Purpose: Evaluation of a hands free crutch. This interesting device is intended for patients who have undergone foot and ankle surgery and should be non-weight bearing. It involves a knee tray attached to a vertical beam with a rubber foot. The crutch is strapped to the lower limb and weight is transferred though the proximal tibia. Methods: Five Volunteers were assessed using the crutch, the K9 walker and 2 standard crutches in a simulated environment. A comparison was made between this device and the K9 walker which has been shown to be a liberating walking aid indoors. Tasks from activities of daily living, productivity and transfers were included. Assessment was undertaken by the Occupational Therapy Team. The hands free crutch was also compared with non weight bearing using two crutches to gauge performance outdoors. Assessment of ease of use and safety was undertaken by the Physiotherapy Team. Results: Domestic chores including cleaning, cooking and shopping were possible using this device. Sitting activities were noted to be more difficult, because of the necessity to remove the crutch on each occasion. Although speed was significantly greater (p< 0.0001.) using two crutches, the hands free crutch permitted safe outdoor mobilisation on even or uneven ground, up and down slopes with a gradient of 1 in 10 and up and down stairs. Good single leg stance stability was predictive of ease of use and safety for the hands free crutch. Discussion: The hands free crutch is suited to motivated and physically able patients. Other lower limb pathology contraindicates the use of this device, but in patients with upper limb pathology it would permit non-weight bearing mobilisation. Good balance is paramount and perhaps a falls risk assessment should be performed prior to use

Introduction. Modern forearm crutches have evolved little since their invention last century. We evaluated comfort and user satisfaction of 2 spring-loaded crutches compared with existing crutch designs. Methods. 25 healthy subjects (11 male, average age 26.2 years; 14 female, average age 22.7 years) participated. Each used 5 different crutches in a randomly allocated order:. standard forearm crutch (ergonomic grip);. spring-loaded crutch (soft spring, ergonomic grip);. spring-loaded crutch (firm spring, ergonomic grip);. standard forearm crutch (normal grip);. axillary crutch. Participants completed a purpose built course at the Pedestrian Accessibility and Movement LAboratory, UCL (PAMELA). The course consisted of a mixture of slopes (transverse and longitudinal), sprint, slalom, and a slow straight. All participants completed questionnaires relating to crutch user preference and design features. Results. Crutches were ranked in order of preference. The crutch least favoured was the axillary design, irrespective of subject weight, followed by the standard forearm crutch with normal grip. The 3 crutches with ergonomic handles all scored similarly. Preferences were also analysed in two weight controlled groups and compared against the soft and firm spring-loaded crutches. Of the lighter group 80% preferred the softer spring. Of the heavier group 56% preferred the firmer spring. Over 50% of subjects rated handle/cuff comfort as a key feature in crutch design. Conclusions. Preference for different spring tensions depended on subject weight, which should be the focus of further research. The least favoured crutches were the axillary and standard issue forearm grip crutch. Comfort was the most important feature in crutch design with preference for ergonomic handles, followed by cuff design ranked the most important. Spring-loaded crutches performed comparably to the other crutches with ergonomic handles

Introduction: Pedobarograph systems are used to measure foot pressure characteristics during gait. These measurements help clinicians diagnose pathology and assess treatment outcome. While most patients can walk across the Pedobarograph footplate unaided, some patients ask if they can use their crutch. Aim: The aim of this study was to assess the effect of using a crutch on pedobarograh measurements. Materials and Methods: A Musgrave Pedobarograph system was used to measure the foot pressure characteristics of twenty feet in ten normal subjects. The group’s mean age and weight were 31 years (SD=6) and 78 kg (SD=12), respectively. Each subject had each of their feet measured 3 times as they walked across the foot plate unaided. These measurements were then repeated with the subject using a crutch on the contralateral side to that being measured. The force through the crutch was recorded using a set of scales to ensured consistency between measurements. Results: The main foot pressure characteristics are listed below. The table shows the mean value of the normal parameter, along with the percentage difference of the mean values when the crutch was used. The results of a paired-t test are also given to indicate the statistical significance of the change. In addition to the above quantitative changes, qualitative assessment of the data showed an alteration in the loading pattern with reduced push off forces. However, eighteen of the twenty feet showed no alteration in the pattern of pressure distribution. Conclusion: These results show that a crutch affects normal gait by generally increasing the time parameters and reducing the load and pressure parameters. The only parameters not significantly affected by the crutch were “Push off duration” and “Time to peak heel strike pressure”

