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Association of chronic enteropathy activity index, blood urea concentration, and risk of death in dogs with protein‐losing enteropathy

BACKGROUND: Malnutrition is associated with increased risk of premature death in humans with inflammatory bowel disease. HYPOTHESIS/OBJECTIVE: To determine if historical, clinical, and laboratory markers of malnutrition in dogs at the time of histologic diagnosis of protein‐losing enteropathy (PLE)...

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Autores principales: Kathrani, Aarti, Sánchez‐Vizcaíno, Fernando, Hall, Edward J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6430906/
https://www.ncbi.nlm.nih.gov/pubmed/30784115
http://dx.doi.org/10.1111/jvim.15448
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author Kathrani, Aarti
Sánchez‐Vizcaíno, Fernando
Hall, Edward J.
author_facet Kathrani, Aarti
Sánchez‐Vizcaíno, Fernando
Hall, Edward J.
author_sort Kathrani, Aarti
collection PubMed
description BACKGROUND: Malnutrition is associated with increased risk of premature death in humans with inflammatory bowel disease. HYPOTHESIS/OBJECTIVE: To determine if historical, clinical, and laboratory markers of malnutrition in dogs at the time of histologic diagnosis of protein‐losing enteropathy (PLE) caused by chronic enteropathy (CE) or lymphangiectasia are associated with increased risk of death. ANIMALS: Seventy‐one client‐owned dogs diagnosed with PLE. METHODS: The medical records were retrospectively searched for cases of PLE, diagnosed with CE or lymphangiectasia on the basis of histopathology of intestinal biopsies at a referral hospital. For each case, various variables at the time of diagnostic investigation were recorded and follow‐up obtained by telephone contact with the referring veterinarian. RESULTS: A multivariable cox model indicated that canine chronic enteropathy activity index (CCEAI) and blood urea concentration were significantly associated with death (P values <.01). For each unit increase in CCEAI, the hazard of death increased by 22.9% (confidence interval [CI]: 6.9%‐41.2%). Dogs with a CCEAI of ≤8 and dogs with urea ≤7 mmol/L survived 256 days longer (P = .001, CI: 106.7‐405.4 days) and 279 days longer (P = .009, CI: 70.0‐488.7 days) than those with a CCEAI of >8 and urea >7 mmol/L on average, respectively, when followed up for 647 days. CONCLUSIONS AND CLINICAL IMPORTANCE: Increased CCEAI and blood urea concentration at the time of diagnosis might be predictive of death in dogs with PLE caused by CE or lymphangiectasia.
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spelling pubmed-64309062019-04-04 Association of chronic enteropathy activity index, blood urea concentration, and risk of death in dogs with protein‐losing enteropathy Kathrani, Aarti Sánchez‐Vizcaíno, Fernando Hall, Edward J. J Vet Intern Med SMALL ANIMAL BACKGROUND: Malnutrition is associated with increased risk of premature death in humans with inflammatory bowel disease. HYPOTHESIS/OBJECTIVE: To determine if historical, clinical, and laboratory markers of malnutrition in dogs at the time of histologic diagnosis of protein‐losing enteropathy (PLE) caused by chronic enteropathy (CE) or lymphangiectasia are associated with increased risk of death. ANIMALS: Seventy‐one client‐owned dogs diagnosed with PLE. METHODS: The medical records were retrospectively searched for cases of PLE, diagnosed with CE or lymphangiectasia on the basis of histopathology of intestinal biopsies at a referral hospital. For each case, various variables at the time of diagnostic investigation were recorded and follow‐up obtained by telephone contact with the referring veterinarian. RESULTS: A multivariable cox model indicated that canine chronic enteropathy activity index (CCEAI) and blood urea concentration were significantly associated with death (P values <.01). For each unit increase in CCEAI, the hazard of death increased by 22.9% (confidence interval [CI]: 6.9%‐41.2%). Dogs with a CCEAI of ≤8 and dogs with urea ≤7 mmol/L survived 256 days longer (P = .001, CI: 106.7‐405.4 days) and 279 days longer (P = .009, CI: 70.0‐488.7 days) than those with a CCEAI of >8 and urea >7 mmol/L on average, respectively, when followed up for 647 days. CONCLUSIONS AND CLINICAL IMPORTANCE: Increased CCEAI and blood urea concentration at the time of diagnosis might be predictive of death in dogs with PLE caused by CE or lymphangiectasia. John Wiley & Sons, Inc. 2019-02-19 2019 /pmc/articles/PMC6430906/ /pubmed/30784115 http://dx.doi.org/10.1111/jvim.15448 Text en © 2019 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
Kathrani, Aarti
Sánchez‐Vizcaíno, Fernando
Hall, Edward J.
Association of chronic enteropathy activity index, blood urea concentration, and risk of death in dogs with protein‐losing enteropathy
title Association of chronic enteropathy activity index, blood urea concentration, and risk of death in dogs with protein‐losing enteropathy
title_full Association of chronic enteropathy activity index, blood urea concentration, and risk of death in dogs with protein‐losing enteropathy
title_fullStr Association of chronic enteropathy activity index, blood urea concentration, and risk of death in dogs with protein‐losing enteropathy
title_full_unstemmed Association of chronic enteropathy activity index, blood urea concentration, and risk of death in dogs with protein‐losing enteropathy
title_short Association of chronic enteropathy activity index, blood urea concentration, and risk of death in dogs with protein‐losing enteropathy
title_sort association of chronic enteropathy activity index, blood urea concentration, and risk of death in dogs with protein‐losing enteropathy
topic SMALL ANIMAL
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6430906/
https://www.ncbi.nlm.nih.gov/pubmed/30784115
http://dx.doi.org/10.1111/jvim.15448
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