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

被引:56
作者
Robatel, C
Decosterd, LA
Biollaz, J
Eckert, P
Schaller, MD
Buclin, J
机构
[1] Univ Lausanne Hosp, Div Clin Pharmacol, Lausanne, Switzerland
[2] Univ Lausanne Hosp, Div Intens Care Med, Lausanne, Switzerland
[3] Univ Lausanne Hosp, Dept Med, Lausanne, Switzerland
关键词
continuous venovenous hemodiafiltration; meropenem; acute renal failure; pharmacokinetics;
D O I
10.1177/0091270003260286
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
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 (3 %). 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.
引用
收藏
页码:1329 / 1340
页数:12
相关论文
共 26 条
[1]   THE PHARMACOKINETICS OF MEROPENEM IN VOLUNTEERS [J].
BAX, RP ;
BASTAIN, W ;
FEATHERSTONE, A ;
WILKINSON, DM ;
HUTCHISON, M ;
HAWORTH, SJ .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 1989, 24 :311-320
[2]  
BURMAN LA, 1991, J ANTIMICROB CHEMOTH, V27, P219
[3]   PHARMACOKINETICS OF MEROPENEM IN PATIENTS WITH VARIOUS DEGREES OF RENAL-FUNCTION, INCLUDING PATIENTS WITH END-STAGE RENAL-DISEASE [J].
CHIMATA, M ;
NAGASE, M ;
SUZUKI, Y ;
SHIMOMURA, M ;
KAKUTA, S .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1993, 37 (02) :229-233
[4]   PHARMACOKINETICS OF MEROPENEM IN SUBJECTS WITH VARIOUS DEGREES OF RENAL IMPAIRMENT [J].
CHRISTENSSON, BA ;
NILSSONEHLE, I ;
HUTCHISON, M ;
HAWORTH, SJ ;
OQVIST, B ;
NORRBY, SR .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1992, 36 (07) :1532-1537
[5]  
DRUSANO GL, 1995, SCAND J INFECT DIS, P11
[6]   Current concepts: Continuous hemofiltration in the treatment of acute renal failure [J].
Forni, LG ;
Hilton, PJ .
NEW ENGLAND JOURNAL OF MEDICINE, 1997, 336 (18) :1303-1309
[7]   STABILITY OF MEROPENEM AND EFFECT OF 1-BETA-METHYL SUBSTITUTION ON ITS STABILITY IN THE PRESENCE OF RENAL DEHYDROPEPTIDASE-I [J].
FUKASAWA, M ;
SUMITA, Y ;
HARABE, ET ;
TANIO, T ;
NOUDA, H ;
KOHZUKI, T ;
OKUDA, T ;
MATSUMURA, H ;
SUNAGAWA, M .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1992, 36 (07) :1577-1579
[8]   MEROPENEM - INVITRO ACTIVITY AND KINETICS OF ACTIVITY AGAINST ORGANISMS OF THE BACTEROIDES-FRAGILIS GROUP [J].
GARCIARODRIGUEZ, JA ;
SANCHEZ, JEG ;
TRUJILLANO, I ;
LORENZO, ASD .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 1991, 27 (05) :599-606
[9]   Pharmacokinetics of meropenem in intensive care unit patients receiving continuous veno-venous hemofiltration or hemodiafiltration [J].
Giles, LJ ;
Jennings, AC ;
Thomson, AH ;
Creed, G ;
Beale, RJ ;
McLuckie, A .
CRITICAL CARE MEDICINE, 2000, 28 (03) :632-637
[10]   Meropenem - A review of its use in patients in intensive care [J].
Hurst, M ;
Lamb, HM .
DRUGS, 2000, 59 (03) :653-680