土耳其裔、摩洛哥裔、苏里南裔和荷兰-加勒比裔癌症患者的诊断、治疗和预后:系统的文献回顾。

IF 2 Q3 HEALTH POLICY & SERVICES Journal of Cancer Policy Pub Date : 2023-11-19 DOI:10.1016/j.jcpo.2023.100455
Asiye Gedik , Esther van Meerten , Milou J.P. Reuvers , Olga Husson , Winette T.A. van der Graaf
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引用次数: 0

摘要

背景:世界范围内的国际移民人数正在增加。荷兰的四个主要非西方民族是土耳其人、摩洛哥人、苏里南人和荷属加勒比人。本文回顾了有关这四个民族的癌症患者对癌症诊断、治疗和预后的看法的科学文献。方法:采用EMBASE、Medline Web of Science和Cochrane Central Register数据库进行系统文献综述。研究纳入了土耳其、摩洛哥、苏里南和荷兰-加勒比血统的患者。包括定性和定量研究,并进行专题分析。使用混合方法评估工具评估方法学质量。结果:在土耳其对土耳其癌症患者进行了13项研究,而在荷兰对土耳其和摩洛哥癌症患者进行了3项研究。从纳入的研究中出现了四个主题:诊断披露、沟通、信息提供和决策。土耳其的大多数癌症患者希望获得有关其诊断和治疗的信息。然而,在土耳其,很少与癌症患者讨论癌症诊断的披露,而在荷兰,这是直接提供的。东道国和原籍国的家庭成员对沟通和决策都有很大的影响。没有关于苏里南或荷兰-加勒比癌症患者这一主题的文献。结论:虽然主要的少数民族生活在东道国,但缺乏对患者及其家属的最佳沟通和癌症信息披露的知识。政策总结:进一步研究不同种族对如何沟通癌症的看法,对于确保每位患者获得最佳护理和治疗至关重要。
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The views of cancer patients of Turkish, Moroccan, Surinamese, and Dutch-Caribbean descent on diagnosis, treatment and prognosis: A systematic literature review

Background

The number of international migrants is increasing worldwide. The four major non-western ethnic groups in the Netherlands are Turkish, Moroccan, Surinamese, and Dutch-Caribbean. This review examined the scientific literature on the views of cancer patients from these four ethnic groups on cancer diagnosis, treatment, and prognosis.

Methods

A systematic literature review was conducted using the databases EMBASE, Medline Web of Science, and Cochrane Central Register. Studies with patients who were of Turkish, Moroccan, Surinamese, and Dutch-Caribbean descent were included. Both qualitative and quantitative studies were included, and thematic analysis was performed. The methodological quality was assessed using the Mixed Methods Appraisal Tool.

Results

Thirteen studies were conducted in Turkey on Turkish cancer patients, while three were conducted in the Netherlands on Turkish and Moroccan cancer patients. Four themes emerged from the included studies: disclosure of diagnosis, communication, information provision, and decision-making. The majority of cancer patients in Turkey wanted information regarding their diagnosis and treatment. However, disclosure of a cancer diagnosis was rarely discussed with cancer patients in Turkey, whereas in the Netherlands it was provided directly. Family members in both the host and native countries had a strong influence on communication and decision-making. No literature on this topic for Surinamese or Dutch-Caribbean cancer patients was found.

Conclusion

Although major ethnic groups live in host countries, there is a lack of knowledge on optimal communication and information disclosure on cancer to patients and their families.

Policy summary

Further research into the views of ethnic groups on how to communicate about cancer is essential to ensuring that every patient receives optimal care and treatment.

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来源期刊
Journal of Cancer Policy
Journal of Cancer Policy Medicine-Health Policy
CiteScore
2.40
自引率
7.70%
发文量
47
审稿时长
65 days
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