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参与者对药物基因组学的理解和看法:梅奥诊所 RIGHT 方案(正确的药物、正确的剂量、正确的时间)。

Participant-perceived understanding and perspectives on pharmacogenomics: the Mayo Clinic RIGHT protocol (Right Drug, Right Dose, Right Time).

机构信息

Department of Health Sciences Research, Mayo Clinic, Rochester, Minnesota, USA.

Center for Individualized Medicine, Mayo Clinic, Rochester, Minnesota, USA.

出版信息

Genet Med. 2017 Jul;19(7):819-825. doi: 10.1038/gim.2016.192. Epub 2017 Jan 5.

Abstract

PURPOSE

To examine predictors of understanding preemptive CYP2D6 pharmacogenomics test results and to identify key features required to improve future educational efforts of preemptive pharmacogenomics testing.

METHODS

One thousand ten participants were surveyed after receiving preemptive CYP2D6 pharmacogenomics test results.

RESULTS

Eighty-six percent (n = 869) of patients responded. Of the responders, 98% were white and 55% were female; 57% had 4 years or more of post-secondary education and an average age of 58.9 ± 5.5 years. Twenty-six percent said that they only somewhat understood their results and 7% reported they did not understand them at all. Only education predicted understanding. The most common suggestion for improvement was the use of layperson's terms when reporting results. In addition, responders suggested that results should be personalized by referring to medications that they were currently using. Of those reporting imperfect drug adherence, most (91%) reported they would be more likely to use medication as prescribed if pharmacogenomic information was used to help select the drug or dose.

CONCLUSION

Despite great efforts to simplify pharmacogenomic results (or because of them), approximately one-third of responders did not understand their results. Future efforts need to provide more examples and tailor results to the individual. Incorporation of pharmacogenomics is likely to improve medication adherence.Genet Med advance online publication 05 January 2017.

摘要

目的

探讨理解预先 CYP2D6 药物基因组学检测结果的预测因素,并确定改进预先药物基因组学检测教育工作所需的关键特征。

方法

对 1100 名接受预先 CYP2D6 药物基因组学检测结果的患者进行了调查。

结果

86%(n=869)的患者做出了回应。在应答者中,98%为白人,55%为女性;57%具有 4 年或以上的高等教育背景,平均年龄为 58.9±5.5 岁。26%的人表示他们只是部分理解了检测结果,7%的人表示他们根本不理解。只有教育程度可预测理解程度。最常见的改进建议是在报告结果时使用通俗易懂的术语。此外,应答者建议应通过参考他们正在使用的药物来个性化结果。在报告药物依从性不理想的人群中,大多数(91%)表示如果使用药物基因组学信息来帮助选择药物或剂量,他们更有可能按照医嘱使用药物。

结论

尽管在简化药物基因组学结果方面做出了巨大努力(或者正是因为这些努力),但大约三分之一的应答者仍然不理解他们的检测结果。未来的工作需要提供更多的例子,并根据个人情况调整结果。药物基因组学的纳入可能会提高药物依从性。遗传医学在线发表 2017 年 1 月 5 日。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d348/5498279/ef592bc9671b/nihms827445f1.jpg

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