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Clinicopathologic and radiographic features in 33 cats with aspiration and 26 cats with bronchopneumonia (2007‐2017)

BACKGROUND: Aspiration pneumonia (AP) and bronchopneumonia (BP) are poorly characterized diseases in cats that share clinical similarities to inflammatory airway disease (IAD). OBJECTIVES: Describe clinicopathologic, radiographic, and microbiologic features in cats with AP and BP and compare finding...

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Autores principales: Dear, Jonathan D., Vernau, William, Johnson, Eric G., Hulsebosch, Sean E., Johnson, Lynelle R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7848386/
https://www.ncbi.nlm.nih.gov/pubmed/33315286
http://dx.doi.org/10.1111/jvim.16005
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author Dear, Jonathan D.
Vernau, William
Johnson, Eric G.
Hulsebosch, Sean E.
Johnson, Lynelle R.
author_facet Dear, Jonathan D.
Vernau, William
Johnson, Eric G.
Hulsebosch, Sean E.
Johnson, Lynelle R.
author_sort Dear, Jonathan D.
collection PubMed
description BACKGROUND: Aspiration pneumonia (AP) and bronchopneumonia (BP) are poorly characterized diseases in cats that share clinical similarities to inflammatory airway disease (IAD). OBJECTIVES: Describe clinicopathologic, radiographic, and microbiologic features in cats with AP and BP and compare findings to those in cats with IAD. ANIMALS: Thirty‐three cats with AP and 26 with BP; 44 cats with IAD. METHODS: Retrospective case‐control study. Results extracted for all cats included signalment, physical examination findings, historical details, and potential risk factors for aspiration. Diagnostic test results were summarized including CBC, bronchoalveolar (BAL) fluid analysis and microbial culture. Radiographs were reviewed in masked fashion and scored for severity. Results of BAL fluid analysis were assessed for evidence of septic inflammation. RESULTS: Cats with AP were less likely to be presented for evaluation of cough (P < .001) and more likely to be hypothermic (P = .01) than were cats with IAD or BP. Median duration of signs was significantly shorter in cats with AP (12 days) compared to cats with BP or IAD (270 and 180 days; P = .01). Radiographically, cats with AP were more likely to have an alveolar pattern and higher total score than were cats with BP or IAD. Mycoplasma spp. were the organisms most commonly cultured from BAL fluid in cats with BP, but were not cultured from any cats with AP. CONCLUSION AND CLINICAL IMPORTANCE: Pneumonia must be distinguished from IAD in cats with cough and AP should be considered in cats with acute onset of tachypnea.
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spelling pubmed-78483862021-02-05 Clinicopathologic and radiographic features in 33 cats with aspiration and 26 cats with bronchopneumonia (2007‐2017) Dear, Jonathan D. Vernau, William Johnson, Eric G. Hulsebosch, Sean E. Johnson, Lynelle R. J Vet Intern Med SMALL ANIMAL BACKGROUND: Aspiration pneumonia (AP) and bronchopneumonia (BP) are poorly characterized diseases in cats that share clinical similarities to inflammatory airway disease (IAD). OBJECTIVES: Describe clinicopathologic, radiographic, and microbiologic features in cats with AP and BP and compare findings to those in cats with IAD. ANIMALS: Thirty‐three cats with AP and 26 with BP; 44 cats with IAD. METHODS: Retrospective case‐control study. Results extracted for all cats included signalment, physical examination findings, historical details, and potential risk factors for aspiration. Diagnostic test results were summarized including CBC, bronchoalveolar (BAL) fluid analysis and microbial culture. Radiographs were reviewed in masked fashion and scored for severity. Results of BAL fluid analysis were assessed for evidence of septic inflammation. RESULTS: Cats with AP were less likely to be presented for evaluation of cough (P < .001) and more likely to be hypothermic (P = .01) than were cats with IAD or BP. Median duration of signs was significantly shorter in cats with AP (12 days) compared to cats with BP or IAD (270 and 180 days; P = .01). Radiographically, cats with AP were more likely to have an alveolar pattern and higher total score than were cats with BP or IAD. Mycoplasma spp. were the organisms most commonly cultured from BAL fluid in cats with BP, but were not cultured from any cats with AP. CONCLUSION AND CLINICAL IMPORTANCE: Pneumonia must be distinguished from IAD in cats with cough and AP should be considered in cats with acute onset of tachypnea. John Wiley & Sons, Inc. 2020-12-14 2021 /pmc/articles/PMC7848386/ /pubmed/33315286 http://dx.doi.org/10.1111/jvim.16005 Text en © 2020 The Authors. Journal of Veterinary Internal Medicine published by Wiley Periodicals LLC. 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
Dear, Jonathan D.
Vernau, William
Johnson, Eric G.
Hulsebosch, Sean E.
Johnson, Lynelle R.
Clinicopathologic and radiographic features in 33 cats with aspiration and 26 cats with bronchopneumonia (2007‐2017)
title Clinicopathologic and radiographic features in 33 cats with aspiration and 26 cats with bronchopneumonia (2007‐2017)
title_full Clinicopathologic and radiographic features in 33 cats with aspiration and 26 cats with bronchopneumonia (2007‐2017)
title_fullStr Clinicopathologic and radiographic features in 33 cats with aspiration and 26 cats with bronchopneumonia (2007‐2017)
title_full_unstemmed Clinicopathologic and radiographic features in 33 cats with aspiration and 26 cats with bronchopneumonia (2007‐2017)
title_short Clinicopathologic and radiographic features in 33 cats with aspiration and 26 cats with bronchopneumonia (2007‐2017)
title_sort clinicopathologic and radiographic features in 33 cats with aspiration and 26 cats with bronchopneumonia (2007‐2017)
topic SMALL ANIMAL
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7848386/
https://www.ncbi.nlm.nih.gov/pubmed/33315286
http://dx.doi.org/10.1111/jvim.16005
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