Primary care physicians rely on radiology reports to confirm a scoliosis diagnosis and inform the need for spine specialist referral. In turn, spine specialists use these reports for triage decisions and planning of care. To be a valid predictor of disease and management, radiographic evaluation should include frontal and lateral views of the spine and a complete view of the pelvis, leading to accurate Cobb angle measurements and Risser staging. The study objectives were to determine 1) the adequacy of index images to inform treatment decisions at initial consultation by generating a score and 2) the utility of index radiology reports for appropriate triage decisions, by comparing reports to corresponding images. We conducted a retrospective chart and radiographic review including all idiopathic scoliosis patients seen for initial consultation, aged three to 18 years, between January 1-April 30, 2021. A score was generated based on the adequacy of index images to provide accurate Cobb angle measurements and determine skeletal maturity (view of full spine, coronal=two, lateral=one, pelvis=one, ribcage=one). Index images were considered inadequate if repeat imaging was necessary. Comparisons were made between index radiology report, associated imaging, and new imaging if obtained at initial consultation. Major discrepancies were defined by inter-reader difference >15°, discordant Risser staging, or inaccuracies that led to inappropriate triage decisions. Location of index imaging, hospital versus community-based private clinic, was evaluated as a risk factor for inadequate or discrepant imaging. There were 94 patients reviewed with 79% (n=74) requiring repeat imaging at initial consultation, of which 74% (n=55) were due to insufficient quality and/or visualization of the sagittal profile, pelvis or ribcage. Of index images available for review at initial consult (n=80), 41.2% scored five out of five and 32.5% scored two or below. New imaging showed that 50.0% of those patients had not been triaged appropriately, compared to 18.2% of patients with a full score. Comparing index radiology reports to initial visit evaluation with <60 days between imaging (n=49), discrepancies in Cobb angle were found in 24.5% (95% CI 14.6, 38.1) of patients, with 18.4% (95% CI 10.0, 31.4) categorized as major discrepancies. Risser stage was reported in only 14% of index radiology reports. In 13.8% (n=13) of the total cohort, surgical or brace treatment was recommended when not predicted based on index radiology report. Repeat radiograph (p=0.001, OR=8.38) and discrepancies (p=0.02, OR=7.96) were increased when index imaging was obtained at community-based private clinic compared to at a hospital. Re-evaluation of available index imaging demonstrated that 24.6% (95% CI 15.2, 37.1) of Cobb angles were mis-reported by six to 21 degrees. Most pre-referral paediatric spine radiographs are inadequate for idiopathic scoliosis evaluation. Standardization of spine imaging and reporting should improve measurement accuracy, facilitate triage and decrease unnecessary radiation exposure.
Cobalt chrome femoral head has been used widely in total hip arthroplasty and has shown favorable outcome. However, there is still of concern of potential metal toxicity from the wear debris. In the other hand, titanium is well known for its biocompatibility but it is not used in bearing surface of arthroplasty due to its brittleness. Recently, coating of the prosthesis using plasma electrolytic oxidation (PEO) has shown favorable surface protection. Thus, in this study, we tried to find out whether the PEO coating on the titanium surface would provide surface protection. Five Titanium alloy (Ti-6Al-4V) ball mimicking femoral head was manufactured and was coted using plasma electrolytic oxidation. Wear rate was tested using validated wear tester with 10N compression force at 80rpm. The amount of wear was detected by measuring change of weight after wear test was completed. This was compared with femoral head manufactured with titanium alloy without PEO coating. Toxicity of the debris was also tested using MTT assay with human osteoblast cell line.Introduction
Materials and methods
