An evaluation of risk factors to predict target concentration non-attainment in critically ill patients prior to empiric β-lactam therapy

被引:0
|
作者
Sahand Imani
Hergen Buscher
Richard Day
Sheridan Gentili
Graham R. D. Jones
Debbie Marriott
Ross Norris
Indy Sandaradura
机构
[1] University of Notre Dame Australia,School of Medicine
[2] SydPath,Department of Clinical Microbiology
[3] St Vincent’s Hospital,Department of Intensive Care Medicine
[4] St Vincent’s Hospital,St Vincent’s Clinical School, Faculty of Medicine
[5] University of New South Wales,Department of Clinical Pharmacology and Toxicology
[6] St Vincent’s Hospital,School of Pharmacy and Medical Sciences, Sansom Institute for Health Research
[7] University of South Australia,Department of Chemical Pathology
[8] SydPath,Discipline of Clinical Pharmacology, School of Medicine & Public Health
[9] St Vincent’s Hospital,Centre for Infectious Diseases and Microbiology
[10] University of Newcastle,undefined
[11] Hunter Medical Research Institute,undefined
[12] Westmead Hospital,undefined
来源
European Journal of Clinical Microbiology & Infectious Diseases | 2018年 / 37卷
关键词
Beta-lactam antibiotics; Therapeutic drug monitoring; Empiric prescribing; Critically ill; Risk factors; Target concentration non-attainment;
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学科分类号
摘要
To determine whether target concentration non-attainment can be anticipated in critically ill patients prior to initiating empiric β-lactam antibiotic therapy based on readily available clinical factors. Retrospective review of consecutive patients treated with piperacillin or meropenem and who underwent therapeutic drug monitoring (TDM) at St Vincent’s Hospital (Sydney, Australia) between January 2013 and December 2015 was performed. Predefined subgroups were patients who received continuous renal replacement therapy (CRRT) and those who did not (non-CRRT). Potential risk factors were evaluated by correlation with β-lactam antibiotic trough concentrations (Cmin) lower than or equal to targeted minimum inhibitory concentration (MIC). Only the first drug concentration after initiation of the antibiotic treatment was included to reflect empirical dose selection. A total of n = 249 patients (piperacillin, n = 169; meropenem, n = 80) were investigated. For non-CRRT patients (n = 210), multivariate analysis demonstrated the following: male gender (p = 0.006); younger age (p = 0.015); prescribed daily antibiotic dose less than 1.5 times the product information recommendations (p = 0.004); lack of positive microbiology (p = 0.006); lower overall illness severity (p = 0.005); and estimated glomerular filtration rate (eGFR) ≥ 90 mL/min/1.73 m2 (p < 0.001), to be associated with Cmin ≤ MIC. No predictor variable was found to be significantly associated with Cmin ≤ MIC for the CRRT cohort. Evaluating the risk of target concentration non-attainment using simple clinical factors is possible at the bedside for non-CRRT patients prior to empiric antibiotic initiation. Clinicians should be wary of selecting doses based on the product information especially when treating younger male patients with apparently ‘normal’ renal function.
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页码:2171 / 2175
页数:4
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