pubmed-article:18757956 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:18757956 | lifeskim:mentions | umls-concept:C0086511 | lld:lifeskim |
pubmed-article:18757956 | lifeskim:mentions | umls-concept:C0008976 | lld:lifeskim |
pubmed-article:18757956 | lifeskim:mentions | umls-concept:C2587213 | lld:lifeskim |
pubmed-article:18757956 | lifeskim:mentions | umls-concept:C0681906 | lld:lifeskim |
pubmed-article:18757956 | pubmed:issue | 9 | lld:pubmed |
pubmed-article:18757956 | pubmed:dateCreated | 2008-9-1 | lld:pubmed |
pubmed-article:18757956 | pubmed:abstractText | We 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 |
pubmed-article:18757956 | pubmed:commentsCorrections | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:18757956 | pubmed:language | eng | lld:pubmed |
pubmed-article:18757956 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:18757956 | pubmed:citationSubset | AIM | lld:pubmed |
pubmed-article:18757956 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:18757956 | pubmed:month | Sep | lld:pubmed |
pubmed-article:18757956 | pubmed:issn | 0301-620X | lld:pubmed |
pubmed-article:18757956 | pubmed:author | pubmed-author:LearmonthII | lld:pubmed |
pubmed-article:18757956 | pubmed:author | pubmed-author:PotterAA | lld:pubmed |
pubmed-article:18757956 | pubmed:author | pubmed-author:LingardEE | lld:pubmed |
pubmed-article:18757956 | pubmed:author | pubmed-author:WyldeVV | lld:pubmed |
pubmed-article:18757956 | pubmed:author | pubmed-author:BettinsonKK | lld:pubmed |
pubmed-article:18757956 | pubmed:issnType | Print | lld:pubmed |
pubmed-article:18757956 | pubmed:volume | 90 | lld:pubmed |
pubmed-article:18757956 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:18757956 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:18757956 | pubmed:pagination | 1172-9 | lld:pubmed |
pubmed-article:18757956 | pubmed:dateRevised | 2010-11-10 | lld:pubmed |
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pubmed-article:18757956 | pubmed:year | 2008 | lld:pubmed |
pubmed-article:18757956 | pubmed:articleTitle | Patient-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:18757956 | pubmed:affiliation | University of Bristol, Bristol Implant Research Centre, Avon Orthopaedic Centre, Southmead Hospital, Bristol BS10 5NB, UK. V.Wylde@bristol.ac.uk | lld:pubmed |
pubmed-article:18757956 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:18757956 | pubmed:publicationType | Randomized Controlled Trial | lld:pubmed |
pubmed-article:18757956 | pubmed:publicationType | Multicenter Study | lld:pubmed |
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