Purpose: Use of six-axis analysis and computer assisted deformity correction via a circular external fixator is a new method for deformity correction. We investigated its accuracy and safety in reconstruction of femoral deformity in children and young adults.

Method: We retrospectively reviewed all cases including the indications for use and the methodology of application of the computer assisted six-axis analysis and circular external fixator for reconstruction of 22 femora in 20 patients. Twelve patients were female, and 8 were male. The average age was 13.9 (range, 5.9–24.6). Etiology included traumatic (7), idiopathic (6), multiple enchondromatosis (2), rickets (2), congenital femoral deficiency (2), spondyloepiphyseal dysplasia (1), congenital pseudohypoparathyroidisim (1), and multifocal osteomyelitis (1). Clinical and radiographic data were analyzed.

Results: Average follow-up was 14.4 months (range, 4.5–32). Average time in frame was 6.2 months (range, 2.6–19). Bone lengthening of 3.9 cm (range, 1–8.5) was performed in 12 femora. In genu valgum patients, the mLDFA improved from a mean of 73.7° to a mean of 89°. In genu varum patients, the mLDFA improved from a mean of 99.8° to a mean of 89.5°. Complications included pin tract infection in 6, knee stiffness in 3, delayed union in 2, skin irritation in 1, posterior knee subluxation in 2, both of which had stable knees preoperatively. One patient was lost to follow-up and returned back with deformity. No complications occurred in 8 patients.

Conclusion: Computer assisted femoral deformity correction with six-axis analysis and application of circular external fixator is a useful technique with the advantage of managing multiplanar deformities in children and young adults. It has the potential complications of the use of any external fixator. Close follow-up is necessary to avoid subluxation of the knee joint even in patients with stable knees. Accurate and safe correction can be achieved in almost all patients.

We suggested a new concept of buffered implant fixation. It is a cementless fixation using a buffer instead of the cement between the bone and the implant. We investigated the feasibility of the buffered implant fixation using a rat model. In our previous study, we measured the amount of bone around the implant to compare the buffered implant fixation with the cemented fixation. The results showed the difference in change of Bone Volume/Total Volume (BV/TV) with time between the buffered fixation and the cemented fixation. Now, in this study, we are comparing the mechanical interface strength between two fixations.

After micro CT scanning, the specimens were used for mechanical push-out test to measure the interface shear strength at the buffer-bone or cement-bone interface. The distal side of the femur was carefully removed to expose the whole distal region of the implant while the proximal side of femur was cut carefully with diamond saw (Metsaw, R& B Inc., Korea) until the proximal end of cement or buffer is exposed. The femur was embedded into a push-out jig with a plaster. The push-out jig was mounted in a material testing machine (KSU-10M, Kyungsung testing machine, Korea) and loaded at a rate of 0.01mm/s. The apparent interface strength was calculated by dividing the peak force by the surface area of the buffer or cement.

After 2 weeks, the apparent interface strength is 217.0 ± 280.0(average ± standard deviation) for buffer and 472.4 ± 381.1 for cement; after 4 weeks, 92.9 ± 67.6 and 268.1 ± 197.9; after 12 weeks, 441.9 ± 467.1 and 201.8 ± 132.3, respectively. The buffered fixation showed gain in strength with time while the cemented fixation showed reverse tendency but the interaction by ANOVA was not significant (p=0.125). Even though the excellence of buffer fixation was not clearly confirmed because of small sample size and high variance, the feasibility of the buffer fixation was shown.

However, further studies are necessary to improve the buffered implant fixation. To enhance the cell adhesion and biocompatibility, it is necessary to modify the surface of polyetheretherketone (PEEK) such as by plasma treatment or biological coating. Also, an animal test using a higher level animal such as dog or pig is necessary.

Purpose: Waterproof casts have been shown to be a safe and effective means of immobilization in children with minimally displaced fractures. The purpose of this study was to determine if waterproof Gore-Tex-lined casts are as effective as traditional cotton-lined casts in the immediate postoperative period after closed reduction of displaced distal radius fractures in children.

Method: We performed a retrospective review of distal radius fractures that underwent closed reduction and application of a long-arm cast between June 2004 and December 2006. A total of 124 cases were included (55 Gore-Tex; 69 traditional cotton-lined). The primary outcome measure was redisplacement in the cast. The cast index was also used to assess the quality of cast molding. Data was analyzed using repeated measures ANOVA. Power analyses were also conducted.

