智力发育障碍学生申请教育、保健和护理计划的等待时间不平等:一份简短报告。

IF 2.1 2区 医学 Q1 EDUCATION, SPECIAL
Irene O Lee, Jeanne Wolstencroft, Harriet Housby, Marianne B M van den Bree, Samuel J R A Chawner, Jeremy Hall, Michael J Owen, David H Skuse
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引用次数: 0

摘要

背景:患有智力和发育障碍(IDDs)的儿童和青少年在生活的各个方面都面临挑战,需要大量的支持,特别是在教育领域。在联合王国,教育、保健和护理计划(EHCPs)为学校中有特殊教育需要的人提供支持。在我们的国家教育系统中,idd学生必须等待多长时间才能获得EHCP,但社会人口统计学对这些差异的影响目前尚不清楚。延迟提供EHCP支持会导致负面的教育、福祉和发展结果。使用来自国家小学生数据库(NPD)的数据,我们检查了EHCP提供等待时间的变异性,以及与SEN分类、家庭社会经济地位、居住地区和种族等潜在影响变量的相关性。方法:这项全国性研究招募了2131名与遗传疾病相关的idd患者[6-28岁,平均(SD) = 14.1(4.4)岁]。家长们同意让研究小组审查他们孩子的教育记录。所有参与者在英国接受全日制教育期间都曾接受过EHCP。我们访问了NPD(由英国教育部提供),以了解参与者的主要SEN类型,免费校餐资格,种族和他们获得EHCP的学年的详细信息。根据他们的家庭住址邮编,我们给每个家庭分配了多重剥夺指数(IMD)得分。根据NPD的数据,我们计算了孩子们从推荐EHCP到接受EHCP的等待时间。我们将这些数据与IMD分数、小学SEN类型、免费校餐资格、英语居住地区、种族和性别进行比较。我们使用线性回归模型来检验预测因子(上述人口统计学自变量)与儿童接受EHCP所需时间之间的关系。结果:与儿童SEN类型的NPD分类无关,生活在英格兰社会最贫困地区的遗传病因性IDDs患者等待EHCP支持的时间比生活在最贫困地区的患者更长。孩子的种族和性别都没有额外的影响。无论他们的IMD状态如何,生活在伦敦的参与者比生活在英国其他地方的参与者更快地获得了EHCP。结论:在全国范围内,为已知遗传病因的智力障碍儿童和青少年提供ehcp所需的时间不一致。地方教育当局可获得的资金的地区不平等可能是一个主要因素。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Inequalities of the Waiting Time for Education Health and Care Plan Provision for Pupils With Intellectual Developmental Disabilities: A Brief Report.

Background: Children and young people with intellectual and developmental disabilities (IDDs) face challenges across various aspects of their lives and require significant support, particularly in the field of education. In the United Kingdom, Education, Health and Care Plans (EHCPs) support those with special educational needs (SEN) in schools. Disparities exist throughout our national educational system with respect to how long pupils with IDDs must wait for an EHCP, but the socio-demographic influences on those disparities are currently unknown. Delays in providing EHCP support result in negative educational, wellbeing and developmental outcomes. Using data from the National Pupil Database (NPD), we examined variabilities in waiting times for EHCP provision, and correlations with potentially influential variables such as SEN classification, family socio-economic status, region of domicile and ethnicity.

Methods: This national study recruited 2131 participants [6-28 years old, mean (SD) = 14.1 (4.4) years] with IDDs associated with a genetic condition. Families gave consent for their child's educational records to be reviewed by the research team. All participants had received an EHCP at some point during their full-time education in England. We accessed the NPD (provided by the UK Department for Education), for details of participants' primary SEN type, free school meal eligibility, ethnicity and the academic year in which they received an EHCP. Based on their home address postcode, we assigned to each family an index of multiple deprivation (IMD) score. From the NPD, we calculated the waiting time between a child's recommendation for an EHCP and the time they received it. We compared these data with IMD scores, primary SEN type, free school meal eligibility, English region of domicile, ethnicity, and sex. We used linear regression models to examine the associations between the predictors (the above demographic independent variables) and the duration of time it took for children to receive an EHCP.

Results: Participants with IDDs of genetic aetiology who lived in the most socially deprived regions of England waited longer for EHCP support than those in the least deprived regions, irrespective of the NPD classification of the child's SEN type. Neither the child's ethnicity nor their sex had any added impact. Whatever their IMD status, participants living in London obtained an EHCP more quickly than those living elsewhere in England.

Conclusions: There are nationwide inconsistencies in the time taken to provide EHCPs to children and young people whose intellectual impairments are of known genetic aetiology. Regional inequalities in the funds available to local education authorities could be a major contributory factor.

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来源期刊
CiteScore
5.60
自引率
5.60%
发文量
81
期刊介绍: The Journal of Intellectual Disability Research is devoted exclusively to the scientific study of intellectual disability and publishes papers reporting original observations in this field. The subject matter is broad and includes, but is not restricted to, findings from biological, educational, genetic, medical, psychiatric, psychological and sociological studies, and ethical, philosophical, and legal contributions that increase knowledge on the treatment and prevention of intellectual disability and of associated impairments and disabilities, and/or inform public policy and practice. Expert reviews on themes in which recent research has produced notable advances will be included. Such reviews will normally be by invitation.
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