Periprosthetic femoral fractures (PFFs) remain a major concern following cementless total hip arthroplasty (THA). This study aimed to evaluate the association between different types of cementless tapered stems and the risk of postoperative PFF. A retrospective review of primary THAs performed at a single center from January 2011 to December 2018 included 3,315 hips (2,326 patients). Cementless stems were classified according to their design geometry using the system proposed by Radaelli et al. The incidence of PFF was compared between flat taper porous-coated stems (type A), rectangular taper grit-blasted stems (type B1), and quadrangular taper hydroxyapatite-coated stems (type B2). Multivariate regression analyses were performed to identify independent factors related to PFF. The mean follow-up duration was 61 months (range, 12‒139 months). Overall, 45 (1.4%) postoperative PFFs occurred. The incidence of PFF was significantly higher in type B1 stems than in type A and type B2 stems (1.8 vs. 0.7 vs. 0.7%; P=0.022). Additionally, more surgical treatments (1.7 vs. 0.5 vs. 0.7%; P=0.013) and femoral revisions (1.2 vs. 0.2 vs. 0%; P=0.004) were required for PFF in type B1 stems. After controlling for confounding variables, older age (P<0.001), diagnosis of hip fracture (P<0.001), and use of type B1 stems (P=0.001) were significant factors associated with PFF. Type B1 rectangular taper stems were found to have higher risks for postoperative PFF and PFF requiring surgical management than type A and type B2 stems in THA. Femoral stem geometry should be considered when planning for cementless THA in elderly patients with compromised bone quality.
Obesity is associated with poor outcomes and increased risk of failure after rotator cuff (RC) repair surgery. The effect of diet-induced obesity (DIO) on enthesis healing has not been well characterised and whether its effects can be reversed with dietary intervention is unknown. We hypothesised that DIO would result in inferior enthesis healing in a rat model of RC repair and that dietary intervention in the peri-operative period would improve enthesis healing. A total of 78 male Sprague-Dawley rats were divided into three weight-matched groups from weaning and fed either: control diet (CD), high-fat diet (HFD), or HFD until surgery, then CD thereafter (HF-CD). After 12 weeks the left supraspinatus tendon was detached, followed by immediate surgical repair. At 2 and 12 weeks post-surgery, animals were cullers and RCs harvested for biomechanical and histological evaluation. Body composition and metabolic markers were assessed via DEXA and plasma analyses, respectively. DIO was established in the HFD and HF-CD groups prior to surgery, and subsequently reversed in the HF-CD group after surgery. At 12 weeks post-surgery, plasma leptin concentrations were higher in the HFD group compared to the CD group (5.28 vs. 2.91ng/ml, P=0.003). Histologically, the appearance of the repaired entheses was poorer in both the HFD and HF-CD compared to the CD group at 12 weeks (overall histological score 6.20 (P=0.008), 4.98 (P=0.001) and 8.68 out of 15, respectively). The repaired entheses in the HF-CD group had significantly lower (26.4 N, P=0.028) load-at-failure 12 weeks post-surgery compared to the CD group (34.4 N); while the HFD group was low, but not significantly different (28.1 N, P=0.096). Body mass at the time of surgery, plasma leptin and body fat percentage were negatively correlated with histological scores and plasma leptin with load-at-failure 12 weeks post-surgery. DIO impaired enthesis healing in this rat RC repair model, with inferior biomechanical and histological outcomes. Restoring normal weight with dietary change after surgery did not improve healing outcomes. Exploring interventions that improve the metabolic state of obese patients and counselling patients appropriately about their modest expectations after repair should be considered.
We hypothesised that diet-induced obesity (DIO) would result in inferior enthesis healing in a rat model of rotator cuff (RC) repair and that dietary intervention in the peri-operative period would improve enthesis healing. A total of 78 male Sprague-Dawley rats were divided into three weight-matched groups from weaning and fed either: control diet (CD), high-fat diet (HFD), or HFD until surgery, then CD thereafter (HF-CD). After 12 weeks, the left supraspinatus tendon was detached, followed by immediate surgical repair. At 2 and 12 weeks post-surgery, animals were culled, and RCs harvested for biomechanical and histological evaluation. Body composition and metabolic markers were assessed via DEXA and plasma analyses, respectively. DIO was established in the HFD and HF-CD groups before surgery and subsequently reversed in the HF-CD group after surgery. Histologically, the appearance of the repaired entheses was poorer in both the HFD and HF-CD groups compared with the CD group at 12 weeks after surgery, with semiquantitative scores of 6.2 (P<0.01), 4.98 (P<0.01), and 8.7 of 15, respectively. The repaired entheses in the HF-CD group had a significantly lower load to failure (P=0.03) at 12 weeks after surgery compared with the CD group, while the load to failure in the HFD group was low but not significantly different (P=0.10). Plasma leptin were negatively correlated with histology scores and load to failure at 12 weeks after surgery. DIO impaired enthesis healing in this rat RC repair model, with inferior biomechanical and histological outcomes. Restoring normal weight with dietary change after surgery did not improve healing outcomes. Circulating levels of leptin significantly correlated with poor healing outcomes. This pre-clinical rodent model demonstrates that obesity is a potentially modifiable factor that impairs RC healing and increases the risk of failure after RC surgery.
