Contemporary acetabular reconstruction in major acetabular bone loss often involves the use of porous metal augments, a cup-cage construct or custom implant. The aims of this study were: To determine the reproducibility of a reconstruction algorithm in major acetabular bone loss. To determine the subsequent success of reconstruction performed in terms of re-operation, all-cause revision and Oxford Hip Score (OHS) and to further define the indications for custom implants in major acetabular bone loss.

Consecutive series of Paprosky Type III defects treated according to a reconstruction algorithm. IIIA defects were planned to use a superior augment and hemispherical cup.

IIIB defects were planned to receive either augment and cup, cup-cage or custom implant.

105 procedures in cohort 100 patients (5 bilateral) with mean age 73 years (42–94).

IIIA defects (50 cases) − 72.0% (95%CI 57.6–82.1) required a porous metal augment the remainder treated with a hemispherical cup alone. IIIB defects (55 cases) 71.7% (95%CI 57.6–82.1) required either augments or cup-cage. 20 patients required a hemispherical cup alone and 6 patients received a custom-made implant.

Mean follow up of 7.6 years. 6 re-revisions were required (4 PJI, 2 peri-prosthetic fractures & 1 recurrent instability) with overall survivorship of 94.3% (95% CI 97.4–88.1) for all cause revision. Single event dislocations occurred in 3 other patients so overall dislocation rate 3.8%. Mean pre-op OHS 13.8 and mean follow-up OHS 29.8.

Custom implants were used in: Mega-defects where AP diameter >80mm, complex discontinuity and massive bone loss in a small pelvis (i.e., unable to perform cup-cage)

A reconstruction algorithm can >70% successfully predict revision construct which thereafter is durable with a low risk of re-operation. Jumbo cup utilized <1/3 of cases when morphology allowed. The use of custom implants has been well defined in this series and accounts for <5% of cases.

Hypochlorous acid (HOCl) is a potent anti-bacterial agent which could reduce periprosthetic joint infection. Early infection complications in joint replacements are often considered to be due to local contamination at the time of surgery and result in a significant socioeconomic cost. Current theatre cleaning procedures produce “clean” operating theatres which still contain bacteria (colony forming units, CFU). Reducing this bacterial load may reduce local contamination at the time of surgery. HOCl is produced naturally in the human neutrophil and has been implicated as the primary agent involved in bacterial killing during this process. In vitro research confirms its efficacy against essentially all clinically relevant bacteria. The recent advent of commercial production of HOCl, delivered as a fog, has resulted in extensive use in the food industry. Reported lack of corrosion and high anti-bacterial potency are seen as two key factors for the use of HOCl in the orthopaedic environment. Prior work by the authors comparing human cell toxicity of HOCl, chlorhexidine and iodine solutions shows favourable results.

This study evaluates use of neutral HOCl applied as a dry room fog to decrease bacteria in the operating theatre environment. Using an animal operating theatre as the test site, bacterial swabs were taken from ten 100cm² sample areas before standard cleaning with detergent, after standard cleaning, and again after 60 minutes exposure to HOCl fog.

After standard cleaning, 6 of 10 sample sites recorded significant bacterial growth (>10 CFU/100cm²). After exposure to HOCl fog, growth in all 10 sites was below detection limits (<10 CFU/100cm²). This was repeated with specific exposure to Staphylococcus aureus and Escherichia coli.

We can conclude that HOCl is effective when used as a fogging agent to reduce bacterial loading within an operating theatre environment and as such has significant potential to reduce intraoperative contamination and periprosthetic infection.

Aim

To review the outcome of deep prosthetic infection in patients following hip hemiarthroplasty surgery.

Purpose of Study: This study was done to assess the efficacy of EQ5D (EuroQol), a simple quality of life (QOL) score. The study was designed to test the feasibility and reliability of using this simple QOL score alongside Constant score following arthroscopic shoulder surgery. Though Constant score gives a shoulder related outcome it does not provide a patient perspective of outcome in relation to their quality of life.

