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首页> 外文期刊>Palliative medicine >Effect of caregiving at end of life on grief, quality of life and general health: A prospective, longitudinal, comparative study
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Effect of caregiving at end of life on grief, quality of life and general health: A prospective, longitudinal, comparative study

机译:悲伤在生活结束时悲伤,生活质量和一般健康效果:前瞻性,纵向,比较研究

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Background: Determining the effect of caregiving and bereavement remains a challenge. To date, no study has employed a comparison group to investigate caregivers' grief, quality of life and general health in relation to non-caregivers. Aim: We aimed to determine how caregivers' grief, quality of life and general health changed following death compared to non-caregivers and whether pre-death grief predicted these outcomes. Design: A prospective, longitudinal study of family caregivers and a comparison group matched for age, gender and postcode was conducted. All participants completed questionnaires at four points - once pre-death and three times post-death (3-4 months, 6-7 months and 9-10 months). Setting/participants: Participants (N = 70) were family caregivers of persons receiving palliative care, mostly for cancer, recruited from three palliative care providers in Western Australia and matched comparisons recruited from advertisements. Results: There were significant differences between the caregivers' and comparisons' grief, general health and quality of life at pre-death, 3-4 months and 6-7 months post-death, but not at 9-10 months post-death. The rate of progression in these constructs following death was independent from the intensity of pre-death grief. However, caregiver prolonged grief score significantly predicted prolonged grief score at 6-7 and 9-10 months post-death. Conclusion: It took 9-10 months for the caregivers' grief, general health and quality of life to correspond to the comparison group. These findings present an opportunity for palliative care research and practice to consider how best to support the majority of caregivers without grief complications so that their pre- and post-death support needs are realised.
机译:背景:确定护理和丧亲丧失的效果仍然是一个挑战。迄今为止,没有研究聘用了一个比较小组来调查护理人员的悲伤,生活质量和与非照顾者有关的一般健康。目的:我们旨在确定与非照顾者相比,死亡人员如何悲伤,生活质量和一般健康状况如何发生变化,以及预防死亡悲伤是否预测了这些结果。设计:对家庭护理人员的前瞻性,纵向研究,与年龄,性别和邮政编码相匹配的比较组。所有参与者完成了四点的问卷 - 一旦死亡前和死后三次(3-4个月,6-7个月和9-10个月)。设定/参与者:参与者(n = 70)是接受姑息治疗的人的家庭照顾者,主要用于癌症,从西澳大利亚西澳大利亚的三个姑息治疗提供者招募,并征收广告的比较。结果:在死亡后3-4个月和6-7个月之前,护理人员与比较,生活质量和生活质量之间存在显着差异,死后3-4个月和6-7个月,但死后9-10个月。死亡后这些构建体中的进展率独立于死亡前悲伤的强度。然而,由于死后6-7和9-10个月,照顾者长期悲伤得分明显预测延长悲伤。结论:护理人员悲伤,一般健康和生活质量花费了9-10个月,以对应于比较组。这些调查结果为姑息治疗的研究和实践提供了一个姑息性的研究和实践,以考虑如何最好地支持大多数护理人员而没有悲伤并发症,以实现他们的前后和后期的支持需求。

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