The purpose of this study is to compare the mid-term outcomes between rotating platform(RP) and posterior cruciate substitute(PS) bearings in LCS-total knee arthroplasty (TKA). This is a prospective randomized matched-pairs case–control study of patients who underwent primary TKAs with a minimum 2 years follow-up. The inclusion criteria was degenerative arthritis, and exclusion criteria was arthritis other than degeneration, previous operations such as osteotomy, body mass index (BMI) over 30 kg/m2. The matching criteria were set as age, BMI, preoperative ROM, gender, and the Knee Society (KS) and Hospital for Special Surgery (HSS) scores. After 1:1 matching, 50 cases involved the LCS RP bearing system as group 1 and 50 cases involved LCS PS bearing system group as group 2. Clinical and radiographic outcomes were evaluated.Purpose
Methods
The fourth generation ceramic, in which zirconia is incorporated into the alumina matrix, was developed to reduce the risk of ceramic fractures. The purpose of this study was to evaluate the survivorship, clinical and radiographic results, and bearing-related failures associated with total hip arthroplasty using zirconia-toughened alumina ceramic-on-ceramic bearings over a minimum follow-up of 5 years. We retrospectively analysed 135 patients (151 hips) who underwent cementless total hip arthroplasty using zirconia-toughened alumina ceramic-on-ceramic bearings. There were 58 men and 77 women with mean age of 55.9 years (range, 20 to 82 years) at index surgery. Acetabular and femoral components were cementless in all hips. A 36 mm head was used in 81 of 151 hips and a 32 mm head was used in 70 hips with smaller acetabular shells. The mean duration of follow-up was 6.1 years (range, 5 to 6.8 years).Purpose
Materials and methods
The use of tranexamic acid (TXA) in primary total hip arthroplasty (THA) is supported by many studies that confirm its efficacy for decreasing blood loss, but the comparison between topical intra-articular (IA) and intra-venous (IV) is unclear, especially combined with chemical prophylaxis. The purpose of this study is to verify non-inferior efficacy of topical IA TXA compared with IV TXA in primary THA. A single center, randomized, controlled clinical trial was performed to compare topical IA TXA (2 g of TXA in 100 cc of normal saline) with two IV doses of TXA (1 g dose before surgery and another 1 g dose 3 hours later) on blood loss. The primary outcome was total blood loss as calculated from the difference between the preoperative hemoglobin (Hb) and the lowest postoperative Hb. The secondary outcome included drained blood loss, transfusion volume, and thromboembolic events. The sample size of 112 patients was calculated to give a statistical power of 99% for demonstrating inferiority. Fifty-six patients each was assigned to receive topical IA TXA (IA group) and IV TXA (IV group). There were no significant differences in demographics and preoperative laboratory values between the two groups. Non-inferiority was estimated by comparing the confidence interval with a delta of 10%. All subjects took oral direct factor Xa inhibitor to prevent venous thromboembolism included during 2 weeks after surgery.Introduction
Methods & Methods
The range of motion (ROM) obtained after total knee arthroplasty (TKA) is an important measurement to evaluate the postoperative outcomes impacting other measures such as postoperative function and satisfaction. Flexion contracture is a recognized complication of TKA, which reduces ROM or stability and is a source of morbidity for patients. The purpose of this study was to evaluate the influence of intra-operative soft tissue release on correction of flexion contracture in navigated TKA.Introduction
Objectives
As the proximal femoral bone is generally compromised in failed total hip arthroplasty, achievement of solid fixation with a new component can be technically demanding. Clinical studies have demonstrated good medium-term results after revision total hip arthroplasty using modular fluted and tapered distal fixation stems, but, to our knowledge, long-term outcomes have been rarely reported in the literature. The purpose of this study was to report the minimum ten-year results of revision total hip arthroplasty using a modular fluted and tapered distal fixation stem. We analyzed 40 revision THAs performed in using a modular fluted and tapered distal fixation stem (Fig. 1) between December 1998 and February 2004. There were 11 men (12 hips) and 28 women (28 hips) with a mean age of 59 years (range, 38 to 79 years) at the time of revision THA. According to the Paprosky classification of femoral defects, 5 were Type II, 24 were Type IIIA, and 11 were Type IIIB. An extended trochanteric osteotomy was carried out in 21 (52%) of the 40 hips. Patients were followed for a mean of 11.7 years (range, 10 to 15 years).Introduction
Materials & Methods
