Introduction

Trial reduction while performing total hip replacement is an essential step of the procedure. This is to check the stability of the hip joint with the selected implant sizes and to assess the leg length to avoid discrepancy.

Disengagement of the femoral head trial from the femoral rasp stem, with subsequent migration of the trial head into the pelvic cavity is a rare occurrence, but can be a very frustrating complication to both the surgeon and occasionally the patient.

We present our experience with this exceptional situation and different management options, together with systematic review of the literature.

Purpose. Minimally invasive anterolateral approach (ALA) for total hip arthroplasty (THA) has gained popularity in recent years as better postoperative functional recovery and lower risk of postoperative dislocation are claimed. However, difficulties for femur exposure and intraoperative complications during femoral canal preparation and component placement have been reported. This study analyzes the anatomical factors likely to be related with intraoperative complications and the difficulties of access noted by the surgeons through a modified minimally invasive ALA. The aim is to define the profile for patient at risk of intraoperative complications during minimally invasive ALA. Methods. We retrospectively included 310 consecutive patients (100 males, 210 females) who had primary unilateral THA using the same technique in all cases. The approach was performed between the tensor fascia lata and the gluteus medius and minimus, without incising or detaching muscles and tendons. Posterior translation was combined to external rotation for proximal femur exposure (Fig. 1). All patients were reviewed clinically and radiologically. For the radiological evaluation, all patients underwent pre- and postoperative standing and sitting full-body EOS acquisitions. Pelvic [Sacral slope, Pelvic incidence (PI), Anterior pelvic plane angle] and femoral parameters were measured preoperatively. We assessed all intraoperative and postoperative complications for femoral preparation and implantation. Intraoperative complications included the femoral fractures and difficulties for femoral exposure (limitations for exposure and lateralization of the proximal femur). The patients were divided into two groups: patients with or without intraoperative complications. Results. Ten patients (3.2%) had intraoperative femoral fractures (greater trochanter: 2 cases, calcar: 8 cases). Five fractures required additional wiring. Difficult access to proximal femur was reported in the operative records for 10 other patients (3.2%). There was no difference in diagnosis, age, sex, BMI between the patients with or without intraoperative complications. No significant group differences were found for surgical time, and blood loss. Patients with intraoperative complication, presented a significantly lower pelvic incidence than patients without intraoperative complications (mean PI: 39.4° vs 56.9°, p<0.001). The relative risk of intraoperative complications in patients with low PI (PI<45°) was more than thirteen times (relative risk; 13.3, 95% CI= 8.2 to 21.5. p<0.001) the risk for patients with normal and high PI (PI>45°). Conclusions. Anterolateral approach for THA implantation in lateral decubitus is reported to have anatomical and functional advantages. Nevertheless, the exposure of the femur remains a limitation. This study highlights a significant increased risk in case of low PI less than 45°. This specific anatomical pattern reduces the local working space as the possibility for posterior translation and elevation of the proximal femur is less on a narrow pelvis. This limitation is due to the length and the orientation of the hip abductor and short external rotator muscles related to the relative positions of iliac wing and greater trochanter (Fig. 2). This study points out the importance of pelvic incidence for the detection of anatomically less favourable patients for THA implantation using ALA. For any figures or tables, please contact the authors directly

The reconstruction of peri-acetabular defects after severe bone loss or pelvic resection for tumor is among the most challenging surgical intervention. The Lumic® prosthesis (Implantcast, Buxtehude, Germany) was first introduced in 2008 in an effort to reduce the mechanical complications encountered with the classic peri-acetabular reconstruction techniques and to improve functional outcomes. Few have evaluated the results associated with the use of this recent implant. A retrospective study from five Orthopedic Oncology Canadian centers was conducted. Every patient in whom a Lumic® endoprosthesis was used for reconstruction after peri-acetabular resection or severe bone loss with a minimal follow-up of three months was included. The charts were reviewed and data concerning patients’ demographics, peri-operative characteristics and post-operative complications was collected. Surgical and functional outcomes were also assessed. Sixteen patients, 11 males and five females, were included and were followed for 28 months [3 – 60]. Mean age was 55 [17–86], and mean BMI reached 28 [19.6 – 44]. Twelve patients (75%) had a Lumic® after a resection of a primary sarcoma, two following pelvic metastasis, one for a benign tumor and one after a comminuted acetabular fracture with bone loss. Twelve patients (75%) had their surgery performed in one stage whereas four had a planned two-stage procedure. Mean surgical time was 555 minutes [173-1230] and blood loss averaged 2100 mL [500-5000]. MSTS score mean was 60.3 preoperatively [37.1 – 97] and 54.3 postoperatively [17.1-88.6]. Five patients (31.3%) had a cemented Lumic® stem. All patients got the dual mobility bearing, and 10 patients (62.5%) had the largest acetabular cup implanted (60 mm). In seven of these 10 patients the silver coated implant was used to minimize risk of infection. Five patients (31.3%) underwent capsular reconstruction using a synthetic fabric aiming to reduce the dislocation risk. Five patients had per-operative complications (31.3%), four were minor and one was serious (comminuted iliac bone fracture requiring internal fixation). Four patients dislocated within a month post-operatively and one additional patient sustained a dislocation one year post-operatively. Eight patients (50%) had a post-operative surgical site infection. All four patients who had a two-stage surgery had an infection. Ten patients (62.5%) needed a reoperation (two for fabric insertion, five for wash-outs, and three for implant exchange/removal). One patient (6.3%) had a septic loosening three years after surgery. At the time of data collection, 13 patients (81.3%) were alive with nine free of disease. Silver coating was not found to reduce infection risk (p=0.2) and capsuloplasty did not prevent dislocation (p=1). These results are comparable to the sparse data published. Lumic® endoprosthesis is therefore shown to provide good functional outcomes and low rates of loosening on short to medium term follow-up. Infection and dislocation are common complications but we were unable to show benefits of capsuloplasty and of the use of silver coated implants. Larger series and longer follow-ups are needed

