What factors are associated with informal carers' psychological morbidity during end-of-life home care? A systematic review and thematic synthesis of observational quantitative studies.

Tracey Shield, Kerin Bayliss, Alexander Hodkinson, Maria Panagioti, Alison Wearden, Jackie Flynn, Christine Rowland, Penny Bee, Morag Farquhar, Danielle Harris, Gunn Grande
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Understanding what factors may affect carers' mental health is important in developing strategies to maintain their psychological well-being during caregiving.</p><p><strong>Aim: </strong>To conduct a systematic review and thematic evidence synthesis of factors related to carers' mental health during end-of-life caregiving.</p><p><strong>Method: </strong>Searches of MEDLINE, CINAHL, PsychINFO, Social Sciences Citation Index, EMBASE, Cochrane Central Register of Controlled Trials and Database of Abstracts of Reviews of Effects 1 January 2009-24 November 2019. We included observational quantitative studies focusing on adult informal/family carers for adult patients at end of life cared for at home considering any factor related to carer mental health (anxiety, depression, distress and quality of life) pre-bereavement. Newcastle-Ottawa Quality Assessment Scale was used. 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Patients' other symptoms and functional impairment may relate to carer mental health, but findings were unclear. <b>Impact of caring responsibilities</b> (14 studies): impact on carers' lives, task difficulty and general burden had clear associations with worse carer mental health. <b>Relationships</b> (8 studies): family dynamics and the quality of the carer-patient relationship may be important for carer mental health and are worthy of further investigation. <b>Finance</b> (6 studies): insufficient resources may relate to carers' mental health and warrant further study. <b>Carers' psychological processes</b> (13 studies): self-efficacy and preparedness were related to better mental health. However, findings regarding coping strategies were mixed. <b>Support</b> (18 studies): informal support given by family and friends may relate to better carer mental health, but evidence on formal support is limited. 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引用次数: 1

Abstract

Background: Family carers are central in supporting patients nearing end of life. As a consequence, they often suffer detrimental impacts on their own mental health. Understanding what factors may affect carers' mental health is important in developing strategies to maintain their psychological well-being during caregiving.

Aim: To conduct a systematic review and thematic evidence synthesis of factors related to carers' mental health during end-of-life caregiving.

Method: Searches of MEDLINE, CINAHL, PsychINFO, Social Sciences Citation Index, EMBASE, Cochrane Central Register of Controlled Trials and Database of Abstracts of Reviews of Effects 1 January 2009-24 November 2019. We included observational quantitative studies focusing on adult informal/family carers for adult patients at end of life cared for at home considering any factor related to carer mental health (anxiety, depression, distress and quality of life) pre-bereavement. Newcastle-Ottawa Quality Assessment Scale was used. Thematic analysis with box score presentation, and meta-analysis were done where data permitted.

Results: Findings from 63 included studies underpinned seven emergent themes. Patient condition (31 studies): worse patient psychological symptoms and quality of life were generally associated with worse carer mental health. Patient depression was associated with higher depression in carers (standardised mean difference = 0.59, 95% confidence interval 0.32 to 0.87, I2 = 77%). Patients' other symptoms and functional impairment may relate to carer mental health, but findings were unclear. Impact of caring responsibilities (14 studies): impact on carers' lives, task difficulty and general burden had clear associations with worse carer mental health. Relationships (8 studies): family dynamics and the quality of the carer-patient relationship may be important for carer mental health and are worthy of further investigation. Finance (6 studies): insufficient resources may relate to carers' mental health and warrant further study. Carers' psychological processes (13 studies): self-efficacy and preparedness were related to better mental health. However, findings regarding coping strategies were mixed. Support (18 studies): informal support given by family and friends may relate to better carer mental health, but evidence on formal support is limited. Having unmet needs was related to worse mental health, while satisfaction with care was related to better mental health. Contextual factors (16 studies): older age was generally associated with better carer mental health and being female was associated with worse mental health.

Limitations: Studies were mainly cross-sectional (56) rather than longitudinal (7) which raises questions about the likely causal direction of relationships. One-third of studies had samples < 100, so many had limited statistical power to identify existing relationships.

