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One of the major concerns of biomedical engineers and biomedical industry operators is to date the reduction of risk related to human implantation of biomedical devices, as heart valves, artificial hearts, VAD Systems, stents, bypass grafts, etc. In fact, if from one side the modern technology has successfully tested innovative biocompatible materials, from the other side it is recognised that the nature and characteristics of the blood motion modified by the implanted device still remains, for major items, under investigation.
Actually, flow properties, most notably shear stress, turbulence, in terms of small scale vortices, high temporal and spatial velocity gradients as well as localised stagnation, have been implicated in several ventricular assist device problems including blood cell damage, thrombus formation, calcification and infection. On the side of the heart valves, the elevated flow stresses and regions of recirculation of blood origin thrombogenicity due to platelet activation.
Today, no integrated high-performance system in support to design of these biomedical devices and monitoring phases exists at industrial level. As well, no adequate systems are in practise of hospitals and clinics to provide researcher and operators with a mean for verification of patient constraints before surgery intervention or device implantation.