Background

Reverse Geometry shoulder replacement requires fixation of a base plate (called a metaglene) to the glenoid to which a convex glenosphere is attached. Most systems use screws to achieve this fixation. The suprascapular nerve passes close to the glenoid and is known to be at risk of injury when devices and sutures are inserted into the glenoid. We investigate the risk posed to the suprascapular nerve by placement of metaglene fixation screws.

Purpose: Biomaterial-related infections continue to hamper the success of reconstructive and arthroplasty procedures in orthopaedic surgery. Staphylococci are the most common etiologic agents, with biofilm formation representing a major virulence factor. Environmental stress factors and sub-inhibitory concentration of some antibiotics have been identified to trigger staphylococcal biofilm formation through increased icaADBC expression. In staphylococci, production of polysaccharide intercellular adhesin (PIA) by the enzyme products of the icaADBC operon is the best understood mechanism of biofilm development, making the ica genes a potential target for biofilm inhibitors. Aims of the current study were

Determine the minimum inhibitory concentration (MIC) of Povidone-iodine.

Method: MIC of povidone – iodine for both reference strains and strains isolated from infected orthopaedic implants was determined. Biofilm assay was performed at different Povidone-iodine concentrations using 96-well polystyrene plates. Total RNA for cDNA synthesis was isolated from bacteria at different twofold dilutions of Povidone-iodine concentrations. Real time polymerase chain reaction was used to quantify effects of Povidone-iodine on gene expression pattern of the icaADBC operon using the constitutively expressed gyrB gene as internal control

Results: The MIC of povidone-iodine was 1.4% for all bacterial strains. Clinical in-use doses of povidone-iodine prevented biofilm formation.

A step-wise reduction of biofilm was observed at increasing sub-inhibitory doses of povidone-iodine (p< 0.0001).

IcaA expression correlated with biofilm formation in staphylococcal organisms. Decrease in icaA expression was strongly associated with an increase in expression in the biofilm repressor gene, icaR.

The repressive effect of povidone-iodine on biofilm formation by Staphylococcal bacteria is by a separate mechanism from its bacteriostatic mechanism of action.

Conclusion: This study shows that icaR is a potential therapeutic target through which the ability of Staphylococcal bacterial to form biofilm may be reduced. These data reveal an additional therapeutic benefit of povidone-iodine and suggest that studies to evaluate the suitability of povidone-iodine as biomaterial coating agent to reduce device-related infection rates are merited.

Background: The success of the increasing number of arthroplasty, spinal instrumentation and other implanted orthopaedic devices is hampered by device-related infections. More than half of these infections are caused by staphylococcal biofilm mediated antibiotic resistance. The hope of preventing prosthetic joint infection by antibiotic loaded cement is threatened by emerging resistant organisms. No bacterial resistance to betadine has been reported.

Current intervention strategy is focussed on prevention of initial device colonisation and inhibition of genes encoding biofilm formation.

Aim:

Determine the minimum inhibitory concentration (MIC) of betadine.

Methods: MIC of betadine for both reference strains and strains isolated from infected orthopaedic implants was determined. Biofilm assay was performed at different betadine concentrations using 96-well polystyrene plates.

Total RNA for cDNA synthesis was isolated from bacterial at different twofold dilutions of betadine concentrations.

Real time polymerase chain reaction was used to quantify effects of betadine on gene expression pattern of the icaADBC operon using the constitutively expressed gyrB gene as internal control.

Bacterial was cultivated on polystyrene plates coated with different sub-inhibitory and clinical in-use doses of betadine to assess surface adherence.

Results: The MIC of betadine was 1.4% for all bacterial strains. Clinical in-use doses of betadine prevented biofilm formation.

A step-wise reduction of biofilm was observed at increasing sub-inhibitory doses of betadine (p< 0.0001).

IcaA expression correlated with biofilm formation in staphylococcal organisms. Decrease in icaA expression was strongly associated with an increase in expression in the biofilm repressor gene, icaR.

The repressive effect of betadine on biofilm formation by Staphylococcal bacteria is by a separate mechanism from its bacteriostatic mechanism of action.

Conclusion: This study shows that icaR is a potential therapeutic target through which the ability of Staphylococcal bacterial to form biofilm may be reduced. Sub-inhibitory dose of betadine inhibited biofilm formation.

