Guest guest Posted June 10, 2004 Report Share Posted June 10, 2004 It was arrogant and unfeeling of me to use language I did in my initial postings. Especially the guinea pig comment. Sorry. There is no published evidence to show BHR/Cormet 2000 superior to others. No evidence to contrary either. A scientific trial to demonstrate conclusively that one is better than the other almost impossible to conduct because so many variables. If such studies were possible to conduct easily, we would not have present turmoil in THR market. Would not like to try and count the total number of THR devices ever released onto the market. Some have not been very good at all. It is patients that have largely paid the price of these designs, that were released with the best of intentions? Whose fault is that? OS? Or does innovation have to come at such a cost? The stakes in hip resurfacing are particularly high as patients are younger. Genuinely worried about proliferation of new resurfacing devices. Is this OK or will we eventually end up in same situation as Total Hip Replacement market? Unfortunately ( and this my own fault) comments were construed as direct attack on C+. Accept that Dr Amstutz has made a pioneering contribution to Hip resurfacing and but for him many of you would have had THR. Accept that C+ is device with a worthy track record. Was wrong of me to imply otherwise. Pity that US insurance companies will not fund Hip resurfacing. It was difficult to get insurance companies to fund hip resurfacing in UK until National Institute for Clinical Exellence (NICE) released a guide cautiously approving concept of MOM resurfacing. http://www.nice.org.uk/page.aspx?o=33560. In US which regulatory body holds key to release of new devices? I understand it is FDA? Is this for devices originating both inside and outside US? What do you all make of high profile media campaign re Jack Nicklaus ceramic-on-ceramic hip replacement? Quote Link to comment Share on other sites More sharing options...
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