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罕见病社交媒体群组参与者对与遗传咨询师互动的看法:混合方法研究。

Perspectives of Rare Disease Social Media Group Participants on Engaging With Genetic Counselors: Mixed Methods Study.

机构信息

Department of Genetics, Stanford University School of Medicine, Stanford, CA, United States.

Stanford Center for Biomedical Ethics, Stanford University School of Medicine, Stanford, CA, United States.

出版信息

J Med Internet Res. 2022 Dec 21;24(12):e42084. doi: 10.2196/42084.

Abstract

BACKGROUND

Social media provides a potential avenue for genetic counselors to address gaps in access to reliable genetics information for rare disease communities. However, only limited research has examined patient and family attitudes toward engaging with genetic counselors through social media.

OBJECTIVE

Our study assessed the attitudes of members of rare disease social media groups toward engaging with genetic counselors through social media, characteristics associated with greater interest, and the benefits and potential pitfalls of various approaches to such engagement.

METHODS

We conducted a mixed methods survey of patients and family members recruited from a systematic sample of rare disease Facebook groups. Patient characteristics and their associations with interest in engagement with genetic counselors were evaluated using univariate and bivariate statistics. Responses to open-ended questions were analyzed using thematic content analysis.

RESULTS

In total, 1053 individuals from 103 rare disease groups participated. The median overall interest in engaging with genetic counselors on social media was moderately high at 7.0 (IQR 4.0-9.0, range 0-10). No past experience with a genetic counselor was associated with greater interest in engaging with one through social media (µ=6.5 vs 6.0, P=.04). Participants expressed greatest interest (median 9.0, IQR 5.0-10.0) in engagement models allowing direct communication with genetic counselors, which was corroborated by the majority (n=399, 61.3%) of individuals who responded to open-ended questions explicitly stating their interest in 1-on-1 interactions. When asked what forms of support they would request from genetic counselors through social media, participants desired individualized support and information about how to access services. However, participants also expressed concerns regarding privacy and confidentiality.

CONCLUSIONS

Patients and family members in rare disease social media groups appear interested in engaging with genetic counselors through social media, particularly for individualized support. This form of engagement on social media is not meant to replace the current structure and content of genetic counseling (GC) services, but genetic counselors could more actively use social media as a communication tool to address gaps in knowledge and awareness about genetics services and gaps in accessible patient information. Although encouraging, concerns regarding privacy and feasibility require further consideration, pointing to the need for professional guidelines in this area.

摘要

背景

社交媒体为遗传咨询师提供了一个潜在的途径,可以解决罕见病社区获取可靠遗传信息方面的差距。然而,只有有限的研究探讨了患者和家属对通过社交媒体与遗传咨询师互动的态度。

目的

我们的研究评估了罕见病社交媒体群组的成员对通过社交媒体与遗传咨询师互动的态度、与更大兴趣相关的特征,以及各种互动方式的好处和潜在陷阱。

方法

我们对从罕见病 Facebook 群组的系统抽样中招募的患者和家属进行了混合方法调查。使用单变量和双变量统计评估患者特征及其与对与遗传咨询师互动的兴趣的关联。对开放式问题的回答进行主题内容分析。

结果

共有 103 个罕见病群组的 1053 人参与了研究。对通过社交媒体与遗传咨询师互动的总体兴趣中位数较高,为 7.0(四分位距 4.0-9.0,范围 0-10)。过去没有与遗传咨询师的接触与通过社交媒体与遗传咨询师互动的更大兴趣相关(µ=6.5 与 6.0,P=.04)。参与者对允许与遗传咨询师直接沟通的互动模式表现出最大的兴趣(中位数 9.0,四分位距 5.0-10.0),这与大多数(n=399,61.3%)回答开放式问题的人明确表示对一对一互动感兴趣的人一致。当被问及他们希望通过社交媒体从遗传咨询师那里获得哪些形式的支持时,参与者希望获得个性化的支持和有关如何获得服务的信息。然而,参与者也对隐私和保密性表示担忧。

结论

罕见病社交媒体群组的患者和家属似乎对通过社交媒体与遗传咨询师互动感兴趣,特别是对于个性化支持。这种形式的社交媒体互动并不是要取代遗传咨询服务的当前结构和内容,而是遗传咨询师可以更积极地将社交媒体用作沟通工具,以解决关于遗传服务的知识和意识差距以及可获得的患者信息差距。尽管令人鼓舞,但对隐私和可行性的担忧需要进一步考虑,这表明在这一领域需要专业指南。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ac0/9813816/95ff29836899/jmir_v24i12e42084_fig1.jpg

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