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住院患者华法林迅速达到治疗目标的相关因素及安全性:一项回顾性队列研究。

Associated factors and safety of the rapidly achieving first therapeutic target of warfarin in hospitalized patients: a retrospective cohort study.

机构信息

Department of Pharmacy, Second Affiliated Hospital, Zhejiang University School of Medicine, 310009, Hangzhou, China.

College of Pharmacy, Hangzhou Medical College, 310053, Hangzhou, China.

出版信息

Int J Clin Pharm. 2022 Aug;44(4):939-946. doi: 10.1007/s11096-022-01404-9. Epub 2022 Apr 21.

DOI:10.1007/s11096-022-01404-9
PMID:35449349
Abstract

BACKGROUND

Warfarin is a commonly used anticoagulant drug in clinical practice. Rapidly achieving the first therapeutic international normalized ratio (INR) of warfarin may reduce the hospital length of stay. However, little research has been carried out to evaluate the influencing factors and the safety of rapidly achieving the first therapeutic INR target of warfarin.

AIM

To investigate the associated factors and the safety of rapidly achieving the first therapeutic INR target of warfarin.

METHOD

A retrospective cohort study was conducted in inpatients who took warfarin from November 2018 to October 2019. Patients' information was retrieved from medical records.

RESULTS

487 patients were included. The mean achieving first therapeutic target time was 6.0 ± 3.2 days (median, 5.0 days). Age > 65 years, body mass index < 24 kg/m, and initial warfarin dose ≥ 3 mg/d were independent factors associated with the rapidly achieving first INR target of warfarin therapy. The incidence of INR ≥ 4 was higher in patients achieving the first INR target rapidly than those achieving the first INR target slowly, while there were no significant differences in bleeding events between the two groups.

CONCLUSION

Hospitalized patients aged > 65 years, with a body mass index < 24 kg/m, or receiving an initial warfarin dose ≥ 3 mg/d were more likely to achieve the first INR target of warfarin rapidly. Closer INR monitoring and appropriate warfarin dose adjustment are recommended to improve the safety for patients achieving the first INR ≥ 1.8 within 6 days after beginning oral warfarin.

摘要

背景

华法林是临床实践中常用的抗凝药物。快速达到华法林的首次治疗国际标准化比值(INR)可能会缩短住院时间。然而,对于快速达到华法林首次治疗 INR 目标的影响因素及其安全性的研究甚少。

目的

探讨快速达到华法林首次治疗 INR 目标的相关因素及安全性。

方法

回顾性队列研究纳入 2018 年 11 月至 2019 年 10 月服用华法林的住院患者,从病历中提取患者信息。

结果

共纳入 487 例患者,达到首次治疗目标的平均时间为 6.0±3.2 天(中位数为 5.0 天)。年龄>65 岁、体质量指数(BMI)<24kg/m2、初始华法林剂量≥3mg/d 是快速达到华法林治疗首次 INR 目标的独立影响因素。与缓慢达到首次 INR 目标的患者相比,快速达到首次 INR 目标的患者 INR≥4 的发生率更高,两组出血事件无显著差异。

结论

年龄>65 岁、BMI<24kg/m2 或初始华法林剂量≥3mg/d 的住院患者更有可能快速达到华法林的首次 INR 目标。建议更密切地监测 INR,并适当调整华法林剂量,以提高在开始口服华法林后 6 天内达到首次 INR≥1.8 的患者的安全性。

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