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The number of primary hip replacement procedures performed worldwide is expected to be roughly 1.7 million in 2018.
April 30, 2018
By: DePuy Synthes Inc.
DePuy Synthes, part of the Johnson & Johnson Medical Devices Companies, announced today clinical results associated with the use of its CORAIL Hip System Femoral Stems. Results showed that both the collarless and collared versions of the CORAIL Cementless Stem performed in line with industry expectations and that the CORAIL Standard Collared stem was associated with a 29 percent lower revision risk when compared to all other cementless stems on the National Joint Registry (NJR) for England, Wales, Northern Ireland and the Isle of Man.1,2 This analysis was independently conducted based on Nnational Joint Registry (NJR) data. “While the entire CORAIL Hip portfolio has a long and successful clinical heritage, this latest information is significant as it reinforces that using a proven, robust construct design with a strong supportive evidence base may help reduce the revision risk for patients and the associated cost burden to healthcare systems,” said Torbjorn Sköld, vice president, DePuy Synthes EMEA Joint Reconstruction. The results of this analysis come at a time when the number of primary hip replacement procedures performed around the world is anticipated to be approximately 1.7 million in 2018.3 DePuy Synthes commissioned this analysis, known as a Bespoke Implant Report, to provide the orthopedic community with new outcomes data on one of its most widely used implants. Since 1986, the CORAIL Hip System has been provided for more than 2 million patients around the world4 and is an integral part of the DePuy Synthes hip portfolio. In this analysis, the survivorship rates of the CORAIL Standard Collared and Collarless Femoral Stems were retrospectively compared to all other cementless femoral stems in the NJR. In all, the analysis encompassed more than 130,000 CORAIL Femoral Stem Implantations. Results at 10 years showed:
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