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华法林起始方案用于国际标准化比值目标为2.0至3.0的评估。

Evaluation of an Initiation Regimen of Warfarin for International Normalized Ratio Target 2.0 to 3.0.

作者信息

Mohamed Sahimi, Mei Fong Chan, Jie Ming Yew, Naila Kori Ahlam, Abdul Wahab Sopian, Mohd Ali Zarina

机构信息

Hospital Tengku Ampuan Afzan, Kuantan, Pahang, Malaysia.

University Malaysia Pahang, Kuantan, Pahang, Malaysia.

出版信息

J Pharm Technol. 2021 Dec;37(6):286-292. doi: 10.1177/87551225211034175. Epub 2021 Aug 5.

Abstract

he number of patients on warfarin therapy is rising steadily. Although warfarin is beneficial, it carries a high risk of bleeding, especially if the international normalized ratio (INR) values exceed 3.0. Currently, no warfarin initiation regimens have been developed for the Asian population, especially for Malaysians. This article describes the efficacy and safety of a new initiation regimen for warfarin among warfarin-naive patients. Data were retrospectively collected from the ambulatory and inpatient settings. A total of 165 patients who each had a target INR of 2.0 to 3.0 were included in the study. The mean age was 57.2 years and 94 patients were male. A total of 108 patients used Regimen 1 (5 mg/5 mg/3mg) and the rest of the patients used Regimen 2 (5 mg/3 mg/3 mg). Most patients used warfarin either for atrial fibrillation (52.1%) or for venous thromboembolism (29.7%). Overall, 88 of the patients had INR values above 50% from the baseline on Day 4. Additionally, 13 patients had INR values of >3.2, which required withholding and lower dose of warfarin. The predicted weekly maintenance warfarin dose (23 ± 0.5 mg/week) was found to have correlated closely with the actual maintenance dose (22.8 ± 0.5 mg/week; = 0.75). Nearly two thirds (70.3%) of the patients achieved the target INR on Day 11. The warfarin initiation regimens in this study was simple, safe, and suitable to be used in both ambulatory and inpatient settings for managing warfarin therapy.

摘要

接受华法林治疗的患者数量正在稳步上升。尽管华法林有益,但它具有很高的出血风险,特别是当国际标准化比值(INR)超过3.0时。目前,尚未为亚洲人群,尤其是马来西亚人制定华法林起始方案。本文描述了一种对华法林初治患者的新起始方案的疗效和安全性。数据是从门诊和住院环境中回顾性收集的。共有165名目标INR为2.0至3.0的患者纳入研究。平均年龄为57.2岁,男性患者94名。共有108名患者使用方案1(5毫克/5毫克/3毫克),其余患者使用方案2(5毫克/3毫克/3毫克)。大多数患者使用华法林治疗房颤(52.1%)或静脉血栓栓塞(29.7%)。总体而言,88名患者在第4天的INR值比基线高出50%以上。此外,13名患者的INR值>3.2,这需要停用并降低华法林剂量。发现预测的每周维持华法林剂量(23±0.5毫克/周)与实际维持剂量(22.8±0.5毫克/周;r = 0.75)密切相关。近三分之二(70.3%)的患者在第11天达到目标INR。本研究中的华法林起始方案简单、安全,适用于门诊和住院环境中管理华法林治疗。

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