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Construction of meanings during life‐limiting illnesses and its impacts on palliative care: Ethnographic study in an African context

机译:危及生命疾病中含义的构建及其对姑息治疗的影响:非洲语境中的民族图研究

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Abstract Objective Knowledge about how people make meaning in cancer, palliative, and end‐of‐life care is particularly lacking in Africa, yet it can provide insights into strategies for improving palliative care (PC). This study explored ways in which cancer patients, their families, and health care professionals (HCPs) construct meaning of their life‐limiting illnesses and how this impact on provision and use of PC in a Nigerian hospital. Methods This ethnographic study utilised participant observation, informal conversations during observation, and interviews to gather data from 39 participants, comprising service users and HCPs in a Nigerian hospital. Data were analysed using Spradley's framework for ethnographic data analysis. Results Meaning‐making in life‐limiting illness was predominantly rooted in belief systems. Most patients and their families, including some HCPs, perceived that cancer was caused by the devil, mystical, or supernatural beings. They professed that these agents manifested in the form of either spiritual attacks or that wicked people in society used either poison or acted as witches/wizards to inflict cancer on someone. These beliefs contributed to either nonacceptance of, or late presentation for, PC by most of patients and their families, while some professionals depended on supernatural powers for divine intervention and tacitly supporting religious practices to achieve healing/cure. Conclusions Findings revealed that cultural and religious world views about life‐limiting illnesses were used in decision‐making process for PC. This, therefore, provided evidence that could improve the clinicians' cultural competence when providing PC to individuals of African descent, especially Nigerians, both in Nigerian societies and in foreign countries.
机译:摘要关于人们如何在癌症中发出意义的客观知识,非洲尤其缺乏植物群体,姑息,尤其缺乏,但它可以为改善姑息治疗(PC)的策略提供见解。本研究探讨了癌症患者,家庭和医疗保健专业人员(HCP)的方式构建其生命限制疾病的意义以及如何对尼日利亚医院提供和使用PC的影响。方法采用参与者观察,观察期间的非正式谈话,以及从39名参与者收集数据,包括服务用户和尼日利亚医院的HCP的访谈。使用Spradley的民族图数据分析框架进行分析数据。结果在生活限制疾病中的意义主要植根于信仰系统。大多数患者及其家庭,包括一些HCP,认为癌症是由魔鬼,神秘或超自然的生物引起的。他们宣称,这些代理人以精神袭击的形式表现为或社会中的邪恶人员使用毒药或担任巫师/巫师,以对某人造成癌症。这些信念促成了大多数患者及其家庭的PC的非承认,或者延迟介绍,而一些专业人员则取决于神圣干预的超自然权力,并默默地支持宗教施法以实现愈合/治愈。结论发现表明,在PC的决策过程中使用了关于终身疾病的文化和宗教世界观。因此,这提供了可以改善临床医生的文化能力的证据,当为尼日利亚社会和国外提供非洲人血统,尤其是尼日利亚人的个人时。

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