Results: There were no significant differences between the two groups with regards to translation of the radius or angulation of the radius on anterior-posterior (AP) and lateral radiographs at the time of injury, postreduction, or cast removal. Redisplacement as measured by the change in translation of the radius and angulation of the radius on AP and lateral radiographs from the time of reduction to cast removal was also not significantly different between the two groups. The mean cast index for the Gore-Tex and traditional cotton-lined groups was 0.882 and 0.873 respectively, which was not a significant difference.

Conclusion: A waterproof Gore-Tex-lined cast will maintain fracture reduction as well as a cotton-lined cast for closed reductions of distal radius fractures in children in the immediate postreduction period. Waterproof casts also provide extensive benefits to the patient with regards to bathing, hygiene, and participation in aquatic activities

Spontaneous osteonecrosis of the knee (SPONK) usually involves a single condyle or plateau. The medial femoral condyle is most often involved and spontaneous osteonecrosis of medial tibial plateau is a rare condition, representing only 2 % of all necrosis reported in the knee. Therefore, SPONK with both involvement of medial femoral condyle(MFC) and medial tibial plateau(MTP) might be extremely rare. SPONK in each MFC or MTP respectively might be extended into corresponding side of the knee at their advanced final stage, howevere, in that situations, significant degenerative change would accompany and it might be difficult to differentiate final staged SPONK form severe osteoarthritis. To the best of our knowledge, SPONK affecting both medial femoral condyle and medial tibial plateau without significant secondary osteoarthritis changes is not reported, even though it was difficult to know which occurred first. We experienced 3 patients with histologically proven osteonecrosis of the medial tibial condyle and medial tibial plateau, and report their radiologic features. All 3 patients showed similar ridiograhic patterns. Medial portion of medial tibial plateau and lateral portion of medial femoral condyle showed longitudinal fracture like-subchondral collapse. Standing anteroposterior radiograph at 30 degree knee flexion showed well fitted features such as “locked” medial condyle. Varus angulation was present. Significant degenerative changes was not shown except for subchondral sclerosis. T1-weighted coronal and Fat suppressed T2-weighted MR images showed subchondral collapse with ill-defined diffuse bone marrow edema changes on both tibial and femoral condyles. At surgical findings, longitudinal track-like groove was shown in both medial femoral condyle and medial tibial plateau. Articular cartilage was denuded and showed glistening surface with bone defect of lateral side of medial femoral condyle and medial side of tibial articular surface. Histological analysis shows necrotic bone, surrounded by an area of fibrovascular granulation tissue on both femoral and tibial sides. Total knee arthoplasty was performed in all 3 patients. As a result of very low prevalence of both involvement of MFC and MTP and limited number of our cases, we could not conclude that radiologic features in our cases are typical radiologic pattern of both involvement. However, based on our cases, we believe that this characteristic radiologic features may considered as one of the possible various radiologic findings of simultaneous involvement in MFC and MTP and allow diagnosis for SPONK with both involvement in MFC and MTP to be facilitated.

Purpose: Porous tantalum has been shown to be very effective in achieving bone ingrowth. However, in some circumstances, bone quality or quantity is insufficient to allow adequate bone ingrowth. We hypothesized that the addition of alendronate to porous tantalum would enhance the ability of porous tantalum to achieve bone ingrowth in these challenging situations, such as when a gap exists between the implant and bone. We evaluated the effect of alendronate coated porous tantalum on new bone formation in an animal model incorporating a gap between implant and bone.

Method: Thirty-six cylindrical porous tantalum implants were bilaterally implanted into the distal femur of 18 rabbits for 4 weeks. There were 3 groups of implants inserted; a control group of porous tantalum with no coatings, porous tantalum with micro-porous calcium phosphate coating, and porous tantalum coated with micro-porous calcium phosphate and alendronate. Subcutaneous fluorescent labeling was used to track new bone formation. Bone formation was analyzed by backscattered electron microscopy and fluorescent microscopy on undecalcified samples.

Results: The relative increase in mean volume of gap filling, bone ingrowth and total bone formation was 143% (p< 0.001), 259% (p< 0.001) and 193% (p< 0.001) respectively in the alendronate coated porous tantalum compared with the uncoated porous tantalum controls. The relative increase in the percentage of new bone-implant contact length was increased by 804% on average in the alendronate coated porous tantalum compared with the uncoated tantalum controls.

