The Moral Dimensions of Family Caregiving for Patients with Advanced Cancer: A Qualitative Study

IF 1.8 4区 医学 Q3 HEALTH CARE SCIENCES & SERVICES
Aline Sarradon-Eck, Aurelia Mathiot, Seth M. Holmes, Elise Gilbert, Géraldine Capodano, Aurélien Proux
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Abstract

Background. Family caregivers in charge of patients with advanced cancer play an essential role. The psychosocial cost of these caregiving activities has been studied, and psychosocial interventions have been developed to improve the quality of life of family caregivers. A deeper understanding of caregivers’ burden is essential in order to enhance the benefits of these interventions. The aim of this study was to explore the socioeconomic and cultural factors responsible for shaping the complex personal experience of family caregiving and to analyse the moral dimensions of the caring experience so as to understand its effects on family caregivers more clearly. Materials and Methods. A qualitative study based on in-depth interviews was conducted with patients with advanced cancer (n = 20) and their family caregivers (n = 19) from 2017 to 2020. These interviews were analysed using an inductive approach and an iterative procedure. A thematic analysis was then performed using Tronto’s “ethic of care” framework in order to identify the various levels of responsibility and the relationships and effects involved. Results. Providing patients with advanced cancer with informal care is highly valuable work requiring various moral qualities, including attentiveness, responsibility, competence, and responsiveness. The mental load resulting from the moral aspects of care results from the cumulative effects of carers’ attentiveness and the responsibilities they have taken on. Conclusion. The present findings could guide healthcare professionals to develop best practice resources and guidelines in order to alleviate the hitherto underestimated effects of caring and promote a coordinated public health approach addressing the needs of caregivers. These efforts are particularly important as contemporary health policies tend to promote the shift from inpatient to outpatient treatment, which increases the importance of informal caregiving and the burden involved.
晚期癌症患者家庭照顾的道德维度:一项质性研究
背景。负责晚期癌症患者的家庭照顾者发挥着至关重要的作用。已经研究了这些照料活动的社会心理成本,并开发了社会心理干预措施来改善家庭照料者的生活质量。为了提高这些干预措施的效益,更深入地了解护理人员的负担至关重要。本研究的目的是探讨社会经济和文化因素负责塑造复杂的个人家庭照顾经验,并分析照顾经验的道德维度,以便更清楚地了解其对家庭照顾者的影响。材料与方法。通过深度访谈对2017 - 2020年晚期癌症患者(n = 20)及其家庭照顾者(n = 19)进行定性研究。使用归纳方法和迭代程序对这些访谈进行分析。然后使用Tronto的“关怀伦理”框架进行专题分析,以确定责任的各个层面以及所涉及的关系和影响。结果。为晚期癌症患者提供非正式护理是一项非常有价值的工作,需要各种道德品质,包括关注、责任、能力和反应能力。由于照顾者的道德方面而产生的心理负担是由于照顾者的注意力和他们所承担的责任的累积效应造成的。结论。本研究结果可以指导医疗保健专业人员开发最佳实践资源和指南,以减轻迄今为止被低估的护理效果,并促进协调一致的公共卫生方法,解决照顾者的需求。这些努力尤其重要,因为当代卫生政策倾向于促进从住院治疗转向门诊治疗,这增加了非正式护理的重要性和所涉及的负担。
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来源期刊
European Journal of Cancer Care
European Journal of Cancer Care 医学-康复医学
CiteScore
4.00
自引率
4.80%
发文量
213
审稿时长
3 months
期刊介绍: The European Journal of Cancer Care aims to encourage comprehensive, multiprofessional cancer care across Europe and internationally. It publishes original research reports, literature reviews, guest editorials, letters to the Editor and special features on current issues affecting the care of cancer patients. The Editor welcomes contributions which result from team working or collaboration between different health and social care providers, service users, patient groups and the voluntary sector in the areas of: - Primary, secondary and tertiary care for cancer patients - Multidisciplinary and service-user involvement in cancer care - Rehabilitation, supportive, palliative and end of life care for cancer patients - Policy, service development and healthcare evaluation in cancer care - Psychosocial interventions for patients and family members - International perspectives on cancer care
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