Patients with osteonecrosis of the femoral head are typically younger, more active, and often require high rates of revision following primary total hip arthroplasty. However, outcomes of revision hip arthroplasty in this patient population have been rarely reported in the literature. The purpose of this study was to report the intermediate-term clinical and radiographic outcomes of revision hip arthroplasty in patients with osteonecrosis of the femoral head. Between November 1994 and December 2009, 187 revision hip arthoplasty were performed in 137 patients who had a diagnosis of osteonecrosis of the femoral head. Exclusion criteria included infection, recurrent instability, isolated polyethylene liner exchange, and inadequate follow-up (less than 3 years). The final study cohort of this retrospective review consisted of 72 patients (75 hips) with a mean age of 53.3 years (range, 34 to 76). Components used for the acetabular revision included a cementless porous-coated cup in 58 hips and an acetabular cage in 2 hips. Components used for the femoral revision included a fully grit-blasted tapered stem in 30 hips and a proximally porous-coated modular stem in 9 hips. The mean duration of follow-up was 7 years (range, 3 to 17).Introduction
Materials & Methods
The purpose of this study is to investigate the relationship between the angles made by the reference axes on the computerized tomography (CT) images and comparison of the knee alignment between healthy young adults and patients who is scheduled to have total knee arthroplasty. This study was conducted in 102 patients with osteoarthritis of knee joint who underwent preoperative computerized tomography (CT). The control group included 50 patients having no arthritis who underwent CT of knee. Axial CT image of the distal femur were used to measure the angles among the the anteroposterior (AP) axis, the posterior condylar axis (PCA), clinical transepicondylar axis (cTEA) and the surgical transepicondylar axis (sTEA). Then, the differences in amounts of rotation between normal and osteoarthritic knee was evaluated.Purpose
Materials and Methods
Management of the patella with poor bone stock remains a challenge in revision total knee arthroplasty (TKA). The purpose of this study was to evaluate the results of a novel surgical technique in which widely available wires and acrylic bone cement are used in the reconstruction of a deficient patella. Twenty-eight patients (30 knees) underwent revision TKA in which a deficient patella was treated with an onlay-type prosthesis and bone-augmenting procedure, using transcortical wiring. The technique was indicated when the thickness of remnant patella was less than 8mm with variable amounts of the peripheral rim. The remaining patellar height ranged from 3.2mm to 7.3mm. Follow-up was available for all patients with a mean of 36.6 months (range, 24 to 55 months). The respective mean Knee Society scores for knee and function improved from 34.2 points (range, 18 to 65 points) and 23 points (range, 18 to 46 points) preoperatively to 73.5 points (range, 30 to 88 points) and 61points (range, 34 to 80 points) at final follow-up. The mean thickness of the patellar construct was 14.6mm (range, 12.2 – 18.3mm). One patient experienced patellar fracture during knee flexion one week after surgery. There were no complications associated with implanted hardware. A patellar bone-augmenting procedure using transcortical wiring is a straightforward technique that potentially allows firm fixation. Considering the satisfactory short- to mid-term results, we believe that this technique provides a good alternative option in addressing this challenging problem in revision TKA.
Modern ceramic-on-ceramic bearings have become attractive alternatives to conventional polyethylene due to their low wear and minimal particle production. However, ceramic-on-ceramic implants have been associated with ceramic fracture and squeaking. To address these issues, large ceramic heads with a titanium-alloy sleeve have been introduced although limited data are available on their clinical outcomes. The purpose of this study was to report the midterm results of primary total hip arthroplasty using a 32mm with a titanium-alloy sleeve. We reviewed 245 patients who had 274 total hip arthroplasties with a 32 mm ceramic head with a titanium-alloy sleeve and had been followed for more than 5 years (average, 6.5 years; range, 5–9 years). The mean patient age at the time of surgery was 55.1 years (range, 16–82 years). All operations were performed at a single center. All of the ceramic implants were hot isostatic pressed, laser-marked, proof-tested third-generation alumina (Fig. 1). We determined the implant survival, Harris hip scores, incidence of ceramic fracture or noisy hips, and presence of osteolysis.Introduction
Materials & Methods
Management of the patella with poor bone stock remains a challenge in revision total knee arthroplasty (TKA). The purpose of this study was to evaluate the results of a novel surgical technique in which widely available wires and acrylic bone cement are used in the reconstruction of a deficient patella. Twenty-eight patients (30 knees) underwent revision TKA in which a deficient patella was treated with an onlay-type prosthesis and bone-augmenting procedure, using transcortical wiring. The technique was indicated when the thickness of remnant patella was less than 8mm with variable amounts of the peripheral rim. The remaining patellar height ranged from 3.2mm to 7.3mm. Follow-up was available for all patients with a mean of 36.6 months (range, 24 to 55 months).Background
Methods
