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Fig. 1 | BMC Pulmonary Medicine

Fig. 1

From: Baseline characteristics and comorbidities in the CAnadian REgistry for Pulmonary Fibrosis

Fig. 1

Percent ILD diagnosis overall and by CARE-PF site. 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

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