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A growing animal model for neonatal repair of large diaphragmatic defects to evaluate patch function and outcome

OBJECTIVES: We aimed to develop a more representative model for neonatal congenital diaphragmatic hernia repair in a large animal model, by creating a large defect in a fast-growing pup, using functional pulmonary and diaphragmatic read outs. BACKGROUND: Grafts are increasingly used to repair congen...

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Autores principales: Eastwood, Mary Patrice, Joyeux, Luc, Pranpanus, Savitree, Van der Merwe, Johannes, Verbeken, Eric, De Vleeschauwer, Stephanie, Gayan-Ramirez, Ghislaine, Deprest, Jan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5373533/
https://www.ncbi.nlm.nih.gov/pubmed/28358826
http://dx.doi.org/10.1371/journal.pone.0174332
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author Eastwood, Mary Patrice
Joyeux, Luc
Pranpanus, Savitree
Van der Merwe, Johannes
Verbeken, Eric
De Vleeschauwer, Stephanie
Gayan-Ramirez, Ghislaine
Deprest, Jan
author_facet Eastwood, Mary Patrice
Joyeux, Luc
Pranpanus, Savitree
Van der Merwe, Johannes
Verbeken, Eric
De Vleeschauwer, Stephanie
Gayan-Ramirez, Ghislaine
Deprest, Jan
author_sort Eastwood, Mary Patrice
collection PubMed
description OBJECTIVES: We aimed to develop a more representative model for neonatal congenital diaphragmatic hernia repair in a large animal model, by creating a large defect in a fast-growing pup, using functional pulmonary and diaphragmatic read outs. BACKGROUND: Grafts are increasingly used to repair congenital diaphragmatic hernia with the risk of local complications. Growing animal models have been used to test novel materials. METHODS: 6-week-old rabbits underwent fiberoptic intubation, left subcostal laparotomy and hemi-diaphragmatic excision (either nearly complete (n = 13) or 3*3cm (n = 9)) and primary closure (Gore-Tex patch). Survival was further increased by moving to laryngeal mask airway ventilation (n = 15). Sham operated animals were used as controls (n = 6). Survivors (90 days) underwent chest X-Ray (scoliosis), measurements of maximum transdiaphragmatic pressure and breathing pattern (tidal volume, Pdi). Rates of herniation, lung histology and right hemi-diaphragmatic fiber cross-sectional area was measured. RESULTS: Rabbits surviving 90 days doubled their weight. Only one (8%) with a complete defect survived to 90 days. In the 3*3cm defect group all survived to 48 hours, however seven (78%) died later (16–49 days) from respiratory failure secondary to tracheal stricture formation. Use of a laryngeal mask airway doubled 90-day survival, one pup displaying herniation (17%). Cobb angel measurements, breathing pattern, and lung histology were comparable to sham. Under exertion, sham animals increased their maximum transdiaphragmatic pressure 134% compared to a 71% increase in patched animals (p<0.05). Patched animals had a compensatory increase in their right hemi-diaphragmatic fiber cross-sectional area (p<0.0001). CONCLUSIONS: A primarily patched 3*3cm defect in growing rabbits, under laryngeal mask airway ventilation, enables adequate survival with normal lung function and reduced maximum transdiaphragmatic pressure compared to controls.
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spelling pubmed-53735332017-04-07 A growing animal model for neonatal repair of large diaphragmatic defects to evaluate patch function and outcome Eastwood, Mary Patrice Joyeux, Luc Pranpanus, Savitree Van der Merwe, Johannes Verbeken, Eric De Vleeschauwer, Stephanie Gayan-Ramirez, Ghislaine Deprest, Jan PLoS One Research Article OBJECTIVES: We aimed to develop a more representative model for neonatal congenital diaphragmatic hernia repair in a large animal model, by creating a large defect in a fast-growing pup, using functional pulmonary and diaphragmatic read outs. BACKGROUND: Grafts are increasingly used to repair congenital diaphragmatic hernia with the risk of local complications. Growing animal models have been used to test novel materials. METHODS: 6-week-old rabbits underwent fiberoptic intubation, left subcostal laparotomy and hemi-diaphragmatic excision (either nearly complete (n = 13) or 3*3cm (n = 9)) and primary closure (Gore-Tex patch). Survival was further increased by moving to laryngeal mask airway ventilation (n = 15). Sham operated animals were used as controls (n = 6). Survivors (90 days) underwent chest X-Ray (scoliosis), measurements of maximum transdiaphragmatic pressure and breathing pattern (tidal volume, Pdi). Rates of herniation, lung histology and right hemi-diaphragmatic fiber cross-sectional area was measured. RESULTS: Rabbits surviving 90 days doubled their weight. Only one (8%) with a complete defect survived to 90 days. In the 3*3cm defect group all survived to 48 hours, however seven (78%) died later (16–49 days) from respiratory failure secondary to tracheal stricture formation. Use of a laryngeal mask airway doubled 90-day survival, one pup displaying herniation (17%). Cobb angel measurements, breathing pattern, and lung histology were comparable to sham. Under exertion, sham animals increased their maximum transdiaphragmatic pressure 134% compared to a 71% increase in patched animals (p<0.05). Patched animals had a compensatory increase in their right hemi-diaphragmatic fiber cross-sectional area (p<0.0001). CONCLUSIONS: A primarily patched 3*3cm defect in growing rabbits, under laryngeal mask airway ventilation, enables adequate survival with normal lung function and reduced maximum transdiaphragmatic pressure compared to controls. Public Library of Science 2017-03-30 /pmc/articles/PMC5373533/ /pubmed/28358826 http://dx.doi.org/10.1371/journal.pone.0174332 Text en © 2017 Eastwood et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://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
Eastwood, Mary Patrice
Joyeux, Luc
Pranpanus, Savitree
Van der Merwe, Johannes
Verbeken, Eric
De Vleeschauwer, Stephanie
Gayan-Ramirez, Ghislaine
Deprest, Jan
A growing animal model for neonatal repair of large diaphragmatic defects to evaluate patch function and outcome
title A growing animal model for neonatal repair of large diaphragmatic defects to evaluate patch function and outcome
title_full A growing animal model for neonatal repair of large diaphragmatic defects to evaluate patch function and outcome
title_fullStr A growing animal model for neonatal repair of large diaphragmatic defects to evaluate patch function and outcome
title_full_unstemmed A growing animal model for neonatal repair of large diaphragmatic defects to evaluate patch function and outcome
title_short A growing animal model for neonatal repair of large diaphragmatic defects to evaluate patch function and outcome
title_sort growing animal model for neonatal repair of large diaphragmatic defects to evaluate patch function and outcome
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5373533/
https://www.ncbi.nlm.nih.gov/pubmed/28358826
http://dx.doi.org/10.1371/journal.pone.0174332
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