Behçet disease

Behcet's syndrome: Bechet disease (BD) is a chronic, relapsing, multisystemic vasculitis characterized by mucocutaneous lesions, as well as articular, vascular, ocular and central nervous system manifestations.

Endpoint definition

Name M13_BEHCET
Long name Behçet disease
Hospital Discharge registry ICD-10: M352
Cause of Death registry ICD-10: M352
Level in the ICD-hierarchy 4
First defined in version DF2
Latin name Morbus Behçet

Summary Statistics

Key figures

All Female Male
Number of individuals 51 40 11
Unadjusted prevalence (%) 0.02 0.03 0.01
Mean age at first event (years) 47.09 46.47 49.36
Case fatality at 5-years (%) 3.92 5.00 0.00

Longitudinal metrics

All Female Male
Median nb. of events per indiv. 2.0 3.5 1.0
Recurrence at 6 months (%) 52.94 57.50 36.36

Survival analyses between endpoints

Plot

before Behçet disease
after Behçet disease

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