Methodology: A prospective cohort study of 100 consecutive patients listed for arthroscopic shoulder surgery between May and December 2005 were recruited. Assessments were undertaken both preoperatively and at 6 months post operatively. EuroQol is a simple 5 question self administered questionnaire and the Constant score was recorded by the treating physician who was blinded to the result of the EuroQol. Data was assessed for normality and non parametric tests were used. Statistical significance was assumed at the p< 0.05 level.

Results: The median age of 54 years (32 to 79). 60% were male. The median pre operative EuroQol score was 0.26 with a median post operative score of 0.71. Preoperatively, the median constant score was 31.0 with a postoperative score of 72.0 The difference between pre and post operative scores in both the EuroQol and Constant scores was shown to be statistically significant (p< 0.0001 in each group). In the 200 paired observations the two scores were also shown to be closely correlated RS statistic 0.71 (p< 0.0001).

Conclusion: EQ5D is easily completed by the patient by a self administered questionnaire and reflects the quality of life improvement attained after shoulder surgery. It is very easy to use compared to other available QOL scores like SF12, SF36. We recommend its routine usage along with Constant Shoulder score as there is a strong positive correlation.

Surgical options in the treatment of acute acromio-clavicular joint (Rockwood Type III and IV) dislocations are many and controversial. We evaluated our technique using TIGHTROPE connecting the base of the coracoid to the proximal fragment of the clavicle. Between March 2006 and December 2006, ten young and active adult patients with acute ACJ dislocations were treated with arthroscopically assisted ARTHREX TIGHTROPE fixation. The dislocation was reduced with traction and manual reduction with the patient in beach-chair position. The base of the coracoid was identified and isolated using a radiofrequency ablator placed through the anterior portal while visualizing through the lateral portal. An ACL guide was placed percutaneously supero-medial to the coracoid over the distal with the inferior end of the ACL guide placed through a posterior portal, approximated against the prepared base of the coracoid. The Arthrex Tightrope braided fibre-wire was introduced through the pre-drilled distal clavicle passed to the base of the coracoid and manually tensioned to achieve stable reduction. Standard rehabilitation protocol was utilised as for internal fixation of distal clavicular fractures. Patients were evaluated clinically using Constant Score, which ranged from 75 to 83 and radiologically at 6 weeks and 3 months. We present the functional results and the technical difficulties faced highlighting on the probable reasons for failure of fixation in two of our early patients who had revision fixations. We also describe the additional intra-operative techniques used in the last few patients to prevent such complications and achieve a secure reduction. We conclude that Arthroscopic Reconstruction of dislocated Acromio-Clavicular joint using TIGHTROPE may require additional repair of the ligaments in carefully selected patients to prevent failure of fixation.

Aim: The purpose of this study was to assess the various subtrochanteric fracture classification systems particularly in relation to their predictive value for choice of treatment and outcome.

Methods: A comprehensive search of various data sources extending from 1966 to October 2003 was conducted to identify appropriate studies using specific search terms. Articles of all languages were considered. From these articles and those referenced within them, the use of, and any description of fracture classifications were recorded. Abstracts and studies reporting on less than ten fractures were excluded. A methodological scoring system adapted from that of Detsky was used to assess the quality of studies. For each classification system, features such as proximal and distal margin of subtrochanteric fractures, number of subdivisions, advice for fractures which cross the described anatomical boundaries, number of publications using that classification system, published articles showing value in predicting outcome and published articles showing inter-observer variation were analysed.

Results: 110 studies involving 2725 fractures were identified. 16 different classification methods were analysed. The actual length of femur defined as the subtrochanteric zone varied from 3 cms to12 cms. There was no agreement between the different classifications regarding the proximal and distal borders, or for classifying fractures that traverse anatomical boundaries. None of the classifications systems was shown to be of value in determining treatment or for predicting outcome.

Conclusion: There is a need for a universally accepted definition for subtrochanteric fractures and sub-classifying such fractures is questionable. Indicators to a simple yet valid classification system which takes into account the variations of this fracture and which would assist in determination of treatment and prediction of outcome are proposed.