Abstract

BackgroundEarly and appropriate antibiotic dosing is associated with improved clinical outcomes in critically ill patients, yet target attainment remains a challenge. Traditional antibiotic dosing is not suitable in critically ill patients, since these patients undergo physiological alterations that strongly affect antibiotic exposure. For beta-lactam antibiotics, the unbound plasma concentrations above at least one to four times the minimal inhibitory concentration (MIC) for 100% of the dosing interval (100%ƒT > 1–4×MIC) have been proposed as pharmacodynamic targets (PDTs) to maximize bacteriological and clinical responses. The objectives of this study are to describe the PDT attainment in critically ill patients and to identify risk factors for target non-attainment.MethodsThis prospective observational study was performed in two ICUs in the Netherlands. We enrolled adult patients treated with the following beta-lactam antibiotics: amoxicillin (with or without clavulanic acid), cefotaxime, ceftazidime, ceftriaxone, cefuroxime, and meropenem. Based on five samples within a dosing interval at day 2 of therapy, the time unbound concentrations above the epidemiological cut-off (ƒT > MICECOFF and ƒT > 4×MICECOFF) were determined. Secondary endpoints were estimated multivariate binomial and binary logistic regression models, for examining the association of PDT attainment with patient characteristics and clinical outcomes.ResultsA total of 147 patients were included, of whom 63.3% achieved PDT of 100%ƒT > MICECOFF and 36.7% achieved 100%ƒT > 4×MICECOFF. Regression analysis identified male gender, estimated glomerular filtration rate (eGFR) ≥ 90 mL/min/1.73 m2, and high body mass index (BMI) as risk factors for target non-attainment. Use of continuous renal replacement therapy (CRRT) and high serum urea significantly increased the probability of target attainment. In addition, we found a significant association between the 100%ƒT > MICECOFF target attainment and ICU length of stay (LOS), but no significant correlation was found for the 30-day survival.ConclusionsTraditional beta-lactam dosing results in low target attainment in the majority of critically ill patients. Male gender, high BMI, and high eGFR were significant risk factors for target non-attainment. These predictors, together with therapeutic drug monitoring, may help ICU clinicians in optimizing beta-lactam dosing in critically ill patients.Trial registrationNetherlands Trial Registry (EXPAT trial), NTR 5632. Registered on 7 December 2015.

Highlights

  • Large multicenter studies have reported antibiotic use in 64 to 71% of patients during their stay in the intensive care unit (ICU) [1, 2]

  • Pharmacokinetic parameters Box-and-whisker plots of unbound trough plasma concentrations observed for the different antibiotics are shown in Fig. 1, and peak plasma concentration plots can be found in Additional file 1

  • This study provides additional pharmacodynamic targets (PDTs) attainment data and risk factors associated with target non-attainment to support beta-lactam antibiotic dosing in critically ill patients

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Summary

Introduction

Large multicenter studies have reported antibiotic use in 64 to 71% of patients during their stay in the intensive care unit (ICU) [1, 2]. To adequately prevent and treat severe infections in critically ill patients, it is important that patients are treated with an appropriate dosing regimen of antibiotics [3,4,5]. Critically ill patients represent a highly heterogeneous population with a wide distribution of patients’ ages, severities of illness, co-morbidities, source of infections, and outcomes [8]. These challenging conditions make it difficult to achieve optimal exposure in critically ill patients when using standard dosing regimens for beta-lactam antibiotics. And appropriate antibiotic dosing is associated with improved clinical outcomes in critically ill patients, yet target attainment remains a challenge. The objectives of this study are to describe the PDT attainment in critically ill patients and to identify risk factors for target non-attainment

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