Westbrook L E, Silver E J, Stein R E
Department of Pediatrics, Albert Einstein College of Medicine, Bronx, New York 10461, USA.
Pediatrics. 1998 Jun;101(6):1025-30. doi: 10.1542/peds.101.6.1025.
To test how prevalence estimates and characteristics of children vary by the way that disability is defined. Specifically, to determine 1) the proportions of children identified as disabled by one particular operationalization of disability based on parental reports of three types of consequences (i.e., functional limitations [FL]), dependence on compensatory mechanisms (CD), and service use or need beyond routine [SU/N]), and 2) whether children identified as disabled by these three types of consequences differ by type of disorder or condition, age, socioeconomic status, or race.
We analyzed a national dataset representing a random sample of 712 households with 1388 children. The Questionnaire for Identifying Children with Chronic Conditions (QuICCC) was used to identify children with disabling conditions. We divided the QuICCC items into three discrete sets, reflecting three definitional components of disability, and compared the proportions and characteristics of children fitting these components separately and in combination.
Using the QuICCC definition of disability, SU/N identified the largest proportion of children (72%), followed by CD (55%) and FLs (49%). Forty-four percent of children were identified by only one component, 36% by two components in any combination, and 20% by all three components. The type of disorder or condition generally did not vary by the three definitional components, although the FL component may be more effective at identifying children with sensory impairments. Children identified by two or more components were more likely to have multiple conditions and had more pervasive disorders than those identified by only one component. The youngest children (0 to 3 years old) may be less likely to be identified as disabled than children of other ages, especially by FLs. FLs also were more likely to identify children from the poorest and least educated families.
Although the specific findings reported here pertain to a single definitional approach (the QuICCC), the data highlight that who will be classified as disabled (and who will not) may be dependent on how disability is defined. The implications of using different definitions and definitional components on both the prevalence and the characteristics of children with disabilities need to be considered before data can be applied responsibly and appropriately.
检验儿童患病率估计值和特征如何因残疾定义方式的不同而有所差异。具体而言,确定:1)根据父母报告的三种后果(即功能受限[FL]、对代偿机制的依赖[CD]以及超出常规的服务使用或需求[SU/N]),通过一种特定的残疾操作化定义所确定的残疾儿童比例;2)被这三种后果确定为残疾的儿童在疾病或状况类型、年龄、社会经济地位或种族方面是否存在差异。
我们分析了一个全国性数据集,该数据集代表了712户有1388名儿童的随机样本。使用慢性病儿童识别问卷(QuICCC)来识别有残疾状况的儿童。我们将QuICCC项目分为三个离散组,反映残疾的三个定义要素,并分别及综合比较符合这些要素的儿童比例和特征。
采用QuICCC残疾定义,SU/N确定的儿童比例最大(72%),其次是CD(55%)和FL(49%)。44%的儿童仅由一个要素确定为残疾,36%由任意两个要素组合确定为残疾,20%由所有三个要素确定为残疾。疾病或状况类型一般不因这三个定义要素而有所不同,不过FL要素在识别有感官障碍的儿童方面可能更有效。由两个或更多要素确定为残疾的儿童比仅由一个要素确定为残疾的儿童更可能患有多种疾病且障碍更普遍。最小的儿童(0至3岁)比其他年龄段的儿童更不容易被确定为残疾,尤其是通过FL要素。FL要素也更有可能识别出来自最贫困和受教育程度最低家庭的儿童。
尽管此处报告的具体研究结果仅涉及一种定义方法(QuICCC),但数据突出表明谁将被归类为残疾(以及谁不会被归类为残疾)可能取决于残疾的定义方式。在能够负责任且恰当地应用数据之前,需要考虑使用不同定义和定义要素对残疾儿童患病率及特征的影响。