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感到困惑?探讨药物基因组学结果对医疗管理、披露和患者行为的影响。

Perplexed by PGx? Exploring the impact of pharmacogenomic results on medical management, disclosures and patient behavior.

机构信息

Department of Genetic Counselling, The Hospital for Sick Children, University of Toronto, Toronto, Ontario, Canada.

Department of Molecular Genetics, University of Toronto, Toronto, Ontario, Canada.

出版信息

Pharmacogenomics. 2019 Apr;20(5):319-329. doi: 10.2217/pgs-2018-0179. Epub 2019 Apr 15.

Abstract

Pharmacogenomic (PGx) tests represent significant advances in precision medicine. Our aim was to explore perceptions following the return of PGx results, medication management, and disclosure to providers. We surveyed clients who had PGx testing and conducted a chart review of PGx results. Respectively, 84% and 94% of participants found pre- and post-test genetic counseling helpful. There was a significant difference in disclosure, while 6% disclosed results to a pharmacist, 50% disclosed to a physician. Qualitative analysis identified three themes: 1) psychological response; 2) perceived utility; 3) experiences with disclosure. Our study supports the provision of genetic counseling for a non-disease related genetic test. Benefits of PGx testing can be optimized by the collaboration of physicians, pharmacists, genetic counselors and patients.

摘要

药物基因组学(PGx)检测代表了精准医学的重大进展。我们的目的是探讨 PGx 结果返回后、药物管理和向提供者披露的情况。我们对接受过 PGx 检测的客户进行了调查,并对 PGx 结果进行了图表审查。分别有 84%和 94%的参与者认为测试前后的遗传咨询很有帮助。披露情况存在显著差异,而 6%的参与者向药剂师披露了结果,50%的参与者向医生披露了结果。定性分析确定了三个主题:1)心理反应;2)感知效用;3)披露经验。我们的研究支持为非疾病相关的基因检测提供遗传咨询。通过医生、药剂师、遗传咨询师和患者的合作,可以优化 PGx 检测的益处。

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