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Bone & Joint Research
Vol. 2, Issue 10 | Pages 220 - 226
1 Oct 2013
Chang Y Tai C Hsieh P Ueng SWN

Objectives

The objective of this study is to determine an optimal antibiotic-loaded bone cement (ALBC) for infection prophylaxis in total joint arthroplasty (TJA).

Methods

We evaluated the antibacterial effects of polymethylmethacrylate (PMMA) bone cements loaded with vancomycin, teicoplanin, ceftazidime, imipenem, piperacillin, gentamicin, and tobramycin against methicillin-sensitive Staphylococcus aureus (MSSA), methicillin-resistant Staph. aureus (MRSA), coagulase-negative staphylococci (CoNS), Escherichia coli, Pseudomonas aeruginosa, and Klebsiella pneumoniae. Standardised cement specimens made from 40 g PMMA loaded with 1 g antibiotics were tested for elution characteristics, antibacterial activities, and compressive strength in vitro.


Orthopaedic Proceedings
Vol. 86-B, Issue SUPP_III | Pages 265 - 265
1 Mar 2004
Ridgeway S Steinlechner C Tai C Graevett-Ball C Carey-Smith R Harrison D
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Aims: To study the outcome of lumbar spinal fusions in patients with chronic lower back pain due to degenerative spinal disorders. Methods: 85 patients with DSD’s, a mean age of 46.4 years, back pain for at least 2 years (mean=7.7years) and failed conservative treatment for at least 1 year were admitted to the study. Questionnaires recorded socio-demographic characteristics; changes in pain, clinical findings, disability (Oswestry (ODI)), employment, radiographic fusion, patient satisfaction and complications. All patients had 3, 6, 12 and 24-month follow-ups. Results: There were 37 males (44.9years) and 48 females (47.6 years) with a mean BMI of 24.8; 49% were smokers. Pain improved significantly at 3months (p< 0.001); no deterioration at 2 years with 38.4% having no back pain. Motor (p< 0.01), sensory (p< 0.05) and Oswestry Disability (0.001) improved significantly at 3 months and continued throughout. Unemployment improved significantly 30.4% to 16.5% at 2 years (p< 0.04). Radiographic fusion occurred in 91.8%, instrument failure in 11.8% and 9.4% required re-operation. Patient satisfaction revealed a significant increase in excellent (p< 0.02) and poor (p< 0.03) results. Instrument failure correlated strongly with ODI (r=0.94, p< 0.04). No other significant correlations. Conclusions:With the correct patient selection, lumbar fusions for DSD’s lead to a significantly improved outcome at 2 years, with an acceptable complication rate. There is no correlation between radiographic fusion and outcome, but instrument failure leads to significantly worse outcome


Orthopaedic Proceedings
Vol. 86-B, Issue SUPP_III | Pages 245 - 245
1 Mar 2004
Ridgeway S Tai C Carey-Smith R Graevett-Ball C Harrison H
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Aims: To investigate the functional outcome with different autologous bone graft weights in posterolateral lumbar spine instrumentation for DSD’s. Methods: A total of 79 patients (mean age of 47.2) with chronic lower back pain for at least 2 years, with at least 1 year of failed conservative treatment and who were undergoing pos-terolateral spinal instrumentation for DSD’s were admitted to the trial. Patients were randomised into three groups to receive bone graft weights of 25g (Group A=26 patients), 50g (Group B=30 patients) and 100g (Group C=23 patients) per segment. Pain, clinical characteristics, disability (Oswestry), radiographic fusion, patient satisfaction and complications were recorded at 3, 6, 12 and 24-month follow-ups. Results: At 2 years, Group B (50g) had a significantly improved Oswestry Index, pain intensity, motor and sensory changes, and overall patient satisfaction than Group C (100g), which was significantly better than Group A (25g). There was no correlation between bone graft weight and radiographic fusion, between fusion and outcome, nor smoking and fusion or bone graft weight. Complications were similar. Conclusions: Patients had significantly better functional and clinical outcomes with bone graft weights of 50g. Bone graft weights of 25g had the worse outcomes and 100g did not seem to have any beneficial affect over 50g. We recommend autologous bone graft weights of 50g per fused spinal segments in this group of surgical patients.


