Samran Sheriff, Maryam Vizheh, Romika Patel, Samantha Spanos, Klay Lamprell, Jeffrey Braithwaite, Janet C Long
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引用次数: 0
Abstract
The integration of genetic testing into primary care is influencing healthcare practices, yet little is known about consumers' knowledge, attitudes, and experiences with genetic testing services or the practitioners who provide them. This systematic review synthesizes peer-reviewed studies on consumers' perspectives regarding the role of primary health professionals in delivering genomic medicine in primary care settings. Six databases (PubMed, Scopus, Embase, CINAHL, Cochrane Library and PsycINFO) were systematically searched. Inclusion criteria focused on studies that addressed consumers' knowledge, attitudes, and experiences related to Primary Care Providers' (PCP) roles in genomic medicine. Data relevant to the review objective, including key article characteristics, barriers and facilitators of implementation, and recommendations for advancement or optimisation, were extracted and analysed using thematic analysis. We reviewed 19 studies meeting the inclusion criteria involving 3557 participants. Thematic analysis identified two overarching themes: consumer views on genomic testing irrespective of setting, comprising three sub-themes, and consumer views on genomic testing in the primary care setting, comprising four sub-themes. Consumers' trust in PCPs as familiar and approachable professionals was a major concern. Consumers often reported positive experiences when PCPs were well-informed and communicative, but negative experiences were common when there was a perceived lack of knowledge or confidence from the PCP. As reported in other healthcare settings, concerns about privacy, data security, and the cost of genomic testing were also prominent. Integrating genomic medicine into primary care requires trust-building between PCPs and consumers, enhancing PCP education and resources, addressing privacy and cost concerns and strengthening collaboration with genetic specialists to improve consumer experiences.
期刊介绍:
The European Journal of Human Genetics is the official journal of the European Society of Human Genetics, publishing high-quality, original research papers, short reports and reviews in the rapidly expanding field of human genetics and genomics. It covers molecular, clinical and cytogenetics, interfacing between advanced biomedical research and the clinician, and bridging the great diversity of facilities, resources and viewpoints in the genetics community.
Key areas include:
-Monogenic and multifactorial disorders
-Development and malformation
-Hereditary cancer
-Medical Genomics
-Gene mapping and functional studies
-Genotype-phenotype correlations
-Genetic variation and genome diversity
-Statistical and computational genetics
-Bioinformatics
-Advances in diagnostics
-Therapy and prevention
-Animal models
-Genetic services
-Community genetics