Highly cross-linked polyethylene has been introduced to decrease osteolysis secondary to polyethylene wear debris generation, but there are few long-term data on revision total hip arthroplasty using highly cross-linked polyethylene liners. The purpose of this study was to report the long-term radiographic and clinical outcomes of a highly cross-linked polyethylene liner in revision total hip arthroplasty. We analyzed 63 revision total hip arthoplasties that were performed in 63 patients using a highly cross-linked polyethylene liner between April 2000 and February 2005. Of these, nine died and four were lost to follow-up before the end of the 10-year evaluation. Thus, the final study cohort consisted of 50 patients (50 hips). There were 26 males and 24 females with a mean age at time of revision total hip arthoplasty of 53 years (range, 27–75 years). Mean duration of follow-up was 11 years (range, 10–14 years).Introduction
Materials & Methods
A large proportion of patients with osteoarthritis of the knee, present with bilateral symptoms at the outpatient department. A simultaneous total knee arthroplasty (TKA) procedure is available for such patients. The first operation in a simultaneous surgery may provide information to the operator to determine component size, soft tissue balancing, and estimate gap size for the second operation, while the second team usually conducts an operation in a confined space on the contralateral side during closure for the first operation, which can disturb cooperation during the second operation and may lead to more intra-operative surgical errors. We hypothesized that the circumstances of the two consecutive operations of a simultaneous bilateral TKA are different, could lead to different outcomes of overlapping bilateral TKAs. We therefore addressed the following research questions to determine whether there would be differences in short-term clinical outcomes, radiographic results, and implanted component size between the two sides A retrospective review of 451 consecutive patients, who underwent simultaneous bilateral TKA between January 2011 and April 2012, was conducted. Bilateral TKAs were performed with the senior surgeon conducting the main procedure (from skin incision to implantation of first prosthesis until prior closure of the first knee) on the right side first and subsequently the left side with a second team. At 1 year after surgery, clinical outcome scores (the Knee Society Knee and Function scores, WOMAC score), radiologic findings were evaluated and clinical results as postoperative blood loss, operation time were compared between bilateral sides.Introduction
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
The outcome of previous cemented total hip arthroplasty has been reported to be inferior in renal transplant patients because of poor bone stock resulting from long-term steroid use. Moreover, as renal transplant patients remain on immunosuppressant therapy for life, higher levels of overall morbidity must be considered. We evaluated the mid-term results of cementless total hip arthroplasty in renal transplant recipients with osteonecrosis of the femoral head, and compared those with age and sex matched osteonecrosis patients that had not undergone organ transplantation or been treated with long-term steroid. Between October 1997 and October 2008, 45 consecutive primary cementless total hip arthroplasties were performed in 30 patients with advanced osteonecrosis of the femoral head after renal transplantation. There were 18 males (27 hips) and 12 females (18 hips) of overall mean age 44 years (22 to 68). The clinical and radiographic results of cementless total hip arthroplasty in these 45 hips were compared with those of 96 sex and age-matched osteonecrotic hips of 72 patients that had not undergone organ transplantation or long-term steroid use. Patients were evaluated at surgery and at a mean of 7.2 years (range, 2–13 years) postoperatively.Introduction:
Materials & Methods:
Ceramic head with titanium-alloy sleeve offers a modular ceramic head solution for the damaged taper in revision total hip arthroplasty (THA). It can also be used in primary THA to reduce the risk of ceramic head fracture. The purpose of the present study was to report the intermediate-term outcomes of primary ceramic-on-ceramic THA with use of ceramic head with titanium-alloy sleeve. We evaluated 244 patients (271 hips) who had undergone primary ceramic-on-ceramic THA with use of BIOLOX® forte 32 mm ceramic head with titanium-alloy sleeve between November 2005 and August 2009. There were 158 males (175 hips) and 86 female (96 hips) patients with a mean age of 55.5 years. Clinical and radiographic evaluation was performed at a mean of 4.6 years (range, 2–7 years) postoperatively.Introduction:
Materials & Methods:
The management strategy regarding optimally addressing polyethylene wear with a well-fixed acetabular shell remains controversial. The purpose of the present study was to document outcomes of cementation of a highly cross-linked polyethylene (PE) liner into a well-fixed acetabular metal shell in 36 hips We identified 37 patients (39 hips) who had undergone revision THA by cementation of a highly cross-linked PE liner into a well-fixed metal shell between June 2004 and April 2009. Of these patients, one (1 hip) died before the end of the 3-year evaluation and another was lost to follow-up. Thus, the study cohort consisted of 35 patients (36 hips). There were 23 males (24 hips) and 12 female (12 hips) patients with a mean age at time of revision surgery of 57.6 years (range, 38–79 years). All operations were performed by a single surgeon using only one type of liner. Clinical and radiographic evaluation was performed at a mean of 6.1 years (range, 3–8 years) postoperatively.Introduction:
