Clinic for Autism and Neurodevelopment (CAN) research, Brain and Mind Centre, Children's Hospital Westmead Clinical School, Faculty of Medicine and Health, University of Sydney, Sydney, New South Wales, Australia.
Child Neurodevelopment and Mental Health Team, Brain and Mind Centre, University of Sydney, Sydney, New South Wales, Australia.
BMJ Open. 2023 Feb 1;13(2):e069500. doi: 10.1136/bmjopen-2022-069500.
Early developmental assessment is crucial for effective support and intervention. This study examined factors that contribute to (a) older child age when caregivers first became concerned about their child's development and (b) older child age at the point of entry into developmental and diagnostic assessment. We also quantified how factors contributed to risk of children not receiving an assessment by 5 years and considered the acceptability of electronic data capture for families.
This cross-sectional study collected information about caregiver developmental concerns, family history and child characteristics.
Children and families entered a large, publicly funded hospital-based paediatric developmental assessment service.
Consecutively enrolled children (N=916) aged 6 months to 17 years with neurodevelopmental concerns and their caregivers.
A developmental history questionnaire completed by caregivers.
The average age that caregivers identified developmental concerns was 3.0 years of age but the average age of a receiving a developmental assessment was 6.6 years. Only 46.4% of children received a diagnostic assessment by 5 years of age, even though 88.0% of caregivers were concerned about their child's development by that age. Parental age, relationship status, education level, prior use of support services and being from a culturally and linguistically diverse background contributed to age at identification of concern, age at diagnostic assessment and the likelihood of receiving a diagnostic assessment by 5 years. Electronic data capture had high acceptability, with 88.2% of caregivers reporting a preference for electronic completion of questionnaires.
The study shows a substantial delay in diagnostic assessments that leaves most vulnerable children without an assessment by school age and highlights contributors to delays. These delays highlight the complexity of delivering early intervention and support policies that rely on swift and appropriate developmental assessment to vulnerable families.
早期发育评估对于提供有效支持和干预至关重要。本研究旨在探讨以下两个方面的因素:(a)照顾者首次对其子女发育问题产生关注时,子女的年龄;(b)进入发育和诊断评估的年龄。我们还量化了导致部分儿童在 5 岁前未接受评估的因素,并考虑了电子数据采集对家庭的可接受性。
本横断面研究收集了照顾者对子女发育问题的关注、家庭史和儿童特征的信息。
儿童及其家庭入组了一家大型、公共资助的医院儿科发育评估服务机构。
连续入组的有神经发育问题的 6 个月至 17 岁儿童及其照顾者(共 916 名)。
照顾者填写的发育史问卷。
照顾者识别发育问题的平均年龄为 3.0 岁,但接受发育评估的平均年龄为 6.6 岁。尽管 88.0%的照顾者在该年龄时已对其子女的发育表示担忧,但仅有 46.4%的儿童在 5 岁前接受了诊断评估。父母年龄、关系状况、教育水平、既往使用支持服务情况和来自文化和语言多样化背景均与识别问题的年龄、诊断评估的年龄以及 5 岁前接受诊断评估的可能性相关。电子数据采集具有较高的可接受性,88.2%的照顾者表示更愿意通过电子方式完成问卷。
研究表明,诊断评估存在较大延迟,导致大多数弱势儿童在学龄期前未接受评估,并强调了延迟的原因。这些延迟突显了向弱势家庭提供早期干预和支持政策的复杂性,这些政策依赖于对弱势家庭进行迅速和适当的发育评估。