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Nomogram based on actual body weight for estimation of vancomycin maintenance dose in infants
Pavla Pokorná1,2,3, Martin Šíma1, Olga Černá2
1a Institute of Pharmacology, First Faculty of Medicine , Charles University and General University Hospital in Prague , Prague , Czech Republic.
Insights
Optimizing vancomycin dosing in infants is crucial. Actual body weight is the best predictor for vancomycin clearance, enabling a new dosing nomogram for effective sepsis treatment.
Area of Science:
- Pediatric Pharmacology
- Infectious Diseases
- Antibiotic Stewardship
Background:
- Vancomycin is the primary antibiotic for infants with resistant gram-positive bacterial infections.
- Optimal vancomycin dosing in infants remains a clinical challenge despite extensive use.
- This study addresses the need for improved vancomycin dosing strategies in pediatric sepsis.
Purpose of the Study:
- To identify predictors of vancomycin clearance in infants.
- To develop an evidence-based method for optimal maintenance dosing of vancomycin.
- To create a practical tool for guiding vancomycin therapy in pediatric sepsis.
Main Methods:
- Pharmacokinetic analysis using a one-compartmental model based on serum concentrations.
- Linear regression to identify covariates associated with vancomycin clearance.
- Development of a dosing nomogram based on predictive variables.
Main Results:
- Twenty-two infants were included in the study.
- Vancomycin clearance was significantly associated with actual body weight, height, body surface area, gestational age, postnatal age, postmenstrual age, and estimated glomerular filtration rate.
- Actual body weight emerged as the strongest predictor of vancomycin clearance.
Conclusions:
- An easy-to-use dosing nomogram was developed, utilizing actual body weight.
- The nomogram facilitates maintaining a target vancomycin average steady-state concentration of 22.5 mg/L.
- This tool aims to optimize vancomycin therapy in infants with suspected or confirmed sepsis.
Background:
Vancomycin is the first-choice antibiotic for infants with β-lactam-resistant gram-positive bacterial infection. Despite long experience of prescribing of this drug optimal dosing is still challenging. This study aimed at investigating variables predicting vancomycin clearance in order to propose optimal maintenance dosing in infants treated for suspected or culture-proven sepsis.
Methods:
Vancomycin pharmacokinetics was calculated in a one-compartmental model based on serum concentrations. A linear regression model was used to explore relationships between vancomycin clearance and expected covariates.
Results:
Twenty-two patients were enrolled into the study. Median (IQR) postnatal age was 157 (112-238) days. The median (IQR) volume of distribution and clearance for vancomycin were 0.50 (0.39-0.94) L/kg and 0.112 (0.095-0.133) L/h/kg, respectively. Vancomycin clearance was associated with actual body weight, height, body surface area, gestational age, postnatal age, postmenstrual age and estimate glomerular filtration rate. Actual body weight was the best predictive variable for vancomycin clearance. Daily maintenance dose (mg) calculated as 76.28 × actual body weight (kg) - 41.57 most closely approximated optimal dosing based on individual pharmacokinetics. This relationship was used to construct a dosing nomogram.
Conclusions:
We developed an easy-to-use dosing nomogram for maintaining a vancomycin average steady-state concentration of 22.5 mg/L based on actual body weight.
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