Materials & Methods:
A functional total knee replacement has to be well aligned, which implies that it should lie along the mechanical axis and in the correct axial and rotational planes. Incorrect alignment will lead to abnormal wear, early mechanical loosening, and patellofemoral problems. There has been increased interest of late in total knee arthroplasty with robot assistance. This study was conducted to determine if robot-assisted total knee arthroplasty is superior to the conventional surgical method with regard to the precision of implant positioning. Twenty knee replacements of ten robot-assisted and another ten conventional operations were performed on ten cadavers. Two experienced surgeons performed the surgery. Both procedures were undertaken by one surgeon on each cadaver. The choice of which was to be done first was randomized. After the implantation of the prosthesis, the mechanical-axis deviation, femoral coronal angle, tibial coronal angle, femoral sagittal angle, tibial sagittal angle, and femoral rotational alignment were measured via three-dimensional CT scanning. These variants were then compared with the preoperative planned values. In the robot-assisted surgery, the mechanical-axis deviation ranged from −1.94 to 2.13° (mean: −0.21°), the femoral coronal angle ranged from 88.08 to 90.99° (mean: 89.81°), the tibial coronal angle ranged from 89.01 to 92.36° (mean: 90.42°), the tibial sagittal angle ranged from 81.72 to 86.24° (mean: 83.20°), and the femoral rotational alignment ranged from 0.02 to 1.15° (mean: 0.52°) in relation to the transepicondylar axis. In the conventional surgery, the mechanical-axis deviation ranged from −3.19 to 3.84°(mean: −0.48°), the femoral coronal angle ranged from 88.36 to 92.29° (mean: 90.50°), the tibial coronal angle ranged from 88.15 to 91.51° (mean: 89.83°), the tibial sagittal angle ranged from 80.06 to 87.34° (mean: 84.50°), and the femoral rotational alignment ranged from 0.32 to 4.13° (mean: 2.76°) in relation to the transepicondylar axis. In the conventional surgery, there were two cases of outlier outside the range of 3° varus or valgus of the mechanical-axis deviation. The robot-assisted surgery showed significantly superior femoral-rotational-alignment results compared with the conventional surgery (p=0.006). There was no statistically significant difference between robot-assisted and conventional total knee arthroplasty in the other variants. All the variants were measured with high intraobserver and interobserver reliability. In conclusion, Robot-assisted total knee arthroplasty showed excellent precision in the sagittal and coronal planes of the three-dimensional CT. Especially, better accuracy in femoral rotational alignment was shown in the robot-assisted surgery than in the conventional surgery despite the fact that the surgeons who performed the operation were more experienced and familiar with the conventional surgery than with robot-assisted surgery. It can thus be concluded that robot-assisted total knee arthroplasty is superior to the conventional total knee arthroplasty.
We compared extrusion of the allograft after
medial and lateral meniscal allograft transplantation and examined
the correlation between the extent of extrusion and the clinical
outcome. A total of 73 lateral and 26 medial meniscus allografts
were evaluated by MRI at a mean of 32 months (24 to 59) in 99 patients
(67 men, 32 women) with a mean age of 35 years (21 to 52). The absolute
values and the proportional widths of extruded menisci as a percentage were
measured in coronal images that showed maximum extrusion. Functional
assessments were performed using Lysholm scores. The mean extrusion
was 4.7 mm (1.8 to 7.7) for lateral menisci and 2.9 mm (1.2 to 6.5)
for medial menisci (p <
0.001), and the mean percentage extrusions
were 52.0% (23.8% to 81.8%) and 31.2% (11.6% to 63.4%), respectively
(p <
0.001). Mean Lysholm scores increased significantly from
49.0 (10 to 83) pre-operatively to 86.6 (33 to 99) at final follow-up
for lateral menisci (p = 0.001) and from 50.9 (15 to 88) to 88.3
(32 to 100) for medial menisci (p <
0.001). The final mean Lysholm
scores were similar in the two groups (p = 0.312). Furthermore,
Lysholm scores were not found to be correlated with degree of extrusion
(p = 0.242). Thus, transplanted lateral menisci extrude more significantly
than transplanted medial menisci. However, the clinical outcome
after meniscal transplantation was not found to be adversely affected
by extrusion of the allograft.
The purpose of this study was to evaluate the
long-term functional and radiological outcomes of arthroscopic removal
of unstable osteochondral lesions with subchondral drilling in the
lateral femoral condyle. We reviewed the outcome of 23 patients
(28 knees) with stage III or IV osteochondritis dissecans lesions
of the lateral femoral condyle at a mean follow-up of 14 years (10
to 19). The functional clinical outcomes were assessed using the Lysholm
score, which improved from a mean of 38.1 ( We found radiological evidence of degenerative changes in the
third or fourth decade of life at a mean of 14 years after arthroscopic
excision of the loose body and subchondral drilling for an unstable
osteochondral lesion of the lateral femoral condyle. Clinical and
functional results were more satisfactory.
