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Evaluating the Relationship between Vancomycin Trough Concentration and 24-Hour Area under the Concentration-Time
Sheng-Hsuan Tseng1, Chuan Poh Lim2, Qi Chen3
1Department of Pharmacy, National University of Singapore, Singapore tseng.sheng.hsuan@u.nus.edu lim.chuan.poh@sgh.com.sg.
Abstract:
Bacterial sepsis is a major cause of morbidity and mortality in neonates, especially those involving methicillin-resistant Staphylococcus aureus (MRSA). Guidelines by the Infectious Diseases Society of America recommend the vancomycin 24-h area under the concentration-time curve to MIC ratio (AUC24/MIC) of >400 as the best predictor of successful treatment against MRSA infections when the MIC is ≤1 mg/liter. The relationship between steady-state vancomycin trough concentrations and AUC24 values (mg·h/liter) has not been studied in an Asian neonatal population. We conducted a retrospective chart review in Singapore hospitals and collected patient characteristics and therapeutic drug monitoring data from neonates on vancomycin therapy over a 5-year period. A one-compartment population pharmacokinetic model was built from the collected data, internally validated, and then used to assess the relationship between steady-state trough concentrations and AUC24 A Monte Carlo simulation sensitivity analysis was also conducted. A total of 76 neonates with 429 vancomycin concentrations were included for analysis. Median (interquartile range) was 30 weeks (28 to 36 weeks) for postmenstrual age (PMA) and 1,043 g (811 to 1,919 g) for weight at the initiation of treatment. Vancomycin clearance was predicted by weight, PMA, and serum creatinine. For MRSA isolates with a vancomycin MIC of ≤1, our major finding was that the minimum steady-state trough concentration range predictive of achieving an AUC24/MIC of >400 was 8 to 8.9 mg/liter. Steady-state troughs within 15 to 20 mg/liter are unlikely to be necessary to achieve an AUC24/MIC of >400, whereas troughs within 10 to 14.9 mg/liter may be more appropriate.
Insights
For neonatal MRSA sepsis, a vancomycin trough concentration of 8-8.9 mg/L is recommended for optimal treatment. Higher levels (15-20 mg/L) are likely unnecessary, suggesting 10-14.9 mg/L may be more appropriate.
Area of Science:
- Neonatal pharmacokinetics and pharmacodynamics
- Infectious disease management in neonates
- Antimicrobial stewardship
Background:
- Bacterial sepsis, particularly from MRSA, poses significant risks to neonates.
- Current guidelines recommend vancomycin AUC24/MIC >400 for MRSA treatment, but data in Asian neonates is limited.
- Understanding vancomycin trough concentrations' relationship with AUC24 is crucial for effective dosing.
Purpose of the Study:
- To determine the relationship between steady-state vancomycin trough concentrations and AUC24 values in Asian neonates.
- To identify optimal vancomycin trough targets for achieving therapeutic AUC24/MIC ratios against MRSA.
- To inform vancomycin dosing strategies in neonatal populations.
Main Methods:
- Retrospective chart review of vancomycin therapy in neonates across Singapore hospitals.
- Development and internal validation of a one-compartment population pharmacokinetic model.
- Monte Carlo simulation for sensitivity analysis to assess AUC24/MIC achievement.
Main Results:
- Analysis included 76 neonates with 429 vancomycin concentrations; median PMA was 30 weeks.
- Vancomycin clearance was influenced by weight, PMA, and serum creatinine.
- A minimum steady-state trough of 8-8.9 mg/L predicted AUC24/MIC >400 for MRSA (MIC ≤1 mg/L); troughs of 10-14.9 mg/L may be more appropriate than 15-20 mg/L.
Conclusions:
- The study establishes a target vancomycin trough range of 8-8.9 mg/L for neonates with MRSA infections (MIC ≤1 mg/L).
- Current higher trough targets (15-20 mg/L) may not be necessary, with 10-14.9 mg/L potentially being more suitable.
- Findings support refined vancomycin dosing guidelines for Asian neonates to optimize MRSA treatment efficacy and safety.
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