A Novel Global Assessment Scale for Wilson's Disease (GAS for WD)

被引:97
作者
Aggarwal, Annu [2 ]
Aggarwal, Nitin [3 ]
Nagral, Aabha [4 ]
Jankharia, Govindji [5 ]
Bhatt, Mohit [1 ,2 ]
机构
[1] Kokilaben Dhirubhai Ambani Hosp & Med Res Inst, Movment Disorder Clin, Dept Neurol, Bombay 400053, Maharashtra, India
[2] Jaslok Hosp & Res Ctr, Dept Neurol, Movement Disorder Clin, Bombay, Maharashtra, India
[3] Univ Illinois, Coordinated Sci Lab, Urbana, IL 61801 USA
[4] Jaslok Hosp & Res Ctr, Dept Gastroenterol, Bombay, Maharashtra, India
[5] Jaslok Hosp & Res Ctr, Dept Radiol, Bombay, Maharashtra, India
关键词
Wilson's disease; disability scale; reliability; responsiveness; validation; NEUROLOGICAL MANIFESTATIONS; DIAGNOSIS; SCORE;
D O I
10.1002/mds.22231
中图分类号
R74 [神经病学与精神病学];
学科分类号
100204 [神经病学];
摘要
Wilson's disease (WD) is an inherited disorder of copper meutbolism. Despite being treatable, patients with WD suffer severe disabilities due to delay in initiation and difficulty in monitoring treatment. We propose a two tier, Global Assessment Scale for Wilson's Disease (GAS for WD) that grades the multisystemic manifestations of the disease. Tier 1 scores the global disability in four domains: Liver, Cognition and behavior. Motor, and Osseomuscular. Tier 2 is multidimensional scale for a fine grained evaluation of the neurological dysfunction. We prospectively validated this scale in 30 patients with WD. Both tiers hada high inter-rater reliability (Intraclass correlation coefficient ICC (A. 2) = 0.96-1.0). Tier 2 items were internally consistent (Cronbach's alpha = 0.89) and factorial analysis showed that 90.3% of the Tier 2 total score variance was determined by seven factors. Scores of both tiers were commensurate with the disease burden as assessed by standard disability scales (Child Pugh, UPDRS, SS3, and CGI) and satisfied criteria for validity. Longitudinal follow-up over 1.5 years showed that the scale was sensitive to clinical change. This suggests that GAS for WD is a practical tool with potential applications in management of patients, and in testing and comparison of treatment regimens. (C) 2008 Movement Disorder Society
引用
收藏
页码:509 / 518
页数:10
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