Rocha Heather Mae, Savatt Juliann M, Riggs Erin Rooney, Wagner Jennifer K, Faucett W Andrew, Martin Christa Lese
Genomic Medicine Institute, Geisinger, 100 N Academy Ave, MC 26-20, Danville, PA, 17822, USA.
Autism & Developmental Medicine Institute, Geisinger, Lewisburg, PA, USA.
J Genet Couns. 2018 Apr;27(2):470-480. doi: 10.1007/s10897-017-0170-z. Epub 2017 Nov 13.
Patients with newly-described or rare genetic findings are turning to social media to find and connect with others. Blogs, Facebook groups, and Twitter have all been reported as tools for patients to connect with one another. However, the preferences for social media use and privacy among patients, their families, and these communities have not been well characterized. To explore preferences about privacy and membership guidelines, an online survey was administered to two web-based patient registries, Simons Variation in Individuals Project ( www.simonsvipconnect.org ) and GenomeConnect ( www.genomeconnect.org ). Over a three-month period, invitations were sent to 2524 individuals and 103 responses (4%) were received and analyzed. Responses indicate that Facebook is the most popular resource accessed within this sample population (99%). Participants used social media to look for information about their diagnosis or test results (83%), read posts from rare disease groups or organizations (73%), participate in conversations about their diagnosis (67%), and connect with others to find support (58%). Focusing on privacy issues in social media, respondents indicate that membership and access impact the level of comfort in sharing personal or medical information. Nearly 60% of respondents felt uncomfortable sharing photos or medical information within a public Facebook group, whereas only 12% of respondents felt uncomfortable sharing in private group targeted to families alone. Using this preliminary data concerning social media use and privacy, we developed points for genetic counselors to incorporate when discussing available support resources for patients with a new, or rare, genetic diagnosis or genetic test result. Genetic counselors are trained to provide anticipatory guidance to families adapting to new genetic information, and are well-equipped to help patients consider their preferences about using social media as a source of information and support.
有新发现的或罕见基因检测结果的患者开始转向社交媒体来寻找他人并与之建立联系。博客、脸书群组和推特都被报道为患者相互联系的工具。然而,患者、其家人以及这些群体对社交媒体使用和隐私的偏好尚未得到充分描述。为了探究对隐私和成员准则的偏好,我们对两个基于网络的患者登记处进行了在线调查,即西蒙斯个体变异项目(www.simonsvipconnect.org)和基因组连接项目(www.genomeconnect.org)。在三个月的时间里,我们向2524人发送了邀请,共收到103份回复(4%)并进行了分析。回复表明,脸书是该样本群体中最常访问的资源(99%)。参与者利用社交媒体来查找有关其诊断或检测结果的信息(83%)、阅读罕见病群体或组织发布的帖子(73%)、参与有关其诊断的讨论(67%)以及与他人建立联系以寻求支持(58%)。聚焦于社交媒体中的隐私问题,受访者表示成员资格和访问权限会影响分享个人或医疗信息时的舒适程度。近60%的受访者在公共脸书群组中分享照片或医疗信息时感到不舒服,而只有12%的受访者在仅面向家人的私密群组中分享时感到不舒服。利用这些关于社交媒体使用和隐私的初步数据,我们制定了要点,供基因咨询师在讨论为新诊断出罕见基因或有罕见基因检测结果的患者提供可用支持资源时纳入考虑。基因咨询师经过培训,可为适应新基因信息的家庭提供前瞻性指导,并且具备充分条件来帮助患者考虑其对将社交媒体用作信息和支持来源的偏好。