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文化、社区与癌症:索韦托女性基于非亲身经历对乳腺癌的认知

Culture, community, and cancer: Understandings of breast cancer from a non-lived experience among women living in Soweto.

作者信息

Malope Seemela D, Norris Shane A, Joffe Maureen

机构信息

University of the Witwatersrand.

University of Southampton.

出版信息

Res Sq. 2024 Aug 28:rs.3.rs-4797158. doi: 10.21203/rs.3.rs-4797158/v1.

Abstract

BACKGROUND

Individual perceptions compounded with socio-cultural beliefs and health system factors are key determinants of people's health seeking behavior and are widely cited as the causes of delayed breast cancer diagnosis among women from structurally vulnerable settings. Asking: "how do women with a non-lived experience of cancer understand the disease and, what informs their health seeking behaviors?", we explored individual, sociocultural and health system elements from a conceptual model derived from the Socioecological, Health Belief and Cancer Stigma Frameworks, to understand perspectives of breast cancer in a South African urban community setting.

METHODS

Using a deductive approach, we conducted a qualitative study consisting of 6 focus group discussions among 34 women from Soweto, Johannesburg (aged 35-74 years) and followed-up with 20 semi-structured in-depth interviews.

RESULTS

Findings revealed some awareness of breast and other cancers, but confusion and gaps in understanding of the disease, resulting in socio-culturally influenced misperceptions of risks, causes, and outcomes following treatment of breast cancer. This fueled perceptions of profound fear and stigma against people with breast and other cancers. These findings together with participant perceptions of primary healthcare providers being unwelcoming, under-resourced, and insufficiently trained to deal with breast cancer, resulted in women reporting being reluctant to participating in screening/early detection care seeking behavior. They only accessed primary care when experiencing extreme pain or ill-health. Participants suggested as solutions for future interventions, the need for sustained community engagement, harnessing existing clinic and community stakeholders and resources to provide clear and understandable breast cancer information and encouragement for screening uptake.

CONCLUSIONS

Health literacy gaps surrounding breast cancer fuels socio-culturally influenced misperceptions, fear, stigma, and fatalism among community women from Soweto, South Africa. Women perceive primary care providers of having insufficient knowledge, skills, and resources to provide effective breast cancer screening services. Participants suggested the need for greater community engagement involving primary clinics and existing community stakeholders working hand in hand. Clear, understandable, and consistent information about breast cancer must be regularly disseminated and communities must be regularly encouraged to utilise breast cancer screening services.

摘要

背景

个人认知与社会文化信仰及卫生系统因素相互交织,是人们就医行为的关键决定因素,并且被广泛认为是导致结构脆弱环境中女性乳腺癌诊断延迟的原因。我们提出问题:“没有患过癌症经历的女性如何理解这种疾病,以及是什么影响了她们的就医行为?”,并从社会生态、健康信念和癌症耻辱框架衍生出的概念模型中探究个体、社会文化和卫生系统要素,以了解南非城市社区环境中乳腺癌的相关观点。

方法

采用演绎法,我们进行了一项定性研究,包括对约翰内斯堡索韦托的34名女性(年龄在35 - 74岁之间)进行6次焦点小组讨论,并随后进行了20次半结构化深度访谈。

结果

研究结果显示,人们对乳腺癌和其他癌症有一定认识,但对疾病的理解存在困惑和差距,这导致了受社会文化影响的对乳腺癌治疗后风险、病因和结果的误解。这加剧了对乳腺癌和其他癌症患者的深深恐惧和耻辱感。这些发现以及参与者认为初级医疗服务提供者不热情、资源不足且缺乏应对乳腺癌的充分培训,导致女性表示不愿参与筛查/早期检测的就医行为。她们只有在经历极度疼痛或健康状况不佳时才会去寻求初级医疗服务。参与者建议,作为未来干预措施的解决方案,需要持续的社区参与,利用现有的诊所和社区利益相关者及资源,提供清晰易懂的乳腺癌信息,并鼓励进行筛查。

结论

围绕乳腺癌的健康素养差距加剧了南非索韦托社区女性受社会文化影响的误解、恐惧、耻辱感和宿命论。女性认为初级医疗服务提供者缺乏提供有效乳腺癌筛查服务的知识、技能和资源。参与者建议需要加强社区参与,让初级诊所和现有的社区利益相关者携手合作。必须定期传播关于乳腺癌的清晰、易懂且一致的信息,并且必须经常鼓励社区利用乳腺癌筛查服务。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c197/11384026/9ab6f0f39ead/nihpp-rs4797158v1-f0001.jpg

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