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Lay Understanding of Familial Risk of Common Chronic Diseases: A Systematic Review and Synthesis of Qualitative Research

机译:对常见的慢性病的家族风险有深刻的了解:系统的综述和定性研究的综合

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摘要

>PURPOSE Although the family history is increasingly used for genetic risk assessment of common chronic diseases in primary care, evidence suggests that lay understanding about inheritance may conflict with medical models. This study systematically reviewed and synthesized the qualitative literature exploring understanding about familial risk held by persons with a family history of cancer, coronary artery disease, and diabetes mellitus.>METHODS Twenty-two qualitative articles were found after a comprehensive literature search and were critically appraised; 11 were included. A meta-ethnographic approach was used to translate the studies across each other, synthesize the translation, and express the synthesis.>RESULTS A dynamic process emerged by which a personal sense of vulnerability included some features that mirror the medical factors used to assess risk, such as the number of affected relatives. Other features are more personal, such as experience of a relative’s disease, sudden or premature death, perceived patterns of illness relating to gender or age at death, and comparisons between a person and an affected relative. The developing vulnerability is interpreted using personal mental models, including models of disease causation, inheritance, and fatalism. A person’s sense of vulnerability affects how that person copes with, and attempts to control, any perceived familial risk.>CONCLUSIONS Persons with a family history of a common chronic disease develop a personal sense of vulnerability that is informed by the salience of their family history and interpreted within their personal models of disease causation and inheritance. Features that give meaning to familial risk may be perceived differently by patients and professionals. This review identifies key areas for health professionals to explore with patients that may improve the effectiveness of communication about disease risk and management.
机译:>目的尽管家族病史越来越多地用于初级保健中常见慢性疾病的遗传风险评估,但有证据表明,对遗传的外行理解可能与医学模型相抵触。本研究系统地回顾和综合了定性文献,探讨了对具有癌症,冠心病和糖尿病家族史的人所具有的家族风险的理解。>方法文献检索并受到严格评估;其中包括11个。使用元民族志方法将研究相互翻译,合成翻译并表达合成。>结果出现了一个动态过程,在此过程中,个人的脆弱感包括一些与医学相似的特征用于评估风险的因素,例如受影响亲戚的数量。其他特征更具个人性,例如亲戚的疾病经历,猝死或过早死亡,与性别或死亡年龄有关的可感知疾病模式以及人与受影响亲戚之间的比较。使用个人心理模型(包括疾病因果关系,遗传和宿命论模型)来解释发展中的脆弱性。一个人的脆弱感会影响该人应对和试图控制任何已知的家族风险的方式。>结论有常见慢性病家族病史的人会形成个人的脆弱感,这种脆弱感会因他们的家族史的显着性,并在他们的疾病因果关系和遗传模型中得到解释。患者和专业人员对家庭风险的理解可能有所不同。这篇综述确定了卫生专业人员与患者一起探索的关键领域,这些领域可能会提高疾病风险和管理方面的沟通效率。

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