Introduction. Reverse Total Shoulder Arthroplasty (rTSA) is currently advised against in patient populations with movement disorders, due to potential premature failure of the implants from the use of walking assistive devices. The objective of this study is to measure the amount of displacement induced by the simulated loading of axillary crutches on a rTSA assembly in a laboratory mimicking immediate postoperative conditions. Methods. 8 reverse shoulder baseplate/glenosphere assemblies (Equinoxe, Exactech, Inc) were fixated to 15 lb/ft3 density rigid polyurethane bone substitute blocks. Displacement of the assemblies in the A/P and S/I axes was measured using digital displacement indicators by applying a physiologically relevant 357N shear load parallel to the face of the glenosphere, and a nominal 50N compressive axial load perpendicular to the glenosphere. Westerhoff et al. reported in vivo shoulder loads while ambulating with axillary crutches had a maximum resultant force of 170% times the patient's bodyweight with the arm at 45.25° of abduction1. This was recreated by applying a 1435.4N compressive load (Average bodyweight of 86.1kg*170%) to a humeral liner and reverse shoulder assembly in an Instron testing apparatus at 45.25° of abduction as shown in Figure 1. The glenosphere was rotated about the humeral component through the arc of the axillary crutch swing, from −5° of extension to 30° of flexion as shown in Figure 2 for 183,876 cycles2. The number of cycles was based on number of steps taken in a day from pedometer data reported by Tudor Locke et al. for patients with movement disorders, extrapolated out to a 6 week postoperative recovery period3. A Student's one-tailed, paired t-test was used to identify whether or not significant displacement occurred, where p<0.05 denoted a significant difference. Results. Displacement in the A/P and S/I axes before and after cyclic loading are presented in Table 1. The S/I direction showed no significant difference in displacement (p≤.0801), whereas the A/P direction showed significant increase in displacement (p≤.0340). The average increase in displacement in the A/P and S/I directions was 43.5 and 35.8 microns, respectively. Discussion and Conclusions. This study was designed to represent a worst case scenario, as a patient is unlikely to bear full bodyweight on crutches immediately postoperatively, and is also unlikely to take as many steps as a healthy individual until full recovery occurs. For these reasons, early results indicate statistically significant displacement could occur if a patient bears full bodyweight on axillary crutches immediately postoperatively. This risk could be lowered after the postoperative recovery period in combination with non-full weight bearing devices such as a cane or a walker. To view tables/figures, please contact authors directly

Unilateral musculoskeletal below knee injuries occur with great frequency. Patients who cannot bear weight on an injured limb usually mobilise with standard crutches. However when the patient also has an upper limb injury, mobilisation may be impossible and can result in a lengthy in-patient stay. We present its value in facilitating early discharge in patients with both upper and lower limb injuries. We show the cost benefit of the saving in in-patient stay that the hands free crutch provides. We present our experience in which this innovative crutch was used and discuss the potential of this device to be used more often in orthopaedic surgery

Introduction. In the US over half a million people are prescribed crutches each year. More than 750,000 wheelchair users exist in the UK and wheelchair and crutch users commonly develop shoulder pathology. The purpose of this study was to determine the influence of complex topographies on heart rate (HR) and thus energy expenditure, using a wheelchair and differing crutch designs on the exertional body stress. Method. Two Paralympics Athletes from the GB amputee football squad were assessed in a Lomax Active wheelchair and 5 different types of crutches in a randomly allocated order over a course representing everyday complex terrains at the Pedestrian Accessibility and Movement Environment Laboratory (PAMELA), University College London. In addition results were compared over the same course with the athletes using their own personal pair of crutches. The PAMELA course consisted of a mixture of 4% and 2.5% cross falls (transverse) and a simulated road crossing, sprint, slalom and a slow straight. Results. Initial findings show both athletes needed to work harder, thus spend more energy (13% more) to cope with the wheelchair tasks (2.6) than with the crutches(2.3). The Total Heart Beat Index (THBI) revealed that trying to ambulate with the crutches was more difficult in 4% cross fall (3.3) than on the longitudinal slopes (3.2), followed by 2.5% cross fall (2.85), slalom (2.1) and sprint (1.8). For the same tasks executed using a wheelchair the 2.5% gradient was shown to be the higher energy demanding (3.8), followed by the 4% (3.5), slopes (2.9), slalom (2.2) and sprint (2.1). Both participants reached a lower THBI (2.2) during the same task when using their own crutches. Conclusion. The results of this study imply that ambulation with crutches puts less burden than wheelchair. This might be due to the time these athletes spend with crutches, either in training or activities of daily living. Furthermore, the physical strain which they underwent during the complex terrains was clearly reflected on their heart rate. The setting of longer distances to collect more consistent HR data should be the focus of further research. The comparison in performance between athletes and the general population should also be investigated