Conclusion: This study demonstrated the significant enhancement of bone-implant gap filling and bone ingrowth which can be achieved by coating porous tantalum with alendronate. It is proposed that, when faced with the clinical problem of revision joint replacement in the face of bone loss (at the hip, knee or elsewhere), the addition of an alendronate-delivery surface coating would enhance biological fixation of the implant and promote the healing of bone defects.

The cemented and cementless implant fixations are popular in orthopaedic arthroplasty. However, these implant fixations have some problems such as cement failure, wear debris, stress shielding, revision and so on. To overcome these problems, we are developing a new concept of buffered implant fixation which uses a bone-friendly buffer between the implant and the bone. In this study, we performed a finite element analysis to evaluate the buffered implant fixation in comparison with cemented and cementless implant fixations in mechanical aspects. In addition, we investigated the effect of buffer taper angle to the stress distribution in the buffered implant fixation.

Three-dimensional FEA of the cemented, cementless and buffered fixation were performed using the ABAQUS program. In these FEA, the ‘standardized femur’, which is the composite femur model supplied by Pacific Research Lab., was used as the bone model and the CPT stem and the Versys Fibermetal Midcoat stem were modeled for the cemented fixation and the cementless fixation, respectively. These three-dimensional models were meshed using the tetrahedral elements with 4 nodes (C3D4) and the additional contact definitions. The buffered implant fixation is similar with the polished cemented fixation except the material between the implant and the bone. The polyetheretherketone (PEEK) was selected as the buffer material. Also, several taper angles of buffer were simulated to change the stress distributions in the buffered fixation. The external load three times of mean body weight (74.3 kg) was cyclically loaded at the femoral head with the angle of 20° in adduction and 6° in flexion while the distal end of femur was fixed.

In the buffered implant fixation, the taper-locked effects were observed. The buffered fixation had greater cyclic compression for the bone compared to the cemented fixation. Also, the failure probability of the buffer in the buffered fixation was less than that of the cement in the cemented fixation. The risk factors in the buffer were 0.148 for the tension and 0.176 for the compression while, the risk factors of cement in the polished cemented implant fixation were over than 1. Moreover, the buffered fixation had widely distributed compression compared to the cementless fixation and the stress distribution could be modified easily to change the taper angle of buffer. The FEA results showed that the buffered implant fixation would provide an appropriate mechanical environment.

The anterior pelvic plane has been introduced as a concept of the reference plane to image free navigation-assisted cup placement of total hip arthroplasty. With the neutral pelvis, the anteversion relative to the conventional coordinate system is equal to the that of relation to the anatomical coordinate system. This is the rationale of image free navigation system. But, currently, two major concerns about image-free navigation assisted total hip arthroplasty are tilting of anatomic coordinate system and the cutaneous palpation procedure. Therefore, it was the goal of this study to provide both the bone anterior pelvic plane (Bone_APP) and the overlying soft tissue plane (Soft_APP) simultaneously, and to find possible correlations of biometrical parameters and effect of ante-version were an additional motivation of this study. 23 Korean adult patients underwent image-free navigation-assisted total hip arthroplasty. The tilting of Bone_APP, soft tissue thickness on ASIS, pubis, and then tilting of Soft_APP, and anteversion of cup were measured with reconstructed CT and 3D workstation system.

The average age was 66.1 years, the average height was 162.5cm at a weight of 59.2 kg. The average body mass index was 22.3. And the average lumbar lordosis was measured as 30.4 degrees. The soft tissue on the level of the pubis was 17.6 mm thicker than that on the level of ASIS in average. In all cases, Soft_APP was positive, that is from 3.5 to 16.5 degrees of backward rotation. We also found a high-intersubject variability in the Bone_APP from 13.4 of forward rotatation to 23 degrees of backward rotation. Overall, there are no correlation between biometrical parameters and difference of navigated data to others measured on CT. Averaged navigated data was 22.4 degrees. The average anatomic, operative, and planar anteversion were 29.2, 27.2 and 21.3 degrees respectively. The value of anteversion measured on the transverse plane and sagittal plane shows higher than navigated anteversion in paired comparison. This could be comprehended that the navigation system had under-estimated the anteversion than that of transverse and sagittal plane, This means navigation assessed pelvic plane as back ward tilting rather than forward tilting intraoperatively.

