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Ex vivo assessment and simulation to guide cefepime-taniborbactam dosing recommendations for patients receiving continuous renal replacement therapy
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DOI：10.1128/aac.00061-25.png)
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Abstract
En 中文
Cefepime-taniborbactam dosing in patients undergoing continuous renal replacement therapy (CRRT) is unknown. We employed an ex vivo CRRT model to characterize transmembrane clearance (CLTM) and derive optimal dosing regimens for patients supported by CRRT. CLTM was determined in CVVH and CVVHD modes using the Prismaflex ST150 and HF1400 hemofilter sets. Samples were collected over 60 minutes to determine cefepime and taniborbactam concentrations at increasing effluent flow rates (ER). Sieving (SC) and saturation (SA) coefficients were measured and used to calculate CLTM. Multiple linear regression determined cefepime and taniborbactam CLTM as a function of ER, hemofilter, and mode. An established population pharmacokinetic model was integrated with the CLTM, and a 1,000 patient Monte Carlo Simulation was conducted to determine exposures of potential dosing regimens for pneumonia. The overall mean +/- SD SC/SA across CRRT modes, hemofilters, and ERs were 1.13 +/- 0.08 and 1.03 +/- 0.07 for cefepime and taniborbactam, respectively. ER was the primary driver (P < 0.001) of CLTM for both drugs. For ER <3.5 L/h, cefepime and taniborbactam 1 g-0.25g q8h and 2 g-0.5g q12h as 4 h infusions achieved high probability of pharmacodynamic target attainment while keeping area under the curve exposures consistent with the proposed dose in pneumonia in non-CRRT patients. For ER >= 3.5 L/h, the optimum regimen was cefepime and taniborbactam 2 g-0.5 g q8h as a 4 h infusion. When incorporated into a population pharmacokinetic model, these CLTM data were used to propose dosing recommendations for cefepime and taniborbactam as a function of ER in patients undergoing CRRT.
Keywords:
pharmacokinetics
pharmacodynamics
renal impairment
antibiotic dosing
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