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Utility of serum amyloid A in monitoring clinical response to antimicrobial treatment in horses with bacterial pneumonia

BACKGROUND: Serum amyloid A (SAA) is a major acute phase protein in horses which could be a useful tool for assessing clinical response to treatment of bacterial pneumonia in adult horses. OBJECTIVES: To monitor SAA concentration in response to treatment and identify associations among SAA concentra...

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Autores principales: Hepworth‐Warren, Kate L., Estell, Krista, Cowles, Bobby, Amodie, Deborah, Crisman, Mark
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10473010/
https://www.ncbi.nlm.nih.gov/pubmed/37522636
http://dx.doi.org/10.1111/jvim.16818
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author Hepworth‐Warren, Kate L.
Estell, Krista
Cowles, Bobby
Amodie, Deborah
Crisman, Mark
author_facet Hepworth‐Warren, Kate L.
Estell, Krista
Cowles, Bobby
Amodie, Deborah
Crisman, Mark
author_sort Hepworth‐Warren, Kate L.
collection PubMed
description BACKGROUND: Serum amyloid A (SAA) is a major acute phase protein in horses which could be a useful tool for assessing clinical response to treatment of bacterial pneumonia in adult horses. OBJECTIVES: To monitor SAA concentration in response to treatment and identify associations among SAA concentration, WBC and neutrophil counts, and fibrinogen in bacterial pneumonia in adult horses. ANIMALS: Eighteen adult horses with bacterial pneumonia. METHODS: Prospective clinical study. Horses hospitalized with bacterial pneumonia were enrolled and SAA concentration and vital signs were assessed daily. SAA concentration was measured by a handheld meter. CBC and plasma fibrinogen were assessed on days 0, 1, and 2, then every 3 days until discharge. Data were not normally distributed and therefore were log transformed. Log‐transformed data were analyzed and comparisons were performed on LSMeans by the 2‐sided Student's t‐test at the 5% level of significance. RESULTS: Geometric mean SAA concentration on day 0 was 537 μg/mL (SE 383 μg/mL). Geometric mean SAA concentration decreased significantly over time (P = .0001), peaking at day 2 (geomean 1038 μg/mL, SE 261.7 μg/mL) and decreasing until discharge. Plasma concentration of fibrinogen (P = .06), neutrophil count (P = .48), and WBC count (P = .07) did not change significantly over time. CONCLUSIONS AND CLINICAL IMPORTANCE: SAA concentration decreased significantly over the course of treatment and correlated with clinical improvement of pneumonia whereas fibrinogen, neutrophil, and WBC counts did not.
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spelling pubmed-104730102023-09-02 Utility of serum amyloid A in monitoring clinical response to antimicrobial treatment in horses with bacterial pneumonia Hepworth‐Warren, Kate L. Estell, Krista Cowles, Bobby Amodie, Deborah Crisman, Mark J Vet Intern Med EQUINE BACKGROUND: Serum amyloid A (SAA) is a major acute phase protein in horses which could be a useful tool for assessing clinical response to treatment of bacterial pneumonia in adult horses. OBJECTIVES: To monitor SAA concentration in response to treatment and identify associations among SAA concentration, WBC and neutrophil counts, and fibrinogen in bacterial pneumonia in adult horses. ANIMALS: Eighteen adult horses with bacterial pneumonia. METHODS: Prospective clinical study. Horses hospitalized with bacterial pneumonia were enrolled and SAA concentration and vital signs were assessed daily. SAA concentration was measured by a handheld meter. CBC and plasma fibrinogen were assessed on days 0, 1, and 2, then every 3 days until discharge. Data were not normally distributed and therefore were log transformed. Log‐transformed data were analyzed and comparisons were performed on LSMeans by the 2‐sided Student's t‐test at the 5% level of significance. RESULTS: Geometric mean SAA concentration on day 0 was 537 μg/mL (SE 383 μg/mL). Geometric mean SAA concentration decreased significantly over time (P = .0001), peaking at day 2 (geomean 1038 μg/mL, SE 261.7 μg/mL) and decreasing until discharge. Plasma concentration of fibrinogen (P = .06), neutrophil count (P = .48), and WBC count (P = .07) did not change significantly over time. CONCLUSIONS AND CLINICAL IMPORTANCE: SAA concentration decreased significantly over the course of treatment and correlated with clinical improvement of pneumonia whereas fibrinogen, neutrophil, and WBC counts did not. John Wiley & Sons, Inc. 2023-07-31 /pmc/articles/PMC10473010/ /pubmed/37522636 http://dx.doi.org/10.1111/jvim.16818 Text en © 2023 The Authors. Journal of Veterinary Internal Medicine published by Wiley Periodicals LLC on behalf of American College of Veterinary Internal Medicine. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle EQUINE
Hepworth‐Warren, Kate L.
Estell, Krista
Cowles, Bobby
Amodie, Deborah
Crisman, Mark
Utility of serum amyloid A in monitoring clinical response to antimicrobial treatment in horses with bacterial pneumonia
title Utility of serum amyloid A in monitoring clinical response to antimicrobial treatment in horses with bacterial pneumonia
title_full Utility of serum amyloid A in monitoring clinical response to antimicrobial treatment in horses with bacterial pneumonia
title_fullStr Utility of serum amyloid A in monitoring clinical response to antimicrobial treatment in horses with bacterial pneumonia
title_full_unstemmed Utility of serum amyloid A in monitoring clinical response to antimicrobial treatment in horses with bacterial pneumonia
title_short Utility of serum amyloid A in monitoring clinical response to antimicrobial treatment in horses with bacterial pneumonia
title_sort utility of serum amyloid a in monitoring clinical response to antimicrobial treatment in horses with bacterial pneumonia
topic EQUINE
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10473010/
https://www.ncbi.nlm.nih.gov/pubmed/37522636
http://dx.doi.org/10.1111/jvim.16818
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