Fig. 2
From: Baseline characteristics and comorbidities in the CAnadian REgistry for Pulmonary Fibrosis
a Patient-reported exposure overall and by ILD subtype. Other ILD includes: Vasculitis, diffuse alveolar hemorrhage, drug related, pneumoconiosis, post-acute respiratory disease syndrome, aspiration, eosinophilic pneumonia, pleuroparenchymal fibroelastosis, lymphangioleiomyomatosis, Langerhan’s cell histiocytosis, neuroendocrine cell hyperplasia, pulmonary alveolar proteinosis. Abbreviations: CTD-ILD, connective tissue disease-associated ILD; HP, hypersensitivity pneumonitis; IIP, idiopathic interstitial pneumonia; ILD, interstitial lung disease; IPF, idiopathic pulmonary fibrosis. b Patient-reported organic exposures for the overall cohort