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在一家大型学术医疗中心,对部分接受依诺肝素治疗的患者使用抗Xa因子监测。

The use of anti-factor Xa monitoring in a selection of patients receiving enoxaparin at a large academic medical center.

作者信息

Sacha Gretchen L, Greenlee Katie M, Ketz Jeffrey M

机构信息

Cleveland Clinic, 9500 Euclid Ave/JJN1-200, Cleveland, OH, 44195, USA.

出版信息

J Thromb Thrombolysis. 2016 Nov;42(4):479-85. doi: 10.1007/s11239-016-1384-x.

Abstract

Therapeutic enoxaparin is commonly used over heparin because of its favorable pharmacokinetic profile and ease of administration. Monitoring of the anticoagulant response, if necessary, is done with anti-factor Xa levels. Currently, it is suggested that monitoring may be beneficial in patients who are overweight and those with renal dysfunction. This study aimed to characterize the use of enoxaparin at a large-academic medical center in patients >150 kg, <45 kg and in those with renal dysfunction, and to describe the rate of anti-factor Xa monitoring in these patients. There were 273 patients included in the study: n = 96 for <45 kg arm, n = 111 for >150 kg arm and n = 66 for renal dysfunction arm. Less than 30 % of patients in each arm had low molecular weight heparin anti-factor Xa levels drawn. Of these only half were drawn as peak levels (4 h post dose). Overall rates of anti-factor Xa monitoring was low. It was found that obese patients achieved therapeutic anticoagulation with lower than recommended doses; underweight patients were often subtherapeutic on the recommended doses; and patients with renal dysfunction tended to have therapeutic to subtherapeutic anti-factor Xa levels. Ultimately, this evaluation showed that enoxaparin has unpredictable pharmacokinetics in these three high-risk patient populations and anti-factor Xa monitoring may be necessary to ensure therapeutic levels and appropriate dosing.

摘要

由于依诺肝素具有良好的药代动力学特性且易于给药,因此在治疗中其使用通常优于肝素。如有必要,可通过抗Xa因子水平监测抗凝反应。目前,建议在超重患者和肾功能不全患者中进行监测可能有益。本研究旨在描述一家大型学术医疗中心对体重>150 kg、<45 kg的患者以及肾功能不全患者使用依诺肝素的情况,并描述这些患者中抗Xa因子监测的比例。该研究共纳入273例患者:体重<45 kg组有96例,体重>150 kg组有111例,肾功能不全组有66例。每组中不到30%的患者检测了低分子量肝素抗Xa因子水平。其中只有一半检测的是峰值水平(给药后4小时)。抗Xa因子监测的总体比例较低。研究发现,肥胖患者使用低于推荐剂量即可达到治疗性抗凝;体重过轻的患者按推荐剂量用药时往往达不到治疗效果;肾功能不全患者的抗Xa因子水平往往处于治疗至亚治疗范围。最终,该评估表明依诺肝素在这三类高危患者群体中的药代动力学不可预测,可能需要进行抗Xa因子监测以确保达到治疗水平并合理给药。

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