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1642. Vancomycin AUC(24) Estimation Using First Order Pharmacokinetic Methods in Pediatric Patients
BACKGROUND: The 2020 guidelines for the monitoring of vancomycin emphasize the importance of timely assessment of AUC(24) for both efficacy and safety in pediatric patients. However, real-world data supporting the feasibility of vancomycin AUC(24) in pediatric patients using first-order equations is...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10677463/ http://dx.doi.org/10.1093/ofid/ofad500.1476 |
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author | Wallace, Katie L Burgess, David Olney, Katie B Brandon, Hope |
author_facet | Wallace, Katie L Burgess, David Olney, Katie B Brandon, Hope |
author_sort | Wallace, Katie L |
collection | PubMed |
description | BACKGROUND: The 2020 guidelines for the monitoring of vancomycin emphasize the importance of timely assessment of AUC(24) for both efficacy and safety in pediatric patients. However, real-world data supporting the feasibility of vancomycin AUC(24) in pediatric patients using first-order equations is lacking. [Figure: see text] METHODS: This is a single-center, retrospective cohort study of hospitalized pediatric patients (< 18 years) receiving intravenous (IV) vancomycin between 1/1/2020 and 8/20/2022. Patients were included if they received at least 24 hours of IV vancomycin with peak and trough concentrations obtained in the first 96 hours of therapy. Patients with baseline renal dysfunction were excluded. First-order equations were utilized to estimate K(e), V(d), Cl, and AUC(24.) RESULTS: Overall, 219 patients (68% male, 87% Caucasian, 24% critically ill, median age of 6 years (IQR 1-12)) met inclusion criteria. Of the total patients, 9% were neonates (age ≤ 28 days), 11% were infants (age 29 days to < 1 year), 58% were children (age 1 to 12 years), and 22% were adolescents (age 13 to 17 years). The pharmacokinetic parameters for each group are outlined in Table 1. The estimated AUC(24) was within the therapeutic range of 400-600 mg*hr/L for the majority of patients. However, when comparing age groups, adolescents had the lowest (53%) while neonates had the greatest (79%) percentage of patients within the therapeutic range CONCLUSION: Our results reinforce the variability in vancomycin PK seen across pediatric age groups, confirming the need to tailor empiric dosing regimens by patient age. For patients with AUC(24) outside the therapeutic range, more patients had SUPRAtherapeutic rather than SUBtherapeutic AUC(24). In response to results of this study, institutional empiric vancomycin dosing will be decreased for all age groups outside the neonatal group to better align with the 2020 guideline recommended AUC(24) of 400 - 600 mg*hr/L for pediatric patients. DISCLOSURES: Katie B. Olney, PharmD, BCIDP, The Society of Infectious Diseases Pharmacists (SIDP): Grant/Research Support |
format | Online Article Text |
id | pubmed-10677463 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-106774632023-11-27 1642. Vancomycin AUC(24) Estimation Using First Order Pharmacokinetic Methods in Pediatric Patients Wallace, Katie L Burgess, David Olney, Katie B Brandon, Hope Open Forum Infect Dis Abstract BACKGROUND: The 2020 guidelines for the monitoring of vancomycin emphasize the importance of timely assessment of AUC(24) for both efficacy and safety in pediatric patients. However, real-world data supporting the feasibility of vancomycin AUC(24) in pediatric patients using first-order equations is lacking. [Figure: see text] METHODS: This is a single-center, retrospective cohort study of hospitalized pediatric patients (< 18 years) receiving intravenous (IV) vancomycin between 1/1/2020 and 8/20/2022. Patients were included if they received at least 24 hours of IV vancomycin with peak and trough concentrations obtained in the first 96 hours of therapy. Patients with baseline renal dysfunction were excluded. First-order equations were utilized to estimate K(e), V(d), Cl, and AUC(24.) RESULTS: Overall, 219 patients (68% male, 87% Caucasian, 24% critically ill, median age of 6 years (IQR 1-12)) met inclusion criteria. Of the total patients, 9% were neonates (age ≤ 28 days), 11% were infants (age 29 days to < 1 year), 58% were children (age 1 to 12 years), and 22% were adolescents (age 13 to 17 years). The pharmacokinetic parameters for each group are outlined in Table 1. The estimated AUC(24) was within the therapeutic range of 400-600 mg*hr/L for the majority of patients. However, when comparing age groups, adolescents had the lowest (53%) while neonates had the greatest (79%) percentage of patients within the therapeutic range CONCLUSION: Our results reinforce the variability in vancomycin PK seen across pediatric age groups, confirming the need to tailor empiric dosing regimens by patient age. For patients with AUC(24) outside the therapeutic range, more patients had SUPRAtherapeutic rather than SUBtherapeutic AUC(24). In response to results of this study, institutional empiric vancomycin dosing will be decreased for all age groups outside the neonatal group to better align with the 2020 guideline recommended AUC(24) of 400 - 600 mg*hr/L for pediatric patients. DISCLOSURES: Katie B. Olney, PharmD, BCIDP, The Society of Infectious Diseases Pharmacists (SIDP): Grant/Research Support Oxford University Press 2023-11-27 /pmc/articles/PMC10677463/ http://dx.doi.org/10.1093/ofid/ofad500.1476 Text en © The Author(s) 2023. Published by Oxford University Press on behalf of Infectious Diseases Society of America. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Abstract Wallace, Katie L Burgess, David Olney, Katie B Brandon, Hope 1642. Vancomycin AUC(24) Estimation Using First Order Pharmacokinetic Methods in Pediatric Patients |
title | 1642. Vancomycin AUC(24) Estimation Using First Order Pharmacokinetic Methods in Pediatric Patients |
title_full | 1642. Vancomycin AUC(24) Estimation Using First Order Pharmacokinetic Methods in Pediatric Patients |
title_fullStr | 1642. Vancomycin AUC(24) Estimation Using First Order Pharmacokinetic Methods in Pediatric Patients |
title_full_unstemmed | 1642. Vancomycin AUC(24) Estimation Using First Order Pharmacokinetic Methods in Pediatric Patients |
title_short | 1642. Vancomycin AUC(24) Estimation Using First Order Pharmacokinetic Methods in Pediatric Patients |
title_sort | 1642. vancomycin auc(24) estimation using first order pharmacokinetic methods in pediatric patients |
topic | Abstract |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10677463/ http://dx.doi.org/10.1093/ofid/ofad500.1476 |
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