Early target attainment of continuous infusion piperacillin/tazobactam and meropenem in critically ill patients: A prospective observational study

被引:29
作者
Dhaese, Sofie A. M. [1 ]
Thooft, Alexander D. J. [2 ]
Farkas, Andras [3 ]
Lipman, Jeffrey [4 ,5 ]
Verstraete, Alain G. [6 ,7 ]
Stove, Veronique [6 ,7 ]
Roberts, Jason A. [4 ,5 ,8 ,9 ]
De Waele, Jan J. [1 ]
机构
[1] Ghent Univ Hosp, Dept Intens Care Med, Ghent, Belgium
[2] Univ Ghent, Ghent, Belgium
[3] Mt Sinai West Hosp, Dept Pharm, New York, NY USA
[4] Univ Queensland, Ctr Clin Res, Brisbane, Qld, Australia
[5] Royal Brisbane & Womens Hosp, Dept Intens Care Med, Brisbane, Qld, Australia
[6] Ghent Univ Hosp, Dept Lab Med, Ghent, Belgium
[7] Univ Ghent, Dept Diagnost Sci, Ghent, Belgium
[8] Royal Brisbane & Womens Hosp Brisbane, Dept Pharm, Brisbane, Qld, Australia
[9] Univ Queensland, Sch Pharm, Ctr Translat Antiinfect Pharmacodynam, Brisbane, Qld, Australia
基金
英国医学研究理事会;
关键词
Critically ill patients; Continuous infusion; Target attainment; Piperacillin; Meropenem; Empirical therapy; AUGMENTED RENAL CLEARANCE; AUSTRALIAN INDIGENOUS PATIENTS; BETA-LACTAM ANTIBIOTICS; PHARMACOKINETICS; SEPSIS; INTERMITTENT; TISSUE; BOLUS;
D O I
10.1016/j.jcrc.2019.04.013
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
Purpose: To evaluate target attainment of empirically dosed continuous infusion piperacillin/tazobactam (TZP) and meropenem (MER) in critically ill patients. Patients and methods: Patients were sampled on a daily basis. TZP or MER concentrations were evaluated during the first two days antibiotic therapy. The lower limit of the target range was defined as unbound concentrations equaling 4 times the epidemiological cutoff value of P. aeruginosa. The upper limit of the target range was based on the risk of toxicity, i.e. unbound concentrations >160 mg/L for TZP and >45 mg/L for MER. Multivariable logistic regression was used to evaluate factors associated with target attainment. Results: Data from 253 patients were analyzed. Overall, 76/205 (37.1%) and 36/48 (75%) of the patients receiving TZP or MER respectively, attained target concentrations. In multivariable analysis, estimated creatinine clearance was identified as a risk factor for target non-attainment (OR 0.988, 95%CI [0.982;0.994]). Patients receiving MER were more likely to attain target concentrations compared with patients receiving TZP (OR 6.02, 95%CI [2.12;18.4]). Conclusion: Target attainment of empiric antibiotic therapy in critically ill patients was low (37%) for TZP and moderate (75%) for MER, despite the use of a loading dose and despite optimization of the mode of infusion. (C) 2019 Elsevier Inc. All rights reserved.
引用
收藏
页码:75 / 79
页数:5
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