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Establishing a pre-clinical growing animal model to test a tissue engineered valved pulmonary conduit

BACKGROUND: Many valvular pathologies of the heart may be only sufficiently treated by replacement of the valve if a reconstruction is not feasible. However, structural deterioration, thrombosis with thromboembolic events and infective endocarditis are commonly encountered complications over time an...

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Autores principales: Knirsch, Walter, Krüger, Bernard, Fleischmann, Thea, Malbon, Alexandra, Lipiski, Miriam, Lemme, Frithjof, Sauer, Mareike, Cesarovic, Niko, Dave, Hitendu, Hübler, Michael, Schweiger, Martin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: AME Publishing Company 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7138975/
https://www.ncbi.nlm.nih.gov/pubmed/32274175
http://dx.doi.org/10.21037/jtd.2019.12.70
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author Knirsch, Walter
Krüger, Bernard
Fleischmann, Thea
Malbon, Alexandra
Lipiski, Miriam
Lemme, Frithjof
Sauer, Mareike
Cesarovic, Niko
Dave, Hitendu
Hübler, Michael
Schweiger, Martin
author_facet Knirsch, Walter
Krüger, Bernard
Fleischmann, Thea
Malbon, Alexandra
Lipiski, Miriam
Lemme, Frithjof
Sauer, Mareike
Cesarovic, Niko
Dave, Hitendu
Hübler, Michael
Schweiger, Martin
author_sort Knirsch, Walter
collection PubMed
description BACKGROUND: Many valvular pathologies of the heart may be only sufficiently treated by replacement of the valve if a reconstruction is not feasible. However, structural deterioration, thrombosis with thromboembolic events and infective endocarditis are commonly encountered complications over time and often demand a re-operation. In congenital heart disease the lack of small diameter valves with the potential to grow poses additional challenges and limits treatment options to homo- or xenograft implants. METHODS: In this study, a chronic sheep model (24 months follow-up), a self-constructed valved conduit was created out of a tissue engineered (TE) patch (CorMatrix® Cardiovascular, Inc, USA) and implanted in orthotopic right ventricular (RV)-pulmonary artery (PA) position. Thereafter, the sheep were regularly monitored by clinical, laboratory and echocardiographic examinations to evaluate cardiac function and the implanted RV-PA-conduit. DISCUSSION: Here, we summarize the study protocol and our experiences during the perioperative phase and the follow up period and explain how we constructed a valved conduit out of a commercially available TE patch. TRIAL REGISTRATION: License number: ZH 284/14.
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spelling pubmed-71389752020-04-09 Establishing a pre-clinical growing animal model to test a tissue engineered valved pulmonary conduit Knirsch, Walter Krüger, Bernard Fleischmann, Thea Malbon, Alexandra Lipiski, Miriam Lemme, Frithjof Sauer, Mareike Cesarovic, Niko Dave, Hitendu Hübler, Michael Schweiger, Martin J Thorac Dis Study Protocal BACKGROUND: Many valvular pathologies of the heart may be only sufficiently treated by replacement of the valve if a reconstruction is not feasible. However, structural deterioration, thrombosis with thromboembolic events and infective endocarditis are commonly encountered complications over time and often demand a re-operation. In congenital heart disease the lack of small diameter valves with the potential to grow poses additional challenges and limits treatment options to homo- or xenograft implants. METHODS: In this study, a chronic sheep model (24 months follow-up), a self-constructed valved conduit was created out of a tissue engineered (TE) patch (CorMatrix® Cardiovascular, Inc, USA) and implanted in orthotopic right ventricular (RV)-pulmonary artery (PA) position. Thereafter, the sheep were regularly monitored by clinical, laboratory and echocardiographic examinations to evaluate cardiac function and the implanted RV-PA-conduit. DISCUSSION: Here, we summarize the study protocol and our experiences during the perioperative phase and the follow up period and explain how we constructed a valved conduit out of a commercially available TE patch. TRIAL REGISTRATION: License number: ZH 284/14. AME Publishing Company 2020-03 /pmc/articles/PMC7138975/ /pubmed/32274175 http://dx.doi.org/10.21037/jtd.2019.12.70 Text en 2020 Journal of Thoracic Disease. All rights reserved. https://creativecommons.org/licenses/by-nc-nd/4.0/Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) .
spellingShingle Study Protocal
Knirsch, Walter
Krüger, Bernard
Fleischmann, Thea
Malbon, Alexandra
Lipiski, Miriam
Lemme, Frithjof
Sauer, Mareike
Cesarovic, Niko
Dave, Hitendu
Hübler, Michael
Schweiger, Martin
Establishing a pre-clinical growing animal model to test a tissue engineered valved pulmonary conduit
title Establishing a pre-clinical growing animal model to test a tissue engineered valved pulmonary conduit
title_full Establishing a pre-clinical growing animal model to test a tissue engineered valved pulmonary conduit
title_fullStr Establishing a pre-clinical growing animal model to test a tissue engineered valved pulmonary conduit
title_full_unstemmed Establishing a pre-clinical growing animal model to test a tissue engineered valved pulmonary conduit
title_short Establishing a pre-clinical growing animal model to test a tissue engineered valved pulmonary conduit
title_sort establishing a pre-clinical growing animal model to test a tissue engineered valved pulmonary conduit
topic Study Protocal
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7138975/
https://www.ncbi.nlm.nih.gov/pubmed/32274175
http://dx.doi.org/10.21037/jtd.2019.12.70
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