Thorac Cardiovasc Surg 2017; 65(S 01): S1-S110
DOI: 10.1055/s-0037-1598810
Oral Presentations
Monday, February 13th, 2017
DGTHG: Miscellaneous
Georg Thieme Verlag KG Stuttgart · New York

Three-dimensional Construction of Tissue Casting Molds for Aortic Arch Reconstruction in Hypoplastic Left Heart Syndrome

C. Haller
1   Cardiovascular Surgery, The Hospital for Sick Children, Toronto, Canada
,
S.J. Yoo
3   Diagnostic Imaging, The Hospital for Sick Children, Toronto, Canada
,
G. Van Arsdell
1   Cardiovascular Surgery, The Hospital for Sick Children, Toronto, Canada
,
O. Honjo
1   Cardiovascular Surgery, The Hospital for Sick Children, Toronto, Canada
› Author Affiliations
Further Information

Publication History

Publication Date:
03 February 2017 (online)

Objectives: Aortic arch reconstruction is a key step of the Norwood operation in hypoplastic left heart syndrome (HLHS). Inadequate geometry leads to significant morbidity. We assessed aortic geometry and growth after arch reconstruction and developed a computational model to generate tissue casting molds.

Methods: A computational model was developed based on anatomic dimensions derived by echocardiography. Software engineering was performed with Matlab R2015b (Mathworks, Natick, MA, United States). Mimics (Materialise, Leuven, Belgium) was used for three-dimensional reconstruction of CT data. CAD postprocessing was performed with SketchUp Make (Trimble Navigation Ltd., Sunnyvale, CA, United States).

Results: The algorithm included diameters of the hypoplastic ascending aorta, main pulmonary artery and descending aorta. Furthermore, geometry was defined by height of the native aortic arch and distance between pulmonary artery and descending aorta. To respect the spatial relations of the ascending aorta, the pulmonary artery and the descending aorta, the model incorporated the angle between the ascending and descending aorta with regard to the pulmonary artery. Further adaptations had to be performed to account for the larger proximal neoaortic dimensions due to the Damus-Kay-Stansel anastomosis. Alignment of the non-parallel orientation of the pulmonary artery to descending aorta axis and the ascending to descending aorta axis was achieved by tilting of the construct. Export functions to the STereoLithography (STL) file format were added to enable export to CAD software, postprocessing and printing of sterilizable models. Virtual reconstruction was performed after data export. The tissue scaffold was virtually fused with the native anatomy of a patient with HLHS to evaluate adequacy of the theoretical approach and the computer algorithm.

Conclusion: We developed a software tool that is close to its clinical application. The parameters used can be acquired easily in patients with HLHS and do not necessitate complex diagnostic procedures. Three-dimensional printing offers the possibility to sterilize the tissue scaffold and to use it as an individualized, readily available casting mold for customized patches.