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Evaluation of Hemostatic Abnormalities in Canine Spirocercosis and Its Association with Systemic Inflammation

BACKGROUND: Canine spirocercosis is caused by the nematode Spirocerca lupi and is characterized by esophageal fibro‐inflammatory nodules that may undergo neoplastic transformation. No sensitive and specific laboratory assays other than histopathology have been reported to differentiate non‐neoplasti...

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Autores principales: Pazzi, P., Goddard, A., Kristensen, A.T., Dvir, E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4895557/
https://www.ncbi.nlm.nih.gov/pubmed/24147754
http://dx.doi.org/10.1111/jvim.12220
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author Pazzi, P.
Goddard, A.
Kristensen, A.T.
Dvir, E.
author_facet Pazzi, P.
Goddard, A.
Kristensen, A.T.
Dvir, E.
author_sort Pazzi, P.
collection PubMed
description BACKGROUND: Canine spirocercosis is caused by the nematode Spirocerca lupi and is characterized by esophageal fibro‐inflammatory nodules that may undergo neoplastic transformation. No sensitive and specific laboratory assays other than histopathology have been reported to differentiate non‐neoplastic from neoplastic disease. HYPOTHESIS/OBJECTIVES: Dogs with spirocercosis will have evidence of hypercoagulability based on thromboelastography (TEG)‐derived maximal amplitude (MA); increased MA will be correlated with increased acute phase protein (APP) concentrations (C‐reactive protein [CRP] and fibrinogen); increased MA and APPs will be exacerbated with neoplastic spirocercosis. ANIMALS: Thirty‐nine client‐owned dogs with naturally occurring spirocercosis and 15 sex‐matched healthy controls. METHODS: A prospective comparative study evaluating TEG, activated partial thromboplastin time, prothrombin time, antithrombin (AT) activity, platelet count and D‐dimer concentration, and APPs of dogs with non‐neoplastic (n = 24) and neoplastic (n = 15) spirocercosis compared to control dogs. RESULTS: Median MA was significantly increased in the non‐neoplastic group (P < .01) and neoplastic group (P < .01) compared to the controls. Both APPs were significantly increased in the neoplastic group compared to the non‐neoplastic and control groups. MA was strongly correlated with fibrinogen (r = 0.85, P < .001) and CRP (r = 0.73, P < .001). An MA >76 mm provided 96% specificity and 73% sensitivity for differentiation of disease state. CONCLUSIONS AND CLINICAL IMPORTANCE: Canine spirocercosis is associated with increased TEG variables, MA and α, and decreased AT activity, which may indicate a hypercoagulable state seemingly more severe with neoplastic transformation. MA was correlated with APP in dogs with spirocercosis and can be used as an adjunctive test to support the suspicion of neoplastic transformation.
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spelling pubmed-48955572016-06-22 Evaluation of Hemostatic Abnormalities in Canine Spirocercosis and Its Association with Systemic Inflammation Pazzi, P. Goddard, A. Kristensen, A.T. Dvir, E. J Vet Intern Med Standard Articles BACKGROUND: Canine spirocercosis is caused by the nematode Spirocerca lupi and is characterized by esophageal fibro‐inflammatory nodules that may undergo neoplastic transformation. No sensitive and specific laboratory assays other than histopathology have been reported to differentiate non‐neoplastic from neoplastic disease. HYPOTHESIS/OBJECTIVES: Dogs with spirocercosis will have evidence of hypercoagulability based on thromboelastography (TEG)‐derived maximal amplitude (MA); increased MA will be correlated with increased acute phase protein (APP) concentrations (C‐reactive protein [CRP] and fibrinogen); increased MA and APPs will be exacerbated with neoplastic spirocercosis. ANIMALS: Thirty‐nine client‐owned dogs with naturally occurring spirocercosis and 15 sex‐matched healthy controls. METHODS: A prospective comparative study evaluating TEG, activated partial thromboplastin time, prothrombin time, antithrombin (AT) activity, platelet count and D‐dimer concentration, and APPs of dogs with non‐neoplastic (n = 24) and neoplastic (n = 15) spirocercosis compared to control dogs. RESULTS: Median MA was significantly increased in the non‐neoplastic group (P < .01) and neoplastic group (P < .01) compared to the controls. Both APPs were significantly increased in the neoplastic group compared to the non‐neoplastic and control groups. MA was strongly correlated with fibrinogen (r = 0.85, P < .001) and CRP (r = 0.73, P < .001). An MA >76 mm provided 96% specificity and 73% sensitivity for differentiation of disease state. CONCLUSIONS AND CLINICAL IMPORTANCE: Canine spirocercosis is associated with increased TEG variables, MA and α, and decreased AT activity, which may indicate a hypercoagulable state seemingly more severe with neoplastic transformation. MA was correlated with APP in dogs with spirocercosis and can be used as an adjunctive test to support the suspicion of neoplastic transformation. John Wiley and Sons Inc. 2013-10-21 2014 /pmc/articles/PMC4895557/ /pubmed/24147754 http://dx.doi.org/10.1111/jvim.12220 Text en Copyright © 2013 by the American College of Veterinary Internal Medicine
spellingShingle Standard Articles
Pazzi, P.
Goddard, A.
Kristensen, A.T.
Dvir, E.
Evaluation of Hemostatic Abnormalities in Canine Spirocercosis and Its Association with Systemic Inflammation
title Evaluation of Hemostatic Abnormalities in Canine Spirocercosis and Its Association with Systemic Inflammation
title_full Evaluation of Hemostatic Abnormalities in Canine Spirocercosis and Its Association with Systemic Inflammation
title_fullStr Evaluation of Hemostatic Abnormalities in Canine Spirocercosis and Its Association with Systemic Inflammation
title_full_unstemmed Evaluation of Hemostatic Abnormalities in Canine Spirocercosis and Its Association with Systemic Inflammation
title_short Evaluation of Hemostatic Abnormalities in Canine Spirocercosis and Its Association with Systemic Inflammation
title_sort evaluation of hemostatic abnormalities in canine spirocercosis and its association with systemic inflammation
topic Standard Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4895557/
https://www.ncbi.nlm.nih.gov/pubmed/24147754
http://dx.doi.org/10.1111/jvim.12220
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