Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/35553
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dc.contributor.authorLi, Andrew-
dc.contributor.authorTeoh, Alan-
dc.contributor.authorTroy, Lauren-
dc.contributor.authorGlaspole, Ian-
dc.contributor.authorWilsher, Margaret L-
dc.contributor.authorde Boer, Sally-
dc.contributor.authorWrobel, Jeremy-
dc.contributor.authorMoodley, Yuben P-
dc.contributor.authorThien, Francis-
dc.contributor.authorGallagher, Henry-
dc.contributor.authorGalbraith, Michelle-
dc.contributor.authorChambers, Daniel C-
dc.contributor.authorMackintosh, John-
dc.contributor.authorGoh, Nicole S L-
dc.contributor.authorKhor, Yet Hong-
dc.contributor.authorEdwards, Adrienne-
dc.contributor.authorRoyals, Karen-
dc.contributor.authorGrainge, Christopher-
dc.contributor.authorKwan, Benjamin-
dc.contributor.authorKeir, Gregory J-
dc.contributor.authorOng, Chong-
dc.contributor.authorReynolds, Paul N-
dc.contributor.authorVeitch, Elizabeth-
dc.contributor.authorChai, Gin Tsen-
dc.contributor.authorNg, Ziqin-
dc.contributor.authorTan, Geak Poh-
dc.contributor.authorJackson, Dan-
dc.contributor.authorCorte, Tamera-
dc.contributor.authorJo, Helen-
dc.date2024-
dc.date.accessioned2024-10-21T05:18:48Z-
dc.date.available2024-10-21T05:18:48Z-
dc.date.issued2024-10-16-
dc.identifier.citationThorax 2024-10-16; 79(11)en_US
dc.identifier.issn1468-3296-
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/35553-
dc.description.abstractLung function testing remains a cornerstone in the assessment and management of interstitial lung disease (ILD) patients. The clinical implications of the Global Lung function Initiative (GLI) reference equations and the updated interpretation strategies remain uncertain. Adult patients with ILD with baseline forced vital capacity (FVC) were included from the Australasian ILD registry and the National Healthcare Group ILD registry, Singapore.The European Coal and Steel Community and Miller reference equations were compared with the GLI reference equations to assess (a) differences in lung function percent predicted values; (b) ILD risk prediction models and (c) eligibility for ILD clinical trial enrolment. Among 2219 patients with ILD, 1712 (77.2%) were white individuals. Idiopathic pulmonary fibrosis (IPF), connective tissue disease-associated ILD and unclassifiable ILD predominated.Median FVC was 2.60 (2.01-3.36) L, forced expiratory volume in 1 s was 2.09 (1.67-2.66) L and diffusing capacity of the lungs for carbon monoxide (DLCO) was 13.60 (10.16-17.60) mL/min/mm Hg. When applying the GLI reference equations, the mean FVC percentage predicted was 8.8% lower (87.7% vs 78.9%, p<0.01) while the mean DLCO percentage predicted was 4.9% higher (58.5% vs 63.4%, p<0.01). There was a decrease in 19 IPF and 119 non-IPF patients who qualified for the nintedanib clinical trials when the GLI reference equations were applied. Risk prediction models performed similarly in predicting mortality using both reference equations. Applying the GLI reference equations in patients with ILD leads to higher DLCO percentage predicted values and smaller lung volume percentage predicted values. While applying the GLI reference equations did not impact on prognostication, fewer patients met the clinical trial criteria for antifibrotic agents.en_US
dc.language.isoeng-
dc.subjectConnective tissue disease associated lung diseaseen_US
dc.subjectIdiopathic pulmonary fibrosisen_US
dc.subjectInterstitial Fibrosisen_US
dc.subjectPulmonary vasculitisen_US
dc.subjectRare lung diseasesen_US
dc.titleImplications of the 2022 lung function update and GLI global reference equations among patients with interstitial lung disease.en_US
dc.typeJournal Articleen_US
dc.identifier.journaltitleThoraxen_US
dc.identifier.affiliationDepartment of Medicine, Respiratory Service, Woodlands Health, Singapore.;Department of Respiratory and Sleep Medicine, Royal Prince Alfred Hospital, Camperdown, New South Wales, Australia.;Department of Respiratory and Critical Care Medicine, Tan Tock Seng Hospital, Singapore.en_US
