Journal article
Diagnosis and management of connective tissue disease-associated interstitial lung disease in Australia and New Zealand: A position statement from the Thoracic Society of Australia and New Zealand*
AS Jee, R Sheehy, P Hopkins, TJ Corte, C Grainge, LK Troy, K Symons, LM Spencer, PN Reynolds, S Chapman, S de Boer, T Reddy, AE Holland, DC Chambers, IN Glaspole, HE Jo, JF Bleasel, JP Wrobel, L Dowman, MJS Parker Show all
Respirology | WILEY | Published : 2021
DOI: 10.1111/resp.13977
Abstract
Pulmonary complications in CTD are common and can involve the interstitium, airways, pleura and pulmonary vasculature. ILD can occur in all CTD (CTD-ILD), and may vary from limited, non-progressive lung involvement, to fulminant, life-threatening disease. Given the potential for major adverse outcomes in CTD-ILD, accurate diagnosis, assessment and careful consideration of therapeutic intervention are a priority. Limited data are available to guide management decisions in CTD-ILD. Autoimmune-mediated pulmonary inflammation is considered a key pathobiological pathway in these disorders, and immunosuppressive therapy is generally regarded the cornerstone of treatment for severe and/or progressi..
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Funding Acknowledgements
This work was supported by the NHMRC Centre of Research Excellence in Pulmonary Fibrosis, Australia, which is funded by the NHMRC and supported by Foundation partner Boehringer Ingelheim and Program Partners Roche and Galapagos.