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 congenit...

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Main Authors: Mary Patrice Eastwood, Luc Joyeux, Savitree Pranpanus, Johannes Van der Merwe, Eric Verbeken, Stephanie De Vleeschauwer, Ghislaine Gayan-Ramirez, Jan Deprest
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2017-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC5373533?pdf=render
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spelling doaj-8d8fc6c4f1ce44769a7d57a465b2cb512020-11-25T02:12:29ZengPublic Library of Science (PLoS)PLoS ONE1932-62032017-01-01123e017433210.1371/journal.pone.0174332A growing animal model for neonatal repair of large diaphragmatic defects to evaluate patch function and outcome.Mary Patrice EastwoodLuc JoyeuxSavitree PranpanusJohannes Van der MerweEric VerbekenStephanie De VleeschauwerGhislaine Gayan-RamirezJan DeprestOBJECTIVES: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.http://europepmc.org/articles/PMC5373533?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Mary Patrice Eastwood
Luc Joyeux
Savitree Pranpanus
Johannes Van der Merwe
Eric Verbeken
Stephanie De Vleeschauwer
Ghislaine Gayan-Ramirez
Jan Deprest
spellingShingle Mary Patrice Eastwood
Luc Joyeux
Savitree Pranpanus
Johannes Van der Merwe
Eric Verbeken
Stephanie De Vleeschauwer
Ghislaine Gayan-Ramirez
Jan Deprest
A growing animal model for neonatal repair of large diaphragmatic defects to evaluate patch function and outcome.
PLoS ONE
author_facet Mary Patrice Eastwood
Luc Joyeux
Savitree Pranpanus
Johannes Van der Merwe
Eric Verbeken
Stephanie De Vleeschauwer
Ghislaine Gayan-Ramirez
Jan Deprest
author_sort Mary Patrice Eastwood
title 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_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_sort growing animal model for neonatal repair of large diaphragmatic defects to evaluate patch function and outcome.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2017-01-01
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.
url http://europepmc.org/articles/PMC5373533?pdf=render
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