School-recorded special educational needs provision in children with major congenital anomalies: A linked administrative records study of births in England, 2003-2013.
Maria Peppa, Kate M Lewis, Bianca De Stavola, Pia Hardelid, Ruth Gilbert
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引用次数: 0
Abstract
Background: Children with major congenital anomalies (MCAs) disproportionately experience complex health problems requiring additional health and educational support.
Objectives: To describe survival to the start of school and recorded special educational needs (SEN) provision among children with and without administrative record-identified MCAs in England. We present results for 12 system-specific MCA subgroups and 25 conditions. We also describe the change of prevalence in recorded SEN provision before and after SEN reforms in 2014, which were implemented to improve and streamline SEN provision.
Methods: We created a birth cohort of 6,180,400 singleton children born in England between 1 September 2003 and 31 August 2013 using linked administrative records from the ECHILD database. MCAs were identified using hospital admission and mortality records during infancy. SEN provision in primary school was defined by one or more recording of SEN provision in state-school records during years 1 to 6 (ages 5/6 years to 10/11 years).
Results: Children with any MCA had a 5-year survival rate of 95.1% (95% confidence interval (CI) 95.0, 95.2) compared with 99.7% (95% CI 99.7, 99.7) among children without an MCA. 41.6% (75,381/181,324) of children with an MCA had any recorded SEN provision in primary school compared with 25.7% (1,285,572/5,008,598) of unaffected children. Of the 12 system-specific MCA subgroups, children with chromosomal, nervous system and eye anomalies had the highest prevalence of recorded SEN provision. The prevalence of recorded SEN provision decreased by 4.8% (99% CI -5.4, -4.3) for children with any MCA compared with a reduction of 4.2% (99% CI -4.3, -4.2) for unaffected children, when comparing pupils in year 1 before and after 2014.
Conclusion: We observed that approximately two fifths of children with MCAs have some type of SEN provision recorded during primary school, but this proportion varied according to condition and declined following the 2014 SEN reforms, similar to children unaffected by MCAs.
背景:患有严重先天性异常(MCAs)的儿童不成比例地经历复杂的健康问题,需要额外的健康和教育支持。目的:描述在英格兰有和没有行政记录的mca儿童中生存到学校开始和记录的特殊教育需求(SEN)提供。我们提出了12个系统特定的MCA亚组和25个条件的结果。我们还描述了2014年为改善和简化SEN提供而实施的SEN改革前后记录SEN提供的流行率的变化。方法:我们使用来自ECHILD数据库的相关行政记录,创建了2003年9月1日至2013年8月31日期间在英格兰出生的6180,400名独生子女的出生队列。根据婴儿时期的住院和死亡率记录确定mca。小学的特殊教育条件是由公立学校1至6年级(5/6岁至10/11岁)的一次或多次特殊教育条件记录来定义的。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)。41.6%(75,381/181,324)的MCA儿童在小学有任何记录的SEN规定,而未受影响的儿童为25.7%(1,285,572/5,008,598)。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有最高的SEN提供率。对比2014年前后的一年级学生,任何MCA儿童的SEN提供率下降了4.8% (99% CI -5.4, -4.3),而未受影响儿童的SEN提供率下降了4.2% (99% CI -4.3, -4.2)。结论:我们观察到,大约五分之二的MCAs儿童在小学期间记录了某种类型的SEN规定,但这一比例因情况而异,并在2014年SEN改革后下降,类似于未受MCAs影响的儿童。