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Autism. 2025 Aug;29(8):2097-2110. doi: 10.1177/13623613251335702. Epub 2025 May 9.
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本文引用的文献

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Acad Pediatr. 2023 Jul;23(5):904-912. doi: 10.1016/j.acap.2023.03.013. Epub 2023 Mar 31.
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The earlier the better: An RCT of treatment timing effects for toddlers on the autism spectrum.越早越好:一项关于自闭症谱系幼儿治疗时机效果的随机对照试验。
Autism. 2023 Mar 15;27(8):13623613231159153. doi: 10.1177/13623613231159153.
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Parent-to-parent support among parents of children with autism: A review of the literature.自闭症儿童父母之间的亲职间支持:文献综述。
Autism. 2024 Feb;28(2):263-275. doi: 10.1177/13623613221146444. Epub 2023 Jan 1.
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Advancing translational science education.推进转化科学教育。
Clin Transl Sci. 2022 Nov;15(11):2555-2566. doi: 10.1111/cts.13390. Epub 2022 Sep 10.
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Achieving Diagnostic Resolution in Young Children with Social Communication Concerns in a Predominantly Low-Income Population.在以低收入人群为主的环境中,对存在社会交往沟通问题的幼儿进行诊断并得出结论。
J Health Care Poor Underserved. 2021;32(3):1359-1371. doi: 10.1353/hpu.2021.0137.
6
A first-hand experience of co-design in mental health service design: Opportunities, challenges, and lessons.精神卫生服务设计中的共同设计第一手经验:机遇、挑战和教训。
Int J Ment Health Nurs. 2021 Dec;30(6):1693-1702. doi: 10.1111/inm.12925. Epub 2021 Aug 13.
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Reducing Barriers to Autism Screening in Community Primary Care: A Pragmatic Trial Using Web-Based Screening.在社区初级保健中减少自闭症筛查障碍:使用基于网络的筛查进行的实用试验。
Acad Pediatr. 2022 Mar;22(2):263-270. doi: 10.1016/j.acap.2021.04.017. Epub 2021 Apr 23.
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Understanding the "Swiss Cheese Model" and Its Application to Patient Safety.理解“瑞士奶酪模型”及其在患者安全中的应用。
J Patient Saf. 2022 Mar 1;18(2):119-123. doi: 10.1097/PTS.0000000000000810.
9
Evidence-Based Practices for Children, Youth, and Young Adults with Autism: Third Generation Review.自闭症儿童、青少年和年轻人的循证实践:第三代综述。
J Autism Dev Disord. 2021 Nov;51(11):4013-4032. doi: 10.1007/s10803-020-04844-2. Epub 2021 Jan 15.
10
Effect of Family Navigation on Diagnostic Ascertainment Among Children at Risk for Autism: A Randomized Clinical Trial From DBPNet.家庭导航对自闭症风险儿童诊断确定的影响:来自 DBPNet 的一项随机临床试验。
JAMA Pediatr. 2021 Mar 1;175(3):243-250. doi: 10.1001/jamapediatrics.2020.5218.

在一个为文化和语言背景多样的家庭服务的非营利性社区组织内,共同设计一条新颖的服务提供途径,以增加获得自闭症诊断和护理的机会。

Co-designing a novel service delivery pathway to increase access to autism identification and care within a non-profit community organization serving culturally and linguistically diverse families.

作者信息

Attar Shana M, Benavidez Hannah, Gicheru Carol, Alabi Colleen, Sapano Risho, L Stone Wendy

机构信息

Department of Psychology, University of Washington, Seattle, USA.

Mother Africa, USA.

出版信息

Autism. 2025 Aug;29(8):2097-2110. doi: 10.1177/13623613251335702. Epub 2025 May 9.

