Authors Affiliations: School of Health and Caring Sciences, Faculty of Health and Life Sciences, Linnaeus University, Kalmar (Drs Schildmeijer and Ekstedt); and Department of Learning, Informatics, Management, and Ethics, Karolinska Institutet, Stockholm (Drs Frykholm and Ekstedt); Department of Health Care Sciences, Ersta Sköndal University, Stockholm (Dr Kneck), Sweden.
Cancer Nurs. 2019 Jan/Feb;42(1):E36-E43. doi: 10.1097/NCC.0000000000000559.
Cancer and its treatment can severely impact quality of life, giving rise to complex needs with respect to follow-up care. To support patient needs and increase efficiency of care with limited resources, the Swedish government has launched national reforms to redesign cancer care pathways.
The aim of this study was to explore how prostate cancer patients experience their journey through the healthcare system when their care is provided according to the standardized care pathway, as described in healthcare policy documents.
A qualitative, descriptive approach with individual interviews was used. A template of a standardized prostate cancer pathway, created together with healthcare professionals, was used during interviews. Fourteen interviews were conducted with prostate cancer patients all operated on at a midsized hospital in southeast Sweden between October 2015 and April 2016. The interviews were analyzed with qualitative content analysis and illustrated in a patient journey map.
We identified an overall theme, "walking a tightrope," consisting of 4 categories: "waiting," "becoming familiar with a troublesome body," "adjusting to a different life," and "information challenges."
The clinical implementation of the standardized care pathway is described as a straight path through care, but patients described their experiences as walking a tightrope. Lack of information, especially about cancer treatment and its adverse effects, was the most common experience.
Our findings indicate areas where further healthcare tools could improve patient experiences of cancer treatment. This could include offering individualized information and tools to increase patient empowerment, as well as patient/caregiver collaboration (co-care).
癌症及其治疗会严重影响生活质量,引发对后续护理的复杂需求。为了满足患者的需求并在资源有限的情况下提高护理效率,瑞典政府启动了国家改革,重新设计癌症护理路径。
本研究旨在探讨当患者按照医疗政策文件中描述的标准化护理路径接受护理时,他们如何体验整个医疗系统之旅。
采用个体访谈的定性描述方法。使用与医疗保健专业人员共同创建的标准化前列腺癌路径模板进行访谈。2015 年 10 月至 2016 年 4 月,在瑞典东南部的一家中型医院对 14 名前列腺癌患者进行了访谈。访谈采用定性内容分析法进行分析,并以患者旅程图进行说明。
我们确定了一个总体主题,“走钢丝”,由 4 个类别组成:“等待”、“熟悉有问题的身体”、“适应不同的生活”和“信息挑战”。
标准化护理路径的临床实施被描述为一条贯穿护理的直线路径,但患者描述他们的经历是走钢丝。缺乏信息,特别是关于癌症治疗及其不良反应的信息,是最常见的经历。
我们的发现表明,在某些领域需要进一步的医疗工具来改善患者对癌症治疗的体验。这可能包括提供个性化的信息和工具来增强患者的权能,以及患者/护理人员的合作(共同护理)。