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For certain cardiovascular diseases, cannulas are implanted into the blood circuit. To match the patients individual anatomy of the heart, there is research for cannulas to be custom-designed and manufactured aided by 3D printing. However, cannulas have to hold very high standards with regard to the smoothness of their surfaces, as rough patches can lead to formation of
blood clots. Therefore, this work uses computer vision to detect such patches as part of quality assurance. First, the produced cannula is scanned using a precise CT scanner and transformed into a 3D mesh object. Rough patches in an otherwise smooth but curved surface are detected by using cosine similarity between neighboring faces and a statistical evaluation. In the end, this method is able to raise a warning when curved surfaces are not smooth enough and visualizes the problematic patches. However, there is just limited access to test data currently and the scanner used needs to be upgraded.
Some children are born with a univentricular heart, meaning their heart has only one pumping chamber instead of two. To improve circulation, patients often undergo the Fontan procedure, which reroutes blood flow — but this can put stress on other organs. In some cases, ventricular assist devices, or VADs, are used to support the heart’s pumping function. This involves an artificial pump connected directly to the patient's heart via silicone-based cannulas. Unique anatomical conditions introduce special challenges for cannula geometry. Additive manufacturing offers innovative solutions by enabling the production of personalized medical devices. The aim of the project is to develop the manufacturing workflow for the individualized cannula from digital imaging of the patient and customized design to additive manufacturing. Besides technical feasibility, validating the entire process is crucial for regulatory approval. The selection and testing of suitable additive manufacturing processes and biocompatible materials for individualized silicone cannulas, ensuring compliance with quality standards for high-risk medical products, will be presented.