首页> 外文期刊>International Journal of Integrated Care >What is important to people with multimorbidity and their caregivers? Identifying attributes of person centred primary health care from the user perspective
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What is important to people with multimorbidity and their caregivers? Identifying attributes of person centred primary health care from the user perspective

机译:对于多发病的人及其照料者重要的是什么?从用户角度识别以人为本的基本医疗保健的属性

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Introduction : Health systems worldwide are striving to provide care that is ‘person centred’—aligned with the needs and values of those receiving it. Partnerships and linkages between care settings such as primary care and the community sector (i.e., community based primary health care) has the goal of enabling better care and outcomes for people. It is unclear; however, if within these models, patients and caregivers perceive their care to be person-centered. In this study we capture what matters most to people with complex care needs and their caregivers (i.e., outcomes of importance) and second, we outline the conditions and activities associated with these outcomes. Methods : This is a qualitative descriptive study entailing one-to-one interviews with older adults with complex care needs receiving CBPHC in Ontario, Quebec and New Zealand and caregivers of these types of patients. The data were analyzed using inductive and deductive approaches by four researchers. Core categories were identified from the interviews, each representing an outcome of importance. Results : The majority of patients were female, 65+, with an average of 5 health conditions. A proportion spoke English as their second language. The majority of caregivers were female, a family member or partner of the patient and living in the same household. The outcomes of importance were: feeling heard, appreciated and comfortable; having someone to count on; understanding how to manage health and what to expect; being independent; feeling safe; and easily accessing health and social care. There were a number of activities associated with each outcome including (and not limited to): being treated like a friend; having the contact information of a dedicated and responsive provider; being given clear explanations of different treatment options and why these treatment options were being recommended; having the opportunity to partake in meaningful hobbies; having homes adapted to support physical limitations; and being accompanied to activities (ranging from doctors’ appointments to grocery shopping). Discussion : Through a large international collection of interviews of culturally diverse patients with multi-morbidity and their caregivers, we outline what person centered care means to people as well as specific activities that support these outcomes. Conclusion (w/ key findings) : The importance of comfortable and reliable relationships, being independent, having access to social care resources and the trade-offs that patients and caregivers make as their needs change need to be considered as health care systems seek to better coordinate and integrate care for vulnerable populations and their families. Lessons Learned : Key attributes of good care extend beyond the management of disease. While we focused on the experience of patients and caregivers receiving CBPHC, their experiences extended to other sectors and providers because not all care was available within the models studied. Limitations : We did not conduct a comparative analysis of attributes (e.g., ethnicities, geographies, etc.) which would help to answer important implementation questions including, what works for whom and in what conditions? Suggestions for Future Research : Examining how key attributes vary by sub-groups will provide insight into how to further tailor models of community base d primary health care.
机译:简介:全世界的卫生系统都在努力提供“以人为本”的护理,以与接受该护理的人的需求和价值相一致。诸如初级保健和社区部门(即基于社区的初级保健)等医疗机构之间的伙伴关系和联系的目标是为人们提供更好的护理和结果。目前尚不清楚;但是,如果在这些模型中,患者和护理人员会认为他们的护理以人为本。在这项研究中,我们捕获了对具有复杂护理需求的人及其护理人员(即重要结果)最重要的问题,其次,我们概述了与这些结果相关的条件和活动。方法:这是一项定性描述性研究,需要在安大略省,魁北克省和新西兰对有复杂护理需求的老年人进行CBPHC进行一对一访谈,并对这类患者的护理人员进行访谈。四个研究人员使用归纳和演绎方法对数据进行了分析。从访谈中确定了核心类别,每个类别都代表了重要的结果。结果:大多数患者为65岁以上的女性,平均5种健康状况。一部分人说英语作为第二语言。大多数护理人员是女性,患者的家庭成员或伴侣,并住在同一家庭。重要的结果是:感到被聆听,欣赏和舒适;有人指望了解如何管理健康以及期望什么;独立;觉得安全;并轻松获得健康和社会护理。每个结局都有许多活动,包括(但不限于):像朋友一样被对待;具有专门的响应提供商的联系信息;被明确解释了不同的治疗方案,以及为什么推荐这些治疗方案;有机会参加有意义的爱好;拥有适应身体限制的住房;并参加各种活动(从医生的约会到杂货店购物)。讨论:通过大量的国际访谈,访谈了文化多元的多发病患者及其护理人员,我们概述了以人为中心的护理对人们的意义以及支持这些结果的特定活动。结论(有关键发现):建立舒适,可靠的关系,保持独立,能够获得社会护理资源以及患者和护理人员根据需求变化做出的取舍的重要性,需要在医疗体系寻求更好的基础上加以考虑协调和整合对弱势人群及其家庭的照顾。经验教训:良好护理的关键特性超出了疾病的管理范围。尽管我们专注于接受CBPHC的患者和护理人员的经验,但他们的经验扩展到其他部门和提供者,因为在研究的模型中并非所有护理都可用。局限性:我们没有对属性(例如种族,地域等)进行比较分析,这有助于回答重要的实施问题,包括哪些对谁有效以及在什么条件下起作用?未来研究的建议:研究各子组的关键属性如何变化将提供有关如何进一步定制社区基础初级保健模型的见识。

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