Endpoint definition
↥| Name | IPF |
|---|---|
| Long name | Idiopathic pulmonary fibrosis |
| Hospital Discharge registry | ICD-10: J841 |
| Cause of Death registry | ICD-10: J841 |
| First defined in version | DF5 |
| Latin name | Morbus pulmonum interstitialis cum fibrosi |
Idiopathic pulmonary fibrosis
idiopathic pulmonary fibrosis: Idiopathic pulmonary fibrosis (IPF) is a nonneoplastic pulmonary disease that is characterized by the formation of scar tissue within the lungs in the absence of any known cause.
Summary Statistics
↥Key figures
| All | Female | Male | |
|---|---|---|---|
| Number of individuals | 1028 | 378 | 650 |
| Unadjusted prevalence (%) | 0.47 | 0.31 | 0.69 |
| Mean age at first event (years) | 68.75 | 66.97 | 69.79 |
| Case fatality at 5-years (%) | 19.65 | 16.67 | 21.38 |
Longitudinal metrics
| All | Female | Male | |
|---|---|---|---|
| Median nb. of events per indiv. | 4.0 | 4.0 | 5.0 |
| Recurrence at 6 months (%) | 65.27 | 63.49 | 66.31 |
Survival analyses between endpoints
↥Plot
before Idiopathic pulmonary fibrosis
after Idiopathic pulmonary fibrosis
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Table
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