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Bereavement Care最新文献

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The M Word M字
Q3 Nursing Pub Date : 2020-01-02 DOI: 10.1080/02682621.2020.1728161
M. Higgins
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引用次数: 0
Diversity challenges from urban West Africa: How Senegalese family deaths illuminate dominant understandings of ‘bereavement’ 西非城市面临的多样性挑战:塞内加尔家庭死亡如何阐明对“丧亲之痛”的主流理解
Q3 Nursing Pub Date : 2019-09-02 DOI: 10.1080/02682621.2019.1679468
J. McCarthy, R. Evans, S. Bowlby
ABSTRACT Based on interviews with Senegalese people living in four contemporary urban neighbourhoods, who had experienced the death of an adult family member, we explore how the research challenged and surprised the White, British members of the research team. Such challenges help to shed light on some dominant, taken-for-granted understandings of ‘bereavement’ based in ‘Western’ perspectives. The surprises include how the death was discussed and explained; patterns of family living and the implications for how individuals responded to the death; the emotional significance of particular religious expectations; and the emotional implications of material hardships. After exploring how interviewees responded to the deaths in Senegal, we consider how these responses compare with expectations and taken-for-granted assumptions about ‘bereavement’ in the contemporary UK. We conclude by discussing the implications for bereavement support and professional practice, in relation to diverse responses to death.
基于对生活在四个当代城市社区的塞内加尔人的采访,我们探讨了这项研究如何挑战和惊讶于研究团队的英国白人成员。这些挑战有助于揭示基于“西方”视角的对“丧亲”的一些主流的、理所当然的理解。这些惊喜包括如何讨论和解释死亡;家庭生活模式及其对个人如何应对死亡的影响;特殊宗教期望的情感意义;以及物质困难的情感暗示。在探索了受访者对塞内加尔死亡的反应之后,我们考虑了这些反应如何与当代英国对“丧亲之痛”的期望和想当然的假设进行比较。最后,我们讨论了与死亡的不同反应有关的丧亲支持和专业实践的影响。
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引用次数: 4
Editorial 编辑
Q3 Nursing Pub Date : 2019-09-02 DOI: 10.1080/02682621.2019.1679485
C. M. Parkes
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引用次数: 0
UK childhood bereavement services: A reflection on their development and cultural influence 英国儿童丧亲服务的发展及其文化影响
Q3 Nursing Pub Date : 2019-09-02 DOI: 10.1080/02682621.2019.1679483
L. Rolls
Abstract Childhood bereavement services are a relatively recent form of child welfare provision in the UK. They are predicated on assumptions about the development of children and on an increasing research base that describes the potential impact of childhood bereavement and that support following bereavement is beneficial. UK services largely began as a result of practitioners responding to the needs of bereaved children. Over time, services have become more formalised into an organisational framework, contributing to and influenced by practice based experience, research and training. They have become more sophisticated and wide-ranging in their response to the needs of bereaved children for which there is evidence of a favourable impact on their wellbeing. More importantly, as a structural form of provision now embedded within the UK’s health and social landscape, childhood bereavement services have had a significant impact on social policy and the wider cultural discourse concerning bereaved children.