There is controversy regarding the effect of different approaches on recovery after THR. Collecting detailed relevant data with satisfactory compliance is difficult. Our retrospective observational multi-center study aimed to find out if the data collected via a remote coaching app can be used to monitor the speed of recovery after THR using the anterolateral (ALA), posterior (PA) and the direct anterior approach (DAA). 771 patients undergoing THR from 13 centers using the moveUP platform were identified. 239 had ALA, 345 DAA and 42 PA. There was no significant difference between the groups in the sex of patients or in preoperative HOOS Scores. There was however a significantly lower age in the DAA (64,1y) compared to ALA (66,9y), and a significantly lower Oxford Hip Score in the DAA (23,9) compared to PA(27,7). Step count measured by an activity tracker, pain killer and NSAID use was monitored via the app. We recorded when patients started driving following surgery, stopped using crutches, and their HOOS and Oxford hip scores at 6 weeks. Overall compliance with data request was 80%. Patients achieved their preoperative activity level after 25.8, 17,7 and 23.3 days, started driving a car after 33.6, 30.3 and 31.7 days, stopped painkillers after 27.5, 20.2 and 22.5 days, NSAID after 30.3, 25.7, and 24.7 days for ALA, DAA and PA respectively. Painkillers were stopped and preoperative activity levels were achieved significantly earlier favoring DAA over ALA. Similarly, crutches were abandoned significantly earlier (39.9, 29.7 and 24.4 days for ALA, DAA and PA respectively) favoring DAA and PA over ALA. HOOS scores and Oxford Hip scores improved significantly in all 3 groups at 6 weeks, without any statistically significant difference between groups in either Oxford Hip or HOOS subscores. No final conclusion can be drawn as to the superiority of either approach in this study but the remote coaching platform allowed the collection of detailed data which can be used to advise patients individually, manage expectations, improve outcomes and identify areas for further research

Proximal femoral focal deficiency is a congenital disorder of malformation of the proximal femur and/or the acetabulum. Patients present with limb length discrepancy and clinical features along a spectrum of severity. As these patients progress through to skeletal maturity and on to adulthood, altered biomechanical demands lead to progression of arthropathy in any joint within the lower limb. Abnormal anatomy presents a challenge to surgeons and conventional approaches and implants may not necessarily be applicable. We present a case of a 62-year-old lady with unilateral proximal femoral focal deficiency (suspected Aitken Class A) who ambulated with an equinus prosthesis for her entire life. She presented with ipsilateral knee pain and instability due to knee arthritis but could not tolerate a total knee arthroplasty due to poor quadriceps control. A custom osteointegration prosthesis was inserted with a view to converting to the proximal segment to a total hip replacement if required. The patient went on to develop ipsilateral symptomatic hip arthritis but altered acetabular anatomy required a custom tri-flange component (Ossis, Christchurch, New Zealand) and a custom proximal femoral component to link with the existing osseointegration component (Osseointegration Group of Australia, Sydney, Australia) were designed and implanted. The 18 month follow up of the custom hip components showed that the patient had Oxford hip scores that were markedly improved from pre-operatively. Knee joint heights were successfully restored to equal when the patient's prosthesis was attached. The patient describes feeling like “a normal person”, walks unaided for short distances and can ambulate longer distances with crutches. Advances in design and manufacture of implants have empowered surgeons to offer life improving treatments to patients with challenging anatomy. Using a custom acetabular tri-flange and osseointegration components is one possible solution to address symptomatic ipsilateral hip and knee arthropathy in the context of PFFD in adulthood

Gluteal Tendinopathy is a poorly understood condition that predominantly affects post-menopausal women. It causes lateral hip pain, worse when lying on the affected side or when walking up a hill or stairs. It has been labelled ˜Greater Trochanteric Pain Syndrome” a name that recognises the lack of understanding of the condition. Surgical reconstruction of the gluteal cuff is well established and has been undertaken numerous times over the last 16 years by the senior author (AJL). However, the quality of collagen in the tendons can be very poor and this leads to compromised results. We present the results of gluteal cuff reconstruction combined with augmentation using a bioinductive implant. 14 patients (11 female, 3 male; mean age 74.2 ± 6.3 years) with significant symptoms secondary to gluteal tendinopathy that had failed conservative treatment (ultrasound guided injection and structured physiotherapy) underwent surgical reconstruction by the senior author using an open approach. In all cases the iliotibial band was lengthened and the trochanteric bursa excised. The gluteal cuff was reattached using Healicoil anchors (3–5×4.75mm anchors; single anchors but double row repair) and then augmented using a Regeneten patch. Patients were mobilised fully weight bearing post-operatively but were asked to use crutches until they were no longer limping. All had structured post-surgery rehabilitation courtesy of trained physiotherapists. There were no post-operative complications and all patients reported an improvement in pain levels (Visual Analogue Scale 7.8 pre-op; 2.6 post-op) and functional levels (UCLA Activity Score 3.5 pre-op; 7.1 post-op) at 6 months post surgery. Surgery for gluteal tendinopathy produces good outcomes and the use of Regeneten as an augment for poor quality collagen is seemingly a safe, helpful addition. Further comparative studies would help clarify this

