Developing Standardized Care Pathways for management of autism spectrum disorders in the Ashanti Region

A. Osei-Bonsu, A. Tannor, C. Hammond, J. Dogbe
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Abstract

Background According to the Ghana Multiple Indicator cluster survey 2011, 1 in 4 Ghanaian children aged 36-59 months is estimated to have a delay in their development (cognitive, learning, socioemotional and physical). Although the exact prevalence of autism spectrum disorder (ASD) in the country is unknown, these children are a particularly under-served population in Ghana, suffering from late identification and poor access to evaluation and treatment.Aim: To establish standard care pathways in the public health sector for the management of ASD in the Ashanti Region of Ghana by August 2021. Method A multidisciplinary guiding coalition was established to conduct a fish-bone root cause analysis via one-on-one interviews and focused group discussions with major stakeholders to understand the primary cause of the problem. A simple referral process map was then designed by the group. After an extensive literature search using google scholar and PubMed, the 23Q screening tool, originally designed in Uganda, for developmental assessment of children aged 2-9years was selected and locally validated. The tool was then piloted in 15 schools across 9 out of 43 districts assemblies in the Ashanti Region. Results 23 out of 43 special needs coordinators in Ashanti Region were trained in the use of the screening tool. Across the 15 schools visited, the tool identified developmental disorders in a total of 427 children, aged 3-17years, with an average age of 9years. 18% (n=78) of these children aged between 3 and 17years, were flagged by ASD specific questions with 7% (32) aged between 3-9years. Conclusion Autism awareness is evolving in Ghana. This project seeks to ultimately establish the burden of ASD in Ghana and connect pediatricians, medical officers, special education teachers, therapists, and families in an all teach, all learn collaboration which would set the framework for a national system of coordinated care for children with ASD.
在阿散蒂地区制定管理泛自闭症障碍的标准化护理途径
根据2011年加纳多指标类集调查,估计每4个年龄在36-59个月的加纳儿童中就有1个发育迟缓(认知、学习、社会情感和身体发育)。尽管该国自闭症谱系障碍(ASD)的确切患病率尚不清楚,但在加纳,这些儿童是一个特别得不到服务的群体,他们的诊断较晚,获得评估和治疗的机会也很少。目标:到2021年8月,在加纳阿散蒂地区建立管理自闭症谱系障碍的公共卫生部门标准护理途径。方法建立多学科指导联盟,通过一对一访谈和与主要利益相关者的焦点小组讨论,对问题的根本原因进行鱼刺式分析。然后,该小组设计了一个简单的转诊流程图。在使用google scholar和PubMed进行广泛的文献检索后,最初在乌干达设计的用于2-9岁儿童发育评估的23Q筛选工具被选中并在当地得到验证。该工具随后在阿散蒂地区43个区议会中的9个区的15所学校进行了试点。结果阿散蒂地区43名特殊需要协调员中有23人接受了使用筛查工具的培训。在访问的15所学校中,该工具确定了427名3-17岁儿童的发育障碍,平均年龄为9岁。年龄在3- 17岁之间的儿童中,有18% (n=78)被标记为ASD特定问题,7%(32)的年龄在3-9岁之间。结论:加纳的自闭症意识正在发展。该项目旨在最终在加纳确定自闭症障碍的负担,并将儿科医生、医务人员、特殊教育教师、治疗师和家庭联系在一起,进行全教全学的合作,为自闭症障碍儿童的全国协调护理体系建立框架。
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