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Physical activity and associations with clinical outcome measures in adults with cystic fibrosis; a systematic review

AbstractBackgroundPhysical activity (PA) is important in the management of Cystic Fibrosis (CF) and is associated with a number of beneficial effects. PA assessment is not commonplace or consistent in clinical practice, therefore understanding of PA in adults with CF remains limited. The purpose of...

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Published in:Journal of cystic fibrosis 2019-09, Vol.18 (5), p.590-601
Main Authors: Shelley, James, Boddy, Lynne M, Knowles, Zoe R, Stewart, Claire E, Dawson, Ellen A
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Language:English
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cited_by cdi_FETCH-LOGICAL-c451t-da9adefbb1b152142b2b8df19776c00089a3becd0f45a117f2e3aadf82dd424f3
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container_end_page 601
container_issue 5
container_start_page 590
container_title Journal of cystic fibrosis
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creator Shelley, James
Boddy, Lynne M
Knowles, Zoe R
Stewart, Claire E
Dawson, Ellen A
description AbstractBackgroundPhysical activity (PA) is important in the management of Cystic Fibrosis (CF) and is associated with a number of beneficial effects. PA assessment is not commonplace or consistent in clinical practice, therefore understanding of PA in adults with CF remains limited. The purpose of this review was to evaluate PA levels in this population and compare PA to global recommendations and non-CF peers. MethodsThe Preferred Reporting Items for Systematic Reviews and Meta-analyses guidelines were utilised to inform the review process. Original research was identified and screened against inclusion/exclusion criteria. Quality was assessed, data extracted and a narrative synthesis undertaken to describe the findings. ResultsAdults with CF did not achieve recommended PA guidelines and step count targets in 5/8 studies where assessment was possible. No significant differences in PA were found between CF and non-CF peers in 3/5 studies. Associations between PA and improved lung function were inconsistent with 4/9 studies finding a positive association. Evidence for an association between PA and higher exercise capacity was stronger with all 4 studies reviewed reporting a positive association. Quality ratings were low across all studies. ConclusionsPA in adults with CF is largely comparable to their non-CF peers, despite being insufficiently active to achieve PA recommendations. Assessment tools used and outcomes reported are variable, many of which do not provide sufficient information to assess relevant components of PA. There is a requirement for high quality studies designed specifically to explore PA in adults with CF, ideally employing standardised PA assessment methods.
doi_str_mv 10.1016/j.jcf.2019.03.003
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PA assessment is not commonplace or consistent in clinical practice, therefore understanding of PA in adults with CF remains limited. The purpose of this review was to evaluate PA levels in this population and compare PA to global recommendations and non-CF peers. MethodsThe Preferred Reporting Items for Systematic Reviews and Meta-analyses guidelines were utilised to inform the review process. Original research was identified and screened against inclusion/exclusion criteria. Quality was assessed, data extracted and a narrative synthesis undertaken to describe the findings. ResultsAdults with CF did not achieve recommended PA guidelines and step count targets in 5/8 studies where assessment was possible. No significant differences in PA were found between CF and non-CF peers in 3/5 studies. Associations between PA and improved lung function were inconsistent with 4/9 studies finding a positive association. Evidence for an association between PA and higher exercise capacity was stronger with all 4 studies reviewed reporting a positive association. Quality ratings were low across all studies. ConclusionsPA in adults with CF is largely comparable to their non-CF peers, despite being insufficiently active to achieve PA recommendations. Assessment tools used and outcomes reported are variable, many of which do not provide sufficient information to assess relevant components of PA. There is a requirement for high quality studies designed specifically to explore PA in adults with CF, ideally employing standardised PA assessment methods.</description><identifier>ISSN: 1569-1993</identifier><identifier>EISSN: 1873-5010</identifier><identifier>DOI: 10.1016/j.jcf.2019.03.003</identifier><identifier>PMID: 30926321</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>Exercise ; PRISMA ; Pulmonary/Respiratory ; Quality of life ; Respiratory disease</subject><ispartof>Journal of cystic fibrosis, 2019-09, Vol.18 (5), p.590-601</ispartof><rights>European Cystic Fibrosis Society</rights><rights>2019 European Cystic Fibrosis Society</rights><rights>Copyright © 2019 European Cystic Fibrosis Society. Published by Elsevier B.V. 