Pharmacogenetic information in Swiss drug labels - a systematic analysis

被引:17
作者
Jeiziner, C. [1 ]
Suter, K. [2 ]
Wernli, U. [1 ]
Barbarino, J. M. [3 ]
Gong, L. [3 ]
Whirl-Carrillo, M. [3 ]
Klein, T. E. [3 ,4 ]
Szucs, T. D. [2 ]
Hersberger, K. E. [1 ]
Meyer zu Schwabedissen, H. E. [5 ]
机构
[1] Univ Basel, Dept Pharmaceut Sci, Pharmaceut Care Res Grp, CH-4001 Basel, Switzerland
[2] Univ Basel, European Ctr Pharmaceut Med, Fac Med, CH-4056 Basel, Switzerland
[3] Stanford Univ, Dept Biomed Data Sci, Stanford, CA 94305 USA
[4] Stanford Univ, Dept Med, Stanford, CA 94305 USA
[5] Univ Basel, Dept Pharmaceut Sci, Biopharm, CH-4056 Basel, Switzerland
关键词
CONSORTIUM CPIC GUIDELINE; BIOMARKER INFORMATION; CYP2D6; VARIANTS; GENE; HYPERSENSITIVITY; POLYMORPHISMS; GENOTYPES; HLA; US;
D O I
10.1038/s41397-020-00195-4
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Implementation of pharmacogenetics (PGx) and individualization of drug therapy is supposed to obviate adverse drug reactions or therapy failure. Health care professionals (HCPs) use drug labels (DLs) as reliable information about drugs. We analyzed the Swiss DLs to give an overview on the currently available PGx instructions. We screened 4306 DLs applying natural language processing focusing on drug metabolism (pharmacokinetics) and we assigned PGx levels following the classification system of PharmGKB. From 5979 hits, 2564 were classified as PGx-relevant affecting 167 substances. 55% (n = 93) were classified as "actionable PGx". Frequently, PGx information appeared in the pharmacokinetics section and in DLs of the anatomic group "nervous system". Unstandardized wording, appearance of PGx information in different sections and unclear instructions challenge HCPs to identify and interpret PGx information and translate it into practice. HCPs need harmonization and standardization of PGx information in DLs to personalize drug therapies and tailor pharmaceutical care.
引用
收藏
页码:423 / 434
页数:12
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