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

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TLDR
People 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.
Abstract
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 confl ict 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 identifi es key areas for health professionals to explore with patients that may improve the effectiveness of communication about disease risk and management.

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Citations
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Consolidated criteria for reporting qualitative research (COREQ): a 32-item checklist for interviews and focus groups

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The Consultation: An Approach to Learning and Teaching

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References
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Book

Meta-Ethnography: Synthesizing Qualitative Studies

TL;DR: In this paper, the idea of a meta-ethnography was introduced and a Meta-Ethnographic Approach was proposed to construct META-ETHNOGRAPHIES Reciprocal Translations as Synthesis this paper.
Journal ArticleDOI

Qualitative research methods in health technology assessment: a review of the literature.

TL;DR: Case studies are not necessarily restricted in scope and general concepts can be formulated, which may, upon further investigation, be found to be germane to a wider variety of settings.
Book

Patient-Centered Medicine: Transforming the Clinical Method

TL;DR: In this paper, the authors describe the four components of the patient-centered clinical method: exploring health, disease and the illness experience, understanding the whole person, finding common ground and enhancing the patientclinician relationship.
Journal ArticleDOI

Using meta ethnography to synthesise qualitative research: a worked example.

TL;DR: It is possible to use meta ethnography to synthesise the results of qualitative research, and the worked example has produced middle-range theories in the form of hypotheses that could be tested by other researchers.
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