Clinical cure of ventilator-associated pneumonia treated with piperacillin/tazobactam administered by continuous or intermittent infusion

被引:96
作者
Lorente, Leonardo [1 ]
Jimenez, Alejandro [2 ]
Martin, Maria M. [1 ]
Iribarren, Jose Luis [1 ]
Jose Jimenez, Juan [1 ]
Mora, Maria L. [1 ]
机构
[1] Hosp Univ Canarias, Intens Care Unit, Tenerife 38320, Spain
[2] Hosp Univ Canarias, Res Unit, Tenerife 38320, Spain
关键词
Ventilator-associated pneumonia; Piperacillin; Continuous infusion; Intermittent infusion; Gram-negative bacilli; COMPLICATED INTRAABDOMINAL INFECTION; CYSTIC-FIBROSIS PATIENTS; POPULATION PHARMACOKINETICS; INTENSIVE-CARE; BETA-LACTAMS; OPEN-LABEL; TAZOBACTAM; PHARMACODYNAMICS; STABILITY; CEFTAZIDIME;
D O I
10.1016/j.ijantimicag.2008.10.025
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
The standard mode of administration of piperacillin treatment is by intermittent infusion. However, continuous infusion may be advantageous as beta-lactam antibiotics exhibit time-dependent antibacterial activity. In previous studies, we found a higher rate of clinical cure of ventilator-associated pneumonia (VAP) by continuous infusion rather than intermittent infusion of meropenem and ceftazidime. Therefore, the objective of this historical cohort study was to establish the clinical efficacy of piperacillin/tazobactam (PIP/TAZ) administered by continuous and intermittent infusion in the treatment of VAP in patients without renal failure. Logistic regression analysis showed a higher probability of clinical cure of VAP by continuous compared with intermittent infusion when the microorganism responsible for VAP had a minimum inhibitory concentration (MIC) of 8 mu g/mL [8/9 (88.9%) vs. 6/15 (40.0%); odds ratio (OR) = 10.79, 95% confidence interval (CI) 1.01-588.24; P=0.049] or 16 mu g/mL [7/8 (87.5%) vs. 1/6 (16.7%); OR=22.89, 95% CI 1.19-1880.78; P = 0.03]. Thus, administration of PIP/TAZ by continuous infusion may be considered more effective than intermittent infusion for the treatment of VAP caused by Gram-negative bacteria when the MIC of the microorganism responsible for VAP is 8-16 mu g/mL in patients without renal failure. (C) 2008 Elsevier B.V. and the International Society of Chemotherapy. All rights reserved.
引用
收藏
页码:464 / 468
页数:5
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