Preferences, Needs, and Values of Patients With Chronic Obstructive Pulmonary Disease Attending a Telehealth Service: Qualitative Interview Study.

IF 2.6 Q2 HEALTH CARE SCIENCES & SERVICES
JMIR Human Factors Pub Date : 2024-06-21 DOI:10.2196/53131
Camilla Wong Schmidt, Karen Borgnakke, Anne Frølich, Lars Kayser
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引用次数: 0

Abstract

Background: Digitally assisted health care services and technologies are gaining popularity. They assist patients in managing their conditions, thereby reducing the burden on health care staff. Digital health care enables individuals to receive care that is more tailored to their needs and preferences. When implemented properly, it can promote equity by considering each person's opportunities and limitations in the context of health care needs, preferences, values, and capabilities.

Objective: This study aims to understand the needs, values, and preferences of individuals with chronic obstructive pulmonary disease (COPD) who are provided with a 24/7 digital health care service. Furthermore, we aim to understand the dynamics of the communities to which they belong and how these communities intersect. This will provide us with the essential knowledge to establish new methods of providing education, including the development of educational activities for health professionals to engage, train, and empower people living with COPD.

Methods: The study included 7 informants diagnosed with COPD who received 24/7 digital health care service support from a regional project in Region Zealand, Denmark. The informants were visited 4 times during 2 months, including a "Hello" visit, a day with a semistructured interview, and 2 days with field observations. The informants participated in a semistructured interview, following participant observation and an ethnographic approach. The interview content was analyzed using an inductive methodology to categorize the empirical data.

Results: Using the inductive approach, we identified 3 main categories related to the informants' needs, values, and preferences: (1) Health, (2) Value Creation, and (3) Resources. These 3 main categories were based on 9 subcategories: (1) health and barriers, (2) self-monitoring, (3) medication, (4) behavior, (5) motivation, (6) hobbies, (7) social networks, (8) health professionals, and (9) technology. These findings revealed that the informants placed value on maintaining their daily activities and preserving their sense of identity before the onset of COPD. Furthermore, they expressed a desire not to be defined by their COPD, as conversations about COPD often shifted away from the topic.

Conclusions: Digital health solutions and the health care professionals who offer them should prioritize the individuals they serve, considering their needs, values, and preferences rather than solely focusing on the medical condition. This approach ensures the highest level of daily living and empowerment for those living with long-term health conditions. The communities surrounding individuals must engage in constant interaction and collaboration. They should work together to incorporate people's needs, values, and preferences into future digital health services, thereby promoting empowerment and self-management. New educational programs aimed at developing the digital health service competencies of registered nurses should facilitate collaboration between the 2 communities. This collaboration is essential for supporting patients with long-term health conditions in their daily activities.

参加远程保健服务的慢性阻塞性肺病患者的偏好、需求和价值观:定性访谈研究。
背景:数字辅助医疗保健服务和技术越来越受欢迎。它们能帮助病人控制病情,从而减轻医护人员的负担。数字医疗能让个人获得更符合其需求和偏好的医疗服务。如果实施得当,它可以在医疗保健需求、偏好、价值观和能力的背景下考虑每个人的机会和局限性,从而促进公平:本研究旨在了解慢性阻塞性肺病(COPD)患者对全天候数字医疗服务的需求、价值观和偏好。此外,我们还希望了解他们所属社区的动态以及这些社区之间的交集。这将为我们提供必要的知识,以建立提供教育的新方法,包括为卫生专业人员开展教育活动,让慢性阻塞性肺病患者参与其中,对他们进行培训并增强他们的能力:研究对象包括 7 名被诊断患有慢性阻塞性肺病的信息提供者,他们接受了丹麦新西兰地区一个区域项目提供的全天候数字医疗服务支持。在 2 个月的时间里,我们对这些信息提供者进行了 4 次访问,包括一次 "你好 "访问、一天的半结构化访谈和两天的实地观察。信息提供者在参与观察和人种学方法之后,参加了一次半结构式访谈。我们采用归纳法对访谈内容进行了分析,对经验数据进行了分类:利用归纳法,我们确定了与信息提供者的需求、价值观和偏好相关的三大类别:(1) 健康,(2) 价值创造,(3) 资源。这 3 个主要类别基于 9 个子类别:(1) 健康与障碍,(2) 自我监测,(3) 药物治疗,(4) 行为,(5) 动机,(6) 业余爱好,(7) 社交网络,(8) 医疗专业人员,以及 (9) 技术。这些调查结果显示,受访者重视在慢性阻塞性肺病发病前保持日常活动和身份认同感。此外,他们还表示不希望自己被慢性阻塞性肺病所定义,因为有关慢性阻塞性肺病的谈话经常偏离这个话题:数字医疗解决方案和提供这些解决方案的医疗保健专业人员应优先考虑他们所服务的个人,考虑他们的需求、价值观和偏好,而不是仅仅关注医疗状况。这种方法可确保长期健康状况患者的日常生活达到最高水平,并增强他们的能力。个人周围的社区必须不断进行互动与合作。他们应共同努力,将人们的需求、价值观和偏好纳入未来的数字医疗服务中,从而促进赋权和自我管理。旨在培养注册护士数字医疗服务能力的新教育计划应促进这两个群体之间的合作。这种合作对于支持长期病患者的日常活动至关重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
JMIR Human Factors
JMIR Human Factors Medicine-Health Informatics
CiteScore
3.40
自引率
3.70%
发文量
123
审稿时长
12 weeks
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