Primary-school recorded special educational needs in children born with major congenital anomalies in England: A population-based study using the Education and Child Health Insights from Linked Data database

Kate Lewis, Maria Peppa, Bianca De Stavola, Pia Hardelid, Ruth Gilbert
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 MethodsWe created a cohort of 6,180,400 singleton children born in England between 1 September 2003 and 31 August 2013 using linked administrative health and education records (from the ‘ECHILD’ database). MCAs were identified using hospital admission and mortality records during infancy. We used at least one record of SEN in state-school records as a proxy for SEN provision. We quantified: survival to age 5 using Kaplan-Meier survival analysis; the prevalence of recorded SEN during primary school Years 1 to 6; and the difference in proportion of children with recorded SEN in Year 1 before and after the 2014 government SEN reforms.
 ResultsChildren with any MCA had 5-year survival rates of 95.1% (95% confidence interval, CI, 95.0, 95.2), compared with 99.7% (95% CI 99.7, 99.7) among children without a MCA. 41.5% (75,202/181,328) of children with an MCA attending state-school between Year 1 and 6 had any recorded SEN compared with 25.6% (1,282,979/5,008,624) of children without a MCA. Of the 12 system-specific MCA subgroups, children with chromosomal, nervous system and eye anomalies had the largest prevalence of recorded SEN. The prevalence of recorded SEN decreased by 4.9% (95% CI -5.3, -4.4) for children with any MCA compared with a reduction of 4.3% (95% CI -4.4, -4.2) for children without a MCA, when comparing pupils in Year 1 before and after 2014.
 ConclusionRecorded SEN among children with hospital identified MCAs was markedly higher than for those without MCAs, however more than half had no recorded SEN. Our findings suggest government reform in 2014 reduced SEN provision for children with MCAs.","PeriodicalId":132937,"journal":{"name":"International Journal for Population Data Science","volume":"214 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2023-09-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"International Journal for Population Data Science","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.23889/ijpds.v8i2.2340","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
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Abstract

ObjectivesWe provide a national overview of survival to primary school and recorded special educational needs (SEN) provision among children with hospital identified major congenital anomalies (MCAs) born in England. We also report changes before and after government reform of SEN in 2014. MethodsWe created a cohort of 6,180,400 singleton children born in England between 1 September 2003 and 31 August 2013 using linked administrative health and education records (from the ‘ECHILD’ database). MCAs were identified using hospital admission and mortality records during infancy. We used at least one record of SEN in state-school records as a proxy for SEN provision. We quantified: survival to age 5 using Kaplan-Meier survival analysis; the prevalence of recorded SEN during primary school Years 1 to 6; and the difference in proportion of children with recorded SEN in Year 1 before and after the 2014 government SEN reforms. ResultsChildren with any MCA had 5-year survival rates of 95.1% (95% confidence interval, CI, 95.0, 95.2), compared with 99.7% (95% CI 99.7, 99.7) among children without a MCA. 41.5% (75,202/181,328) of children with an MCA attending state-school between Year 1 and 6 had any recorded SEN compared with 25.6% (1,282,979/5,008,624) of children without a MCA. Of the 12 system-specific MCA subgroups, children with chromosomal, nervous system and eye anomalies had the largest prevalence of recorded SEN. The prevalence of recorded SEN decreased by 4.9% (95% CI -5.3, -4.4) for children with any MCA compared with a reduction of 4.3% (95% CI -4.4, -4.2) for children without a MCA, when comparing pupils in Year 1 before and after 2014. ConclusionRecorded SEN among children with hospital identified MCAs was markedly higher than for those without MCAs, however more than half had no recorded SEN. Our findings suggest government reform in 2014 reduced SEN provision for children with MCAs.
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英国先天性畸形儿童的小学特殊教育需求记录:一项基于人口的研究,使用关联数据数据库中的教育和儿童健康见解
目的:我们对在英国出生的经医院鉴定为主要先天性异常(MCAs)的儿童的小学存活率和特殊教育需求(SEN)提供的记录进行了全国性概述。我们还报告了2014年政府改革SEN前后的变化。 方法:我们使用相关的行政健康和教育记录(来自“ECHILD”数据库)创建了2003年9月1日至2013年8月31日在英格兰出生的6180,400名独生子女队列。根据婴儿时期的住院和死亡率记录确定mca。我们在公立学校的记录中至少使用了一个特殊教育水平的记录作为特殊教育水平提供的代理。我们使用Kaplan-Meier生存分析进行量化:存活至5岁;小学一至六年级的特殊教育情况;以及2014年政府SEN改革前后第一年记录SEN的儿童比例的差异。 结果任何MCA患儿的5年生存率为95.1%(95%可信区间,CI, 95.0, 95.2),而无MCA患儿的5年生存率为99.7% (95% CI, 99.7, 99.7)。41.5%(75,202/181,328)在一年级至六年级就读公立学校的MCA儿童有任何记录的SEN,而没有MCA的儿童为25.6%(1,282,979/5,008,624)。在12个系统特异性MCA亚组中,有染色体、神经系统和眼睛异常的儿童记录SEN的患病率最高。当比较2014年前后的一年级学生时,有任何MCA的儿童记录SEN的患病率下降了4.9% (95% CI -5.3, -4.4),而没有MCA的儿童记录SEN的患病率下降了4.3% (95% CI -4.4, -4.2)。结论医院确定的mca患儿中记录的SEN明显高于非mca患儿,但超过一半的患儿没有记录SEN。我们的研究结果表明,2014年政府改革减少了对mca患儿的SEN提供。
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