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M. Hamman de Vaal 1 , Michael W. Gee 2 and Wolfgang A. Wall 1 Computational Modeling of High Risk Aortic Manipulation during Open-Heart Surgeries Worldwide, approximately 2 million open-heart surgeries are done annually [1]. A major risk factor of these procedures include end-organ ischemia, including stroke, with an incidence of 0.9-13%, depending on the procedural complexity [2]. At least 50% of the peri-operative embolic load is caused by aortic manipulation, including especially aortic occlusion and arterial cannular flow [2,3], as also seen in clinical findings shown here on the right. 1 Institute for Computational Mechanics, Technische Universität München, GERMANY 2 Mechanics and High Performance Computing Group, Technische Universität München, GERMANY Objectives Discussion and Future Challenges Introduction Detailed knowledge of the patient-specific impact of aortic manipulation, especially w.r.t. high risk maneuvers such as arterial cannular flow and aortic occlusion is needed to not only aid in clinical decision making and protocol evaluation, but also for improved product design. Ultrasound image revealing likely aortic manipulation related injury, showing a new intimal tear (1) and a new mobile lesion (2) – adapted from [4] Aortic Occlusion of Calcified Aorta REFERENCES: [1] Pezzella TA, Global Aspects of Cardiothoracic Surgery with Focus on Developing Countries. Asian Cardiovasc Thorac Ann 18(3):299-310, 2010. [2] de Vaal MH, Wildhirt SM, Gee MW, Stock UA, Wall WA, Current state of large deformation aortic manipulation during cardiac surgery In preparation. [3] Stump DA, Jones TJJ, Rorie KD, Neurophysiologic Monitoring and Outcomes in Cardiovascular Surgery. J Cardiothorac Vasc Anesth, 13(5):600-613, 1999. [4] Ura M, Sakata R, Nakayama Y, Goto T, Ultrasonographic Demonstration of Manipulation-related Aortic Injuries After Cardiac Surgery. J Am Coll Cardiol 35:1303-10, 2000. [5] Joubert-Huebner E, Gerdes A, Sievers HH, An in vitro evaluation of a new cannula tip design compared with two clinically established cannula-tip designs regarding aortic arch vessel perfusion characteristics, Perfusion 15:69–76, 2000. [6] Scharfschwerdt M, Richter A, Boehmer K, Repenning D, Sievers HH, Improved hydrodynamics of a new aortic cannula with a novel tip design, Perfusion 19:193–197, 2004. Large deformations caused by occlusion exerts significant high stresses in the arterial wall, of which the magnitude and therefore risk of damage is highly variable, depending unintuitively on the of occluder, occluding location and patient- specific arterial wall constitution. The tip design of arterial cannulas determines the distribution of flow entering the aortic arch, and therefore the cerebral circulation, as well as the amount of damage caused by the dangerous “sand-blasting” effect of the high velocity jet against the arterial wall. No design completely fulfills the requirements of safe arterial return. Future investigations are needed to further improve models that will help to optimize clinical protocol and aid in device design. [7] Maier A, Gee M, Reeps C, Eckstein HH, Wall W. Impact of calcifications on patient-specific wall stress analysis of abdominal aortic aneurysms Biomech Model Mechanobiol, Biomechanics and Modeling in Mechanobiology 9:511-521, 2010. [8] Gee MW, Förster Ch, Wall WA, A Computational Strategy for Prestressing Patient Specific Biomechanical Problems Under Finite Deformation. Comm Num Meth in Eng 26(1):52-72, 2009. Arterial Cannular Flow influenced by Tip Design “DANGER ZONE” b) a) Patient-specific (male, 66 yrs) aortic lumen geometry with major atheroslerotic calcification was extracted from medical CT-data. The three main different types of clinically available arterial cannula tip-designs was considered in an idealized arterial segment. Hybrid tip Side-hole tip End-hole tip [5,6] Each fluid domain was discretized in Harpoon (Sharc Ltd., Manchester, UK) with a HEX-dominant mesh with selective refinement and boundary layer meshes to ensure sufficient resolution especially of flow through the cannula, the jet flow through the vessel prior to hitting the wall and the jet flow where it hits the wall. The blood flow through the cannulas were simulated as an incompressible, newtonian fluid (µ = 0.004 Pa·s), using a stabilized, equal-order, linear FE scheme on our in-house FE solver baci. The maximum flowrate considered was 50% of full CPB flow, i.e. 3 l/min The outer surface of the lumen was meshed selectively to capture the most important features of the vessel deformation during occlusion. On this surface mesh, a pure HEX-mesh could be extruded (4 layers, 2.3 mm total thickness) in CUBIT (Sandia Nat. Labs. Albuquerque, NM, USA), including also an arterial cannula mesh. Standard DeBakey cross-clamps was applied at two different orientations rotated around the vessel axis by 60°. At the same location, an endo-aortic balloon (EAB) was also applied. The aortic wall was modelled with an isotropic, hyperelastic Raghavan&Vorp model developed for aneurysmatic arterial walls (α = 0.174 MPa, β = 1.88 MPa), with regional stiffening at the calcified wall, mapped to and relative to the Houndsfield Units (HU) extracted from the CT-data [7]. Prior to occlusion, the aorta was prestressed to approximate the imaged internal pressure of the aorta using a Modified Updated Lagrangian Formulation [8]. The clamps and the EAB was modelled in a way to mimic the actual clinical load exerted on the artery. The structural contact simulation was performed using a reduced integration, linear FE scheme on our in-house FE solver baci. Geometry Velocity > threshold Profile entering aortic arch Induced WSS WSS > damage threshold Calcification mapping, Occluder configuration EABO Cross-clamp 0° Cross-clamp 60° View 1 Maximum occluder impact View 2 Maximum calcification impact 1225 1122 750 1177 1040 555 1283 Von Mises Stress (kPa) 924 2830 2505 97 77 ? Calcification 1225

