Clinical pharmacist, Hamad Medical Corporation, Doha, Qatar.
College of Pharmacy, QU Health, Qatar University, P.O. Box 2713, Doha, Qatar.
Int J Clin Pharm. 2022 Jun;44(3):599-607. doi: 10.1007/s11096-022-01386-8. Epub 2022 Mar 5.
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.
背景
几十年来,维生素 K 拮抗剂,特别是华法林,一直是唯一被用于口服治疗血栓栓塞性疾病的药物,包括中风和静脉血栓栓塞症(VTE)。一些因素导致华法林剂量的变化,包括遗传和非遗传因素,这使得华法林的管理极具挑战性,尤其是在起始阶段。为了克服华法林起始剂量管理的挑战,除了常规或固定剂量外,还引入并探索了其他剂量策略。
目的
在本叙述性综述中,我们旨在讨论和评价华法林起始时的不同剂量策略,更侧重于基于基因型的华法林剂量以及最近支持和反对其使用的证据。
方法
从 1965 年至 2021 年 7 月,我们在 Medline 数据库中进行了检索。筛选了有关不同华法林剂量方法的文章,以纳入本综述。
结果
有许多方法可用于华法林的起始剂量。由于研究设计、研究人群、对照和测量的结果不同,比较不同起始剂量方法的研究结果存在差异。
结论
从整体上看,华法林起始时使用基因剂量可以带来更好的结果。这些更好的结果是否在临床或经济上有益仍存在争议。