relapsing polychondritis: Relapsing polychondritis (RP) is a rare, clinically heterogeneous, multisystemic inflammatory disease characterized by inflammation of the cartilage and proteoglycan rich structures leading to cartilage damage with joint, ocular and cardiovascular involvement.
| Name | M13_RELAPSPOLYCHONDR |
|---|---|
| Long name | Relapsing polychondritis |
| Hospital Discharge registry | ICD-10: M941 |
| Cause of Death registry | ICD-10: M941 |
| Level in the ICD-hierarchy | 4 |
| First defined in version | DF2 |
| Latin name | Polychondritis recidiva |
| All | Female | Male | |
|---|---|---|---|
| Number of individuals | 32 | 22 | 10 |
| Unadjusted prevalence (%) | 0.01 | 0.02 | 0.01 |
| Mean age at first event (years) | 50.77 | 49.56 | 53.42 |
| Case fatality at 5-years (%) | 0.00 | 0.00 | 0.00 |
| All | Female | Male | |
|---|---|---|---|
| Median nb. of events per indiv. | 4.0 | 4.5 | 2.0 |
| Recurrence at 6 months (%) | 71.88 | 77.27 | 60.00 |
before Relapsing polychondritis
after Relapsing polychondritis
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