Continuous versus intermittent administration of ceftazidime in intensive care unit patients with nosocomial pneumonia

被引:120
作者
Nicolau, DP
McNabb, J
Lacy, MK
Quintiliani, R
Nightingale, CH
机构
[1] Hartford Hosp, Dept Pharm Res, Hartford, CT 06102 USA
[2] Hartford Hosp, Div Infect Dis, Hartford, CT 06102 USA
[3] Univ Nebraska, Med Ctr, Dept Pharm Practice, Omaha, NE 68198 USA
[4] Univ Kansas, Med Ctr, Kansas City, KS 66160 USA
[5] Hartford Hosp, Off Res Adm, Hartford, CT 06102 USA
关键词
ceftazidime; nosocomial pneumonia; tobramycin;
D O I
10.1016/S0924-8579(01)00329-6
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
A prospective, randomized pilot study was undertaken to compare the efficacy of continuous versus intermittent ceftazidime in ICU patients with nosocomial pneumonia. Ceftazidime was administered either as a 3 g/day continuous infusion (CI) or an intermittent infusion (II) of 2 g every 8 h. In addition, all patients received concomitant once-daily tobramycin. The demographics of the evaluable patients (n = 35) were similar between the groups: age (years), CI 46 +/- 16, II 56 +/- 20; Apache score, CI 14 +/- 4, II 16 +/- 6: time (days) from admission to diagnosis, CI 9 +/- 6, II 9 +/- 6. Clinical efficacy, defined as cure/improvement was similar between groups [n (%), Cl 16/17 (94), II 15/18 (83)], while microbiological response was also comparable [n (%), CI 10/13 (76). II 12/15 (80)]. Minimal inhibitory concentrations (MICs) for all isolates were measured throughout the treatment course; there was no development of resistance during therapy for either regimen. While limited clinical data exist, our results suggest that the use of ceftazidime by CI administration maintains clinical efficacy, optimizes the pharmacodynamic profile and uses less antibiotic compared with the standard 2 g every 8 h intermittent dosing regimen. (C) 2001 Elsevier Science B.V. and International Society of Chemotherapy. All rights reserved.
引用
收藏
页码:497 / 504
页数:8
相关论文
共 37 条
[31]  
QUINTILIANI R, 1997, INFECT DIS ANTIMICRO, P48
[32]   Nosocomial infections in medical intensive care units in the United States [J].
Richards, MJ ;
Edwards, JR ;
Culver, DH ;
Gaynes, RP .
CRITICAL CARE MEDICINE, 1999, 27 (05) :887-892
[33]   CEFTAZIDIME MONOTHERAPY VS CEFTRIAXONE TOBRAMYCIN FOR SERIOUS HOSPITAL-ACQUIRED GRAM-NEGATIVE INFECTIONS [J].
RUBINSTEIN, E ;
LODE, H ;
GRASSI, C .
CLINICAL INFECTIOUS DISEASES, 1995, 20 (05) :1217-1228
[34]   Continuous infusion of ceftazidime in cystic fibrosis patients during home treatment: Clinical outcome, microbiology and pharmacokinetics [J].
Vinks, AATMM ;
Brimicombe, RW ;
Heijerman, HGM ;
Bakker, W .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 1997, 40 (01) :125-133
[35]   EPIDEMIOLOGY AND CONTROL OF NOSOCOMIAL INFECTIONS IN ADULT INTENSIVE-CARE UNITS [J].
WEINSTEIN, RA .
AMERICAN JOURNAL OF MEDICINE, 1991, 91 :S179-S184
[36]   Comparison of strategies using cefpirome and ceftazidime for empiric treatment of pneumonia in intensive care patients [J].
Wolff, M .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1998, 42 (01) :28-36
[37]   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