Prevention of bacterial surface attachment as demonstrated by this study is suggestive that these compounds could be developed as a surface coating agents for orthopaedic implants.

Backgroud: Revision total knee arthroplasty (TKA) consumes considerably more resources than primary TKA. Management of infected arthroplasty has been shown to require even more resources in terms of inpatient stay, microbiological investigation, multiple stage procedures and more complex implants than treatment of aseptic failures. We investigated the trends in cost of revision TKA over a 10 year period.

Patients and Methods: Between 1997 and 2006, 189 patients underwent revision total knee arthroplasty in our institution. The perioperative data was available for 181 of these (95.77%). Data collected included age, gender, diagnosis, number of revisions length of stay, operative time, blood loss, number of units of blood transfused and ASA grade. Financial data included cost of implants and instrumentation, cost and number of bed-days, investigations and treatment. In the case of 2 stage revisions involving 2 admissions, the cumulative data was compiled as a single episode.

Results: The study group comprised 123 females (65.07%) and 66 males (34.93%). The mean age for both groups was 68.97 (range of 20 to 91years), with a 6.7% increase in mean age over the ten year period (66.75 to 71.19). The mean ASA score dropped from 2.67 in 1997 to 2.23 in 2006. The number of revision surgeries per year increased over the study period from 8 to 36. The number of TKA revisions for infection over the 10 years was 18(9.5%).

The mean length of stay for revision due to aseptic loosening in 1997 was 14.3 days. The average length of stay for revision for infected arthroplasty was 35 days. In 2006, the length of stay increased to 65 days for infected arthroplasty and 15.03 days for aseptic cases.

The mean total cost of aseptic revision per patient was 12,409.92 (range 8,822.58–13,559.65) euro in 1997 with revisions for infection costing 20,888.66 euro, a difference of 68.32%.

The industry cost of implants increased by 32–35% (€3119–€4371 and €4216–€5800) between 1999 and 2006 depending on implant selection. There was a 20– 42% increase in generic hospital costs (admission, investigation and treatment related costs) in the same period.

Conclusion: With increasing life expectancy and increased indication for primary arthroplasty more patients are coming to revision surgery. The cost of Revision TKR has increased steadily over the last 10 years. Revision TKR for infection remains significantly more expensive than revision for aseptic loosening or other causes and provides a significant financial burden on orthopaedic services. Infected arthroplasty incurs significantly greater cost and every precaution should be taken to avoid infection in total knee arthroplasty.

Introduction: Duchenne’s Muscular Dystrophy (DMD) is a progresssive sex linked recessive disorder predominantly involving skeletal muscle. Scoliosis is almost universal in patients with DMD. Surgical stabilisation carries significant risks and complications with per-operative mortality of < 6%. Cardiopulmonary complications along with severe intraoperative blood loss requiring massive nlood transfusion are the major cause of morbidity.

Aim: To evaluate the efficacy of single rod fusion technique in reducing the peroperative and post operative complications especially blood loss, duration of surgery and progression of curve.

Materials and Methods: Retrospective review- 32 patients with scoliosis secondary to DMD with an average age of 14 years (range, 11–18) underwent either single rod fusion technique (19 patients) using Isola rod system or Hartshill rectangle/double rod fusion technique (13 patients). Blood loss was measured directly from the peroperative suction and postoperative drainage, indirectly by weighing swabs. Vapour free hypotensive anaesthesia was used in all cases. Progression of curve was followed up in the outpatients.

Results: The mean operative time was 130 minutes (range, 80–180) for the single rod fusion technique in comparison to 250 minutes (range, 170–300) for the Hartshill/Double rod technique. The average blood loss for the single rod fusion technique was reduced, 2.2 L (range 0.4–4) versus 3.1L (0.8–4). The mean follow up was 35 months (range, 5–72). The inpatient stay was 12 days (range, 6–23). Seven patients developed complications: 3 ileus, 2 respiratory tract infections, one patient had loosening and migration of the rod, which required revision under LA, and one patient developed a superficial wound infection, which resolved with intravenous antibiotics.

