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. 2019 Aug 5;5(2):e000933. doi: 10.1136/rmdopen-2019-000933

Table 2.

Uveitis follow-up

All uveitis (n=147) ANA+JIA (n=58) ANA−JIA
(n=24)
ERA
(n=9)
Idiopathic (n=36) Sarcoidosis (n=9) Others uveitis* (n=11)
Uveitis in remission off steroids†
 Number of cases, n (%) 45 (30) 18 (31) 5 (20) 5 (55) 11 (30) 3 (33) 3 (27)
 Follow-up (month), mean±SD (median) 48±32 (48) 58±36 (51.5) 46±37 (60) 31±31 (13) 56±43 (48) 51±29 (48) 45±39 (48)
 Age (years) at last consultation, mean (median) 11.4 (11) 10 (10) 10 (9) 13.8 (15) 14.1 (14) 17 13.2 (11)
 DMARDs 13 (27) 10 (55) 0 0 1 (9) 1 (33) 1 (10)
 Biological therapy 13 (29) 5 (27) 1 (25) 2 (33) 1 (9) 0 2 (20)
  Adalimumab 8 3 1 2 1 0 1
  Etanercept 3 2 1 0 0 0 0
  Abatacept 1 0 0 0 0 0 0
  Anakinra 1 0 0 0 0 0 1
  Infliximab 1 1 0 0 0 0 0
 Duration of remission (month) 24±20 (6 – 76) 22±19 (12) 38±29(24) 15±8 (12) 25±2124 12 (12) 30±36 (6)
Inactive uveitis on topical steroids‡
 Number of cases, n (%) 56 (39) 21 (35) 13 (54) 2 (22) 13 (36) 2 (22) 5 (45)
 Follow-up (month), mean±SD (median) 51.4±39 (42) 67±43 (72) 51±38.5 (42) 22±10 (22.5) 35±2630 69.5±20 (69.5) 40.6±5218
 Age at last consultation (years), mean (n–N) 12 (2–21) 11.4 (2–16) 10.7 (5–18) 15(14–15) 12.6 (2.5–17) 16.25 (11.5–21) 14.4 (5–21)
 Topical corticosteroids 56 21 13 2 13 2 5
 Systemic corticosteroids 10 (21) 1 (5) 1 (8) 0 2 (17) 2 4 (44)
 DMARDs 37 (66) 18 (86) 11(85) 0 6 (50) 1 (50) 1 (11)
 Biological therapy 26 (45) 13 (62) 9 (70) 0 2 (17) 0 2 (11)
  Adalimumab 23 13 7 0 2 0 1
  Etanercept 2 0 2 0 0 0 0
  Anakinra 1 0 0 0 0 0 1
  Infliximab 1 0 1 0 0 0 0
 Duration of remission/inactivity (month), mean±SD (median) 13.8±11 (4 – 48) 14.5±11 (12) 19.5±16 (12) 9±4.2 (9) 9.6±8.6 (3) 9±4.2 (9) 9.6±3.2 (2)
Active uveitis§
 Number of cases, n (%) 46 (31) 19 (33) 6 (26) 2 (11) 12 (34) 4 (44) 3 (27)
 Follow-up (month), mean±SD (median) 54±41 (6 –168) 64±40 (66) 73.5±46 (60) 3 30.7±22 (27) 45.6±31 (24) 45.6±33.8 (33)
 Age at last consultation (years), mean (n–N) 11.4 (4–18) 10 (4–17) 11.5 (6.5–17) 14.5 10.8 (6.5–17) 13.7 (9.5–8) 14.6 (12.5–18)
 Topical corticosteroids 48 19 6 1 12 4 5
 Systemic corticosteroids 9 (19) 4 (21) 1 (17) 0 4 (33) 2 (50) 0
 DMARDs 31 (73) 15 (79) 6 (100) 0 6 (50) 3 (75) 4 (40)
 Biological therapy 25 (52) 15 (79) 4 (67) 0 4 (33) 2 (50) 1 (10)
  Adalimumab 24 15 4 3 1 1
  Etanercept 2 1 1 0 0 0
  Abatacept 2 0 1 0 1 0
  Tocilizumab 0 0 0 1 0 0
  Infliximab 5 2 1 1 1 0
 SUN classification, cells, n (%)
  0+ 0 0 0 0 0 0 0
  0.5+ 27 (58) 13 (68) 4 (67) 1 7 (58) 1 (75) 1 (33)
  1+ 19 (42) 6 (32) 2 (33) 1 5 (42) 3 (25) 2 (67)

*Other aetiologies: 4 Behçet disease, 1 Muckle-Wells syndrome, 1 Cogan syndrome, 2 TINU syndrome, 2 Vogt-Koyanagi-Harada syndrome, 1 systemic-onset JIA.

†According to SUN criteria: patients with inactive disease for at least 6 months after discontinuing all topical steroids.

‡According to SUN criteria: grade >0.5 cells apply to the anterior chamber.

§According to SUN criteria: grade 0 cells apply to the anterior chamber.

¶No patient had a score of >1 at the latest follow-up.

ANA, antinuclear antibody; DMARD, disease-modifying antirheumatic drug; ERA, enthesitis-related arthritis; JIA, juvenile idiopathic arthritis.