DOI:10.1177/13623613251335702
PMID:40346799
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12263326/
Abstract

Culturally and linguistically diverse families experience greater challenges accessing timely, autism-specialized care relative to non-culturally and linguistically diverse families, and ultimately experience less optimal health outcomes. Alternative pathways to access autism care for culturally and linguistically diverse families are needed; however, the features of a novel pathway remain unclear. A co-design process was used with a culturally embedded non-profit community organization to develop a novel service delivery pathway for increasing access to autism services for culturally and linguistically diverse families in the United States. Twenty-three individuals participated in eight, 2-hour co-design sessions. Participants included front-line staff (seven non-specialist providers), management leaders (two program supervisors and two organization directors), and eight end-users (caregivers) from seven understudied cultural and linguistic groups (i.e. Somali Mai Mai, Swahili, Arabic, Dari/Pashto, French, Amharic, and Tigrinya) and four autism specialists. The co-design identified five key design features: respecting diversity, prioritizing caregiver agency, increasing accessibility, minimizing stigma, and maximizing feasibility. These features informed the co-development of a novel pathway to access autism identification and care for culturally and linguistically diverse families that pairs navigation services with the dissemination of brief, culturally sensitive, and evidence-based parenting and coping strategies. This power-sharing, community-academic partnership may serve as a model for improving equity in autism care.Lay AbstractEarly, specialized support is important for helping young autistic children learn and develop. However, families from different cultural backgrounds often find it challenging to access this early help. A university lab and a community organization worked together to create a new way for these families to access autism services. We used a co-design approach, which involves gathering feedback from a variety of people involved in autism care, including service providers, community leaders, caregivers, and autism experts. Twenty-three individuals participated in eight co-design sessions that were two hours each. Participants were from different language groups, including Somali Mai Mai, Swahili, Arabic, Dari/Pashto, French, Amharic, and Tigrinya. These sessions helped us identify five important factors important for improving access to needed services: being mindful about cultural differences between groups, empowering caregivers, providing information and support for accessing services, reducing stigma around autism, and ensuring the service is practical to use. Based on these factors, we developed a new pathway for families to access autism care. This new approach includes providing help in navigating the medical and educational systems and provides short, culturally appropriate advice for parenting and coping. This project shows how working together with communities can create more fair and effective ways to provide autism support.

摘要

与文化和语言背景单一的家庭相比,文化和语言背景多元的家庭在获得及时的自闭症专科护理方面面临更大挑战,最终健康结果也不太理想。需要为文化和语言背景多元的家庭开辟获得自闭症护理的替代途径;然而,新途径的特点仍不明确。我们与一个融入文化的非营利社区组织共同开展了一个协同设计过程,以开发一种新的服务提供途径,增加美国文化和语言背景多元家庭获得自闭症服务的机会。23人参加了8次为时2小时的协同设计会议。参与者包括一线工作人员(7名非专科提供者)、管理负责人(2名项目主管和2名组织主任),以及来自7个研究不足的文化和语言群体(即索马里迈迈族、斯瓦希里族、阿拉伯族、达里语/普什图语、法语、阿姆哈拉语和提格雷尼亚语)的8名最终用户(照顾者)和4名自闭症专家。协同设计确定了五个关键设计特征:尊重多样性、优先考虑照顾者的自主权、提高可及性、尽量减少污名化以及最大化可行性。这些特征为共同开发一种新途径提供了依据,该途径用于让文化和语言背景多元的家庭获得自闭症诊断和护理,将导航服务与传播简短、具有文化敏感性且基于证据的育儿和应对策略相结合。这种权力共享的社区 - 学术伙伴关系可作为改善自闭症护理公平性的典范。

摘要早期的专业支持对于帮助自闭症幼儿学习和发展很重要。然而,来自不同文化背景的家庭往往发现获得这种早期帮助具有挑战性。一个大学实验室和一个社区组织合作,为这些家庭创造了一种获得自闭症服务的新方式。我们采用了协同设计方法,即从参与自闭症护理的各类人员那里收集反馈,包括服务提供者、社区领袖、照顾者和自闭症专家。23人参加了8次每次为时两小时的协同设计会议。参与者来自不同语言群体,包括索马里迈迈族、斯瓦希里族、阿拉伯族、达里语/普什图语、法语、阿姆哈拉语和提格雷尼亚语。这些会议帮助我们确定了五个对于改善获得所需服务的机会很重要的因素:关注群体间的文化差异、赋予照顾者权力、提供获取服务的信息和支持、减少对自闭症的污名化以及确保服务便于使用。基于这些因素,我们为家庭开发了一条获得自闭症护理的新途径。这种新方法包括在医疗和教育系统中提供导航帮助,并提供简短、适合文化背景的育儿和应对建议。这个项目展示了与社区合作如何能够创造出更公平、有效的方式来提供自闭症支持。