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Primary Care Physician Experiences with Integrated Population-Scale Genetic Testing: A Mixed-Methods Assessment

机译:初级保健医师与综合人口规模遗传检测经验:混合方法评估

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摘要

The scalable delivery of genomic medicine requires collaboration between genetics and non-genetics providers. Thus, it is essential to investigate and address the perceived value of and barriers to incorporating genetic testing into the clinical practice of primary care providers (PCPs). We used a mixed-methods approach of qualitative interviews and surveys to explore the experience of PCPs involved in the pilot DNA-10K population genetic testing program. Similar to previous research, PCPs reported low confidence with tasks related to ordering, interpreting and managing the results of genetic tests, and identified the need for additional education. PCPs endorsed high levels of utility for patients and their families but noted logistical challenges to incorporating genetic testing into their practice. Overall PCPs were not familiar with the United States’ Genetic Information Nondiscrimination Act and they expressed high levels of concern for patient data privacy and potential insurance discrimination. This PCP feedback led to the development and implementation of several processes to improve the PCP experience with the DNA-10K program. These results contribute to the knowledge base regarding genomic implementation using a mixed provider model and may be beneficial for institutions developing similar clinical programs.
机译:基因组医学的可扩展性递送需要遗传学和非遗传提供者之间的合作。因此,必须研究和解决将遗传测试纳入初级保健提供者(PCP)的临床实践的感知和障碍。我们使用了定性访谈和调查的混合方法方法,探讨了涉及试点DNA-10K人口遗传测试计划的PCP的经验。与以前的研究类似,PCP向有关订购,解释和管理遗传检验结果的任务报告了低信任,并确定了需要额外教育的需求。 PCP为患者及其家人提供了高水平的效用,但注意到将遗传测试纳入其实践的后勤挑战。整体PCP不熟悉美国的遗传信息无耻行为,他们对患者数据隐私和潜在保险歧视表示高度关注。这种PCP反馈导致了多个流程的开发和实施,以改善DNA-10K程序的PCP体验。这些结果有助于使用混合提供者模型的基因组实施的知识库,并且可能有利于制定类似临床计划的机构。

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