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引用次数: 0
摘要
在一个高度制度化的死亡环境中,垂死的人如何在家中得到良好的护理?例如,台湾的卫生福利部(Ministry of Health and Welfare)推动了临终关怀家庭护理,并尊重病人的自主权,以提高临终体验的质量。然而,这项研究发现临终关怀不会自动个性化或赋予患者权力。本研究从照护实务的理论角度,强调家庭照护者无形工作对病患达成这些目标的重要性。通过深入访谈和在台湾北部一家医疗中心为期12个月的参与者观察,这项研究发现,家庭护理人员会细致地根据患者的病情提供护理,包括重新安排地点、协调资源和其他护理人员,以及实践护理。本文揭示了安宁疗护的实践不仅依赖于患者的自主权,还依赖于家庭照护者和医疗团队的工作,这在医疗保险制度中是相对不可见的。
Attuning to the Erratic End of Life: The Logic of Care in Hospice at Home
How do dying people receive good care at home in a highly institutionalized death context? The Ministry of Health and Welfare in Taiwan, for example, has promoted hospice home care and respecting patient autonomy to improve the quality of end-of-life experiences. However, this study finds that end-of-life care is not automatically personalized or empowering for patients. From the theoretical perspective of care practices, this study accentuates the importance of family carers’ invisible work in achieving these goals for patients. Drawing from in-depth interviews and twelve months of participant observation in a medical center in northern Taiwan, the study found that family caregivers are meticulously attuned to the patient’s condition to provide care, which includes rearranging the place, coordinating resources and other carers, and practicing care. This paper reveals that the practice of hospice home care does not depend merely on the patient’s autonomy but also on the family caregivers’ and medical team’s work, which is relatively invisible within the health insurance system.