Moving towards meaningful measurement: Rasch analysis of the North Star Ambulatory Assessment in Duchenne muscular dystrophy

被引:99
作者
Mayhew, Anna [1 ]
Cano, Stefan [2 ]
Scott, Elaine [3 ]
Eagle, Michelle [1 ]
Bushby, Kate [1 ]
Muntoni, Francesco [4 ]
机构
[1] Newcastle Univ, Inst Human Genet, Int Ctr Life, Newcastle Upon Tyne NE1 3BZ, Tyne & Wear, England
[2] Peninsula Coll Med & Dent, Plymouth, Devon, England
[3] Muscular Dystrophy Campaign, London, England
[4] UCL, Inst Child Hlth, Dubowitz Neuromuscular Ctr, London, England
基金
英国医学研究理事会;
关键词
MULTIPLE-SCLEROSIS;
D O I
10.1111/j.1469-8749.2011.03939.x
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
Aim Reliable measurement of disease progression and the effect of therapeutic interventions in Duchenne muscular dystrophy (DMD) require clinically meaningful and scientifically sound rating scales. Therefore, we need robust evidence to support such tools. The North Star Ambulatory Assessment (NSAA) is a promising, clinician-rated scale with potential uses spanning clinical practice and clinical trials. In this study, we used Rasch analysis to test its suitability in these roles as a measurement instrument. Method NSAA data from 191 ambulant boys (mean age at assessment 7y 8mo, SD 2y 4mo; range 3y 6mo-15y 5mo) with a confirmed diagnosis of DMD were examined for psychometric properties including clinical meaning, targeting, response categories, model fit, reliability, dependency, stability, and raw to interval-level measurement. All analyses were performed using the Rasch Unidimensional Measurement Model. Results Overall, Rasch analysis supported the NSAA as being a reliable (high Person Separation Index of 0.91) and valid (good targeting, little misfit, no reversed thresholds) measure of ambulatory function in DMD. One item displayed misfit (lifts head, fit residual 6.9) and there was evidence for some local dependency (stand on right/left leg, climb and descend box step right/left leg, and hop on right/left leg, residual correlations > 0.40), which we provide potential solutions for in future use of the NSAA. Importantly, our findings supported good clinical validity in that the hierarchy of items within the scale produced by the analyses was supported by clinical opinion, thus increasing the clinical interpretability of scale scores. Interpretation In general, Rasch analysis supported the NSAA as a psychometrically robust scale for use in DMD clinical research and trials. This study also demonstrates how Rasch analysis is a useful instrument to detect and understand the key measurement issues of rating scales.
引用
收藏
页码:535 / 542
页数:8
相关论文
共 27 条
[1]
ANDRICH D, 1989, PROCEEDINGS OF THE XXIV INTERNATIONAL CONGRESS OF PSYCHOLOGY, VOL 4, P7
[2]
Bradley D.M., 1998, Seminars in Neonatology, V3, P27, DOI DOI 10.1016/S1084-2756(98)80146-2
[3]
Diagnosis and management of Duchenne muscular dystrophy, part 1: diagnosis, and pharmacological and psychosocial management [J].
Bushby, Katharine ;
Finkel, Richard ;
Birnkrant, David J. ;
Case, Laura E. ;
Clemens, Paula R. ;
Cripe, Linda ;
Kaul, Ajay ;
Kinnett, Kathi ;
McDonald, Craig ;
Pandya, Shree ;
Poysky, James ;
Shapiro, Frederic ;
Tomezsko, Jean ;
Constantin, Carolyn .
LANCET NEUROLOGY, 2010, 9 (01) :77-93
[4]
Watch out, watch out, the FDA are about [J].
Cano, Stefan J. ;
Hobart, Jeremy C. .
DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY, 2008, 50 (06) :408-409
[5]
Cronbach LJ, 1951, PSYCHOMETRIKA, V16, P297
[6]
Neonatal screening for Duchenne muscular dystrophy: A novel semiquantitative application of the bioluminescence test for creatine kinase in a pilot national program in cyprus [J].
Drousiotou, A ;
Ioannou, P ;
Georgiou, T ;
Mavrikiou, E ;
Christopoulos, G ;
Kyriakides, T ;
Voyasianos, M ;
Argyriou, A ;
Middleton, L .
GENETIC TESTING, 1998, 2 (01) :55-60
[7]
Emery A E, 1991, Neuromuscul Disord, V1, P19, DOI 10.1016/0960-8966(91)90039-U
[8]
Is the Sense of Coherence-instrument applicable on adolescents? A latent trait analysis using Rasch-modelling [J].
Hagquist, C ;
Andrich, D .
PERSONALITY AND INDIVIDUAL DIFFERENCES, 2004, 36 (04) :955-968
[9]
Improving the evaluation of therapeutic interventions in multiple sclerosis: the role of new psychometric methods [J].
Hobart, J. ;
Cano, S. .
HEALTH TECHNOLOGY ASSESSMENT, 2009, 13 (12) :1-+
[10]
Getting the measure of spasticity in multiple sclerosis: the Multiple Sclerosis Spasticity Scale (MSSS-88) [J].
Hobart, JC ;
Riazi, A ;
Thompson, AJ ;
Styles, IM ;
Ingram, W ;
Vickery, PJ ;
Warner, M ;
Fox, PJ ;
Zajicek, JP .
BRAIN, 2006, 129 :224-234