为 1 型糖尿病青少年及其父母设计的共同决策糖尿病管理计划工具:原型开发和试点测试。

Q2 Medicine
Tamara S Hannon, Courtney M Moore, Erika R Cheng, Dustin O Lynch, Lisa G Yazel-Smith, Gina Em Claxton, Aaron E Carroll, Sarah E Wiehe
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引用次数: 0

摘要

背景:患有 1 型糖尿病的青少年很难达到最佳血糖控制效果,部分原因是相互竞争的优先事项干扰了糖尿病患者的自我护理。与糖尿病相关的家庭冲突经常发生,青少年对糖尿病管理的想法和感受可能被忽视。如果青少年能参与决策过程,以患者为中心的糖尿病治疗效果可能会更好:我们的研究目的是与青少年患者和家长咨询委员会共同设计一种诊所干预措施,利用共同决策来解决糖尿病自我护理问题:患者和家长咨询委员会由我院儿科糖尿病项目招募的 6 名 12 至 18 岁 1 型糖尿病青少年(青少年)及其家长组成。青少年和家长提供了知情同意书,并参加了患者和家长咨询委员会的两次会议中的一次或两次,每次会议持续 3 到 4 个小时。会议 1 的主题是:(1)与生活质量相关的以患者为中心的结果、家长与青少年共同管理糖尿病以及共同的家庭经历;(2)以患者为中心的糖尿病护理计划干预的实施和可接受性,其中使用了共同决策。我们分析了录音、笔记和其他资料,以确定和提取与制定以患者为中心的糖尿病管理计划相关的观点。这些数据被直观地编码成类似的主题。我们利用这些信息开发了糖尿病管理计划工具的原型,并在第二部分进行了试点测试:会议 1 确定了 6 个主要的以患者为中心的生活质量测量领域:压力、恐惧和担忧、进餐时间的挣扎、假设和判断、感觉不正常和冲突。我们确定了糖尿病管理计划干预的两个主要目标:(1) 将干预重点放在糖尿病困扰和冲突解决策略上;(2) 努力实现一个口头化的共同目标。在第二部分中,我们根据这些发现创建了糖尿病管理计划工具,并将其用于临床试验,目的是协助以患者为中心设定目标:结论:1 型糖尿病患者可以有效参与以患者为中心的研究设计。1 型糖尿病青少年患者在其人生的这个阶段,将减少家庭冲突和融入社会环境置于健康结果之上。在设计干预措施以改善 1 型糖尿病青少年患者的健康状况时,必须认识到这一点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Codesigned Shared Decision-Making Diabetes Management Plan Tool for Adolescents With Type 1 Diabetes Mellitus and Their Parents: Prototype Development and Pilot Test.

Codesigned Shared Decision-Making Diabetes Management Plan Tool for Adolescents With Type 1 Diabetes Mellitus and Their Parents: Prototype Development and Pilot Test.

Background: Adolescents with type 1 diabetes mellitus have difficulty achieving optimal glycemic control, partly due to competing priorities that interfere with diabetes self-care. Often, significant diabetes-related family conflict occurs, and adolescents' thoughts and feelings about diabetes management may be disregarded. Patient-centered diabetes outcomes may be better when adolescents feel engaged in the decision-making process.

Objective: The objective of our study was to codesign a clinic intervention using shared decision making for addressing diabetes self-care with an adolescent patient and parent advisory board.

Methods: The patient and parent advisory board consisted of 6 adolescents (teens) between the ages 12 and 18 years with type 1 diabetes mellitus and their parents recruited through our institution's Pediatric Diabetes Program. Teens and parents provided informed consent and participated in 1 or both of 2 patient and parent advisory board sessions, lasting 3 to 4 hours each. Session 1 topics were (1) patient-centered outcomes related to quality of life, parent-teen shared diabetes management, and shared family experiences; and (2) implementation and acceptability of a patient-centered diabetes care plan intervention where shared decision making was used. We analyzed audio recordings, notes, and other materials to identify and extract ideas relevant to the development of a patient-centered diabetes management plan. These data were visually coded into similar themes. We used the information to develop a prototype for a diabetes management plan tool that we pilot tested during session 2.

Results: Session 1 identified 6 principal patient-centered quality-of-life measurement domains: stress, fear and worry, mealtime struggles, assumptions and judgments, feeling abnormal, and conflict. We determined 2 objectives to be principally important for a diabetes management plan intervention: (1) focusing the intervention on diabetes distress and conflict resolution strategies, and (2) working toward a verbalized common goal. In session 2, we created the diabetes management plan tool according to these findings and will use it in a clinical trial with the aim of assisting with patient-centered goal setting.

Conclusions: Patients with type 1 diabetes mellitus can be effectively engaged and involved in patient-centered research design. Teens with type 1 diabetes mellitus prioritize reducing family conflict and fitting into their social milieu over health outcomes at this time in their lives. It is important to acknowledge this when designing interventions to improve health outcomes in teens with type 1 diabetes mellitus.

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来源期刊
Journal of Participatory Medicine
Journal of Participatory Medicine Medicine-Medicine (miscellaneous)
CiteScore
3.20
自引率
0.00%
发文量
8
审稿时长
12 weeks
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