Understanding the potential factors affecting carers’ mental health during end-of-life home care: a meta synthesis of the research literature

G. Grande, Tracey Shield, K. Bayliss, Christine Rowland, Jackie Flynn, P. Bee, A. Hodkinson, M. Panagioti, M. Farquhar, Danielle Harris, A. Wearden
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Reviews of the qualitative, observational and intervention literature were conducted to address this.\n \n \n \n (1) to review trials of carer interventions to improve our understanding of factors related to carer mental health identified in earlier qualitative and observational reviews; (2) to synthesise the evidence from our qualitative, observational and intervention reviews on factors related to carers’ mental health during end-of-life caregiving.\n \n \n \n We carried out searches of MEDLINE, Cumulative Index to Nursing and Allied Health Literature (CINAHL), PsycINFO® (American Psychological Association, Washington, DC, USA), Social Sciences Citation Index, EMBASE, Cochrane Central Register of Controlled Trials (CENTRAL) and Database of Abstracts of Reviews of Effects (DARE) from 1 January 2009 to 24 November 2019. We included studies into adult informal/family carers for adult patients at the end of life cared for at home that considered any factor related to carer mental health (anxiety, depression, distress, quality of life) pre bereavement. The quality appraisal used Critical Appraisal Skills Programme (CASP) checklists and the Newcastle–Ottawa Scale. The qualitative review analysis developed themes that then provided a framework for the quantitative review analyses. Findings from all three reviews were mapped onto a single framework, informed by a carer Review Advisory Panel.\n \n \n \n A total of 31 qualitative, 60 observational, 12 intervention and 3 mixed-methods studies were identified. Factors associated with carer mental health were as follows: (1) patient condition, particularly psychological symptoms and quality of life; (2) impact of caring responsibilities, particularly life changes, workload and carer burden; (3) relationships, particularly with the patient; (4) finances, whether sufficient or not; (5) internal processes, particularly self-efficacy; (6) support, particularly adequacy and quality of support; (7) contextual factors, particularly age and gender. The three types of literature were reflected in most themes and yielded similar or complementary results, adding validity to findings. Only observational studies investigated contextual factors. Intervention studies focused on modifiable factors, but added little evidence on the causal direction between factors and mental health owing to design and analysis limitations. Relationships and finance received little attention overall. There was limited research into ethnicity, race or culture. 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Future research needs more (1) work on defining and measuring concepts; (2) longitudinal design, repeated measurement and path analysis, to move beyond evidence of association towards an understanding of causal relationships; (3) focus on factors that matter to carers rather than what is easily measured or manipulated; and (4) investigation of relationships, finance, ethnicity, race and culture.\n \n \n \n This study is registered as PROSPERO CRD42019130279.\n \n \n \n This project was funded by the National Institute for Health and Care Research (NIHR) Health and Social Care Delivery Research programme and will be published in Health and Social Care Delivery Research. 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引用次数: 1

