• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

相似文献

1
Lessons learned from a statewide needs assessment of Asian American families of children with developmental disabilities.从对发育障碍儿童的亚裔美国家庭进行的全州需求评估中吸取的经验教训。
Int J Dev Disabil. 2023 Dec 21;71(5):788-792. doi: 10.1080/20473869.2023.2286404. eCollection 2025.
2
Factors that influence parents' and informal caregivers' views and practices regarding routine childhood vaccination: a qualitative evidence synthesis.影响父母和非正式照顾者对常规儿童疫苗接种看法和做法的因素:定性证据综合分析。
Cochrane Database Syst Rev. 2021 Oct 27;10(10):CD013265. doi: 10.1002/14651858.CD013265.pub2.
3
Parent training interventions for parents with intellectual disability.针对智障父母的家长培训干预措施。
Cochrane Database Syst Rev. 2018 Jul 13;7(7):CD007987. doi: 10.1002/14651858.CD007987.pub3.
4
"Living Independently Means Everything to Me": The Voice of Australian Autistic Adults.“独立生活对我来说意味着一切”:澳大利亚成年自闭症患者的心声。
Autism Adulthood. 2024 Sep 16;6(3):312-320. doi: 10.1089/aut.2022.0102. eCollection 2024 Sep.
5
Patient navigator programmes for children and adolescents with chronic diseases.慢性病患儿和青少年的患者导航员计划。
Cochrane Database Syst Rev. 2024 Oct 9;10(10):CD014688. doi: 10.1002/14651858.CD014688.pub2.
6
Child, family and professional views on valued communication outcomes for non-verbal children with neurodisability: A qualitative meta-synthesis.儿童、家庭和专业人员对神经发育障碍的非言语儿童有价值的沟通结果的看法:定性元分析。
Int J Lang Commun Disord. 2024 Nov-Dec;59(6):2946-2984. doi: 10.1111/1460-6984.13121. Epub 2024 Oct 17.
7
Community Member Views on Autism Intervention: Effects of Closeness to Autistic People with Intellectual Disabilities And Nonspeaking Autistic People.社区成员对自闭症干预的看法:与智障自闭症患者及无语言能力自闭症患者亲近程度的影响。
Autism Adulthood. 2024 Sep 16;6(3):253-271. doi: 10.1089/aut.2023.0202. eCollection 2024 Sep.
8
Parents' and informal caregivers' views and experiences of communication about routine childhood vaccination: a synthesis of qualitative evidence.父母及非正式照料者关于儿童常规疫苗接种沟通的观点与经历:定性证据综述
Cochrane Database Syst Rev. 2017 Feb 7;2(2):CD011787. doi: 10.1002/14651858.CD011787.pub2.
9
Understanding Barriers to Engagement With a Prostate Cancer Research and Genetic Risk Service Among UK Men of Black African or Black Caribbean Ancestry.了解英国非洲裔或加勒比裔黑人男性参与前列腺癌研究和遗传风险服务的障碍。
Health Expect. 2025 Jun;28(3):e70282. doi: 10.1111/hex.70282.
10
Creating the conditions for meaningful and effective PPIE in community-based public health research: learning from a UK-wide lived experience panel.为基于社区的公共卫生研究中开展有意义且有效的公众及患者参与、介入与合作创造条件:借鉴全英生活经历小组的经验
Res Involv Engagem. 2025 Jul 17;11(1):85. doi: 10.1186/s40900-025-00727-x.

引用本文的文献

1
The Effect of Self-Regulation on Spiritual Well-Being Among Parents of Children with Hearing Impairment in China: Does Resilience Function as a Mediator?自我调节对中国听力障碍儿童家长精神幸福感的影响:心理韧性是否起中介作用?
J Relig Health. 2025 Apr 23. doi: 10.1007/s10943-025-02310-w.

