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A Community-Based Qualitative Assessment of Knowledge, Barriers, and Promoters of Communicating about Family Cancer History among African-Americans

机译:基于社区的定性评估对非裔美国人在非洲裔美国人沟通的知识,障碍和启动子的定性评估

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Family cancer history (FCH) can shape prevention and early detection behaviors to decrease cancer risk. However, many individuals are unaware of increased risk for cancers based on family patterns. For some African-American communities, communication about FCH is rare and barriers have not been well studied. To optimize the use of FCH, it is crucial to understand how patients gather and share FCH with relatives and healthcare providers. We conducted four focus groups (n = 40) and seven key informant interviews (n = 9) to investigate knowledge, experiences, and barriers/promoters of FCH in the East Baltimore African-American community. Thematic analysis identified 14 distinct themes across six communication domains: participants' understanding of FCH, past FCH communication with family and providers, barriers to FCH communication, promoters of FCH communication, suggestions for future communication, and community health priorities. FCH was most often defined by narratives of family cancer experiences, and the majority of participants had shared little FCH with family members. Five psychosocial domains were commonly reported as barriers to sharing FCH: fear/denial, pride/dignity, selflessness/self-sacrifice, cancer fatalism, and distrust/skepticism of medical care. Diagnosis/death and caregiving/social support promoted FCH communication and encouraged cancer prevention behaviors such as screening. Although most participants had experienced cancer in their families, communication about FCH was low and psychosocial barriers were common. Understanding these communication domains in minority populations is crucial to developing interventions to address disparities in cancer prevention and control, particularly where effective screening and care recommendations exist for those with positive family histories.
机译:家庭癌症历史(FCH)可以塑造预防和早期检测行为,以降低癌症风险。然而,许多人不知道基于家庭模式的癌症的风险增加。对于一些非裔美国人的社区,关于FCH的沟通是罕见的,并且没有得到很好的研究障碍。为了优化FCH的使用,了解患者如何与亲戚和医疗保健提供者分享FCH至关重要。我们进行了四个焦点小组(n = 40)和七个关键信息面试(n = 9),以调查东巴尔的摩非洲裔美国社区FCH的知识,经验和障碍/启动子。主题分析确定了六个通信领域的14个不同的主题:参与者对FCH的理解,与家庭和提供者的障碍,FCH通信的障碍,FCH通信的推动者,未来通信的建议,以及社区健康优先事项。 FCH最常被家庭癌症经历的叙述定义,大多数参与者与家庭成员共享了小型费。五个心理社会域通常被报告为分享FCH的障碍:恐惧/拒绝,骄傲/尊严,无私/自我牺牲,癌症致命主义和医疗护理的不信任/怀疑。诊断/死亡和护理/社会支持促进了FCH沟通,并鼓励癌症预防行为如筛选。虽然大多数参与者在家庭中经历了癌症,但关于FCH的沟通是低,心理社会障碍是常见的。了解少数民族人口中的这些通信领域对于开发癌症预防和控制差异的干预措施至关重要,特别是那么存在具有阳性家庭历史的人的有效筛查和护理建议。

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