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.
Filter registries Inpat., Oupat., Death
Check pre-conditions None
Include endpoints None
Check conditions None
Apply sex-specific rule None
IPF
Extra metadata
List of similar endpoints to
Idiopathic pulmonary fibrosis
based on the number of shared cases.
Broader endpoints:
Narrower endpoints:
None
| All | Female | Male | |
|---|---|---|---|
| Number of individuals | 1176 | 426 | 750 |
| Unadjusted prevalence (%) | 0.45 | 0.29 | 0.66 |
| Mean age at first event (years) | 68.31 | 65.96 | 69.65 |
| Follow-up | Absolute risk | HR [95% CI] | p | N |
|---|---|---|---|---|
| 1998–2019 | - | - | - | - |
| 15 years | - | - | - | - |
| 5 years | - | - | - | - |
| 1 year | - | - | - | - |
Index endpoint: IPF – Idiopathic pulmonary fibrosis
GWS hits: 7
before Idiopathic pulmonary fibrosis
after Idiopathic pulmonary fibrosis
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