Vol. 38 No. 3 (2021): Junio
Antimicrobial

Impact of the vancomycin and amikacin therapeutic monitoring in the optimization of antimicrobial dose in pediatric patients

Paula Francisca Chávez Montoya
Universidad de Chile- Hospital Clínico San Borja Arriarán
Bio
Ayvlis Fernández Herrera
Universidad de Chile- Hospital Clínico San Borja Arriarán
Bio
Rubén Hernández M
Hospital Clínico San Borja Arriarán
Bio
Luis Delpiano Méndez
Hospital Clínico San Borja Arriarán
Bio

Published 2021-07-09

How to Cite

1.
Chávez Montoya PF, Fernández Herrera A, Hernández M R, Delpiano Méndez L. Impact of the vancomycin and amikacin therapeutic monitoring in the optimization of antimicrobial dose in pediatric patients. Rev. Chilena. Infectol. [Internet]. 2021 Jul. 9 [cited 2025 Nov. 13];38(3). Available from: https://revinf.cl/index.php/revinf/article/view/888

Abstract

Background: The monitoring of antimicrobial therapy through plasma levels makes it possible to determine the optimal dosage of antimicrobials, an essential approach in pediatrics. Aim: To describe the monitoring of plasma antimicrobial levels and dose adjustment in the pediatric population to determine if the doses used reach therapeutic ranges. Methods: Retrospective, descriptive study using a database with measurement of plasma levels of amikacin and vancomycin in pediatric patients at San Borja Arriarán Hospital between 2015-2018. The number of patients who reached the therapeutic range with the initial dose, how many required adjustment and their characteristics were determined. Results: 104 total levels were monitored. For vancomycin 65 plasmatic levels were baseline, being outside the therapeutic range 56.5%; 25% of those requiring adjustment were neonates with a higher probability of being out of range versus others (p = 0.022). For amikacin, Cpeak was in range in 60% of measurements; 15.4% required adjustment, including patients with cystic fibrosis and cancer, without adjustments in patients without comorbidity. Conclusion: Measurement of plasma levels is necessary to individually adjust the dose, especially in pediatric patients with cystic fibrosis, oncology and in neonatology where it is more likely not to reach a therapeutic range with initial doses.