Sarcoidosis

obsolete_sarcoidosis: ['An idiopathic inflammatory disorder characterized by the formation of non-necrotizing epithelioid granulomas which contain giant cells. It usually affects the lungs, lymph nodes, liver, and skin.', 'An idiopathic systemic inflammatory granulomatous disorder comprised of epithelioid and multinucleated giant cells with little necrosis. It usually invades the lungs with fibrosis and may also involve lymph nodes, skin, liver, spleen, eyes, phalangeal bones, and parotid glands.']

Endpoint definition

Name D3_SARCOIDOSIS
Long name Sarcoidosis
Hospital Discharge registry ICD-10: D86, ICD-9: 135, ICD-8: 135
Cause of Death registry ICD-10: D86, ICD-9: 135, ICD-8: 135
KELA reimboursements codes 132
Level in the ICD-hierarchy 3
First defined in version DF2
Latin name Sarcoidosis

Summary Statistics

Key figures

All Female Male
Number of individuals 2046 1144 902
Unadjusted prevalence (%) 0.94 0.93 0.96
Mean age at first event (years) 45.87 46.73 44.79
Case fatality at 5-years (%) 1.12 0.87 1.44

Longitudinal metrics

All Female Male
Median nb. of events per indiv. 4.0 4.0 4.0
Recurrence at 6 months (%) 67.50 67.40 67.63

Survival analyses between endpoints

Plot

before Sarcoidosis
after Sarcoidosis

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