The reconstruction of peri-acetabular defects after severe bone loss or pelvic resection for tumor is among the most challenging surgical intervention. The Lumic® prosthesis (Implantcast, Buxtehude, Germany) was first introduced in 2008 in an effort to reduce the mechanical complications encountered with the classic peri-acetabular reconstruction techniques and to improve functional outcomes. Few have evaluated the results associated with the use of this recent implant. A retrospective study from five Orthopedic Oncology Canadian centers was conducted. Every patient in whom a Lumic® endoprosthesis was used for reconstruction after peri-acetabular resection or severe bone loss with a minimal follow-up of three months was included. The charts were reviewed and data concerning patients’ demographics, peri-operative characteristics and post-operative complications was collected. Surgical and functional outcomes were also assessed. Sixteen patients, 11 males and five females, were included and were followed for 28 months [3 – 60]. Mean age was 55 [17-86], and mean BMI reached 28 [19.6 – 44]. Twelve patients (75%) had a Lumic® after a resection of a primary sarcoma, two following pelvic metastasis, one for a benign tumor and one after a comminuted acetabular fracture with bone loss. Twelve patients (75%) had their surgery performed in one stage whereas four had a planned two-stage procedure. Mean surgical time was 555 minutes [173-1230] and blood loss averaged 2100 mL [500-5000]. MSTS score mean was 60.3 preoperatively [37.1 – 97] and 54.3 postoperatively [17.1-88.6]. Five patients (31.3%) had a cemented Lumic® stem. All patients got the dual mobility bearing, and 10 patients (62.5%) had the largest acetabular cup implanted (60 mm). In seven of these 10 patients the silver coated implant was used to minimize risk of infection. Five patients (31.3%) underwent capsular reconstruction using a synthetic fabric aiming to reduce the dislocation risk. Five patients had per-operative complications (31.3%), four were minor and one was serious (comminuted iliac bone fracture requiring internal fixation). Four patients dislocated within a month post-operatively and one additional patient sustained a dislocation one year post-operatively. Eight patients (50%) had a post-operative surgical site infection. All four patients who had a two-stage surgery had an infection. Ten patients (62.5%) needed a reoperation (two for fabric insertion, five for wash-outs, and three for implant exchange/removal). One patient (6.3%) had a septic loosening three years after surgery. At the time of data collection, 13 patients (81.3%) were alive with nine free of disease. Silver coating was not found to reduce infection risk (p=0.2) and capsuloplasty did not prevent dislocation (p=1). These results are comparable to the sparse data published. Lumic® endoprosthesis is therefore shown to provide good functional outcomes and low rates of loosening on short to medium term follow-up. Infection and dislocation are common complications but we were unable to show benefits of capsuloplasty and of the use of silver coated implants. Larger series and longer follow-ups are needed

The use of total hip arthroplasty in adolescents for end-stage degenerative hip disease is controversial with few reported outcomes in the literature. The purpose of the study was to report the outcomes of total hip arthroplasty in a cohort of adolescents managed by a multidisciplinary team of paediatric and adult orthopaedic surgeons from a single centre. A multidisciplinary clinic consisting of paediatric and adult hip surgeons was established in 2013 to identify, treat and prospectively follow adolescents who would potentially beneift from a total hip arthoplasty. To date 29 consecutive adolescent patients (20 female, 9 male, 32 hips) with end stage degenerative hip disease have undergone cementless primary total hip arthroplasty. Mean age at decision to treat was 15.7 years (age 11.4–18.5). Ten different underlying paediatric specific pathologies were documented including DDH, cerebral palsy, JIA, skeletal dysplasias, SCFE and idiopathic chondrolysis. Three patients had bilateral staged procedures. Clinical baseline and outcomes were measured using Oxford Hip Score (OHS), WOMAC score and ASKp scores. Radiographic follow-up was conducted at 6 weeks, 6 months and yearly thereafter. Post-operative complications were recorded. Twenty-five hips were eligible for minimum 2-year follow-up scoring at a mean 2.7 years (2.0–3.6 years). No intraoperative complications occurred. One case of recalcitrant postoperative psoas tendonitis occured. OHS improved from 25 (7–43) to 41 (23–48). WOMAC improved from 48 (12–8) to 12 (1–44), and ASKp improved from 78% (33–98%) to 93% (73–100%). Radiographic review revealed acceptable alignment of all components with no signs of loosening or wear. No revision of components was required. One patient died at 6 months post op from an unrelated condition. The early term results of total hip arthroplasty in adolescents from our multidisciplinary program are encouraging. Improvements in quality of life to normal values were seen as were hip scores consistent with satisfactory joint function. Depite the range of complex and varied causes of arthritis seen in this population the establishment of combined paediatric and adult orthopaedic surgical teams appears to be a successful model to manage end-stage degenerative hip disease in adolescents

The primary objective of this study was to establish a safety profile for an all-arthroscopic anatomic glenoid reconstruction via iliac crest autograft augmentation for the treatment of shoulder instability with glenoid bone loss. Short-term clinical and radiological outcomes were also evaluated. This study involved a retrospective analysis of prospectively collected data for 14 patients (male 8, female 6) who were treated for shoulder instability with bone loss using autologous iliac crest bone graft between 2014 and 2018. Of 14 patients, 11 were available for follow-up. The safety profile was established by examining intra-operative and post-operative complications such as neurovascular injuries, infections, major bleeding, and subluxations. Assessment of pre-operative and post-operative Western Ontario Shoulder Instability (WOSI) index, radiographs, and CT scans comprised the evaluation of clinical and radiological outcomes. A good safety profile was observed. There was no occurrence of intraoperative complications, neurovascular injuries, adverse events, or major bleeding. One patient did develop an infection in the neurovascular injuries, adverse events, or major bleeding. One patient did develop an infection in the treated shoulder post-surgery. There were no subluxations or positive apprehension tests on clinical examination post-operatively. Short-term clinical outcomes were seen to be favorable WOSI scores at the most recent follow-up were significantly higher than pre-operative scores, with a mean increase of 39.6 ± 10.60 (p = 0.00055). The average follow-up for CT scan was 4.66 (SD± 2.33) months, where all patients showed bone graft union. Arthroscopic treatment of shoulder instability with bone loss via autologous iliac crest bone graft is shown to be a safe operative procedure that results in favorable short-term clinical and radiological outcomes. Further investigations must be done to evaluate the longevity of these positive health outcomes

