TY - JOUR
T1 - In vivo implantation of 3-dimensional printed customized branched tissue engineered vascular graft in a porcine model
AU - Yeung, Enoch
AU - Inoue, Takahiro
AU - Matsushita, Hiroshi
AU - Opfermann, Justin
AU - Mass, Paige
AU - Aslan, Seda
AU - Johnson, Jed
AU - Nelson, Kevin
AU - Kim, Byeol
AU - Olivieri, Laura
AU - Krieger, Axel
AU - Hibino, Narutoshi
N1 - Publisher Copyright:
© 2019 The American Association for Thoracic Surgery
PY - 2020/5
Y1 - 2020/5
N2 - Background: The customized vascular graft offers the potential to simplify the surgical procedure, optimize physiological function, and reduce morbidity and mortality. This experiment evaluated the feasibility of a flow dynamic–optimized branched tissue engineered vascular graft (TEVG) customized based on medical imaging and manufactured by 3-dimensional (3D) printing for a porcine model. Methods: We acquired magnetic resonance angiography and 4-dimensional flow data for the native anatomy of the pigs (n = 2) to design a custom-made branched vascular graft of the pulmonary bifurcation. An optimal shape of the branched vascular graft was designed using a computer-aided design system informed by computational flow dynamics analysis. We manufactured and implanted the graft for pulmonary artery (PA) reconstruction in the porcine model. The graft was explanted at 4 weeks after implantation for further evaluation. Results: The custom-made branched PA graft had a wall shear stress and pressure drop (PD) from the main PA to the branch PA comparable to the native vessel. At the end point, magnetic resonance imaging revealed comparable left/right pulmonary blood flow balance. PD from main PA to branch between before and after the graft implantation was unchanged. Immunohistochemistry showed evidence of endothelization and smooth muscle layer formation without calcification of the graft. Conclusions: Our animal model demonstrates the feasibility of designing and implanting image-guided, 3D-printed, customized grafts. These grafts can be designed to optimize both anatomic fit and hemodynamic properties. This study demonstrates the tremendous potential structural and physiological advantages of customized TEVGs in cardiac surgery.
AB - Background: The customized vascular graft offers the potential to simplify the surgical procedure, optimize physiological function, and reduce morbidity and mortality. This experiment evaluated the feasibility of a flow dynamic–optimized branched tissue engineered vascular graft (TEVG) customized based on medical imaging and manufactured by 3-dimensional (3D) printing for a porcine model. Methods: We acquired magnetic resonance angiography and 4-dimensional flow data for the native anatomy of the pigs (n = 2) to design a custom-made branched vascular graft of the pulmonary bifurcation. An optimal shape of the branched vascular graft was designed using a computer-aided design system informed by computational flow dynamics analysis. We manufactured and implanted the graft for pulmonary artery (PA) reconstruction in the porcine model. The graft was explanted at 4 weeks after implantation for further evaluation. Results: The custom-made branched PA graft had a wall shear stress and pressure drop (PD) from the main PA to the branch PA comparable to the native vessel. At the end point, magnetic resonance imaging revealed comparable left/right pulmonary blood flow balance. PD from main PA to branch between before and after the graft implantation was unchanged. Immunohistochemistry showed evidence of endothelization and smooth muscle layer formation without calcification of the graft. Conclusions: Our animal model demonstrates the feasibility of designing and implanting image-guided, 3D-printed, customized grafts. These grafts can be designed to optimize both anatomic fit and hemodynamic properties. This study demonstrates the tremendous potential structural and physiological advantages of customized TEVGs in cardiac surgery.
KW - 3D printing graft
KW - CFD optimization
KW - customized branched TEVG
KW - in vivo implantation of TEVG
KW - neotissue formation
UR - https://www.scopus.com/pages/publications/85074390572
UR - https://www.scopus.com/pages/publications/85074390572#tab=citedBy
U2 - 10.1016/j.jtcvs.2019.09.138
DO - 10.1016/j.jtcvs.2019.09.138
M3 - Article
C2 - 31864694
AN - SCOPUS:85074390572
SN - 0022-5223
VL - 159
SP - 1971-1981.e1
JO - Journal of Thoracic and Cardiovascular Surgery
JF - Journal of Thoracic and Cardiovascular Surgery
IS - 5
ER -