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Academic attainment findings in children with sickle cell disease

机译:镰状细胞病患儿的学业成绩调查结果

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BACKGROUND: Children with sickle cell disease (SCD) demonstrate deficits in cognitive and academic functioning. This study compared the academic attainment of children with SCD relative to national, state, and local school district rates for African American students. METHODS: A retrospective chart review of children with SCD was completed and academic information was collected from caregiver report and school records. One-sample tests of proportions were calculated to compare academic attainment rates in children with SCD relative to national, state, and local school district normative data of African American students. RESULTS: Overall, 197 patient records were reviewed. A higher proportion of children with SCD were retained a grade relative to national, state, and local school district rates for African American students. In addition, a higher proportion of children with SCD received special education services relative to the national, state, and local school district rates for African American students. CONCLUSION: Children with SCD demonstrate higher rates of special education services and grade retention relative to African American peers. Overall, children with SCD demonstrate poorer academic attainment relative to healthy, African American peers highlighting the need for increased focus on special education services to address school performance issues within this population.
机译:背景:镰状细胞疾病(SCD)的儿童表现出认知和学术功能方面的缺陷。这项研究比较了SCD儿童相对于非裔美国学生的国家,州和当地学区费用的学业状况。方法:完成了对SCD儿童的回顾性图表审查,并从看护人报告和学校记录中收集了学术信息。计算了一个样本的比例测试,以比较SCD儿童相对于非裔美国学生的国家,州和地方学区规范数据的学业达到率。结果:总共检查了197例患者记录。相对于国家,州和当地学区非裔美国学生的学费,有较高比例的SCD儿童被保留为年级。此外,相对于非裔美国学生的国家,州和地方学区费用,患有SCD的儿童接受特殊教育服务的比例更高。结论:与非裔美国同龄人相比,患有SCD的儿童表现出更高的特殊教育服务和年级保留率。总体而言,相对于健康的非洲裔美国人同龄人而言,患有SCD的儿童的学业成绩较差,这突出表明需要更加关注特殊教育服务,以解决该人群中的学校表现问题。

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