Introduction. Total hip arthroplasty (THA) using the direct anterior approach (DAA) in a supine position is a minimally invasive surgery that reduces postoperative dislocation. Excellent exposure of both the acetabulum and proximal femoral part is important to reduce intraoperative complications. Generally, two surgical assistants need to hold four retractors to maintain excellent exposure of the acetabulum. We examined intra- and postoperative complications as indicators of the efficiency of using the “Magic Tower” (MT) device compared with a non-MT group. Material and Method. Twenty consecutive DAA THAs using MT were analyzed, and 20 DAA THAs not using MT were also analyzed. MT is a retractor-holding device, and has an arm structure that can be moved in a wide variety of directions. This device holds a retractor stably, and each movement of the arm can be locked by one click. Operating time, blood loss, length of skin incision, intraoperative complications, and number of assistants were recorded. Postoperative radiographs were obtained to evaluate implant position. Results. Mean operating time was 105 min in the MT group and 118 min in the non-MT group. Mean blood loss was 232 g in the MT group and 233 g in the non-MT group. Mean length of skin incision was 80 mm in the MT group and 85 mm in the non-MT group. Mean cup inclination was 45.8° in the MT group and 47.3° in the non-MT group. Postoperative implant position was also excellent in both groups. In all comparisons, no significant differences were seen between groups. No intraoperative complications were encountered. Two assistants were required in the non-MT group, and one in the MT group. Discussion. A majority of the complications reported with THA can be attributed to access issues, i.e., difficulties in exposure and accurate component implantation. To achieve excellent exposure at the acetabulum, four retractors (anterior, posterior, cranial, and caudal) are desirable. In such procedures, two surgical assistants are needed to hold retractors. One of these assistants needs to hold the anterior retractor and cranial/caudal retractor from the opposite side of the surgery beyond the abdomen of the patient. However, the assistant on the opposite side cannot achieve good exposure, as strong retraction of the anterior part of the acetabulum may cause complications of femoral nerve palsy. The MT is able to hold a retractor firmly by applying pressure toward the acetabulum instead of traction, and also reduces the number of surgical assistants required. While preparing the femur, exposure of the femoral canal was also better than in the non-MT group. Conclusion. In primary DAA THA, no significant differences between groups were identified. However, the MT is clearly a useful device that allows maintenance of excellent exposure, reducing the number of surgical assistants required

Introduction. In total knee arthroplasty, the alignment of leg depends on the alignment of the component. In unicompartmental knee arthroplasty, it is determined by the thickness of the implant relative to the bone excised mostly. After initial scepticism, UKA is increasingly accepted as a reliable procedure for unicompartmental knee osteoarthritis with the improvements in implant design, surgical technique and appropriate patient selection. Recently, computer assisted UKA is helpful in accuracy and less invasive procedure. But, fixed bearing or mobile bearing in UKA is still controversy. We compared the early clinical and radiological results of robot-assisted unicompartmental knee arthroplasty using a fixed bearing design versus a mobile type bearing design. Materials and Methods. A data set of 50 cases of isolated compartmental degenerative disease that underwent robot-assisted UKA using a fixed bearing design were compared to a data set of 50 cases using a mobile bearing type design. The operations were performed by one-senior author with the same robot system. The clinical evaluations included the Knee Society Score (knee score, functional score) and postoperative complications. The radiological evaluations was assessed by 3-foot standing radiographs using the technique of Kennedy and White to determine the mechanical axis and femoro-tibial angle for knee alignment. Operative factors were evaluated including length of skin incision, operation time, blood loss, hospital stay and intraoperative complications. Results. There were no statistically significant differences in operation time, skin incision size, blood loss and hospital stay. (p > 0.05) There were no significant differences in Knee Society Scores at last follow up. An average preoperative femorotibial alignment was varus alignment of −1° in both groups. Postoperative patients with fixed-bearing implants had an average +2.1° valgus and the patients with mobile bearing implants had +5.4° valgus in femorotibial alignment, which was different.(p<0.05) There was one case of medial tibia plateau fracture in fixed bearing group in 3 months postoperatively. And there were one case of liner dislocation with unstable knee in 6 weeks postoperatively and one case of femoral component loosening in 1 year postoperatively in mobile bearing group. There was no intraoperative complication. The average preoperative knee score was 45.8, which improved to 89.5 in fixed bearing group and 46.5, which improved to 91.2 in mobile bearing group at last followup. The average preoperative function score was 62.4 which improved to 86.5 in fixed bearing group and 60.7 which improved to 88.2 in mobile bearing group at last followup. Conclusion. In ourearly experience, two types of bearing of robot-assisted UKA groups showed no statistical differences in clinical assessment but there was statistical difference in postoperative radiological corrected alignment. But in aspect of early complications, we think that mobile bearing seems to be requiring more attention in surgery

