Oduro Elisha Baafi, Jackson Amy, Fu Yunting, Carpenter Joan G
Organizational System and Adult Health, University of Maryland School of Nursing, Baltimore, MD, USA.
Am J Hosp Palliat Care. 2025 Aug;42(8):735-745. doi: 10.1177/10499091241273403. Epub 2024 Aug 14.
BackgroundPatients from underrepresented racial and ethnic groups (URGs) in the United States (US) experience disparities in accessing palliative care (PC) at the end of life (EOL). Additionally, little effort has been made to understand their experiences with PC.ObjectivesTo identify and synthesize existing literature on PC experiences among adults from URGs in nursing homes, community settings, and hospitals in the US.MethodsGuided by the Joanna Briggs Institute methodological recommendation and Preferred Reporting Items for Systematic Reviews and Meta-Analyses Extension for Scoping Reviews, we conducted a scoping review. We searched PubMed, EMBASE, CINAHL, Scopus, and ProQuest Dissertations & Theses Global from inception to January 2024.ResultsWe included five studies representing Hispanic/Latino, American Indian, African/Black American, and Chinese individuals. Data were organized around two themes: navigating PC pathway and choices and practices during PC. Navigating PC pathway theme highlights that despite the several barriers URGs face when accessing PC, they seek PC services due to their limited formal family assistance in managing their chronic conditions and pain. The choices and practices during PC theme emphasize the roles URG family members play in EOL care, the patient's care preferences, and their spiritual practices and beliefs related to EOL care.ConclusionThis scoping review reveals limited literature about URG experiences with PC and highlights the need for more studies to focus on making PC services more accessible to URGs and providing culturally sensitive care to meet the needs of the diverse growing US population.
背景
在美国,来自代表性不足的种族和族裔群体(URGs)的患者在临终时获得姑息治疗(PC)方面存在差异。此外,人们对他们接受PC的经历了解甚少。
目的
识别并综合关于美国养老院、社区环境和医院中URGs成年人PC经历的现有文献。
方法
在乔安娜·布里格斯研究所的方法学建议和系统评价与Meta分析扩展版的首选报告项目的指导下,我们进行了一项范围综述。我们检索了从创刊到2024年1月的PubMed、EMBASE、CINAHL、Scopus和ProQuest Dissertations & Theses Global。
结果
我们纳入了五项研究,涉及西班牙裔/拉丁裔、美国印第安人、非裔/美国黑人以及华裔个体。数据围绕两个主题进行组织:在PC途径中导航以及PC期间的选择和实践。在PC途径中导航这一主题强调,尽管URGs在获得PC时面临诸多障碍,但由于他们在管理慢性病和疼痛方面获得的正式家庭援助有限,他们仍寻求PC服务。PC期间的选择和实践这一主题强调了URG家庭成员在临终护理中的作用、患者的护理偏好以及他们与临终护理相关的精神实践和信仰。
结论
这项范围综述揭示了关于URGs接受PC经历的文献有限,并强调需要更多研究聚焦于使URGs更容易获得PC服务,以及提供具有文化敏感性的护理,以满足美国不断增长的多样化人口的需求。