儿童丧亲服务是英国儿童福利提供的一种相对较新的形式。它们是基于对儿童发展的假设和越来越多的研究基础,这些研究描述了童年丧亲之痛的潜在影响,以及丧亲之痛后的支持是有益的。英国的服务很大程度上是由于从业者对失去亲人的儿童的需求作出反应而开始的。随着时间的推移,服务已经变得更加形式化,成为一个组织框架,为基于实践的经验、研究和培训做出贡献并受到其影响。在对失去亲人的儿童的需要作出反应方面,它们已变得更加复杂和广泛,有证据表明,这对他们的福祉产生了有利的影响。更重要的是,作为一种结构性的提供形式,儿童丧亲服务现已融入联合王国的健康和社会格局,对社会政策和有关丧亲儿童的更广泛的文化话语产生了重大影响。
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引用次数: 0
Do the Welsh have it? Evaluating a bereavement support service supporting people bereaved by dementia 威尔士人有吗?评估为痴呆症患者提供的丧亲支持服务
Q3 Nursing Pub Date : 2019-09-02 DOI: 10.1080/02682621.2019.1679481
Caity Roleston, K. West, R. Shaw
Abstract Accumulating evidence suggests that a dementia diagnosis, for many, triggers feelings of grief, and often marks the first of many losses that will be experienced by both the person who has received the diagnosis and their loved ones, as the disease progresses. Previous research has also revealed that carers who report higher levels of pre-death grief are at greater risk of complicated grief after their loved one has died. Despite this evidence, appropriate bereavement support for people bereaved by dementia is a significant unmet need. The Bereaved by Dementia project was delivered collaboratively by Cruse Cymru and Alzheimer’s Cymru to address the bereavement needs of people bereaved by dementia throughout Wales. This paper draws on an independent evaluation of the Bereaved by Dementia Project conducted by Aston University and the University of Bristol. We summarise our main findings, recommendations, and suggestions for future research.
摘要越来越多的证据表明,对许多人来说,痴呆症的诊断会引发悲伤,并且往往标志着随着疾病的发展,接受诊断的人和他们的亲人将经历的许多损失中的第一个。先前的研究还表明,报告死亡前悲伤程度较高的护理人员在亲人去世后发生复杂悲伤的风险更大。尽管有这些证据,但为痴呆症患者提供适当的丧亲支持是一项尚未满足的重大需求。Cruse Cymru和Alzheimer’s Cymru合作开展了痴呆症患者丧亲项目,以满足威尔士各地痴呆症患者的丧亲需求。本文借鉴了阿斯顿大学和布里斯托尔大学对痴呆症患者丧亲项目的独立评估。我们总结了我们的主要发现、建议和对未来研究的建议。
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引用次数: 0
Cruse Bereavement Care at 60 – strengths, challenges and new directions 60岁的丧亲护理——优势、挑战和新方向
Q3 Nursing Pub Date : 2019-09-02 DOI: 10.1080/02682621.2019.1679541
K. Mitchell
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引用次数: 0
Equal bereavement for same sex partners 同性伴侣平等丧亲
Q3 Nursing Pub Date : 2019-09-02 DOI: 10.1080/02682621.2019.1679473
R. O'Leary
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引用次数: 0
Early studies of bereavement and Cruse Bereavement Care 丧亲之痛与临终关怀的早期研究
Q3 Nursing Pub Date : 2019-09-02 DOI: 10.1080/02682621.2019.1679476
C. M. Parkes
Abstract In this article Cruse Life President Colin Murray Parkes describes the early days of Cruse and how pioneers brought about the science of the care of the dying and bereaved, tracing the development of grief counselling and the body of Cruse volunteers who provide today’s invaluable work.
在这篇文章中,Cruse Life主席Colin Murray Parkes描述了Cruse的早期,以及先驱们如何带来了临终和丧亲之人的护理科学,追溯了悲伤咨询的发展和Cruse志愿者的身体,他们提供了今天宝贵的工作。
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引用次数: 0
Digital legacies with people affected by motor neurone disease: The views, experiences and perceptions of healthcare professionals, specialists and experts for use with bereaved young people 运动神经元疾病患者的数字遗产:供丧亲年轻人使用的保健专业人员、专家和专家的观点、经验和看法
Q3 Nursing Pub Date : 2019-09-02 DOI: 10.1080/02682621.2019.1679461
O. Clabburn, K. Knighting, M. O'brien, B. Jack
Abstract Background: Motor neurone disease is a terminal neurological illness with no known cure. It is often referred to as a ‘family disease’ with the ripples causing additional implications for children and young people. As such, little is known about how to best support young people (24 years old and under) (WHO, 2019)) when a family member dies from the disease. One potential solution is through use of a digital legacy whereby videos which document a person’s life, memories and achievements are purposefully recorded by an adult during their illness. However, due to this being an emerging area of research, little is known about whether a digital legacy may support or hinder bereavement for young people affected by the disease. Aim: To investigate healthcare professionals, specialists and experts views, perceptions and experiences of using digital legacies with bereaved young people due to motor neurone disease. Design: A qualitative study underpinned by interpretative phenomenological analysis. Setting/participants: Twenty healthcare professionals, specialists and experts were recruited using a maximum purposive sampling method. Open-ended interviews were conducted in participants’ place of work either over the telephone or by the lead researcher. Ethical approval was granted by a university ethics committee and Health Research Authority (HRA). Findings: Two key overarching themes were identified from the data: perceived benefit and value for bereaved young people using a digital legacy and challenges and barriers for bereaved young people using a digital legacy. Conclusion: A number of potential challenges and considerations were identified. However, the use of a digital legacy was perceived to be a feasible and valuable method of support for young people bereaved as a result of motor neurone disease.