INTRODUCTION. Cementless femoral component designs supplemented with hydroxyapatite (HA) coating have been hypothesised to enhance osseointegration, thereby improving stability and clinical outcomes. We herein offer interim results at 5 years from a prospective, multi-centre study of a femoral stem (SL-PLUS™ Hip Stem Prosthesis), forged from titanium alloy (Ti6Al7Nb) and consisting of a titanium plasma sprayed coating (0.3mm) with an additional 0.05mm layer of HA. METHODS. Investigators at 2 centres enrolled patients between 18–75 years of age who underwent primary total hip arthroplasty (THA) with this HA-coated stem. The study's primary outcome was the clinical efficacy of the stem, as measured by the Harris Hip Score (HHS), Western Ontario & McMaster Universities Osteoarthritis (WOMAC) Score calculated out of Hip Disability and Osteoarthritis Outcome Score (HOOS), and the EuroQol EQ-5D-3L index score and visual analogue scale (VAS). Its secondary outcomes included a radiographic assessment of implant position and fixation, and overall safety, as measured by intraoperative/early postoperative complications and survivorship calculated using Kaplan-Meier estimates. RESULTS. Ninety-three patients (94 hips) were enrolled in the study. At the time of surgery, the study population had a mean age of 60.1 years (standard deviation [SD], 8.4), a mean body mass index of 27.9 kg/m. 2. (SD, 4.75), and 54.8% were female. Indications for surgery include primary osteoarthritis (74.5%), dysplasia (17.5%), femoral head necrosis (6.4%), and other (2.1%). Patients were followed up through 5 years in the ongoing safety and performance analysis. Between preoperative baseline and final follow up, there were notable improvements in the mean scores for all primary clinical outcomes: HHS (51.6 to 91.4, respectively), WOMAC from HOOS (42.6 to 91.0, respectively), mean EQ-5D-3L index score (0.7 to 0.9, respectively), and EQ-5D-3L VAS (54.7 to 80.2, respectively). The majority of patients rated their satisfaction as excellent (84.2% of treated hips), with an additional 14.5% of treated hips being mostly satisfied. Five years after surgery, radiographic findings showed an overall stability of the device, with 100% unchanged stem positions (no movement in varus/valgus or subsidence) and no stem was classified as loose. Intraoperative complications were observed in 3 patients (3.2%), consisting of 2 cases of trochanteric fracture and 1 case of leg lengthening. There were no general early postoperative complications reported in any patient. Two revision surgeries of the study device were reported, both due to infection, resulting in a survivorship of 97.5% (95% confidence interval: 90.3% – 99.4%) at 5 years. CONCLUSION. These results confirm the safety and efficacy of this HA-coated femoral stem at 5 years. All clinical outcomes showed significant improvement between baseline and midterm follow up, with mean HHS in particular meeting the 90-point range considered “excellent.” Additionally, revision rates met the accepted benchmarks for a successful THA device. For any figures or tables, please contact authors directly

The brief answer is no….I do not believe that outpatient total joint arthroplasty is the emergent standard of care. However, for some patients and some surgeons I do believe that outpatient total joint arthroplasty can be performed safely and with greater comfort and convenience for the patient. Further, for the surgeon, it can provide greater control over the care environment if performed at an ambulatory surgery center. Patient selection is paramount in my opinion for safely performing outpatient total joint arthroplasty. While some have attempted to define specific criteria, our own criteria include patients with simple orthopaedic problems who are healthy, trustworthy and have a good support system of family or friends to assist them. As surgeons we must also be self-aware as the margin for error, particularly at a freestanding ambulatory surgery center, is narrow. Operative times should be reliably brief and blood loss should be minimal to allow for a safe discharge on the same day. Further the incidence of intraoperative complications such as fractures at the time of total hip arthroplasty or ligament injuries during total knee arthroplasty should be low. The surgeon should also be prepared with the equipment to address these common issues, if they do occur. In our review of the NSQIP data set we matched 1,236 outpatient TJA 1:1 with inpatients based on propensity scores. The risk of 30-day readmissions and complications was no different between groups, although inpatients had a higher rate of VTE and outpatients had a higher risk of re-operation. Risk factors for adverse events included patient age > 85 years old, diabetes and BMI > 35. Likewise in a review of results from my own practice, we have seen no difference in the risk of complications. As health care providers we must keep the safety of our patients paramount at all times. Further, we must be fiscally responsible to avoid costly complications, reoperations and readmissions. With conservative patient selection and careful surgical technique I believe that outpatient TJA offers an attractive alternative that is safe, cost effective and associated with high satisfaction for both patients and surgeons

Introduction. The hip hemiarthroplasty in posterior approach is a common surgical procedure at the femoral neck fractures in the elderly patients. However, the postoperative hip precautions to avoid the risk of dislocations are impeditive for early recovery after surgery. We used MIS posterior approach lately known as conjoined tendon preserving posterior (CPP) approach, considering its enhancement of joint stability, and examined the intraoperative and postoperative complications, retrospectively. Methods. We performed hip hemiarthroplasty using CPP approach in 30 patients, and hip hemiarthroplasty using conventional posterior approach in 30 patients, and both group using lateral position with the conventional posterior skin incision. The conjoined tendon (periformis, obturator internus, and superior/inferior gemellus tendon) was preserved and the obturator externus tendon was incised in CPP approach without any hip precautions postoperatively. The conjoined tendon was incised in conventional approach using hip abduction pillow postoperatively. Results. There was no difference between CPP approach group and conventional approach group in the mean age of patients (81.8 years, and 80.3 years, respectively), and in the mean operative time (68.8 minutes, and 64.9 minutes, respectively). In 4 cases of CPP approach, the avulsion fracture at femoral attachment of the conjoined tendon occured during hip reduction manoeuvres. No dislocations occured in both groups in the follow-up period (2 years). Discussion. Lately, the number of hip surgery in muscle sparing approach is increasing. However, in general, MIS approach induces the intraoperative complications, and requires the skillful procedure. The hip reduction manoeuvres would be more difficult in the CPP approach, than in conventional posterior approach, because the preserved conjoined tendon would inhibit hip reduction, considering those avulsion fractures of the femoral attachment. Nevertheless, CPP approach did not require no extended time compared to conventional approach, and no postoperative hip precautions. Due to these results, CPP approach could be a good MIS procedure including early recovery after surgery based on the enhancement of joint stability, excluding the difficulties in hip reduction manoeuvres. We could not show the difference in dislocation rate between two groups, because of small numbers. We are planning to increase the number of patients in the future study

