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Fluid–structure interaction simulation of visceral perfusion and impact of different cannulation methods on aortic dissection

Hemodynamics in aortic dissection (AD) is closely associated with the risk of aortic aneurysm, rupture, and malperfusion. Altered blood flow in patients with AD can lead to severe complications such as visceral malperfusion. In this study, we aimed to investigate the effect of cannulation flow on he...

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Autores principales: Lee, Gyu-Han, Heo, Woon, Lee, Youngjin, Kim, Tae-Hoon, Huh, Hyungkyu, Song, Suk-Won, Ha, Hojin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9860063/
https://www.ncbi.nlm.nih.gov/pubmed/36670162
http://dx.doi.org/10.1038/s41598-023-27855-2
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author Lee, Gyu-Han
Heo, Woon
Lee, Youngjin
Kim, Tae-Hoon
Huh, Hyungkyu
Song, Suk-Won
Ha, Hojin
author_facet Lee, Gyu-Han
Heo, Woon
Lee, Youngjin
Kim, Tae-Hoon
Huh, Hyungkyu
Song, Suk-Won
Ha, Hojin
author_sort Lee, Gyu-Han
collection PubMed
description Hemodynamics in aortic dissection (AD) is closely associated with the risk of aortic aneurysm, rupture, and malperfusion. Altered blood flow in patients with AD can lead to severe complications such as visceral malperfusion. In this study, we aimed to investigate the effect of cannulation flow on hemodynamics in AD using a fluid–structure interaction simulation. We developed a specific-idealized AD model that included an intimal tear in the descending thoracic aorta, a re-entry tear in the left iliac artery, and nine branches. Two different cannulation methods were tested: (1) axillary cannulation (AC) only through the brachiocephalic trunk and (2) combined axillary and femoral cannulation (AFC) through the brachiocephalic trunk and the right common iliac artery. AC was found to result in the development of a pressure difference between the true lumen and false lumen, owing to the difference in the flow rate through each lumen. This pressure difference collapsed the true lumen, disturbing blood flow to the celiac and superior mesenteric arteries. However, in AFC, the pressure levels between the two lumens were similar, and no collapse occurred. Moreover, the visceral flow was higher than that in AC. Lastly, the stiffness of the intimal flap affected the true lumen's collapse.
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spelling pubmed-98600632023-01-22 Fluid–structure interaction simulation of visceral perfusion and impact of different cannulation methods on aortic dissection Lee, Gyu-Han Heo, Woon Lee, Youngjin Kim, Tae-Hoon Huh, Hyungkyu Song, Suk-Won Ha, Hojin Sci Rep Article Hemodynamics in aortic dissection (AD) is closely associated with the risk of aortic aneurysm, rupture, and malperfusion. Altered blood flow in patients with AD can lead to severe complications such as visceral malperfusion. In this study, we aimed to investigate the effect of cannulation flow on hemodynamics in AD using a fluid–structure interaction simulation. We developed a specific-idealized AD model that included an intimal tear in the descending thoracic aorta, a re-entry tear in the left iliac artery, and nine branches. Two different cannulation methods were tested: (1) axillary cannulation (AC) only through the brachiocephalic trunk and (2) combined axillary and femoral cannulation (AFC) through the brachiocephalic trunk and the right common iliac artery. AC was found to result in the development of a pressure difference between the true lumen and false lumen, owing to the difference in the flow rate through each lumen. This pressure difference collapsed the true lumen, disturbing blood flow to the celiac and superior mesenteric arteries. However, in AFC, the pressure levels between the two lumens were similar, and no collapse occurred. Moreover, the visceral flow was higher than that in AC. Lastly, the stiffness of the intimal flap affected the true lumen's collapse. Nature Publishing Group UK 2023-01-20 /pmc/articles/PMC9860063/ /pubmed/36670162 http://dx.doi.org/10.1038/s41598-023-27855-2 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Lee, Gyu-Han
Heo, Woon
Lee, Youngjin
Kim, Tae-Hoon
Huh, Hyungkyu
Song, Suk-Won
Ha, Hojin
Fluid–structure interaction simulation of visceral perfusion and impact of different cannulation methods on aortic dissection
title Fluid–structure interaction simulation of visceral perfusion and impact of different cannulation methods on aortic dissection
title_full Fluid–structure interaction simulation of visceral perfusion and impact of different cannulation methods on aortic dissection
title_fullStr Fluid–structure interaction simulation of visceral perfusion and impact of different cannulation methods on aortic dissection
title_full_unstemmed Fluid–structure interaction simulation of visceral perfusion and impact of different cannulation methods on aortic dissection
title_short Fluid–structure interaction simulation of visceral perfusion and impact of different cannulation methods on aortic dissection
title_sort fluid–structure interaction simulation of visceral perfusion and impact of different cannulation methods on aortic dissection
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9860063/
https://www.ncbi.nlm.nih.gov/pubmed/36670162
http://dx.doi.org/10.1038/s41598-023-27855-2
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