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Abstract Number: 2018

Juvenile Idiopathic Arthritis in Adulthood: Evaluation of Disease Activity, Damage and Quality of Life

Alessandra Salmaso1, Lorenzo Ceri2, Serena Capannini2, Francesco La Torre3, Maurizio Gattinara4, Irene Pontikaki1, Pier Luigi Meroni5, Fernanda Falcini2 and Valeria Gerloni1, 1Pediatric Rheumatology, G. Pini Institute, Department and Chair of Rheumatology, Milan, Italy, 2Department of Internal Medicine, Rheumatology Section, Transition Clinic, University of Florence, Firenze, Italy, 3DIMIMP-University, Rheumatologic Section, Bari, Italy, 4Pediatric Rheumatology, Pediatric Rheumatology, G. Pini Institute, Department and Chair of Rheumatology, Milan, Italy, 5Dept. of clinical and community science, Division of Rheumatology, Istituto G. Pini, University of Milan, Milano, Italy

Meeting: ACR/ARHP Annual Meeting 2012

Keywords: juvenile idiopathic arthritis (JIA)

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Session Information

Title: Pediatric Rheumatology - Clinical and Therapeutic Aspects: Juvenile Idiopathic Arthritis and Other Pediatric Rheumatic Diseases

Session Type: Abstract Submissions (ACR)

Background/Purpose: : Health outcomes in Juvenile Idiopathic Arthritis (JIA) have been a very active area of research in the past several years. Altogether, the available data indicate that a considerable number of patients with JIA enters adulthood with persistently active disease and a significant proportion of them may develop severe physical disability. In general children with polyarticular course are more likely to have erosive radiological damage on follow-up. The comparison of earlier studies with those published in the last decade shows a decline in the frequency of patients with severe physical disability over the years; however, patients who enter adulthood with active disease do not seem to be diminished. The purpose of this study is to evaluate in patients with JIA in adulthood the functional and anatomic damage and the quality of life.

Methods: All consecutive JIA patients aged >18 yrs, afferent to three different paediatric rheumatology centres in the last year, were assessed with: HAQ; SF36; active joint count; VAS (0-100 mm) for pain, patient and physician global health assessment; radiological evaluation (Steinbrocker classification).

Results: 347 patients with JIA in adulthood, age >18 yrs, were enrolled. The collected data are shown in the following table

JIA IN ADULTHOOD, age >18 yrs

JIA all

Syst

Poly RF+

Poly RF-

Oligo pers

Oligo ext

Psor

ERA

# pts

347

41

22

60

122

50

14

38

Mean age

27(17-52)

30(18-52)

26(18-42)

27(18-51)

26(18-44)

28(18-46)

28(19-44)

25(18-39)

Mean disease duration

19(3-51)

21(3-48)

15(4-30)

18(3-51)

19(6-40)

22(6-43)

22(6-43)

14(3-31)

Active arthritis(%)

40

46

43

48

38

38

29

32

Mean VAS pain

24(0-100)

36(0-100)

25(0-70)

24(0-88)

22(0-82)

21(0-88)

22(0-62)

22(0-84)

Mean patient GH

71(0-100)

62(0-100)

77(30-100)

70(0-100)

74(24-100)

72(10-100)

65(40-90)

72(20-100)

Mean VAS physician

15(0-100)

22(0-100)

19(0-75)

17(0-90)

12(0-70)

15(0-50)

17(0-94)

12(0-60)

% anatomic class III-IV

45

72

71

53

25

60

50

30

% pts with protesis

11

49

10

12

1

15

21

0

Mean HAQ

0,5(0-3)

0,8(0-3)

0,4(0-2)

0,4(0-3)

0,2(0-1,6)

0,3(0-1,3)

0,4(0-1,8)

0,1(0-0,8)

Mean SF36 physical health

62(1-99)

50(1-97)

62(25-97)

62(11-99)

65(13-99)

66(15-99)

50(22-80)

59(12-98)

Mean SF36 mental health

63(12-100)

61(12-93)

63(22-99)

62(11-99)

64(13-100)

68(20-100)

51(21-90)

60(30-98)

Conclusion: this hospital-based study clearly shows a selection bias toward the most serious cases, but underlines the high rate of JIA patients with disease still active in adulthood, confirming the need of a more aggressive and precocious treatment, to improve outcome in the future.


Disclosure:

A. Salmaso,
None;

L. Ceri,
None;

S. Capannini,
None;

F. La Torre,
None;

M. Gattinara,
None;

I. Pontikaki,
None;

P. L. Meroni,
None;

F. Falcini,
None;

V. Gerloni,
None.

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