Aims

Safety concerns surrounding osseointegration are a significant barrier to replacing socket prosthesis as the standard of care following limb amputation. While implanted osseointegrated prostheses traditionally occur in two stages, a one-stage approach has emerged. Currently, there is no existing comparison of the outcomes of these different approaches. To address safety concerns, this study sought to determine whether a one-stage osseointegration procedure is associated with fewer adverse events than the two-staged approach.

Aims. The aim of this study was to assess the clinical and radiological results of patients who were revised using a custom-made triflange acetabular component (CTAC) for component loosening and pelvic discontinuity (PD) after previous total hip arthroplasty (THA). Methods. Data were extracted from a single centre prospective database of patients with PD who were treated with a CTAC. Patients were included if they had a follow-up of two years. The Hip Disability and Osteoarthritis Outcome Score (HOOS), modified Oxford Hip Score (mOHS), EurQol EuroQoL five-dimension three-level (EQ-5D-3L) utility, and Numeric Rating Scale (NRS), including visual analogue score (VAS) for pain, were gathered at baseline, and at one- and two-year follow-up. Reasons for revision, and radiological and clinical complications were registered. Trends over time are described and tested for significance and clinical relevance. Results. A total of 18 females with 22 CTACs who had a mean age of 73.5 years (SD 7.7) were included. A significant improvement was found in HOOS (p < 0.0001), mOHS (p < 0.0001), EQ-5D-3L utility (p = 0.003), EQ-5D-3L NRS (p = 0.013), VAS pain rest (p = 0.008), and VAS pain activity (p < 0.0001) between baseline and final follow-up. Minimal clinically important improvement in mOHS and the HOOS Physical Function Short Form (HOOS-PS) was observed in 16 patients (73%) and 14 patients (64%), respectively. Definite healing of the PD was observed in 19 hips (86%). Complications included six cases with broken screws (27%), four cases (18%) with bony fractures, and one case (4.5%) with sciatic nerve paresthesia. One patient with concurrent bilateral PD had revision surgery due to recurrent dislocations. No revision surgery was performed for screw failure or implant breakage. Conclusion. CTAC in patients with THA acetabular loosening and PD can result in stable constructs and significant improvement in functioning and health-related quality of life at two years' follow-up. Further follow-up is necessary to determine the mid- to long-term outcome. Cite this article: Bone Jt Open 2023;4(2):53–61

The objective of this study was to assess the clinical and radiological results of patients who were revised using a new generation custom-made triflange acetabular component (CTAC) for component loosening and large acetabular defect (Paprosky 3A and 3B) after previous total hip arthroplasty (THA). New generation CTACs involve the use of patient-specific drill guides and incorporate three-dimensional printed bone models, enhancing precision during surgical implantation. Data were extracted from a single centre prospective database of patients with large acetabular defects who were treated with a new generation CTAC. Patients were included if they had a minimum follow-up of five years. The modified Oxford Hip Score (mOHS), EurQol EuroQoL five-dimension three-level (EQ-5D-3L) utility, and Numeric Rating Scale (NRS), including visual analogue score (VAS) for pain, were gathered at baseline, and at two- and five-year follow-up. Reasons for revision, and radiological and clinical complications were registered. Trends over time are described and tested for significance (p<0.05). A total of 49 (70%) of 70 patients with a mean age of 73.5 years (SD 7.7) had a complete follow-up of 5 years. A significant improvement was found in HOOS, mOHS, EQ-5D-3L utility and NRS, VAS pain rest and activity between baseline and final follow-up. Complications included 8 cases with loosening screws, 4 with bony fractures, 4 periprosthetic infections and 2 cases with dislocation. One patient with bilateral pelvic discontinuity had revision surgery due to recurrent dislocations. No revision surgery was performed for screw failure or implant breakage. New generation CTAC in patients with THA acetabular loosening and massive acetabular bone loss (Paprosky 3A and 3B) can result in stable constructs and significant improvement in functioning and health-related quality of life at five years’ follow-up

