Evaluation of pharmacogenetic automated clinical decision support for clopidogrel

被引:0
|
作者
Massmann, Amanda [1 ,2 ]
Van Heukelom, Joel [1 ,2 ]
Weaver, Max [1 ]
Schultz, April [1 ,2 ]
Figueroa, Debbie M. [2 ,3 ]
Stys, Adam [2 ,4 ]
Stys, Tomasz P. [2 ,4 ]
Christensen, Kurt D. [5 ,6 ]
机构
[1] Sanford Imagenet, Sioux Falls, SD 57105 USA
[2] Univ South Dakota, Sch Med, Dept Internal Med, Vermillion, SD 57069 USA
[3] Sanford Med Genet Lab, Sioux Falls, SD 57105 USA
[4] Sanford Cardiovasc Inst, Sioux Falls, SD 57105 USA
[5] Harvard Pilgrim Hlth Care Inst, Precis Med Translat Res PROMoTeR Ctr, Dept Populat Med, Boston, MA 02215 USA
[6] Harvard Med Sch, Boston, MA 02215 USA
关键词
clinical; clopidogrel; decision support systems; electronic health records; genetic testing; patient safety; pharmacogenetics; pharmacy; platelet aggregation inhibitors; precision medicine; CYP2C19; GENOTYPE; IMPLEMENTATION; OUTCOMES; THERAPY;
D O I
10.1080/14622416.2024.2394014
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Aim: Clopidogrel requires CYP2C19 activation to have antiplatelet effects. Pharmacogenetic testing to identify patients with impaired CYP2C19 function can be coupled with clinical decision support (CDS) alerts to guide antiplatelet prescribing. We evaluated the impact of alerts on clopidogrel prescribing. Materials & methods: We retrospectively analyzed data for 866 patients in which CYP2C19-clopidogrel CDS was deployed at a single healthcare system during 2015-2023. Results: Analyses included 2,288 alerts. CDS acceptance rates increased from 24% in 2015 to 63% in 2023 (p < 0.05). Adjusted analyses also showed higher acceptance rates when clopidogrel had been ordered for a percutaneous intervention (OR: 28.7, p < 0.001) and when cardiologists responded to alerts (OR: 2.11, p = 0.001). Conclusion: CDS for CYP2C19-clopidogrel was effective in reducing potential drug-gene interactions. Its influence varied by clinician specialty and medication indications.
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页数:9
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