Introduction. Treatment of non-union in open tibial fractures Gustilo-Anderson(GA)-3A/3B fractures remains a challenging problem. Most of these can be dealt using treatment methods that requires excision of the non-union followed by bone grafting, masquelet technique, or acute shortening. Circular fixators with closed distraction or bone transport also remains a useful option. However, sometimes due to patient specific factors these cannot be used. Recently antibiotic loaded bone substitutes have been increasingly used for repairing infected non-unions. They provide local antibiotic delivery, fill dead space, and act as a bone conductive implant, which is resorted at the end of a few months. We aimed to assess the outcome of percutaneous injection of bone substitute while treating non-union of complex open tibial fractures. Materials & Methods. Three cases of clinical and radiological stiff tibial non-union requiring further intervention were identified from our major trauma open fracture database. Two GA-3B cases, treated with a circular frame developed fracture-related-infection(FRI) manifesting as local cellulitis, loosened infected wires/pins with raised blood-markers, and one case of GA-3A treated with an intramedullary nail. At the time of removal of metalwork/frame, informed consent was obtained and Cerament-G. TM. (bone-substitute with gentamicin) was percutaneously injected through a small cortical window using a bone biopsy(Jamshedi needle). All patients were allowed to weight bear as tolerated in a well-fitting air-cast boot and using crutches. They were followed up at 6 weekly intervals with clinical assessment of their symptoms and radiographs. Fracture union was assessed using serial radiographs with healing defined as filling of fracture gap, bridging callus and clinical assessment including return to full painless weight bearing. Results. Follow-up at 6 months showed all fractures had healed with no defect or gaps with evidence of new trabecular bone and significant resorption of Cerament-G. TM. at final follow-up. There was no evidence of residual infection with restoration of normal limb function. Fractures with no internal fixation showed a mild deformity that had developed during the course of the healing, presumed due to mild collapse in the absence of fixation. These were less than 10 degrees in sagittal and coronal planes and were clinically felt to be insignificant by the patients. Conclusions. Cerament-G's unique combination of high dose antibiotics and hydroxy apatite matrix provided by calcium sulphate might help provide an osteoconductive environment to allow these stiff non-unions to heal. The matrix appears to provide a scaffold-like structure that allows new bone in-growth with local release of antibiotics helping reduce deep-seated infections. The final deformation at fracture site underlines the need for fixation- and it is very unlikely that this technique will work in mobile nonunions. Whilst similar fractures may heal without the use of bone substitute injections, the speed of healing in presence of significant fracture gap suggests the use of these bone substitutes did help in our cases. Further studies with a larger cohort, including RCTs, to evaluate the effectiveness of this technique compared to other methods are needed