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M. Hamman de Vaal1, Michael W. Gee2 and Wolfgang A. Wall1

Computational Modeling of High Risk Aortic Manipulation

during Open-Heart Surgeries

Worldwide, approximately 2 million open-heart surgeries are done annually [1]. A major risk factor of theseprocedures include end-organ ischemia, including stroke, with an incidence of 0.9-13%, depending on theprocedural complexity [2]. At least 50% of the peri-operative embolic load is caused by aorticmanipulation, including especially aortic occlusion and arterial cannular flow [2,3], as also seen in clinicalfindings shown here on the right.

1 Institute for Computational Mechanics, Technische Universität München, GERMANY2 Mechanics and High Performance Computing Group, Technische Universität München, GERMANY

Objectives

Discussion and Future Challenges

Introduction

Detailed knowledge of the patient-specificimpact of aortic manipulation, especiallyw.r.t. high risk maneuvers such as arterialcannular flow and aortic occlusion isneeded to not only aid in clinical decisionmaking and protocol evaluation, but alsofor improved product design.

Ultrasound image revealing likely aortic manipulation related injury, showing a new intimal tear (1) and a new mobile lesion (2) – adapted from [4]

Aortic Occlusion of Calcified Aorta

REFERENCES:

[1] Pezzella TA, Global Aspects of Cardiothoracic Surgery with Focus on Developing Countries. Asian Cardiovasc Thorac

Ann 18(3):299-310, 2010.

[2] de Vaal MH, Wildhirt SM, Gee MW, Stock UA, Wall WA, Current state of large deformation aortic manipulation during

cardiac surgery In preparation.

[3] Stump DA, Jones TJJ, Rorie KD, Neurophysiologic Monitoring and Outcomes in Cardiovascular Surgery. J Cardiothorac

Vasc Anesth, 13(5):600-613, 1999.

