Table 1.
Type of Interstitial Lung Disease | Participants [No. (%)] |
---|---|
Idiopathic pulmonary fibrosis | 15 (11.9) |
Connective tissue disease | 23 (18.3) |
Rheumatoid arthritis | 7 (5.6) |
Systemic sclerosis | 9 (7.1) |
Systemic lupus erythematosus | 1 (0.8) |
Primary Sjögren syndrome | 1 (0.8) |
Myositis | 4 (3.2) |
Mixed connective tissue disease | 1 (0.8) |
Other interstitial lung disease | 36 (28.6) |
Idiopathic nonspecific idiopathic pneumonia | 11 (8.7) |
Hypersensitivity pneumonitis | 13 (10.3) |
Vasculitis | 1 (0.8) |
Chronic eosinophilic pneumonia | 1 (0.8) |
Chemotherapy/radiation therapy | 2 (1.6) |
Combined pulmonary fibrosis and emphysema | 5 (4.0) |
Idiopathic pleuroparenchymal fibroelastosis | 1 (0.8) |
Familial pulmonary fibrosis | 1 (0.8) |
Inflammatory bowel disease related | 1 (0.8) |
Unclassifiable idiopathic interstitial pneumoniaa | 52 (41.3) |
Based on American Thoracic Society/European Respiratory Society definition of idiopathic interstitial pneumonia with either inadequate or discordant clinical, radiologic, and pathologic data to support a specific interstitial lung disease subtype diagnosis.