Investigating how patients with lupus nephritis access and trust health information: Results from a Canadian survey of patients with lupus nephritis.
作者信息
Cardwell Francesca S, Elliott Susan J, Barber Megan Rw, Cheema Kim, George Sydney, Boucher Adrian, Clarke Ann E
机构信息
Department of Geography and Environmental Management, University of Waterloo, Waterloo, ON, Canada.
Division of Rheumatology, Cumming School of Medicine, University of Calgary, Calgary, AB, Canada.
出版信息
Lupus. 2025 Feb;34(2):217-219. doi: 10.1177/09612033251313578. Epub 2025 Jan 10.
Abstract
摘要
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本文引用的文献
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Canadian patient experiences of lupus nephritis: a qualitative analysis.加拿大狼疮肾炎患者的体验：一项定性分析。
Lupus Sci Med. 2023 Dec 9;10(2):e000982. doi: 10.1136/lupus-2023-000982.
2
Listening to Patients With Lupus: Why Not Proactively Integrate the Internet as a Resource to Drive Improved Care?倾听狼疮患者的声音：为何不主动将互联网整合为资源，以推动改善护理？
J Med Internet Res. 2023 Mar 29;25:e44660. doi: 10.2196/44660.
3
Health information use by patients with systemic lupus erythematosus (SLE) pre and during the COVID-19 pandemic.系统性红斑狼疮患者在 COVID-19 大流行前及期间对健康信息的使用。
Lupus Sci Med. 2022 Oct;9(1). doi: 10.1136/lupus-2022-000755.
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The Danger of Misinformation in the COVID-19 Crisis.新冠疫情危机中错误信息的危害
Mo Med. 2020 Nov-Dec;117(6):510-512.
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Public Health and Online Misinformation: Challenges and Recommendations.公共卫生与网络错误信息：挑战与建议。
Annu Rev Public Health. 2020 Apr 2;41:433-451. doi: 10.1146/annurev-publhealth-040119-094127. Epub 2019 Dec 24.
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Assessing the quality, reliability and readability of online health information regarding systemic lupus erythematosus.评估关于系统性红斑狼疮的在线健康信息的质量、可靠性和可读性。
Lupus. 2018 Oct;27(12):1911-1917. doi: 10.1177/0961203318793213. Epub 2018 Aug 16.
7
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J Am Soc Nephrol. 2004 Feb;15(2):241-50. doi: 10.1097/01.asn.0000108969.21691.5d.
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