Abstract

(1) Purpose of this study: To determine whether patient weight influences the probability of target attainment (PTA) over 72 h of initial therapy with beta-lactam (cefepime, ceftazidime, piperacillin/tazobactam) and carbapenem (imipenem, ertapenem, meropenem) antibiotics in the critical care setting. This is the first paper to address the question of whether patient size affects antibiotic PTA in the ICU. (2) Methods: We performed a post hoc analysis of Monte Carlo simulations conducted in virtual critically ill patients receiving antibiotics and continuous renal replacement therapy. The PTA was calculated for each antibiotic on the following pharmacodynamic (PD) targets: (a) were above the target organism’s minimum inhibitory concentration (≥%fT≥1×MIC), (b) were above four times the MIC (≥%fT≥4×MIC), and (c) were always above the MIC (≥100%fT≥MIC) for the first 72 h of antibiotic therapy. The PTA was analyzed in patient weight quartiles [Q1 (lightest)-Q4 (heaviest)]. Optimal doses were defined as the lowest dose achieving ≥90% PTA. (3) Results: The PTA for fT≥1×MIC led to similarly high rates regardless of weight quartiles. Yet, patient weight influenced the PTA for higher PD targets (100%fT≥MIC and fT≥4×MIC) with commonly used beta-lactams and carbapenems. Reaching the optimal PTA was more difficult with a PD target of 100%fT≥MIC compared to fT≥4×MIC. (4) Conclusions: The Monte Carlo simulations showed patients in lower weight quartiles tended to achieve higher antibiotic pharmacodynamic target attainment compared to heavier patients.

Highlights

  • Continuous renal replacement therapy (CRRT) is the preferred renal replacement therapy (RRT) over intermittent hemodialysis in patients with acute kidney injury (AKI)due to hemodynamic instability [1]

  • Since the antibiotic doses were used in both intensity arms, some suggested that patients with intensive CRRT may have had lower overall antibiotic exposures due to a higher drug removal rate [3,4]

  • This is noteworthy because altered volume of distribution (Vd) in AKI patients receiving CRRT can cause high interindividual and interoccasion variability in antibiotic serum concentrations [7]

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Summary

Introduction

Continuous renal replacement therapy (CRRT) is the preferred renal replacement therapy (RRT) over intermittent hemodialysis in patients with acute kidney injury (AKI)due to hemodynamic instability [1]. Institutes of Health Acute Renal Failure Trial Network Study (ATN trial) showed that there was no difference in clinical outcomes when patients received less-intensive or intensive effluent rates for CRRT [2]. Since the antibiotic doses were used in both intensity arms, some suggested that patients with intensive CRRT may have had lower overall antibiotic exposures due to a higher drug removal rate [3,4]. Increased Vd leads to a lower plasma concentration, requiring higher doses of a drug. This is noteworthy because altered Vd in AKI patients receiving CRRT can cause high interindividual and interoccasion variability in antibiotic serum concentrations [7]. Interindividual variability was noted with piperacillin and tazobactam trough levels by

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