Incorporation of pharmacogenomics into routine clinical practice: the Clinical Pharmacogenetics Implementation Consortium (CPIC) guideline development process.
Incorporation of pharmacogenomics into routine clinical practice: the Clinical Pharmacogenetics Implementation Consortium (CPIC) guideline development process.
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DOI:
10.2174/1389200215666140130124910
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发表时间:
2014-02
影响因子:
2.3
通讯作者:
Johnson SG
中科院分区:
文献类型:
--
作者:
Caudle KE;Klein TE;Hoffman JM;Muller DJ;Whirl-Carrillo M;Gong L;McDonagh EM;Sangkuhl K;Thorn CF;Schwab M;Agundez JA;Freimuth RR;Huser V;Lee MT;Iwuchukwu OF;Crews KR;Scott SA;Wadelius M;Swen JJ;Tyndale RF;Stein CM;Roden D;Relling MV;Williams MS;Johnson SG
The Clinical Pharmacogenetics Implementation Consortium (CPIC) publishes genotype-based drug guidelines to help clinicians understand how available genetic test results could be used to optimize drug therapy. CPIC has focused initially on well-known examples of pharmacogenomic associations that have been implemented in selected clinical settings, publishing nine to date. Each CPIC guideline adheres to a standardized format and includes a standard system for grading levels of evidence linking genotypes to phenotypes and assigning a level of strength to each prescribing recommendation. CPIC guidelines contain the necessary information to help clinicians translate patient-specific diplotypes for each gene into clinical phenotypes or drug dosing groups. This paper reviews the development process of the CPIC guidelines and compares this process to the Institute of Medicine’s Standards for Developing Trustworthy Clinical Practice Guidelines.
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