Department of Nursing, Brock University, St. Catharines, Canada.
College of Nursing, University of Manitoba, Winnipeg, Canada.
BMC Psychiatry. 2018 Sep 24;18(1):307. doi: 10.1186/s12888-018-1882-9.
Most persons with dementia die in long term care (LTC) homes, where palliative approaches are appropriate. However, palliative approaches have not been widely implemented and there is limited understanding of staff and family experiences of dying and bereavement in this context.
This descriptive qualitative study explored family and staff experiences of end of life and end of life care for persons with dementia in LTC homes. Eighteen focus groups were conducted with 77 staff members and 19 relatives of persons with dementia at four LTC homes in four Canadian provinces.
Three themes emerged: knowing the resident, the understanding that they are all human beings, and the long slow decline and death of residents with dementia.
Intimate knowledge of the person with dementia, obtained through longstanding relationships, was foundational for person-centred end of life care. Health care aides need to be included in end of life care planning to take advantage of their knowledge of residents with dementia. There were unmet bereavement support needs among staff, particularly health care aides. Persons with dementia were affected by death around them and existing rituals for marking deaths in LTC homes may not fit their needs. Staff were uncomfortable answering relatives' questions about end of life.
Longstanding intimate relationships enhanced end of life care but left health care aides with unmet bereavement support needs. Staff in LTC homes should be supported to answer questions about the trajectory of decline of dementia and death. Further research about residents' experiences of deaths of other residents is needed.
大多数痴呆症患者都在长期护理(LTC)院死亡,姑息治疗方法在这些地方是合适的。然而,姑息治疗方法尚未广泛实施,并且对于在这种情况下工作人员和家属的临终和丧亲体验知之甚少。
本描述性定性研究探讨了长期护理院中痴呆症患者的临终和临终关怀的家属和工作人员的经验。在加拿大四个省的四个长期护理院进行了 18 个焦点小组,共有 77 名工作人员和 19 名痴呆症患者的家属参加。
出现了三个主题:了解居民,认识到他们都是人类,以及痴呆症居民的长期缓慢衰退和死亡。
通过长期的关系而获得的对痴呆症患者的深入了解,是以人为本的临终关怀的基础。需要将医疗保健助手纳入临终关怀计划,以利用他们对痴呆症患者的了解。工作人员存在未满足的丧亲支持需求,尤其是医疗保健助手。痴呆症患者受到周围死亡的影响,长期护理院中现有的死亡标记仪式可能不符合他们的需求。工作人员对回答家属关于临终的问题感到不舒服。
长期的亲密关系增强了临终关怀,但使医疗保健助手的丧亲支持需求未得到满足。应支持长期护理院的工作人员回答有关痴呆症和死亡轨迹的问题。需要进一步研究其他居民的死亡经历。