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Manual therapies in cystic fibrosis care: a scoping review
OBJECTIVES: To review the use of manual therapies (MT) for pain, respiratory muscle strength and pulmonary function in cystic fibrosis (CF) care. METHODS: A search with a systematic approach was conducted by two independent reviewers, using the databases Medline, PubMed, Scopus and Cinahl from their...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9903555/ https://www.ncbi.nlm.nih.gov/pubmed/36747207 http://dx.doi.org/10.1186/s12998-023-00478-0 |
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author | Sposato Sinderholm, Niklas Bjerså, Kristofer |
author_facet | Sposato Sinderholm, Niklas Bjerså, Kristofer |
author_sort | Sposato Sinderholm, Niklas |
collection | PubMed |
description | OBJECTIVES: To review the use of manual therapies (MT) for pain, respiratory muscle strength and pulmonary function in cystic fibrosis (CF) care. METHODS: A search with a systematic approach was conducted by two independent reviewers, using the databases Medline, PubMed, Scopus and Cinahl from their respective inception dates to March 2021. RESULTS: A total of 199 publications were initially screened by title and abstract, after which 190 were excluded. Following a full-text review of the remaining articles, six studies with a total of 234 participants were included. Decreased pain levels following MT were observed in two studies and, in three studies, patient reports on improvement in ease of breathing and peak airflow were presented. No significant effects on spirometry measures were observed and none of the included studies investigated respiratory muscle strength. CONCLUSION: Current research on MT in CF care indicates positive trends based on subjective measures. However, research in this context is sparse and disparate in terms of both interventions and methodology. Further investigations including MT as part of multimodal interventions are therefore suggested before any specific recommendations for clinical implementation of MT in CF can be provided. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12998-023-00478-0. |
format | Online Article Text |
id | pubmed-9903555 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-99035552023-02-08 Manual therapies in cystic fibrosis care: a scoping review Sposato Sinderholm, Niklas Bjerså, Kristofer Chiropr Man Therap Scoping Reviews OBJECTIVES: To review the use of manual therapies (MT) for pain, respiratory muscle strength and pulmonary function in cystic fibrosis (CF) care. METHODS: A search with a systematic approach was conducted by two independent reviewers, using the databases Medline, PubMed, Scopus and Cinahl from their respective inception dates to March 2021. RESULTS: A total of 199 publications were initially screened by title and abstract, after which 190 were excluded. Following a full-text review of the remaining articles, six studies with a total of 234 participants were included. Decreased pain levels following MT were observed in two studies and, in three studies, patient reports on improvement in ease of breathing and peak airflow were presented. No significant effects on spirometry measures were observed and none of the included studies investigated respiratory muscle strength. CONCLUSION: Current research on MT in CF care indicates positive trends based on subjective measures. However, research in this context is sparse and disparate in terms of both interventions and methodology. Further investigations including MT as part of multimodal interventions are therefore suggested before any specific recommendations for clinical implementation of MT in CF can be provided. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12998-023-00478-0. BioMed Central 2023-02-06 /pmc/articles/PMC9903555/ /pubmed/36747207 http://dx.doi.org/10.1186/s12998-023-00478-0 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Scoping Reviews Sposato Sinderholm, Niklas Bjerså, Kristofer Manual therapies in cystic fibrosis care: a scoping review |
title | Manual therapies in cystic fibrosis care: a scoping review |
title_full | Manual therapies in cystic fibrosis care: a scoping review |
title_fullStr | Manual therapies in cystic fibrosis care: a scoping review |
title_full_unstemmed | Manual therapies in cystic fibrosis care: a scoping review |
title_short | Manual therapies in cystic fibrosis care: a scoping review |
title_sort | manual therapies in cystic fibrosis care: a scoping review |
topic | Scoping Reviews |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9903555/ https://www.ncbi.nlm.nih.gov/pubmed/36747207 http://dx.doi.org/10.1186/s12998-023-00478-0 |
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