视角-狼疮患者赋权的最重要影响

Laniyati Hamijoyo, Jonathan Paul Consignado, Sandra V. Navarra
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引用次数: 0

摘要

患者授权在狼疮是一个过程,其中患者积极参与决策与医疗保健专业人员和承担责任,为自己的条件。为了有效地参与医疗护理并取得最佳治疗效果,患者必须具备足够的知识和对狼疮及其复杂性的理解。此外,每个国家的家庭和照顾者、其他卫生保健专业人员和支持系统以及政策制定者的重要作用对健康结果和整体生活质量产生巨大影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Perspective—The Paramount Impact of Lupus Patient Empowerment
Patient empowerment in lupus is a process wherein patients actively participate in decision-making with healthcare professionals and take responsibility for their own condition. In order to effectively be involved in their medical care and achieve the best treatment outcomes, patients have to be equipped with a sufficient body of knowledge and understanding of lupus and its intricacies. Furthermore, the significant roles of families and caregivers, other healthcare professionals and support systems, and policymakers in each country have an immense impact on health outcomes and the overall quality of life.
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