Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/20497
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dc.contributor.authorBurgess, Andrew-
dc.contributor.authorGoon, Ken-
dc.contributor.authorBrannan, John D-
dc.contributor.authorAttia, John-
dc.contributor.authorPalazzi, Kerrin-
dc.contributor.authorOldmeadow, Christopher-
dc.contributor.authorCorte, Tamera J-
dc.contributor.authorGlaspole, Ian-
dc.contributor.authorGoh, Nicole S L-
dc.contributor.authorKeir, Gregory-
dc.contributor.authorAllan, Heather-
dc.contributor.authorChapman, Sally-
dc.contributor.authorCooper, Wendy-
dc.contributor.authorEllis, Samantha-
dc.contributor.authorHopkins, Peter-
dc.contributor.authorMoodley, Yuben-
dc.contributor.authorReynolds, Paul-
dc.contributor.authorZappala, Chris-
dc.contributor.authorMacansh, Sacha-
dc.contributor.authorGrainge, Christopher-
dc.date2019-03-28-
dc.date.accessioned2019-04-02T01:07:32Z-
dc.date.available2019-04-02T01:07:32Z-
dc.date.issued2019-10-
dc.identifier.citationRespirology (Carlton, Vic.) 2019; 24(10): 988-995en_US
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/20497-
dc.description.abstractPublicly funded therapy for idiopathic pulmonary fibrosis (IPF) relies on percentage predicted values from pulmonary function testing, for example Australian patients must have a forced vital capacity ≥50% (%FVC), transfer factor of the lung for carbon monoxide ≥ 30% (%TLco) and forced expiratory volume in 1 s (FEV1 )/FVC ratio > 0.7. Despite defined cut-off values, no jurisdiction prescribes a reference equation for use; multiple equations exist. We hypothesized that access to subsidized treatment varies depending on the chosen equation. The %FVC and %TLco from different commonly used reference equations across general respiratory patients, and IPF-specific patients, were compared. FVC and TLco measurements from a large general respiratory laboratory and the Australian Idiopathic Pulmonary Fibrosis Registry (AIPFR) database were analysed using multiple equations. Differences between %FVC and %TLco for each equation were calculated, with particular interest in classification of patients (%) at the threshold for subsidized treatment. A total of 20 378 general respiratory database results were analysed. The %FVC ≥ 50% increased from 86% with the Roca equation to 96% with Quanjer (European Coal and Steal Community, ECSC) and %TLco≥30% increased from 91% with Paoletti to 98% with Thompson. However, overall increase in eligibility for subsidized treatment was modest, varying from 48.2% to 49.2%. A total of 545 AIPFR database results were analysed. The %FVC ≥ 50% increased from 73% with Roca to 94% with Quanjer (ECSC) and %TLco≥30% increased from 87% with Paoletti to 96% with Miller. Overall eligibility for subsidized treatment in the AIPFR group varied from 73.6% to 82.8% between surveyed interstitial lung disease (ILD) centres based entirely on the equation used. Substantial variability exists between reference equations, impacting access to subsidized treatment. Treating clinicians should be aware of this when assessing patients around public funding thresholds.en_US
dc.language.isoeng-
dc.subjectfibrosisen_US
dc.subjectlung functionen_US
dc.subjectpredicted equationsen_US
dc.subjecttreatmenten_US
dc.titleEligibility for anti-fibrotic treatment in idiopathic pulmonary fibrosis depends on the predictive equation used for pulmonary function testing.en_US
dc.typeJournal Articleen_US
dc.identifier.journaltitleRespirology (Carlton, Vic.)en_US
dc.identifier.affiliationDepartment of Respiratory Medicine, Royal Prince Alfred Hospital, Sydney, NSW, Australiaen_US
dc.identifier.affiliationFaculty of Medicine, University of Sydney, Sydney, NSW, Australiaen_US
dc.identifier.affiliationRespiratory Department, John Hunter Hospital (JHH), Newcastle, NSW, Australiaen_US
dc.identifier.affiliationSchool of Medicine, Newcastle University, Newcastle, NSW, Australiaen_US
dc.identifier.affiliationHunter Medical Research Institute (HMRI), Newcastle, NSW, Australiaen_US
dc.identifier.affiliationAustralian Idiopathic Pulmonary Fibrosis Registry (AIPFR), Brisbane, QLD, Australiaen_US
dc.identifier.affiliationLung Foundation Australia, Brisbane, QLD, Australiaen_US
dc.identifier.affiliationDepartment of Thoracic Medicine, Royal Brisbane and Women's Hospital, Brisbane, QLD, Australiaen_US
dc.identifier.affiliationDepartment of Respiratory Medicine, Royal Adelaide Hospital, Adelaide, SA, Australiaen_US
dc.identifier.affiliationDepartment of Respiratory Medicine, Fiona Stanley Hospital, Perth, WA, Australiaen_US
dc.identifier.affiliationSchool of Medicine, University of Queensland, Brisbane, QLD, Australiaen_US
dc.identifier.affiliationQueensland Lung Transplant Service, The Prince Charles Hospital, Brisbane, QLD, Australiaen_US
dc.identifier.affiliationDepartment of Radiology, The Alfred Hospital, Melbourne, VIC, Australiaen_US
dc.identifier.affiliationTissue pathology and Diagnostic Oncology, Royal Prince Alfred Hospital, Sydney, NSW, Australiaen_US
dc.identifier.affiliationSchool of Medicine, Western Sydney University, Sydney, NSW, Australiaen_US
dc.identifier.affiliationDepartment of Respiratory Medicine, Princess Alexandria Hospital, Brisbane, QLD, Australiaen_US
dc.identifier.affiliationDepartment of Allergy and Respiratory Medicine, The Alfred Hospital, Melbourne, VIC, Australiaen_US
dc.identifier.affiliationRespiratory and Sleep Medicineen_US
dc.identifier.affiliationInstitute for Breathing and Sleepen_US
dc.identifier.affiliationFaculty of Medicine, Monash University, Melbourne, VIC, Australiaen_US
dc.identifier.doi10.1111/resp.13540en_US
dc.type.contentTexten_US
dc.identifier.orcid0000-0001-7218-2091en_US
dc.identifier.orcid0000-0002-7096-9365en_US
dc.identifier.orcid0000-0002-5118-2890en_US
dc.identifier.orcid0000-0003-2065-4346en_US
dc.identifier.orcid0000-0001-9979-8726en_US
dc.identifier.orcid0000-0002-9310-7258en_US
dc.identifier.orcid0000-0002-0777-1196en_US
dc.identifier.orcid0000-0002-2273-1774en_US
dc.identifier.orcid0000-0002-6565-9928en_US
dc.identifier.pubmedid30924257-
dc.type.austinJournal Article-
local.name.researcherGoh, Nicole S L
item.grantfulltextnone-
item.openairetypeJournal Article-
item.languageiso639-1en-
item.fulltextNo Fulltext-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.cerifentitytypePublications-
crisitem.author.deptRespiratory and Sleep Medicine-
crisitem.author.deptInstitute for Breathing and Sleep-
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