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家长对学龄期儿童近期发病1型糖尿病教育及心理社会干预的看法:一项定性研究

Parent Perspectives on Educational and Psychosocial Intervention for Recent-Onset Type 1 Diabetes in Their School-Age Child: A Qualitative Study.

作者信息

Marker Arwen M, Monzon Alexandra D, Goggin Kathy, Clements Mark A, Patton Susana R

机构信息

University of Kansas, Lawrence, KS.

Children's Mercy-Kansas City, Kansas City, MO.

出版信息

Diabetes Spectr. 2021 May;34(2):166-174. doi: 10.2337/ds20-0058. Epub 2021 Dec 23.

Abstract

OBJECTIVE

The recent-onset period of type 1 diabetes (T1D) in early school-age children should include comprehensive, parent-focused T1D education as well as family-centered resources and support to help with adjustment. Here, we present parent/caregiver perspectives on specific areas of concern during the recent-onset period of T1D and their preferred timing for different topics related to T1D education.

METHODS

Parents/caregivers of 5- to 9-year-old children with T1D completed a card-sorting task and qualitative interview to describe ongoing areas of concern and preferred educational topics during the first year after T1D diagnosis.

RESULTS

Thirteen parents/caregivers (aged 35.1 ± 6.9 years) of a child with T1D (aged 8.9 ± 0.8 years, 11.3 ± 7.0 months post-diagnosis) completed the card-sorting task, and 11 completed the qualitative interview. Parents/caregivers endorsed four preferred stages of education: basic education and T1D survival skills during month 1 post-diagnosis, application and practice of T1D skills from months 1-3, access to community supports to cope with anxiety and distress from months 3-6, and support to build autonomy and manage burnout beyond month 6 post-diagnosis. Parents/caregivers endorsed four main themes for ongoing concerns: anxiety, autonomy, distress, and support.

CONCLUSION

Parents endorsed four time points for education and psychosocial services within the first year of a T1D diagnosis. Parents/caregivers may benefit the most from psychosocial interventions 3-6 months post-diagnosis, once they have had sufficient time to develop basic T1D management skills. These findings support the need for regular parent psychosocial screening and access to scalable psychosocial interventions in the first year post-diagnosis of T1D.

摘要

目的

小学低年级儿童1型糖尿病(T1D)发病初期应开展全面的、以家长为重点的T1D教育,以及以家庭为中心的资源和支持,以帮助他们进行调整。在此,我们阐述家长/照顾者对T1D发病初期特定关注领域的看法,以及他们对T1D教育不同主题的首选时机。

方法

对5至9岁T1D患儿的家长/照顾者进行卡片分类任务和定性访谈,以描述T1D诊断后第一年持续关注的领域和首选教育主题。

结果

13名T1D患儿(年龄8.9±0.8岁,诊断后11.3±7.0个月)的家长/照顾者(年龄35.1±6.9岁)完成了卡片分类任务,11人完成了定性访谈。家长/照顾者认可四个首选教育阶段:诊断后第1个月的基础教育和T1D生存技能,第1至3个月T1D技能的应用和实践,第3至6个月获得社区支持以应对焦虑和痛苦,以及诊断后6个月后支持建立自主性和应对倦怠。家长/照顾者认可持续关注的四个主要主题:焦虑、自主性、痛苦和支持。

结论

家长认可T1D诊断后第一年内教育和心理社会服务的四个时间点。家长/照顾者在诊断后3至6个月,一旦有足够时间掌握基本的T1D管理技能,可能从心理社会干预中获益最多。这些发现支持在T1D诊断后第一年对家长进行定期心理社会筛查并提供可扩展的心理社会干预的必要性。

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