Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/32660
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dc.contributor.authorWong, Alyson W-
dc.contributor.authorSun, Huiying-
dc.contributor.authorCox, Ingrid A-
dc.contributor.authorFisher, Jolene H-
dc.contributor.authorKhalil, Nasreen-
dc.contributor.authorJohannson, Kerri A-
dc.contributor.authorMarcoux, Veronica-
dc.contributor.authorAssayag, Deborah-
dc.contributor.authorManganas, Helene-
dc.contributor.authorKolb, Martin-
dc.contributor.authorPalmer, Andrew J-
dc.contributor.authorde Graaff, Barbara-
dc.contributor.authorWalters, E Haydn-
dc.contributor.authorHopkins, Peter-
dc.contributor.authorZappala, Christopher-
dc.contributor.authorGoh, Nicole S-
dc.contributor.authorMoodley, Yuben-
dc.contributor.authorNavaratnam, Vidya-
dc.contributor.authorCorte, Tamera J-
dc.contributor.authorRyerson, Christopher J-
dc.contributor.authorZhang, Wei-
dc.date2023-
dc.date.accessioned2023-04-14T02:47:37Z-
dc.date.available2023-04-14T02:47:37Z-
dc.date.issued2023-03-
dc.identifier.citationPloS One 2023; 18(3)en_US
dc.identifier.issn1932-6203-
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/32660-
dc.description.abstractFibrotic interstitial lung disease (ILD) includes a large group of conditions that lead to scarring of the lungs. The lack of available 5-level EuroQol 5D (EQ5D) data has limited the ability to conduct economic evaluations in ILD. The purpose of this study was to develop and validate a mapping algorithm that predicts EQ5D utilities from commonly collected pulmonary function measurements (forced vital capacity [FVC] and diffusing capacity of the lung for carbon monoxide [DLCO]) in fibrotic ILDs. EQ5D utility and pulmonary function measurements from the Canadian Registry for Pulmonary Fibrosis were included. Ordinary least squares (OLS), beta regression, two-part, and tobit models were used to map EQ5D utilities from FVC or DLCO. Model performance was assessed by comparing the predicted and observed utilities. Subgroup analyses were also conducted to test how well models performed across different patient characteristics. The models were then externally validated in the Australian Idiopathic Pulmonary Fibrosis Registry. The OLS model performed as well as other more complex models (root mean squared error: 0.17 for FVC and 0.16 for DLCO). As with the other models, the OLS algorithm performed well across the different subgroups (except for EQ5D utilities < 0.5) and in the external validation cohort. We developed a mapping algorithm that predicts EQ5D utilities from FVC and DLCO, with the intent that this algorithm can be applied to clinical trial populations and real-world cohorts that have not prioritized collection of health-related utilities. The mapping algorithm can be used in future economic evaluations of potential ILD therapies.en_US
dc.language.isoeng-
dc.titleMapping EQ5D utilities from forced vital capacity and diffusing capacity in fibrotic interstitial lung disease.en_US
dc.typeJournal Articleen_US
dc.identifier.journaltitlePloS Oneen_US
dc.identifier.affiliationDepartment of Medicine, University of British Columbia, Vancouver, British Columbia, Canada.;Centre for Heart Lung Innovation, St. Paul's Hospital, Vancouver, British Columbia, Canada.en_US
dc.identifier.affiliationCentre for Health Evaluation and Outcome Sciences, Vancouver, British Columbia, Canada.en_US
dc.identifier.affiliationMenzies Institute for Medical Research, University of Tasmania, Hobart, Tasmania, Australia.en_US
dc.identifier.affiliationDepartment of Medicine, University of Toronto, Toronto, ON, Canada.en_US
dc.identifier.affiliationDepartment of Medicine, University of Calgary, Calgary, AB, Canada.en_US
dc.identifier.affiliationDepartment of Medicine, University of Saskatchewan, Saskatoon, Saskatchewan, Canada.en_US
dc.identifier.affiliationDepartment of Medicine, McGill University, Montreal, Quebec, Canada.en_US
dc.identifier.affiliationDépartement de Médecine, Centre Hospitalier de l'Université de Montréal, Montreal, QC, Canada.en_US
dc.identifier.affiliationDepartment of Medicine, Firestone Institute for Respiratory Health, McMaster University, Hamilton, ON, Canada.en_US
dc.identifier.affiliationSchool of Medicine, University of Tasmania, Hobart, Tasmania, Australia.en_US
dc.identifier.affiliationLung Transplant Unit, The Prince Charles Hospital, Brisbane, Australia.en_US
dc.identifier.affiliationDept of Thoracic Medicine, Royal Brisbane and Women's Hospital, Brisbane, Australia.en_US
dc.identifier.affiliationRespiratory and Sleep Medicineen_US
dc.identifier.affiliationDepartment of Respiratory Medicine, Fiona Stanley Hospital, Murdoch, Australia.en_US
dc.identifier.affiliationLung Transplant Unit, The Prince Charles Hospital, Brisbane, Australia.en_US
dc.identifier.affiliationDepartment of Respiratory and Sleep Medicine, Royal Prince Alfred Hospital, Sydney, NSW, Australia.;Centre of Research Excellence for Pulmonary Fibrosis, University of Sydney, Sydney, NSW, Australia.en_US
dc.identifier.affiliationCentre for Health Evaluation and Outcome Sciences, Vancouver, British Columbia, Canada.;School of Population and Public Health, University of British Columbia, Vancouver, British Columbia, Canada.en_US
dc.identifier.doi10.1371/journal.pone.0283110en_US
dc.type.contentTexten_US
dc.identifier.orcid0000-0003-4910-1948en_US
dc.identifier.pubmedid37000790-
dc.description.volume18-
dc.description.issue3-
dc.description.startpagee0283110-
dc.subject.meshtermssecondaryLung Diseases, Interstitial/drug therapy-
dc.subject.meshtermssecondaryIdiopathic Pulmonary Fibrosis/drug therapy-
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-
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