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“在脸书和社交媒体出现之前……我们不认识其他有这种情况的人”:家长对儿科临床基因检测过程中互联网和社交媒体使用的看法。

"Before Facebook and before social media…we did not know anybody else that had this": parent perspectives on internet and social media use during the pediatric clinical genetic testing process.

作者信息

Barton Krysta S, Wingerson Andrew, Barzilay Julie R, Tabor Holly K

机构信息

Treuman Katz Center for Pediatric Bioethics, Seattle Children's Research Institute, Seattle, Washington, USA.

Keck School of Medicine of the University of Southern California, Los Angeles, CA, USA.

出版信息

J Community Genet. 2019 Jul;10(3):375-383. doi: 10.1007/s12687-018-0400-6. Epub 2018 Dec 19.

DOI:10.1007/s12687-018-0400-6
PMID:30569339
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6591503/
Abstract

Parents of children who undergo clinical genetic testing have significant informational and emotional support needs at different stages of the testing process. We analyzed parent views about use of both the internet and social media to help meet these needs. We interviewed 20 parents of children who underwent clinical genetic testing and analyzed transcripts to identify themes related to internet and social media use. Parents described using the internet to search for information at three stages of the genetic testing process: before testing, pending results return, and after results return. Each stage corresponded to different information vacuums and needs. Parents also described using condition-specific Facebook groups to learn more about their child's condition and to find support networks of families with similar experiences in ways that were challenging using non-social media approaches. Both the internet and social media play important roles in meeting informational and support needs in pediatric genetic testing, especially for rare conditions. Providers should consider engaging parents at different stages of the testing process about their use of the internet and social media, and consider directing them to vetted sites and groups as part of shared decision making and to improve satisfaction and outcomes.

摘要

接受临床基因检测的儿童的家长在检测过程的不同阶段有重大的信息和情感支持需求。我们分析了家长对于利用互联网和社交媒体来满足这些需求的看法。我们采访了20位其子女接受临床基因检测的家长,并对访谈记录进行分析,以确定与互联网和社交媒体使用相关的主题。家长们描述了在基因检测过程的三个阶段利用互联网搜索信息:检测前、等待结果返回期间以及结果返回之后。每个阶段对应着不同的信息空白和需求。家长们还描述了利用特定疾病的脸书群组来更多地了解孩子的病情,并以非社交媒体方法难以做到的方式找到有类似经历的家庭支持网络。互联网和社交媒体在满足儿科基因检测中的信息和支持需求方面都发挥着重要作用,尤其是对于罕见病。医疗服务提供者应考虑在检测过程的不同阶段与家长探讨他们对互联网和社交媒体的使用情况,并考虑将他们引导至经过审核的网站和群组,作为共同决策的一部分,以提高满意度和检测结果。

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