作者
Munir Pirmohamed, Girvan Burnside, Niclas Eriksson, Andrea L Jorgensen, Cheng Hock Toh, Toby Nicholson, Patrick Kesteven, Christina Christersson, Bengt Wahlström, Christina Stafberg, J Eunice Zhang, Julian B Leathart, Hugo Kohnke, Anke H Maitland-van der Zee, Paula R Williamson, Ann K Daly, Peter Avery, Farhad Kamali, Mia Wadelius
发表日期
2013/12/12
期刊
New England Journal of Medicine
卷号
369
期号
24
页码范围
2294-2303
出版商
Massachusetts Medical Society
简介
Background
The level of anticoagulation in response to a fixed-dose regimen of warfarin is difficult to predict during the initiation of therapy. We prospectively compared the effect of genotype-guided dosing with that of standard dosing on anticoagulation control in patients starting warfarin therapy.
Methods
We conducted a multicenter, randomized, controlled trial involving patients with atrial fibrillation or venous thromboembolism. Genotyping for CYP2C9*2, CYP2C9*3, and VKORC1 (−1639G→A) was performed with the use of a point-of-care test. For patients assigned to the genotype-guided group, warfarin doses were prescribed according to pharmacogenetic-based algorithms for the first 5 days. Patients in the control (standard dosing) group received a 3-day loading-dose regimen. After the initiation period, the treatment of all patients was managed according to routine clinical practice. The primary outcome …
引用总数
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学术搜索中的文章
M Pirmohamed, G Burnside, N Eriksson, AL Jorgensen… - New England Journal of Medicine, 2013