{"title":"First generation migrants' experiences of terminal illness: a systematic review of diasporic dying.","authors":"Tim Sedgley, Joanne Alexander, Liz Forbat","doi":"10.1186/s12904-025-01789-0","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Migration is an established global phenomenon. While many newly arrived migrants have better health than the general population of the country they have moved to, migrants also have their own healthcare needs and face particular issues when diagnosed with a terminal illness. First generation migrants are less likely to have social, financial, and medical supports when faced with a terminal illness. These factors make first generation migrants an important group to understand in order to inform service commissioning and delivery.</p><p><strong>Methods: </strong>The systematic review was an international qualitative evidence synthesis of English language papers from 2000 to 2023. The primary research question underpinning this novel review was: What are the experiences of first-generation migrants who live with or who are supporting a relative with a terminal illness in the country to which they have moved? Databases (MEDLINE; CINAHL; PsycINFO; SocIndex; Web of Science) were searched in August 2023. Records of 1593 publications were screened, resulting in 39 included papers. CASP was used to inform quality appraisal.</p><p><strong>Results: </strong>First generation migrants struggled with accessing suitable health services and treatments. Structural barriers, such as lack of support for translation/interpreting and for navigating care was visible alongside limited social support networks. Financial precarity ran as a thread through the data, with participants needing to work while unwell, and being unable to return to their country of origin for their own death or to bear witness to the deaths of relatives. First generation migrants experienced caregiving through the lens of difference; maintaining autonomy in the country they would die in, intersected with cultural practices and expectations such as not sharing the prognosis, and mis-matched ideas regarding quality of care provided. The identity of 'migrant' is heterogenous, poorly defined, and may have resulted in identifying studies conducted in the global north.</p><p><strong>Conclusions: </strong>Diasporic dying is not a new phenomenon, yet services and policies fail to meet people's needs. Services urgently need to identify and dismantle structures which uphold and perpetuate inequality, including this population who suffer multiple disadvantages and risks.</p><p><strong>Protocol registration: </strong>CRD42023457054.</p>","PeriodicalId":48945,"journal":{"name":"BMC Palliative Care","volume":"24 1","pages":"152"},"PeriodicalIF":2.5000,"publicationDate":"2025-05-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12107898/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"BMC Palliative Care","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1186/s12904-025-01789-0","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"HEALTH CARE SCIENCES & SERVICES","Score":null,"Total":0}
引用次数: 0
Abstract
Background: Migration is an established global phenomenon. While many newly arrived migrants have better health than the general population of the country they have moved to, migrants also have their own healthcare needs and face particular issues when diagnosed with a terminal illness. First generation migrants are less likely to have social, financial, and medical supports when faced with a terminal illness. These factors make first generation migrants an important group to understand in order to inform service commissioning and delivery.
Methods: The systematic review was an international qualitative evidence synthesis of English language papers from 2000 to 2023. The primary research question underpinning this novel review was: What are the experiences of first-generation migrants who live with or who are supporting a relative with a terminal illness in the country to which they have moved? Databases (MEDLINE; CINAHL; PsycINFO; SocIndex; Web of Science) were searched in August 2023. Records of 1593 publications were screened, resulting in 39 included papers. CASP was used to inform quality appraisal.
Results: First generation migrants struggled with accessing suitable health services and treatments. Structural barriers, such as lack of support for translation/interpreting and for navigating care was visible alongside limited social support networks. Financial precarity ran as a thread through the data, with participants needing to work while unwell, and being unable to return to their country of origin for their own death or to bear witness to the deaths of relatives. First generation migrants experienced caregiving through the lens of difference; maintaining autonomy in the country they would die in, intersected with cultural practices and expectations such as not sharing the prognosis, and mis-matched ideas regarding quality of care provided. The identity of 'migrant' is heterogenous, poorly defined, and may have resulted in identifying studies conducted in the global north.
Conclusions: Diasporic dying is not a new phenomenon, yet services and policies fail to meet people's needs. Services urgently need to identify and dismantle structures which uphold and perpetuate inequality, including this population who suffer multiple disadvantages and risks.
背景:移民是一个公认的全球现象。虽然许多新抵达的移徙者的健康状况比移徙国的一般人口要好,但移徙者也有自己的保健需求,在被诊断患有绝症时面临特殊问题。第一代移民在面对绝症时不太可能获得社会、经济和医疗支持。这些因素使第一代移民成为需要了解的重要群体,以便为服务调试和交付提供信息。方法:对2000 ~ 2023年国际上发表的英语文献进行系统评价和定性证据综合。支撑这篇新颖综述的主要研究问题是:在移居的国家,第一代移民与身患绝症的亲属同住或抚养他们的亲属,他们的经历是什么?数据库(MEDLINE;CINAHL;PsycINFO;SocIndex;Web of Science)于2023年8月被检索。对1593份出版物的记录进行了筛选,结果纳入了39篇论文。采用CASP进行质量评价。结果:第一代移民难以获得适当的卫生服务和治疗。结构性障碍,如缺乏对翻译/口译和导航护理的支持,以及有限的社会支持网络,都是显而易见的。经济不稳定贯穿整个数据,参与者需要在身体不适的情况下工作,并且无法返回原籍国,因为他们自己的死亡或见证亲属的死亡。第一代移民通过不同的视角体验照顾;在他们将死去的国家保持自主权,与文化习俗和期望交织在一起,比如不分享预后,以及对所提供的护理质量的不匹配的想法。“移民”的身份是异质的,定义不清,可能导致在全球北方进行的识别研究。结论:散居死亡并不是一个新现象,但服务和政策未能满足人们的需求。服务部门迫切需要确定和拆除维护和延续不平等的结构,包括遭受多重不利条件和风险的人口。协议注册:CRD42023457054。
期刊介绍:
BMC Palliative Care is an open access journal publishing original peer-reviewed research articles in the clinical, scientific, ethical and policy issues, local and international, regarding all aspects of hospice and palliative care for the dying and for those with profound suffering related to chronic illness.