正常导航:为小儿肾移植受者和护理人员设计个人健康可视化。

IF 4.7 2区 医学 Q1 COMPUTER SCIENCE, INFORMATION SYSTEMS Journal of the American Medical Informatics Association Pub Date : 2024-07-30 DOI:10.1093/jamia/ocae206
Lily V Jeffs, Julia C Dunbar, Sanaa Syed, Chelsea Ng, Ari H Pollack
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引用次数: 0

摘要

目标:包括肾病在内的慢性病患者在评估自己的健康状况时,会考虑自己的正常感。虽然这一概念是他们自我决定健康状况的关键指标,但他们很难理解自己的经历是否具有典型性。为了应对这一挑战,我们开始探索如何设计个人健康可视化方法,帮助参与者更好地了解他们移植后的经历,识别正常感的障碍,并实现他们期望的医疗结果:小儿肾移植患者及其护理人员参加了三次异步设计会议,包括分享经验、展示象征性物品和提供可视化反馈,以了解他们对移植后正常生活的看法。对设计环节 1 和 2 的数据分析包括演绎和归纳分析。我们使用亲和图来确定参与者移植经历的主题领域。我们还对设计环节三正常状态可视化的理解进行了评估:结果:参与者有效地参与了设计环节,对他们的经历表达了不同的观点。我们发现,患者和护理人员非常需要描述正常状态的可视化产品,以更好地了解他们的健康状况:讨论:正常状态可视化应包含三个关键的设计原则:个人价值观、促进同伴和自我比较以及无缝传达抽象概念,以帮助青少年肾移植受者理解他们的移植经历是否正常以及正常状态对他们意味着什么:结论:通过将患者和护理人员生活的方方面面融入个人健康可视化中,他们可以认识到自己的正常化进程,并有能力做出有助于他们感觉正常的决定。
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Navigating normalcy: designing personal health visualizations for pediatric kidney transplant recipients and caregivers.

Objectives: Patients with chronic illnesses, including kidney disease, consider their sense of normalcy when evaluating their health. Although this concept is a key indicator of their self-determined well-being, they struggle to understand if their experience is typical. To address this challenge, we set out to explore how to design personal health visualizations that aid participants in better understanding their experiences post-transplant, identifying barriers to normalcy, and achieving their desired medical outcomes.

Materials and methods: Pediatric kidney transplant patients and their caregivers participated in three asynchronous design sessions involving sharing experiences, presenting symbolic objects, and providing feedback on visualizations to understand their perceptions of normalcy post-transplant. Data analysis of design session 1 and 2 comprised deductive and inductive analysis. We used affinity diagramming to identify thematic areas about participants' transplant experiences. Comprehension of design session three normalcy visualizations was also evaluated.

Results: Participants effectively engaged in the design sessions, revealing diverse perspectives on their experiences. We found there is a significant need for visualizations that depict normalcy to better inform patients and caregivers about their health.

Discussion: Normalcy Visualizations should incorporate three key design principles: personal values, facilitating peer and self-comparison, and seamlessly communicating abstract concepts to help youth kidney transplant recipients comprehend and contextualize if their transplant experience is normal and what normalcy means to them.

Conclusion: By incorporating holistic aspects of patients' and caregivers' lives into personal health visualizations, they can be cognizant of their progress to normalcy and empowered to make decisions that help them feel normal.

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来源期刊
Journal of the American Medical Informatics Association
Journal of the American Medical Informatics Association 医学-计算机:跨学科应用
CiteScore
14.50
自引率
7.80%
发文量
230
审稿时长
3-8 weeks
期刊介绍: JAMIA is AMIA''s premier peer-reviewed journal for biomedical and health informatics. Covering the full spectrum of activities in the field, JAMIA includes informatics articles in the areas of clinical care, clinical research, translational science, implementation science, imaging, education, consumer health, public health, and policy. JAMIA''s articles describe innovative informatics research and systems that help to advance biomedical science and to promote health. Case reports, perspectives and reviews also help readers stay connected with the most important informatics developments in implementation, policy and education.
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