Nottingham University Business School, Nottingham, UK.
Health Expect. 2021 Apr;24(2):628-637. doi: 10.1111/hex.13209. Epub 2021 Feb 6.
Increased self-management is a suggested solution to the burden on health-care services of long-term conditions (LTCs). This requires effective sharing of knowledge between health-care professionals and patients, and is an underexplored area.
To understand how patients and health-care professionals (HCPs) share and utilize knowledge in the social context of health-care interactions within long-term condition management.
Thematic analysis of 93 hours of observations of health-care interactions and 33 semi-structured interviews involving patients, carers and HCPs.
3 themes were identified: normative social roles, differing professional roles and the value of knowledge. Knowledge sharing was a complex process heavily influenced by social and cultural norms within the health-care context. Not all knowledge was easily shared within routine health-care interactions.
The social context in which health-care is practised influences what knowledge is shared and how this is achieved. It favours sharing of clinical knowledge from HCPs to patients and disadvantages patients in their ability to share their unique knowledge based on lived experience of illness. The opportunities for patients to be supported in their knowledge, skills and confidence within routine health-care interactions are limited.
Both patients and HCPs need support to recognize the characteristics of the social context of health care and their understandings of their roles within this in order for them to move beyond accepted behaviours to develop more effective partnership working.
Patients were involved in initial design of the study, particularly ethics of ethnographic observation.
增加自我管理是解决长期疾病(LTCs)对医疗服务负担的一种建议方案。这需要医护人员和患者之间有效共享知识,而这是一个尚未充分探索的领域。
了解患者和医疗保健专业人员(HCPs)如何在长期疾病管理的医疗保健互动的社会背景下共享和利用知识。
对 93 小时的医疗保健互动观察和 33 次半结构化访谈进行主题分析,涉及患者、护理人员和 HCPs。
确定了 3 个主题:规范的社会角色、不同的专业角色和知识的价值。知识共享是一个复杂的过程,受到医疗保健环境中社会和文化规范的严重影响。并非所有知识都能在常规医疗保健互动中轻松共享。
医疗保健实践的社会背景影响着共享哪些知识以及如何实现这一目标。它有利于 HCP 向患者共享临床知识,而不利于患者根据疾病的亲身经历来分享他们独特的知识。患者在常规医疗保健互动中获得知识、技能和信心支持的机会有限。
患者和 HCPs 都需要支持,以认识到医疗保健社会背景的特点及其对自身角色的理解,以便他们超越可接受的行为,发展更有效的合作工作。
患者参与了研究的最初设计,特别是人种学观察的伦理学。