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

被引:21
|
作者
Lemke, Amy A. [1 ]
Amendola, Laura M. [2 ]
Kuchta, Kristine [3 ]
Dunnenberger, Henry M. [1 ]
Thompson, Jennifer [1 ]
Johnson, Christian [1 ,4 ]
Ilbawi, Nadim [5 ]
Oshman, Lauren [5 ]
Hulick, Peter J. [1 ]
机构
[1] NorthShore Univ HealthSyst, Neaman Ctr Personalized Med, Evanston, IL 60201 USA
[2] Univ Washington, Div Med Genet, Seattle, WA 98115 USA
[3] NorthShore Univ HealthSyst, Ctr Biomed Res Informat, Evanston, IL 60201 USA
[4] Univ Chicago, Dept Med, 5841 S Maryland Ave, Chicago, IL 60637 USA
[5] NorthShore Univ HealthSyst, Dept Family Med, Evanston, IL 60201 USA
来源
JOURNAL OF PERSONALIZED MEDICINE | 2020年 / 10卷 / 04期
关键词
genomic screening; precision medicine; primary care; clinical implementation; genomics education; PROVIDERS; PERCEPTIONS; KNOWLEDGE; ATTITUDES;
D O I
10.3390/jpm10040165
中图分类号
R19 [保健组织与事业(卫生事业管理)];
学科分类号
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.
引用
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页码:1 / 13
页数:13
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