Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/35461
Full metadata record
DC FieldValueLanguage
dc.contributor.authorDowman, Leona M-
dc.contributor.authorHolland, Anne E-
dc.date2024-
dc.date.accessioned2024-09-12T00:42:23Z-
dc.date.available2024-09-12T00:42:23Z-
dc.date.issued2024-09-01-
dc.identifier.citationCurrent Opinion in Pulmonary Medicine 2024-09-01; 30(5)en_US
dc.identifier.issn1531-6971-
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/35461-
dc.description.abstractThis review synthesizes the expanding evidence for pulmonary rehabilitation that has led to its recommended inclusion in the holistic care of people with idiopathic pulmonary fibrosis (IPF), as well as discussing strategies that may maximize and sustain benefits. Pulmonary rehabilitation is an effective intervention leading to significant improvements in exercise tolerance, symptoms, and quality of life for people with IPF. Improvements in symptoms and quality of life can persist longer term, whereas functional capacity does not; therefore, strategies to preserve functional capacity are an important area of research. Referral early in the disease course is encouraged to promote longer lasting effects. Evidence that high-intensity interval training may optimize benefits of exercise training is emerging. Supplemental oxygen is frequently used to manage exercise-induced desaturation, although its use as an adjunct therapy requires more evidence. Current evidence strongly supports the inclusion of pulmonary rehabilitation in the standard holistic care of IPF, with early participation encouraged. Further research is needed to establish the optimal exercise strategies, modalities and adjunct therapies that enhance outcomes of pulmonary rehabilitation and promote longer lasting effects.en_US
dc.language.isoeng-
dc.titlePulmonary rehabilitation in idiopathic pulmonary fibrosis.en_US
dc.typeJournal Articleen_US
dc.identifier.journaltitleCurrent Opinion in Pulmonary Medicineen_US
dc.identifier.affiliationSchool of Translational Medicine, Monash University.;Departments of Physiotherapy and Respiratory and Sleep Medicine, Austin Healthen_US
dc.identifier.affiliationSchool of Translational Medicine, Monash University.;Institute for Breathing and Sleep.;Departments of Physiotherapy and Respiratory Medicine, Alfred Health, Melbourne, Australia.en_US
dc.identifier.affiliationInstitute for Breathing and Sleepen_US
dc.identifier.doi10.1097/MCP.0000000000001094en_US
dc.type.contentTexten_US
dc.identifier.pubmedid38958566-
dc.description.volume30-
dc.description.issue5-
dc.description.startpage516-
dc.description.endpage522-
dc.subject.meshtermssecondaryIdiopathic Pulmonary Fibrosis/rehabilitation-
dc.subject.meshtermssecondaryIdiopathic Pulmonary Fibrosis/physiopathology-
dc.subject.meshtermssecondaryIdiopathic Pulmonary Fibrosis/therapy-
dc.subject.meshtermssecondaryExercise Tolerance/physiology-
dc.subject.meshtermssecondaryExercise Therapy/methods-
item.grantfulltextnone-
item.openairetypeJournal Article-
item.fulltextNo Fulltext-
item.languageiso639-1en-
item.cerifentitytypePublications-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
crisitem.author.deptPhysiotherapy-
crisitem.author.deptInstitute for Breathing and Sleep-
crisitem.author.deptInstitute for Breathing and Sleep-
crisitem.author.deptPhysiotherapy-
Appears in Collections:Journal articles
Show simple item record

Page view(s)

18
checked on Oct 21, 2024

Google ScholarTM

Check


Items in AHRO are protected by copyright, with all rights reserved, unless otherwise indicated.