Weight-based antibiotic dosing in a real-world European study of complicated skin and soft-tissue infections due to methicillin-resistant Staphylococcus aureus
Related Experiment Video
Updated: Apr 6, 2026

Subcutaneous Infection of Methicillin Resistant Staphylococcus Aureus MRSA
Published on: February 9, 2011
W Lawson1, D Nathwani2, C Eckmann3
1Hammersmith Hospital, Imperial College Healthcare NHS Trust, London, UK.
Abstract:
We aimed to characterize real-world dosing of weight-based intravenous (IV) antibiotic therapy in patients hospitalized for methicillin-resistant Staphylococcus aureus (MRSA) complicated skin and soft-tissue infections (cSSTIs). This was a subgroup analysis of a retrospective chart review that captured data from 12 European countries. The study included patients ≥18 years old, hospitalized with an MRSA cSSTI between 1 July 2010 and 30 June 2011 and discharged alive by 31 July 2011. Patients treated with IV vancomycin, teicoplanin or daptomycin at any stage during hospitalization were included in this analysis. Analyses were conducted at the regimen level (dosing in mg/kg or in mg, frequency, and total daily dose (TDD)), with potentially multiple regimens per patient, and the patient level, categorizing patients into low, standard (labelled) and high dosing groups according to their initial MRSA-targeted regimen. Among the 1502 patients in the parent study, 998 patients contributed a total of 1050 daptomycin, teicoplanin or vancomycin regimens. Across all regimens, the mean initial TDDs were 6.3 ± 1.9 mg/kg for daptomycin, 10.5 ± 4.9 mg/kg for teicoplanin and 28.5 ± 11.5 mg/kg for vancomycin. A total of 789 patients received first-line therapy with one of the above antibiotics. The majority of patients receiving first-line teicoplanin and daptomycin (96% and 80%, respectively) received higher than labelled cSSTI doses, whereas vancomycin doses were lower than labelled doses in >40% of patients. These real-world data reveal significant deviation from labelled antibiotic dosing in 12 European countries and the potential for suboptimal outcomes in patients with MRSA cSSTIs.
Insights
Real-world antibiotic dosing for methicillin-resistant Staphylococcus aureus (MRSA) complicated skin and soft-tissue infections (cSSTIs) in Europe often deviates from labeled recommendations. Many patients received higher or lower doses than standard, potentially impacting treatment outcomes.
Area of Science:
- Infectious Diseases
- Pharmacology
- Clinical Pharmacy
Background:
- Methicillin-resistant Staphylococcus aureus (MRSA) complicated skin and soft-tissue infections (cSSTIs) require effective antibiotic treatment.
- Intravenous (IV) antibiotic dosing strategies are crucial for managing severe MRSA cSSTIs.
- Understanding real-world antibiotic administration practices is essential for optimizing patient care.
Purpose of the Study:
- To characterize the actual weight-based IV antibiotic dosing regimens used in hospitalized patients with MRSA cSSTIs across 12 European countries.
- To compare real-world dosing of vancomycin, teicoplanin, and daptomycin against their labeled recommendations for MRSA cSSTIs.
- To identify deviations in antibiotic dosing and their potential implications for patient outcomes.
Main Methods:
- Retrospective chart review of patients hospitalized with MRSA cSSTIs between July 2010 and June 2011.
- Inclusion of patients treated with IV vancomycin, teicoplanin, or daptomycin.
- Analysis of dosing regimens (mg/kg, frequency, total daily dose) at both regimen and patient levels, categorizing doses as low, standard, or high.
Main Results:
- Analysis included 998 patients and 1050 antibiotic regimens.
- Mean total daily doses (TDDs) were 6.3 mg/kg for daptomycin, 10.5 mg/kg for teicoplanin, and 28.5 mg/kg for vancomycin.
- A high percentage of patients received higher-than-labeled doses for teicoplanin (96%) and daptomycin (80%), while over 40% received lower-than-labeled vancomycin doses.
Conclusions:
- Significant deviations from labeled antibiotic dosing practices for MRSA cSSTIs were observed in real-world European settings.
- The observed dosing variations, including both supra- and sub-therapeutic levels, may lead to suboptimal clinical outcomes.
- Further research is warranted to establish optimal dosing strategies and their impact on treatment efficacy and safety.
Related Concept Videos
Clinical Significance of Antibiotic Resistance
Mechanism of Antibiotic Resistance in MRSA
Staphylococcal Skin Infections
Estimation of k and VD of Aminoglycosides
Determination of Multiple Dosing Parameters: Steady-State, Minimum and Maximum Concentrations
Dosage Interval and Administration Route: Determination Methods