Previous scientific studies have highlighted how coupling is an important element affecting total hip arthroplasty's survival. This study aims to evaluate whether metal-on-metal (MOM) coupling could be a statistically significant risk factor. The data from the regional joint registry (Registro dell'Impiantologia Protesica Ortopedica, RIPO) was used for analysis. The data collection accuracy of this registry was 97.2% in 2017. We retrospective evaluate all MOM total hip arthroplasties (THAs) implanted in our department between January 01st 2000 and December 31st 2011. We used a control group composed by all other prosthesis implanted in our Department in the same time lapse. We registered 660 MOM THAs. Mean age of patients was 66.9 years. 603 patients have a >36mm head, while 78 a <36 mm one. Neck modularity was present in half of patients. 676 implants were cementless. We registered 69 revisions, especially due to aseptic mobilization (16 THAs), implant breakage (9 THAs) and periprosthetic fracture (6 THAs). The MOM THAs overall Kaplan-Meier survival rate was 87.2 at 15 years, and the difference between MOM THAs and other implants two curves is statistically significant (p<0.05). Male sex is a significant risk factors. Further evaluations are in progress to establish the presence of any additional risk factors. We think weight and/or BMI may be included in this category. Our study confirms the data currently present in the literature regarding a lower survival of metal-on-metal hip prostheses. The male sex is a statistically significant risk factor (p<0.05), while age, head size and modularity of the prosthetic neck are not statistically significant (p>0.05). Any new finds will be presented at the congress venue

Pelvic discontinuity (PD) is a detrimental complication following total hip arthroplasty (THA). The aim of this study was to assess the clinical and radiological results of patients with PD who were revised using a custom-made triflange acetabular component (CTAC). This is a single centre prospective study of patients with PD following THA who were treated with a CTAC. The Hip Disability and Osteoarthritis Outcome Score (HOOS), modified Oxford Hip Score (mOHS), EurQol five-dimension three-level (EQ-5D-3L) utility, and Numeric Rating Scale (NRS), including visual analogue score (VAS) for pain, were gathered at baseline, and at one- and two-year follow-up. Clinical and radiological complications, including reasons for revisions were registered. Trends over time are described and tested for significance and clinical relevance. 18 females with 22 CTACs were included with a mean age of 73.5 years (SD 7.7). There were significant improvements between baseline and final follow-up in HOOS (p<0.01), mOHS (p<0.01), EQ-5D-3L utility (p<0.01), EQ-5D-3L NRS (p<0.01), VAS pain rest (p<0.01), and VAS pain activity (p<0.01). A minimal clinically important improvement in mOHS and the HOOS was observed in 16 patients (73%) and 14 patients (64%), respectively. Definite healing of the PD was observed in 19 hips (86%). Complications included six cases with broken screws (27%), four cases (18%) with bony fractures, and one case (4.5%) with sciatic nerve paresthesia. One patient with concurrent bilateral PD had revision surgery due to recurrent dislocations. No revision surgery was performed for screw failure or implant breakage. This is the first prospective assessment in clinical outcome of patients with PD who were treated with a CTAC. We have demonstrated that CTAC in patients with THA acetabular loosening and PD can result in stable constructs with no mechanical failures. Moreover, clinically relevant improvements in health-related quality of life at two years’ follow-up was observed

Introduction. Osseointegration is a potential treatment option for transfemoral amputees experiencing socket related problems. Till this date, there is little data assessing the feasibility and advantages of osseointegration in individuals with transtibial amputations. Materials and Methods. We prospectively followed 91 patients undergoing transtibial osseointegration from 2014–2018 who either 1) reported pain or mobility dissatisfaction with socket prosthesis; 2) had an intact limb with incapacitating pain, complex deformity, or profound distal weakness or 3) were recent amputees preferring osseointegration. Adverse events were monitored including infection, periprosthetic fracture, implant breakage, aseptic loosening, revision surgery/additional amputation and death. Functional outcomes were measured using the Questionnaire of persons with a Trans-femoral amputation (Q-TFA) and mobility was assessed using Six Minute Walk Test (6MWT) and Time Up and Go (TUG). Results. Following osseointegration surgery, there was a significant increase in the Q-TFA global score, the 6MWT and the K-levels during follow-up. At one year following Osseointegration surgery, all patients were pain-free, the 11 patients who were wheelchair-bound prior to surgery were ambulatory, and the other 27 patient unable to walk prior to surgery, demonstrated improved mobility. There were 7 cases of implant removals due to pain and loosening and 10 cases of revisions within an average of 1.8 years, of which 1 was aseptic loosening, 6 due to infection, 1 failure to integrate and 2 implant fractures. No periprosthetic bone fractures occurred. Conclusions. Transtibial osseointegration results in improved functional outcomes after amputation. Complications are manageable and should decrease with surgical and implant improvements

