Behavioural and Psychological Functioning of Children and Adults with Sagittal Synostosis

Pub Date : 2023-10-13 DOI:10.1007/s40817-023-00149-1
Amanda J. Osborn, Rachel M. Roberts, Diana S. Dorstyn, Ben G. Grave, David J. David
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Abstract

Abstract Research examining the behavioural and psychological functioning of children and adults with sagittal synostosis (SS) is scarce, often disparate, and lacks well-matched control groups. Clinicians are therefore often unable to provide families with guidance about their child’s anticipated functioning. Social media channels were used to recruit community-based parents of children with SS, or adults with SS ( n = 56) and an age- and sex-matched control group ( n = 56). Families completed an online survey encompassing a range of demographic and clinical variables and a comprehensive battery of validated questionnaires. Surveys were either parent-rated (children 2 to < 5 years), both parent-rated and self-reported (children 5 to ≤ 18 years), or self-reported only (adults ≥ 19 years). Results show that for both unadjusted and adjusted (SES) analyses, children and adults were functioning at a similar level to their peers. Whilst mean parent-rated scores generally indicated that children with SS were experiencing slightly more difficulties, group differences were not statistically significant. Most adjusted Hedges’ g effect sizes were trivial ( g = .10) to small ( g = .20). Nonetheless, more children with SS were assessed as having clinically significant problems on each composite of the Behavior Assessment System for Children 3 rd Ed. In addition, screening rates of Attention Deficit Hyperactivity Disorder (18%; Behavior Rating Inventory of Executive Function 2) and Autism Spectrum Disorder (15%; Social Responsiveness Scale-2), in children with SS, were high. Findings suggest that children with SS should be monitored and referrals for appropriate support made readily available, as required.
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矢状面滑膜闭锁儿童和成人的行为和心理功能
研究检查儿童和成人矢状面滑膜闭锁(SS)的行为和心理功能是稀缺的,往往是不同的,并且缺乏良好匹配的对照组。因此,临床医生通常无法向家庭提供有关其孩子预期功能的指导。使用社交媒体渠道招募以社区为基础的患有孤独症儿童的父母,或患有孤独症的成年人(n = 56),以及年龄和性别匹配的对照组(n = 56)。家庭完成了一项在线调查,其中包括一系列人口统计和临床变量以及一系列全面的有效问卷。调查是由家长评定的(孩子2岁到11岁);5岁),父母评定和自我报告(5至≤18岁的儿童),或仅自我报告(成人≥19岁)。结果表明,在未调整和调整(SES)分析中,儿童和成人的功能水平与其同龄人相似。虽然父母评定的平均分数一般表明,患有孤独症的儿童遇到的困难稍微多一些,但组间差异没有统计学意义。大多数调整后对冲的g效应大小从微不足道(g = 0.10)到很小(g = 0.20)不等。尽管如此,更多的SS儿童被评估为在儿童行为评估系统第三版的每个组合中存在临床显著问题。此外,注意缺陷多动障碍的筛查率(18%;执行功能行为评定量表(2)和自闭症谱系障碍(15%;社会反应量表(Social Responsiveness Scale-2)在孤独症儿童中表现较高。研究结果表明,应监测患有自闭症的儿童,并根据需要随时提供适当的支持。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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