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Updated: May 27, 2025

A Novel Method to Determine the Longitudinal Antibacterial Activity of Drug-Eluting Materials
Published on: March 3, 2023
Empirical dosage determination of vancomycin for a target area under the concentration-time curve of 400 μg·h/mL in
Kazutaka Oda1,2, Yoko Hiyama3, Takashi Ueda4
1Department of Pharmacy, Kumamoto University Hospital, Kumamoto city, Kumamoto, Japan.
Aim:
Area under the concentration-time curve (AUC)-guided dosing is recommended in vancomycin therapy. This study aims to determine the empirical dosing for achieving an AUC on the first day (AUCf24h) and the optimal number of samplings for Bayesian estimation.
Methods:
A multicentric prospective study was conducted across five hospitals. Critically ill patients were included, with rich sampling conducted on the first day and/or days 3-5 of therapy. Cumulative dose on the first day for the trapezoidal AUCf24h > 400 μg·h/mL and the predictive performances of AUC and clearance in limited sampling were evaluated. The probability of adherence to AUCf24h within 400-600 μg·h/mL in the guidelines-compliant or non-compliant doses were also evaluated.
Results:
The study included 27 patients and 395 samplings were performed. The mean cumulative dose (standard deviation) on the first day was higher in the group with AUCf24h > 400 μg·h/mL at 49.3 (4.5) mg/kg compared to the group with AUCf24h < 400 μg·h/mL at 42.1 (6.8) mg/kg (P = 0.01) for patients with creatinine clearance > 90 mL/min, respectively. The biases and variations of Bayesian posterior AUC by using only a trough concentration were improved by using two-point concentrations at trough and peak. The probability of adherence to AUCf24h was significantly higher in the guidelines-compliant group (66.7%) than in the non-compliant group (11.1%, P < .01).
Conclusion:
This study suggested an empirical dosage of about 50 mg/kg on the first day of vancomycin therapy and the use of two-point sampling in Bayesian estimations to enhance accuracy.
Trial Registration:
Not applicable because this is a non-intervention study.
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