Title
Diagnosis and Management of Still’s Disease, Comprising Systemic Juvenile Idiopathic Arthritis and Adult-Onset Still’s Disease
Authoring Organization
Publication Month/Year
September 24, 2024
Last Updated Month/Year
October 1, 2024
Supplemental Implementation Tools
Document Type
Consensus
Country of Publication
European
Document Objectives
Systemic juvenile idiopathic arthritis (sJIA) and adult-onset Still's disease (AOSD) are considered the same disease, but a common approach for diagnosis and management is still missing. EULAR and PReS endorsed a proposal for a joint task force (TF) to develop recommendations for the diagnosis and management of sJIA and AOSD. The TF agreed during a first meeting to address four topics: similarity between sJIA and AOSD, diagnostic biomarkers, therapeutic targets and strategies and complications including macrophage activation syndrome (MAS). Systematic literature reviews were conducted accordingly. These recommendations are the first consensus for the diagnosis and management of children and adults with Still's disease.
Inclusion Criteria
Male, Female, Adolescent, Adult, Child, Older adult
Health Care Settings
Ambulatory
Intended Users
Nurse, nurse practitioner, physician, physician assistant
Scope
Diagnosis, Assessment and screening, Management
Diseases/Conditions (MeSH)
D016706 - Still's Disease, Adult-Onset
Keywords
arthritis, Still's disease
Source Citation
Fautrel B, Mitrovic S, De Matteis A, et alEULAR/PReS recommendations for the diagnosis and management of Still’s disease, comprising systemic juvenile idiopathic arthritis and adult-onset Still’s diseaseAnnals of the Rheumatic Diseases Published Online First: 24 September 2024. doi: 10.1136/ard-2024-225851