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Cardiac cachexia in cats with congestive heart failure: Prevalence and clinical, laboratory, and survival findings
BACKGROUND: Cardiac cachexia is common in people and dogs with congestive heart failure (CHF). However, the prevalence and effects of cardiac cachexia in cats are unknown. OBJECTIVES: To determine the prevalence of cachexia and its associations with clinical laboratory and survival data in cats with...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley & Sons, Inc.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6979101/ https://www.ncbi.nlm.nih.gov/pubmed/31837182 http://dx.doi.org/10.1111/jvim.15672 |
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author | Santiago, Sasha L. Freeman, Lisa M. Rush, John E. |
author_facet | Santiago, Sasha L. Freeman, Lisa M. Rush, John E. |
author_sort | Santiago, Sasha L. |
collection | PubMed |
description | BACKGROUND: Cardiac cachexia is common in people and dogs with congestive heart failure (CHF). However, the prevalence and effects of cardiac cachexia in cats are unknown. OBJECTIVES: To determine the prevalence of cachexia and its associations with clinical laboratory and survival data in cats with CHF. ANIMALS: One hundred twenty‐five cats with CHF. METHODS: Medical records of cats evaluated during a 40‐month period were retrospectively reviewed to identify cats with cardiac cachexia using 7 different definitions. Clinical, laboratory, and survival data were compared between cats with and without cachexia. RESULTS: Prevalence of cachexia ranged from 0 to 66.7% for the 7 definitions, with a prevalence of 41.6% using muscle condition score (MCS). Cats with cachexia (determined by MCS) were older (P < .001), more likely to have pleural effusion (P = .003), had significantly higher blood urea nitrogen (P < .001) and neutrophil concentrations (P = .01), and significantly lower body condition score (P < .001), body weights (P < .001), hematocrit (P = .007), and hemoglobin concentrations (P = .009). Survival time for cats with cachexia (determined by MCS) was significantly shorter than for cats without cachexia (P = .03). Cats that were underweight (P = .002) and cats with dilated cardiomyopathy (DCM) also had shorter survival times (P = .04). CONCLUSIONS AND CLINICAL IMPORTANCE: The association between cachexia and reduced survival time emphasizes the importance of identifying and addressing this common problem in cats with CHF. |
format | Online Article Text |
id | pubmed-6979101 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | John Wiley & Sons, Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-69791012020-01-28 Cardiac cachexia in cats with congestive heart failure: Prevalence and clinical, laboratory, and survival findings Santiago, Sasha L. Freeman, Lisa M. Rush, John E. J Vet Intern Med SMALL ANIMAL BACKGROUND: Cardiac cachexia is common in people and dogs with congestive heart failure (CHF). However, the prevalence and effects of cardiac cachexia in cats are unknown. OBJECTIVES: To determine the prevalence of cachexia and its associations with clinical laboratory and survival data in cats with CHF. ANIMALS: One hundred twenty‐five cats with CHF. METHODS: Medical records of cats evaluated during a 40‐month period were retrospectively reviewed to identify cats with cardiac cachexia using 7 different definitions. Clinical, laboratory, and survival data were compared between cats with and without cachexia. RESULTS: Prevalence of cachexia ranged from 0 to 66.7% for the 7 definitions, with a prevalence of 41.6% using muscle condition score (MCS). Cats with cachexia (determined by MCS) were older (P < .001), more likely to have pleural effusion (P = .003), had significantly higher blood urea nitrogen (P < .001) and neutrophil concentrations (P = .01), and significantly lower body condition score (P < .001), body weights (P < .001), hematocrit (P = .007), and hemoglobin concentrations (P = .009). Survival time for cats with cachexia (determined by MCS) was significantly shorter than for cats without cachexia (P = .03). Cats that were underweight (P = .002) and cats with dilated cardiomyopathy (DCM) also had shorter survival times (P = .04). CONCLUSIONS AND CLINICAL IMPORTANCE: The association between cachexia and reduced survival time emphasizes the importance of identifying and addressing this common problem in cats with CHF. John Wiley & Sons, Inc. 2019-12-03 2020 /pmc/articles/PMC6979101/ /pubmed/31837182 http://dx.doi.org/10.1111/jvim.15672 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-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 | SMALL ANIMAL Santiago, Sasha L. Freeman, Lisa M. Rush, John E. Cardiac cachexia in cats with congestive heart failure: Prevalence and clinical, laboratory, and survival findings |
title | Cardiac cachexia in cats with congestive heart failure: Prevalence and clinical, laboratory, and survival findings |
title_full | Cardiac cachexia in cats with congestive heart failure: Prevalence and clinical, laboratory, and survival findings |
title_fullStr | Cardiac cachexia in cats with congestive heart failure: Prevalence and clinical, laboratory, and survival findings |
title_full_unstemmed | Cardiac cachexia in cats with congestive heart failure: Prevalence and clinical, laboratory, and survival findings |
title_short | Cardiac cachexia in cats with congestive heart failure: Prevalence and clinical, laboratory, and survival findings |
title_sort | cardiac cachexia in cats with congestive heart failure: prevalence and clinical, laboratory, and survival findings |
topic | SMALL ANIMAL |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6979101/ https://www.ncbi.nlm.nih.gov/pubmed/31837182 http://dx.doi.org/10.1111/jvim.15672 |
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