父母和专业人士对唐氏综合症儿童残疾程度的看法

Mukta Bhattacharya, Peter Sidebotham
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引用次数: 4

摘要

目的、对象和方法进行了一项研究,以确定患有唐氏综合症的儿童的父母是否认为他们的孩子的残疾程度与他们的医学评估不同。根据标准的医学评估,向72名年龄在0-18岁的唐氏综合症儿童的父母发送了调查问卷。儿童最近的医疗评估数据来自儿童健康计算机的特殊需要模块。结果从收到的47份问卷中,父母和专业人员对儿童行动能力、手功能和听力的评估无显著差异。父母认为孩子的视力、行为、健康和成长以及个人护理受到的损害比医生严重得多,但他们认为孩子的言语和语言受到的损害较小。结论本研究提示父母对唐氏综合症儿童残疾水平的评估与专业评估存在一定差异,医学评估可以采取更以家庭为导向的方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Parental and professional perceptions of the levels of disability in children with Down's syndrome

Objectives, subjects and methods A study was undertaken to determine whether parents of children with Down's syndrome view their child's levels of disability differently from their medical assessments. Questionnaires, based on a standard medical assessment were sent to the parents of 72 children with Down's syndrome aged 0–18 years. Data on the children's most recent medical assessment were obtained from the special needs module of the child health computer.

Results From the 47 returned questionnaires, there were no significant differences in parental and professional assessments of the children's mobility, hand function or hearing. Parents rated their child's vision, behaviour, health and growth, and personal care as significantly more impaired than did the doctors, but rated their speech and language as less impaired.

Conclusions This study suggests that there are some differences between parental and professional assessments of disability levels in children with Down's syndrome and that medical assessments could take a more family-orientated approach.

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