BACKGROUND. Total hip revision surgery in cases with previous multiple reconstructive procedures is a challenging treatment due to difficulties in treatment huge bone defects with standard revision prosthetic combinations. A new specially made production system in Electron-Beam Melting (EBM) technology based on a precise analysis of patients' preoperative CT scans has been developed. METHODS. Objectives of design customization in difficult cases are to correctly evaluate patient's anatomy, to plan a surgical procedure and to obtain an optimal fixation to a poor bone stock. The 3D Printing (EBM) technology permits to create an extremely flexible patient matching implant and instrument, with material performances not viable with standard manufacturing process. Dedicated visual 3D tools and instrumentations improve implants congruency according to preoperative plan. Primary stability is enhanced and tailored on patient's anatomy by means of press-fit, iliac stems and the high friction performances of Trabecular Titanium matrix. The use of bone screws and their position is designed to enhance primary stability, even in critical bone conditions, avoiding implant stress shielding and allowing bone integration. 4 cases (2 men and 2 women) of acetabular customized implants were performed. Mean age at surgery was 51.5 years (range 25–72). Patients were reviewed clinically and radiographically at follow-up. RESULTS. No signs of miss-match between intraoperative bone conditions and pre-operative planning were observed. No additional bone grafts or further native bone removal were needed. Biomechanical parameters were restored by using internal modularity (i.e. face-changers / angled spacers). Face-changers allow to correct coverage and anteversion of the acetabular system. Incompatibility or impingement between the stems and new acetabular component was not observed and stem revision was performed in one case. On-table stability proved excellent and no intraoperative complications were observed. All patients underwent an immediate mobilization with full weight-bearing. Mean Harris Hip Score increased significantly from 13.9 (range 6.9–20.6) preoperatively to 75.8 (range 53.9–94) at last follow-up (mean 17.5, range: 10–33), showing an improvement in terms of both pain relief, function and joint mobility. Radiographically neither signs of instability, migration nor tilting were observed. No case of dislocation nor infection were recorded. CONCLUSION. A detailed anatomical reconstruction, in-depth preoperative planning, custom-implant design, high performance of the 3D-printing technology, system modularity and patient-specific surgical tools permitted an effective restoration of the biomechanical joint parameters in these complex revision cases. The optimal primary stability of the implants promoted an early osseointegration with the remaining bone stock. Further studies shall be necessary to assess the performance of these Implants at long-term follow-up

Introduction. There is a high prevalence of obesity in the United States and the numbers are increasing. These patients comprise a significant portion of the shoulder arthroplasty patient population. There are several reports of outcomes in the literature on obese patients after total knee or hip replacement, however, this data is lacking in the shoulder arthroplasty patient population. The purpose of this study is to compare the functional outcomes and complications of obese patients undergoing shoulder arthroplasty with the non-obese population. Methods. Between 2009 to 2010, 76 patients that had a primary total shoulder replacement were grouped according to their Body Mass Index (BMI) and followed prospectively for 2 years. The groups were divided as normal (BMI <25, N=26), overweight (25 to 30 BMI, N=25), and obese (>30 BMI, N=25) according to the World Health Organization classifications. Preoperative demographics, age, comorbidities and postoperative complications were recorded. Perioperative operating room and hospital data were analyzed. Functional outcome measurements including ASES, SF-36 physical component (PC) scores, mental component (MC) scores and visual analog scale along with general health and fatigue were evaluated at the 0 and 2 year time period. Statistical analyses were performed. Results. Functional outcome: In the normal BMI group: Average ASES scores improved from 38.4 +/− 15.5 (pre-op) to 80.2 +/− 19.4 (2 yr), SF-36 Physical Component (PC) scores improved from 38.3 +/− 6.5 (pre-op) to 53.7 +/− 11.3 (2 yr), and VAS decreased from 62 to 12 (2 yr). There were no intraoperative complications and two patients required revision of components. In the overweight BMI group: Average ASES scores improved from 37.4 +/− 18.1 (pre-op) to 75.2 +/− 24.9 (2 yr), SF-36 Physical Component (PC) scores improved from 36.1 +/− 8.0 (pre-op) to 39.8 +/− 12.2 (2 yr), and VAS decreased from 68 to 18. One patient had deep infection that required surgical irrigation/debridement, one intraoperative glenoid fracture converted to hemiarthroplasty and two patients required revision of components. In the obese BMI group: Average ASES scores improved from 35.8 +/− 12.5 (pre-op) to 80.0 +/− 20.6 (2 yr), SF-36 Physical Component (PC) scores improved from 36.3 +/− 8.4 (pre-op) to 40.7 +/− 12.4 (2 yr), and VAS decreased from 66 to 11 (2 yr). There were no intraoperative complications and no patients required revision surgery. * Statistical analysis showed significant difference in the SF-36 PC scores between both the overweight and the obese group compared to the normal BMI group. No statistical difference was seen between the three groups with the perioperative OR/hospital data, SF-36 MC scores, general health and fatigue scales. Conclusion. Shoulder arthroplasty in all three groups were associated with significant improvements in ASES scores and decrease in overall pain. Obese and overweight patients after TSA had significantly less overall physical functional improvements compared to the normal BMI group. Both intraoperative and postoperative complications were minimal after TSA in all three BMI groups. OR time and intraoperative blood loss was higher in the obese group, but overall ASA scores and number of days of hospital stay were similar in all three groups

