Warfarin dosing strategies evolution and its progress in the era of precision medicine, a narrative review

被引:13
作者
Fahmi, Amr Mohamed [1 ]
Elewa, Hazem [2 ,3 ]
El Jilany, Islam [4 ]
机构
[1] Hamad Med Corp, Doha, Qatar
[2] Qatar Univ, Coll Pharm, QU Hlth, POB 2713, Doha, Qatar
[3] Qatar Univ, Biomed & Pharmaceut Res Unit, QU Hlth, Doha, Qatar
[4] Univ Florida, Sch Pharm, Gainesville, FL USA
关键词
Genetic-guided warfarin dosing; Warfarin clinical dosing; Warfarin dosing algorithms; Warfarin fixed dosing; ANTICOAGULATION CONTROL; RANDOMIZED-TRIAL; CLINICAL FACTORS; PHARMACOGENOMICS; AGE; POLYMORPHISM; MANAGEMENT; PREDICT; WEIGHT; 10-MG;
D O I
10.1007/s11096-022-01386-8
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Background For decades, vitamin K antagonists and specifically warfarin, have been the sole agents used orally to manage thromboembolic conditions, including stroke and venous thromboembolism (VTE). Several factors lead to warfarin dose variability, including genetic and non-genetic factors which made warfarin management challenging especially at the initiation phase. To overcome the challenges with warfarin dosing at initiation, strategies other than conventional or fixed dosing were introduced and explored. Aim In this narrative review, we aim to discuss and critique the different dosing strategies for warfarin at initiation with more focus on genotype-guided warfarin dosing and the most recent supporting evidence for and against its use. Method Medline database was searched from 1965 to July 2021. Articles addressing different warfarin dosing methods were screened for inclusion. Results A number of methods exist for warfarin initiation. Studies comparing different dosing methods for initiation yielded conflicting outcomes due to differences in study design, population studied, comparator, and outcomes measured. Conclusions Looking at the big picture, the use of genetic dosing for warfarin initiation can lead to better outcomes. Whether these better outcomes are clinically or economically beneficial remains controversial.
引用
收藏
页码:599 / 607
页数:9
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