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Hemodynamic effects of perfusion level of peripheral ECMO on cardiovascular system
BACKGROUND: Peripheral ECMO is an effective cardiopulmonary support in clinical. The perfusion level could directly influence the performances and complications. However, there are few studies on the effects of the perfusion level on hemodynamics of peripheral ECMO. METHODS: The geometric model of c...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5944029/ https://www.ncbi.nlm.nih.gov/pubmed/29743080 http://dx.doi.org/10.1186/s12938-018-0493-5 |
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author | Gu, Kaiyun Zhang, Zhe Gao, Bin Chang, Yu Wan, Feng |
author_facet | Gu, Kaiyun Zhang, Zhe Gao, Bin Chang, Yu Wan, Feng |
author_sort | Gu, Kaiyun |
collection | PubMed |
description | BACKGROUND: Peripheral ECMO is an effective cardiopulmonary support in clinical. The perfusion level could directly influence the performances and complications. However, there are few studies on the effects of the perfusion level on hemodynamics of peripheral ECMO. METHODS: The geometric model of cardiovascular system with peripheral ECMO was established. The blood assist index was used to classify the perfusion level of the ECMO. The flow pattern from the aorta to the femoral artery and their branches, blood flow rate from aorta to brain and limbs, flow interface, harmonic index of blood flow, wall shear stress and oscillatory shear index were chosen to evaluate the hemodynamic effects of peripheral ECMO. RESULTS: The results demonstrated that the flow rate of aorta outlets increased and perfusion condition had been improved. And the average flow to the upper limbs and brain has a positive correlation with BAI (r = 0.037, p < 0.05), while there is a negative correlation with lower limbs (r = − 0.054, p < 0.05). The HI has negative correlation with BAI (p < 0.05, r < 0). The blood interface is further from the heart with the BAI decrease. And the average WSS has negative correlation with BAI (p < 0.05, r = − 0.983) at the bifurcation of femoral aorta and has positive correlation with BAI (p < 0.05, r = 0.99) at the inner aorta. The OSI under different BAI is higher (reaching 0.4) at the inner wall of the aortic arch, the descending aorta and the femoral access. CONCLUSIONS: The pathogenesis of peripheral ECMO with different perfusion levels varies; its further research will be thorough and extensive. |
format | Online Article Text |
id | pubmed-5944029 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-59440292018-05-14 Hemodynamic effects of perfusion level of peripheral ECMO on cardiovascular system Gu, Kaiyun Zhang, Zhe Gao, Bin Chang, Yu Wan, Feng Biomed Eng Online Research BACKGROUND: Peripheral ECMO is an effective cardiopulmonary support in clinical. The perfusion level could directly influence the performances and complications. However, there are few studies on the effects of the perfusion level on hemodynamics of peripheral ECMO. METHODS: The geometric model of cardiovascular system with peripheral ECMO was established. The blood assist index was used to classify the perfusion level of the ECMO. The flow pattern from the aorta to the femoral artery and their branches, blood flow rate from aorta to brain and limbs, flow interface, harmonic index of blood flow, wall shear stress and oscillatory shear index were chosen to evaluate the hemodynamic effects of peripheral ECMO. RESULTS: The results demonstrated that the flow rate of aorta outlets increased and perfusion condition had been improved. And the average flow to the upper limbs and brain has a positive correlation with BAI (r = 0.037, p < 0.05), while there is a negative correlation with lower limbs (r = − 0.054, p < 0.05). The HI has negative correlation with BAI (p < 0.05, r < 0). The blood interface is further from the heart with the BAI decrease. And the average WSS has negative correlation with BAI (p < 0.05, r = − 0.983) at the bifurcation of femoral aorta and has positive correlation with BAI (p < 0.05, r = 0.99) at the inner aorta. The OSI under different BAI is higher (reaching 0.4) at the inner wall of the aortic arch, the descending aorta and the femoral access. CONCLUSIONS: The pathogenesis of peripheral ECMO with different perfusion levels varies; its further research will be thorough and extensive. BioMed Central 2018-05-09 /pmc/articles/PMC5944029/ /pubmed/29743080 http://dx.doi.org/10.1186/s12938-018-0493-5 Text en © The Author(s) 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Gu, Kaiyun Zhang, Zhe Gao, Bin Chang, Yu Wan, Feng Hemodynamic effects of perfusion level of peripheral ECMO on cardiovascular system |
title | Hemodynamic effects of perfusion level of peripheral ECMO on cardiovascular system |
title_full | Hemodynamic effects of perfusion level of peripheral ECMO on cardiovascular system |
title_fullStr | Hemodynamic effects of perfusion level of peripheral ECMO on cardiovascular system |
title_full_unstemmed | Hemodynamic effects of perfusion level of peripheral ECMO on cardiovascular system |
title_short | Hemodynamic effects of perfusion level of peripheral ECMO on cardiovascular system |
title_sort | hemodynamic effects of perfusion level of peripheral ecmo on cardiovascular system |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5944029/ https://www.ncbi.nlm.nih.gov/pubmed/29743080 http://dx.doi.org/10.1186/s12938-018-0493-5 |
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