To evaluate prospectively the mid-term results of the Zimmer Unicondylar Knee arthoplasty (UKA). Between 2005 and 2012, 187 unicompartmental knee arthroplasties (UKA) were performed by a single surgeon using a fixed-bearing prosthesis (Zimmer). 37 cases were excluded as either were lost to follow-up or had less than six months follow-up. The study included 150 UKAs. Deformity, if present, was correctable. Patellofemoral joint (PFJ) disease was not considered as an absolute contraindication. The average patient age at the time of surgery was 66 years (range 42–88 years); 78 of which were male. Mean follow-up time was 3.6 years (range 7–81 months). Mean Body Mass Index (BMI) was 29 (range 21–41). Clinical and conventional radiological evaluations were carried out at six months, one, two and five years postoperatively. 147 cases were medial compartment replacement and three were lateral. 86 patients had grade III OA and 64 had grade IV (Kellgren and Lawrence). 113 patients had an element of PFJ disease. The mean Knee Society knee and function scores had an improvement from 55 and 54 points pre-operatively to 95 and 94 points respectively at time of most recent evaluation. The average flexion improved from 116 degrees pre-operatively to 127 degrees. Two cases were revised, one due to progression of osteoarthritis in the lateral compartment of the knee and the other was due to arthrofibrosis. The Zimmer unicompartmental knee arthroplasty provided excellent pain relief and restoration of function in carefully selected patients. However, long-term studies are necessary to investigate the survival rate for this prothesis.
To audit the routine measurement of Vitamin B12 levels prior to cervical decompressive surgery Retrospective analysis of medical records and pathology results of patients who underwent decompressive cervical surgery for myelopathy over a 6 month period 26 patients were identified from theatre records. 21 out of 26 patients did not have vitamin B12 levels checked prior to their decompressive surgery The reports in the literature of co-existent B12 deficient myelopathy and mechanical compression are a cause for concern. Although the incidence of this is unknown and unlikely to be common, good clinical practice would suggest that we should be routinely monitoring B12 levels in myelopathic patients. We have introduced new standards for routinely checking B12 levels pre-operatively and intend to re-audit the effectiveness of these in six months time.
To establish the current practice of spinal cord monitoring in units carrying out scoliosis surgery in the UK. To illustrate the benefit of routinely monitoring motor evoked potentials (MEPs). Questionaire: Nationwide survey of spinal monitoring modalities used by spinal units carrying out deformity surgery. 10 out of 27 units routinely measure motor evoked potentials (MEPs), the remainder use only sensory potentials (SEPs). There is significant variability in use of monitoring around the UK and we have compared this to the practice elsewhere in the world. We report the case of a thirteen year old girl who underwent posterior instrumentation for correction of an idiopathic scoliosis. Intra-operatively there was a significant reduction in the amplitude of the MEPs without any corresponding change in the SEPs. These changes reversed when the correction was released. The surgery was abandoned and was carried out as a staged procedure, initially anteriorly then posteriorly. There was no loss of motor potentials during either operation and no post operative neurological abnormalities. We propose that the changes noted initially were due to transient ischaemia of the cord which would not have been detected without MEPs and may have led to long term sequelae. This highlights the safety benefit of routinely using MEPs in scoliosis surgery. Nationally there is wide variation in the monitoring of spinal cord function during scoliosis surgery. We feel that monitoring of motor potentials is a vital component in ensuring scoliosis surgery is as safe as possible.
We assessed polyethylene wear and osteolysis in 15 patients (30 hips) undergoing staged bilateral total hip arthroplasty, who had a cemented hip arthroplasty on one side and a hybrid arthroplasty on the other. All factors apart from mode of acetabular component fixation were matched. Wear was measured radiographically using Livermore’s technique. The mean clinical and radiological follow-up was 11.2 years for the cemented arthroplasties and 10.7 years for the hybrid arthroplasties. Mean annual linear wear rate for the cemented cups was 0.09mm/year, and 0.14mm/year for the uncemented cups. This difference was statistically significant (p=0.03), confirming previous reports that polyethylene wear in uncemented cups is greater than in cemented cups. Polyethylene wear in the uncemented cup exceeded wear in the cemented cup by more than >
0.1mm/year in 5 patients, 4 of whom had a BMI of greater than 30. No periacetabular osteolysis was noted. Femoral osteolysis was present in 5 hybrid arthroplasties and 2 cemented arthroplasties. Zone 7 femoral osteolysis occurred in 3 patients on the side of the hybrid arthroplasty, multifocal femoral osteolysis not involving zone 7 was seen in 2 patients in both hips.
