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Parenterally administered vancomycin in 29 dogs and 7 cats (2003‐2017)

BACKGROUND: Vancomycin is commonly used to treat resistant bacterial infections in people. Reported adverse effects of vancomycin in people include acute kidney injury (AKI), neutropenia, and systemic allergic reaction. Given the increased incidence of vancomycin‐resistant bacterial infections in pe...

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Autores principales: DeStefano, Ian M., Wayne, Annie S., Rozanski, Elizabeth A., Babyak, Jonathan M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6335575/
https://www.ncbi.nlm.nih.gov/pubmed/30499215
http://dx.doi.org/10.1111/jvim.15357
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author DeStefano, Ian M.
Wayne, Annie S.
Rozanski, Elizabeth A.
Babyak, Jonathan M.
author_facet DeStefano, Ian M.
Wayne, Annie S.
Rozanski, Elizabeth A.
Babyak, Jonathan M.
author_sort DeStefano, Ian M.
collection PubMed
description BACKGROUND: Vancomycin is commonly used to treat resistant bacterial infections in people. Reported adverse effects of vancomycin in people include acute kidney injury (AKI), neutropenia, and systemic allergic reaction. Given the increased incidence of vancomycin‐resistant bacterial infections in people, support is growing for restriction of vancomycin. OBJECTIVES: To evaluate the use of intravenous (IV) vancomycin in a university teaching hospital and to describe potential adverse effects. ANIMALS: Twenty‐nine dogs and 7 cats. METHODS: Medical records of dogs and cats treated with IV vancomycin at the Foster Hospital for Small Animals between January 2003 and October 2017 were reviewed. Information recorded included signalment, infection source, vancomycin dosing, potential adverse effects, and outcome. RESULTS: Vancomycin was used to treat infections from a range of sources with a variety of dosing intervals. The most common bacterial isolates susceptible to vancomycin included Enterococcus sp. (11/36, 30.6%), methicillin‐resistant Staphylococcus aureus (8/36, 22.2%), and methicillin‐resistant Staphylococcus pseudintermedius (2/36, 5.6%). AKI occurred in 6 of 36 patients (16.7%) during vancomycin treatment but could not definitively be attributed to vancomycin treatment in any patients because of illness severity, additional nephrotoxic treatments, or both. Neutropenia or allergic reaction was not documented in any animal. In 2 of 36 patients (5.6%), susceptibility data documented an infection that was only susceptible to vancomycin. Most patients survived to discharge (25/36, 69.4%). CONCLUSIONS AND CLINICAL IMPORTANCE: Adverse effects attributable to vancomycin were infrequent in dogs and cats. In most cases, there were potential alternative effective antimicrobials or lack of susceptibility data to support vancomycin treatment.
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spelling pubmed-63355752019-01-23 Parenterally administered vancomycin in 29 dogs and 7 cats (2003‐2017) DeStefano, Ian M. Wayne, Annie S. Rozanski, Elizabeth A. Babyak, Jonathan M. J Vet Intern Med SMALL ANIMAL BACKGROUND: Vancomycin is commonly used to treat resistant bacterial infections in people. Reported adverse effects of vancomycin in people include acute kidney injury (AKI), neutropenia, and systemic allergic reaction. Given the increased incidence of vancomycin‐resistant bacterial infections in people, support is growing for restriction of vancomycin. OBJECTIVES: To evaluate the use of intravenous (IV) vancomycin in a university teaching hospital and to describe potential adverse effects. ANIMALS: Twenty‐nine dogs and 7 cats. METHODS: Medical records of dogs and cats treated with IV vancomycin at the Foster Hospital for Small Animals between January 2003 and October 2017 were reviewed. Information recorded included signalment, infection source, vancomycin dosing, potential adverse effects, and outcome. RESULTS: Vancomycin was used to treat infections from a range of sources with a variety of dosing intervals. The most common bacterial isolates susceptible to vancomycin included Enterococcus sp. (11/36, 30.6%), methicillin‐resistant Staphylococcus aureus (8/36, 22.2%), and methicillin‐resistant Staphylococcus pseudintermedius (2/36, 5.6%). AKI occurred in 6 of 36 patients (16.7%) during vancomycin treatment but could not definitively be attributed to vancomycin treatment in any patients because of illness severity, additional nephrotoxic treatments, or both. Neutropenia or allergic reaction was not documented in any animal. In 2 of 36 patients (5.6%), susceptibility data documented an infection that was only susceptible to vancomycin. Most patients survived to discharge (25/36, 69.4%). CONCLUSIONS AND CLINICAL IMPORTANCE: Adverse effects attributable to vancomycin were infrequent in dogs and cats. In most cases, there were potential alternative effective antimicrobials or lack of susceptibility data to support vancomycin treatment. John Wiley & Sons, Inc. 2018-11-30 2019 /pmc/articles/PMC6335575/ /pubmed/30499215 http://dx.doi.org/10.1111/jvim.15357 Text en © 2018 The Authors. Journal of Veterinary Internal Medicine published by Wiley Periodicals, Inc. on behalf of the American College of Veterinary Internal Medicine. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle SMALL ANIMAL
DeStefano, Ian M.
Wayne, Annie S.
Rozanski, Elizabeth A.
Babyak, Jonathan M.
Parenterally administered vancomycin in 29 dogs and 7 cats (2003‐2017)
title Parenterally administered vancomycin in 29 dogs and 7 cats (2003‐2017)
title_full Parenterally administered vancomycin in 29 dogs and 7 cats (2003‐2017)
title_fullStr Parenterally administered vancomycin in 29 dogs and 7 cats (2003‐2017)
title_full_unstemmed Parenterally administered vancomycin in 29 dogs and 7 cats (2003‐2017)
title_short Parenterally administered vancomycin in 29 dogs and 7 cats (2003‐2017)
title_sort parenterally administered vancomycin in 29 dogs and 7 cats (2003‐2017)
topic SMALL ANIMAL
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6335575/
https://www.ncbi.nlm.nih.gov/pubmed/30499215
http://dx.doi.org/10.1111/jvim.15357
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