As the proximal femoral bone is generally compromised in failed hip arthroplasty, achievement of solid fixation with a new component can be technically demanding. Recent studies have demonstrated good short-term clinical results after revision total hip arthroplasty using modular distal fixation stems, but, to our knowledge, none have included clinical follow-up of greater than 5 years. The purpose of this study was to report the clinical and radiographic outcomes assessed 5 to 10 years following revision total hip arthroplasty with a modular tapered distal fixation stem. We retrospectively evaluated 50 revision total hip arthroplasties performed using a modular tapered distal fixation stem Between December 1998 and November 2003. There were 15 men (16 hips) and 34 women (34 hips) with a mean age of 59 years (range, 36 to 80 years). The index operation was the first femoral revision for 46 hips, the second for 3 hips, and the fifth for 1 hip. According to the Paprosky classification, 5 femoral defects were Type II, 31 were Type IIIA, and 14 were Type IIIB. An extended trochanteric osteotomy was carried out in 24 (48%) of the 50 hips. Patients were followed both clinically and radiographically for a mean of 7.2 years. The mean Harris hip score improved from 54 points preoperatively to 94 points at the time of the latest follow-up. The mean stem subsidence was 1.5mm. Three stems subsided more than 5 mm, but all have stabilized in their new positions. During follow-up, a total of 4 hips required additional surgery. One hip had two-stage re-revision due to deep infection, one had liner and head exchange for alumina ceramic head fracture, and the other two underwent isolated cup re-revision because of aseptic cup loosening and recurrent dislocation, respectively. No repeat revision was performed due to aseptic loosening of the femoral component. Complications included 6% intraoperative fractures, 4% cortical perforations, and 4% dislocations. There were no stem fractures at the modular junction. The medium-term clinical results and mechanical stability obtained with this modular tapered distal fixation stem were excellent in these challenging revision situations with femoral bone defects.
A number of causes have been advanced to explain the destructive discovertebral (Andersson) lesions that occur in ankylosing spondylitis, and various treatments have been proposed, depending on the presumed cause. The purpose of this study was to identify the causes of these lesions by defining their clinical and radiological characteristics. We retrospectively reviewed 622 patients with ankylosing spondylitis. In all, 33 patients (5.3%) had these lesions, affecting 100 spinal segments. Inflammatory lesions were found in 91 segments of 24 patients (3.9%) and traumatic lesions in nine segments of nine patients (1.4%). The inflammatory lesions were associated with recent-onset disease; a low modified Stoke ankylosing spondylitis spine score (mSASSS) due to incomplete bony ankylosis between vertebral bodies; multiple lesions; inflammatory changes on MRI; reversal of the inflammatory changes and central bony ankylosis at follow-up; and a good response to anti-inflammatory drugs. Traumatic lesions were associated with prolonged disease duration; a high mSASSS due to complete bony ankylosis between vertebral bodies; a previous history of trauma; single lesions; nonunion of fractures of the posterior column; acute kyphoscoliotic deformity with the lesion at the apex; instability, and the need for operative treatment due to that instability. It is essential to distinguish between inflammatory and traumatic Andersson lesions, as the former respond to medical treatment whereas the latter require surgery.
Hip resurfacing has many advantages such as proximal bone conservation and easy revision including conversion to total hip arthroplasty. The major complication in the hip resurfacing is notching at the lateral cortical bone and fracture of the neck. In this research, we simulated the range of direction of reaming without causing notch. One left femur model was used for the simulation. The femoral head was fitted by a sphere and the origin of Cartesian coordinate was set at the center of the sphere. The simulation was made by imposing a cylindrical cut to the femoral head in varying direction and location. The existence of notching was decided comparing the maximum distance from reaming axis to neck section contour and the radius of cylindrical cut. If the maximum distance is bigger than the radius of cut, the notching exists and vice versa. We simulated existence of notching by varying inclination(α) from 20 to 70 degrees, anteversion(β) from 0 to 30 degree and depth passing through the head center(d) from 0 to 5mm. The implant used for the simulation was Durom®, Zimmer©. We selected the implant size that is close to the fitted sphere of femoral head. No notching was made for any direction when the depth d was less than 2mm. When the depth was 3mm, notching did not generate in the range of α from 43 degrees to 60 degrees and β from 0 to 25 degrees. When the range of depth was from 4mm to 5mm, notching did not generate in ranges of α from 41 degrees to 60 degrees and β from 0 to 29 degrees. The no-notching angle range had tendency increasing slightly when the depth was increased. The angle between the stem of the implant and the neck shaft axis without notching can be calculated from the angle α. When the depth was from 4mm to 5mm, the corresponding angle between stem of implant and the shaft axis was from 120 degrees to 139 degrees.
We hypothesized that navigation can help provide a well-balanced knee, through real-time feedback of alignment accuracies and gap sizes in flexion and extension. The purpose of this study was to evaluate in vivo stabilities of mediolateral laxity in full extension and anteroposterior laxities in 90° of flexion after navigation-assisted total knee arthroplasty, and to determine the nature of the correlations between these and range of motion (ROM). Forty-two total knee arthroplasties performed using a navigation system with a minimum two-year follow-up were included. The following were measured at final follow-ups; mediolateral laxities at extension and anteroposterior laxities at 90 degrees of flexion (using stress radiographs and a Telos arthrometer), modified HSS scores (excluding laxity and range of motion), and range of motion (ROM). At final follow-up the mean modified HSS score was 82% of total points and mean postoperative ROM was 128.1 ± 10.4°. Mean medial laxity was 3.5 ± 1.4°, mean lateral laxity 4.4 ± 2.2°, and mean anteroposterior laxity 7.1 ± 4.1 mm. We found no significant correlation between mediolateral laxity and postoperative ROM. However, a significant correlation was found between postoperative ROM and anteroposterior laxity. In the present study, the use of a navigation system in total knee arthroplasty was found to improve in vivo stability and produce promising short-term clinical results.
