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Implications of the 2022 lung function update and GLI global reference equations among patients with interstitial lung disease.
Li, Andrew; Teoh, Alan; Troy, Lauren; Glaspole, Ian; Wilsher, Margaret L; de Boer, Sally; Wrobel, Jeremy; Moodley, Yuben P; Thien, Francis; Gallagher, Henry; Galbraith, Michelle; Chambers, Daniel C; Mackintosh, John; Goh, Nicole; Khor, Yet Hong; Edwards, Adrienne; Royals, Karen; Grainge, Christopher; Kwan, Benjamin; Keir, Gregory J; Ong, Chong; Reynolds, Paul N; Veitch, Elizabeth; Chai, Gin Tsen; Ng, Ziqin; Tan, Geak Poh; Jackson, Dan; Corte, Tamera; Jo, Helen.
Afiliação
  • Li A; Department of Medicine, Respiratory Service, Woodlands Health, Singapore.
  • Teoh A; Department of Respiratory and Sleep Medicine, Royal Prince Alfred Hospital, Camperdown, New South Wales, Australia.
  • Troy L; Department of Respiratory and Critical Care Medicine, Tan Tock Seng Hospital, Singapore.
  • Glaspole I; Department of Respiratory and Sleep Medicine, Royal Prince Alfred Hospital, Camperdown, New South Wales, Australia.
  • Wilsher ML; Department of Respiratory and Sleep Medicine, Westmead Hospital, Sydney, New South Wales, Australia.
  • de Boer S; Department of Respiratory and Sleep Medicine, Royal Prince Alfred Hospital, Camperdown, New South Wales, Australia.
  • Wrobel J; Sydney Medical School, University of Sydney, Sydney, New South Wales, Australia.
  • Moodley YP; Alfred Hospital, Melbourne, Victoria, Australia.
  • Thien F; Respiratory Services, Auckland District Health Board, Auckland, New Zealand.
  • Gallagher H; Green Lane Respiratory Services, Auckland City Hospital, Auckland, New Zealand.
  • Galbraith M; Department of Respiratory Medicine, Fiona Stanley Hospital, Murdoch, Western Australia, Australia.
  • Chambers DC; Department of Medicine, University of Notre Dame Australia, Fremantle, Perth, Australia.
  • Mackintosh J; Department of Respiratory Medicine, Fiona Stanley Hospital, Murdoch, Western Australia, Australia.
  • Goh N; Centre for Respiratory Health, Institute for Respiratory Health, Nedlands, Western Australia, Australia.
  • Khor YH; Department of Respiratory Medicine, Eastern Health and Monash University, Box Hill, Victoria, Australia.
  • Edwards A; Waikato Hospital, Hamilton, New Zealand.
  • Royals K; Waikato Hospital, Hamilton, New Zealand.
  • Grainge C; Queensland Lung Transplant Service, The Prince Charles Hospital, Chermside, Queensland, Australia.
  • Kwan B; Faculty of Medicine, The University of Queensland, Brisbane, Queensland, Australia.
  • Keir GJ; Department of Thoracic Medicine, The Prince Charles Hospital, Chermside, Queensland, Australia.
  • Ong C; Respiratory and Sleep Medicine Department, Austin Health, Heidelberg, Victoria, Australia.
  • Reynolds PN; Respiratory and Sleep Medicine, Austin Hospital, Heidelberg, Victoria, Australia.
  • Veitch E; Institute for Breathing and Sleep, Monash University, Melbourne, Victoria, Australia.
  • Chai GT; Faculty of Medicine, University of Melbourne, Melbourne, Victoria, Australia.
  • Ng Z; Respiratory Research@ALfred, Central Clinical School, Monash University, Melbourne, Victoria, Australia.
  • Tan GP; Respiratory Department, Christchurch Hospital, Christchurch, Canterbury, New Zealand.
  • Jackson D; Department for Health and Ageing, Respiratory Nursing Service, Adelaide, South Australia, Australia.
  • Corte T; University of Newcastle, Callaghan, New South Wales, Australia.
  • Jo H; Department of Respiratory and Sleep Medicine, Sutherland Hospital, Caringbah, New South Wales, Australia.
Thorax ; 79(11): 1024-1032, 2024 Oct 16.
Article em En | MEDLINE | ID: mdl-39317451
ABSTRACT

BACKGROUND:

Lung 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.

METHODS:

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.

RESULTS:

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.

CONCLUSION:

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.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doenças Pulmonares Intersticiais Limite: Aged / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doenças Pulmonares Intersticiais Limite: Aged / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2024 Tipo de documento: Article