Abstract

Family carers are central in supporting patients nearing the end of life, but this often has an impact on their own mental health. Understanding what factors may affect carers’ mental health is important in developing strategies to maintain mental health, through identifying carers at risk who may need added monitoring and support or developing interventions to change modifiable factors. Reviews of the qualitative, observational and intervention literature were conducted to address this. (1) to review trials of carer interventions to improve our understanding of factors related to carer mental health identified in earlier qualitative and observational reviews; (2) to synthesise the evidence from our qualitative, observational and intervention reviews on factors related to carers’ mental health during end-of-life caregiving. We carried out searches of MEDLINE, Cumulative Index to Nursing and Allied Health Literature (CINAHL), PsycINFO® (American Psychological Association, Washington, DC, USA), Social Sciences Citation Index, EMBASE, Cochrane Central Register of Controlled Trials (CENTRAL) and Database of Abstracts of Reviews of Effects (DARE) from 1 January 2009 to 24 November 2019. We included studies into adult informal/family carers for adult patients at the end of life cared for at home that considered any factor related to carer mental health (anxiety, depression, distress, quality of life) pre bereavement. The quality appraisal used Critical Appraisal Skills Programme (CASP) checklists and the Newcastle–Ottawa Scale. The qualitative review analysis developed themes that then provided a framework for the quantitative review analyses. Findings from all three reviews were mapped onto a single framework, informed by a carer Review Advisory Panel. A total of 31 qualitative, 60 observational, 12 intervention and 3 mixed-methods studies were identified. Factors associated with carer mental health were as follows: (1) patient condition, particularly psychological symptoms and quality of life; (2) impact of caring responsibilities, particularly life changes, workload and carer burden; (3) relationships, particularly with the patient; (4) finances, whether sufficient or not; (5) internal processes, particularly self-efficacy; (6) support, particularly adequacy and quality of support; (7) contextual factors, particularly age and gender. The three types of literature were reflected in most themes and yielded similar or complementary results, adding validity to findings. Only observational studies investigated contextual factors. Intervention studies focused on modifiable factors, but added little evidence on the causal direction between factors and mental health owing to design and analysis limitations. Relationships and finance received little attention overall. There was limited research into ethnicity, race or culture. Quantitative research missed some factors highlighted by carers in qualitative studies (e.g. quality aspects of formal support), and focused more on ‘self-management’ within internal processes (emphasised less by carers). Findings are from Organisation for Economic Co-operation and Development (OECD) country English-language publications on adult carers and patients in the home setting and limited to these contexts. Literature heterogeneity (study focus, objectives, methods, variables, measures) hindered meta-synthesis. Future work requires broad stakeholder engagement to address the diverse range of factors associated with carers’ mental health. Project findings will be disseminated accordingly. Future research needs more (1) work on defining and measuring concepts; (2) longitudinal design, repeated measurement and path analysis, to move beyond evidence of association towards an understanding of causal relationships; (3) focus on factors that matter to carers rather than what is easily measured or manipulated; and (4) investigation of relationships, finance, ethnicity, race and culture. This study is registered as PROSPERO CRD42019130279. This project was funded by the National Institute for Health and Care Research (NIHR) Health and Social Care Delivery Research programme and will be published in Health and Social Care Delivery Research. See the NIHR Journals Library website for further project information.
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了解临终家庭护理期间影响护理人员心理健康的潜在因素:研究文献的元综合
家庭照顾者在支持接近生命尽头的病人方面发挥着核心作用,但这往往会对他们自己的心理健康产生影响。了解哪些因素可能影响护理人员的心理健康,对于制定维持心理健康的策略非常重要,方法是确定可能需要额外监测和支持的高危护理人员,或制定干预措施以改变可改变的因素。为了解决这个问题,我们回顾了定性、观察和干预方面的文献。(1)回顾照顾者干预的试验,以提高我们对早期定性和观察性评价中确定的照顾者心理健康相关因素的理解;(2)综合我们对临终关怀过程中与照顾者心理健康相关因素的定性、观察和干预评价的证据。从2009年1月1日至2019年11月24日,我们检索了MEDLINE、护理和相关健康文献累积索引(CINAHL)、PsycINFO®(美国心理学会,华盛顿特区,美国)、社会科学引文索引、EMBASE、Cochrane中央对照试验注册库(Central)和疗效评价摘要数据库(DARE)。我们纳入了对成年患者在家中接受临终关怀的成人非正式/家庭护理者的研究,这些研究考虑了与护理者心理健康(焦虑、抑郁、痛苦、生活质量)相关的任何因素。质量评估使用了关键评估技能计划(CASP)清单和纽卡斯尔-渥太华量表。定性审查分析发展了主题,然后为定量审查分析提供了框架。所有三次审查的结果都被映射到一个单一的框架中,由护理人员审查咨询小组提供信息。共纳入31项定性研究、60项观察研究、12项干预研究和3项混合方法研究。与护理人员心理健康相关的因素如下:(1)患者状况,特别是心理症状和生活质量;(2)照顾责任,特别是生活变化、工作量和照顾者负担的影响;(3)关系,特别是与病人的关系;(四)财务状况,是否充足;(5)内部过程,尤其是自我效能;(6)支持,特别是支持的充分性和质量;(7)语境因素,尤其是年龄和性别。这三种类型的文献反映在大多数主题中,并产生相似或互补的结果,增加了发现的有效性。只有观察性研究调查了环境因素。干预研究侧重于可改变的因素,但由于设计和分析的限制,几乎没有证据表明因素与心理健康之间的因果关系。总体而言,人际关系和财务很少受到关注。对民族、种族或文化的研究有限。定量研究忽略了定性研究中护理人员强调的一些因素(例如,正式支持的质量方面),而更多地关注内部流程中的“自我管理”(护理人员较少强调)。研究结果来自经济合作与发展组织(OECD)国家关于家庭环境中成人护理人员和患者的英语出版物,并且仅限于这些背景。文献异质性(研究焦点、目标、方法、变量、测量)阻碍了meta综合。未来的工作需要广泛的利益相关者参与,以解决与护理人员心理健康相关的各种因素。项目调查结果将据此散发。未来的研究需要做更多的工作:(1)概念的定义和测量;(2)纵向设计、重复测量和路径分析,从关联证据转向对因果关系的理解;(3)关注对护理人员重要的因素,而不是容易测量或操纵的因素;(4)人际关系、财务、民族、种族和文化的调查。本研究注册号为PROSPERO CRD42019130279。该项目由国家卫生和保健研究所(NIHR)卫生和社会保健提供研究方案资助,并将发表在《卫生和社会保健提供研究》上。请参阅NIHR期刊图书馆网站了解更多项目信息。
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