Validation and clinical significance of the childhood myositis assessment scale for assessment of muscle function in the juvenile idiopathic inflammatory myopathies

被引:140
作者
Huber, AM
Feldman, BM
Rennebohm, RM
Hicks, JE
Lindsley, CB
Perez, MD
Zemel, LS
Wallace, CA
Ballinger, SH
Passo, MH
Reed, AM
Summers, RM
White, PH
Katona, IM
Miller, FW
Lachenbruch, PA
Rider, LG
机构
[1] IWK Hlth Ctr, Halifax, NS B3J 3G9, Canada
[2] Dalhousie Univ, Halifax, NS, Canada
[3] Hosp Sick Children, Toronto, ON M5G 1X8, Canada
[4] Univ Toronto, Toronto, ON, Canada
[5] Ohio State Univ, Columbus, OH 43210 USA
[6] Columbus Childrens Hosp, Columbus, OH USA
[7] NIH, Ctr Clin, Bethesda, MD USA
[8] Univ Kansas, Kansas City, KS USA
[9] Baylor Coll Med, Houston, TX 77030 USA
[10] Texas Childrens Hosp, Houston, TX 77030 USA
[11] Univ Connecticut, Hartford, CT 06112 USA
[12] Connecticut Childrens Med Ctr, Hartford, CT USA
[13] Childrens Hosp, Seattle, WA USA
[14] Univ Washington, Seattle, WA 98195 USA
[15] James Whitcomb Riley Hosp Children, Indianapolis, IN 46202 USA
[16] Indiana Univ, Indianapolis, IN 46204 USA
[17] Childrens Hosp, Cincinnati, OH 45229 USA
[18] Univ Cincinnati, Cincinnati, OH USA
[19] Mayo Clin, Rochester, MN USA
[20] Childrens Natl Med Ctr, Washington, DC 20010 USA
[21] Uniformed Serv Univ Hlth Sci, Bethesda, MD 20814 USA
[22] Natl Inst Environm Hlth Sci, NIH, Bethesda, MD USA
[23] US FDA, Ctr Biol Evaluat & Res, Rockville, MD USA
来源
ARTHRITIS AND RHEUMATISM | 2004年 / 50卷 / 05期
关键词
D O I
10.1002/art.20179
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective. To examine the measurement characteristics of the Childhood Myositis Assessment Scale (CMAS) in children with juvenile idiopathic inflammatory myopathy (juvenile IIM), and to obtain preliminary data on the clinical significance of CMAS scores. Methods. One hundred eight children with juvenile IIM were evaluated on 2 occasions, 7-9 months apart, using various measures of physical function, strength, and disease activity. Interrater reliability, construct validity, and responsiveness of the CMAS were examined. The minimum clinically important difference (MID) and CMAS scores corresponding to various degrees of physical disability were estimated. Results. The intraclass correlation coefficient for 26 patients assessed by 2 examiners was 0.89, indicating very good interrater reliability. The CMAS score correlated highly with the Childhood Health Assessment Questionnaire (C-HAQ) score and with findings on manual muscle testing (MMT) (r(s) = -0.73 and 0.73, respectively) and moderately with physician-assessed global disease activity and skin activity, parent-assessed global disease severity, and muscle magnetic resonance imaging (rs = -0.44 to -0.61), thereby demonstrating good construct validity. The standardized response mean was 0.81 (95% confidence interval 0.53, 1.09) in patients with at least 0.8 cm improvement on a 10-cm visual analog scale for physician-assessed global disease activity, indicating strong responsiveness. In bivariate regression models predicting physician-assessed global disease activity, MMT remained significant in models containing the CMAS (P = 0.03) while the C-HAQ did not (P = 0.4). Estimates of the MID ranged from 1.5 to 3.0 points on a 0-52-point scale. CMAS scores corresponding to no, mild, mild-to-moderate, and moderate physical disability, respectively, were 48, 45, 39, and 30. Conclusion. The CMAS exhibits good reliability, construct validity, and responsiveness, and is therefore a valid instrument for the assessment of physical function, muscle strength, and endurance in children with juvenile IIM. Preliminary data on MID and corresponding levels of disability should aid in the clinical interpretation of CMAS scores when assessing patients with juvenile IIM.
引用
收藏
页码:1595 / 1603
页数:9
相关论文
共 24 条
[1]   Evaluating changes in health status: Reliability and responsiveness of five generic health status measures in workers with musculoskeletal disorders [J].
Beaton, DE ;
HoggJohnson, S ;
Bombardier, C .
JOURNAL OF CLINICAL EPIDEMIOLOGY, 1997, 50 (01) :79-93
[2]   POLYMYOSITIS AND DERMATOMYOSITIS .1. [J].
BOHAN, A ;
PETER, JB .
NEW ENGLAND JOURNAL OF MEDICINE, 1975, 292 (07) :344-347
[3]  
Dempster H, 2001, ARTHRITIS RHEUM, V44, P1768, DOI 10.1002/1529-0131(200108)44:8<1768::AID-ART312>3.0.CO
[4]  
2-Q
[5]   Minimal difference in pain associated with change in quality of life in children with rheumatic disease [J].
Dhanani, S ;
Quenneville, J ;
Perron, M ;
Abdolell, M ;
Feldman, BM .
ARTHRITIS & RHEUMATISM-ARTHRITIS CARE & RESEARCH, 2002, 47 (05) :501-505
[6]   Decreased aerobic capacity in children with juvenile dermatomyositis [J].
Hicks, JE ;
Drinkard, B ;
Sunmers, RM ;
Rider, LG .
ARTHRITIS & RHEUMATISM-ARTHRITIS CARE & RESEARCH, 2002, 47 (02) :118-123
[7]  
HINDERER KA, 1993, MUSCLE STRENGTH, P93
[8]  
Huber AM, 2001, J RHEUMATOL, V28, P1106
[9]  
Josefson A, 1996, J RHEUMATOL, V23, P1380
[10]  
Kendall F.P., 1993, MUSCLES TESTING FUNC