Introduction. Post-meniscectomy syndrome is broadly characterised by intractable pain following the partial or total removal of a meniscus. There is a large treatment gap between the first knee pain after meniscectomy and the eligibility for a TKA. Hence, there is a strong unmet need for a solution that will relieve this post-meniscectomy pain. Goal of this first-in-man study was to evaluate the safety and performance of an anatomically shaped artificial medial meniscus prosthesis and the accompanying surgical technique. Methods. A first-in-man, prospective, multi-centre, single arm clinical investigation was intended to be performed on 18 post-medial meniscectomy syndrome patients with limited underlying cartilage damage (Kellgren Lawrence scale 0–3) in the medial compartment and having a normal lateral compartment. Eventually 5 patients received a polycarbonate urethane mediale meniscus prosthesis (Trammpolin® medial meniscus prosthesis; ATRO Medical B.V., the Netherlands) which was clicked onto two titanium screws fixated at the native horn attachments on the tibia. PROMs were collected at baseline and at 6 weeks, 3, 6, 12 and 24 months following the intervention including X-rays at 6, 12 and 24 Months. MRI scans were repeated after 12 and 24 months. Results. The surgical technique to select the appropriately sized implant and correct positioning of the fixation screws and meniscus prosthesis onto the tibia was demonstrated feasible and reproducible. The surgeries showed that in particular the positioning of the posterior screw is crucial for correct positioning of the prosthesis. Inclusion stopped after 5 patients, who reached the 6 months evaluation. The PROMs did not improve in the first 6 months after surgery. All patients reported knee joint stiffness and slight effusion in their knee at 6 months follow-up. In case of symptomatic patients an evaluation of the device position and integrity was performed by MRI. In three patients the implants were removed because of implant failure and in one patient the implant was removed because of persistent pain and extension deficit. At present one patient has the implant still in situ. The explantations of the implants demonstrated no articular cartilage damage and the fixation screws were securely anchored. Discussion. This is the first clinical study with an artificial meniscus-like prosthesis. Except one, all implants were removed due to implant breakage or discomfort of the patient. Analysis of the torn implants showed fatigue failure resulting from the lack of loadsharing between implant and cartilage: the implant was too stiff and carried all the load in the medial compartment of the knee. Furthermore, the fixation with screws seemed too rigid which restricted the motion of the posterior horn. Based on previous in vitro and animal experiments, we expected more creep of the material and more motion on the screw fixation. Conclusion. This first-in-man clinical study demonstrates that the investigated device design is not safe and did not perform as expected. Therefore, modification of the meniscus prosthesis design and fixation technique is required to allow for more motion of the meniscus prosthesis during knee joint movement

Aim: Compressive forces on the medial femoral cortex and tensile forces at the lateral femoral cortex along with cortical comminution lead to a high risk of failure of surgical fixation of subtrochanteric fractures. The purpose of the study was to correlate the incidence of fracture healing complications to the surgical stabilisation method used. Methods: A comprehensive search of various data sources extending from 1966 to October 2003 was conducted to identify appropriate studies using specific search terms. We also scanned the reference lists of eligible studies for potentially relevant reports. Articles of all languages were considered. Studies with a follow-up of less than six months, pathological fractures, fractures treated non-operatively and studies reporting on less than ten fractures were excluded. Abstracts were also excluded. Each eligible study was independently reviewed by authors for methodological quality. A methodological scoring system adapted from that of Detsky was used. Guidelines for reporting of meta-analysis, adapted from QUOROM statement were followed. Results: 39 studies including 1835 fractures were analysed. For extramedullary devices, the incidence of non-union (35/673 – 5.2%), delayed union (11/221 – 4.7%), implant breakage ( 24/444 – 5.1%) and deep infection (14/459 – 3.0%) was statistically significantly higher than non-union (14/506 – 2.7%), delayed union (5/529 – 0.94%), implant breakage (12/628 –1.9%) and deep infection (9/764 – 1.2%) for intramedullary devices. Mortality and superficial infection were higher for extramedullary than intramedullary devices. However, this was not statistically significant. Malunion, shortening and implant cut out were higher for intramedullary than extramedullary devices. This was not statistically significant. Conclusion: The incidence of fracture healing complications appear to be significantly less with intramedullary than extramedullary devices. Based on this study, we advocate the use of intramedullary surgical fixation devices for subtrochanteric fractures

