Polyarteritis Nodosa: ['A necrotizing vasculitis that affects medium-sized arteries, it is usually idiopathic, and may be triggered by viral infections (Hepatitis B, also others). A multisystem disease, it most commonly affects skin (nodules, livedo reticularis) and peripheral nerves; higher morbidity is associated with gastrointestinal, central nervous system, cardiac, and/or other organ involvement. Anti-neutrophil cytoplasmic antibodies (ANCA) are typically negative. [ NCI ]']
| Name | M13_POLYARTERETAL |
|---|---|
| Long name | Polyarteritis nodosa and related conditions |
| Hospital Discharge registry | ICD-10: M30 |
| Cause of Death registry | ICD-10: M30 |
| Include | M13_POLNODOSA, M13_CHURGSTRAUSS, M13_JUVEPOLYNOD, M13_KAWASAKI, M13_POYARTOTH |
| Level in the ICD-hierarchy | 3 |
| First defined in version | DF2 |
| Latin name | Polyarteritis nodosa et condiciones cognatae |
| All | Female | Male | |
|---|---|---|---|
| Number of individuals | 164 | 101 | 63 |
| Unadjusted prevalence (%) | 0.08 | 0.08 | 0.07 |
| Mean age at first event (years) | 48.26 | 46.50 | 51.07 |
| Case fatality at 5-years (%) | 9.15 | 5.94 | 14.29 |
| All | Female | Male | |
|---|---|---|---|
| Median nb. of events per indiv. | 1.0 | 2.0 | 1.0 |
| Recurrence at 6 months (%) | 43.29 | 46.53 | 38.10 |
before Polyarteritis nodosa and related conditions
after Polyarteritis nodosa and related conditions
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