Department of Pharmaceutical Sciences, Division of Pharmacoepidemiology & Clinical Pharmacology, Utrecht University, Utrecht, The Netherlands.
Pharmacogenomics. 2012 Sep;13(12):1405-17. doi: 10.2217/pgs.12.124.
Genotyping patients for CYP2C9 and VKORC1 polymorphisms can improve the accuracy of dosing during the initiation of anticoagulation with vitamin K antagonists (coumarin derivatives). The anticipated degree of improvement in the safety of anticoagulation with coumarins through genotyping may vary depending on the quality of patient care, which varies both with and among countries. The management and the cost of anticoagulant care can therefore influence the cost-effectiveness of genotyping within any given country. In this article, we provide an overview of the cost-effectiveness of pharmacogenetics-guided dosing of coumarin derivatives. We describe the organization of anticoagulant care in the UK, Sweden, The Netherlands, Greece, Germany and Austria, where a genotype-guided dosing algorithm is currently being investigated as part of the EU-PACT trial. We also explore the costs of anticoagulant care for the treatment of atrial fibrillation in these countries.
对 CYP2C9 和 VKORC1 基因多态性进行基因分型可以提高维生素 K 拮抗剂(香豆素衍生物)起始抗凝治疗时的剂量准确性。通过基因分型提高香豆素抗凝安全性的预期程度可能因患者护理质量的不同而有所不同,而这种质量的不同既存在于国家之间,也存在于国家内部。因此,抗凝治疗管理和成本可能会影响特定国家内基因分型的成本效益。在本文中,我们概述了香豆素衍生物药物基因组学指导剂量的成本效益。我们描述了英国、瑞典、荷兰、希腊、德国和奥地利的抗凝治疗管理情况,在这些国家,正在作为 EU-PACT 试验的一部分研究一种基于基因型的给药算法。我们还探讨了这些国家治疗心房颤动的抗凝治疗成本。