Physiologically based pharmacokinetic-pharmacodynamic evaluation of meropenem plus fosfomycin in paediatrics

Aims The objective of the current study was to evaluate paediatric dosing regimens for meropenem plusfosfomycinthat generate sufficient coverage against multidrug-resistant bacteria. Methods The physiologically based pharmacokinetic (PBPK) models of meropenem and fosfomycin were developed from previously published pharmacokinetic studies in five populations: healthy subjects of Japanese origin, and healthy adults, geriatric, paediatric and renally impaired of primarily Caucasian origins. Pharmacodynamic (PD) analyses were carried out by evaluating dosing regimens that achieved a >= 90% joint probability of target attainment (PTA), which was defined as the minimum of the marginal probabilities to achieve the target PD index of each antibiotic. For meropenem, the percentage of time over a 24-hour period wherein the free drug concentration was above the minimum inhibitory concentration (fT > MIC) of at least 40% was its PD target. The fosfomycin PD index was described byfAUC/MIC of at least 40.8. Results For coadministration consisting of 20 mg/kg meropenem q8h as a 3-hour infusion and 35 mg/kg fosfomycin q8h also as a 3-hour infusion in a virtual paediatric population between 1 month and 12 years of age with normal renal function and a corresponding body weight between 3 and 50 kg, a joint PTA >= 90% is achieved at MICs of 16 and 64 mg/L for meropenem and fosfomycin coadministration, respectively, againstKlebsiella pneumoniaeandPseudomonas aeruginosa. Conclusion The current study identified potentially effective paediatric dosing regimens for meropenem plus fosfomycin coadministration against multidrug-resistant bacteria.

Automated summary

This study evaluated paediatric dosing regimens for meropenem plus fosfomycin against multidrug-resistant bacteria, using PBPK models and PD analyses to identify effective dosing regimens for Klebsiella pneumoniae and Pseudomonas aeruginosa.