None of cases showed the Bone_APP was parallel to conventional coordinate system. Comparing the variable bone APP tilt, all of cases showed an backward tilted soft tissue plane. There were no correlation between bone APP and biometrical parameters. Overall, navigated data were less than anatomic and operative anteversion. Rather than anatomic coordinate system (Bone-APP), backward tilting due to overlying soft tissue (Soft-APP) might to make the navigated data have the tendency to under-estimated the anteversion of cup measured with CT. In conclusion, anterior pelvic plane does not satisfactory reliability with should be easily identified during operation. Image-free navigation system would take into account variations of individuals including both bone tilt and soft tissue plane.

Introduction and Objectives: We analyzed the physical and health status of patients with ankle arthritis that underwent arthrodesis or total ankle replacement and determined which alternative provided a greater perception of improvement in quality of life and whether there was any difference in the perception of the patients that underwent either of these two procedures.

Materials and Methods: This is a comparative-prospective study in patients that underwent arthrodesis (16 cases) or total ankle replacement (14 cases) in which clinical-functional variables were assessed by means of the AOFAS score and quality of life was measured using SF-36 at 2 years of follow-up and this was compared with preoperative assessment.

Results: The study was carried out with 2 series of comparable patients, both surgical techniques showed a statistically significant improvement on clinical assessment and on quality of life assessment in comparison with preoperative status after 2 years of follow-up. The group of patients that underwent arthrodesis changed from mid-range AOFAS values of 37.12 to 45.62 (p=0.055) and mid-range SF-36 values of 32.96 to 46.25 (p=0.008). The group that underwent arthroplasties changed from mid-range AOFAS values of 33 to 62 (p=0.024) and mid-range SF-36 values of 33.62 to 59.84 (p=0.001). The improvement was statistically greater in the group that underwent arthroplasties than in the group that underwent arthrodesis (p=0.48 for AOFAS, and p=0.026 for SF-36)

Discussion and Conclusions: Both procedures are good treatment options, they ‘significantly improve patient’s status both clinically and in their perception of their health and quality of life. The medium term perception of quality of life and general health on the part of patients with ankle arthritis is better when they undergo ankle arthroplasty than when they undergo surgical fusion.

We report the outcome at ten to 15 years of two-stage revision for hip infection in 99 patients using the Prostalac articulated hip spacer system.

All the patients were contacted to determine their current functional and infection status using the Oxford-12, Short form-12, and Western Ontario and McMaster University Osteoarthritis Index questionnaires. A total of 11 of the 99 patients had a further infection, of whom seven responded to repeat surgery with no further sequelae. The mean interval between the stages was five months (1 to 36). We were able to review 48 living patients, with a mean age of 72 years (46 to 86), 34 (71%) of whom provided health-related quality-of-life outcome scores.

The mean follow-up was 12 years (10 to 15). The long-term success rate was 89% and with additional surgery this rose to 96%. The mean global Western Ontario and McMaster University Osteoarthritis Index score was 80.6 (sd 18.3). The mean Oxford-12 score was 74.0 (sd 22.3), and the mean Short form-12 score was 53.1 (sd 9.4) (mental) and 33.5 (sd 13.5) (physical). The mean satisfaction score was 90.5 (sd 15.3).

Two-stage revision for hip infection using a Prostalac interim spacer offers a predictable and lasting solution for patients with this difficult problem.

There is an ever-increasing clinical need for the regeneration and replacement of tissue to replace soft tissue lost due to trauma, disease and cosmetic surgery. A potential alternative to the current treatment modalities is the use of tissue engineering applications using mesenchymal stem cells that have been identified in many tissue including the infrapatellar fat pad. In this study, stem cells isolated from the infrapatellar fat pad were characterised to ascertain their origin, and allowed to undergo adipogenic differentiation to confirm multilineage differentiation potential.

The infrapatellar fat pad was obtained from total knee replacement for osteoarthritis. Cells were isolated and expanded in monolayer culture. Cells at passage 2 stained strongly for CD13, CD29, CD44, CD90 and CD105 (mesenchymal stem cell markers). The cells stained poorly for LNGFR and STRO1 (markers for freshly isolated bone marrow derived stem cells), and sparsely for 3G5 (pericyte marker). Staining for CD34 (haematopoetic marker) and CD56 (neural and myogenic lineage marker) was negative.