Neck modularity has been proposed to improve THA accuracy, thanks to the close restoration of anatomy, however it has been associated with issues like early breakages or corrosion. Our Hospital has been using neck modularity since the 90s, so we analyzed retrospectively implants performed between January 2000 and December 2014. The minimum follow up was 1Y. The cohort was composed of 1,033 THAs or 951 patients (82 bilateral), of which 643 females and 390 males. Average patient age was 67.7Y. THA indications were primary Osteoarthritis (80.9%), Fracture (9.0%), Congenital Dysplasia or Congenital Luxation (4.2%), Osteonecrosis (3.2%), other causes (2,7%). The stems used were all cementless, 381 anatomically shaped (36.9%), 635 straight (61.5%), 17 short MIS (1.6%). All necks used were made of Titanium alloy. 419 implants (40.5%) were manufactured by Wright Medical, while 614 (59.5%) were produced by Adler Ortho. A total of 37 revisions has been reported, mainly due to periprosthetic fractures (32.4%), luxation (24.3%), implant mobilization (18.9%) and implant breakage (16.2%). We have recorded 3 modular neck breakages. 4 patients required re-revisions, because of luxations (3) and neck breakage (1). The overall survival rate was 96.4%. We did not observe any component corrosion, probably thanks to the exclusive use of Titanium necks. We had a neck breakages rate of 0.29% and a luxation rate of 0.87%, lower than normally reported in the literature. In conclusion, our experience suggests as neck modularity could be a safe and effective way to reconstruct the proximal femur in THA patients

Ceramic on ceramic (CoC) Total Hip Replacement revisions give specific problems and no consensus is made on the way to perform it. The aim of this study was to report the results of THA CoC revisions and to identify the specific concerns. Between April 2007 and May 2016, 50 consecutive revisions have been performed on average 2.8 years after the THA, in 46 patients (28 males, 18 females) at a mean age of 55 years. The main reasons for revision were loosening (34%), pain without loosening (20%), infection (12%), implant breakage (10%), and instability (8%). There were 41 implant revisions, five revisions without implant change (10%) and four revisions for head change (8%). Revisions were performed without bone reconstruction in 68% of hips and with a CoC couple in 83% of hips. Three patients have died and three were lost to follow up. There were six intraoperative femoral fractures, one early and two late non−recurrent dislocations. Eight hips (16%) had re−revision with implant replacement. At a mean follow-up of 5.5 years, the mean PMA, Harris and WOMAC scores were 14.8, 72 and 23. 80% of patients were satisfied of the procedure and 89% were ready to re-do the surgery if necessary. 16% of hips experienced a noise. There were no complete lucent lines, no osteolysis, and no implant migration. Wear was not measurable. The 6-year survival rate was 82 % and 90 % if the end-point was implant revision for any cause and for fixation failure, respectively. CoC THA failure mainly affects a young population and occurs early. Failure is not wear-related but possibly related to inadequate technique. It is often possible to perform THA revision without any bone graft, using standard implants and CoC couple, provided the implants are matched

The anterior/Hueter approach to the hip was first described in 1883. It was then popularised in the 1940s by Judet in France using an orthopaedic positioning table which at the time was also used to treat a variety of orthopaedic injuries. In North America its use for joint replacements was limited to a few surgeons such as Kris Keggi in Connecticut using a regular surgical table as well as a select few surgeons (Joel Matta) who had trained with Emile Letournel, a student of Judet. It is fair to say that this anatomical approach to the hip was never forgotten but rather put aside as industry and clinicians focused on critical issues of implant breakage and failure as well as the larger problem of wear-related osteolysis. As we have made significant improvements in implant durability and fixation, the focus has now shifted on optimizing patient recovery and minimizing length of stay while providing the same quality of care. In these regards, the anterior approach provides a valid alternative to standard approaches to the hip due to its low risk of dislocation and minimal disruption to the musculature. In addition, the capacity of intra-operative imaging with the patient in the supine position provides assessment of component orientation as well as leg lengths. More importantly, like the advent of better instrumentation for the anterior approach, the use and optimization of the positioning table facilitates the execution of the anterior approach i.e. one assistant and no soft tissue release

Aims

The aim of this study was to investigate the safety and efficacy of 3D-printed modular prostheses in patients who underwent joint-sparing limb salvage surgery (JSLSS) for malignant femoral diaphyseal bone tumours.

Aims

National joint registries under-report revisions for periprosthetic joint infection (PJI). We aimed to validate PJI reporting to the Australian Orthopaedic Association National Joint Arthroplasty Registry (AOANJRR) and the factors associated with its accuracy. We then applied these data to refine estimates of the total national burden of PJI.

