TY - JOUR
T1 - Effects of cardiac function alterations on the risk of postoperative thrombotic complications in patients receiving endovascular aortic repair
AU - Sun, Xiaoning
AU - Li, Siting
AU - He, Yuan
AU - Liu, Yuxi
AU - Ma, Tianxiang
AU - Zeng, Rong
AU - Liu, Zhili
AU - Chen, Yu
AU - Zheng, Yuehong
AU - Liu, Xiao
N1 - Publisher Copyright:
Copyright © 2023 Sun, Li, He, Liu, Ma, Zeng, Liu, Chen, Zheng and Liu.
PY - 2023/1/10
Y1 - 2023/1/10
N2 - Introduction: Chronic heart disease (CHD) is a common comorbidity of patients receiving endovascular aneurysm repair (EVAR) for abdominal aortic aneurysms (AAA). The explicit relationship between ventricular systolic function and EVAR complication of thrombotic events is unknown. Methods: In this study, we proposed a three-dimensional numerical model coupled with the lumped-elements heart model, which is capable of simulating thrombus formation in diverse systolic functions. The relation of cardiac functions and the predicted risk of thrombus formation in the aorta and/or endograft of 4 patients who underwent EVAR was investigated. Relative risks for thrombus formation were identified using machine-learning algorithms. Results: The computational results demonstrate that thrombus tended to form on the interior side of the aorta arch and iliac branches, and cardiac function can affect blood flow field and affect thrombus formation, which is consistent with the four patients' post-operative imaging follow-up. We also found that RRT, OSI, TAWSS in thrombosis area are lower than whole average. In addition, we found that the thrombus formation has negative correlations with the maximum ventricular contractile force (r = −.281 ±.101) and positive correlations with the minimum ventricular contractile force (r =.238 ±.074), whereas the effect of heart rate (r = −.015 ±.121) on thrombus formation is not significant. Conclusion: In conclusion, changes in ventricular systolic function may alter the risk of thrombotic events after EVAR repair, which could provide insight into the selection of adjuvant therapy strategies for AAA patients with CHD.
AB - Introduction: Chronic heart disease (CHD) is a common comorbidity of patients receiving endovascular aneurysm repair (EVAR) for abdominal aortic aneurysms (AAA). The explicit relationship between ventricular systolic function and EVAR complication of thrombotic events is unknown. Methods: In this study, we proposed a three-dimensional numerical model coupled with the lumped-elements heart model, which is capable of simulating thrombus formation in diverse systolic functions. The relation of cardiac functions and the predicted risk of thrombus formation in the aorta and/or endograft of 4 patients who underwent EVAR was investigated. Relative risks for thrombus formation were identified using machine-learning algorithms. Results: The computational results demonstrate that thrombus tended to form on the interior side of the aorta arch and iliac branches, and cardiac function can affect blood flow field and affect thrombus formation, which is consistent with the four patients' post-operative imaging follow-up. We also found that RRT, OSI, TAWSS in thrombosis area are lower than whole average. In addition, we found that the thrombus formation has negative correlations with the maximum ventricular contractile force (r = −.281 ±.101) and positive correlations with the minimum ventricular contractile force (r =.238 ±.074), whereas the effect of heart rate (r = −.015 ±.121) on thrombus formation is not significant. Conclusion: In conclusion, changes in ventricular systolic function may alter the risk of thrombotic events after EVAR repair, which could provide insight into the selection of adjuvant therapy strategies for AAA patients with CHD.
KW - abdominal aortic aneurysms
KW - computational model
KW - hemodynamics
KW - thrombus
KW - ventricular systolic function
UR - https://www.scopus.com/pages/publications/85146909497
U2 - 10.3389/fphys.2022.1114110
DO - 10.3389/fphys.2022.1114110
M3 - 文章
AN - SCOPUS:85146909497
SN - 1664-042X
VL - 13
JO - Frontiers in Physiology
JF - Frontiers in Physiology
M1 - 1114110
ER -