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评估肥胖症患者的依诺肝素给药方案。

Assessing an enoxaparin dosing protocol in morbidly obese patients.

作者信息

Lalama Jeffrey T, Feeney Megan E, Vandiver Jeremy W, Beavers K Diane, Walter Leah N, McClintic Jacqueline R

机构信息

Regis University School of Pharmacy, 3333 Regis Blvd H-28, Denver, CO, 80221-1099, USA,

出版信息

J Thromb Thrombolysis. 2015 May;39(4):516-21. doi: 10.1007/s11239-014-1117-y.

Abstract

The effect of obesity on the pharmacokinetics of enoxaparin is not clearly understood and traditional treatment doses in morbidly obese patients (body mass index [BMI] > 40 kg/m(2)) can lead to over anticoagulation. Our institution developed an inpatient protocol with reduced enoxaparin doses (0.75 mg/kg/dose based on actual body weight) for patients with a weight >200 kg or BMI > 40 kg/m(2). The primary objective was to determine if modified enoxaparin treatment doses would achieve therapeutic anti-Xa levels (goal range 0.6-1.0 IU/mL) in morbidly obese patients. Thirty-one patients were included in our study and had a median body weight of 138 kg (range 105-197) and a median BMI of 46.2 kg/m(2) (range 40.1-62). The initial peak anti-Xa levels were in therapeutic range in 15 of 31 patients (48 %) with an initial mean anti-Xa level of 0.92 IU/mL. Twenty-four patients (77 %) achieved therapeutic anti-Xa levels in goal range during their hospitalization, with a mean enoxaparin dose of 0.71 mg/kg. Bleeding and thrombotic events were minimal and all patients that achieved an anti-Xa level in goal range did so with a dose less than 1 mg/kg of enoxaparin.

摘要

肥胖对依诺肝素药代动力学的影响尚不清楚,病态肥胖患者(体重指数[BMI]>40kg/m²)的传统治疗剂量可能导致抗凝过度。我们机构为体重>200kg或BMI>40kg/m²的患者制定了一项降低依诺肝素剂量(基于实际体重0.75mg/kg/剂量)的住院治疗方案。主要目的是确定调整后的依诺肝素治疗剂量是否能使病态肥胖患者达到治疗性抗Xa水平(目标范围0.6-1.0IU/mL)。我们的研究纳入了31名患者,中位体重为138kg(范围105-197),中位BMI为46.2kg/m²(范围40.1-62)。31名患者中有15名(48%)的初始抗Xa峰值水平在治疗范围内,初始平均抗Xa水平为0.92IU/mL。24名患者(77%)在住院期间达到了目标范围内的治疗性抗Xa水平,依诺肝素平均剂量为0.71mg/kg。出血和血栓形成事件极少,所有达到目标范围内抗Xa水平的患者所用依诺肝素剂量均低于1mg/kg。

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