Takayasu arteritis: Takayasu arteritis (TAK) is a rare inflammatory large-vessel vasculitis primarily affecting the aorta and its major branches, but also other large vessels, causing stenosis, occlusion, or aneurysm.
| Name | M13_TAKAYASU |
|---|---|
| Long name | Aortic arch syndrome [Takayasu] |
| Hospital Discharge registry | ICD-10: M314 |
| Cause of Death registry | ICD-10: M314 |
| Level in the ICD-hierarchy | 4 |
| First defined in version | DF2 |
| Latin name | Syndroma arcus aortae |
| All | Female | Male | |
|---|---|---|---|
| Number of individuals | 26 | 20 | 6 |
| Unadjusted prevalence (%) | 0.01 | 0.02 | 0.01 |
| Mean age at first event (years) | 48.60 | 48.01 | 50.55 |
| Case fatality at 5-years (%) | 0.00 | 0.00 | 0.00 |
| All | Female | Male | |
|---|---|---|---|
| Median nb. of events per indiv. | 10.0 | 10.5 | 8.0 |
| Recurrence at 6 months (%) | 69.23 | 70.00 | 66.67 |
before Aortic arch syndrome [Takayasu]
after Aortic arch syndrome [Takayasu]
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