Lie H R, Börjeson M C, Lagerkvist B, Rasmussen F, Hagelsteen J H, Lagergren J
Social and Health Administration, Municipality of Aarhus, Denmark.
Dev Med Child Neurol. 1994 Nov;36(11):1000-9. doi: 10.1111/j.1469-8749.1994.tb11796.x.
Family dynamics and social conditions were studied of 527 children with myelomeningocele aged four to 18 years from Denmark, Finland, Norway and Sweden; the control group was a representative sample of 7792 children of the same age-range and from the same countries. Information was obtained from postal questionnaires and from patients' charts. Overall, there were more similarities than differences between index and control families, the major difference occurring in measures related to the mothers' situation. Variations within groups of index families were in many respects more important than differences between index and control families. In spite of the different welfare systems developed to support families with disabled children, this study clearly showed that the responsibility for the care of the disabled child still lies primarily with the mother. Increased efforts must be made to meet the needs of these mothers.
对来自丹麦、芬兰、挪威和瑞典的527名4至18岁患有脊髓脊膜膨出的儿童的家庭动态和社会状况进行了研究;对照组是来自相同国家、相同年龄范围的7792名儿童的代表性样本。信息通过邮政问卷和患者病历获取。总体而言,指数家庭和对照家庭之间的相似之处多于差异,主要差异出现在与母亲状况相关的指标上。指数家庭组内的差异在许多方面比指数家庭和对照家庭之间的差异更重要。尽管已建立了不同的福利体系来支持残疾儿童家庭,但这项研究清楚地表明,照顾残疾儿童的责任仍然主要落在母亲身上。必须加大力度满足这些母亲的需求。