Humeral retroversion is variable among individuals, and there are several measurement methods. This study was conducted to compare the concordance and reliability between the standard method and 5 other measurement methods on Twodimensional (2D) computed tomography (CT) scans. CT scans from 21 patients who underwent shoulder arthroplasty (19 women and 2 men; mean age, 70.1 years [range, 42 to 81 years]) were analyzed. The elbow transepicondylar axis was used as a distal reference. Proximal reference points included the central humeral head axis (standard method), the axis of the humeral center to 9 mm posterior to the posterior margin of the bicipital groove (method 1), the central axis of the bicipital groove –30° (method 2), the base axis of the triangular shaped metaphysis +2.5° (method 3), the distal humeral head central axis +2.4° (method 4), and contralateral humeral head retroversion (method 5). Measurements were conducted independently by two orthopedic surgeons.Background
Methods
There are still some controversies over the routine use of negative suction drainage after primary total hip arthroplasty (THA). In this study we are to know the benefits of new suction drainage management strategy after primary THA. From 2010 to 2012, two hundred patients who had unilateral primary THA were randomly allocated into two groups. One group had negative suction drainage immediately after THA (Group 1). In the other group, the suction drainage was inserted but negative pressure was applied more than 12 hours after surgery, in the morning postoperative day one (Group 2). All surgeries were performed by one single hip surgeon using the same technique and postoperative rehabilitation protocol was all same. We checked the amount of blood loss, changes in hemoglobin (Hb), volume of blood transfusion, superficial or deep wound infection and hematoma. Clinical results were evaluated using HHS score.Purpose
Materials and methods
Ultra high molecular weight polyethylene (UHMWPE) has been used successfully as a bearing material in hip, knee, and shoulder joint replacements. However, there are problems to cause a failure in UHMWPE component, which are wear behavior and creep deformation. Continuous bearing motion and dynamic load have occurred to UHMWPE wear debris caused osteolysis in periprosthetic tissue and to plastic deformation of joint component, and subsequent aseptic loosening of components. Therefore, many studies have being carried out in order to reduce wear debris and to improve mechanical strength from UHMWPE, and there is tremendous improvement of mechanical property in UHMWPE from gamma irradiated conventional UHMWPE (GIPE), highly crosslinked PE (XLPE), and XLPE with vitamin E1, 2. Friction has a significant one of the factors effect on the wear and creep deformation. In this study, the short-term frictional behaviors of three typical types of GIPE, remelted XLPE (R-XLPE), and s annealed XLPE (A-XLPE), and XLPE with Vitamin E against Co-Cr alloy were compared under three levels of contact pressures which occured in hip, knee, and shoulder joints. Friction tests were conducted with UHMWPE against Co-Cr alloy by using pin-on-disk type triboteter. For test, tribotester performed in a repeat pass rotational slidintg motion with a velocity of 60rpm. Applied contact pressure selected three kinds of levels, 5, 10, and 20MPa which were within the range of maximum contact pressures for total hip, knee, and shoulder joint replacements. To analyze the frictional effect of UHMWPE type, it conducted t-test and p-values less than 0.05 were used to determine the statistically significant difference.Introduction
Methods
Total hip arthroplasty (THA) is the most common surgery performed for complications of bipolar arthroplasty. The present study evaluated the functional results and complications associated with this surgery. Forty eight hips (48 patients) who had conversion of bipolar arthroplasty to THA between 1998 June and 2013 June, and who were followed-up for more than one year were evaluated. Twenty one hips had conversion surgery to THA using a Fitmore cup with metal-on-metal articulation (28 mm head). Six hips had surgery using the SecurFit cup and three hips, using the Lima LTO cup with ceramic-on-ceramic articulation (28 mm or 32 mm head). Eighteen hips had surgery using a large head metal-on-metal bearing: –MMC (seven hips), ACCIS (six hips) and Magnum (five hips). The average time of follow-up duration was 3.9 years (range, 1.0–11.3). There were 22 men and 26 women between the ages of 28 and 80 years (average, 68.9 years) at the time of conversion surgery. Conversion arthroplasty was performed for acetabular erosion without femoral stem loosening in 19 hips, acetabular cartilage erosion with femoral stem loosening in 13 hips, periprosthetic fracture in 12 hips, and recurrent dislocation in four hips. Results were evaluated using Harris hip score (HHS) and Western Ontario McMaster Universities Osteoarthritis Index (WOMAC) score. The radiographs were analyzed for evidence of acetabular and femoral osteolysis or loosening. The complications were evaluated.Introduction
