UHMWPE
4
th International Meeting
UHMWPE for arthroplasty: from powder to debris Satellite Meeting UHMWPE and Medical Devices: from production to the Hospital Turin, 16 -18 September 2009 Honorary President Dept. Orthopaedics and Traumatology AO CTO - Turin University IFM Chemistry Department Ultra High Molecular Weight Polyethylene (UHMWPE) is to date an essential biomaterial for arthroplasty, still now without alternatives for the knee. Methods available to improve its quality are still being discussed. In particular, stabilization using vitamin E to avoid oxidative degradation, and consequently its wearing, is a very relevant subject following the recent approval of ASTM norms. Debris and its consequences inside the organism are the subject of many studies that aim to prevent the disastrous biological effects that we unfortunately still witness when the implantation of a prosthesis fails. The IV International Congress on UHMWPE organized in Turin will be followed by a Satellite Symposium verging on evaluation procedures, and the subsequent acquisition, of prosthetic materials by Italian Hospital companies. This meeting will ensure the opportunity for an essential scientific confrontation among Orthopaedists, researchers and health related companies. PRELIMINARY PROGRAMME September 16 Afternoon Welcome address Chairman: Panel Discussion Invited speaker: Speakers: Selected papers Chairman: Panel Discussion Invited speaker: Selected papers September 17 Morning Chairman Panel Discussion Invited speakers: Selected papers Chairman: Panel Discussion Invited speakers: Selected papers Afternoon Chairman: Panel Discussion Invited speakers: del Prever, Selected papers Chairmen: Panel Discussion Selected papers September 18 Morning Satellite Meeting organized by Welcome address Competition procedures for the acquisition of prosthetic components, Past experiences: Polyethylene quality and the ministerial recommendation of March 5 Norms concerning the certification and classification of medical devices and creation of the National Classification of Medical Devices, Device certification and production quality, Panel Discussion The contribution of Registers, The researcher's view, Industry's view - The orthopaedic view, The voice of patients, ARESS (Regional Agency for Health Services) and Technology Assessment, Legal aspects in an international perspective, The role of administrations and their discretional powers, Conclusions * To be confirmed Congress web site Informations 011505730 F +39 011590940 e-mail