Abstract
Antimicrobial treatment in critically ill patients remains challenging. The aim of this study
was to develop a population pharmacokinetic model for linezolid in critically ill patients and to
evaluate the adequacy of current dosing recommendation (600 mg/12 h). Forty inpatients were
included, 23 of whom were subjected to continuous renal replacement therapies (CRRT). Blood and
effluent samples were drawn after linezolid administration at defined time points, and linezolid
levels were measured. A population pharmacokinetic model was developed, using NONMEM 7.3.
The percentage of patients that achieved the pharmacokinetic/pharmacodynamic (PK/PD) targets
was calculated (AUC24/MIC > 80 and 100% T>MIC). A two‐compartment model best described the
pharmacokinetics of linezolid. Elimination was conditioned by the creatinine clearance and by the
extra‐corporeal clearance if the patient was subjected to CRRT. For most patients, the standard dose
of linezolid did not cover infections caused by pathogens with MIC ≥