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首页> 外文期刊>Primary health care research & development >Diagnosis and management of chronic fatigue syndrome/myalgic encephalitis in black and minority ethnic people: a qualitative study
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Diagnosis and management of chronic fatigue syndrome/myalgic encephalitis in black and minority ethnic people: a qualitative study

机译:黑人和少数民族慢性疲劳综合征/肌性脑炎的诊断和处理:定性研究

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Aim: This study aims to explore the possible reasons for the lower levels of diagnosis of chronic fatigue syndrome/myalgic encephalitis (CFS/ME) in the black and minority ethnic (BME) population, and the implications for management. Background: Population studies suggest CFS/ME is more common in people from BME communities compared with the White British population. However, the diagnosis is made less frequently in BME groups. Methods: Semi-structured qualitative interviews were conducted with 35 key stakeholders in NW England. Interviews were analysed using open explorative thematic coding. Findings: There are barriers at every stage to the diagnosis and management of CFS/ME in people from BME groups. This begins with a lack of awareness of CFS/ME among BME respondents. Religious beliefs and the expectation of roles in the family and community mean that some people in BME groups may choose to manage their symptoms outside primary care using alternative therapies, prayer or spiritual healing. When accessing primary care, all participants recognised the possible influence of language barriers in reducing the likelihood of a diagnosis of CFS/ME. Stereotypical beliefs, including labels such as 'lazy' or 'work shy' were also believed to act as a barrier to diagnosis. Patients highlighted the importance of an on-going relationship with the general practitioner (GP), but perceived a high turnover of GPs in inner city practices, which undermined the holistic approach necessary to achieve a diagnosis. Conclusion: Training is required for health professionals to challenge inaccurate assumptions about CFS/ME in BME groups. The focus on the individual in UK primary care may not be appropriate for this group due to the role played by the family and community in how symptoms can be presented and managed. Culturally sensitive, educational resources for patients are also needed to explain symptoms and legitimise consultation.
机译:目的:本研究旨在探讨黑人和少数民族(BME)人群诊断慢性疲劳综合征/肌性脑炎(CFS / ME)水平较低的可能原因及其对管理的意义。背景:人口研究表明,与白人英国人相比,CFS / ME在BME社区的人中更为常见。但是,在BME组中诊断的频率较低。方法:对英格兰西北地区的35个主要利益相关者进行了半结构化的定性访谈。使用公开探索性主题编码对访谈进行了分析。研究结果:BME组患者在诊断和管理CFS / ME的每个阶段都存在障碍。这首先是由于BME受访者对CFS / ME缺乏了解。宗教信仰以及对家庭和社区角色的期望意味着BME组中的某些人可以选择使用替代疗法,祈祷或精神疗法来在初级保健之外管理症状。在接受初级保健时,所有参与者都认识到语言障碍可能会降低诊断CFS / ME的可能性。包括“懒惰”或“害羞的工作”等刻板印象的信念也被认为是诊断的障碍。患者强调了与全科医生(GP)保持持续关系的重要性,但认为市区内实践中GP的离职率很高,这破坏了实现诊断所需的整体方法。结论:卫生专业人员必须接受培训,以挑战BME组中关于CFS / ME的不正确假设。由于家庭和社区在如何表现和管理症状方面所起的作用,因此在英国初级保健中对个人的关注可能不适用于该人群。还需要具有文化敏感性的患者教育资源,以解释症状和使咨询合法化。

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