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. 2016 Sep 22;2(2):e000304. doi: 10.1136/rmdopen-2016-000304

Table 2.

Classification according to adult rheumatic diseases

Onset ILAR category Adult rheumatic disease classification at the last visit
RA AS USpA EA PsA ASD Non-classifiable
Systemic, n=39 2 (5.1%) 0 0 0 0 36 (92.3%) 1 (2.6%)
RF− poly, n=63 36 (57.1%) 2 (3.8%) 2 (3.8%) 0 8 (12.7%) 0 15 (23.8%)
RF+ poly, n=68 65 (95.6%) 1 (1.5%) 0 0 1 (1.5%) 0 1 (1.5%)
P. oligo, n=66 4 (6.1%) 5 (7.6%) 9 (13.6%) 4 (6.1%) 5 (7.6%) 0 39 (59.1%)
E. oligo, n=54 21 (38.9%) 2 (3.7%) 10 (18.5%) 1 (1.9%) 1 (1.9%) 0 19 (35.2%)
ERA, n=76 0 41 (53.9%) 21 (27.6%) 4 (5.3%) 6 (7.9%) 0 4 (5.3%)
PsA, n=13 0 0 0 0 12 (92.3%) 0 1 (7.7%)
Undif, n=6 3 (50%) 1 (16.7%) 0 1 (16.7%) 0 0 1 (16.7%)
Total 131 (34%) 52 (13.5%) 42 (10.9%) 10 (2.6%) 33 (8.6%) 36 (9.4%) 81 (21%)

AS, ankylosing spondylitis; ASD, adult Still disease; E. Oligo, extended oligoarthritis; EA, enteropathic arthritis; ERA, enthesitis-related arthritis; ILAR, International League of Associations for Rheumatology; JIA, juvenile idiopathic arthritis; P. Oligo, persistent oligoarthritis; PsA, psoriatic arthritis; RA, rheumatoid arthritis; RF− Poly, rheumatoid factor negative polyarthritis; RF+ poly, rheumatoid factor positive polyarthritis; Undif, undifferentiated arthritis; USpA, undifferentiated spondyloarthritis.