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In vivo biomechanical responses of neonatal brachial plexus when subjected to stretch

Neonatal brachial plexus palsy (NBPP) results from over-stretching of the neonatal brachial plexus during complicated birthing scenarios. The lack of information on the biomechanical response of the neonatal brachial plexus complex when subjected to stretch limits our understanding of the NBPP injur...

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Autores principales: Singh, Anita, Orozco, Virginia, Balasubramanian, Sriram
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10468090/
https://www.ncbi.nlm.nih.gov/pubmed/37647327
http://dx.doi.org/10.1371/journal.pone.0290718
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author Singh, Anita
Orozco, Virginia
Balasubramanian, Sriram
author_facet Singh, Anita
Orozco, Virginia
Balasubramanian, Sriram
author_sort Singh, Anita
collection PubMed
description Neonatal brachial plexus palsy (NBPP) results from over-stretching of the neonatal brachial plexus during complicated birthing scenarios. The lack of information on the biomechanical response of the neonatal brachial plexus complex when subjected to stretch limits our understanding of the NBPP injury mechanism. This study aims to fill that critical gap by using a neonatal piglet animal model and providing the in vivo biomechanical properties of the neonatal brachial plexus complex when subjected to stretch. Forty-seven brachial plexus levels (identified by the four brachial plexus terminal nerve branches namely musculocutaneous, median, ulnar, and radial), obtained from 16 neonatal Yorkshire piglets (3–5 days old), were subjected to stretch-induced failure. The average maximum load and corresponding strain were reported to be 16.6 ± 1.3 N and 36.1 ± 1.6%, respectively. Maximum loads reported at the musculocutaneous level were significantly lower than the median and radial levels. No differences in strains at failure were reported at all four tested levels. Proximal or distal failure locations were reported in 83% of the tests with 17% mid-length ruptures that were primarily reported at the bifurcation of the median and ulnar brachial plexus levels. Histological studies reported an overall loss of wavy pattern of the nerve fibers, an increase in nerve spacing, fiber disruptions, and blood vessel ruptures in the stretched tissue. This in vivo piglet animal study offers insight into the NBPP mechanism by reporting biomechanical, injury location, and structural damage responses in neonatal brachial plexus when subjected to stretch.
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spelling pubmed-104680902023-08-31 In vivo biomechanical responses of neonatal brachial plexus when subjected to stretch Singh, Anita Orozco, Virginia Balasubramanian, Sriram PLoS One Research Article Neonatal brachial plexus palsy (NBPP) results from over-stretching of the neonatal brachial plexus during complicated birthing scenarios. The lack of information on the biomechanical response of the neonatal brachial plexus complex when subjected to stretch limits our understanding of the NBPP injury mechanism. This study aims to fill that critical gap by using a neonatal piglet animal model and providing the in vivo biomechanical properties of the neonatal brachial plexus complex when subjected to stretch. Forty-seven brachial plexus levels (identified by the four brachial plexus terminal nerve branches namely musculocutaneous, median, ulnar, and radial), obtained from 16 neonatal Yorkshire piglets (3–5 days old), were subjected to stretch-induced failure. The average maximum load and corresponding strain were reported to be 16.6 ± 1.3 N and 36.1 ± 1.6%, respectively. Maximum loads reported at the musculocutaneous level were significantly lower than the median and radial levels. No differences in strains at failure were reported at all four tested levels. Proximal or distal failure locations were reported in 83% of the tests with 17% mid-length ruptures that were primarily reported at the bifurcation of the median and ulnar brachial plexus levels. Histological studies reported an overall loss of wavy pattern of the nerve fibers, an increase in nerve spacing, fiber disruptions, and blood vessel ruptures in the stretched tissue. This in vivo piglet animal study offers insight into the NBPP mechanism by reporting biomechanical, injury location, and structural damage responses in neonatal brachial plexus when subjected to stretch. Public Library of Science 2023-08-30 /pmc/articles/PMC10468090/ /pubmed/37647327 http://dx.doi.org/10.1371/journal.pone.0290718 Text en © 2023 Singh 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
Singh, Anita
Orozco, Virginia
Balasubramanian, Sriram
In vivo biomechanical responses of neonatal brachial plexus when subjected to stretch
title In vivo biomechanical responses of neonatal brachial plexus when subjected to stretch
title_full In vivo biomechanical responses of neonatal brachial plexus when subjected to stretch
title_fullStr In vivo biomechanical responses of neonatal brachial plexus when subjected to stretch
title_full_unstemmed In vivo biomechanical responses of neonatal brachial plexus when subjected to stretch
title_short In vivo biomechanical responses of neonatal brachial plexus when subjected to stretch
title_sort in vivo biomechanical responses of neonatal brachial plexus when subjected to stretch
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10468090/
https://www.ncbi.nlm.nih.gov/pubmed/37647327
http://dx.doi.org/10.1371/journal.pone.0290718
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