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Morbidity and Mortality of Heterotopic Partial Heart Transplantation in Rodent Models

Unrepairable congenital heart valve disease is an unsolved problem in pediatric cardiac surgery because there are no growing heart valve implants. Partial heart transplantation is a new type of transplant that aims to solve this problem. In order to study the unique transplant biology of partial hea...

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Autores principales: Skidmore, Savannah, Hill, Morgan A., Bishara, Katherine, Konsek, Haley, Kwon, Jennie H., Brockbank, Kelvin G. M., Rajab, Taufiek Konrad
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10299259/
https://www.ncbi.nlm.nih.gov/pubmed/37367399
http://dx.doi.org/10.3390/jcdd10060234
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author Skidmore, Savannah
Hill, Morgan A.
Bishara, Katherine
Konsek, Haley
Kwon, Jennie H.
Brockbank, Kelvin G. M.
Rajab, Taufiek Konrad
author_facet Skidmore, Savannah
Hill, Morgan A.
Bishara, Katherine
Konsek, Haley
Kwon, Jennie H.
Brockbank, Kelvin G. M.
Rajab, Taufiek Konrad
author_sort Skidmore, Savannah
collection PubMed
description Unrepairable congenital heart valve disease is an unsolved problem in pediatric cardiac surgery because there are no growing heart valve implants. Partial heart transplantation is a new type of transplant that aims to solve this problem. In order to study the unique transplant biology of partial heart transplantation, animal models are necessary. This study aimed to assess the morbidity and mortality of heterotopic partial heart transplantation in rodent models. This study assessed two models. The first model involved transplanting heart valves from donor animals into the abdominal aortic position in the recipient animals. The second model involved transplanting heart valve leaflets into the renal subcapsular position of the recipient animals. A total of 33 animals underwent heterotopic partial heart transplantation in the abdominal aortic position. The results of this model found a 60.61% (n = 20/33) intraoperative mortality rate and a 39.39% (n = 13/33) perioperative mortality rate. Intraoperative mortality was due to vascular complications from the procedure, and perioperative mortality was due to graft thrombosis. A total of 33 animals underwent heterotopic partial heart transplantation in the renal subcapsular position. The results of this model found a 3.03% (n = 1/33) intraoperative mortality rate, and the remaining 96.97% survived (n = 32/33). We conclude that the renal subcapsular model has a lower mortality rate and is technically more accessible than the abdominal aortic model. While the heterotopic transplantation of valves into the abdominal aortic position had significant morbidity and mortality in the rodent model, the renal subcapsular model provided evidence for successful heterotopic transplantation.
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spelling pubmed-102992592023-06-28 Morbidity and Mortality of Heterotopic Partial Heart Transplantation in Rodent Models Skidmore, Savannah Hill, Morgan A. Bishara, Katherine Konsek, Haley Kwon, Jennie H. Brockbank, Kelvin G. M. Rajab, Taufiek Konrad J Cardiovasc Dev Dis Article Unrepairable congenital heart valve disease is an unsolved problem in pediatric cardiac surgery because there are no growing heart valve implants. Partial heart transplantation is a new type of transplant that aims to solve this problem. In order to study the unique transplant biology of partial heart transplantation, animal models are necessary. This study aimed to assess the morbidity and mortality of heterotopic partial heart transplantation in rodent models. This study assessed two models. The first model involved transplanting heart valves from donor animals into the abdominal aortic position in the recipient animals. The second model involved transplanting heart valve leaflets into the renal subcapsular position of the recipient animals. A total of 33 animals underwent heterotopic partial heart transplantation in the abdominal aortic position. The results of this model found a 60.61% (n = 20/33) intraoperative mortality rate and a 39.39% (n = 13/33) perioperative mortality rate. Intraoperative mortality was due to vascular complications from the procedure, and perioperative mortality was due to graft thrombosis. A total of 33 animals underwent heterotopic partial heart transplantation in the renal subcapsular position. The results of this model found a 3.03% (n = 1/33) intraoperative mortality rate, and the remaining 96.97% survived (n = 32/33). We conclude that the renal subcapsular model has a lower mortality rate and is technically more accessible than the abdominal aortic model. While the heterotopic transplantation of valves into the abdominal aortic position had significant morbidity and mortality in the rodent model, the renal subcapsular model provided evidence for successful heterotopic transplantation. MDPI 2023-05-26 /pmc/articles/PMC10299259/ /pubmed/37367399 http://dx.doi.org/10.3390/jcdd10060234 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Skidmore, Savannah
Hill, Morgan A.
Bishara, Katherine
Konsek, Haley
Kwon, Jennie H.
Brockbank, Kelvin G. M.
Rajab, Taufiek Konrad
Morbidity and Mortality of Heterotopic Partial Heart Transplantation in Rodent Models
title Morbidity and Mortality of Heterotopic Partial Heart Transplantation in Rodent Models
title_full Morbidity and Mortality of Heterotopic Partial Heart Transplantation in Rodent Models
title_fullStr Morbidity and Mortality of Heterotopic Partial Heart Transplantation in Rodent Models
title_full_unstemmed Morbidity and Mortality of Heterotopic Partial Heart Transplantation in Rodent Models
title_short Morbidity and Mortality of Heterotopic Partial Heart Transplantation in Rodent Models
title_sort morbidity and mortality of heterotopic partial heart transplantation in rodent models
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10299259/
https://www.ncbi.nlm.nih.gov/pubmed/37367399
http://dx.doi.org/10.3390/jcdd10060234
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