[4] Ura M, Sakata R, Nakayama Y, Goto T, Ultrasonographic Demonstration of Manipulation-related Aortic Injuries After

Cardiac Surgery. J Am Coll Cardiol 35:1303-10, 2000.

[5] Joubert-Huebner E, Gerdes A, Sievers HH, An in vitro evaluation of a new cannula tip design compared with two clinically

established cannula-tip designs regarding aortic arch vessel perfusion characteristics, Perfusion 15:69–76, 2000.

[6] Scharfschwerdt M, Richter A, Boehmer K, Repenning D, Sievers HH, Improved hydrodynamics of a new aortic cannula

with a novel tip design, Perfusion 19:193–197, 2004.

Large deformations caused by occlusion exerts significant high stresses in the

arterial wall, of which the magnitude and therefore risk of damage is highly variable,

depending unintuitively on the of occluder, occluding location and patient-

specific arterial wall constitution.

The tip design of arterial cannulas determines the distribution of flow entering the

aortic arch, and therefore the cerebral circulation, as well as the amount of damage

caused by the dangerous “sand-blasting” effect of the high velocity jet against the

arterial wall. No design completely fulfills the requirements of safe arterial return.

Future investigations are needed to further improve models that will help to optimize

clinical protocol and aid in device design.

[7] Maier A, Gee M, Reeps C, Eckstein HH, Wall W. Impact of calcifications on patient-specific wall stress analysis of abdominal

aortic aneurysms Biomech Model Mechanobiol, Biomechanics and Modeling in Mechanobiology 9:511-521, 2010.

[8] Gee MW, Förster Ch, Wall WA, A Computational Strategy for Prestressing Patient Specific Biomechanical Problems Under Finite

Deformation. Comm Num Meth in Eng 26(1):52-72, 2009.

Arterial Cannular Flow influenced by Tip Design

“DANGER ZONE”

b)a)Patient-specific (male,66 yrs) aortic lumengeometry with majoratherosleroticcalcification wasextracted frommedical CT-data.

The three main different types of clinicallyavailable arterial cannula tip-designs wasconsidered in an idealized arterial segment.

Hybrid tip Side-hole tip End-hole tip

[5,6]

Each fluid domain was discretized in Harpoon(Sharc Ltd., Manchester, UK) with a HEX-dominantmesh with selective refinement and boundary layermeshes to ensure sufficient resolution especially offlow through the cannula, the jet flow through thevessel prior to hitting the wall and the jet flow whereit hits the wall.

The blood flow through the cannulas were simulated as an incompressible, newtonianfluid (µ = 0.004 Pa·s), using a stabilized, equal-order, linear FE scheme on our in-houseFE solver baci. The maximum flowrate considered was 50% of full CPB flow, i.e. 3 l/min

The outer surface of the lumen was meshed selectively tocapture the most important features of the vesseldeformation during occlusion. On this surface mesh, a pureHEX-mesh could be extruded (4 layers, 2.3 mm totalthickness) in CUBIT (Sandia Nat. Labs. Albuquerque, NM,USA), including also an arterial cannula mesh. StandardDeBakey cross-clamps was applied at two differentorientations rotated around the vessel axis by 60°. At thesame location, an endo-aortic balloon (EAB) was alsoapplied.

The aortic wall was modelled with an isotropic, hyperelastic Raghavan&Vorp modeldeveloped for aneurysmatic arterial walls (α = 0.174 MPa, β = 1.88 MPa), with regionalstiffening at the calcified wall, mapped to and relative to the Houndsfield Units (HU)extracted from the CT-data [7]. Prior to occlusion, the aorta was prestressed toapproximate the imaged internal pressure of the aorta using a Modified UpdatedLagrangian Formulation [8]. The clamps and the EAB was modelled in a way to mimicthe actual clinical load exerted on the artery. The structural contact simulation wasperformed using a reduced integration, linear FE scheme on our in-house FE solverbaci.

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