使用参与式设计调查和支持复杂医疗决策中的患者和护理人员感知。

IF 1.9 Q3 HEALTH CARE SCIENCES & SERVICES MDM Policy and Practice Pub Date : 2023-01-01 DOI:10.1177/23814683231164988
Sarah Fadem
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引用次数: 0

摘要

背景。面对复杂健康决策的患者和护理人员必须理解不熟悉的、情感上具有挑战性的信息和经历。对于恶性血液病患者,骨髓移植(BMT)可能是治愈的最佳机会,但有显著的发病率和死亡率风险。本研究旨在调查和支持患者和护理人员在考虑BMT时的意义生成。方法。10名BMT患者和5名护理人员参与了远程参与式设计(PD)研讨会。参与者绘制了他们在BMT之前的难忘经历的时间表。然后,他们用透明纸标注他们的时间表,并设计改进这一过程。结果。对图纸和抄本的专题分析揭示了一个三阶段的意义生成过程。在第一阶段,参与者被介绍给BMT,并将其理解为一种可能性,而不是不可避免的。在第二阶段,他们专注于满足先决条件,包括缓解和捐赠者识别。参与者开始相信他们需要移植,因此将BMT描述为不是在可行的选择之间的决定,而是移植是他们生存的“唯一机会”。在第三阶段,参与者参加了一个详细介绍移植风险的培训,导致焦虑和怀疑。参与者设计了解决方案,为那些正在努力应对移植改变生活影响的人提供了保证。结论。对于患者和护理人员来说,做出复杂的健康决定是一个动态的、持续的过程,它会影响期望和情感健康。以保证和风险信息为目标的干预措施可以减轻情绪影响,促进期望的发展。PD和语义生成方法的整合使参与者能够创建整体的、有形的经验表示,同时授权利益相关者参与干预设计。这种方法可以应用于其他复杂的医疗环境,以了解生活经验和制定有效的支持干预措施。重点:骨髓移植患者和护理人员经历了一个不断发展的,情感上具有挑战性的过程,逐渐了解移植程序及其风险。参与者设计的解决方案以提供安心和风险信息为中心,表明未来的干预措施可以针对情感支持,因为患者试图满足先决条件,并努力应对潜在治疗过程的风险。通过观察复杂医疗决策在意义构建方面的挑战,并应用参与式设计等视觉方法,研究人员可以促进动态的、多方面的、情感的体验成分的表达,并授权利益相关者参与干预设计。
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Investigating and Supporting Patient and Caregiver Sensemaking in Complex Medical Decisions Using Participatory Design.

Background. Patients and caregivers facing complex health decisions must make sense of unfamiliar, emotionally challenging information and experiences. For patients with hematological malignancy, bone marrow transplant (BMT) may be the best chance for a cure but has significant risk of morbidity and mortality. This study aimed to investigate and support patient and caregiver sensemaking as they consider BMT. Methods. Ten BMT patients and 5 caregivers engaged in remote participatory design (PD) workshops. Participants drew timelines of their memorable experiences leading up to BMT. Then, they used transparency paper to annotate their timelines and design improvements to this process. Results. Thematic analysis of drawings and transcripts revealed a 3-phase sensemaking process. In phase 1, participants were introduced to BMT and understood it as a possibility, not an inevitability. In phase 2, they focused on meeting prerequisites including remission and donor identification. Participants came to believe they needed transplant, consequently describing BMT not as a decision between viable options, but that transplant was their "only chance" for survival. In phase 3, participants attended an orientation detailing the extensive risks of transplant, leading to anxiety and doubt. Participants designed solutions that provided reassurance to those grappling with the life-altering impacts of transplant. Conclusions. For patients and caregivers navigating complex health decisions, sensemaking is a dynamic, ongoing process that affects expectations and emotional well-being. Interventions targeting reassurance alongside risk information can alleviate emotional impact and facilitate expectation development. The integration of PD and sensemaking methodologies enables participants to create holistic, tangible representations of experiences while empowering stakeholder engagement in intervention design. This method could be applied to other complex medical contexts to understand lived experiences and develop effective support interventions.

Highlights: Bone marrow transplant patients and caregivers experienced an evolving, emotionally challenging process of gradually understanding the transplant procedure and its risks.The solutions that participants designed centered on providing reassurance alongside risk information, suggesting future interventions could target emotional support as patients attempt to meet prerequisites and grapple with the risks of the potentially curative procedure.By viewing the challenges of complex medical decisions in terms of sensemaking and applying visual methods such as participatory design, researchers can facilitate expression of the dynamic, multifaceted, emotional components of experience and empower stakeholder involvement in intervention design.

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来源期刊
MDM Policy and Practice
MDM Policy and Practice Medicine-Health Policy
CiteScore
2.50
自引率
0.00%
发文量
28
审稿时长
15 weeks
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