General practitioners' (GPs) experience, attitudes and needs on clinical genetic services: a systematic review.

IF 2.6 3区 医学 Q1 PRIMARY HEALTH CARE
Cheryl Siow Bin Ong, Rose Wai-Yee Fok, Ryo Chee Ann Tan, Si Ming Fung, Shirley Sun, Joanne Yuen Yie Ngeow
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引用次数: 2

Abstract

Objective: The proliferation and growing demands of genetic testing are anticipated to revolutionise medical practice. As gatekeepers of healthcare systems, general practitioners (GPs) are expected to play a critical role in the provision of clinical genetic services. This paper aims to review existing literature on GPs' experience, attitudes and needs towards clinical genetic services.

Design: A systematic mixed studies review of papers published between 2010 and 2022.

Eligibility criteria: The inclusion criterion was peer-reviewed articles in English and related to GPs' experience, views and needs on any genetic testing.

Information sources: The PubMed, PsycINFO, Cochrane, EMBASE databases were searched using Mesh terms, Boolean and wildcards combinations to identify peer-reviewed articles published from 2010 to 2022. Study quality was assessed using Mixed Methods Appraisal Tool. Only articles that fulfilled the inclusion criteria were selected. A thematic meta-synthesis was conducted on the final sample of selected articles to identify key themes.

Results: A total of 62 articles were included in the review. Uncertainty over GPs' role in providing genetic services were attributed by the lack of confidence and time constraints and rarity of cases may further exacerbate their reluctance to shoulder an expanded role in clinical genetics. Although educational interventions were found to increasing GPs' knowledge and confidence to carry out genetic tasks, varied interest on genetic testing and preference for a shared care model with other genetic health professionals have resulted in minimal translation to clinical adoption.

Conclusion: This review highlights the need for deeper exploration of GPs' varied experience and attitudes towards clinical genetic services to better facilitate targeted intervention in the adoption of clinical genetics.

全科医生对临床遗传服务的经验、态度和需求:系统综述。
目的:基因检测的扩散和日益增长的需求预计将彻底改变医疗实践。作为医疗保健系统的守门人,全科医生(全科医生)有望在提供临床遗传服务中发挥关键作用。本文旨在回顾现有文献对全科医生的经验,态度和对临床遗传服务的需求。设计:对2010年至2022年间发表的论文进行系统的混合研究综述。入选标准:入选标准是同行评议的英文文章,并与全科医生对任何基因检测的经验、观点和需求有关。信息来源:检索PubMed, PsycINFO, Cochrane, EMBASE数据库,使用Mesh术语,布尔和通配符组合来识别2010年至2022年发表的同行评议文章。采用混合方法评价工具评价研究质量。只选择符合纳入标准的文章。对选定文章的最后样本进行主题综合,以确定关键主题。结果:共纳入62篇文献。全科医生在提供遗传服务方面的作用的不确定性归因于缺乏信心和时间限制,以及病例的罕见可能进一步加剧他们不愿在临床遗传学中承担更大的作用。虽然教育干预被发现增加了全科医生的知识和信心来执行遗传任务,但对基因检测的不同兴趣和对与其他遗传健康专业人员共享护理模式的偏好导致极少转化为临床采用。结论:本综述强调有必要深入探讨全科医生对临床遗传学服务的不同经验和态度,以更好地促进临床遗传学应用的针对性干预。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
9.70
自引率
0.00%
发文量
27
审稿时长
19 weeks
期刊介绍: Family Medicine and Community Health (FMCH) is a peer-reviewed, open-access journal focusing on the topics of family medicine, general practice and community health. FMCH strives to be a leading international journal that promotes ‘Health Care for All’ through disseminating novel knowledge and best practices in primary care, family medicine, and community health. FMCH publishes original research, review, methodology, commentary, reflection, and case-study from the lens of population health. FMCH’s Asian Focus section features reports of family medicine development in the Asia-pacific region. FMCH aims to be an exemplary forum for the timely communication of medical knowledge and skills with the goal of promoting improved health care through the practice of family and community-based medicine globally. FMCH aims to serve a diverse audience including researchers, educators, policymakers and leaders of family medicine and community health. We also aim to provide content relevant for researchers working on population health, epidemiology, public policy, disease control and management, preventative medicine and disease burden. FMCH does not impose any article processing charges (APC) or submission charges.
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