Computational Fluid Dynamics and Vascular Access

• Published in: Artificial organs Vol. 26; no. 7; pp. 571 - 575
• Main Authors: Krueger, Ulf, Zanow, Juergen, Scholz, Hans
• Format: Journal Article
• Language: English
• Published: Boston, MA, USA Blackwell Science Inc 01-07-2002
• Subjects: Algorithms; Anastomotic intimal hyperplasia; Arm - blood supply; Arteriovenous Anastomosis; Arteriovenous grafts; Blood Flow Velocity; Blood Vessel Prosthesis; Computational Biology; Computer Simulation; Dialysis access graft; Hemodynamics - physiology; Hemorheology; Humans; Hyperplasia - prevention & control; Models, Cardiovascular; Regional Blood Flow; Renal Dialysis; Stress, Mechanical; Tunica Intima - pathology; Vascular Patency
• ISSN: 0160-564X; 1525-1594
• DOI: 10.1046/j.1525-1594.2002.07078.x

: Anastomotic intimal hyperplasia caused by unphysiological hemodynamics is generally accepted as a reason for dialysis access graft occlusion. Optimizing the venous anastomosis can improve the patency rate of arteriovenous grafts. The purpose of this study was to examine, evaluate, and characterize the local hemodynamics and, in particular, the wall shear stresses in conventional venous end‐to‐side anastomosis and in patch form anastomosis (Venaflo) by three‐dimensional computational fluid dynamics (CFD). We investigated the conventional form of end‐to‐side anastomosis and a new patch form by numerical simulation of blood flow. The numerical simulation was done with a finite volume‐based algorithm. The anastomotic forms were constructed with usual size and fixed walls. Subdividing the flow domain into multiple control volumes solved the fundamental equations. The boundary conditions were identical for both forms. The velocity profile of the patch form is better than that for the conventional form. The region of high static pressure caused by flow stagnation is reduced on the vein floor. The anastomotic wall shear stress is decreased. The results of this study strongly support patch form use to reduce the incidence of intimal hyperplasia and venous anastomotic stenoses.