Beom Joon Myeoung, Ju Hyun Park, Byung Joo Lee, Hyeok Jun Jeong, Aran Kim, Min Wook So, Seung-Geun Lee
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引用次数: 0
摘要
本研究分析了在一家三级医院风湿病科就诊的风湿病患者通过社交媒体(SM)获取医疗信息的情况及其对医疗服务利用率的影响。在这项单中心横断面调查中,我们连续评估了 102 名风湿病患者。通过面对面调查,我们询问了患者获取医疗信息的来源、影响他们到三级医院就诊的因素以及通过SM获取RD医疗信息的潜在影响。SM指的是YouTube、Facebook、Instagram、Kakao Channel、Naver Band和X。最常见的疾病是强直性脊柱炎(45.1%),其次是类风湿性关节炎(20.6%)。除风湿免疫科医生外,获取有关研发人员的医疗信息最常用的方法是互联网门户网站(47.8%),其次是 SM(40.2%)。影响患者决定去三级医院就诊的最重要因素是医生(51%);只有 1%的患者回答 SM 是决定其就诊的最关键因素。大多数患者(77.5%)回答说,通过 SM 获取医疗信息有助于他们控制疾病。我们的数据显示,有相当比例的种族歧视患者通过 SM 获取医疗信息。然而,SM对到三级医院就诊的影响微乎其微,这表明SM已成为医疗信息的主流来源,但其可靠性仍相对较低。风湿病学会应建立能够提供高质量医疗信息的SM平台。
Social media has become a mainstream source of medical information for patients with rheumatic diseases: a cross-sectional survey of patients.
This study analyzed the status of medical information acquisition through social media (SM) and its impact on healthcare utilization among patients with rheumatic diseases (RDs) who visited the rheumatology department of a tertiary hospital. We consecutively evaluated 102 patients with RDs in this single-center cross-sectional survey. Using a face-to-face survey, patients were asked about the sources they used to acquire medical information, factors influencing their visits to tertiary hospitals, and the potential impact of acquiring medical information on RDs through SM. SM refers to YouTube, Facebook, Instagram, Kakao Channel, Naver Band, and X. The mean age was 42.3 years and 39% were female. The most common disease was ankylosing spondylitis (45.1%), followed by rheumatoid arthritis (20.6%). The most frequent method for acquiring medical information regarding RDs, except for rheumatologists, was internet portal sites (47.8%), followed by SM (40.2%). The most important factor influencing the decision to visit a tertiary hospital was medical doctors (51%); only 1% of the patients responded that SM was the most crucial factor in determining their visit. Most patients (77.5%) responded that acquiring medical information through SM would help them manage their diseases. Our data revealed that a substantial proportion of patients with RDs obtained medical information through SM. However, the impact of SM on visiting a tertiary hospital was minimal, suggesting that SM has become a mainstream source of medical information, yet the reliability of SM remains relatively low. Rheumatology societies should establish SM platforms capable of providing high-quality medical information.
期刊介绍:
RHEUMATOLOGY INTERNATIONAL is an independent journal reflecting world-wide progress in the research, diagnosis and treatment of the various rheumatic diseases. It is designed to serve researchers and clinicians in the field of rheumatology.
RHEUMATOLOGY INTERNATIONAL will cover all modern trends in clinical research as well as in the management of rheumatic diseases. Special emphasis will be given to public health issues related to rheumatic diseases, applying rheumatology research to clinical practice, epidemiology of rheumatic diseases, diagnostic tests for rheumatic diseases, patient reported outcomes (PROs) in rheumatology and evidence on education of rheumatology. Contributions to these topics will appear in the form of original publications, short communications, editorials, and reviews. "Letters to the editor" will be welcome as an enhancement to discussion. Basic science research, including in vitro or animal studies, is discouraged to submit, as we will only review studies on humans with an epidemological or clinical perspective. Case reports without a proper review of the literatura (Case-based Reviews) will not be published. Every effort will be made to ensure speed of publication while maintaining a high standard of contents and production.
Manuscripts submitted for publication must contain a statement to the effect that all human studies have been reviewed by the appropriate ethics committee and have therefore been performed in accordance with the ethical standards laid down in an appropriate version of the 1964 Declaration of Helsinki. It should also be stated clearly in the text that all persons gave their informed consent prior to their inclusion in the study. Details that might disclose the identity of the subjects under study should be omitted.