For adipogenic differentiation, cells were cultured in adipogenic inducing medium consisting of basic medium with 10ug/ml insulin, 1uM dexamthasone, 100uM indomethacin and 500uM 3-isobutyl-1-methyl xanthine. By day 16, many cells had lipid vacuoles occupying most of the cytoplasm. On gene expression analyses, the cells cultured under adipogenic conditions had almost a 1,000 fold increase in expression of peroxisome proliferator-activated receptor gamma-2 (PPAR gamma-2) and 1,000,000 fold increase in expression of lipoprotein lipase (LPL). Oil red O staining confirmed the adipogenic nature of the observed vacuoles and showed failure of staining in control cells.

Our results show that the human infrapatellar fat pad is a viable potential autogeneic source for mesenchymal stem cells capable of adipogenic differentiation as well as previously documented ostegenic and chondrogenic differentiation. This cell source has potential use in tissue engineering applications.

Purpose of Study: We aimed to reduce the work intensity involved in auditing high volume procedures (eg knee arthroscopy) by developing and validating a tool which uses routinely acquired hospital data, to target those patients most likely to have developed an undesirable post-operative outcome.

Methodology: The work was a collaboration effort between the Orthopaedic and Clinical Effectiveness departments. During the period 1997–2003, 2926 elective knee arthroscopies were identified as having been performed in our unit. Linkage of routinely collected data held on the hospital’s computerized Patient Administrative System (PAS), hospital theatre system and A& E system, with data from the Office of National Statistics concerning death, high-lighted 183 cases (Core group) meeting one or more of four indicators: readmission < 28 days, return to theatre < 28 days, return to A& E < 28 days, and length of stay 4+ days (Graph 1). The accuracy of the tool to identify undesirable post-operative outcomes was made comparing the Core group and a Random sample (N=240).

Results: Accuracy of OPCS-4 coding for arthroscopic procedure performed was 77.1% in the core group and 96.4% in the random sample. The new tool yielded a sensitivity of 38% and specificity of 95%. Where major complications were concerned the sensitivity rose to 100%. For major complications the proposed model indicated a 0.6% complication rate vs 0.5% actual rate. For minor complications the proposed model indicated a 1.4% rate vs 3.8% actual rate. Overall complication rate within our unit was comparable to the published literature.

Conclusion: The tool has achieved its aim of identifying all major complications and undesirable events, along with many minor complications. As the tool identifies additional information it must be used as an aid to identifying patients for case note review. However, in our study it reduced the number needed to less than 7% of the total.

Fractures of the odontoid in children with an open basilar synchondrosis differ from those which occur in older children and adults. We have reviewed the morphology of these fractures and present a classification system for them.

There were four distinct patterns of fracture (types IA to IC and type II) which were distinguished by the site of the fracture, the degree of displacement and the presence or absence of atlantoaxial dislocation. Children with a closed synchondrosis were classified using the system devised by Anderson and D’Alonzo. Those with an open synchondrosis had a comparatively lower incidence of traumatic brain injury, a higher rate of missed diagnosis and a shorter mean stay in hospital. Certain subtypes (type IA and type II) are likely to be missed on plain radiographs and therefore more advanced imaging is recommended. We suggest staged treatment with initial stabilisation in a Halo body jacket and early fusion for those with unstable injuries, severe displacement or neurological involvement.

Rotator cuff tears are a common cause of shoulder pain and dysfunction. Therefore, the purpose of this in-vitro biomechanical study was conducted to determine the effects of simulated tears and subsequent repairs of the rotator cuff tendons on joint kinematics.

Eight paired fresh-frozen cadaveric shoulder specimens (mean age: 66.0 ± 8.7 years) were tested using a custom loading apparatus designed to simulate unconstrained motion of the humerus. Cables were sutured to the rotator cuff tendons and the deltoid. Loads were applied to the cables based on variable ratios of electromyographic (EMG) data and average physiological cross-sectional area (pCSA) of the muscles. An electromagnetic tracking device (Flock of Birds, Ascension Technologies, VT) was used to provide real-time feedback of abduction angle, to which the loading ratio was varied correspondingly. 2 and 4cm tears were made starting at the rotator cuff interval and extending posteriorly. Specimens were randomised to receive either single or double suture anchor repair. In order to quantify repeatability, five successive tests on each of the intact, torn, and repaired cases were performed. Statistical significance was established using One- and Two-way Repeated Measured ANOVAs (p< 0.05).