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PA assessment is not commonplace or consistent in clinical practice, therefore understanding of PA in adults with CF remains limited. The purpose of this review was to evaluate PA levels in this population and compare PA to global recommendations and non-CF peers. MethodsThe Preferred Reporting Items for Systematic Reviews and Meta-analyses guidelines were utilised to inform the review process. Original research was identified and screened against inclusion/exclusion criteria. Quality was assessed, data extracted and a narrative synthesis undertaken to describe the findings. ResultsAdults with CF did not achieve recommended PA guidelines and step count targets in 5/8 studies where assessment was possible. No significant differences in PA were found between CF and non-CF peers in 3/5 studies. Associations between PA and improved lung function were inconsistent with 4/9 studies finding a positive association. Evidence for an association between PA and higher exercise capacity was stronger with all 4 studies reviewed reporting a positive association. Quality ratings were low across all studies. ConclusionsPA in adults with CF is largely comparable to their non-CF peers, despite being insufficiently active to achieve PA recommendations. Assessment tools used and outcomes reported are variable, many of which do not provide sufficient information to assess relevant components of PA. There is a requirement for high quality studies designed specifically to explore PA in adults with CF, ideally employing standardised PA assessment methods.</description><subject>Exercise</subject><subject>PRISMA</subject><subject>Pulmonary/Respiratory</subject><subject>Quality of life</subject><subject>Respiratory disease</subject><issn>1569-1993</issn><issn>1873-5010</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><recordid>eNp9kUuLFTEQhRtRnHH0B7iRLN10W5X0kwFBBl8woKCuQzqpMLn2Y-xKz9D_3rR3rgsXrlIU5xxS38mylwgFAtZvDsXB-kICdgWoAkA9ys6xbVReAcLjNFd1l2PXqbPsGfMBABto2qfZmYJO1kriebZ-vdk4WDMIY2O4C3ETZnLCMM82mBjmicV9iDfCDmH6o5vXaOeRxEiG14VYhEkYtw7xJNw4Bit86JeZA18KIzitaDT7eqG7QPfPsyfeDEwvHt6L7MeH99-vPuXXXz5-vnp3nduywpg70xlHvu-xx0piKXvZt85j1zS1BYC2M6on68CXlUFsvCRljPOtdK6UpVcX2etj7u0y_1qJox4DWxoGM9G8spYSoOmaGlWS4lFq07d5Ia9vlzCaZdMIeqetDzrR1jttDUon2snz6iF-7Udyfx0nvElweRRQOjIdvmi2gSZLLixko3Zz-G_823_cpxJ-0kZ8mNdlSvQ0apYa9Le97r1tbFVC06L6DWSfp9I</recordid><startdate>20190901</startdate><enddate>20190901</enddate><creator>Shelley, James</creator><creator>Boddy, Lynne M</creator><creator>Knowles, Zoe R</creator><creator>Stewart, Claire E</creator><creator>Dawson, Ellen A</creator><general>Elsevier B.V</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0003-4351-0361</orcidid></search><sort><creationdate>20190901</creationdate><title>Physical activity and associations with clinical outcome measures in adults with cystic fibrosis; a systematic review</title><author>Shelley, James ; Boddy, Lynne M ; Knowles, Zoe R ; Stewart, Claire E ; Dawson, Ellen A</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c451t-da9adefbb1b152142b2b8df19776c00089a3becd0f45a117f2e3aadf82dd424f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Exercise</topic><topic>PRISMA</topic><topic>Pulmonary/Respiratory</topic><topic>Quality of life</topic><topic>Respiratory disease</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Shelley, James</creatorcontrib><creatorcontrib>Boddy, Lynne M</creatorcontrib><creatorcontrib>Knowles, Zoe R</creatorcontrib><creatorcontrib>Stewart, Claire E</creatorcontrib><creatorcontrib>Dawson, Ellen A</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of cystic fibrosis</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Shelley, James</au><au>Boddy, Lynne M</au><au>Knowles, Zoe R</au><au>Stewart, Claire E</au><au>Dawson, Ellen A</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Physical activity and associations with clinical outcome measures in adults with cystic fibrosis; a systematic review</atitle><jtitle>Journal of cystic fibrosis</jtitle><addtitle>J Cyst Fibros</addtitle><date>2019-09-01</date><risdate>2019</risdate><volume>18</volume><issue>5</issue><spage>590</spage><epage>601</epage><pages>590-601</pages><issn>1569-1993</issn><eissn>1873-5010</eissn><abstract>AbstractBackgroundPhysical activity (PA) is important in the management of Cystic Fibrosis (CF) and is associated with a number of beneficial effects. PA assessment is not commonplace or consistent in clinical practice, therefore understanding of PA in adults with CF remains limited. The purpose of this review was to evaluate PA levels in this population and compare PA to global recommendations and non-CF peers. MethodsThe Preferred Reporting Items for Systematic Reviews and Meta-analyses guidelines were utilised to inform the review process. Original research was identified and screened against inclusion/exclusion criteria. Quality was assessed, data extracted and a narrative synthesis undertaken to describe the findings. ResultsAdults with CF did not achieve recommended PA guidelines and step count targets in 5/8 studies where assessment was possible. No significant differences in PA were found between CF and non-CF peers in 3/5 studies. Associations between PA and improved lung function were inconsistent with 4/9 studies finding a positive association. Evidence for an association between PA and higher exercise capacity was stronger with all 4 studies reviewed reporting a positive association. Quality ratings were low across all studies. ConclusionsPA in adults with CF is largely comparable to their non-CF peers, despite being insufficiently active to achieve PA recommendations. Assessment tools used and outcomes reported are variable, many of which do not provide sufficient information to assess relevant components of PA. There is a requirement for high quality studies designed specifically to explore PA in adults with CF, ideally employing standardised PA assessment methods.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>30926321</pmid><doi>10.1016/j.jcf.2019.03.003</doi><tpages>12</tpages><orcidid>https://orcid.org/0000-0003-4351-0361</orcidid><oa>free_for_read</oa></addata></record>
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subjects Exercise
PRISMA
Pulmonary/Respiratory
Quality of life
Respiratory disease
title Physical activity and associations with clinical outcome measures in adults with cystic fibrosis; a systematic review
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