TDR: Safety and favourable outcomes obersved with Kineflex|C artificial disc .
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OrthoEvidence Journal (OE Journal) - ACE Report
OE Journal. 2013;1(18):32 J Neurosurg Spine. 2011 Oct;15(4):348-58. doi: 10.3171/2011.5.SPINE10769. Epub 2011 Jun 24269 patients were randomized to determine the efficacy and safety of cervical arthroplasty with the Kineflex|C artificial disc in treatment of cervical radiculopathy. Patients were allocated to receive either cervical total disc replacement with the Kineflex|C cervical disc or anterior cervical discectomy and fusion, and were followed-up for a minimum of 24 months. Results at 24 month follow-up indicated that clinical success, range of motion, and status of adjacent-level deterioration were all improved in the Kineflex|C group compared to ACDF. Clinical outcomes assessing pain and disability were similar between treatments. Reoperation rates were similar between groups.
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