Rotator cuff tears caused alteration in glenohumeral kinematics. A 2cm tear caused the humerus to consistently move posterior through the arc of abduction; however, as the tear increased to 4cm the humerus moved anteriorly, returning towards the intact state. Double row suture anchor repairs more accurately reproduced the kinematics of the intact specimen compared to single row suture anchor repair.

The initial posterior displacement in the plane of elevation with the sectioning of the supraspinatus is related to the diminished anterior moment on the glenohumeral joint. As the tear proceeds into the infraspinatus, the anterior and posterior forces become more balanced and a return to near normal intact kinematics was observed. This study demonstrates that double row suture anchor repair more accurately reproduces active shoulder kinematics of the intact shoulder specimens.

This study compared the effect of a computer-assisted and a traditional surgical technique on the kinematics of the glenohumeral joint during passive abduction after hemiarthroplasty of the shoulder for the treatment of fractures. We used seven pairs of fresh-frozen cadaver shoulders to create simulated four-part fractures of the proximal humerus, which were then reconstructed with hemiarthroplasty and reattachment of the tuberosities. The specimens were randomised, so that one from each pair was repaired using the computer-assisted technique, whereas a traditional hemiarthroplasty without navigation was performed in the contralateral shoulder. Kinematic data were obtained using an electromagnetic tracking device.

The traditional technique resulted in posterior and inferior translation of the humeral head. No statistical differences were observed before or after computer-assisted surgery.

Although it requires further improvement, the computer-assisted approach appears to allow glenohumeral kinematics to more closely replicate those of the native joint, potentially improving the function of the shoulder and extending the longevity of the prosthesis.

Purpose: To investigate the potential value of titanium anterior interbody cages compared to morselized rib graft for anterior interbody fusion in combination with posterior instrumentation, correction and fusion for Scheuermann’s kyphosis.

Methods and Materials: A Non-Randomised historic cohort study of two surgical techniques in matched subjects was carried out.15 patients with identical pre-operative radiographic and physical variables (age, gender, height, weight, BMI ) were managed with combined anterior release, interbody fusion, posterior instrumentation, correction and fusion . Group A (n=8) had morsilized rib graft inserted into each intervertebral disc space. Group B (n=7) had titanium interbody cages packed with bone graft inserted at each level. The posterior instrumentation extended from T2 to L2 in both groups. Pre- and post-operative curve morphometry was studied on plain radiographs by two independent observers. The indices studied included Cobb angle, Ferguson’s angle(FA) , Voutsinas index(VI), Sagittal Vertical Axis (SVA), Sacral Inclination (SI) and Lumbar Lordosis (LL). Interbody Fusion was assessed at final follow up. Each patient was reviewed at 3, 6, 12, 24, 48 and 60 months following surgery with standing radiographs. Wilcoxon-matched pairs test and Mann-Whit-ney test were used for statistical analysis.

Results: The average follow-up for groups A was 70 and Group B,66 months. For the whole group, the pre-operative : postoperative median Cobb angle, FA, VI, SVA and SI were 86: 42degrees, 50 : 28.4degrees, 28.7 :13, −3.5 : −4.0 centimetres and 40 : 34 degrees respectively. There were significant differences for all variables [p< 0.01] indicating good correction. At four-year follow-up, fusion criteria were satisfied in 12 / 15 cases (80%). Three patients had distal junctional kyphosis. There was no significant difference with respect to the variables between the two groups and both retained the post-operative correction achieved.

Conclusion: There was no significant advantage in the use of anterior titanium interbody cages over the use of morselized rib graft in the surgical management of Scheuermann’s Kyphosis.

Purpose: To identify patients in whom anterior scoliosis correction was not possible and to determine pre-operative factors that may predict such an outcome.

Methods: From 1999–2005, 257 patients were listed for anterior correction with the Kaneda Anterior Spine System (KASS). Of these 246 were completed successfully. However in 11 cases it was not possible to complete the procedure.

We performed a retrospective review of case notes and X-rays. A control group of 22 patients, in whom anterior surgery was completed, matched to age, sex and type of curve, was used.

Results: Two reasons for abandoning anterior instrumentation were identified; loss of cord signal (7) and failure to achieve adequate correction after anterior release and reduction (4).

