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pubmed-article:18757956pubmed:abstractTextWe compared patient-reported outcomes of the Kinemax fixed- and mobile-bearing total knee replacement in a multi-centre randomised controlled trial. Patients were randomised to the fixed- or the mobile-bearing prosthesis via a sealed envelope method after the bone cuts had been made in the operating theatre. Randomisation was stratified by centre and diagnosis. Patients were assessed pre-operatively and at eight to 12 weeks, one year and two years post-operatively. Validated questionnaires were used which included the Western Ontario MacMasters University, Short-Form 12, Mental Health Index-5, Knee Injury and Osteoarthritis Outcome Score for Knee-Related Quality of Life and Function in Sport and Recreation scales and a validated scale of satisfaction post-operatively. In total, 242 patients (250 knees) with a mean age of 68 years (40 to 80) were recruited from four NHS orthopaedic centres. Of these, 132 patients (54.5%) were women. No statistically significant differences could be identified in any of the patient-reported outcome scores between patients who received the fixed-bearing or the mobile-bearing knee up to two-years post-operatively.lld:pubmed
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pubmed-article:18757956pubmed:dateRevised2010-11-10lld:pubmed
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pubmed-article:18757956pubmed:articleTitlePatient-reported outcomes after fixed- versus mobile-bearing total knee replacement: a multi-centre randomised controlled trial using the Kinemax total knee replacement.lld:pubmed
pubmed-article:18757956pubmed:affiliationUniversity of Bristol, Bristol Implant Research Centre, Avon Orthopaedic Centre, Southmead Hospital, Bristol BS10 5NB, UK. V.Wylde@bristol.ac.uklld:pubmed
pubmed-article:18757956pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:18757956pubmed:publicationTypeRandomized Controlled Triallld:pubmed
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