interstitial lung disease: A diverse group of lung diseases that affect the lung parenchyma. They are characterized by an initial inflammation of pulmonary alveoli that extends to the interstitium and beyond leading to diffuse pulmonary fibrosis. Interstitial lung diseases are classified by their etiology (known or unknown causes), and radiological-pathological features.
| Name | ILD |
|---|---|
| Long name | Interstitial lung disease |
| Hospital Discharge registry | ICD-10: J84, ICD-9: 515/516, ICD-8: 48499|51701 |
| Cause of Death registry | ICD-10: J84, ICD-9: 515/516, ICD-8: 48499 |
| First defined in version | DF5 |
| Latin name | Alii morbi interstitiales pulmonum |
| All | Female | Male | |
|---|---|---|---|
| Number of individuals | 1969 | 812 | 1157 |
| Unadjusted prevalence (%) | 0.91 | 0.66 | 1.23 |
| Mean age at first event (years) | 64.70 | 62.65 | 66.14 |
| Case fatality at 5-years (%) | 13.97 | 10.10 | 16.68 |
| All | Female | Male | |
|---|---|---|---|
| Median nb. of events per indiv. | 4.0 | 4.0 | 4.0 |
| Recurrence at 6 months (%) | 66.18 | 65.15 | 66.90 |
before Interstitial lung disease
after Interstitial lung disease
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