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Updated: May 15, 2026

Multiplex Therapeutic Drug Monitoring by Isotope-dilution HPLC-MS/MS of Antibiotics in Critical Illnesses
Published on: August 30, 2018
Pharmacokinetics of meropenem in critically ill patients with severe infections
Lutz Binder1, Harald Schwörer, Sebastian Hoppe
1Department of Clinical Chemistry, University Medical Center Göttingen, Göttingen, Germany.
Background:
Meropenem is an effective β-lactam antibiotic that is frequently used to treat serious infections in both intensive care unit (ICU) and febrile neutropenic hematology/oncology (Hem/Onc) patients. Studies suggest that to be effective, meropenem concentrations must be maintained above the inhibitory concentrations for the majority of a dosing interval. However, the pharmacokinetics (PK) of meropenem seem to differ in critically ill patients compared with healthy or less ill subjects used to select labeled dosing regimens.
Objectives:
This study was designed to investigate meropenem PK in critically ill patients and to see how often standard dosing regimens produced adequate plasma concentrations. A secondary objective was to investigate how achieved concentrations were related to outcomes (morbidity and mortality) in these patients.
Methods:
Meropenem plasma concentrations over time were measured using a high pressure liquid chromatography assay in febrile Hem/Onc and ICU patients who were treated with standard meropenem dosing schedules. Outcomes such as fever control and survival were assessed in these patients and compared with individual meropenem PK data and with recommended target concentrations.
Results:
A total of 25 subjects including 10 febrile Hem/Onc and 15 ICU patients with a variety of serious illnesses and baseline renal function were studied. Mean peak concentrations were less variable than were pre-dose concentrations. Post peak and trough concentrations were often below recommended minimum inhibitory concentrations. Both clearance and volumes of distribution were greater than reported in less ill subjects, only in part explained by increased renal clearance. Therefore, serum concentrations often did not exceed recommended concentration targets even for moderately sensitive organisms. Inadequate concentrations were especially common in the mostly ill, febrile neutropenic Hem/Onc subjects and seemed to explain at least some therapeutic failures. Conversely, drug accumulation occurred in ICU subjects with decreased renal function.
Conclusions:
Standard meropenem dosing regimens were inadequate in many critically ill febrile, neutropenic Hem/Onc, and septic ICU patients. These data suggest a role for meropenem concentration monitoring in such patients.
Insights
Standard meropenem dosing is often inadequate for critically ill patients, leading to sub-therapeutic concentrations. Therapeutic drug monitoring of meropenem may be necessary in these vulnerable populations to ensure efficacy.
Area of Science:
- Pharmacology
- Infectious Diseases
- Critical Care Medicine
Background:
- Meropenem is a vital antibiotic for serious infections in ICU and febrile neutropenic hematology/oncology (Hem/Onc) patients.
- Effective meropenem therapy requires concentrations above minimum inhibitory levels for most of the dosing interval.
- Pharmacokinetics (PK) of meropenem may differ significantly in critically ill patients compared to standard populations.
Purpose of the Study:
- To evaluate meropenem PK in critically ill patients.
- To determine the adequacy of standard meropenem dosing regimens in achieving therapeutic concentrations.
- To explore the relationship between achieved meropenem concentrations and patient outcomes (morbidity/mortality).
Main Methods:
- Meropenem plasma concentrations were measured using high-performance liquid chromatography (HPLC).
- Study included febrile Hem/Onc and ICU patients receiving standard meropenem doses.
- Outcomes (fever control, survival) were assessed and correlated with PK data and target concentrations.
Main Results:
- Twenty-five critically ill patients (10 Hem/Onc, 15 ICU) were studied.
- Post-peak and trough meropenem concentrations frequently fell below recommended minimum inhibitory concentrations.
- Increased meropenem clearance and volume of distribution were observed in critically ill patients, leading to inadequate concentrations and potential therapeutic failures, especially in Hem/Onc patients. Drug accumulation occurred in ICU patients with renal impairment.
Conclusions:
- Standard meropenem dosing regimens are frequently insufficient for critically ill Hem/Onc and ICU patients.
- These findings support the need for therapeutic drug monitoring of meropenem in critically ill populations.
- Optimizing meropenem dosing may improve treatment outcomes in severe infections.
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