背景:运动神经元疾病是一种晚期神经系统疾病,目前尚无治愈方法。它通常被称为“家庭疾病”,其涟漪效应会对儿童和年轻人造成额外影响。因此,当家庭成员死于该病时,人们对如何最好地支持年轻人(24岁及以下)(世卫组织,2019年)知之甚少。一种可能的解决方案是通过使用数字遗产,由成年人在他们生病期间有目的地录制记录一个人的生活、记忆和成就的视频。然而,由于这是一个新兴的研究领域,对于数字遗产是否会支持或阻碍受疾病影响的年轻人的丧亲之痛,人们知之甚少。目的:调查医疗保健专业人员、专家和专家对因运动神经元疾病而失去亲人的年轻人使用数字遗产的看法、看法和经验。设计:以解释性现象学分析为基础的定性研究。环境/参与者:采用最大目的抽样方法招募了20名医疗保健专业人员、专家和专家。在参与者的工作地点通过电话或由首席研究员进行开放式访谈。伦理批准由大学伦理委员会和卫生研究管理局(HRA)批准。调查结果:从数据中确定了两个关键的总体主题:失去亲人的年轻人使用数字遗产的感知利益和价值,以及失去亲人的年轻人使用数字遗产的挑战和障碍。结论:确定了一些潜在的挑战和考虑因素。然而,使用数字遗产被认为是支持因运动神经元疾病而失去亲人的年轻人的一种可行和有价值的方法。
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引用次数: 0
The meaning of ‘things’: The evolution of an ethic of care in the return of personal effects after disaster 2001–2019 “事物”的含义:2001年至2019年灾难后个人物品归还中关怀伦理的演变
Q3 Nursing Pub Date : 2019-09-02 DOI: 10.1080/02682621.2019.1679465
L. Easthope
Abstract The right to the return of personal effects belonging to loved ones after sudden death requires both protection and promotion. It is a fragile ‘right’ that can easily be undermined, and may require support from policy and legislation. The author has championed the return of personal effects after bereavement throughout her career in disaster response and was influenced by early examples of poor treatment and destruction. This article provides an evaluation of the historic picture and a reflection on the ongoing work to ensure that property is protected and restored. It also discusses whether the UK now has an ‘ethic of care’ in this area. This piece considers a number of recent case studies drawing on the author’s own experiences of working on incidents between 2001 and the present day, with specific examination of the work of the Metropolitan Police’s Property Restoration Team in 2005.
猝死后归还亲人个人物品的权利需要保护和促进。这是一项脆弱的“权利”,很容易受到破坏,可能需要政策和立法的支持。在她的救灾生涯中,提交人一直支持在丧亲之痛后归还个人物品,并受到早期恶劣待遇和破坏的影响。本文对这幅历史画卷进行了评估,并对正在进行的确保财产得到保护和修复的工作进行了反思。它还讨论了英国现在在这一领域是否有“关爱伦理”。这篇文章考虑了最近的一些案例研究,这些案例研究借鉴了作者自己在2001年至今处理事件的经验,并具体审查了伦敦警察局财产修复小组在2005年的工作。
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引用次数: 1
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Bereavement Care
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