“
“In recent years total hip replacement using large diameter metal-on-metal

bearings (MOMHR), either as a hip resurfacing procedure or using a stemmed femoral prosthesis, has become a common alternative to conventional total hip arthroplasty (THA) for the treatment of young and active arthritis patients because of click here advantages of lower volumetric wear and dislocation risk [1]. However, the clinical outcomes of hip replacement using these prostheses have been mixed. Data from the National Joint Register for England and Wales (2008) demonstrated a 3-year revision rate for hip resurfacing of 4.4% (95%CI 4.0 to 5.0) compared with 1.3% (1.2 to 1.4) for cemented THA (www.njrcentre.org.uk). The Australian Arthroplasty Register (1997 to 2005) also reported a higher 3-year revision rate for hip resurfacing versus THA (3.1% (2.7 to 3.6) versus 2.1% (1.9 to 2.5%) www.dmac.adelaide.edu.au/aoanjrr). The most common adverse events necessitating revision surgery after

MOMHR include early periprosthetic fracture, osteolysis, failure SPTLC1 of prosthesis buy MK-1775 osseo-integration resulting in aseptic loosening, unexplained pain, and inflammatory masses [2], [3], [4], [5], [6] and [7]. Circulating physiological levels of cobalt and chromium are normally < 0.25 μg/L (0.005 μM). Elevated levels of cobalt and chromium occur in both the hip synovial fluid and in peripheral blood after MOMHR. Whole blood concentrations of cobalt and chromium after MOMHR of up to 4.6 μM and 2.3 μM, respectively [8], and local

hip synovial fluid levels of up to 30 μM and 25 μM, respectively, have been measured in-vivo [9]. Whilst circulating metal levels are usually highest over the first few months after implantation, persistent elevation occurs as late as 10 years after surgery [10]. Previous studies have shown that short-term exposure to these metal species may affect human osteoclast and osteoblast survival and function. High concentrations of cobalt2+ (Co2+), chromium3+ (Cr3+), and chromium6+ (Cr6+) ions is toxic to osteoblasts and reduces cell activity in-vitro [11], [12] and [13].