Rationale for Using Social Media to Collect Patient-Reported Outcomes in Patients with Celiac Disease.

Kt Park, Merissa Harris, Nasim Khavari, Chaitan Khosla
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引用次数: 10

Abstract

Patients with celiac disease (CD) are increasingly interconnected through social media, exchanging patient experiences and health-tracking information between individuals through various web-based platforms. Social media represents potentially unique communication interface between gastroenterologists and active social media users - especially young adults and adolescents with celiac disease-regarding adherence to the strict gluten-free diet, gastrointestinal symptoms, and meaningful discussion about disease management. Yet, various social media platforms may be underutilized for research purposes to collect patient-reported outcomes data. In this commentary, we summarize the scientific rationale and potential for future growth of social media in patient-reported outcomes research, focusing on college freshmen with celiac disease as a case study and provide overview of the methodological approach. Finally, we discuss how social media may impact patient care in the future through increasing mobile technology use.

使用社交媒体收集乳糜泻患者报告结果的理由
乳糜泻(CD)患者越来越多地通过社交媒体相互联系,通过各种基于网络的平台在个人之间交换患者经验和健康跟踪信息。社交媒体代表了胃肠病学家和活跃的社交媒体用户之间潜在的独特交流界面——特别是患有乳糜泻的年轻人和青少年——关于严格遵守无麸质饮食、胃肠道症状和关于疾病管理的有意义的讨论。然而,各种社交媒体平台可能没有充分利用于收集患者报告的结果数据的研究目的。在这篇评论中,我们总结了社会媒体在患者报告结果研究中的科学原理和未来增长的潜力,并以患有乳糜泻的大学新生为例进行了研究,并概述了方法方法。最后,我们讨论了社交媒体如何通过增加移动技术的使用来影响未来的患者护理。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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