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Hypercoagulability in dogs with chronic enteropathy and association with serum albumin concentration
BACKGROUND: Dogs with protein‐losing enteropathy (PLE) are at risk of developing a hypercoagulable state, but the prevalence of hypercoagulability in dogs with chronic enteropathies (CE) and normal serum albumin concentration is unknown. HYPOTHESIS: Dogs with CE are predisposed to a hypercoagulable...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley & Sons, Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7995358/ https://www.ncbi.nlm.nih.gov/pubmed/33527508 http://dx.doi.org/10.1111/jvim.16044 |
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author | Dixon, Amy Hall, Edward J. Adamantos, Sophie Kathrani, Aarti McGrath, Ciara Black, Vicki |
author_facet | Dixon, Amy Hall, Edward J. Adamantos, Sophie Kathrani, Aarti McGrath, Ciara Black, Vicki |
author_sort | Dixon, Amy |
collection | PubMed |
description | BACKGROUND: Dogs with protein‐losing enteropathy (PLE) are at risk of developing a hypercoagulable state, but the prevalence of hypercoagulability in dogs with chronic enteropathies (CE) and normal serum albumin concentration is unknown. HYPOTHESIS: Dogs with CE are predisposed to a hypercoagulable state as assessed by thromboelastography (TEG) independent of serum albumin concentration. METHODS: Dogs with chronic gastrointestinal signs from suspected inflammatory CE between 2017 and 2019 were included. Thirty‐eight were evaluated; every dog had a CBC, serum biochemistry panel, and abdominal imaging performed. The Canine Inflammatory Bowel Disease Activity Index (CIBDAI) was calculated. Thromboelastography was performed at presentation, and reaction time (R), kinetic time (K), α‐angle, maximal amplitude (MA), and global clot strength (G) were recorded. Dogs were considered hypercoagulable if the G value was ≥25% above the reference interval. RESULTS: Seventeen of 38 (44.7%; 95% confidence interval [CI], 28.6‐61.7%) dogs with CE were hypercoagulable. The G value did not differ between the 19 dogs with normal (≥28 g/L) serum albumin concentrations (9.05 kdyn/cm(2); 95% CI, 7.26‐10.84; SD 3.71) and 19 dogs with hypoalbuminemia (11.3 kdyn/cm(2); 95% CI, 9.04‐13.6, SD; 4.7; P = .11). The G value was negatively correlated with hematocrit, serum albumin concentration, and duration of signs and positively correlated with age. CONCLUSIONS AND CLINICAL IMPORTANCE: Dogs with CE and normal serum albumin concentration can be hypercoagulable as measured by TEG. |
format | Online Article Text |
id | pubmed-7995358 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley & Sons, Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-79953582021-03-30 Hypercoagulability in dogs with chronic enteropathy and association with serum albumin concentration Dixon, Amy Hall, Edward J. Adamantos, Sophie Kathrani, Aarti McGrath, Ciara Black, Vicki J Vet Intern Med SMALL ANIMAL BACKGROUND: Dogs with protein‐losing enteropathy (PLE) are at risk of developing a hypercoagulable state, but the prevalence of hypercoagulability in dogs with chronic enteropathies (CE) and normal serum albumin concentration is unknown. HYPOTHESIS: Dogs with CE are predisposed to a hypercoagulable state as assessed by thromboelastography (TEG) independent of serum albumin concentration. METHODS: Dogs with chronic gastrointestinal signs from suspected inflammatory CE between 2017 and 2019 were included. Thirty‐eight were evaluated; every dog had a CBC, serum biochemistry panel, and abdominal imaging performed. The Canine Inflammatory Bowel Disease Activity Index (CIBDAI) was calculated. Thromboelastography was performed at presentation, and reaction time (R), kinetic time (K), α‐angle, maximal amplitude (MA), and global clot strength (G) were recorded. Dogs were considered hypercoagulable if the G value was ≥25% above the reference interval. RESULTS: Seventeen of 38 (44.7%; 95% confidence interval [CI], 28.6‐61.7%) dogs with CE were hypercoagulable. The G value did not differ between the 19 dogs with normal (≥28 g/L) serum albumin concentrations (9.05 kdyn/cm(2); 95% CI, 7.26‐10.84; SD 3.71) and 19 dogs with hypoalbuminemia (11.3 kdyn/cm(2); 95% CI, 9.04‐13.6, SD; 4.7; P = .11). The G value was negatively correlated with hematocrit, serum albumin concentration, and duration of signs and positively correlated with age. CONCLUSIONS AND CLINICAL IMPORTANCE: Dogs with CE and normal serum albumin concentration can be hypercoagulable as measured by TEG. John Wiley & Sons, Inc. 2021-02-01 2021 /pmc/articles/PMC7995358/ /pubmed/33527508 http://dx.doi.org/10.1111/jvim.16044 Text en © 2021 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 Dixon, Amy Hall, Edward J. Adamantos, Sophie Kathrani, Aarti McGrath, Ciara Black, Vicki Hypercoagulability in dogs with chronic enteropathy and association with serum albumin concentration |
title | Hypercoagulability in dogs with chronic enteropathy and association with serum albumin concentration |
title_full | Hypercoagulability in dogs with chronic enteropathy and association with serum albumin concentration |
title_fullStr | Hypercoagulability in dogs with chronic enteropathy and association with serum albumin concentration |
title_full_unstemmed | Hypercoagulability in dogs with chronic enteropathy and association with serum albumin concentration |
title_short | Hypercoagulability in dogs with chronic enteropathy and association with serum albumin concentration |
title_sort | hypercoagulability in dogs with chronic enteropathy and association with serum albumin concentration |
topic | SMALL ANIMAL |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7995358/ https://www.ncbi.nlm.nih.gov/pubmed/33527508 http://dx.doi.org/10.1111/jvim.16044 |
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