Table 4.
Outcome risk for ILD subgroups
| Unadjusted | Adjusted | ||||
|---|---|---|---|---|---|
| HR | 95% CI | p-value | HR | 95% CI | p-value |
| Ref | Ref | Ref | Ref | Ref | Ref |
| 0.13 | 0.03–0.55 | 0.005 | 0.20 | 0.05–0.84 | 0.03 |
| 0.65 | 0.37–1.12 | 0.12 | 0.68 | 0.38–1.21 | 0.19 |
| 0.09 | 0.03–0.30 | <0.001 | 0.17 | 0.05–0.54 | 0.003 |
| 0.37 | 0.25–0.55 | <0.001 | 0.52 | 0.34–0.80 | 0.003 |
| 1.11 | 0.84–1.46 | 0.47 | 0.70 | 0.51–0.97 | 0.03 |
| Ref | Ref | Ref | Ref | Ref | Ref |
| 0.37 | 0.23–0.61 | <0.001 | 0.46 | 0.28–0.78 | 0.004 |
| 0.10 | 0.02–0.41 | 0.001 | 0.14 | 0.03–0.58 | 0.007 |
| 0.07 | 0.02–0.23 | <0.001 | 0.13 | 0.04–0.42 | 0.001 |
| 0.28 | 0.19–0.42 | <0.001 | 0.43 | 0.27–0.66 | <0.001 |
| 0.83 | 0.62–1.11 | 0.22 | 0.63 | 0.46–0.86 | 0.003 |
Model 1 adjusted for center, race/ethnicity, presence of UIP, immunosuppressant exposure and GAP stage
Model 2 adjusted for center, race/ethnicity, immunosuppressant exposure and GAP stage
Abbreviations: ILD = interstitial lung disease; IPAF = interstitial pneumonia with autoimmune features; MSA = myositis specific antibody; IIM-ILD = idiopathic inflammatory myopathy-associated ILD; IPF = idiopathic pulmonary fibrosis