Jude Mary Cénat, Élisabeth Dromer, Wina Paul Darius, Rose Darly Dalexis, Sarah Elizabeth Furyk, Hannah Poisson, Farid Mansoub Bekarkhanech, David Guangyu Diao, Andi Phaelle Gedeon, Muhammad S Shah, Patrick R Labelle, Emmanuelle Bernheim, Cary S Kogan
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引用次数: 1
Abstract
Objective: Black communities are increasingly concerned about psychosis, a worry echoed by provincial health-care systems across Canada. Responding to the lack of evidence on psychosis in Black communities, this scoping review examined the incidence and prevalence of psychosis, access to care (pathways to care, coercive referrals, interventions, etc.), treatments received, and stigma faced by individuals with psychosis.
Method: To identify studies, a comprehensive search strategy was developed and executed in December 2021 across 10 databases, including APA PsycInfo, CINAHL, MEDLINE and Web of Science. Subject headings and keywords relating to Black communities, psychosis, health inequalities, Canada and its provinces and territories were used and combined. The scoping review was conducted in accordance with Preferred Reporting Items for Systematic Reviews and Meta-Analyses for Scoping review (PRISMA-ScR) reporting standard.
Results: A total of 15 studies met the inclusion criteria, all of them conducted in Ontario and Quebec. Results highlight different disparities in psychosis among Black communities. Compared to other Canadian ethnic groups, Black individuals are more likely to be diagnosed with psychosis. Black individuals with psychosis are more likely to have their first contact with health-care settings through emergency departments, to be referred by police and ambulance services, and to experience coercive referrals and interventions, and involuntary admission. Black individuals experience a lower quality of care and are the ethnic group most likely to disengage from treatment.
Conclusion: This scoping review reveals many gaps in research, prevention, promotion and intervention on psychosis in Black individuals in Canada. Future studies should explore factors related to age, gender, social and economic factors, interpersonal, institutional and systemic racism, and psychosis-related stigma. Efforts should be directed toward developing trainings for health-care professionals and promotion and prevention programs within Black communities. Culturally adapted interventions, racially disaggregated data, and increased research funding are needed.
目标:黑人社区越来越担心精神病,这一担忧在加拿大各地的省级医疗系统中得到了回应。针对黑人社区缺乏精神病证据的问题,这项范围界定审查调查了精神病的发病率和患病率、获得护理的途径(护理途径、强制转诊、干预等)、接受的治疗以及精神病患者面临的耻辱。方法:为了确定研究,于2021年12月在10个数据库中制定并执行了一项全面的搜索策略,包括APA PsycInfo、CINAHL、MEDLINE和Web of Science。使用并合并了与黑人社区、精神病、健康不平等、加拿大及其各省和地区有关的主题标题和关键词。范围审查是根据系统审查首选报告项目和范围审查荟萃分析(PRISMA ScR)报告标准进行的。结果:共有15项研究符合纳入标准,均在安大略省和魁北克省进行。研究结果突出了黑人社区在精神病方面的不同差异。与其他加拿大种族相比,黑人更容易被诊断为精神病。患有精神病的黑人更有可能通过急诊部门首次接触医疗机构,被警察和救护车服务转介,并经历强制转介和干预,以及非自愿入院。黑人的护理质量较低,是最有可能脱离治疗的族裔群体。结论:这篇范围界定综述揭示了加拿大黑人精神病患者在研究、预防、宣传和干预方面的许多差距。未来的研究应探讨与年龄、性别、社会和经济因素、人际、制度和系统性种族主义以及与精神病相关的污名有关的因素。应努力发展对医疗保健专业人员的培训,并在黑人社区内开展宣传和预防计划。需要适应文化的干预措施、按种族分类的数据和增加研究资金。