Introduction. Multiple techniques exist for performance of Total Knee Arthroplasty (TKA). In April 2010, MyKnee® Patient-Specific Instrumentation (Medacta International, SA, Castel San Pietro, Switzerland) was approved for use in TKA in the United States. The present retrospective study seeks to evaluate early results of this technique. 29 consecutive patients (30 consecutive TKA operations) underwent TKA using the MyKnee cutting-blocks. These results were compared to 30 consecutive patients utilizing Standard TKA method. The findings represent the author's first MyKnee patients, and thus early learning curve for this technique. IRB approval for retrospective research was obtained prior to the evaluation of the data. Methods. 30 consecutive patients (14 males, 16 females) underwent TKA using the MyKnee technique. Pre-operative long-standing radiographs were taken and compared to 6-week post-operative radiographs. Intraoperative data includes the femoral and tibial resections thickness: Distal Medial femoral, Distal Lateral femoral, Posterior Medial Femoral, Posterior Lateral femoral, Medial Tibia, and Lateral Tibia. These were compared to the Planned vs. Actual resections. Tourniquet time was recorded as a measure of speed of surgery. These were compared to 30 consecutive patients using Conventional TKA technique. Intraoperative complications were also recorded. Results. For the MyKnee group, 21 patients had pre-operative varus deformities with a mechanical alignment of 7.8° (range 1.2°-15.2°). 7 patients had Pre-operative valgus deformities averaging 6.9° (range 1.3°-14.5°). 2 patients were neutral. Post-operative alignment for all patients (n=23) was varus 1.92° (range 0°-5.8°). 78% of patients were within 3° and 97% of patients were within 3.6°. Only 1 patient was outside 3.6°, measuring 5.4° valgus (Figure 3). In comparison, the Standard TKA group had 21 patients with pre-operative varus deformities averaging 7.3° (range 0°-16.5°) while 7 knees were valgus 6.3° (range 1.2°-10.6°) and one was neutral. Post-operative alignment for these patients measured varus 1.85°. 79% of patients were within 3°; however the outliers were much more dramatic ranging 3.5°-9.2°. 30 Femora and 21 Tibial resections were available for review using the MyKnee technique. The Actual vs. Planned resections for the Distal Medial Femoral resection was 9.5 vs. 9.1mm respectively. Further Actual vs. Planned Femoral resections include Distal Lateral Femoral 8.4 vs. 6.3mm; Posterior Medial Femoral 9.3 vs. 9.5mm; and Posterior Lateral Femoral 8.6 vs. 7.0mm. The Actual vs. Planned Tibial resections recorded include Medial 6.07 vs. 6.29mm and Lateral 9.36 vs. 8.19mm. Statistically, there is no significant difference in post-op degree (1.85° vs. 1.92°). Tourniquet time (TT) averaged 32.97 minutes in the Standard TKA group vs. 37.03 minutes in the MyKnee group, which isn't significantly different. However, the final 15 MyKnee patients had an average time of 33.46 minutes. EBL was minimal each cohort. No intraoperative complications were recorded in either group. Discussion. Many techniques exist for performance of TKA. The present study shows definitively that Intraoperative resections and Post-operative alignments can be accurately achieved with pre-operative CT planning and using Patient-Specific Instrumentation. In conclusion, using Patient-Specific Instrumentation is safe, quick, and accurate in performance of TKA

Background. Acetabular cup malpositioning during total hip arthroplasty (THA) is known to lead to impingement, instability, wear-induced osteolysis, and increased rates of revision surgery. The purpose of this study was to independently evaluate the accuracy of acetabular cup orientation using a novel mechanical navigation device. Methods. Postoperative acetabular cup orientation was reviewed in 47 primary THAs using the HipSextant mechanical navigation device. Angles were measured with a validated two-dimensional/three-dimensional matching application. An outlier was defined as +/− 10 degrees outside of the preoperative plan for inclination and anteversion. Results. Of the 47 THAs, 47 (100%) met our inclination target, 46 (98%) met our anteversion target, and 46 (98%) simultaneously met both targets. There were no outliers for inclination and one outlier (−12.7°) for anteversion (Figure 1). The absolute errors for both inclination and anteversion were significantly less than 10° (p<0.001). There were no intraoperative complications related to the use of this mechanical navigation system. Conclusions. The HipSextant reliably navigates acetabular cup inclination and anteversion according to a preoperative plan that is individualized for each patient. This should decrease the risk of postoperative complications related to acetabular component malposition during THA. Further research is warranted to assess the clinical impact of reducing outliers using this device

