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Collaborative interaction points in post-discharge stroke care

机译:出院后中风护理中的协作互动点

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Introduction: Lack of appropriate electronic tools for supporting patient involvement and collaboration with care professionals is a problem in health care. Methods: Care and rehabilitation processes of post-discharge stroke patients were analysed using the concept of interaction points where patients, next-of-kin and care professionals interact and exchange information. Thirteen interviews with care professionals and five non-participatory observations were performed. Data were analysed using content analysis and modelling of interaction points in the patient journey. Results: Patient participation and interaction patterns vary; patients requiring home care have a passive role and next-of-kin or nurses become advocates by coordinating care on behalf of the patient, whereas patients who are able to visit primary care coordinate their own care by initiating interactions. Important categories of participation include the following: participation in care planning, in monitoring risk factors and in rehabilitation planning. Conclusions: Designing a supportive electronic tool requires understanding the interactions and patients’ activity levels at each interaction point. A tool for patients with higher activity level should support them to coordinate their own care, whereas for a less-active patient group, the tool could focus on supporting next-of-kin and care professionals in motivating, guiding and including passive patients in their care and rehabilitation processes.
机译:简介:缺乏适当的电子工具来支持患者参与和与护理专业人员的合作是医疗保健中的一个问题。方法:使用患者,近亲和护理专业人员进行互动和交换信息的互动点的概念,对出院后中风患者的护理和康复过程进行了分析。对护理专业人员进行了13次访谈和5次非参与性观察。使用内容分析和对患者旅程中的交互点进行建模来分析数据。结果:患者的参与和互动方式各不相同;需要家庭护理的患者扮演着被动的角色,而近亲或护士则通过代表患者协调护理而成为拥护者,而能够访问初级护理的患者则通过互动来协调自己的护理。参与的重要类别包括:参与护理计划,监测危险因素和康复计划。结论:设计支持性电子工具需要了解每个交互点的交互作用和患者的活动水平。活动水平较高的患者的工具应支持他们协调自己的护理,而活动较少的患者群体的工具应侧重于支持近亲和护理专业人员在他们的动机,指导和包括被动患者方面提供支持。护理和康复过程。

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