Clearance of ceftazidime during continuous venovenous haemofiltration in critically ill patients

被引:46
作者
Traunmüller, F
Schenk, P
Mittermeyer, C
Thalhammer-Scherrer, R
Ratheiser, K
Thalhammer, F
机构
[1] Univ Vienna, Dept Internal Med 1, Div Infect Dis, A-1090 Vienna, Austria
[2] Univ Vienna, Dept Internal Med 4, Intens Care Unit, A-1090 Vienna, Austria
[3] Univ Vienna, Dept Lab Med, A-1090 Vienna, Austria
[4] Univ Vienna, Dept Virol, A-1090 Vienna, Austria
关键词
D O I
10.1093/jac/49.1.129
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Published recommendations for the optimal dosing regimen of ceftazidime in critically ill patients with continuous venovenous haemofiltration (CVVH) differ. The aim of this prospective study was to analyse the pharmacokinetic and pharmacodynamic parameters of ceftazidime during CVVH with a high-flux polysulphone membrane, and derive a dosage recommendation. Twelve critically ill patients (five female, seven male) with acute renal failure undergoing CVVH using a 0.7 m(2) polysulphone high-flux membrane were investigated. All patients received ceftazidime 2 g iv q8h. Peak ceftazidime concentrations were 58.2 +/- 11.6 mg/L, with trough concentrations 14.0 +/- 3.2 mg/L at the arterial port. The elimination half-life, haemofiltration clearance, volume of distribution and total removal were 4.3 +/- 0.6 h, 32.1 +/- 7.9 mL/min, 36.4 +/- 6.4 L and 74.5 +/- 6.5%, respectively. Based on these pharmacokinetic parameters and that maximal killing is at 4 x MIC we recommend at least ceftazidime 2 g iv q8h.
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页码:129 / 134
页数:6
相关论文
共 24 条
[2]   Continuous infusion versus intermittent administration of ceftazidime in critically ill patients with suspected gram-negative infections [J].
Benko, AS ;
Cappelletty, DM ;
Kruse, JA ;
Rybak, MJ .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1996, 40 (03) :691-695
[3]   CLINICAL PHARMACOKINETICS DURING CONTINUOUS HEMOFILTRATION [J].
BRESSOLLE, F ;
KINOWSKI, JM ;
DELACOUSSAYE, JE ;
WYNN, N ;
ELEDJAM, JJ ;
GALTIER, M .
CLINICAL PHARMACOKINETICS, 1994, 26 (06) :457-471
[4]   CONTINUOUS INFUSION OF BETA-LACTAM ANTIBIOTICS [J].
CRAIG, WA ;
EBERT, SC .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1992, 36 (12) :2577-2583
[5]   PHARMACOKINETICS OF CEFUROXIME AND CEFTAZIDIME IN PATIENTS WITH ACUTE-RENAL-FAILURE TREATED BY CONTINUOUS ARTERIOVENOUS HEMODIALYSIS [J].
DAVIES, SP ;
LACEY, LF ;
KOX, WJ ;
BROWN, EA .
NEPHROLOGY DIALYSIS TRANSPLANTATION, 1991, 6 (12) :971-976
[6]   ROLE OF PHARMACOKINETICS IN THE OUTCOME OF INFECTIONS [J].
DRUSANO, GL .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1988, 32 (03) :289-297
[7]  
GENTRY LO, 1985, PHARMACOTHERAPY, V5, P254
[8]   Altered pharmacokinetics of ceftazidime in critically ill patients [J].
Gómez, CMH ;
Cordingly, JJ ;
Palazzo, MGA .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1999, 43 (07) :1798-1802
[9]   Intermittent and continuous ceftazidime infusion for critically ill trauma patients [J].
Hanes, SD ;
Wood, GC ;
Herring, V ;
Croce, MA ;
Fabian, TC ;
Pritchard, E ;
Boucher, BA .
AMERICAN JOURNAL OF SURGERY, 2000, 179 (06) :436-440
[10]   MULTIPLE-DOSE PHARMACOKINETICS OF AMIKACIN AND CEFTAZIDIME IN CRITICALLY ILL PATIENTS WITH SEPTIC MULTIPLE-ORGAN FAILURE DURING INTERMITTENT HEMOFILTRATION [J].
KINOWSKI, JM ;
DELACOUSSAYE, JE ;
BRESSOLLE, F ;
FABRE, D ;
SAISSI, G ;
BOUVET, O ;
GALTIER, M ;
ELEDJAM, JJ .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1993, 37 (03) :464-473