In May 2010, MyKnee® patient-specific instrumentation was approved for use in this procedure in the USA. This technique uses a pre-operative CT scan of the lower extremity to plan the surgery. Images of the hip, knee, and ankle are reconstructed digitally to assess pre-operative deformity as well as size of the knee. Surgery is then planned with the goals of restoring a neutral mechanical axis of limb and providing correct sizing and placement of implants after the surgery. From this plan, patient-specific jigs are created to perform the surgery achieving the planned result without sacrificing speed of surgery or increasing complexity of the procedure. The present study seeks to evaluate both intraoperative and radiographic results of this procedure. IRB approval for retrospective research was obtained prior to evaluation of the data. Thirty consecutive patients (14 males, 16 females) underwent TKA using the MyKnee technique by the senior author. Pre-operative long-standing radiographs were taken and compared to 6-week post-operative radiographs. Intraoperative data includes the femoral and tibial resection thickness: distal medial femoral, distal lateral femoral, posterior medial femoral, posterior lateral femoral, medial tibia, and lateral tibia. These were compared to the planned vs. actual resections. Tourniquet time was recorded as a measure of speed of surgery. These were compared to 30 consecutive patients using standard TKA technique by the same author. Intraoperative complications were also recorded. For patients with varus pre-operative deformities (n = 21), the mechanical alignment was 7.8° (range 1.2° to 15.2°). Seven patients had pre-operative valgus deformities averaging 6.93° (range 1.3° to 14.5°). Two patients were neutral. Post-operative alignment for all patients (n = 30) was varus 1.92° (range 0° to 5.8°). Seventy-eight percent of patients were within 3° and 97% of patients were within 3.6°. In comparison, post-operative alignment for standard TKA patients measured varus 1.85°, which was not statistically significant. Seventy-nine percent of patients were within 3°; however the outliers were more dramatic ranging 3.5° to 9.2°. Thirty femoral and 21 tibial resections were available for review using the MyKnee technique. The actual vs. planned resections for the distal medial femoral resection was 9.5 vs. 9.1mm respectively. Further actual vs. planned femoral resections include distal lateral femoral 8.4 vs. 6.3mm; posterior medial femoral 9.3 vs. 9.5mm; and posterior lateral femoral 8.6 vs. 7.0mm. The actual vs. planned tibial resections recorded include medial 6.07 vs. 6.29mm and lateral 9.36 vs. 8.19mm. Tourniquet time averaged 32.97 minutes (range 25 to 54) in the standard TKA group vs. 37.03 minutes (range 1 to 71) in the MyKnee group. This difference was not significant. However, the final 15 MyKnee patients had an average time of 33.46 minutes. No intraoperative complications occurred. Many techniques exist for performance of TKA. Patient-specific cutting blocks allow the surgeon to pre-operatively determine resection depths, rotations, alignment, and sizing prior to the operative procedure itself. The present study shows that intraoperative resections and post-operative alignments can be accurately achieved with pre-operative CT planning and using patient-specific instrumentation. For the typical varus knee deformity, cartilage will exist on the lateral side of the knee. This can cause measurement error when measuring the lateral compartments as the CT scan is based on bone only. This can be seen in 2.1mm and 1.6mm differences in the distal lateral femoral and posterior lateral femoral resections respectively. Thus, this difference can be explained by the false measurement of intact cartilage. More accurate results could be obtained if the cartilage was removed and bone measured. Valgus knees, being diseased in the lateral compartment, did not show such variance as expected in planned vs. actual resections. Intraoperative speed of surgery is important to all participants in TKA: surgeon, hospital, and patient. Obviously accuracy should not be sacrificed for speed so it is important for any new technology introduced to the market to accelerate surgery not compromise results. In the current study, the average times of MyKnee vs. standard TKA surgery were comparative and not significantly different using a two-sample T-test. The standard TKA average tourniquet time may appear faster than other reported literature; however the surgeon is on the end of learning curve with the system. The MyKnee average tourniquet time represents the initial procedures in the learning curve and can be considered slower than what they will eventually be as the author gains more experience with the technique. Efficiency was demonstrated with the decrease in tourniquet time for the last 15 patients. Furthermore, the goals of surgery were maintained radiographically. Regardless of the deformity, the patient's post-operative mechanical axes averaged 1.85° for standard technique and 1.92° for the MyKnee group, not statistically significantly different. These results were obtained via long-standing x-rays, which are well known to be prone to error in alignment secondary to potential flexion and rotation of the extremity. The standardised protocol for acquisition of the X-ray, attempts to prevent these errors and X-rays are routinely re-done if the technician feels error has occurred. The technique also appears safe as no intra-operative complications occurred and were recognised within the first six weeks post-operative. In conclusion, using patient-specific instrumentation (MyKnee) is safe, quick, and accurate in performance of TKA

Purpose. Clinical outocome of revision total elbow arthroplasty(TEA) in rheumatoid arthritis(RA) patients were evaluated. Methods. Clinical outocome of revision TEA that underwent between 2005 and 2013 were evaluated. Causes of revision, implanted revised prosthesis, a clinical score (the Japanese Orthopaedic Association (JOA) elbow assessment score), the arc of motion and complications were investigated. Totally, 6 patients underwent revision TEA. The patients were females with a mean age of 60.4 years (range, 32 to 72). Results. Seventy-two primary TEAs were done in corresponding period. Six out of 72 (8.3%) TEAs were revised. Causes of revision were loosening, instability (dislocation) and breakage of a component in 3, 2 and 1 cases, respectively. A mean duration from initial TEA to revision surgery was 10.3 years (range, 1 to 13). Semi-constrained arthroplasties (5 Coonrad-Morrey, 1 Discovery) were used for revision surgery. A mean JOA elbow assessment score improved from 59 to 81 point at the time of follow up. The mean ROM, flexion was improved 125 degrees, to 131 degrees. Extension, supination and pronation was not changed. A fracture at the time of implant withdrawal occurred as an intraoperative complication. The fractures were recovered by wiring with autologous bone graft from the ilium and a good bone union was achieved in 2 out of 3 cases. However, a re-revision surgery with plate was required in the remaining case. Conclusions. Revision TEA provided a satisfactory functional outcome. An intraoperative fracture was a critical complication in this procedure

INTRODUCTION. Trabecular Titanium is an open-cell regular structure composed by hexagonal cells of controlled pore, manufactured by Electron Beam Melting (EBM) technology, that allows moulding of cellular solid structures. The Lima Delta TT revision cups are One and Revision, which is characterized by a caudal hook and fins. Both allow internal modularity and cranial TT augments. The aim of this prospective study is to evaluate the short to medium-term clinical and radiographic outcomes of acetabular revision cups in TT. METHODS. Between December 2008 and March 2013 we performed 60 cup revisions, 33 with the Revision cup and 27 with the One cup. The bone defect was classified according to Paprosky acetabular classification: type IIb and IIc presenting continent anterior and posterior acetabular wall were treated by Delta One TT; type IIIa and IIIb were treated with Delta TT Revision. In 20 cases (3.3%) stem revision was associated. Causes of revision were: aseptic loosening in 48 cases, periprosthetic acetabular fractures in 5 cases, recurrent dislocation in 5 cases, infection in 2 cases. In 52 cases bone grafts were used to fill cavitary defects (AIR 1–4). Hemispheric TT augments were used in 13 cases with the same aim. Internal modules were used in 39 cases to restore correct offset. The mean age of patients was 69.6 years (range 29–90). The average follow-up was 39 months (range 19–70). RESULTS. Mean Harris Hip Score (HHS) was 39.9 preoperatively and 82.7 at last follow-up. We had no intraoperative complications. We had 2 cases of superficial infection, one of which required revision of the surgical wound. 4 patients suffered dislocation episodes (1 recurrent); none of them required revision. We had 1 case of asymptomatic aseptic loosening, which did not require intervention. In the remaining cases no radiographic evidence of radiolucent lines was noticed at follow up, neither any evidence of aseptic loosening. The graft was considered to be integrated in all cases. DISCUSSION AND CONCLUSION. Trabecular Titanium revision cups showed high capacity of osseointegration, providing good results in short to medium-term follow-up. Further studies are necessary to assess long-term survivorship