Conclusions and future work: Future work must adopt a comprehensive approach to improving carers' mental health because factors relating to carer mental health cover a broad spectrum. The literature on this topic is diverse and difficult to summarise, and the field would benefit from a clearer direction of enquiry guided by explanatory models. Future research should (1) further investigate quality of relationships and finances; (2) better define factors under investigation; (3) establish, through quantitative causal analyses, why factors might relate to mental health; and (4) utilise longitudinal designs more to aid understanding of likely causal direction of associations.

Study registration: This study is registered as PROSPERO registration 2019 CRD42019130279 at https://www.crd.york.ac.uk/prospero/.

Funding: This award was funded by the National Institute for Health and Care Research (NIHR) Health and Social Care Delivery Research programme HSDR 18/01/01 and is published in full in Health and Social Care Delivery Research. See the NIHR Funding and Awards website for further award information.

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在临终家庭护理期间,哪些因素与非正式护理员的心理疾病有关?对观察性定量研究的系统回顾和专题综合。
背景:家庭照顾者在支持接近生命末期的病人方面起着核心作用。因此,他们往往对自己的心理健康造成不利影响。了解哪些因素可能影响照顾者的心理健康,对于制定策略以在照顾期间维持照顾者的心理健康非常重要。目的:对临终照护过程中影响照护者心理健康的相关因素进行系统回顾和专题证据综合。方法:检索MEDLINE、CINAHL、PsychINFO、社会科学引文索引、EMBASE、Cochrane中央对照试验注册库和2009年1月1日- 2019年11月24日综述摘要数据库。我们纳入了观察性定量研究,重点关注在家照顾的成年临终患者的成人非正式/家庭照顾者,并考虑了丧亲前与照顾者心理健康(焦虑、抑郁、痛苦和生活质量)相关的任何因素。采用纽卡斯尔-渥太华质量评估量表。在数据允许的情况下,采用盒子分数表示的主题分析和元分析。结果:包括63项研究的结果支持了七个新兴主题。患者状况(31项研究):患者心理症状和生活质量较差通常与护理人员心理健康状况较差相关。患者抑郁与护理人员抑郁程度较高相关(标准化平均差= 0.59,95%可信区间0.32 ~ 0.87,I2 = 77%)。患者的其他症状和功能障碍可能与护理人员的心理健康有关,但研究结果尚不清楚。照顾责任的影响(14项研究):对照顾者生活、任务困难和一般负担的影响与照顾者心理健康状况的恶化有明显的关联。关系(8项研究):家庭动态和护患关系的质量可能对护理者心理健康很重要,值得进一步调查。财务(6项研究):资源不足可能与照顾者的心理健康有关,值得进一步研究。照顾者的心理过程(13项研究):自我效能感和心理准备与较好的心理健康有关。然而,关于应对策略的调查结果却喜忧参半。支持(18项研究):家庭和朋友提供的非正式支持可能与更好的护理者心理健康有关,但关于正式支持的证据有限。未满足的需求与较差的心理健康有关,而对护理的满意度与较好的心理健康有关。背景因素(16项研究):年龄较大通常与较好的照顾者心理健康有关,而女性与较差的心理健康有关。局限性:研究主要是横断面的(56)而不是纵向的(7),这提出了关于可能的因果关系方向的问题。结论和未来的工作:未来的工作必须采取全面的方法来改善照顾者的心理健康,因为与照顾者心理健康有关的因素涉及范围很广。关于这一主题的文献是多种多样的,难以总结,该领域将受益于解释模型指导下的更清晰的调查方向。未来的研究应该(1)进一步研究人际关系质量与财务状况;(2)更好地界定调查因素;(3)通过定量因果分析,确立与心理健康相关的因素;(4)更多地利用纵向设计来帮助理解关联的可能因果方向。研究注册:本研究注册为PROSPERO注册2019 CRD42019130279,网址为https://www.crd.york.ac.uk/prospero/.Funding:。该奖项由国家卫生与保健研究所(NIHR)卫生与社会保健提供研究计划HSDR 18/01/01资助,全文发表在《卫生与社会保健提供研究》上。有关进一步的奖励信息,请参阅美国国立卫生研究院资助和奖励网站。
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