Pharmacokinetics and Dosage Adaptation of Meropenem during Continuous Venovenous Hemodiafiltration in Critically Ill Patients.

Autor: C. Robatel, L. A. Decosterd, J. Biollaz, P. Eckert, M. D. Schaller, T. Buclin
Předmět:
Zdroj: Journal of Clinical Pharmacology; Dec2003, Vol. 43 Issue 12, p1329-1340, 12p
Abstrakt: Meropenem, a carbapenembroad-spectrumantibiotic, 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. [ABSTRACT FROM AUTHOR]
Databáze: Complementary Index