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Updated: May 27, 2026

A Novel Method to Determine the Longitudinal Antibacterial Activity of Drug-Eluting Materials
Published on: March 3, 2023
Therapeutic drug monitoring of vancomycin
Ana Luisa Robles-Piedras1, Eva Hilda González-López
1Area Académica de Farmacia, del Instituto de Ciencias de la Salud, Universidad Autónoma del Estado de Hidalgo, México. ana0536@yahoo.com
Abstract:
Vancomycin, a glycopeptide antibiotic, was developed-and released in the 1950's for the treatment of aerobic gram-positive infections and has been widely used mainly in the treatment of methicillin-resistant Staphylococcus aureus infections. Early reports regarding the possibility of nephrotoxicity and ototoxicity led to concern about the use of vancomycin and the need to monitor serum concentrations. In Mexico, the National Institute of Cardiology measures serum level of some drugs, such as vancomycin on a routine basis. Nevertheless, although a large number of measurements are made, the quantification of drug in serum is only used by physicians as a empiric parameter for dose adjustment. The aim of this work was to know whether dosing was appropriate taking the therapeutic interval as a commonly accepted baseline and to propose viable alternatives in the case dosing was inadequate. Peak and through vancomycin levels were analyzed retrospectively (n=295), in patients from 18 to 65 yr old with diagnosis of sepsis. The relationship between administered dose and measured blood levels was established. The equation that characterizes the study population was obtained based on a single compartment model considering the proportional relationship between vancomycin and creatinine clearance. The analysis shows that only 44% of C(trough) and 47% of C(peak) values represented therapeutic levels, with the remainder either toxic or ineffective.
Insights
Vancomycin dosing in sepsis patients often falls outside therapeutic ranges, with many treatments being ineffective or toxic. This study analyzed vancomycin levels to assess dosing appropriateness and suggest improvements for better patient outcomes.
Area of Science:
- Pharmacology
- Infectious Diseases
- Clinical Pharmacy
Background:
- Vancomycin, a critical antibiotic for Gram-positive infections like MRSA, has known risks of nephrotoxicity and ototoxicity.
- Monitoring vancomycin serum concentrations is crucial for safe and effective treatment.
- In Mexico, routine vancomycin level monitoring occurs, but its use in dose adjustment is often empirical.
Purpose of the Study:
- To evaluate the appropriateness of vancomycin dosing in sepsis patients based on established therapeutic intervals.
- To identify the proportion of patients receiving sub-therapeutic or toxic vancomycin doses.
- To propose alternative dosing strategies if current regimens are inadequate.
Main Methods:
- Retrospective analysis of 295 vancomycin peak and trough levels in adult sepsis patients (18-65 years).
- Established the relationship between administered vancomycin dose and measured serum concentrations.
- Utilized a single compartment model incorporating creatinine clearance to characterize the study population's pharmacokinetics.
Main Results:
- Only 44% of trough concentrations (C(trough)) and 47% of peak concentrations (C(peak)) fell within the therapeutic range.
- A significant proportion of patients received vancomycin doses resulting in ineffective or toxic drug levels.
- A pharmacokinetic model was developed to describe vancomycin behavior in relation to creatinine clearance.
Conclusions:
- Current vancomycin dosing practices for sepsis patients in this cohort are frequently inadequate, leading to suboptimal therapeutic outcomes.
- There is a need for more precise vancomycin dosing strategies to optimize efficacy and minimize toxicity.
- Pharmacokinetic modeling can aid in understanding and improving vancomycin dose adjustments.
Related Concept Videos
Therapeutic Drug Monitoring: Overview and Classification
Therapeutic Drug Monitoring: Drug Analysis Methods
Therapeutic Drug Monitoring: Affecting Factors
Determination of Multiple Dosing Parameters: Steady-State, Minimum and Maximum Concentrations
Estimation of k and VD of Aminoglycosides
Drug Accumulation During Multiple Dosing: Intermittent IV Infusions

