Population pharmacokinetics of meropenem in critically ill patients

Author:

Rančić Aleksandar1,Milosavljević Miloš N.2ORCID,Rosić Nikola3,Milovanović Dragan2,Folić Marko4,Zečević Dejana Ružić23,Petrović Nemanja23,Čorbić Mirjana Milojević3,Dabanović Vera5,Janković Slobodan M.23

Affiliation:

1. Institute of Public Health Kragujevac , Kragujevac , Serbia

2. Department of Pharmacology and Toxicology, Faculty of Medical Sciences, University of Kragujevac , Svetozara Markovica 69 , Kragujevac , 34000 , Serbia

3. Clinical Pharmacology Department, University Clinical Centre Kragujevac , Kragujevac , Serbia

4. Department of Pharmacy, Faculty of Medical Sciences, University of Kragujevac , Kragujevac , 34000 , Serbia

5. Pharmacy Institution of Montenegro “Montefarm” , Podgorica , Montenegro

Abstract

Abstract Objective The pharmacokinetics of meropenem are significantly altered in critically ill patients. A population pharmacokinetic study was designed to estimate typical values of meropenem clearance in critically ill patients and evaluate potential factors of influence. Methods After meropenem reached a steady state in each patient, two blood samples were taken within the dose interval. The one-compartment pharmacokinetic model based on the data from 101 intensive care unit patients was built using NONMEM software. Results Typical values of meropenem clearance and volume of distribution were 3.80 L/h and 3.52 L, respectively. In the final model, meropenem clearance was influenced by serum concentrations of creatinine (CRE), leukocyte count (WBC), hypertension (HTA), and concomitant use of vancomycin (VAN) or colistimethate (COL): CL (L/h) = 5.29 × CRE ^ 0.000001 × WBCs ^ (−0.165) + 0.000001 × HTA + 0.825 × VAN + 1.28 × COL. Conclusion In order to achieve effective plasma concentrations of meropenem in critically ill patients, the meropenem dosing regimen should be adjusted according to individual values of drug clearance.

Publisher

Walter de Gruyter GmbH

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