Davoody Nadia, Koch Sabine, Krakau Ingvar, Hägglund Maria
Health Informatics Centre, Department of Learning, Informatics, Management and Ethics, Karolinska Institutet, Stockholm, Sweden.
Health Informatics Centre, Department of Learning, Informatics, Management and Ethics. Karolinska Institutet, Stockholm, Sweden.
Int J Integr Care. 2014 Nov 6;14:e032. doi: 10.5334/ijic.1549. eCollection 2014 Oct.
Lack of appropriate electronic tools for supporting patient involvement and collaboration with care professionals is a problem in health care.
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.
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.
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.
在医疗保健领域,缺乏适当的电子工具来支持患者参与并与护理专业人员协作是一个问题。
运用互动点的概念对出院后中风患者的护理和康复过程进行分析,患者、近亲与护理专业人员在这些互动点进行互动和信息交流。对护理专业人员进行了13次访谈,并进行了5次非参与性观察。使用内容分析法和患者就医过程中互动点的建模对数据进行分析。
患者的参与和互动模式各不相同;需要居家护理的患者处于被动角色,近亲或护士通过代表患者协调护理成为倡导者,而能够前往初级护理机构的患者则通过发起互动来协调自己的护理。重要的参与类别包括:参与护理计划、监测危险因素和康复计划。
设计一种支持性电子工具需要了解每个互动点的互动情况和患者的活动水平。对于活动水平较高的患者群体,工具应支持他们协调自己的护理,而对于活动较少的患者群体,工具可以侧重于支持近亲与护理专业人员激励、引导被动患者参与其护理和康复过程并将他们纳入其中。