a National Research Center in Complementary and Alternative Medicine, Department of Community Medicine , Faculty of Health Sciences, UiT The Arctic University of Norway , Tromsø , Norway.
b Primary care research group, Department of Community Medicine , Faculty of Health Sciences, UiT The Arctic University of Norway , Tromsø , Norway.
Int J Qual Stud Health Well-being. 2018 Dec;13(1):1548240. doi: 10.1080/17482631.2018.1548240.
Person-centred care (PCC) is a well-acknowledged goal throughout the western world both within the health care services sector and for the patients themselves. To be able to create a future health care system that includes improved PCC, we need more in-depth knowledge of what matters to patients, how "what matters" might change over time, and tentative descriptions of commonalities across patients' perspectives. The aim of this study is to contribute to this knowledge base.
We conducted a qualitative interview series over one year with nine Norwegian patients who were recently diagnosed with rectal cancer tumor-node-metastasis stage I-III.
We found that: (1) patients have an initial focus on "biological goals" and conventional treatment; (2) pathways are unique and dynamic; (3) family and friends affected patient pathways positively with respect to meaningfulness and quality of life, but for some participants also negatively because there were heavy burdens of caretaking; (4) receiving help in the health care system depended on the patients' navigation skills; (5) pluralism in health-seeking behaviour was important in all patient pathways.
Long lasting illness may be a dynamic and complex journey. These results represent some features of a pathway with cancer and are important because they contribute with knowledge about what matters most seen from the cancer patients' point of view.
以人为本的护理(PCC)在整个西方世界的医疗保健服务部门和患者自身中都得到了广泛认可。为了能够创建一个包含改进的 PCC 的未来医疗保健系统,我们需要更深入地了解患者关心的问题、“重要的事情”如何随时间而变化,以及对患者观点之间的共性进行初步描述。本研究旨在为此知识库做出贡献。
我们在一年的时间里对 9 名最近被诊断患有直肠肿瘤肿瘤-淋巴结-转移 I-III 期的挪威患者进行了一系列定性访谈。
我们发现:(1)患者最初关注“生物目标”和常规治疗;(2)途径是独特且动态的;(3)家庭和朋友对患者的生活意义和生活质量产生了积极影响,但对一些参与者也产生了负面影响,因为存在沉重的照顾负担;(4)在医疗保健系统中获得帮助取决于患者的导航技能;(5)在所有患者的求医行为中,多元化是很重要的。
长期患病可能是一个动态和复杂的过程。这些结果代表了癌症患者路径的一些特征,这很重要,因为它们提供了从癌症患者角度来看最重要的信息。