Introduction. Angular deformities of the distal femur can be corrected by opening, closing and neutral wedge techniques. Opening wedge (OW) and closing wedge (CW) are popular and well described in the literature. CW and OW techniques lead to leg length difference whereas the advantage of neutral wedge (NW) technique has several unique advantages. NW technique maintains limb length, wedge taken from the closing side is utilised on the opening side and since the angular correction is only half of the measured wedge on either side, translation of distal fragment is minimum. Leg lengths are not altered with this technique hence a useful technique in large deformities. We found no reports of clinical outcomes using NW technique. We present a technique of performing external fixator assisted NW correction of large valgus and varus deformities of distal femur and dual plating and discuss the results. Materials & Methods. We have treated 20 (22 limbs – 2 patients requiring staged bilateral corrections) patients for distal femoral varus and valgus deformities with CWDFO between 2019 and 2022. Out of these 4 patients (5 limbs) requiring large corrections of distal femoral angular deformities were treated with Neutral Wedge (NW) technique. 3 patients (four limbs) had distal femoral valgus deformity and one distal femoral varus deformity. Indication for NW technique is an angular deformity (varus or valgus of distal femur) requiring > 12 mm opening/closing wedge correction. We approached the closing side first and marked out the half of the calculated wedge with K – wires in a uniplanar fashion. Then an external fixator with two Schanz screws is applied on the opposite side, inserting the distal screw parallel to the articular surface and the proximal screw 6–7 cm proximal to the first pin and at right angles to the femoral shaft mechanical axis. Then the measured wedge is removed and carefully saved. External fixator is now used to close the wedge and over correct, creating an appropriate opening wedge on the opposite side. A Tomofix (Depuoy Synthes) plate is applied on the closing side with two screws proximal to osteotomy and two distally (to be completed later). Next the osteotomy on the opposite side is exposed, the graft is inserted. mLDFA is measured under image intensifier to confirm satisfactory correction. Closing wedge side fixation is then completed followed by fixation of opposite side with a Tomofix or a locking plate. Results. 3 patients (4 limbs) had genu valgum due to constitutional causes and one was a case of distal femoral varus from a fracture. Preoperative mLDFA ranged from 70–75° and in one case of varus deformity it was 103°. We achieved satisfactory correction of mLDFA in (85–90°) in 4 limbs and one measured 91°. Femoral length was not altered. JLCA was not affected post correction. Patients were allowed to weight bear for transfers for the first six weeks and full weight bearing was allowed at six weeks with crutches until healing of osteotomy. All osteotomies healed at 16–18 weeks (average 16.8 weeks). Patients regained full range of movement. We routinely recommend removal of metal work to facilitate future knee replacement if one is needed. Follow up ranged from 4 months to 2 yrs. Irritation from metal work was noted in 2 patients and resolved after removing the plates at 9 months post-surgery. Conclusions. NWDFO is a good option for large corrections. We describe a technique that facilitates accurate correction of deformity in these complex cases. Osteotomy heals predictably with uniplanar osteotomy and dual plate fixation. Metal work might cause irritation like other osteotomy and plating techniques in this location

Introduction: The Orthopaedic Leg Trolley (OLT) is an alternative to crutches in the management of patients treated non-weight bearing. Advantages of the OLT include ease of use and the avoidance of problems such as painful hands and axillae, thus promoting greater mobility and facilitating early discharge. It also leaves the hands free for other purposes. The aim of this study was to investigate the benefit of the OLT following major elective foot and ankle surgery, using a questionnaire. Methods: A prospective clinical audit was conducted on thirty patients undergoing elective foot and ankle surgery. Post-operatively, each patient was provided with an OLT. A questionnaire, measuring patient experience and satisfaction, was administered after the period of non-weight bearing. Results: There were 13 males and 17 females, mean age 56 years, range 22 to 81 years. All patients had undergone major hindfoot reconstruction, and many had significant co-morbidities which rendered routine crutch use difficult. The mean duration of use was 4 weeks. After one week’s use, 80 of patients reported having no difficulty; 13.3% had slight difficulty; 6.7% had great difficulty; and no patients found the OLT impossible. All patients had used crutches pre-operatively: 76.7% rated the OLT as being easier to use than crutches; 13.3% felt that it was the same; and 10% reported that crutches were easier to use. Overall 53.3% rated the OLT as “invaluable”; 36.6% as being “very helpful”; 6.7% as being “quite helpful”; and 3.3% as being “not at all helpful”. Conclusion: This study shows that the OLT is a useful alternative to crutches. It is particularly helpful in the rehabilitation of patients who are treated non-weight bearing following major foot and ankle surgery and have significant co-morbidities making crutch use difficult

Human bone morphogenetic protein (hBMP) was prepared according to a modified method (Sampath et al). Implants were prepared with 500 μg of hBMP adsorbed onto a composite matrix (1 gm of insoluble collagenous bone matrix and 200 mg of lyophilised human gelatine). The hBMP/collagen composite was used to treat 11 women and 23 men (mean age 36 years). All patients had failed to achieve union despite previous treatment by internal or external fixation, immobilisation in a cast, and/or allogenic or autogenic bone grafting. The mean age of the nonunions was 26 months (1 to 228). At surgery a mean of 2 gm per patient of the composite was inserted at the site of the defect, which was stabilised by internal or external fixation. Supplementary allogenic cancellous bone particles and block configured spongy bone was used in 17 patients. At follow-up 1, 8, 16 and 23 weeks postoperatively, functional results were assessed according to weight-bearing. A score of 0 was given where there was no weight-bearing, a score of 1 for weight-bearing with the assistance of two crutches, 2 for light weight-bearing with one crutch, 3 for full weight-bearing with one crutch and 4 for full weight-bearing without crutches. At a mean follow-up of 17 weeks (8 to 32), the mean score was 3.25, higher than the mean preoperative score of 2.22 and mean one-week follow-up score of 0.5. Of the five patients who suffered recurrent infection, two failed to score above 2 at 17 weeks mean. Present results indicate that hBMP composite implants may represent effective treatment of difficult nonunions