Patients and Methods
Cementless grit-blasted tapered-wedge titanium femoral stems are being used with increasing frequency in hip arthroplasty because of excellent long-term outcomes. However, periprosthetic femur fracture is a potentially worrisome phenomenon in these types of femoral stems. The aim of this study is to report the incidence of stem loosening in association with periprosthetic femur fractures following hip arthroplasty using cementless grit-blasted tapered-wedge stems. A total of 36 Vancouver Type B1 and B2 periprosthetic femur fractures following either hemiarthroplasty or total hip arthroplasty using cementless grit-blasted tapered-wedge titanium femoral stems (GB group) were identified from a retrospective review of the medical records at three participating academic institutions. The control group consisted of 21 Vancouver Type B1 and B2 periprosthetic femur fractures following either hemiarthroplasty or total hip arthroplasty using cementless proximal porous-coated femoral stems (PC group) at the same institutions during the same period of the study. All femoral stems included in this study had been a well-fixed state before the occurrence of periprosthetic femur fractures. All patients in both groups were treated surgically with either open reduction and internal fixation or femoral stem revision. Femoral stem stability was assessed by preoperative radiographs and was confirmed by intraoperative scrutinization. The incidence of stem loosening was compared between the groups.Introduction
Materials & Methods
Micro-arc oxidation (MAO) is an electrochemical method used to treat metal surfaces. It provides nanoporous pits, and thick oxide layers, and incorporates calcium and phosphorus into the coating layer of titanium alloy. This modification on the surface of titanium alloy by MAO coating would improve the ability of cementless stems to osseointegrate. In spite of these structural and chemical advantages, clinical study of total hip arthroplasty (THA) using MAO coated stem has not yet been reported. In this study, we evaluated the clinical and radiographic results associated with cementless grit-blasted tapered-wedge stems that were identical in geometry but differed with regard to surface treatment with or without MAO coating. We performed a retrospective review of 141 THAs using MAO coated stem for a minimum of 5 years and compared them to 219 THAs using the same geometry stem without MAO coating. A cementless Bencox femoral component (Corentec, Seoul, Korea) was used in all hips. It is made of titanium alloy with a straight, double wedged, tapered stem with a rectangular cross-section. Surface treatment was performed using grit blasting with a roughness of 5.5ųm that was available either with or without MAO coating. Clinical and radiographic evaluations were performed preoperatively and at 6 weeks, 3 months, 6 months, and 1 year postoperatively, and then annually.Introduction
Materials & Methods
Constrained condylar knee (CCK) prosthesis offers an implant option for complex revision total knee arthroplasties in which stable varus-valgus constraint as well as rotational control is needed for severe bone defect and ligament insufficiency. The aim of this study was to evaluate the clinical and radiological outcome of CCK prosthesis in revision TKA. Fify-one revision TKAs performed using CCK prosthesis between Jan. 1998 and Feb. 2006 were performed. The mean follow-up period was 5 years and 3 months (2 to 9 years) and the interval between initial and revision TKA was 8 years (4 months to 21 years). The mean age was 67 years. Range of motion (ROM), knee society (KS) score, hospital for special surgery (HSS) score, complication rate and failure rate was evaluated. The tibiofemoral angle and radiolucent line was also evaluated on plain radiograph. The mean ROM improved from 81.9° to 102°. The mean KS score improved from 49.3° to 79.7°, and KS function score from 50.3 to 71.0 (P<
.001). The mean HSS score improved from 50.7 to 78.7 (P<
.001). Tibiofemoral angle improved from valgus 3.1° to valgus 5.6° (P<
.001). Radiolucent line more than 2mm was observed around 4 femoral and 4 tibial components. Complications including 1 skin necrosis, 1 tibial tubercle nonunion, 2 infections, 3 periprosthetic fractures and 5 arthrofibrosis were observed. Overall rating was excellent or good in 88% at the last follow up. Revision TKA using CCK prosthesis showed comparable results with other reports in average 5 years follow-up.