The purpose of this study was to evaluate the effect of decreasing tibial slope on extention gap during posterior stabilized total knee arthroplasty. 110 posterior stabilized total knee arthroplasties were studied for 2 groups;
having flexion contractures(n=35), having no flexion contracture(n=75). In each group, we measured the decrease of tibial slope and frequency of additional distal femoral resecions that were done due to insufficient extension gap in comparison with flexion gap during posterior stabilized total knee arthroplasty. We also compared frequencies of additional distal femoral resections between 2 parts having more and less slope decrease in each groups. In each group, tibial slope decrease were 8.7 degrees, 7.4 degrees(p=0.145) and frequencies of additional resection were 51.4%, 24%(p=0.005) in average. In 2 parts having more and less slope decrease in each group, frequencies of additional resection were 44.4% vs 58.8%(p=0.505), 13.2% vs 35.1%(p=0.032). Results suggested that more decrease of tibial slope reduced frequency of additional distal femoral resection during posterior stabilized total knee arthroplasty in group having no flexion contracture. Decreasing tibial slope can be considered as a factor influencing on extension gap during posterior stabilized total knee arthroplasty. The estimation of predictable tibia slope decrease through preoperative radiologic findings can be beneficial in performing succeful posterior stabilized total knee arthroplasty.
Rivaroxaban, an oral, direct FXa inhibitor has shown in large phase III trials to be both superior to enoxaparin a low molecular weight heparin for VTE prophylaxis in patients undergoing MOS, and to also have a good safety profile. RECORD, a pivotal clinical trial program investigating rivaroxaban for the prevention of VTE after THR and TKR surgery, consists of four multinational, randomized, double-blind, double-dummy phase III studies (RECORD1,2,3 and 4) comparing rivaroxaban 10 mg once-daily with enoxaparin 40 mg once-daily or 30 mg twice-daily. The RECORD program has consistently shown superiority of rivaroxaban to enoxaparin at preventing VTE after major orthopaedic surgery. Results from the RECORD 2 study confirmed the benefit of extended thromboprophylaxis after THR. Rivaroxaban was more effective than enoxaparin at reducing the incidence of VTE and all course mortality in patients undergoing THR, with a relative risk reduction (RRR) of 70% in total VTE (RECORD 1). In the TKR populations, rivaroxaban was superior to both once-daily (RECORD 3) and twice-daily (RECORD 4) enoxaparin, with a RRR of 49% and 31.4%, respectively. It also significantly reduced the incidence of symptomatic VTE in TKR patients (RECORD 3). Rivaroxaban groups had low and similar bleeding rates to enoxaparin across the RECORD program. Thus, with its superior efficacy and a good safety profile, oral, once-daily fixed dosing with rivaroxaban could transform the future of VTE prevention after major orthopaedic surgery and improve the quality and reliability of patients care.
Risk of impingement after total hip resurfacing arthroplasty may be great because femoral head-neck unit is preserved and there is little flexibility to adjust limb length and femoral offset, but this potentially worrisome phenomenon has been rarely reported. Impingement between femoral neck and acetabular cup was observed in a cohort of patients who underwent contemporary total hip resurfacing arthroplasty. We then questioned whether patient demographics, component features or suboptimal position of components would be risk factors for impingement. We reviewed a consecutive series of 51 patients (61 hips) who underwent contemporary total hip resurfacing arthroplasty. The mean age at the time of the index arthroplasty was 38 years (18 to 64). The most common diagnosis leading to the total hip resurfacing arthroplasty was osteonecrosis of the femoral head in 41 hips (67%). All the procedures were performed by single surgeon through an anterolateral approach. All the patients were assessed clinically and radiographically at a mean of 32 months (24 to 53) postoperatively. Femoro-acetabular cup impingement, defined as the presence of bony spur at the femoral neck corresponding to abutment site of the metallic cup, was observed in seven of the 61 hips (11.5%). Of these, five patients reported limitation of activities due to groin pain. The average postoperative Harris hip score of impingement hips was inferior to those of non-impingement hips (p = 0.004). No significant difference was detected between the impingement hips and non-impingement hips with regard to of patient demographics, component features and radiographic measurements including cup inclination, cup version, femoral component version, anterior femoral offset, stem-shaft angle, femoral offset and limb length discrepancy. Our multivariate analysis revealed that only acetabular cup uncoverage ratio had a significant association with femoro-acetabular cup impingement (p = 0.04, odds ratio 1.385 [95% CI, 1.014 – 1.891]). There was no aseptic loosening of components or femoral neck fracture. We found a high incidence of impingement between retained femoral neck and metallic acetabular cup after contemporary total hip resurfacing arthroplasty in association with an increased acetabular cup uncoverage ratio. As patients with femoro-acetabular cup impingement showed inferior clinical results, it is crucial to avoid excessive protrusion of acetabular cup beyond bony margin by proper selection of acetabular component size and appropriate positioning.
