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美罗培南在危重症患者持续静静脉血液透析滤过期间的药代动力学及剂量调整

Pharmacokinetics and dosage adaptation of meropenem during continuous venovenous hemodiafiltration in critically ill patients.

作者信息

Robatel C, Decosterd L A, Biollaz J, Eckert P, Schaller M D, Buclin T

机构信息

Division of Clinical Pharmacology, Department of Medicine, University Hospital, Lausanne, Switzerland.

出版信息

J Clin Pharmacol. 2003 Dec;43(12):1329-40. doi: 10.1177/0091270003260286.

Abstract

Meropenem, a carbapenem broad-spectrum antibiotic, is regularly used in patients undergoing continuous venovenous hemodiafiltration (CVVHDF). Its disposition was studied over one dosage interval in 15 patients under CVVHDF on a steady regimen of 500 or 1000 mg every 8 to 12 hours. Meropenem levels were measured in plasma and filtrate-dialysate by high-performance liquid chromatography (HPLC) with UV detection. The mean CVVHDF flow rates were 7.1 +/- 0.9 L/h for blood (mean +/- SD), 0.5 +/- 0.3 L/h for predilution solution, 1.2 +/- 0.3 L/h for countercurrent dialysate, and 1.8 +/- 0.5 L/h for the total filtrate-dialysate. The pharmacokinetic analysis was based both on a noncompartmental approach and on a four-compartment modeling. The mean (coefficient of variation [CV]) total body clearance, volume of distribution at steady state, and mean residence time were, respectively, 5.0 L/h (46%), 14.3 L (29%), and 4.8 h (36%). The hemodiafiltration clearances calculated from plasma data alone and plasma with filtrate-dialysate data were 1.2 L/h (26%) and 1.6 L/h (39%), respectively. The compartmental model was used to optimize the therapeutic schedule of meropenem, considering reference minimal inhibitory concentration (MIC) of sensitive strains (4 mg/L). The results indicate that two different therapeutic schedules of meropenem are equally applicable to patients receiving CVVHD: either 750 mg tid or 1500 bid.

摘要

美罗培南是一种碳青霉烯类广谱抗生素,常用于接受连续性静脉-静脉血液透析滤过(CVVHDF)的患者。在15例接受CVVHDF且每8至12小时稳定给予500或1000mg剂量的患者中,研究了美罗培南在一个给药间隔内的处置情况。采用高效液相色谱法(HPLC)结合紫外检测法测定血浆和滤出液-透析液中的美罗培南水平。CVVHDF的平均血流速度为7.1±0.9L/h(平均±标准差),预稀释液流速为0.5±0.3L/h,逆流透析液流速为1.2±0.3L/h,总滤出液-透析液流速为1.8±0.5L/h。药代动力学分析基于非房室方法和四房室模型。平均(变异系数[CV])总体清除率、稳态分布容积和平均驻留时间分别为5.0L/h(CV=46%)、14.3L(CV=29%)和4.8h(CV=36%)。仅根据血浆数据和血浆与滤出液-透析液数据计算的血液透析滤过清除率分别为1.2L/h(CV=26%)和1.6L/h(CV=39%)。考虑敏感菌株的参考最低抑菌浓度(MIC)(4mg/L),采用房室模型优化美罗培南的治疗方案。结果表明,两种不同的美罗培南治疗方案对接受CVVHD的患者同样适用:即750mg每日三次或1500mg每日两次。

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