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首页> 外文期刊>Applied neuropsychology. Child >The Discrepancy between Performance-Based Measures and Questionnaires when Assessing Clinical Outcomes and Quality of Life in Pediatric Patients with Neurological Disorders
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The Discrepancy between Performance-Based Measures and Questionnaires when Assessing Clinical Outcomes and Quality of Life in Pediatric Patients with Neurological Disorders

机译:基于绩效措施和问卷的评估评估临床结果和患有神经障碍患者的生活质量的差异

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摘要

In clinical outcome assessment, the relation between performance-based measures and questionnaire ratings of the same domain is weak, but correlations between questionnaires proposed for the evaluation of different domains are strong. The present study aims to illustrate these phenomena in a group of patients with neurofibromatosis type 1 (NF1) and to propose an explanatory hypothesis. A single neuropsychologist interviewed the parents about the child's situation and current difficulties and then assessed this parental view as overall positive or overall negative. The same assessor then administered the Wechsler Intelligence Scales and neuropsychological tests to 78 children and adolescents with NF1 (5-18 years). Parents then completed the Child Behavioral Checklist (CBCL), the Conners' Parent Rating Scale, the Behavior Rating Inventory of Executive Function (BRIEF), as well as questionnaires assessing quality of life, impact of the medical disorder, and their own difficulties. All questionnaires were inter-correlated (r=0.29 - 0.84) and associated with the overall positive or negative parental view of the child's progress (effect size=0.41-1.46). Conversely, questionnaires were weakly or not significantly related to intelligence, cognitive measures, or clinical severity. In conclusion, the parental view of the child's progress was related to the answers to questionnaires assessing quality of life or strengths and difficulties of patients with a neurological disorder. This factor should be assessed independently and taken into account when assessing clinical outcome.
机译:在临床结果评估中,基于绩效的措施与同一领域的问卷评级之间的关系较弱,但提出对不同域评估的问卷之间的相关性强劲。本研究旨在说明一组神经纤维瘤病1(NF1)患者中的这些现象,并提出解释性假设。一位神经心理学家采访了父母关于孩子的情况和目前的困难,然后评估了这种父母视图,作为整体积极或整体负面。然后,相同的评估员将氟斯勒智力尺度和神经心理学检测给78名儿童和青少年进行NF1(5-18岁)。然后父母完成了孩子行为清单(CBCL),康纳的父评级规模,执行职能的行为评级库存(简短),以及评估生活质量,医疗疾病的影响以及他们自己的困难的问卷调查。所有调查问卷都是相关的(r = 0.29 - 0.84),与儿童进展的总体正或负父母视图相关(效果大小= 0.41-1.46)。相反,调查问卷弱或与智力,认知措施或临床严重程度有明显相关。总之,儿童进展的父母观与调查问卷的答案有关评估患有神经疾病患者的生活质量和优质和困难的答案。应在评估临床结果时独立评估该因素,并考虑。

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