本文引用的文献

1
Recruitment and Data Collection Challenges of Research Focused on Older Adults and Family Caregivers from Asian American Communities: A Case Study Series.聚焦美国亚裔社区老年人及家庭照顾者的研究中的招募与数据收集挑战:系列案例研究
Clin Gerontol. 2022 Oct 7:1-15. doi: 10.1080/07317115.2022.2130848.
2
Diagnostic Process and Barriers Among Chinese-American and Korean-American Parents of Children with Autism.中美韩裔父母在儿童自闭症诊断过程中的差异及障碍。
J Dev Behav Pediatr. 2022 Aug 1;43(6):327-334. doi: 10.1097/DBP.0000000000001070. Epub 2022 Mar 3.
3
Brief Report: Impact of the COVID-19 Pandemic on Asian American Families with Children with Developmental Disabilities.简短报告:新冠疫情对有发育障碍儿童的亚裔美国家庭的影响
J Dev Phys Disabil. 2022;34(3):491-504. doi: 10.1007/s10882-021-09810-z. Epub 2021 Sep 1.
4
Understanding Racial and Ethnic Disparities in Autism-Related Service Use Among Medicaid-Enrolled Children.理解在医疗补助计划覆盖的儿童中,自闭症相关服务使用方面的种族和民族差异。
J Autism Dev Disord. 2021 Sep;51(9):3341-3355. doi: 10.1007/s10803-020-04797-6. Epub 2020 Nov 21.
5
Disparities in Documented Diagnoses of Autism Spectrum Disorder Based on Demographic, Individual, and Service Factors.基于人口统计学、个体和服务因素的自闭症谱系障碍记录诊断的差异。
Autism Res. 2020 Mar;13(3):464-473. doi: 10.1002/aur.2255. Epub 2019 Dec 23.
6
Prevalence and Trends of Developmental Disabilities among Children in the United States: 2009-2017.美国儿童发育障碍的患病率和趋势:2009-2017 年。
Pediatrics. 2019 Oct;144(4). doi: 10.1542/peds.2019-0811.
7
Brief Report: Participation of Black and African-American Families in Autism Research.简报:黑人和非裔美国家庭参与自闭症研究。
J Autism Dev Disord. 2020 May;50(5):1841-1846. doi: 10.1007/s10803-019-03926-0.
8
Influence of Community-Level Cultural Beliefs about Autism on Families' and Professionals' Care for Children.社区层面关于自闭症的文化观念对家庭和专业人员照顾儿童的影响。
Transcult Psychiatry. 2018 Oct;55(5):623-647. doi: 10.1177/1363461518779831. Epub 2018 Jul 4.
9
Experiences and Lessons Learned in Using Community-Based Participatory Research to Recruit Asian American Immigrant Research Participants.利用基于社区的参与性研究招募亚裔美国移民研究参与者的经验与教训
J Nurs Scholarsh. 2016 Mar;48(2):210-8. doi: 10.1111/jnu.12194. Epub 2016 Feb 2.
10
Model minority at risk: expressed needs of mental health by Asian American young adults.面临风险的模范少数族裔:美国亚裔青年成年人的心理健康需求表达
J Community Health. 2009 Apr;34(2):144-52. doi: 10.1007/s10900-008-9137-1.

从对发育障碍儿童的亚裔美国家庭进行的全州需求评估中吸取的经验教训。

Lessons learned from a statewide needs assessment of Asian American families of children with developmental disabilities.

作者信息

Wang Yao, Kim Irang, Dababnah Sarah, Reyes Charina, John Aesha

机构信息

University of Maryland School of Social Work, Baltimore, MD, USA.

Tulane University School of Social Work, New Orleans, LA, USA.

出版信息

Int J Dev Disabil. 2023 Dec 21;71(5):788-792. doi: 10.1080/20473869.2023.2286404. eCollection 2025.

DOI:10.1080/20473869.2023.2286404
PMID:40687532
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12272650/
Abstract

The prevalence of developmental disabilities (DDs) has increased in the past decades. As Asian Americans (AA) represent one of the fastest-growing racial groups in the U.S., it is likely that there are a large number of AA children with DD. Racial disparities among individuals with DDs have been well-documented, yet few studies have comprehensively examined AA parents' experiences accessing diagnostic, therapeutic, or support services for their children with DD. This research gap exists, in part, due to the practical and methodological challenges in conducting culturally responsive research with AA families. In this 'Points of View' article, we describe our process of conducting a statewide, community-engaged needs assessment of AA parents of children with DD. We hope the lessons learned from this process will inform and promote future research engaging AA communities, and ultimately, help grow the body of evidence on underrepresented families of children with DD.

摘要

在过去几十年中,发育障碍(DDs)的患病率有所上升。由于亚裔美国人(AA)是美国增长最快的种族群体之一,很可能有大量患有发育障碍的亚裔美国儿童。发育障碍患者之间的种族差异已有充分记录,但很少有研究全面考察亚裔美国父母为其患有发育障碍的孩子获取诊断、治疗或支持服务的经历。这一研究空白的存在,部分原因是对亚裔美国家庭进行具有文化敏感性的研究存在实际和方法上的挑战。在这篇“观点”文章中,我们描述了对患有发育障碍儿童的亚裔美国父母进行全州范围、社区参与的需求评估的过程。我们希望从这个过程中学到的经验教训能为未来涉及亚裔美国社区的研究提供参考并加以推动,最终有助于增加关于发育障碍儿童中代表性不足家庭的证据。