Of the seven patients with lost signal three were syndromic and four were associated with syrinx. In all seven, loss of signal occurred on clamping of segmental vessels. All seven had no residual neurological deficit post-operatively and had uncomplicated posterior correction the following week.

All four patients in whom inadequate correction was achieved after anterior release and repositioning had idiopathic curves. Of these two were thoracic and two were thoracolumbar. Mean pre-operative Cobb angle was 67 (range 59–85) compared to a mean of 56 (range 42–68) in the control group. Mean pre-operative stiffness index was 91% (range 85%–100%) compared to a mean stiffness index of 65% (range 53–80) in the control population.

Conclusion: Whilst a successful outcome is achieved in a majority of KASS instrumentations we have identified two reasons why anterior surgery has to be abandoned. Whilst one often cannot pre-operatively anticipate intra-operative loss of cord signal, we found that in cases with an underlying syrinx there is a particular risk of this occurrence. Our experience has shown particularly stiff curves (Stiffness index ≥ 85%) may not be suitable for stand-alone anterior surgery.

Introduction: There has been an increasing use of orthotic knee braces in the management of knee injuries. To ensure the biomechanics of the knee are not adversely affected, it is important that orthotic knee braces accurately provide the desired angle of immobilisation. The objective of our study was to measure the actual knee flexion angles for a lockable orthotic knee brace, and measure the resulting knee flexion moment.

Materials and methods: Eight healthy male volunteers participated in the study looking at six different types of knee immobilisation: locked in 0, 10, 20, 30 degrees of knee flexion, with the brace unlocked, and without a brace. Force and 3-dimensional motion data were collected using a single Kistler force plate and an eight-camera Qualisys ProReflex motion analysis system.

Results: The kinematic knee flexion angles were significantly different when compared with the angles set at the orthotic knee brace for 0 degrees (p=0.001) and 10 degrees (p=0.011). The kinematic knee flexion angle when no brace was used was significantly different from the angle for the unlocked orthotic knee brace (p= 0.003). The knee flexion moment was directly proportional to the knee flexion angle. There was a statistically significant difference between the knee flexion moment for the six types of immobilisation (p< 0.001).

Discussion: The knee flexion angles measured using the kinematic data did not always correspond with the angle set at the orthotic knee brace. These findings highlight inadequacies in the design of lockable orthotic knee braces, especially at low flexion angles of 0 and 10 degrees. The resulting higher actual knee flexion angles were associated with greater knee flexion moments and joint reaction forces at the tibiofemoral and patellofemoral joints. This can, at best result in increased energy expenditure and decreased agility, and at worse potentially augment injuries to the knee.

Introduction: Achieving durable implant–host bone fixation is the major challenge in uncemented revision hip arthroplasty when significant bone stock deficiencies are encountered. The purpose of this study was 1) to develop an experimental model which would simulate the clinical revision hip scenario and 2) determine the effects of alendronate coating on porous tantalum on gap filling and bone ingrowth in the experimental model.

Methods: Thirty-six porous tantalum plugs were implanted into the distal femur, bilaterally of 18 rabbits for four weeks. There were 3 groups of plugs inserted; control groups of porous tantalum plugs (Ta) with no coating, a 2^nd control group of porous tantalum plugs with micro-porous calcium phosphate coating, (Ta-CaP) and porous tantalum plugs coated with alendronate (Ta-CaP-ALN). Subcutaneous fluorochrome labelling was used to track new bone formation. Bone formation was analysed by backscattered electron microscopy and fluorescence microscopy on undecalcified histological sections.

Results: The relative increase in mean volume of gap filling, bone ingrowth and total bone formation was 124 %, 232 % and 170 % respectively in Ta-CaP-ALN compared with the uncoated porous tantalum (Ta) controls, which was statistically significant. The contact length of new bone formation on porous tantalum implants in Ta-CaP-ALN was increased by 700% (8-fold) on average compared with the uncoated porous tantalum (Ta) controls.

Discussion: Alendronate coated porous tantalum significantly modulated implant bioactivity compared with controls. This study has demonstrated the significant enhancement of bone-implant gap filling and bone ingrowth, which can be achieved by coating porous tantalum with alendronate. It is proposed that, when faced with the clinical problem of revision joint replacement in the face of bone loss, the addition of alendronate as a surface coating would enhance biological fixation of the implant and promote the healing of bone defects.