Development and Validation of a Composite Disease Activity Score for Juvenile Idiopathic Arthritis

被引:606
作者
Consolaro, Alessandro [1 ,2 ]
Ruperto, Nicolino [1 ]
Bazso, Anna [1 ]
Pistorio, Angela [1 ]
Magni-Manzoni, Silvia [3 ]
Filocamo, Giovanni [1 ]
Malattia, Clara [1 ]
Viola, Stefania [1 ]
Martini, Alberto [4 ,5 ]
Ravelli, Angelo [4 ,5 ]
机构
[1] Ist Ricovero & Cura Carattere Sci G Gaslini, Genoa, Italy
[2] Univ Verona, I-37100 Verona, Italy
[3] Fdn Ist Ricovero & Cura Carattere Sci Policlin S, Pavia, Italy
[4] Ist Recovero & Cura Carattere Sci G Gaslini, Genoa, Italy
[5] Univ Genoa, Genoa, Italy
来源
ARTHRITIS & RHEUMATISM-ARTHRITIS CARE & RESEARCH | 2009年 / 61卷 / 05期
关键词
RHEUMATOID-ARTHRITIS; HEALTH-STATUS; ACTIVITY INDEX; CHILDREN; RESPONSIVENESS; QUALITY; TRIAL;
D O I
10.1002/art.24516
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
Objective. To develop and validate a composite disease activity score for juvenile idiopathic arthritis (JIA), the Juvenile Arthritis Disease Activity Score (JADAS). Methods. The JADAS includes 4 measures: physician global assessment of disease activity, parent/patient global assessment of well-being, active joint count, and erythrocyte sedimentation rate. These variables are part of the American College of Rheumatology (ACR) Pediatric 30 (Pedi 30), Pedi 50, and Pedi 70 criteria for improvement. Validation analyses were conducted on >4,500 patients and included assessment of construct validity, discriminant validity, and responsiveness to change. Three versions of the JADAS were tested based on 71-joint (range 0-101), 27-joint (range 0-57), or 10-joint (range 0-40) counts. Statistical performances of the JADAS were compared with those of 2 rheumatoid arthritis composite scores, the Disease Activity Score in 28 joints (DAS28) and the Clinical Disease Activity Index (CDAI). Results. The JADAS demonstrated good construct validity, yielding strong correlations with JIA activity measures not included in the score and moderate correlations with the Childhood Health Assessment Questionnaire. Correlations obtained for the 3 JADAS versions were comparable, but superior to those yielded by the DAS28 and CDAI. The area under the curve of the JADAS predicted long-term disease outcome, measured as radiographic progression over 3 years. In 2 clinical trials, the JADAS discriminated well between ACR Pedi 30, Pedi 50, and Pedi 70 response and revealed strong responsiveness to clinical change. Conclusion. The JADAS was found to be a valid instrument for assessment of disease activity in JIA and is potentially applicable in standard clinical care, observational studies, and clinical trials.
引用
收藏
页码:658 / 666
页数:9
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