Fondazione Gabriele Monasterio, Pisa, Italy.
Interdisciplinary Research Center Health Science, Scuola Superiore Sant'Anna, Pisa, Italy.
BMC Health Serv Res. 2023 May 3;23(1):429. doi: 10.1186/s12913-023-09241-w.
Heart failure impacts patients' quality of life and life expectancy and significantly affects the daily behaviours and feelings of family caregivers. At the end-of-life, the burden for family caregivers depends on their emotional and sentimental involvement, as well as social costs.
The aim of this work is to determine whether and how family caregivers' experiences and expectations vary in relation to the places of care and teams involved in heart failure management.
A systematic literature review was conducted, by screening manuscripts dealing with the experience of Family Care Givers' (FCGs) of patients with Advanced Heart failure. Methods and results were reported following the PRISMA rules. Papers were searched through three databases (PubMed, Scopus and Web of Science). Seven topics were used to synthetize results by reporting qualitative information and quantitative evidence about the experience of FCGs in places of care and with care teams.
Thirty-one papers, dealing with the experience of 814 FCGs, were selected for this systematic review. Most manuscripts came from the USA (N = 14) and European countries (N = 13) and were based on qualitative methods. The most common care setting and provider profile combination at the end of life was home care (N = 22) and multiprofessional teams (N = 27). Family caregivers experienced "psychological issues" (48.4%), impact of patients' condition on their life (38,7%) and "worries for the future" (22.6%). Usually, when family caregivers were unprepared for the future, the care setting was the home, and there was a lack of palliative physicians on the team.
At the end-of-life, the major needs of chronic patients and their relatives are not health related. And, as we observed, non-health needs can be satisfied by improving some key components of the care management process that could be related to care team and setting of care. Our findings can support the design of new policies and strategies.
心力衰竭影响患者的生活质量和预期寿命,并显著影响家庭护理人员的日常行为和感受。在生命末期,家庭护理人员的负担取决于他们的情感投入以及社会成本。
本研究旨在确定家庭护理人员的经历和期望是否以及如何因心力衰竭管理所涉及的护理地点和团队而有所不同。
通过筛选有关心力衰竭晚期患者家庭护理人员(FCG)经历的文献,进行了系统的文献回顾。方法和结果按照 PRISMA 规则进行报告。通过三个数据库(PubMed、Scopus 和 Web of Science)搜索论文。使用七个主题通过报告有关 FCG 在护理地点和护理团队中的经历的定性信息和定量证据来综合结果。
共选择了 31 篇涉及 814 名 FCG 经历的论文进行系统综述。大多数文章来自美国(N=14)和欧洲国家(N=13),并基于定性方法。生命末期最常见的护理环境和护理团队特征组合是家庭护理(N=22)和多专业团队(N=27)。家庭护理人员经历了“心理问题”(48.4%)、患者病情对生活的影响(38.7%)和“对未来的担忧”(22.6%)。通常,当家庭护理人员对未来没有准备时,护理环境是家庭,团队中缺乏姑息治疗医生。
在生命末期,慢性患者及其亲属的主要需求与健康无关。而且,正如我们观察到的,非健康需求可以通过改善护理管理过程中的一些关键组成部分来满足,这些组成部分可能与护理团队和护理环境有关。我们的研究结果可以为新政策和策略的制定提供支持。