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Comparative effects of nonsteroidal anti-inflammatory drugs at castration and tail-docking in neonatal piglets

This study assessed the efficacy of meloxicam, flunixin, and ketoprofen in piglets undergoing routine castration and tail-docking. Six-day-old male piglets (8/group) received one of five randomized treatments: intramuscular saline (SAL PROC), meloxicam (MEL; 0.4 mg/kg), flunixin (FLU; 2.2 mg/kg), ke...

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Detalles Bibliográficos
Autores principales: Nixon, Emma, Carlson, Alexandra R., Routh, Patricia A., Hernandez, Liliana, Almond, Glen W., Baynes, Ronald E., Messenger, Kristen M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8631668/
https://www.ncbi.nlm.nih.gov/pubmed/34847143
http://dx.doi.org/10.1371/journal.pone.0254409
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author Nixon, Emma
Carlson, Alexandra R.
Routh, Patricia A.
Hernandez, Liliana
Almond, Glen W.
Baynes, Ronald E.
Messenger, Kristen M.
author_facet Nixon, Emma
Carlson, Alexandra R.
Routh, Patricia A.
Hernandez, Liliana
Almond, Glen W.
Baynes, Ronald E.
Messenger, Kristen M.
author_sort Nixon, Emma
collection PubMed
description This study assessed the efficacy of meloxicam, flunixin, and ketoprofen in piglets undergoing routine castration and tail-docking. Six-day-old male piglets (8/group) received one of five randomized treatments: intramuscular saline (SAL PROC), meloxicam (MEL; 0.4 mg/kg), flunixin (FLU; 2.2 mg/kg), ketoprofen (KETO; 3.0 mg/kg) or sham (SAL SHAM; saline injection, no processing). Two hours post-dose, piglets were castrated and tail-docked. Plasma cortisol, interstitial fluid (ISF) prostaglandin E2 (PGE2) and activity levels via Actical® monitoring were used to estimate pain. SAL SHAM and FLU exhibited lower cortisol concentrations than SAL PROC at the time of processing (p = 0.003 and p = 0.049, respectively), and all NSAIDs exhibited lower PGE2 than SAL PROC at 3.69 hours (MEL p = 0.050; FLU p = 0.043 and KETO p = 0.031). While not statistically significant, PGE2 was higher in SAL PROC piglets vs. other treatment groups at most time points. There was also a high degree of variability between piglets, especially for SAL PROC. Activity levels were significantly decreased at multiple time points in SAL PROC and MEL piglets following processing. However, FLU and KETO piglets had increased activity levels closer to that of the SAL SHAM group, suggesting that these NSAIDs are more effective than MEL in providing analgesia. These results demonstrate that management strategies including administration of intramuscular flunixin or ketoprofen to reduce pain associated with processing will likely improve piglet health and welfare in the United States.
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spelling pubmed-86316682021-12-01 Comparative effects of nonsteroidal anti-inflammatory drugs at castration and tail-docking in neonatal piglets Nixon, Emma Carlson, Alexandra R. Routh, Patricia A. Hernandez, Liliana Almond, Glen W. Baynes, Ronald E. Messenger, Kristen M. PLoS One Research Article This study assessed the efficacy of meloxicam, flunixin, and ketoprofen in piglets undergoing routine castration and tail-docking. Six-day-old male piglets (8/group) received one of five randomized treatments: intramuscular saline (SAL PROC), meloxicam (MEL; 0.4 mg/kg), flunixin (FLU; 2.2 mg/kg), ketoprofen (KETO; 3.0 mg/kg) or sham (SAL SHAM; saline injection, no processing). Two hours post-dose, piglets were castrated and tail-docked. Plasma cortisol, interstitial fluid (ISF) prostaglandin E2 (PGE2) and activity levels via Actical® monitoring were used to estimate pain. SAL SHAM and FLU exhibited lower cortisol concentrations than SAL PROC at the time of processing (p = 0.003 and p = 0.049, respectively), and all NSAIDs exhibited lower PGE2 than SAL PROC at 3.69 hours (MEL p = 0.050; FLU p = 0.043 and KETO p = 0.031). While not statistically significant, PGE2 was higher in SAL PROC piglets vs. other treatment groups at most time points. There was also a high degree of variability between piglets, especially for SAL PROC. Activity levels were significantly decreased at multiple time points in SAL PROC and MEL piglets following processing. However, FLU and KETO piglets had increased activity levels closer to that of the SAL SHAM group, suggesting that these NSAIDs are more effective than MEL in providing analgesia. These results demonstrate that management strategies including administration of intramuscular flunixin or ketoprofen to reduce pain associated with processing will likely improve piglet health and welfare in the United States. Public Library of Science 2021-11-30 /pmc/articles/PMC8631668/ /pubmed/34847143 http://dx.doi.org/10.1371/journal.pone.0254409 Text en © 2021 Nixon et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Nixon, Emma
Carlson, Alexandra R.
Routh, Patricia A.
Hernandez, Liliana
Almond, Glen W.
Baynes, Ronald E.
Messenger, Kristen M.
Comparative effects of nonsteroidal anti-inflammatory drugs at castration and tail-docking in neonatal piglets
title Comparative effects of nonsteroidal anti-inflammatory drugs at castration and tail-docking in neonatal piglets
title_full Comparative effects of nonsteroidal anti-inflammatory drugs at castration and tail-docking in neonatal piglets
title_fullStr Comparative effects of nonsteroidal anti-inflammatory drugs at castration and tail-docking in neonatal piglets
title_full_unstemmed Comparative effects of nonsteroidal anti-inflammatory drugs at castration and tail-docking in neonatal piglets
title_short Comparative effects of nonsteroidal anti-inflammatory drugs at castration and tail-docking in neonatal piglets
title_sort comparative effects of nonsteroidal anti-inflammatory drugs at castration and tail-docking in neonatal piglets
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8631668/
https://www.ncbi.nlm.nih.gov/pubmed/34847143
http://dx.doi.org/10.1371/journal.pone.0254409
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