A systematic review of consumers' knowledge, attitudes and experiences of primary health professionals' role in genomic medicine.

IF 4.6 2区 生物学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY
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.

对消费者对初级卫生专业人员在基因组医学中的作用的知识、态度和经验进行系统回顾。
将基因检测纳入初级保健正在影响医疗保健实践,但人们对消费者对基因检测服务或提供基因检测服务的从业人员的知识、态度和经验知之甚少。本系统综述综合了同行评议的关于初级卫生专业人员在初级保健环境中提供基因组医学的作用的消费者观点的研究。系统检索PubMed、Scopus、Embase、CINAHL、Cochrane Library和PsycINFO 6个数据库。纳入标准侧重于研究消费者的知识,态度,以及与初级保健提供者(PCP)在基因组医学中的角色相关的经验。与审查目标相关的数据,包括关键文章特征、实施的障碍和促进因素,以及推进或优化的建议,被提取并使用专题分析进行分析。我们回顾了19项符合纳入标准的研究,涉及3557名受试者。专题分析确定了两个总体主题:消费者对基因组检测的看法,无论环境如何,包括三个分主题,以及消费者对初级保健环境中基因组检测的看法,包括四个分主题。消费者对pcp作为熟悉和平易近人的专业人士的信任是一个主要问题。当PCP消息灵通且善于沟通时,消费者通常会报告积极的体验,但当PCP缺乏知识或信心时,负面体验很常见。正如其他医疗保健机构所报告的那样,对隐私、数据安全和基因组检测成本的担忧也很突出。将基因组医学纳入初级保健需要在PCP和消费者之间建立信任,加强PCP教育和资源,解决隐私和成本问题,并加强与遗传专家的合作,以改善消费者体验。
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来源期刊
European Journal of Human Genetics
European Journal of Human Genetics 生物-生化与分子生物学
CiteScore
9.90
自引率
5.80%
发文量
216
审稿时长
2 months
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
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