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

机译:PGX困惑? 探索药物替代结果对医疗管理,披露和患者行为的影响

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摘要

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.
机译:药物替代(PGX)试验代表精密药物的显着进展。 我们的目标是探讨PGX结果,药物管理和向提供商披露的返回后的看法。 我们调查了具有PGX测试的客户,并对PGX结果进行了图表审查。 分别为84%和94%的参与者发现了测试前和后期遗传咨询有用。 公开内容有一个显着差异,而6%的结果向药剂师公开了50%,向医生公开了50%。 定性分析确定了三个主题:1)心理反应; 2)感知效用; 3)披露的经验。 我们的研究支持提供遗传咨询,用于对非疾病相关的遗传测试。 PGX测试的好处可以通过医生,药剂师,遗传辅导员和患者的协作来优化。

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