Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/33523
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dc.contributor.authorSaynor, Zoe L-
dc.contributor.authorGruet, Mathieu-
dc.contributor.authorMcNarry, Melitta A-
dc.contributor.authorButton, Brenda-
dc.contributor.authorMorrison, Lisa-
dc.contributor.authorWagner, Marlies-
dc.contributor.authorSawyer, Abbey-
dc.contributor.authorHebestreit, Helge-
dc.contributor.authorRadtke, Thomas-
dc.contributor.authorUrquhart, Don S-
dc.date2023-
dc.date.accessioned2023-08-16T05:31:34Z-
dc.date.available2023-08-16T05:31:34Z-
dc.date.issued2023-09-30-
dc.identifier.citationEuropean Respiratory Review : an Official Journal of the European Respiratory Society 2023-09-30; 32(169)en_US
dc.identifier.issn1600-0617-
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/33523-
dc.description.abstractRegular exercise testing is recommended for all people with cystic fibrosis (PwCF). A range of validated tests, which integrate both strength and aerobic function, are available and increasingly being used. Together, these tests offer the ability for comprehensive exercise evaluation. Extensive research and expert consensus over recent years has enabled the adaptation and standardisation of a range of exercise tests to aid the understanding of the pathophysiology related to exercise limitation in PwCF and has led to the development of novel exercise tests which may be applied to PwCF. This article provides expert, opinion-based clinical practice guidance, along with test instructions, for a selection of commonly used valid tests which have documented clinimetric properties for PwCF. Importantly, this document also highlights previously used tests that are no longer suggested for PwCF and areas where research is mandated. This collaboration, on behalf of the European Cystic Fibrosis Society Exercise Working Group, represents expert consensus by a multidisciplinary panel of physiotherapists, exercise scientists and clinicians and aims to improve global standardisation of functional exercise testing of PwCF. In short, the standardised use of a small selection of tests performed to a high standard is advocated.en_US
dc.language.isoeng-
dc.titleGuidance and standard operating procedures for functional exercise testing in cystic fibrosis.en_US
dc.typeJournal Articleen_US
dc.identifier.journaltitleEuropean Respiratory Review : an Official Journal of the European Respiratory Societyen_US
dc.identifier.affiliationPhysical Activity, Health and Rehabilitation Thematic Research Group, School of Sport, Health and Exercise Science, Faculty of Science and Health, University of Portsmouth, Portsmouth, UK.;Wessex Cystic Fibrosis Unit, University Hospitals Southampton NHS Foundation Trust, Southampton, UK.en_US
dc.identifier.affiliationLaboratory of the Impact of Physical Activity on Health (IAPS), University of Toulon, Toulon, France.en_US
dc.identifier.affiliationApplied Sports, Technology, Exercise and Medicine Research Centre, Swansea University, Swansea, UK.en_US
dc.identifier.affiliationDepartment of Physiotherapy, Melbourne School of Health Science, University of Melbourne, Melbourne, Australia.en_US
dc.identifier.affiliationWest of Scotland Adult CF Unit, Queen Elizabeth University Hospital, Glasgow, UK.en_US
dc.identifier.affiliationDepartment of Pediatrics and Adolescent Medicine, Medical University of Graz, Graz, Austria.en_US
dc.identifier.affiliationIcahn School of Medicine at Mount Sinai, New York, NY, USA.en_US
dc.identifier.affiliationPaediatric Department, University Hospitals Würzburg, Würzburg, Germany.en_US
dc.identifier.affiliationDivision of Occupational and Environmental Medicine, Epidemiology, Biostatistics and Prevention Institute, University of Zurich and University Hospital Zurich, Zurich, Switzerland.en_US
dc.identifier.affiliationRoyal Hospital for Children and Young People, Edinburgh, UK.;Department of Child Life and Health, University of Edinburgh, Edinburgh, UK.en_US
dc.identifier.affiliationInstitute for Breathing and Sleepen_US
dc.identifier.doi10.1183/16000617.0029-2023en_US
dc.type.contentTexten_US
dc.identifier.orcid0000-0002-1723-1070en_US
dc.identifier.orcid0000-0002-9048-9692en_US
dc.identifier.pubmedid37558263-
dc.description.volume32-
dc.description.issue169-
dc.subject.meshtermssecondaryCystic Fibrosis/diagnosis-
dc.subject.meshtermssecondaryCystic Fibrosis/therapy-
item.fulltextNo Fulltext-
item.openairetypeJournal Article-
item.cerifentitytypePublications-
item.grantfulltextnone-
item.languageiso639-1en-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
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