Background. Currently, stailess steel, titanium and carbon-fiber reinforced polyetheretherketone (CF-PEEK) plates are available for the treatment of distal radius fractures. Since the possibility to create a less rigid fixation may represent an advantage in case of ostheoporotic or poor quality bone, the aim of this study is to compare the biomechanical properties of these three materials in terms of bending stiffness with a single static load and after cyclical loading, simulating physiologic wrist motion. Materials and Methods. Three volar plating systems with fixed angle were tested: Zimmer stainless steel volar lateral column (Warsaw, IN); Hand Innovations titanium DVR (Miami, FL); Lima Corporate CF-PEEK DiPHOS-RM (San Daniele Del Friuli, Udine, Italy). For each type of plate tested four right synthetic composite bone radii were used. An unstable, extraarticular fracture was simulated by making an 8 mm gap with a saw starting 12 mm proximal to the articular surface of the radius on the distal radio-ulnar joint side. The osteotomies were made perpendicular to the long axis of the bone to allow for a consistent fracture gap on the dorsal and volar sides of the radius. Plates were implanted using all the distal and proximal fixation holes [Fig. 1]. Each synthetic radius model was potted in methylmethacrylate and tested in a bi-axial servo-hydraulic test frame (MTS Minibionix 858, universal testing machine) for load to failure by advancing a cobalt chrome sphere centered over the articular surface at a constant rate of displacement of 5 mm/min. The sphere was advanced until the construct failed or the dorsal edges of the fracture met. The resultant force was defined as bending stiffness pre fatigue. Three constructs for each plate were then dynamically loaded for 6000 cycles of fatigue at a frequency of 10Hz, with a load value corresponding to the 50% of the previously calculated bending strength. Finally, the constructs were loaded to failure, measuring the bending stiffness post fatigue. Results. All fracture constructs survived all phases of the cyclic loading testing. The mean bending stiffness pre fatigue was higher for the Zimmer plate (155.23±1.91 N/mm), in comparison to Hand Innovations (138.67±4.72 N/mm), and DiPHOS-RM (124.75±3.60 N/mm) [Fig. 2]. After cyclic loading, stiffness increased significantly of a mean 24% for the Zimmer plate (190.42±4.33 N/mm); 33% for the Hand Innovations (186.57±1.71 N/mm); and 18% for the DiPHOS-RM (146.28±1.52 N/mm) [Fig. 2–3]. Conclusions. CF-PEEK plate is less stiff than stainless steel and titanium plates, with an elastic modulus more similar to bone as well as the ability to withstand prolonged fatigue strain. From these preliminary data it might be assumed that the CF-PEEK plates could provide a sufficiently stable osteosynthesis, flexible enough to unload the implant-bone interface, minimising peak stresses at the bone- implant interface, making them particularly suitable for fracture fixation in osteoporotic patients. A proper patient selection (avoiding incompliant or non collaborative) should be performed using CF-PEEK plates to avoid possible implant breakage consequent to a fall or a second trauma on the injuried wrist until the complete fracture healing. For any figures or tables, please contact authors directly (see Info & Metrics tab above).

Introduction. When translating the principle of intramedullary nailing for trochanteric femoral fractures to Asian patients, design modifications made to adjust for anatomic differences resulted in an PFNA Asia. The primary endpoint of this study was the rate of complications attributable to fracture fixation. Material and methods. A prospective multicenter case series was performed; 176 patients with a median age of 84 with unstable trochanteric fractures treated with a PFNA Asia were included and followed for one year postoperatively. Complications were reviewed by a complication review board (CRB). Intra- and postoperative fracture fixation complications are presented according to type and incidence proportions (risk). Results. The CRB identified a total of three intraoperative (1.7%) and 14 postoperative fracture fixation complications (8%). Intraoperative complications included a problem with distal locking (1) and poor intraoperative reduction (2). Postoperative fracture fixation problems included significant neck shortening (8), implant breakage (3), cut-outs (2), and one severe loss of reduction. Outcome for most complications was adequate and none were classified as definitely related to the implant design but rather to surgical technique. Discussion & Conclusion. The adaptation of size and geometry to Asian patients leads to a low incidence of intra- and postoperative fracture fixation complications comparable to other studies

Aims

This study evaluated the definitions developed by the European Bone and Joint Infection Society (EBJIS) 2021, the International Consensus Meeting (ICM) 2018, and the Infectious Diseases Society of America (IDSA) 2013, for the diagnosis of periprosthetic joint infection (PJI).

