评估初级保健提供者为未得到服务的人群提供基因和基因组服务的准备情况。

IF 1.3 4区 医学 Q4 GENETICS & HEREDITY Public Health Genomics Pub Date : 2021-09-07 DOI:10.1159/000518415
Yashoda Sharma, Livia Cox, Lucie Kruger, Veena Channamsetty, Susanne B Haga
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引用次数: 0

摘要

导言:基因组学知识和获取途径的增加推动了精准医疗和护理服务的发展。随着精准医疗在整个医疗保健领域的应用,遗传学和基因组学将在初级保健服务中发挥更大的作用。健康差异以及不同种族和民族群体的代表性不足,威胁着那些历来得不到充分服务的群体的公平就医。医疗服务提供者对基因组学应用的认识、知识和感知的重要性是决定其使用的重要因素:我们评估了联邦合格医疗中心--社区医疗中心公司(CHCI)的初级医疗服务提供者为服务不足人群提供基因和基因组检测的准备情况。在线调查问题主要涉及医疗服务提供者在基础和临床遗传学方面的教育和培训、对当前基因检测的熟悉程度以及将遗传学和基因组学纳入其当前实践的需求:77 位初级医疗服务提供者中有 50 位(65%)对调查做出了回应。接受过基础或临床遗传学培训(40%)、熟悉特定基因测试(36%)或对收集家族健康史有信心(44%)的人不到一半,70%的人认为患者会从基因测试中受益:尽管存在知识差距,受访者还是认识到了为患者提供这些服务的价值和必要性,不过他们希望在将遗传学和基因组学应用于实践方面得到更多教育,并在讨论与种族或民族相关的风险因素方面得到更多培训。我们进一步证明,医疗服务提供者需要教育资源和标准化指南来为服务不足的人群提供医疗服务,以优化遗传学和基因组学服务的合理使用和转诊,减少医疗服务中的差异。
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Evaluating Primary Care Providers' Readiness for Delivering Genetic and Genomic Services to Underserved Populations.

Introduction: Increased genomics knowledge and access are advancing precision medicine and care delivery. With the translation of precision medicine across health care, genetics and genomics will play a greater role in primary care services. Health disparities and inadequate representation of racial and ethnically diverse groups threaten equitable access for those historically underserved. Health provider awareness, knowledge, and perceived importance are important determinants of the utilization of genomic applications.

Methods: We evaluated the readiness of primary care providers at a Federally Qualified Health Center, the Community Health Center, Inc. (CHCI) for delivering genetic and genomic testing to underserved populations. Online survey questions focused on providers' education and training in basic and clinical genetics, familiarity with current genetic tests, and needs for incorporating genetics and genomics into their current practice.

Results: Fifty of 77 (65%) primary care providers responded to the survey. Less than half received any training in basic or clinical genetics (40%), were familiar with specific genetic tests (36%), or felt confident with collecting family health history (44%), and 70% believed patients would benefit from genetic testing.

Conclusion: Despite knowledge gaps, respondents recognized the value and need to bring these services to their patients, though would like more education on applying genetics and genomics into their practice, and more training about discussing risk factors associated with race or ethnicity. We provide further evidence of the need for educational resources and standardized guidelines for providers caring for underserved populations to optimize appropriate use and referral of genetic and genomic services and to reduce disparities in care.

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来源期刊
Public Health Genomics
Public Health Genomics 医学-公共卫生、环境卫生与职业卫生
CiteScore
2.90
自引率
0.00%
发文量
14
审稿时长
>12 weeks
期刊介绍: ''Public Health Genomics'' is the leading international journal focusing on the timely translation of genome-based knowledge and technologies into public health, health policies, and healthcare as a whole. This peer-reviewed journal is a bimonthly forum featuring original papers, reviews, short communications, and policy statements. It is supplemented by topic-specific issues providing a comprehensive, holistic and ''all-inclusive'' picture of the chosen subject. Multidisciplinary in scope, it combines theoretical and empirical work from a range of disciplines, notably public health, molecular and medical sciences, the humanities and social sciences. In so doing, it also takes into account rapid scientific advances from fields such as systems biology, microbiomics, epigenomics or information and communication technologies as well as the hight potential of ''big data'' for public health.
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