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维生素 K 拮抗剂的最佳剂量方法。

Approaches to optimal dosing of vitamin K antagonists.

机构信息

Clinical Pharmacy Research & Applied Pharmacogenomics, Kaiser Permanente Colorado, Aurora, Colorado 80011, USA.

出版信息

Semin Thromb Hemost. 2012 Oct;38(7):667-72. doi: 10.1055/s-0032-1324713. Epub 2012 Aug 14.

Abstract

Although vitamin K antagonists (VKAs) such as warfarin have been used clinically for decades, evidence supporting how best to manage their use in clinical practice is lacking, but continues to emerge. This article summarizes available information regarding the clinical management of VKAs with focus on dosing strategies. For patients with previously stable international normalized ratio (INR) control, the single mildly out-of-range INR does not warrant a change in VKA dose. For out-of-range INRs, prompt repeat testing is associated with better INR control. After the first or second in-range INR value a maximum recall interval of 28 days is optimal, but after the third or greater consecutive in-range INR, longer recall intervals (up to 12 weeks for very stable patients) can be used. The use of validated VKA dosing nomograms is suggested as a means of reducing unwanted variability in VKA dosing decisions. Ensuring timely INR monitoring, and adjusting VKA doses when necessary, is important when interacting medications are prescribed during VKA therapy. Daily low-dose vitamin K supplementation is unlikely to improve INR control in patients with stable INR control but may be of benefit in VKA patients with unexplainable variability in the INR response. Dosing decisions during VKA therapy should follow a systematic and coordinated process as used in dedicated anticoagulation management services. Patient self-management of VKA therapy offers advantages for motivated patients who can demonstrate competency in self-management including fingerstick INR testing. Most patients with excessive anticoagulation who are not bleeding can be managed without administering vitamin K. There is an ongoing need for research evaluating VKA dosing practices that can consistently improve the outcomes of VKA therapy.

摘要

尽管华法林等维生素 K 拮抗剂 (VKA) 已在临床上应用了数十年,但缺乏最佳管理其临床应用的证据,不过相关证据仍在不断涌现。本文总结了 VKA 临床管理方面的现有信息,重点介绍了剂量策略。对于国际标准化比值 (INR) 控制稳定的患者,单次轻度超出范围的 INR 无需改变 VKA 剂量。对于超出范围的 INR,及时重复检测与更好的 INR 控制相关。首次或第二次在目标范围内的 INR 值后,最长 28 天的最大召回间隔是最佳的,但在第三次或更多次连续在目标范围内的 INR 后,可以使用更长的召回间隔(对于非常稳定的患者最长可达 12 周)。建议使用经过验证的 VKA 剂量图作为减少 VKA 剂量决策中不必要的变异性的方法。在 VKA 治疗期间开处方相互作用药物时,确保及时进行 INR 监测并在必要时调整 VKA 剂量非常重要。在 INR 控制稳定的患者中,每日低剂量维生素 K 补充不太可能改善 INR 控制,但可能对 INR 反应不可解释的变异性的 VKA 患者有益。在 VKA 治疗期间,应遵循专门抗凝管理服务中使用的系统和协调的决策过程。对于有能力进行自我管理(包括指血 INR 检测)并表现出自我管理能力的有动力的患者,VKA 治疗的自我管理具有优势。大多数没有出血的抗凝过度患者无需给予维生素 K 即可得到管理。需要不断开展研究,评估 VKA 剂量实践,以持续改善 VKA 治疗的结果。

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