With the introduction of new technology in orthopaedics, surgeons must balance anticipated benefits in patient outcomes with challenges or complications associated with surgical learning curve for the technology. The purpose of this study was to determine whether surgeon learning curve with a new multi-radius primary TKA system and instruments designed to improve surgical team ease would impact clinical outcomes, surgical time, and complications. From November 2012 to July 2015, 2369 primary TKAs were prospectively enrolled in two multicentre studies across 50 sites in 14 countries with a new knee system (NEW-TKA) evenly balanced across four configurations: cruciate retaining or posterior stabilised with either fixed bearing or rotating platform (CRFB, CRRP, PSFB, PSRP). 2128 knees had a<1 year visit and 1189 had a minimum 1 year visit. These knees were compared to a reference dataset of 843 primary TKAs from three manufacturers in the same four configurations with currently available products (CA-TKA). Demographics for NEW-TKA and CA-TKA were similar and typical for primary TKA. Operative times, clinical outcomes and a series of five patient reported outcomes were compared for NEW-TKA vs. CA-TKA. The first 10 New-TKA subjects for each surgeon were defined as learning curve cases (N=520) and were compared to all later subjects (N=1849). Patient reported outcome measure and clinical outcome analyses were covariate adjusted for patient demographics, pre-op assessment and days post-op. Mean (SD) surgical time for NEW-TKA learning curve cases was 79.1 (24.3) minutes, which reduced thereafter to 73.6 (24.3) (p=0.002). Beyond 10 cases, there was a continued reduction in NEW-TKA surgical time (R-Squared = 0.031). After 10 cases, surgical time was on par with the mean (SD) 71.9 (21.6) for CA-TKA (p=0.078). PROM outcomes of the first 10 learning curve cases for NEW-TKA were not statistically different from later cases at less than 1 year or later when adjusted for relevant covariates including configuration, patient demographics, pre-op functional status, and time post-op (p-values > 0.01). PROM outcomes for NEW-TKA vs. CA-TKA under the same covariate adjustments showed a trend favoring KOOS ADL, Symptoms, and Sport and Recreation subscores at minimum 1 year (p-values < 0.01). The incidence of intraoperative operative site complications was 1.3% for the NEW-TKA learning curve cases which was similar to the 0.6% rate for historical CA-TKA (p=0.231) and the intraoperative complication rate for the NEW-TKA later cases was consistent with learning curve cases (p=0.158). The introduction of new implants into the market place needs to have adequate data to support that they are safe and effective. Except for a minor increase in surgical time during the first 10 patients, this study found that surgeon learning curve with this new primary TKA system does not adversely affect patient short term outcomes and complication rates

Introduction. With the introduction of new technology in orthopaedics, surgeons must balance anticipated benefits in patient outcomes with challenges or complications associated with surgical learning curve for the technology. The purpose of this study was to determine whether the surgeon learning curve with a new multi-radius primary TKA system (primary TKA implant and instruments) designed for surgical team ease would impact clinical outcomes, surgical time and complications. Materials & Methods. From November 2012 to July 2015, 2369 primary TKAs were prospectively enrolled in two multicenter studies across 50 sites in 14 countries with a new knee system (ATTUNE®) evenly balanced across four configurations: cruciate retaining or posterior stabilised with either fixed bearing or rotating platform (CRFB, CRRP, PSFB, PSRP). 2261 knees had a <1 year visit and 1628 had a greater than 1 year visit. These knees were compared to a reference dataset of 845 primary TKAs from three manufacturers in the same four configurations with currently available products (CURRENT-TKA). Demographics for ATTUNE and CURRENT-TKA were similar and typical for primary TKA. Operative times, clinical outcomes and a series of five patient reported outcomes were compared for ATTUNE vs. CURRENT-TKA. The first 10 ATTUNE subjects for each surgeon were defined as learning curve cases (N=520) and were compared to all later subjects (N=1849) and also with the CURRENT-TKA cases (N=845). Patient reported outcome measures and clinical outcome analyses were adjusted for covariates including patient demographics, pre-op assessment and days post-op. Results. Mean (SD) surgical time for ATTUNE learning curve cases was 79.3 (24.7) minutes, which reduced thereafter to 73.6 (24.3) (p<0.001). Beyond 10 cases, there was a continued reduction in ATTUNE surgical time (R-Squared = 0.031). After 10 cases, surgical time was on par with the mean (SD) 72.0 (21.7) for CURRENT-TKA (p=0.097). PROM outcomes of the first 10 learning curve cases for ATTUNE were not statistically different from later cases at less than 1 year or later when adjusted for relevant covariates including configuration, patient demographics, pre-op functional status, and time post-op (p-values > 0.01). PROM outcomes for ATTUNE vs. CURRENT-TKA under the same covariate adjustments showed a trend favoring KOOS ADL, Symptoms, and Sport and Recreation subscores at minimum 1 year (p-values < 0.05). The incidence of intraoperative operative site (knee) complications was 1.3% (7/520) for the ATTUNE learning curve cases which was similar to both the 0.6% (5/845) rate for historical CURRENT-TKA (p=0.230) and the 0.8% (14/1849) intraoperative complication rate for the ATTUNE later cases (p=0.195). Discussion. The introduction of new implants into the market place needs to have adequate data to support that they are safe and effective. Except for a minor increase in surgical time during the first 10 patients, this study found that surgeon learning curve with the new ATTUNE primary TKA system does not adversely affect patient short term outcomes and complication rates