Conclusion: In our experience, single rod stabilisation is a safe and quick method of correcting the DMD scoliotic spine, with less blood loss and complications compared to traditional methods.

Background: Infected total knee arthroplasty causes significant morbidity to patients and also challenges to surgeons to provide a functional mobile knee joint.

Aim: Present a 10-year review (1997 to 2006) of all the revision total knee replacements performed for infection in our centre.

Methods and Materials: Data including the demographics, ASA grade, blood loss, blood transfusions, length of stay, laboratory investigations including culture and sensitivity of the deep swabs. The sensitivity and specificity of pre-operative CRP and ESR were related to culture results. Post operative complication was recorded. The financial implication of the whole treatment was calculated by applying the prescribed cost by the Voluntary health insurance limited.

Results: Revisions for suspected infection constituted 14.8% (28 out of 189 cases) of the total revision knee procedures performed during the period. All the patients underwent 2 staged revision knee Arthroplasty. The mean age was 68.6 (46–83 yrs). The mode for ASA grade was 2. The average blood loss was 2 litres and the mean blood transfusion units per case were 3.8 units. The average length of stay was 42.25 days, a 24.32 days longer than aseptic revisions.

46.4% of the cases had positive cultures from the deep tissues. Staphylococcus species were responsible for 62% of cases, while enterococci, pseudomonas, streptococcus pneumonia, and MRSA have similar occurrences. The mean total cost per case was € 21,895 (13,597 for aseptic revision) a 61% increase in cost for cases revised for non septic reasons.

Conclusion: Revision Total knee replacement for infection remains significantly more expensive than revision for aseptic loosening or other causes and provides a significant financial burden on orthopaedic services. Every precaution should be taken to avoid infection in total knee arthroplasty.

Introduction: Staphylococcal bacteria, especially the coagulase negative Staphylococci, are responsible for the majority of orthopaedic device related infection. These infections are sub acute, and may not present for months or years following surgery. The virulence of these bacteria is related to their ability to form biofilm, a protective slime which allows them to survive the effects of the host immune system and antimicrobial therapy. Treatment of biofilm based infection almost always necessitates removal of the implant.

Recent work has identified environmental stimuli which induce biofilm formation in Staphylococci. These include stressors such as high temperature, high osmolarity, anaerobiosis, nutrient depletion, salt, ethanol and subinhibitory concentrations of certain antimicrobial drugs. Given the ability of these bacteria to survive the “respiratory burst” from the cells of the mononuclear-macrophage system, we hypothesised that oxidative stress may be one such promoter of biofilm formation by Staphylococci.

Methods and Materials: Staphylococcus epidermidis CSF41498 and Staphylococcus aureus RN422O were selected for study as these are known biofilm forming organisms. Hydrogen peroxide (H₂O₂) was used as an oxidizing agent.

Bacteria were incubated for 24 hours at 37°C in Brain-Heart Infusion (BHI, Oxoid) containing progressively weaker concentrations of H₂O₂ to determine a Minimal Inhibitory Concentration (M.I.C.) for the representative strains. Bacterial viability was assessed by measuring the optical density of the incubated culture using a cell density meter (Ultraspec 10, Amersham Biosciences).

The bacteria were then grown as a biofilm on a 96 well microtitre plate (Nunc) in the presence of subinhibitory concentrations of H₂O₂, using pure BHI as a control. Semiquantative determination of biofilm formation was performed by washing the plates, staining the adherent cells with crystal violet, and measuring the light absorbance of the adherent stained cells at 492 nm using a Multiskan plate reader (Flow Laboratories).

Results: The M.I.C. of H₂O₂ was 18 mM for both Staphylococcus epidermidis CSF41498 and Staphylococcus aureus RN422O. Concentrations of H₂O₂ of 16 mM and below had no normal bacterial growth and replication.

There was no difference in biofilm formation by Staphylococcus epidermidis csf41498 in the presence of 15 mM H₂O₂ when compared to that of the control. However, H₂O₂ had a significant inhibitory effect on biofilm formation by Staphylococcus aureus RN422O, even at a concentration well below the M.I.C.

Conclusion: We conclude that oxidative stress may have an antibiofilm action on certain Staphylococcal species, which is independent from its bactericidal effect, and which is manifest at a concentration below the M.I.C. for that species.