The aim of this study was to evaluate the rotational axis of the tibia and the association of its axis to tibial coronal alignment after TKR. TKRs were performed using navigated mobile bearing system (40 knees), conventional mobile bearing (48 knees) and conventional fixed bearing (40 knees) and preoperative and postoperative CT scans were assessed using 3D image reconstruction-analysis program. The tibial AP axis which was defined as the line connecting the middle of the PCL and the medial edge of the patellar tendon attachment was measured relative to the AP axis of distal femur preoperatively and postoperatively, as well as the coronal angle of the tibia and posterior slope. The tibial coronal alignments in navigation, postoperative plain radiograph and CT were compared. The AP axis of the tibia was in 2.10° internally rotated position relative to the AP axis of the femur preoperatively and 3.54° postoperatively (range, 19.5° internal rotation to 16.8° external rotation). The coronal angle of the tibia was 0.46° varus on plain radiograph, 0.72° varus on CT, 0.37° valgus in navigation (p=0.005). Posterior slope was 2.53° on plain radiograph and 0.67° in navigation (p<
0.001). There was no correlation between postoperative rotational position of the tibia relative to the femur and the difference in the tibial coronal angle between navigation data and CT. The proposed anteroposterior axis of the tibia centered between 0 to 5 degrees internally rotated position relative to the femur but showed wide range of deviation. The rotation angle of the tibial cutting in navigated TKR did not influence on the postoperative measurement discrepancy between navigation and CT.
The aim of this study was to evaluate passive kinematics of a mobile-bearing, ultracongruent (UC) total knee design compared with a mobile-bearing, posterior stabilised (PS) design intraoperatively using navigation system. Thirty-four knees of 24 patients which had undergone total knee arthroplasty with UC prosthesis (E-motion®, Aesculap, Tuttlingen, Germany) for primary osteoarthritis and fifteen knees of 14 patients with PS prosthesis (E-motion®) were included in this study. Thirty-one female and seven male patients were included and the mean age was 70.4 years. Patients were followed up for 7.26 months (6 to 12 months). Intraoperative kinematics including valgus/varus rotation, internal/external rotation, and anterior/posterior translation was assessed from 10° to 120° of passive flexion before and after total knee replacement using a surgical navigation system (Orthopilot®, Aesculap). The range of motion (ROM) was measured preoperatively and at the final follow up. The tibiofemoral alignment in 10° flexion changed from varus 5.85° to valgus 0.38° in UC group and changed from varus 7.45° to valgus 1.08° in PS group (p>
0.05), the magnitude of varus rotation during flexion was 0.01° in UC group and 4.08° in PS group (p<
0.05). PS knee showed the tendency to slight varus alignment during flexion but UC knee showed the tendency toward valgus alignment fter midflexion. The mean internal rotation during flexion was 10.3° in UC group and 13.2° in PS group (p>
0.05). The translation of the femur was 4.99mm posteriorly in UC group and 3.24mm posteriorly in PS group at 120° flexion (p>
0.05). The maximum flexion angle at the final follow up was 123° in UC group and 118° in PS group (p>
0.05). Total knee arthroplasty with high flexion PS prosthesis showed good ROM and satisfactory early clinical results. UC total knee design showed less varus rotation during flexion, more valgus pattern in higher flexion angle than PS design, similar internal rotation angle and pattern, and similar posterior translation at 120° flexion with PS design.
