.fl_str_mv 2023-07-28T12:54:35Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
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dc.identifier.citation.fl_str_mv FREGONEZI, Guilherme; AZEVEDO, Ingrid G; RESQUETI, Vanessa R; ANDRADE, Armèle D de; GUALDI, Lucien P; ALIVERTI, Andrea; DOURADO JUNIOR, Mário Emílio Teixeira; PARREIRA, Verônica F. Muscle Impairment in Neuromuscular Disease Using an Expiratory/Inspiratory Pressure Ratio. Respiratory Care, [S.L.], v. 60, n. 4, p. 533-539, 13 jan. 2015. Daedalus Enterprises. http://dx.doi.org/10.4187/respcare.03367. Disponível em: https://rc.rcjournal.com/content/60/4/533. Acesso em: 21 jul. 2023.
dc.identifier.uri.fl_str_mv https://repositorio.ufrn.br/handle/123456789/54254
dc.identifier.doi.none.fl_str_mv https://doi.org/10.4187/respcare.03367
identifier_str_mv FREGONEZI, Guilherme; AZEVEDO, Ingrid G; RESQUETI, Vanessa R; ANDRADE, Armèle D de; GUALDI, Lucien P; ALIVERTI, Andrea; DOURADO JUNIOR, Mário Emílio Teixeira; PARREIRA, Verônica F. Muscle Impairment in Neuromuscular Disease Using an Expiratory/Inspiratory Pressure Ratio. Respiratory Care, [S.L.], v. 60, n. 4, p. 533-539, 13 jan. 2015. Daedalus Enterprises. http://dx.doi.org/10.4187/respcare.03367. Disponível em: https://rc.rcjournal.com/content/60/4/533. Acesso em: 21 jul. 2023.
url https://repositorio.ufrn.br/handle/123456789/54254
https://doi.org/10.4187/respcare.03367
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dc.publisher.none.fl_str_mv Respiratory Care
publisher.none.fl_str_mv Respiratory Care
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