Attitudes on pharmacogenomic results as secondary findings among medical geneticists

被引:0
|
作者
Bartos, Meghan N. [1 ,2 ]
Scott, Stuart A. [1 ,3 ,4 ]
Jabs, Ethylin Wang [1 ]
Naik, Hetanshi [1 ]
机构
[1] Icahn Sch Med Mt Sinai, Dept Genet & Genom Sci, New York, NY 10029 USA
[2] Univ Alabama Birmingham, Heersink Sch Med, Dept Genet, Birmingham, AL 35294 USA
[3] Stanford Univ, Dept Pathol, Stanford, CA 94305 USA
[4] Stanford Hlth Care, Clin Genom Lab, Palo Alto, CA USA
来源
PHARMACOGENETICS AND GENOMICS | 2022年 / 32卷 / 08期
关键词
complex traits; electronic health records; genetic testing; gene panel; laboratory reports; pharmacogenomics; pharmacogenetics; precision medicine; FOR-MOLECULAR-PATHOLOGY; INCIDENTAL FINDINGS; CLINICAL EXOME; RECOMMENDATIONS; COLLEGE; ASSOCIATION; CONTEXT;
D O I
10.1097/FPC.0000000000000479
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Objectives As evidence mounts supporting the utility of pharmacogenomic-guided medication management, incorporating pharmacogenomic genes into secondary finding results from sequencing panels is increasingly under consideration. We studied medical geneticists' attitudes on receiving pharmacogenomic results as secondary finding. Methods Four focus groups with 16 medical geneticists total were conducted followed by thematic analysis. Results All participants ordered genetic sequencing tests; however, the majority had rarely or never ordered pharmacogenomic tests (10/16) or prescribed medications with established response variability (11/16). In total 81.3% expressed low comfort interpreting pharmacogenomic results without appropriate clinical resources (13/16). The positives of receiving pharmacogenomic results as secondary finding included prevention of adverse drug reactions in adults, grateful information-seeking patients, the ability to rapidly prescribe more effective treatments and appreciation of the recent advances in both pharmacogenomic knowledge and available guidelines. Negatives included laboratory reporting issues, exclusivity of pharmacogenomic results to certain populations, lengthy reports concealing pharmacogenomic results in patient charts and laboratories marketing to individuals without prior pharmacogenomic knowledge or targeting inappropriate populations. The most desirable pharmacogenomic resources included a universal electronic health record clinical decision support tool to assist identifying and implementing pharmacogenomic results, a specialized pharmacist as part of the care team, additional pharmacogenomic training during medical/graduate school, and a succinct interpretation of pharmacogenomic results included on laboratory reports. Conclusions The majority of participants agreed that adding certain actionable pharmacogenomic genes to the American College of Medical Genetics and Genomics SF list is reasonable; however, this was qualified with a need for additional resources to support implementation.
引用
收藏
页码:273 / 280
页数:8
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