Other necrotizing vasculopathies (FG)

vasculitis: Vasculitis represents a clinically heterogenous group of diseases of multifactorial etiology characterized by inflammation of either large-sized vessels (large-vessel vasculitis, e.g. Giant-cell arteritis and Takayasu arteritis; see these terms), medium-sized vessels (medium-vessel vasculitis e.g. polyarteritis nodosa and Kawasaki disease; see these terms), or small-sized vessels (small-vessel vasculitis, e.g. granulomatosis with polyangiitis, microscopic polyangiitis, immunoglobulin A vasculitis, and cutaneous leukocytoclastic angiitis; see these terms). Vasculitis occurs at any age, may be acute or chronic, and manifests with general symptoms such as fever, weight loss and fatigue, as well as more specific clinical signs depending on the type of vessels and organs affected. The degree of severity is variable, ranging from life or sight threatening disease (e.g. BehC'et disease, see this term) to relatively minor skin disease.

Summary Statistics

Key figures

All Female Male
Number of individuals 827 507 320
Unadjusted prevalence (%) 0.38 0.41 0.34
Mean age at first event (years) 60.39 60.59 60.08
Case fatality at 5-years (%) 6.77 4.73 10.00

Longitudinal metrics

All Female Male
Median nb. of events per indiv. 3.0 3.0 5.0
Recurrence at 6 months (%) 61.91 59.96 65.00

Survival analyses between endpoints

Plot

before Other necrotizing vasculopathies (FG)
after Other necrotizing vasculopathies (FG)

Loading survival analyses plot…

Drugs most likely to be purchased after Other necrotizing vasculopathies (FG)