Juvenile dermatomyositis

juvenile dermatomyositis: Juvenile dermatomyositis (JDM) is the early-onset form of dermatomyositis (DM, see this term), a systemic, autoimmune inflammatory muscle disorder, characterized by proximal muscle weakness, evocative skin lesion, and systemic manifestations.

Endpoint definition

Name M13_JUVDERMATOMYO
Long name Juvenile dermatomyositis
Hospital Discharge registry ICD-10: M330, ICD-9: 7103A
Cause of Death registry ICD-10: M330, ICD-9: 7103A
Level in the ICD-hierarchy 4
First defined in version DF2
Latin name Dermatomyositis juvenilis

Summary Statistics

Key figures

All Female Male
Number of individuals 19 12 7
Unadjusted prevalence (%) 0.01 0.01 0.01
Mean age at first event (years) 32.46 28.69 38.94
Case fatality at 5-years (%) 0.00 0.00 0.00

Longitudinal metrics

All Female Male
Median nb. of events per indiv. 3.0 4.5 3.0
Recurrence at 6 months (%) 52.63 50.00 57.14

Survival analyses between endpoints

Plot

before Juvenile dermatomyositis
after Juvenile dermatomyositis

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Drugs most likely to be purchased after Juvenile dermatomyositis