Aim. To evaluate the efficacy of infection elimination and functional outcomes of the resection hip arthroplasty (RHA) with m. vastus lateralis flap plasty in patients with chronic recurrent periprosthetic joint infection (PJI) one year or later after the surgery. Method. We retrospectively studied the outcomes of 61 cases with recurrent PJI (more than 3 relapses). All patients underwent RHA with m. vastus lateralis flap plasty from the year 2005 to 2016. There were 35 males (63.6%) and 20 females (36.4%) with the mean age of 54 years. At least in one year after the surgery, the cases were analyzed for the absence of inflammation during the physical exam, functional result with the Harris hip score (HSS), quality of life with the Instrument for measurement of health-related quality of life scale and level of pain with the visual analogue scale (VAS). The results are presented as means with CI95%. Results. The mean follow-up period was 40.8 months. The overall mortality rate was 12.2% (n = 6). Of all patients, 3 (5.5%) had severe concomitant pathology and died due to systemic infection within 90 days after the surgery. Two more patients died during the period of 1–3 years. Prolonged remission of PJI was achieved in 91% (n = 50) patients. In 9% of cases (n = 5) the relapse of infection was achieved. The HHS corresponded to an unsatisfactory outcome with the mean value of 49.3 (45.4–53.3). Most of the patients (56%, n = 31) used 2 crutches while walking, 23% (n = 13) - a cane or a crutch, and 11% (n = 6) – a walker. In 73% of cases (n = 40), the load-bearing capacity of the operated limb was preserved. In 27% of cases (n = 15) the limb was non-supporting, including 10 patients with severe pain syndrome under the load. At the same time, the pain syndrome was absent in the rest of the patients. The mean VAS score was 2.77 (2.3–3.12). Despite the insufficient function of the operated limb, 83.6% of patients noted a satisfactory result with the mean Instrument for measurement of health-related quality of life* score of 57.8 (52.1–63.4). Conclusions. RHA with m. vastus lateralis flap plasty is a technically complex operation that in most cases leads to the elimination of chronic recurrent PJI. Apparently, the improvement of functional capabilities can be ensured by the use of revision arthroplasty or external fixation in order to form a supporting «new joint» (neoarthrosis). * EQ5D

We wanted to solve the problem of acetabular dysplasia with a cementless total hip endoprothesis by using a smaller acetabular cup in order to fit the size of the dysplastic acetabulum without using any additional bone transplantation for superstructure of the acetabulum. By using this type of acetabular reconstruction we can preliminarily conclude that the bone superstructure of the acetabulum can be avoided and that problems may occur if remodelation of the bone transplant has failed. Irregular biomechanical bending in the supraacetabular region can also be avoided. Uncured developmental dysplasia of the hip joint (DDH) is a huge problem to solve in elderly patients. DDH can be expressed in several forms according to stage, i.e., in young and elderly patients we can find different consequences, from slight to moderate supraacetabular dysplasia combined with anterior dysplasia, valgus and anteversion of the proximal femur, to high hip luxation. In efforts to find a better way to solve slight and moderate supraacetabular dysplasia (in some cases combined with high luxation), we have tried to use a smaller acetabular cup that will fit the dysplastic acetabulum, combined with a higher hip centre, dysplastic polyethylene, and a longer femoral neck to avoid leg length discrepancy and weakness of the gluteal musculature. From January 1999 to January 2000 we performed the above-mentioned type of operation in 33 patients (25 females, 8 males) with dysplastic coxarthrosis of the hip. Age range was from 32 to 63 years. In all cases we performed the application of a Zimmer or Biomet smaller acetabular cementless cup after reaming the acetabulum near the internal lamina of the iliac bone. Good primary fixation of the acetabulum was achieved in all of the cases. Supraacetabular reconstruction was not used. In some cases where the dysplasia was very expressive, we left the acetabular cup uncovered for about 0.5 cm. In the postoperative period we advised the patient to load the operated leg over two crutches without full weight bearing for approximately six weeks. After that time period and according to clinical and radiographic findings, we prescribed walking with one crutch, and walking without crutches four months later. The follow-up period is short but preliminary results of our study are satisfactory. There were no early postoperative complications. Incorporation of bone was good in the acetabular cups measured with radiographs and in some cases with Tc99m. In some cases where we left part of the cup uncovered, there was supraacetabular formation of new bone after six months

