Validity of a three-variable Juvenile Arthritis Disease Activity Score in children with new-onset juvenile idiopathic arthritis

被引:109
|
作者
Mcerlane, Flora [1 ,2 ]
Beresford, Michael W. [2 ,3 ]
Baildam, Eileen M. [3 ]
Chieng, S. E. Alice [4 ]
Davidson, Joyce E. [5 ]
Foster, Helen E. [6 ,7 ]
Gardner-Medwin, Janet [5 ]
Lunt, Mark [1 ]
Wedderburn, Lucy R. [8 ,9 ]
Thomson, Wendy [1 ]
Hyrich, Kimme L. [1 ]
机构
[1] Univ Manchester, Arthrit Res UK Epidemiol Unit, Manchester M13 9PT, Lancs, England
[2] Univ Liverpool, Inst Child Hlth, Dept Translat Med, Liverpool L69 3BX, Merseyside, England
[3] Alder Hey Childrens Hosp NHS Fdn Trust, Dept Paediat Rheumatol, Liverpool, Merseyside, England
[4] Royal Manchester Childrens Hosp, Dept Rheumatol, Manchester M27 1HA, Lancs, England
[5] Univ Glasgow, Royal Hosp Sick Children, Dept Paediat Rheumatol, Glasgow, Lanark, Scotland
[6] Newcastle Univ, Musculoskeletal Res Grp, Inst Cellular Med, Newcastle Upon Tyne NE1 7RU, Tyne & Wear, England
[7] Great North Childrens Hosp, Newcastle Upon Tyne, Tyne & Wear, England
[8] UCL, Inst Child Hlth, Rheumatol Unit, London, England
[9] Great Ormond St Hosp NHS Trust, UCL Inst Child Hlth, London, England
关键词
Disease Activity; Juvenile Idiopathic Arthritis; Treatment; REDUCED JOINT COUNTS; RHEUMATOID-ARTHRITIS; PEDIATRIC RHEUMATOLOGY; VALIDATION; ABILITY; FLARE;
D O I
10.1136/annrheumdis-2012-202031
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objectives To investigate the validity and feasibility of the Juvenile Arthritis Disease Activity Score (JADAS) in the routine clinical setting for all juvenile idiopathic arthritis (JIA) disease categories and explore whether exclusion of the erythrocyte sedimentation rate (ESR) from JADAS (the JADAS3') influences correlation with single markers of disease activity. Methods JADAS-71, JADAS-27 and JADAS-10 were determined at baseline for an inception cohort of children with JIA in the Childhood Arthritis Prospective Study. JADAS3-71, JADAS3-27 and JADAS3-10 were determined using an identical formula but with exclusion of ESR. Correlation of JADAS with JADAS3 and single measures of disease activity/severity were determined by category. Results Of 956 eligible children, sufficient data were available to calculate JADAS-71, JADAS-27 and JADAS-10 at baseline in 352 (37%) and JADAS3 in 551 (58%). The median (IQR) JADAS-71, JADAS-27 and JADAS-10 for all 352 children was 11 (5.9-18), 10.4 (5.7-17) and 11 (5.9-17.3), respectively. Median JADAS and JADAS3 varied significantly with the category (Kruskal-Wallis p=0.0001), with the highest values in children with polyarticular disease patterns. Correlation of JADAS and JADAS3 across all categories was excellent. Correlation of JADAS71 with single markers of disease activity/severity was good to moderate, with some variation across the categories. With the exception of ESR, correlation of JADAS3-71 was similar to correlation of JADAS-71 with the same indices. Conclusions This study is the first to apply JADAS to all categories of JIA in a routine clinical setting in the UK, adding further information about the feasibility and construct validity of JADAS. For the majority of categories, clinical applicability would be improved by exclusion of the ESR.
引用
收藏
页码:1983 / 1988
页数:6
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