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Table 5 Diagnoses in ACCORD patients enrolled in the prospective observational registry (n = 57)

From: A novel transition clinic structure for adolescent and young adult patients with childhood onset rheumatic disease improves transition outcomes

Diagnosis Number of patients
n (%)
JIA 36 (63.2)
 Polyarticular RF negative 10 (17.5)
 Polyarticular RF positive 4 (7.0)
 Oligoarticular 8 (14.0)
 Extended 4 (7.0)
 Persistent 4 (7.0)
 Psoriatic 1 (1.8)
 Enthesitis related 3 (5.3)
 Systemic 2 (3.5)
 Undifferentiated 0
 Other 0
SLE 8 (14.0)
MCTD 2 (3.5)
RA 12 (21.1)
Spondylarthritis 1 (1.8)
Psoriatic arthritis 2 (3.5)
Crystal arthropathy* 1 (1.8)
Dermatomyositis/polymyositis/inflammatory myositis 1 (1.8)
Auto inflammatory** 2 (3.5)
APS 0
Systemic Sclerosis 0
Linear scleroderma 0
Sarcoidosis 0
  1. APS antiphospholipid syndrome, JIA juvenile idiopathic arthritis, MCTD mixed connective tissue disease, RA rheumatoid arthritis, RF rheumatoid factor, SLE systemic lupus erythematosus
  2. * Includes: gout
  3. * Includes: adult-onset still’s disease and cryopyrin-associated periodic fever syndrome (CAPS)