A consecutive series of patients who underwent 113 total hip arthroplasty (THA) with minimally invasive surgery (MIS) (63 one-, 50 two-incision cases) were studied. One-incision THA was performed with a posterolateral approach. For the two-incision, the first incision for cup insertion was made over the anterolateral side of the hip and intermuscular dissection was performed between the gluteus medius and the tensor fascia lata. The second incision for stem insertion was made on the posterolateral side along the fiber of the gluteus maximus and intermuscular dissection was made between the gluteus medius and the piriformis. The average length of the skin incision and standard deviation (SD) in the one- and two-incision group was 7.5 ± 0.54 cm and 12.1 ± 0.93 cm (p < 0.001). Average surgical time for the two groups (and SD) was 52 ± 8.5 minutes and 70 ± 10.2 minutes (p = 0.042) in the one and two incision groups respectively. Fluoroscopy was used in the two-incision group for an average 6.0 ± 5.3 seconds. In the one-incision group, the average time was 1.3 ± 2.1 seconds. The patients in the one-incision group could walk on crutches at postoperative 3.7 days on average, and in the two-incision group at 1.6 days on average (p = 0.000). In the one-incision group, patients used crutches for 6 weeks on average, and in the two-incision group, patients used crutches for 3 weeks on average (p = 0.042). Complications that developed within 1 month of surgery in the one-incision group were: 1 case of DVT, 1 case of intra-operative fracture and 1 case of dislocation; for the two incision group there were: 1 case of DVT, 1 case of intra-operative fracture and 1 case of femoral nerve entrapment. Before surgery, the HHS for the one-incision group was 49.8 points, and for the two-incision group it was 49.6 points (p > 0.05). At the time of the follow up review conducted postoperatively 1 year, the average HHS was not significantly different (p > 0.05). However, the average function score in HSS for the two-incision group was superior to that of the one-incision group (p = 0.045). Preoperative WOMAC scores were not different for the two groups (68.7 in one-incision group and 70.9 in two-incision group, respectively, p > 0.05). However, the average WOMAC score for the two-incision group was better, especially for the function score (p = 0.001). The other hip functions, common in oriental persons, were also better in the two-incision group compared to the one-incision group. On the radiographs, the location of the femoral prosthesis inserted in the medullary cavity was usually central in both groups; only 4 cases showed varus in the one-incision group and 2 cases in the two-incision group. The opening angle of the acetabular component was 38.1° in the one-incision group and 39.2° in the two-incision group (p > 0.05). The anteversion of the acetabular component was 21.0° in the one-incision group and 22.2° in two-incision group (p > 0.05). As compared with one-incision MIS-THA, two-incision MIS-THA, although it is a more difficult procedure, produces superior results, recovery was faster and patient satisfaction was higher due to early rehabilitation and reduced soft tissue damage without increasing the complication frequency

Introduction. Total hip arthroplasty (THA) using short design stem is surging with increasing movement of minimally invasive techniques. Short stems are easier to insert through small incisions preserving muscles. We have used these types of short stems since 2010. Almost all of the patients have shown good clinical results. However, two patients developed fatigue fractures on femurs post operatively. We have reviewed the clinical and radiographic results of these patients. Patients and methods. From April 2010, we have performed 621 THAs with short design stems, Microplasty. R. , Biomet, using a muscle preservation approach, the Direct Anterior Approach (DAA). The age ranged from 31 to 88 years old. Case1: 56y.o. male, BMI 23.1kg/m. 2. Preoperative diagnosis was bilateral osteoarthritis. Simultaneous THAs were performed on bilateral hips. He was allowed to bear as much weight as he could tolerate using an assistive device immediately after surgery, and followed standard hip precautions for the first 3 weeks. He was discharged from hospital seven days after surgery and returned to his job two weeks after surgery. He noticed sudden left thigh pain three weeks after surgery without any obvious cause. Crutches were recommended to partially bear his weight. Six weeks after surgery, a fracture line became visible on the radiographs and new callus formation also became visible. Three months after surgery, he felt no pain and was able to walk without any crutches. Case2: 66y.o. female, BMI 27.5 kg/m. 2. Preoperative diagnosis was bilateral osteoarthritis. THAs were performed on the hips at a six month interval. The right hip was operated on first, followed by the left hip. She was discharged from hospital four days after surgery and returned to her job six weeks after surgery. Two months later after left hip surgery, she suddenly felt pain on her left femur without any obvious cause, and was unable to walk. Three weeks later, X-rays showed fatigue fracture lines and new callus formations. After two or three months using crutches, her pain improved and X-rays showed good callus formation and no stem subsidence. Discussions. Several reports showed insufficiency fractures of the pelvis following THA. But most of them occurred due to repetitive stress on fragile bones. But our cases showed no evidence of osteoporosis. They had no history of trauma. But they had some points in common, which were they were bilateral cases and their BMI were not low. The incident rate of fatigue fractures of femur with this short stem THAs was 0.3% in our cases. We suggested that one of the causes of these fatigue fractures was the shortness of the stems. The shortness of the stems concentrate the body weight to limited contact area of the femur, and the stress causes the fatigue fractures. We should consider the risk of fatigue fractures on the patients who are operated on bilaterally. However these two patients showed good callus formations and no stem subsidence after a few weeks of partial weight bearing