Ultra-high molecular weight polyethylene (UHMWPE) has been used for the bearing liner or inlay components in total joint replacements such as total hip, knee, and artificial disk since 1960’s. UHMWPE components generate wear debris during articulation, which play a key role in osteolysis, subsequent aseptic loosening, and eventually revision surgery. Efforts to solve the wear problem in UHMWPE and to quantify the amount of wear have driven many studies. But in vivo radiographic penetration depth measurement is the result of both wear and viscoelastic creep. Previous study reported that over 70% of the dimensional changes in UHMWPE acetabular cups were due to creep. Creep deformation was quantified under the static and dynamic compressive pressures (2, 4, 8Mpa) that are clinically relevant for the hip joint loads in normal motions. However, according to the finite element stress analyses in UHMWPE components under the active motions in hip, knee, and artificial disk replacements, very high level of contact pressures locally ranged from under 10MPa up to over 60Mpa. In this study, we quantified the creep of UHMWPE under the several high levels of dynamic compressive pressures and compared the results from the previous results. For creep tests, UHMWPE rectangular blocks (10mm long, 10mm wide, 8mm thick) were manufactured from molded unirradiated Chirulen® 1020 sheet (MediTECH, Deutchland). MTS 858 hydraulic test machine was used for conducting the dynamic compressive creep tests under the four different sinusoidal (1Hz) maximum pressures of 10, 20, 40, and 60MPa and minimum pressures of 1, 2, 4, and 6MPa, respectively. All tests were conducted for a total duration of 4×103 minutes at ambient conditions. During the test the displacements of crosshead were stored and the changes in thickness of block specimen devided by the initial thickness were calculated to get the creep strain. The mean dynamic compressive creep strain increased as the loading time increased and had a linear relationship (R2=0.96) with the logarithmic scale of time for all maximun pressures. Over 90% of total creep strain occurred within the first 103 minutes. The rates of creep strain (slopes of curve fitting in logarithmic scale of time) for each maximum pressure were listed in Table 1 with the rates of creep strain for low maximum pressures from the previous study [3]. The rates of creep strain increased linearly as the maximum pressure increased for both current study (R2=0.96) and previous study (R2=0.99). The slope of linearity for the current study with high levels of contact pressures was a little larger than that for the previous study with low levels of contact pressures. This difference in the slope of linearity between current and previous studies lies in the creep recovery during measurement of specimen thickness by micrometer in the previous study. Neglecting this difference, the results of current study can be extrapolated to anticipate the creep strain of UHMWPE under the dynamic compression for the low levels of contact pressures.
Clinical experience has shown the needs for high flexion. The aim of this study was to evaluate the clinical and radiological results of a fixed bearing high flexion posterior stabilized (PS) total knee arthroplasty (TKA). Between July 2001 and December 2005, 422 TKAs in 288 patients were performed with high flexion PS prosthesis and 378 knees of 258 patients had been followed up for 2 to 6.5 years (mean: 3 years 11 months). We evaluated range of motion (ROM), Knee rating system of the Hospital for Special Surgery (HSS) and Knee Society (KS) score, and radiological results. The mean flexion improved from 110.1 degrees to 126.7 degrees at the latest follow-up. 333 knees (88 %) showed more than 120 degrees of flexion, 105 knees (28 %) more than 140 degrees of flexion. The mean KS clinical score improved from 39 to 93 points (p<
0.01) and KS function score, from 40 to 85.4 points (p<
0.01). The mean HSS score improved from 41.2 to 86.3 points (p<
0.01). In 28 knees, radiolucent line of 1–2 mm in width was observed at zone 1 without symptoms. Aseptic loosening in 4 knees, Mid-flexion instability in 2 knees, superficial infection in 3 knees and deep infection in 3 knees were observed. Total knee arthroplasty with high flexion PS prosthesis showed good ROM and satisfactory early clinical results. Complication rate was similar to those of other series. Close observation and serial radiological evaluation are needed for long term results.
Recently with the introduction of operations using various instrument of total ankle arthroplasty, we are showing quite satisfactory short term results on the treatment of resolved pain of ankle joint. However, there have been reports of high probability of complication from total ankle arthroplasty to other arthroplasty applied to other joints. Therefore in order to make the results of ankle arthroplasty superior, it is necessary to reduce these complications. We try to analyze complications that occur often and come up with the best results. There were 45 cases of 42 patients of HINTEGRA® (Newdeal SA, Lyon, France) model from November 2004 to August 2006. Follow up averaged 33.5 months, the average age of patients was 61.1 years, with 14 males and 28 females. We evaluated the complications and analyzed the causes of failures. There was a total 15 cases of complications; 5 cases of medical impingement syndrome, 3 cases of varus malposition, 2 cases of delayed healing of wound, 1 case of peroneal nerve problem, medial malleolar fracture, postoperative deep infection and gouty arthritis pain and Achilles tendinitis. Our conclusion is that total ankle arthroplasty had more complication rate than other joint arthroplasty, so we need a more meticulous preoperative and perioperative care.