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为22q11.2缺失综合征患儿家长开发并评估一份关于该病症精神症状的教育资源。

Development and evaluation of an educational resource for parents of children with 22q11.2 deletion syndrome about the psychiatric manifestations of the condition.

作者信息

Blankenship Kayla, Chieffo Stephanie, Morris Emily, Slomp Caitlin, Batallones Rolan, Prijoles Eloise, Hill-Chapman Crystal, Austin Jehannine

机构信息

University of South Carolina Genetic Counseling Program, Columbia, South Carolina, USA.

University of Iowa Hospitals and Clinics, Iowa City, Iowa, USA.

出版信息

J Genet Couns. 2024 Aug;33(4):720-732. doi: 10.1002/jgc4.1779. Epub 2023 Sep 1.

DOI:10.1002/jgc4.1779
PMID:37658574
Abstract

Parents of children with 22q11.2 deletion syndrome (22q11DS) report concern about the psychiatric manifestations of the condition, but typically receive little information about this in clinical encounters and instead find information about it elsewhere. We developed an educational booklet about the psychiatric manifestations of 22q11DS and assessed its utility among parents of children with the condition. First, six parents of individuals with 22q11DS completed cognitive interviews to review an established generic booklet about the genetics of psychiatric conditions-and to suggest 22q11DS-specific adaptations. We used these suggestions to develop a novel booklet specific to psychiatric conditions and 22q1DS. Then, before and 1-month after reading the novel 22q11DS-specific online booklet, 73 parents of children with 22q11DS (with/without psychiatric conditions) completed validated scales (measuring empowerment, stigma, intolerance of uncertainty), an adapted version of a scale measuring worry about their child developing psychiatric illness, and purpose-designed items assessing perceptions of understanding of 22q11DS and mental illness, confidence in recognizing early signs, etc. After reading the 22q11DS online booklet, participants' feelings of empowerment increased (p = 0.002), while feelings of worry about their child developing psychiatric illness decreased (p = 0.05), and they reported better understanding 22q11DS and mental illness, and increased confidence in recognizing early warning signs. There is potential benefit in broadly distributing this educational booklet to parents of children with 22q11DS.

摘要

患有22q11.2缺失综合征(22q11DS)患儿的家长对该病症的精神症状表示担忧,但在临床诊疗过程中通常很少得到这方面的信息,而是在其他地方寻找相关信息。我们编写了一本关于22q11DS精神症状的教育手册,并评估了其在患有该病症患儿家长中的实用性。首先,六名患有22q11DS个体的家长完成了认知访谈,以审查一本关于精神疾病遗传学的既定通用手册,并提出针对22q11DS的改编建议。我们根据这些建议编写了一本专门针对精神疾病和22q1DS的新手册。然后,在阅读这本专门针对22q11DS的在线新手册之前和之后1个月,73名患有22q11DS(有/无精神疾病)患儿的家长完成了经过验证的量表(测量赋权、耻辱感、对不确定性的不耐受)、一个改编版量表,用于测量对孩子患精神疾病担忧程度,以及专门设计的项目,以评估对22q11DS和精神疾病的理解、识别早期症状的信心等。阅读22q11DS在线手册后,参与者的赋权感增强(p = 0.002),而对孩子患精神疾病的担忧感降低(p = 0.05),他们表示对22q11DS和精神疾病有了更好的理解,识别早期预警信号的信心也增强了。广泛向患有22q11DS患儿的家长分发这本教育手册可能会带来益处。

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