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Longitudinal study on morbidity and mortality in white veal calves in Belgium

BACKGROUND: Mortality and morbidity are hardly documented in the white veal industry, despite high levels of antimicrobial drug use and resistance. The objective of the present study was to determine the causes and epidemiology of morbidity and mortality in dairy, beef and crossbred white veal produ...

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Autores principales: Pardon, Bart, De Bleecker, Koen, Hostens, Miel, Callens, Jozefien, Dewulf, Jeroen, Deprez, Piet
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3366893/
https://www.ncbi.nlm.nih.gov/pubmed/22414223
http://dx.doi.org/10.1186/1746-6148-8-26
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author Pardon, Bart
De Bleecker, Koen
Hostens, Miel
Callens, Jozefien
Dewulf, Jeroen
Deprez, Piet
author_facet Pardon, Bart
De Bleecker, Koen
Hostens, Miel
Callens, Jozefien
Dewulf, Jeroen
Deprez, Piet
author_sort Pardon, Bart
collection PubMed
description BACKGROUND: Mortality and morbidity are hardly documented in the white veal industry, despite high levels of antimicrobial drug use and resistance. The objective of the present study was to determine the causes and epidemiology of morbidity and mortality in dairy, beef and crossbred white veal production. A total of 5853 calves, housed in 15 production cohorts, were followed during one production cycle. Causes of mortality were determined by necropsy. Morbidity was daily recorded by the producers. RESULTS: The total mortality risk was 5,3% and was significantly higher in beef veal production compared to dairy or crossbreds. The main causes of mortality were pneumonia (1.3% of the calves at risk), ruminal disorders (0.7%), idiopathic peritonitis (0.5%), enterotoxaemia (0.5%) and enteritis (0.4%). Belgian Blue beef calves were more likely to die from pneumonia, enterotoxaemia and arthritis. Detection of bovine viral diarrhea virus at necropsy was associated with chronic pneumonia and pleuritis. Of the calves, 25.4% was treated individually and the morbidity rate was 1.66 cases per 1000 calf days at risk. The incidence rate of respiratory disease, diarrhea, arthritis and otitis was 0.95, 0.30, 0.11 and 0.07 cases per 1000 calf days at risk respectively. Morbidity peaked in the first three weeks after arrival and gradually declined towards the end of the production cycle. CONCLUSIONS: The present study provided insights into the causes and epidemiology of morbidity and mortality in white veal calves in Belgium, housed in the most frequent housing system in Europe. The necropsy findings, identified risk periods and differences between production systems can guide both veterinarians and producers towards the most profitable and ethical preventive and therapeutic protocols.
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spelling pubmed-33668932012-06-05 Longitudinal study on morbidity and mortality in white veal calves in Belgium Pardon, Bart De Bleecker, Koen Hostens, Miel Callens, Jozefien Dewulf, Jeroen Deprez, Piet BMC Vet Res Research Article BACKGROUND: Mortality and morbidity are hardly documented in the white veal industry, despite high levels of antimicrobial drug use and resistance. The objective of the present study was to determine the causes and epidemiology of morbidity and mortality in dairy, beef and crossbred white veal production. A total of 5853 calves, housed in 15 production cohorts, were followed during one production cycle. Causes of mortality were determined by necropsy. Morbidity was daily recorded by the producers. RESULTS: The total mortality risk was 5,3% and was significantly higher in beef veal production compared to dairy or crossbreds. The main causes of mortality were pneumonia (1.3% of the calves at risk), ruminal disorders (0.7%), idiopathic peritonitis (0.5%), enterotoxaemia (0.5%) and enteritis (0.4%). Belgian Blue beef calves were more likely to die from pneumonia, enterotoxaemia and arthritis. Detection of bovine viral diarrhea virus at necropsy was associated with chronic pneumonia and pleuritis. Of the calves, 25.4% was treated individually and the morbidity rate was 1.66 cases per 1000 calf days at risk. The incidence rate of respiratory disease, diarrhea, arthritis and otitis was 0.95, 0.30, 0.11 and 0.07 cases per 1000 calf days at risk respectively. Morbidity peaked in the first three weeks after arrival and gradually declined towards the end of the production cycle. CONCLUSIONS: The present study provided insights into the causes and epidemiology of morbidity and mortality in white veal calves in Belgium, housed in the most frequent housing system in Europe. The necropsy findings, identified risk periods and differences between production systems can guide both veterinarians and producers towards the most profitable and ethical preventive and therapeutic protocols. BioMed Central 2012-03-14 /pmc/articles/PMC3366893/ /pubmed/22414223 http://dx.doi.org/10.1186/1746-6148-8-26 Text en Copyright ©2012 Pardon et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Pardon, Bart
De Bleecker, Koen
Hostens, Miel
Callens, Jozefien
Dewulf, Jeroen
Deprez, Piet
Longitudinal study on morbidity and mortality in white veal calves in Belgium
title Longitudinal study on morbidity and mortality in white veal calves in Belgium
title_full Longitudinal study on morbidity and mortality in white veal calves in Belgium
title_fullStr Longitudinal study on morbidity and mortality in white veal calves in Belgium
title_full_unstemmed Longitudinal study on morbidity and mortality in white veal calves in Belgium
title_short Longitudinal study on morbidity and mortality in white veal calves in Belgium
title_sort longitudinal study on morbidity and mortality in white veal calves in belgium
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3366893/
https://www.ncbi.nlm.nih.gov/pubmed/22414223
http://dx.doi.org/10.1186/1746-6148-8-26
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