Between January 2003 and December 2004, 14 patients underwent bilateral resurfacing arthroplasty via a Ganz trochanteric osteotomy. This bilateral group was mobilised fully weight-bearing with crutches. During the same period 139 Ganz trochanteric osteotomies were performed for unilateral hip resurfacing. These patients were mobilised with crutches, weight-bearing up to 10 kg on the operated leg. Nine osteotomies (32%) in the bilateral group subsequently developed a symptomatic non union requiring revision of fixation. This compares with 10 patients (7%) in the unilateral group. Applying the Fisher’s exact test, the difference reached significance (p=0.0004). In 2 patients a second revision was required to achieve union. In 1 patient, revision of trochanteric fixation precipitated a deep infection. Protected weight-bearing following a Ganz trochanteric osteotomy is important to the success of the procedure. Simultaneous bilateral hip arthroplasty through a Ganz approach should be avoided. If it is undertaken, we recommend that patients should be non weight-bearing for 6 weeks following surgery. Non union following a Ganz trochanteric osteotomy for arthroplasty carries a significant morbidity

Purpose. The treatment of children with contractures involving the lower limbs is challenging. Many are confined to wheelchairs for several years till their potential to ambulate is discovered. The aim is to review the treatment and outcome of eight children treated for contractures and deformities of the lower limbs following confinement to wheelchairs. Methods. Eight children aged 4–14 years were treated for contractures of the hips, knees and feet between 2005 and 2011. The initial diagnosis was not made in 5 children. All children had never walked previously. Four patients were labelled “cerebral palsy”. All children were seen with a physiotherapist to assess their walking potential. Genetic and paediatric medical assessment was also made. Final diagnosis revealed arthrogryposis (n = 3) pterygium syndrome (n = 1) calcinosis cutis (n = 1) viral neuropathy (n = 1) and cerebral palsy (n = 2). Clinically all children were assessed to have good upper limb function for use of crutches. Surgical correction of the feet was required in 6 patients. Extension osteotomies of the knees were done in 8 patients following serial plaster cast treatment and hamstring release. Hip releases were done in 4 patients. Results. The osteotomies healed well following above knee cast immobilisation. All patients are ambulant with above knee calipers, anterior knee straps and boots. Two children required repeat extension osteotomies. Follow up ranges between 8 months to 5 years. Conclusion. Patients with contractures of the lower limb should have careful clinical assessment. If upper limb function is suitable for holding crutches and the patients have the potential to kneel with the body erect, careful preoperative planning should be undertaken to improve the foot for weight bearing and the knees with extension osteotomies and ambulation. Accurate diagnosis is essential

A seventy-five-year-old female patient presented with pain and deformity of her left leg of three days duration. Hybrid THRA has been done 11 years ago at her left hip for the treatment of osteoarthritis. Massive osteolysis and pathologic fracture were observed on plain radiograph (Fig. 1). Revision THRA using an allograft prosthesis composite (APC) was planned for solution of extensive bone loss of the proximal femur. Surgical exposure was performed through extended trochanteric osteotomy with the patient supine. Step-cut osteotomy was done at the remained proximal part of host femur to make match with the distal part of APC. Meticulous removal of granulation tissues and remaining cement was done. As Acetabular cup was stable, 60 mm sized high-walled polyethylene liner was exchanged. Calcar reconstruction prosthesis was cemented into a proximal femoral allograft measuring 15 cm and cement at the vicinity of the step-cut osteotomy was removed for later bony union at interface. After solid fixation of APC with cement, the distal half of APC was cemented with the host femur. Step-cut osteotomy was wired and autogenous bone grafts from the greater trochanter were added at the interface. Leg length and stability were rechecked using a standard necked 28 mm metal head and reduction was done stably. Greater trochanter was fixed over the trimmed proximal allograft with multiple wiring and paper-thin host femur was enveloped around the femoral allograft using absorbable sutures. Following insertion of the closed suction drainage drains, closure was done as routine fashion and healing of the wound was uneventful (Fig. 2). An abduction brace was applied post operatively for a period of four weeks. Crutch walking with partial weight bearing was started at four weeks and crutch protection was applied for a period of six months. Incorporation of allograft with the host bone was observed on two-year follow-up radiographs. At seven-year follow-up, the patient walks well with a mild limp, and Harris score is 90. We report on a seven-year follow-up case of revision THRA with APC with references (Fig. 3)