Aims

The mid-term results of kinematic alignment (KA) for total knee arthroplasty (TKA) using image derived instrumentation (IDI) have not been reported in detail, and questions remain regarding ligamentous stability and revisions. This paper aims to address the following: 1) what is the distribution of alignment of KA TKAs using IDI; 2) is a TKA alignment category associated with increased risk of failure or poor patient outcomes; 3) does extending limb alignment lead to changes in soft-tissue laxity; and 4) what is the five-year survivorship and outcomes of KA TKA using IDI?

Implant wear and osteolysis have been a major cause of failure of total knee implants. In the mid-1990s, manufacturers recognised the impact of oxidation on wear with implants sterilised by gamma irradiation in air and changed their methods of sterilisation. This has resulted in a dramatic reduction in wear. In retrieval studies, non-irradiated polyethylene has not shown the fatigue type of failure associated with oxidation. The percentage of revisions done at the Anderson Clinic for polyethylene wear for osteolysis has dropped from 44% in the late 1990s to 4% in the past decade. With the continued use of polyethylene free of oxidation, we anticipate a further reduction in the need for revision surgery secondary to wear and osteolysis. Highly cross-linked polyethylene was introduced to further reduce wear with total knee implants. Higher levels of irradiation used increases crosslinking in the polyethylene but the material strength is reduced. Although volumetric wear is reduced, the wear particles are smaller in size and potentially more bio-reactive. The Manufacturer And User Device Experience Database (MAUDE) reports describe early implant breakage and osteolysis of highly cross-linked polyethylene inserts. Implants that were highly crosslinked with quenched free radicals demonstrate increased levels of oxidation after retrieval unlike, never implanted components “off-the-shelf”. Backside wear remains a concern as non-modular implants have better long-term survivorship compared to their modular counterparts. These reports should temper enthusiasm for using highly cross-linked material in knees or modular tibial components until longer term clinical and retrieval studies have been completed

In total hip arthroplasty (THA), acetabular cup orientation is critical for avoiding edge-loading and implant-implant impingement, which may lead to serious complications such as dislocation, mechanical loosening, accelerated wear, or implant breakage. Many studies recommended to place the acetabular cup radiographically at an inclination of <50° to avoid edge-loading. Simultaneously, larger prosthetic ROMs than the patients’ ROM during daily activities are needed to minimize impingement related complications. Several three-dimensional computer simulation studies have been done for optimal cup orientation to avoid prosthetic impingement within possible hip ROMs in the late 1990s. However, the reference angles in the directions of flexion, extension, external rotation and internal rotation at 90 ° flexion as possible hip ROMs have not been consistent in previous simulation studies. Thus, different reference angles of hip ROMs resulted in different optimal cup orientation. Therefore, to give accurate information about the reference hip ROM, we measured passive hip ROMs intraoperatively using a navigation system in 91 patients. Pelvic and femoral coordinate systems referred a functional pelvic plane in the supine position and a retrocondylar plane, respectively. The neutral position of the hip ROM was defined as the position in which corresponding axes of the pelvic and femoral coordinate systems were parallel. Maximum flexion, extension, external rotation and abduction were 120°, 36 °, 43 ° and 55 °, respectively. Moreover, we investigated the hip ROM during five traditional Japanese hip positions which required large hip flexion and internal rotation angles in five healthy female volunteers by a 3D image matching technique using an open-configuration MRI. Maximum flexion was 122 ° and maximum internal rotation was 40 ° at more than 90 ° of flexion position. Therefore, we recommended using 120 ° for flexion, 40 ° for extension, 40 ° for external rotation and 40 ° for internal rotation at 90 ° flexion as the reference ROM when calculating an optimum cup orientation. We calculated radiographic cup anteversion, when radiographic cup inclination was 40 °, without prosthesis impingement in the reference hip ROMs using computer aided design models of prosthesis, which included a cementless CentPillar stem with a head 32mm in diameter and cementless Trident cup with a flat liner. The results showed the optimal cup target zone existed when the stem anteversion was between 20 ° and 45 °. The size of the target zone was widest when the stem anteversion was 30 °, and then it was plus or minus 5 ° of inclination and anteversion from the center of the zone. To eliminate outliers of cup orientation form the target zone, a computer assisted system such as navigation is recommended