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Effects of drying and providing supplemental oxygen to piglets at birth on rectal temperature over the first 24 h after birth()

Neonatal piglets can experience both a decrease in body temperature and hypoxia, increasing risks for pre-weaning mortality. This research evaluated the effects of drying and providing supplemental oxygen to newborn piglets on rectal temperature (RT) over the first 24 h after birth. The study used a...

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Autores principales: Vande Pol, Katherine D, Tolosa, Andres F, Bautista, Raphael O, Willard, Naomi C, Gates, Richard S, Shull, Caleb M, Brown, Catherine B, Alencar, Stephan A S, Lents, Clay A, Ellis, Michael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8280916/
https://www.ncbi.nlm.nih.gov/pubmed/34278236
http://dx.doi.org/10.1093/tas/txab095
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author Vande Pol, Katherine D
Tolosa, Andres F
Bautista, Raphael O
Willard, Naomi C
Gates, Richard S
Shull, Caleb M
Brown, Catherine B
Alencar, Stephan A S
Lents, Clay A
Ellis, Michael
author_facet Vande Pol, Katherine D
Tolosa, Andres F
Bautista, Raphael O
Willard, Naomi C
Gates, Richard S
Shull, Caleb M
Brown, Catherine B
Alencar, Stephan A S
Lents, Clay A
Ellis, Michael
author_sort Vande Pol, Katherine D
collection PubMed
description Neonatal piglets can experience both a decrease in body temperature and hypoxia, increasing risks for pre-weaning mortality. This research evaluated the effects of drying and providing supplemental oxygen to newborn piglets on rectal temperature (RT) over the first 24 h after birth. The study used a CRD with three Intervention Treatments (IT; applied at birth): Control (no intervention), Drying (dried using a desiccant), Oxygen [dried using a desiccant and placed in a chamber (at 40% oxygen concentration) for 20 min]. A total of 42 litters (485 piglets) were randomly allotted to treatments at the start of farrowing. At birth, each piglet was given a numbered ear tag, weighed, and the treatment was applied; RT was measured at 0, 20, 30, 45, 60, 120, and 1440 min after birth. Blood was collected from one piglet from each birth weight quartile within each litter at 24 h after birth to measure plasma immunocrit concentration. There was no effect (P > 0.05) of IT on piglet RT at 0 or 1440 min after birth. Between 20 and 60 min after birth, piglet RT was lower (P ≤ 0.05) for the Control than the Drying treatment, with the Oxygen treatment being intermediate and different (P ≤ 0.05) from the other two IT. The effect of piglet birth weight on responses to IT were evaluated by classifying piglets into Birth Weight Categories (BWC): Light (<1.0 kg), Medium (1.0 to 1.5 kg), or Heavy (>1.5 kg). There were IT by BWC interactions (P ≤ 0.05) for piglet RT at all measurement times between 20 and 120 min after birth. Relative to the Control, the effects of the Drying and Oxygen treatments on RT were greater (P ≤ 0.05) for Light than heavier piglets. Plasma immunocrit concentrations tended (P = 0.07) to be greater for piglets on the Control treatment compared to the other two IT and were lower (P ≤ 0.05) for Light than Heavy piglets, with Medium piglets being intermediate and different (P ≤ 0.05) to the other BWC. In conclusion, drying piglets at birth reduced the extent and duration of RT decline in piglets in the early postnatal period compared to undried piglets, especially for those of low birth weight. However, the combination of drying and placing piglets in an oxygen-rich environment provided no additional benefit over drying alone.
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spelling pubmed-82809162021-07-16 Effects of drying and providing supplemental oxygen to piglets at birth on rectal temperature over the first 24 h after birth() Vande Pol, Katherine D Tolosa, Andres F Bautista, Raphael O Willard, Naomi C Gates, Richard S Shull, Caleb M Brown, Catherine B Alencar, Stephan A S Lents, Clay A Ellis, Michael Transl Anim Sci Housing and Management Neonatal piglets can experience both a decrease in body temperature and hypoxia, increasing risks for pre-weaning mortality. This research evaluated the effects of drying and providing supplemental oxygen to newborn piglets on rectal temperature (RT) over the first 24 h after birth. The study used a CRD with three Intervention Treatments (IT; applied at birth): Control (no intervention), Drying (dried using a desiccant), Oxygen [dried using a desiccant and placed in a chamber (at 40% oxygen concentration) for 20 min]. A total of 42 litters (485 piglets) were randomly allotted to treatments at the start of farrowing. At birth, each piglet was given a numbered ear tag, weighed, and the treatment was applied; RT was measured at 0, 20, 30, 45, 60, 120, and 1440 min after birth. Blood was collected from one piglet from each birth weight quartile within each litter at 24 h after birth to measure plasma immunocrit concentration. There was no effect (P > 0.05) of IT on piglet RT at 0 or 1440 min after birth. Between 20 and 60 min after birth, piglet RT was lower (P ≤ 0.05) for the Control than the Drying treatment, with the Oxygen treatment being intermediate and different (P ≤ 0.05) from the other two IT. The effect of piglet birth weight on responses to IT were evaluated by classifying piglets into Birth Weight Categories (BWC): Light (<1.0 kg), Medium (1.0 to 1.5 kg), or Heavy (>1.5 kg). There were IT by BWC interactions (P ≤ 0.05) for piglet RT at all measurement times between 20 and 120 min after birth. Relative to the Control, the effects of the Drying and Oxygen treatments on RT were greater (P ≤ 0.05) for Light than heavier piglets. Plasma immunocrit concentrations tended (P = 0.07) to be greater for piglets on the Control treatment compared to the other two IT and were lower (P ≤ 0.05) for Light than Heavy piglets, with Medium piglets being intermediate and different (P ≤ 0.05) to the other BWC. In conclusion, drying piglets at birth reduced the extent and duration of RT decline in piglets in the early postnatal period compared to undried piglets, especially for those of low birth weight. However, the combination of drying and placing piglets in an oxygen-rich environment provided no additional benefit over drying alone. Oxford University Press 2021-05-31 /pmc/articles/PMC8280916/ /pubmed/34278236 http://dx.doi.org/10.1093/tas/txab095 Text en © The Author(s) 2021. Published by Oxford University Press on behalf of the American Society of Animal Science. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) ), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Housing and Management
Vande Pol, Katherine D
Tolosa, Andres F
Bautista, Raphael O
Willard, Naomi C
Gates, Richard S
Shull, Caleb M
Brown, Catherine B
Alencar, Stephan A S
Lents, Clay A
Ellis, Michael
Effects of drying and providing supplemental oxygen to piglets at birth on rectal temperature over the first 24 h after birth()
title Effects of drying and providing supplemental oxygen to piglets at birth on rectal temperature over the first 24 h after birth()
title_full Effects of drying and providing supplemental oxygen to piglets at birth on rectal temperature over the first 24 h after birth()
title_fullStr Effects of drying and providing supplemental oxygen to piglets at birth on rectal temperature over the first 24 h after birth()
title_full_unstemmed Effects of drying and providing supplemental oxygen to piglets at birth on rectal temperature over the first 24 h after birth()
title_short Effects of drying and providing supplemental oxygen to piglets at birth on rectal temperature over the first 24 h after birth()
title_sort effects of drying and providing supplemental oxygen to piglets at birth on rectal temperature over the first 24 h after birth()
topic Housing and Management
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8280916/
https://www.ncbi.nlm.nih.gov/pubmed/34278236
http://dx.doi.org/10.1093/tas/txab095
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