Continuous infusion ceftazidime in intensive care: a randomized controlled trial

被引:89
作者
Lipman, J [1 ]
Gomersall, CD
Gin, T
Joynt, GM
Young, RJ
机构
[1] Royal Brisbane Hosp, Intens Care Facil, Herston Rd, Brisbane, Qld 4029, Australia
[2] Univ Queensland, Royal Brisbane Hosp, Div Anaesthesiol & Intens Care, Brisbane, Qld 4029, Australia
[3] Chinese Univ Hong Kong, Prince Wales Hosp, Dept Anaesthesia & Intens Care, Hong Kong, Peoples R China
[4] Christchurch Hosp, Dept Anaesthesia, Christchurch, New Zealand
关键词
D O I
10.1093/jac/43.2.309
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
We randomized 18 critically ill patients to receive ceftazidime 6 g/day by continuous infusion or bolus dosing (2 g 8 hourly), each with a loading dose of 12 mg/kg ceftazidime. During the first 8 h, plasma ceftazidime concentration fell below 40 mg/L in only one patient (trough 38 mg/L) from the infusion group, compared with eight from the bolus group (2-33 mg/L) for periods ranging from 73 to 369 min. Thereafter all infusion patients; remained above 40 mg/L for 40 h of study versus 20-30% of bolus patients. The pharmacokinetic and pharmacodynamic characteristics of ceftazidime suggest that continuous infusions should be clinically investigated in outcome studies.
引用
收藏
页码:309 / 311
页数:3
相关论文
共 10 条
[2]  
CHARMERS HF, 1995, MANDELL DOUGLAS BENN, P234
[3]   CONDITIONS FOR THE EMERGENCE OF RESISTANCE TO CEFPIROME AND CEFTAZIDIME IN EXPERIMENTAL ENDOCARDITIS DUE TO PSEUDOMONAS-AERUGINOSA [J].
FANTIN, B ;
FARINOTTI, R ;
THABAUT, A ;
CARBON, C .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 1994, 33 (03) :563-569
[4]   KILLING OF PSEUDOMONAS-AERUGINOSA DURING CONTINUOUS AND INTERMITTENT INFUSION OF CEFTAZIDIME IN AN IN-VITRO PHARMACOKINETIC MODEL [J].
MOUTON, JW ;
DENHOLLANDER, JG .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1994, 38 (05) :931-936
[5]  
Mouton JW, 1996, J ANTIMICROB CHEMOTH, V38, P5
[6]   Pharmacokinetic-pharmacodynamic modeling of activity of ceftazidime during continuous and intermittent infusion [J].
Mouton, JW ;
Vinks, AATMM ;
Punt, NC .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1997, 41 (04) :733-738
[7]   IMPACT OF THE DOSAGE SCHEDULE ON THE EFFICACY OF CEFTAZIDIME, GENTAMICIN AND CIPROFLOXACIN IN KLEBSIELLA-PNEUMONIAE PNEUMONIA AND SEPTICEMIA IN LEUKOPENIC RATS [J].
ROOSENDAAL, R ;
BAKKERWOUDENBERG, IAJ ;
VANDENBERGHEVANRAFFE, M ;
VINKVANDENBERG, JC ;
MICHEL, MF .
EUROPEAN JOURNAL OF CLINICAL MICROBIOLOGY & INFECTIOUS DISEASES, 1989, 8 (10) :878-887
[8]   ACTIVITIES OF VARIOUS BETA-LACTAMS AND AMINOGLYCOSIDES, ALONE AND IN COMBINATION, AGAINST ISOLATES OF PSEUDOMONAS-AERUGINOSA FROM PATIENTS WITH CYSTIC-FIBROSIS [J].
SCRIBNER, RK ;
MARKS, MI ;
WEBER, AH ;
TARPAY, MM ;
WELCH, DF .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1982, 21 (06) :939-943
[9]   KINETICS OF ANTIMICROBIAL ACTIVITY [J].
VOGELMAN, B ;
CRAIG, WA .
JOURNAL OF PEDIATRICS, 1986, 108 (05) :835-840
[10]   Intermittent bolus dosing of ceftazidime in critically ill patients [J].
Young, RJ ;
Lipman, J ;
Gin, T ;
Gomersall, CD ;
Joynt, GM ;
Oh, TE .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 1997, 40 (02) :269-273