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公众对遗尿症的认知:来自韩国和美国在线社区的见解

Public Perceptions of Enuresis: Insights From Online Communities in South Korea and the United States.

作者信息

Yu Jung Eun, Ko Kwang Jin, Kim Jung Yoon

机构信息

Department of Game and Interactive Media, General Graduate School, Gachon University, Seongnam, Korea.

Department of Urology, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea.

出版信息

Int Neurourol J. 2024 Sep;28(3):239-249. doi: 10.5213/inj.2448318.159. Epub 2024 Sep 30.

Abstract

PURPOSE

To establish a foundation for raising awareness and disseminating accurate information about enuresis-one of the most challenging conditions to discuss openly-this paper examines public perceptions of enuresis.

METHODS

This paper collected title and text data from posts related to enuresis on the top popular online platforms such Naver Cafe in South Korea and Reddit in the United States (US). The data along with the thematic subcommunities where the posts were uploaded, was analyzed and visualized using word cloud, Latent Dirichlet Allocation (LDA) topic modeling, and pyLDAvis.

RESULTS

The findings reveal both similarities and differences in how the patients from the 2 countries addressed enuresis online. In both countries, enuresis symptoms were a daily concern, and individuals used online platforms as a space to talk about their experiences. However, South Koreans were more inclined to describe symptoms within region-based communities or mothers' forums, where they exchanged information and shared experiences before consulting a doctor. In contrast, US patients with medical experience or knowledge frequently discussed treatment processes, lifestyle adjustments, and medication options.

CONCLUSION

South Koreans tend to be cautious when selecting and visiting hospitals, often relying on others for advice and preparation before seeking medical attention. Compared to online communities in the US, Korean users are more likely to seek preliminary diagnoses based on nonprofessional opinions. Consequently, it is important to lower the barriers for patients to access professional medical advice to mitigate the potential harm of relying on nonprofessional opinions. Additionally, there is a need to raise awareness so that adults can recognize and address their symptoms in a timely manner.

摘要

目的

遗尿症是最难公开讨论的病症之一,为提高对其的认识并传播准确信息奠定基础,本文研究公众对遗尿症的看法。

方法

本文收集了韩国的Naver Cafe和美国的Reddit等热门在线平台上与遗尿症相关帖子的标题和文本数据。使用词云、潜在狄利克雷分配(LDA)主题建模和pyLDAvis对数据以及帖子上传的主题子社区进行分析和可视化。

结果

研究结果揭示了这两个国家的患者在网上提及遗尿症方式的异同。在这两个国家,遗尿症症状都是日常关注的问题,人们将在线平台作为谈论自身经历的空间。然而,韩国人更倾向于在基于地区的社区或妈妈论坛中描述症状,在咨询医生之前他们会在这些地方交流信息和分享经验。相比之下,有医疗经验或知识的美国患者经常讨论治疗过程、生活方式调整和药物选择。

结论

韩国人在选择和就医时往往较为谨慎,在寻求医疗帮助之前常常依赖他人的建议和准备。与美国的在线社区相比,韩国用户更有可能根据非专业意见寻求初步诊断。因此,降低患者获取专业医疗建议的障碍以减轻依赖非专业意见的潜在危害非常重要。此外,有必要提高认识,以便成年人能够及时识别并处理自己的症状。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e90f/11450238/72487e3a4568/inj-2448318-159f1.jpg

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