dc.identifier.affiliationRespiratory and Sleep Medicine, Royal Prince Alfred Hospital, Camperdown, New South Wales, Australia.;Department of Respiratory and Sleep Medicine, Westmead Hospital, Sydney, New South Wales, Australia.en_US
dc.identifier.affiliationSydney Medical School, University of Sydney, Sydney, New South Wales, Australia.en_US
dc.identifier.affiliationAlfred Hospital, Melbourne, Victoria, Australia.en_US
dc.identifier.affiliationRespiratory Services, Auckland District Health Board, Auckland, New Zealand.en_US
dc.identifier.affiliationGreen Lane Respiratory Services, Auckland City Hospital, Auckland, New Zealand.en_US
dc.identifier.affiliationDepartment of Respiratory Medicine, Fiona Stanley Hospital, Murdoch, Western Australia, Australia.;Department of Medicine, University of Notre Dame Australia, Fremantle, Perth, Australia.en_US
dc.identifier.affiliationDepartment of Respiratory Medicine, Eastern Health and Monash University, Box Hill, Victoria, Australia.en_US
dc.identifier.affiliationWaikato Hospital, Hamilton, New Zealand.en_US
dc.identifier.affiliationQueensland Lung Transplant Service, The Prince Charles Hospital, Chermside, Queensland, Australia.;Faculty of Medicine, The University of Queensland, Brisbane, Queensland, Australia.en_US
dc.identifier.affiliationDepartment of Thoracic Medicine, The Prince Charles Hospital, Chermside, Queensland, Australia.en_US
dc.identifier.affiliationRespiratory and Sleep Medicineen_US
dc.identifier.affiliationInstitute for Breathing and Sleep, Monash University, Melbourne, Victoria, Australia.;Faculty of Medicine, University of Melbourne, Melbourne, Victoria, Australia.;Respiratory Research@ALfred, Central Clinical School, Monash University, Melbourne, Victoria, Australia.en_US
dc.identifier.affiliationRespiratory Department, Christchurch Hospital, Christchurch, Canterbury, New Zealand.en_US
dc.identifier.affiliationDepartment for Health and Ageing, Respiratory Nursing Service, Adelaide, South Australia, Australia.en_US
dc.identifier.affiliationUniversity of Newcastle, Callaghan, New South Wales, Australia.en_US
dc.identifier.affiliationDepartment of Respiratory and Sleep Medicine, Sutherland Hospital, Caringbah, New South Wales, Australia.en_US
dc.identifier.affiliationUniversity of Queensland, St Lucia, Queensland, Australia.en_US
dc.identifier.affiliationDepartment of Respiratory and Sleep Medicine, St Vincent's Hospital Sydney, Darlinghurst, New South Wales, Australia.en_US
dc.identifier.affiliationDepartment of Respiratory Medicine, Royal Adelaide Hospital, Adelaide, South Australia, Australia.en_US
dc.identifier.affiliationDepartment of Thoracic Medicine, Concord Hospital, Concord, New South Wales, Australia.en_US
dc.identifier.affiliationDepartment of Respiratory and Critical Care Medicine, Tan Tock Seng Hospital, Singapore.en_US
dc.identifier.affiliationSydney Medical School, University of Sydney, Sydney, New South Wales, Australia.en_US
dc.identifier.affiliationDepartment of Respiratory and Sleep Medicine, Royal Prince Alfred Hospital, Camperdown, New South Wales, Australia.;Sydney Medical School, University of Sydney, Sydney, New South Wales, Australia.en_US
dc.identifier.doi10.1136/thorax-2024-221813en_US
dc.type.contentTexten_US
dc.identifier.orcid0000-0003-1516-3454en_US
dc.identifier.orcid0000-0002-5254-4144en_US
dc.identifier.orcid0000-0002-5434-9342en_US
dc.identifier.orcid0000-0003-0758-6895en_US
dc.identifier.pubmedid39317451-
dc.description.volume79-
dc.description.issue11-
dc.description.startpage1024-
dc.description.endpage1032-
dc.subject.meshtermssecondaryLung Diseases, Interstitial/physiopathology-
dc.subject.meshtermssecondaryVital Capacity/physiology-
dc.subject.meshtermssecondaryForced Expiratory Volume/physiology-
item.languageiso639-1en-
item.openairetypeJournal Article-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.fulltextNo Fulltext-
item.grantfulltextnone-
item.cerifentitytypePublications-
crisitem.author.deptRespiratory and Sleep Medicine-
crisitem.author.deptInstitute for Breathing and Sleep-
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