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Impact of implementing a vancomycin protocol to reduce kidney toxicity: A comparative study

Introduction: Vancomycin is a frequently used antibiotic for treating severe infections caused by multidrug-resistant, Gram-positive pathogens. To ensure its effectiveness and minimize the risk of nephrotoxicity, safe administration and dose monitoring are crucial. Understanding the impact of vancom...

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Autores principales: Baiocco, Graziella Gasparotto, Greiner, Stephanie, Rosa, Mário Borges, Flores, Cecília Dias, Barros, Helena M. T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10569023/
https://www.ncbi.nlm.nih.gov/pubmed/37841919
http://dx.doi.org/10.3389/fphar.2023.1154573
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author Baiocco, Graziella Gasparotto
Greiner, Stephanie
Rosa, Mário Borges
Flores, Cecília Dias
Barros, Helena M. T.
author_facet Baiocco, Graziella Gasparotto
Greiner, Stephanie
Rosa, Mário Borges
Flores, Cecília Dias
Barros, Helena M. T.
author_sort Baiocco, Graziella Gasparotto
collection PubMed
description Introduction: Vancomycin is a frequently used antibiotic for treating severe infections caused by multidrug-resistant, Gram-positive pathogens. To ensure its effectiveness and minimize the risk of nephrotoxicity, safe administration and dose monitoring are crucial. Understanding the impact of vancomycin serum levels on clinical outcomes is of paramount importance, necessitating improved knowledge on its use, dose monitoring, nephrotoxicity, and safe administration. Objective: This study aimed to evaluate the incidence of acute kidney injury (AKI) in patients receiving vancomycin before and after the implementation of an institutional protocol for vancomycin administration in a public tertiary hospital in southern Brazil. Materials and methods: A cross-sectional study design was employed, analyzing data from the electronic medical records of 422 patients who received vancomycin. The patient population was divided into two independent cohorts: those treated in 2016 (pre-protocol) and those treated in 2018 (post-protocol), following the implementation of the institutional vancomycin administration protocol. Results: The study included 211 patients in each year of assessment. Patients from both cohorts had a Charlson Comorbidity Index (CCI) score of 4. The post-protocol cohort consisted of older individuals, with a mean age of 62.8 years. In addition, patients in the post-protocol year had higher baseline creatinine levels, higher rates of intensive care unit (ICU) hospitalization, and increased use of vasopressors. In the pre-protocol year, patients received vancomycin therapy for a longer duration. When comparing the incidence of AKI between the two groups, an intervention study revealed rates of 38.4% in group 1 and 20.9% in group 2, indicating a significant reduction (p < 0.001) in the post-protocol group. A logistic regression model was developed to predict AKI, incorporating variables that demonstrated significance (p ≤ 0.250) in bivariate analysis and those recognized in the literature as important factors for AKI, such as the duration of therapy, vancomycin serum level, and ICU hospitalization. The logistic regression classification performance was assessed using a receiver operating characteristic (ROC) curve, yielding an area under the curve of 0.764, signifying acceptable discrimination of the regression model. Conclusion: Implementation of the institutional protocol for vancomycin administration resulted in a significant and cost-effective impact, ensuring appropriate therapeutic dosing, reducing adverse events (e.g., nephrotoxicity), and improving clinical outcomes for patients in the study population.
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spelling pubmed-105690232023-10-13 Impact of implementing a vancomycin protocol to reduce kidney toxicity: A comparative study Baiocco, Graziella Gasparotto Greiner, Stephanie Rosa, Mário Borges Flores, Cecília Dias Barros, Helena M. T. Front Pharmacol Pharmacology Introduction: Vancomycin is a frequently used antibiotic for treating severe infections caused by multidrug-resistant, Gram-positive pathogens. To ensure its effectiveness and minimize the risk of nephrotoxicity, safe administration and dose monitoring are crucial. Understanding the impact of vancomycin serum levels on clinical outcomes is of paramount importance, necessitating improved knowledge on its use, dose monitoring, nephrotoxicity, and safe administration. Objective: This study aimed to evaluate the incidence of acute kidney injury (AKI) in patients receiving vancomycin before and after the implementation of an institutional protocol for vancomycin administration in a public tertiary hospital in southern Brazil. Materials and methods: A cross-sectional study design was employed, analyzing data from the electronic medical records of 422 patients who received vancomycin. The patient population was divided into two independent cohorts: those treated in 2016 (pre-protocol) and those treated in 2018 (post-protocol), following the implementation of the institutional vancomycin administration protocol. Results: The study included 211 patients in each year of assessment. Patients from both cohorts had a Charlson Comorbidity Index (CCI) score of 4. The post-protocol cohort consisted of older individuals, with a mean age of 62.8 years. In addition, patients in the post-protocol year had higher baseline creatinine levels, higher rates of intensive care unit (ICU) hospitalization, and increased use of vasopressors. In the pre-protocol year, patients received vancomycin therapy for a longer duration. When comparing the incidence of AKI between the two groups, an intervention study revealed rates of 38.4% in group 1 and 20.9% in group 2, indicating a significant reduction (p < 0.001) in the post-protocol group. A logistic regression model was developed to predict AKI, incorporating variables that demonstrated significance (p ≤ 0.250) in bivariate analysis and those recognized in the literature as important factors for AKI, such as the duration of therapy, vancomycin serum level, and ICU hospitalization. The logistic regression classification performance was assessed using a receiver operating characteristic (ROC) curve, yielding an area under the curve of 0.764, signifying acceptable discrimination of the regression model. Conclusion: Implementation of the institutional protocol for vancomycin administration resulted in a significant and cost-effective impact, ensuring appropriate therapeutic dosing, reducing adverse events (e.g., nephrotoxicity), and improving clinical outcomes for patients in the study population. Frontiers Media S.A. 2023-09-28 /pmc/articles/PMC10569023/ /pubmed/37841919 http://dx.doi.org/10.3389/fphar.2023.1154573 Text en Copyright © 2023 Baiocco, Greiner, Rosa, Flores and Barros. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Pharmacology
Baiocco, Graziella Gasparotto
Greiner, Stephanie
Rosa, Mário Borges
Flores, Cecília Dias
Barros, Helena M. T.
Impact of implementing a vancomycin protocol to reduce kidney toxicity: A comparative study
title Impact of implementing a vancomycin protocol to reduce kidney toxicity: A comparative study
title_full Impact of implementing a vancomycin protocol to reduce kidney toxicity: A comparative study
title_fullStr Impact of implementing a vancomycin protocol to reduce kidney toxicity: A comparative study
title_full_unstemmed Impact of implementing a vancomycin protocol to reduce kidney toxicity: A comparative study
title_short Impact of implementing a vancomycin protocol to reduce kidney toxicity: A comparative study
title_sort impact of implementing a vancomycin protocol to reduce kidney toxicity: a comparative study
topic Pharmacology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10569023/
https://www.ncbi.nlm.nih.gov/pubmed/37841919
http://dx.doi.org/10.3389/fphar.2023.1154573
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