The Journal of Bone & Joint Surgery British Volume
Vol. 85-B, Issue 7 | Pages 1032 - 1036
1 Sep 2003
Ridgeway S Tai C Alton P Barnardo P Harrison DJ

We studied the use of autologous pre-donated blood transfusion in surgery for scoliosis in 45 patients who were divided into two groups; 27 who pre-donated autologous blood (group 1) and 18 who were planned recipients of allogenic blood (group 2). Normovolaemic haemodilution and intra-operative blood salvage was used in six patients in group 1 and three patients in group 2.

The two groups did not differ significantly with respect to age, American Society of Anaesthesiologists score, mean operative time, number of vertebral segments fused, total blood loss, length of stay in intensive care and length of stay in hospital. The risk of requiring allogenic blood transfusion was found to be significantly less in group 1 (7.4% ν 88.9%, p < 0.001). Only 5.21% of autologous units were wasted. Although intra-operative blood salvage reduced the total blood loss in both groups, it did not affect the need for subsequent allogenic transfusion or reduce the number of pre-donated autologous units which were given (p < 0.67). Autologous blood transfusion required extra time, personnel, resources and cost £28.88 per patient more than allogenic transfusion, however, the projected costs at May 2002 make this programme cost-effective by £51.54 per patient.

Pre-donated autologous blood transfusion is acceptable and safe in scoliosis surgery. It significantly reduces the subsequent requirement of allogenic transfusion. Although the cost is currently more than allogenic transfusion, with the increase in the costs of the latter and the decrease in potential donors which is anticipated, pre-donation of autologous blood will become comparatively cost-effective.


Orthopaedic Proceedings
Vol. 85-B, Issue SUPP_II | Pages 170 - 170
1 Feb 2003
Tai C Want S Quraishi N Batten J Kalra M Hughes S
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Antibiotics are frequently administered prophylactically in spinal procedures to reduce the risk of disc space infection. There is still controversy, however, over which antibiotics are able to penetrate the intervertebral disc effectively and whether the charges on the antibiotics are important in determining their ability to diffuse into the negatively charged intervertebral disc.

In a prospective randomised double blind clinical study, we examined the penetration of two commonly used antibiotics, cefuroxime (negatively charged) and gentamicin (positively charged), into the intervertebral discs. Twenty patients, randomised into two separate groups, received either 1.5g cefuroxime or 5 mg/kg gentamicin prophylactically two hours before their intervertebral discs removed. A blood specimen, from which serum antibiotic levels were determined, was obtained simultaneously with each discectomy.

Clinical therapeutic levels of antibiotic were detectable in the intervertebral discs of all the ten patients who received gentamicin. Only two of the ten patients (20%) who received cefuroxime had quantifiable level of antibiotic in their discs even though serum levels of cefuroxime were at therapeutic levels in all ten patients. Our results showed that cefuroxime does not diffuse into human intervertebral discs as readily as gentamicin and suggest that the charge due to ionisable groups on the antibiotics is important in determining the penetration of antibiotics. We therefore recommend the use of gentamicin in a single prophylactic dose for all spinal procedures to reduce the incidence of post-operative discitis.


The Journal of Bone & Joint Surgery British Volume
Vol. 79-B, Issue 3 | Pages 361 - 365
1 May 1997
Shih C Lee P Chen J Tai C Chen L Wu JS Chang WH

We made a clinical study of polyethylene wear in 240 hips of 187 patients having primary total hip arthroplasties from 1989 to 1990, using uncemented Osteonics components, with a head size of 26 mm. We excluded cups with anteversion of over 20° and measured linear wear by a new method using a digitiser and special software of our design. Follow-up was from two to five years (mean 4.3).

The mean age at operation was 50.3 years, with more men than women (1.4:1). The mean linear wear per year was 0.15 mm; this did not increase with the longevity of the prosthesis (p = 0.54). In 59 hips showing evidence of osteolysis, the mean linear wear rate was significantly higher at 0.23 mm/year (p < 0.001). The mean linear wear rate also correlated significantly with age at the time of operation (p = 0.008), but we found no significant correlations with body-weight, gender, aetiology of the disease, thickness of polyethylene, or cup position.

Our new method of measurement is time-saving and reproducible. The results confirm the greater rate of linear wear of polyethylene in patients showing osteolysis and in those who are younger.