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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)