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What happens when you involve patients as experts? a participatory action research project at a renal failure unit.

机译:当您让患者作为专家时会发生什么?肾衰竭单元的一项参与式行动研究项目。

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Although there is a trend towards developing health care in a patient-centred direction, changes are usually planned by the professionals without involving the patients. This paper presents an ongoing participatory action research project where patients with chronic renal failure, nurses at a specialist renal failure unit, a hospital manager and a researcher worked together to develop patient-centred care. The project combined the expertise of patients in their own experiences of living with a chronic condition with the professional expertise of nurses, the manager and the researcher. As the workload on the unit was uneven, the development work needed to be low in intensity but long-term. Based on a number of dialogues in focus groups, four main development areas were identified; access to test results, prerequisites for postponing the progress of the illness, general awareness and understanding of living with chronic renal failure, and family-focused care. A number of changes have been planned or implemented, such as developing a prototype for a web-based feed-back system, expanding patient education to newly diagnosed patients, steering the nurses' role towards a guiding and family-focused function, and planning a digital story-telling workshop. Involving committed people who have the mandate to change practices were prerequisites for success.
机译:尽管有朝着以患者为中心的方向发展医疗保健的趋势,但是专业人员通常计划在不让患者参与的情况下进行变更。本文提出了一个正在进行的参与性行动研究项目,其中慢性肾功能衰竭患者,专业肾衰竭单位的护士,医院经理和研究人员共同开发了以患者为中心的护理。该项目将患者在慢性病生活中的专业知识与护士,经理和研究人员的专业知识相结合。由于该单元的工作量不均衡,因此开发工作的强度应较低,但需要长期进行。根据焦点小组的一系列对话,确定了四个主要的发展领域。获得测试结果,推迟疾病进展的前提条件,对慢性肾衰竭患者的一般认识和了解以及以家庭为中心的护理。已经计划或实施了许多更改,例如为基于Web的反馈系统开发原型,将患者教育范围扩大到新诊断的患者,将护士的角色引导到以家庭为中心的指导功能以及计划一个数字故事讲习班。让有责任改变实践的忠诚人士参与是成功的前提。

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