School of Health Sciences, University of Greenwich, Southwood Site, Avery Hill Road, Eltham, London, SE9 2UG, UK.
BMC Gastroenterol. 2021 Aug 18;21(1):322. doi: 10.1186/s12876-021-01857-8.
Prevalence of chronic gastrointestinal diseases has been rising amongst ethnic minority populations in Western countries, despite the first-generation migrants originating from countries of low prevalence. Differences caused by genetic, environmental, cultural, and religious factors in each context may contribute towards shaping experiences of ethnic minority individuals living with primary bowel conditions. This review aimed to explore the experiences of ethnic minority patients living with chronic bowel conditions.
We conducted a systematic scoping review to retrieve qualitative, quantitative, and mixed methods studies from eight electronic databases, and manually searched reference lists of frequently cited papers.
Fourteen papers met the inclusion criteria: focussing on inflammatory bowel disease, irritable bowel syndrome, and coeliac disease. Core themes were narratively analysed. South Asians had limited understanding of inflammatory bowel disease and coeliac disease, hindered by language and literacy barriers, particularly for older generations, suggesting that culturally relevant information is needed. Family support was limited, and Muslim South Asians referred to religion to understand and self-manage inflammatory bowel disease. Ethnic minority groups across countries experienced: poor dietary intake for coeliac disease and inflammatory bowel disease, cultural conflict in self-managing diet for inflammatory bowel disease which increased anxiety, and there was a need for better quality of, and access to, healthcare services. British ethnic minority groups experienced difficulties with IBD diagnosis/misdiagnosis.
Cultural, religious, and social contexts, together with language barriers and limited health literacy influenced experiences of health inequalities for ethnic minority patients living with chronic bowel diseases.
尽管第一代移民来自低流行率国家,但西方国家少数民族人群的慢性胃肠道疾病患病率一直在上升。每个背景下由遗传、环境、文化和宗教因素引起的差异可能会影响少数民族人群原发性肠道疾病患者的体验。本综述旨在探讨少数民族慢性肠病患者的患病体验。
我们进行了系统的范围综述,从八个电子数据库中检索定性、定量和混合方法研究,并手动搜索常被引论文的参考文献列表。
符合纳入标准的有 14 篇论文:主要关注炎症性肠病、肠易激综合征和乳糜泻。核心主题进行了叙述性分析。南亚人对炎症性肠病和乳糜泻的了解有限,语言和读写能力障碍阻碍了他们的理解,尤其是对老一辈人而言,这表明需要提供与文化相关的信息。家庭支持有限,穆斯林南亚人则通过宗教来理解和自我管理炎症性肠病。不同国家的少数民族群体经历了:乳糜泻和炎症性肠病患者的饮食摄入不良,炎症性肠病患者在自我管理饮食方面的文化冲突增加了焦虑,他们需要更好的医疗服务质量和获得途径。英国少数民族群体在炎症性肠病的诊断/误诊方面存在困难。
文化、宗教和社会背景,加上语言障碍和有限的健康素养,影响了少数民族慢性肠病患者的健康不平等体验。