What do we need to transfer pharmacogenetics findings into the clinic?

In an ideal world, individual genetic information should be integrated in computer provider order entry (CPOE) systems and/or clinical decision support tools to calculate precise dosing regimens or to establish effectivity or risks of treatment before physicians generate electronic prescriptions. Ac...

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Published in:Pharmacogenomics Vol. 19; no. 7; pp. 589 - 592
Main Authors: Slob, Elise MA, Vijverberg, Susanne JH, Pijnenburg, Mariëlle W, Koppelman, Gerard H, der Zee, Anke-Hilse Maitland-van
Format: Journal Article
Language:English
Published: England Future Medicine Ltd 01-05-2018
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Summary:In an ideal world, individual genetic information should be integrated in computer provider order entry (CPOE) systems and/or clinical decision support tools to calculate precise dosing regimens or to establish effectivity or risks of treatment before physicians generate electronic prescriptions. According to the clinical evidence pyramid, most weight is given to randomized controlled trials (RCTs) that compare pharmacogenetic-guided treatment strategy to usual care. [...]in case of strong observational evidence of genetic variants associated with life-threatening drug-induced toxicities (3), such as CYP2D6 genotype of breastfeeding mothers and codeine-induced neonate mortality (4). [...]it is important to reach consensus what level of evidence is needed to change clinical practice when precision medicine RCTs are not feasible or ethical. [...]we are moving onward towards implementation of pharmacogenetics into clinical practice.
Bibliography:SourceType-Other Sources-1
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ISSN:1462-2416
1744-8042
DOI:10.2217/pgs-2018-0026