Ronen Gabriel M, Streiner David L, Rosenbaum Peter
Department of Pediatrics, McMaster University, Hamilton, Ontario, Canada.
Epilepsia. 2003 Apr;44(4):598-612. doi: 10.1046/j.1528-1157.2003.46302.x.
To answer a need to include and measure accurately the impact and burden of epilepsy as outcomes of interventions with affected children, we developed and validated self-report and parent-proxy respondent health-related quality of life (HRQL) instruments for preadolescent children with epilepsy.
We combined qualitative and quantitative research methods. Items were extracted from focus group discussions involving children with epilepsy and their parents. We created scales formatted with alternative paired options of forced responses and used factor analysis to generate relevant subscales and reduce the number of items. We checked internal consistency, assessed test-retest reliability 10-14 days apart, and documented construct validity.
A sample of 381 children with epilepsy, age 6-15 years, and their parents independently completed a 67-item questionnaire, from which we chose five items for each subscale. The measures share four subscales, but each measure has an additional distinct subscale. The children and parents could discern differences and report differentially between the various aspects of the HRQL. Internal consistency measured with Cronbach's alpha was acceptable for all subscales; construct validity has been demonstrated from the testing of several hypotheses. Test-retest reliability examined with the intraclass correlation coefficient was satisfactory for the parents and for children age 8 years and older. The correlations between the mothers' and children's responses was poor to moderate.
The data demonstrate sound psychometric properties for both related measures, which are easy to administer for children with epilepsy who are 8 years and older and their parents. The subscales encompass HRQL dimensions judged most important by children with epilepsy for the self-report measure and by parents for the proxy response measure. The parent-proxy measure should be useful as a complement to the child self-report measure in evaluating the validity of parental assessment of the child's health status; in longitudinal outcome research; and in HRQL assessment of children who are unable to respond independently.
为满足将癫痫的影响和负担作为干预患病儿童的结果进行准确纳入和衡量的需求,我们开发并验证了针对患有癫痫的青春期前儿童的自我报告和家长代理应答的健康相关生活质量(HRQL)工具。
我们结合了定性和定量研究方法。项目从涉及癫痫患儿及其家长的焦点小组讨论中提取。我们创建了采用强制应答的替代配对选项格式的量表,并使用因子分析来生成相关子量表并减少项目数量。我们检查了内部一致性,在间隔10 - 14天的情况下评估重测信度,并记录了结构效度。
381名年龄在6 - 15岁的癫痫患儿及其家长独立完成了一份67项问卷,我们为每个子量表从中选择了5个项目。这些测量共享四个子量表,但每个测量还有一个额外的独特子量表。患儿和家长能够辨别差异,并在HRQL的各个方面进行不同的报告。用克朗巴赫α系数测量的内部一致性对所有子量表来说都是可接受的;通过对几个假设的检验证明了结构效度。用组内相关系数检验的重测信度对家长以及8岁及以上的患儿来说是令人满意的。母亲和患儿应答之间的相关性较差至中等。
数据表明这两种相关测量具有良好的心理测量特性,对于8岁及以上的癫痫患儿及其家长来说易于实施。子量表涵盖了癫痫患儿认为自我报告测量中最重要的HRQL维度以及家长认为代理应答测量中最重要的维度。家长代理测量在评估家长对孩子健康状况评估的有效性、纵向结局研究以及对无法独立应答的儿童进行HRQL评估时,应可作为儿童自我报告测量的补充。