The SF-36 in multiple sclerosis: why basic assumptions must be tested

被引:104
作者
Hobart, J
Freeman, J
Lamping, D
Fitzpatrick, R
Thompson, A
机构
[1] Inst Neurol, Neurol Outcome Measures Unit, Dept Clin Neurol & Neurorehabil, London WC1N 3BG, England
[2] London Sch Hygiene & Trop Med, Dept Publ Hlth, Hlth Serv Res Unit, London WC1E 7HT, England
[3] Univ Oxford Nuffield Coll, Dept Publ Hlth & Primary Care, Oxford OX1 1NF, England
关键词
SF-36; tests of scaling assumptions; health measurement; multiple sclerosis;
D O I
10.1136/jnnp.71.3.363
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Objectives-To evaluate, in people with multiple sclerosis, two psychometric assumptions that must be satisfied for valid use of the medical outcomes study 36-item short form health survey (SF-36): the data are of high quality and, it is legitimate to generate scores for eight scales and two summary measures using the standard algorithms. Methods-SF-36 data from 438 people representing the full range of multiple sclerosis were examined (mean age 48; 70% women). Data quality (per cent missing data and computable scale and summary scores) were determined, six scaling criteria were tested to determine the legitimacy of generating the eight SF-36 scale scores using Likert's method of summed ratings, and two scaling criteria were tested to determine the appropriateness of the standard SF-36 algorithms for weighting scale scores to generate two summary measures. Results-Data quality was excellent except in the most disabled subgroup where missing responses reached a maximum of 16.5% and summary scores could only be computed for 72%. There was clear support for the generation of SF-36 scale scores. Item response distributions were symmetric, item mean scores and variances were equivalent, corrected item-total correlations were high (range 0.46-0.85) and similar, and definite scaling success rates exceeded 96%. Nevertheless, there were notable floor or ceiling effects in four of the eight scales. Assumptions for generating two SF-36 summary measures were only partially satisfied. Although principal components analysis suggested a two component model, these components explained less than 60% of the total variance in SF-36 scales, and less than 75% of the variance in five of the eight scales. Moreover, scale to component correlations did not support the use of scale weights derived from United States population data. Conclusions-When using the SF-36 as a health measure in multiple sclerosis summary scores should be reported with caution.
引用
收藏
页码:363 / 370
页数:8
相关论文
共 45 条
[1]  
Auty A, 1998, CAN J NEUROL SCI, V25, P31
[2]   VALIDATING THE SF-36 HEALTH SURVEY QUESTIONNAIRE - NEW OUTCOME MEASURE FOR PRIMARY CARE [J].
BRAZIER, JE ;
HARPER, R ;
JONES, NMB ;
OCATHAIN, A ;
THOMAS, KJ ;
USHERWOOD, T ;
WESTLAKE, L .
BMJ-BRITISH MEDICAL JOURNAL, 1992, 305 (6846) :160-164
[3]   SCREE TEST FOR NUMBER OF FACTORS [J].
CATTELL, RB .
MULTIVARIATE BEHAVIORAL RESEARCH, 1966, 1 (02) :245-276
[4]   Validation of the functional assessment of multiple sclerosis quality of life instrument [J].
Cella, DF ;
Dineen, K ;
Arnason, B ;
Reder, A ;
Webster, KA ;
Karabatsos, G ;
Chang, C ;
Lloyd, S ;
Mo, F ;
Stewart, J ;
Stefoski, D .
NEUROLOGY, 1996, 47 (01) :129-139
[5]  
Cronbach LJ, 1951, PSYCHOMETRIKA, V16, P297
[6]   Qualitative comparison of the reliability of health status assessments with the EuroQol and SF-36 questionnaires after stroke [J].
Dorman, P ;
Slattery, J ;
Farrell, B ;
Dennis, M ;
Sandercock, P .
STROKE, 1998, 29 (01) :63-68
[7]  
Fayers PM, 1998, OX MED PUBL, P191
[8]   Clinical appropriateness: a key factor in outcome measure selection: the 36 item short form health survey in multiple sclerosis [J].
Freeman, J ;
Hobart, JC ;
Langdon, DW ;
Thompson, AJ .
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 2000, 68 (02) :150-156
[9]  
Freeman JA, 1996, J NEUROL REHABIL, V10, P185
[10]  
Guttman L, 1954, PSYCHOMETRIKA, V19, P149, DOI DOI 10.1007/BF02289162