Relationships between slow vital capacity and measures of respiratory function on the ALSFRS-R
Autor(a) principal: | |
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Data de Publicação: | 2018 |
Outros Autores: | , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
Texto Completo: | http://hdl.handle.net/10451/54325 |
Resumo: | © 2018 University of Texas Health Science Center at San Antonio. Published by Informa UK Limited, trading as Taylor & Francis Group. This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives License (http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited, and is not altered, transformed, or built upon in any way. |
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Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
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Relationships between slow vital capacity and measures of respiratory function on the ALSFRS-RALSDisease progressionRespiratory functionVital capacity© 2018 University of Texas Health Science Center at San Antonio. Published by Informa UK Limited, trading as Taylor & Francis Group. This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives License (http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited, and is not altered, transformed, or built upon in any way.Objective: As declining respiratory muscle function commonly leads to disability and death in amyotrophic lateral sclerosis (ALS), respiratory measurements such as slow vital capacity (SVC) may predict disease progression. This study evaluated the relationship between SVC and symptoms measured by the revised ALS Functional Rating Scale (ALSFRS-R). Methods: About 453 ALS placebo-treated patients from the EMPOWER trial (NCT01281189) were evaluated. Correlations between %predicted SVC and individual respiratory ALSFRS-R subdomain items, respiratory subdomain score (maximum score of 12), and total ALSFRS-R score (maximum score of 48) were evaluated using the Pearson correlation coefficient. Pearson's chi-squared test was used to evaluate changes from baseline to week 48 in ALSFRS-R respiratory symptom and respiratory subdomain scores in patients with baseline %predicted SVC above/below the median at baseline and with more slowly/more rapidly decreasing %predicted SVC. Results: The %predicted SVC showed significant correlations with dyspnea, orthopnoea, respiratory insufficiency, respiratory subdomain score, and total ALSFRS-R score (all p < 0.0001). Patients with baseline SVC values < median were significantly more likely than those with baseline SVC ≥ median to have a change in total ALSFRS-R respiratory subdomain score from 12 to <12 (40.9% vs. 30.2%, p = 0.0358) and from ≥10 to <10 (41.6% vs. 24.4%, p = 0.0005). Additionally, patients with smaller declines in SVC over time were significantly more likely to have smaller decreases in their respiratory subdomain scores (p < 0.0001). Conclusions: The higher correlation between %predicted SVC and specific ALSFRS-R symptom scores in patients with rapidly versus more slowly progressing disease reinforces the importance of continually monitoring respiratory function throughout the disease course.Taylor & FrancisRepositório da Universidade de LisboaJackson, CarlayneCarvalho, MamedeGenge, AngelaHeiman-Patterson, TerryShefner, Jeremy M.Wei, JennyWolff, Andrew A.2022-09-06T10:57:21Z20182018-01-01T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/10451/54325engAmyotroph Lateral Scler Frontotemporal Degener. 2018 Nov;19(7-8):506-5122167-842110.1080/21678421.2018.14976582167-9223info:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2023-11-08T16:59:59Zoai:repositorio.ul.pt:10451/54325Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T22:04:47.460267Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse |
dc.title.none.fl_str_mv |
Relationships between slow vital capacity and measures of respiratory function on the ALSFRS-R |
title |
Relationships between slow vital capacity and measures of respiratory function on the ALSFRS-R |
spellingShingle |
Relationships between slow vital capacity and measures of respiratory function on the ALSFRS-R Jackson, Carlayne ALS Disease progression Respiratory function Vital capacity |
title_short |
Relationships between slow vital capacity and measures of respiratory function on the ALSFRS-R |
title_full |
Relationships between slow vital capacity and measures of respiratory function on the ALSFRS-R |
title_fullStr |
Relationships between slow vital capacity and measures of respiratory function on the ALSFRS-R |
title_full_unstemmed |
Relationships between slow vital capacity and measures of respiratory function on the ALSFRS-R |
title_sort |
Relationships between slow vital capacity and measures of respiratory function on the ALSFRS-R |
author |
Jackson, Carlayne |
author_facet |
Jackson, Carlayne Carvalho, Mamede Genge, Angela Heiman-Patterson, Terry Shefner, Jeremy M. Wei, Jenny Wolff, Andrew A. |
author_role |
author |
author2 |
Carvalho, Mamede Genge, Angela Heiman-Patterson, Terry Shefner, Jeremy M. Wei, Jenny Wolff, Andrew A. |
author2_role |
author author author author author author |
dc.contributor.none.fl_str_mv |
Repositório da Universidade de Lisboa |
dc.contributor.author.fl_str_mv |
Jackson, Carlayne Carvalho, Mamede Genge, Angela Heiman-Patterson, Terry Shefner, Jeremy M. Wei, Jenny Wolff, Andrew A. |
dc.subject.por.fl_str_mv |
ALS Disease progression Respiratory function Vital capacity |
topic |
ALS Disease progression Respiratory function Vital capacity |
description |
© 2018 University of Texas Health Science Center at San Antonio. Published by Informa UK Limited, trading as Taylor & Francis Group. This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives License (http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited, and is not altered, transformed, or built upon in any way. |
publishDate |
2018 |
dc.date.none.fl_str_mv |
2018 2018-01-01T00:00:00Z 2022-09-06T10:57:21Z |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://hdl.handle.net/10451/54325 |
url |
http://hdl.handle.net/10451/54325 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
Amyotroph Lateral Scler Frontotemporal Degener. 2018 Nov;19(7-8):506-512 2167-8421 10.1080/21678421.2018.1497658 2167-9223 |
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info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
application/pdf |
dc.publisher.none.fl_str_mv |
Taylor & Francis |
publisher.none.fl_str_mv |
Taylor & Francis |
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reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação instacron:RCAAP |
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Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
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RCAAP |
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RCAAP |
reponame_str |
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
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Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
repository.name.fl_str_mv |
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
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1799134599473790976 |