Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/26597
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dc.contributor.authorKhor, Yet H-
dc.contributor.authorHolland, Anne E-
dc.contributor.authorGoh, Nicole S L-
dc.contributor.authorMiller, Belinda R-
dc.contributor.authorVlahos, Ross-
dc.contributor.authorBozinovski, Steven-
dc.contributor.authorLahham, Aroub-
dc.contributor.authorGlaspole, Ian-
dc.contributor.authorMcDonald, Christine F-
dc.date2020-02-28-
dc.date.accessioned2021-05-24T05:45:39Z-
dc.date.available2021-05-24T05:45:39Z-
dc.date.issued2020-07-
dc.identifier.citationChest 2020; 158(1): 234-244en
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/26597-
dc.description.abstractDespite a lack of evidence, ambulatory oxygen therapy is frequently prescribed for patients with interstitial lung disease (ILD) and exertional desaturation. Patients often prefer portable oxygen concentrators to oxygen cylinders. This study aimed to examine the feasibility of conducting a clinical trial of ambulatory oxygen delivered via portable concentrators in patients with ILD. Is it feasible to conduct a clinical trial of ambulatory oxygen delivered via portable concentrators in patients with ILD? In this randomized, triple-blinded, sham-controlled trial, 30 participants with ILD and isolated exertional desaturation to < 90% on 6-minute walk tests were randomized to 12-week ambulatory oxygen or air delivered via portable concentrators, with assessments performed at baseline and weeks 4, 12, and 18. Primary outcomes were trial feasibility and the change in 6-minute walk distance (6MWD) on room air at week 12. Study recruitment was completed within 18 months, with six withdrawals. Participant blinding was successful, with the Bang's Blinding Index being 0 (95% CI, -0.40 to 0.40) for the oxygen group and 0 (95% CI, -0.42 to 0.42) for the sham group. No significant difference in 6MWD was seen between groups at week 12 (mean difference of -34 m [95% CI, -105 to 36], P = .34). For secondary outcomes, compared with the sham group, the oxygen group had a significantly higher Leicester Cough Questionnaire psychological domain score, indicating better cough-related quality of life (mean difference of 0.9 [95% CI, 0.2 to 1.6], P = .01), but a shorter duration of moderate-to-vigorous activities (mean difference of -135 [95% CI, -267 to -3], P = .04) at week 12. Based on the results of this pilot study, a definitive randomized controlled trial with a longer intervention duration is warranted to clarify therapeutic impacts of ambulatory oxygen in patients with ILD. Australian New Zealand Clinical Trials Registry; No.: ACTRN12617000054314; URL: www.anzctr.org.au/.en
dc.language.isoeng
dc.subjectexertional hypoxemiaen
dc.subjectidiopathic pulmonary fibrosisen
dc.subjectinterstitial lung diseaseen
dc.subjectoxygenen
dc.subjectpulmonary fibrosisen
dc.titleAmbulatory Oxygen in Fibrotic Interstitial Lung Disease: A Pilot, Randomized, Triple-Blinded, Sham-Controlled Trial.en
dc.typeJournal Articleen_US
dc.identifier.journaltitleChesten
dc.identifier.affiliationSchool of Medicine, University of Melbourne, Melbourne, Victoria, Australiaen
dc.identifier.affiliationDepartment of Respiratory Medicine, Alfred Health, Melbourne, Victoria, Australiaen
dc.identifier.affiliationDepartment of Medicine, Monash University, Melbourne, Australiaen
dc.identifier.affiliationSchool of Health and Biomedical Sciences, RMIT University, Bundoora, Victoria, Australiaen
dc.identifier.affiliationMenzies Institute for Medical Research, University of Tasmania, Tasmania, Australiaen
dc.identifier.affiliationInstitute for Breathing and Sleepen
dc.identifier.affiliationDepartment of Physiotherapy, Alfred Health and Monash University, Melbourne, Australiaen
dc.identifier.affiliationRespiratory and Sleep Medicineen
dc.identifier.doi10.1016/j.chest.2020.01.049en
dc.type.contentTexten_US
dc.identifier.pubmedid32113924
local.name.researcherGoh, Nicole S L
item.languageiso639-1en-
item.fulltextNo Fulltext-
item.grantfulltextnone-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.cerifentitytypePublications-
item.openairetypeJournal Article-
crisitem.author.deptRespiratory and Sleep Medicine-
crisitem.author.deptInstitute for Breathing and Sleep-
crisitem.author.deptMedicine (University of Melbourne)-
crisitem.author.deptInstitute for Breathing and Sleep-
crisitem.author.deptPhysiotherapy-
crisitem.author.deptRespiratory and Sleep Medicine-
crisitem.author.deptInstitute for Breathing and Sleep-
crisitem.author.deptInstitute for Breathing and Sleep-
crisitem.author.deptRespiratory and Sleep Medicine-
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