Metal-on-metal bearing was re-introduced with the aim of eliminating polyethylene wear and resulting complications of osteolysis and aseptic loosening in total hip arthroplasty (THA). However, authors of recent studies have reported periprosthetic osteolysis and aseptic failure following second-generation metal-on-metal THA. The purpose of this study is to report the results at a minimum of five years following cementless total hip arthroplasty with a contemporary metal-on-metal articulation. Our study included findings of histologic examination on periprosthetic tissues from revised hips and wear and roughness analysis of retrieved implants. A consecutive series of 158 cementless THAs that were performed in 154 patients using a contemporary metal-on-metal bearing were assessed at a mean of 6.5 years (5 to 8). Their mean age at surgery was 53 years (21 to 80). The patients were assessed clinically with use of the Harris hip score, and the hips were assessed radiographically. Histological analysis was performed on specimens retrieved from the revised hips, and wear and roughness measurements were made for the explanted prostheses. The average Harris hip score improved from 45 points preoperatively to 92 points at the final follow-up examination. There was no aseptic loosening of the femoral or acetabular components. One hip was revised because of recurrent dislocation and one was managed with two-stage re-implantation for deep infection. Thirteen hips (8%) had osteolysis; 11 had osteolysis localized within the greater trochanter and two had both femoral and ace-tabular osteolysis. Of these, five patients who had a persistent pain and osteolysis underwent revision operation for the consideration of bearing exchange to a ceramic-on-ceramic or ceramic-on-polyethylene combination. All these revised hips showed extensive synovial-like tissue hypertrophy and perivascular infiltration of lymphocytes on histological examinations. Annual volumetric wear rate measured on one retrieved femoral head was 1.04mm3/yr, and roughness measured on three retrieved femoral heads was consistently very low between 8nm and 117nm. After the revision surgery, all the patients noticed disappearance of pain as well as radiographic evidence of healing of the osteolytic lesion. Our mid-term follow-up of cementless THA using a contemporary metal-on-metal bearing revealed an unexpectedly high rate of periprosthetic osteolysis possibly in association with metal hypersensitivity. In patients with persistent hip pain and osteolysis after contemporary metal-on-metal THA, surgeons should consider an exchange of the articulation surface to a ceramic-on-ceramic or ceramic-on-polyethylene combination because they can be cured only after an elimination of the source of hypersensitivity reaction.
Two-stage reimplantation is currently the most widely accepted method of treatment for a periprosthetic hip infection. However, it remains controversial whether the treatment protocol may be equally effective in the eradication of resistant microorganisms. We compared the results of two-stage reimplantation performed for periprosthetic hip infection caused by resistant microorganisms with those performed for periprosthetic hip infection caused by non-resistant microorganisms. We reviewed a consecutive series of 32 patients (32 hips) who had a culture-proven deep infection at the site of hip arthroplasty and were treated by a two-stage reimplantation protocol. Based on the antibiotic sensitivities of the infecting microorganisms, the patients were divided into two groups. Resistant microorganism group consisted of 20 patients who had an infection with antibiotic-resistant bacterial strains (methicillin-resistant Staphylococcus aureus in 11 and methicillin-resistant Staphylococcus epidermidis in 9). Non-resistant microorganism group consisted of 12 patients who had an infection with antibiotic-sensitive bacterial strains. The treatment was considered a failure if the patient had a persistent infection after the first-stage procedure or a recurrence of infection after reimplantation. The mean duration of follow-up after the index procedure was 45 months (24 to 123). Among the entire series of the 32 patients, the second-stage reimplantation was able to be performed in 29 patients (91%) and the remaining three went on to a permanent resection of the hip because of persistent infections. After the two-stage reimplantation, four patients had a recurrence of infection (relapse of infection with the same microorganism in three and reinfection with different resistant microorganism in one). Thus, overall treatment failure rate was 22% and all these failures occurred among patients with resistant microorganisms. Treatment failure rate of 35% in resistant microorganism group was significantly higher than that of 0% in the non-resistant microorganism group (p = 0.029). None of the variables evaluated in this study was found to be significantly associated with the treatment failure in the resistant microorganism group. Current two-stage reimplantation protocol showed a high rate of treatment failure in our patients who had periprosthetic hip infection caused by methicillin-resistant bacterial strains. Further study is needed to develop optimal treatment strategy for this difficult-to-treat condition.
In the cementless total hip arthroplasty, the position of the stem is pretty much determined by broach and rasping with which the is required for two reasons: one is to align the stem with the femur at the desired position and the orientation. The other is to achieve the conformity between the stem and the prepared proximal cavity surface in the femur. The robotic hip surgery can be a solution for the accurate of femoral canal shaping, but recent reports about the clinical follow-up study of the robotic hip surgery indicated frequent dislocation mainly due to the excessive soft tissue damage during robotic operation. In this paper, a guide being inserted into the femoral canal is proposed to restrict the undesired motion of the rasp inside the femur without extra incision. A set of canal guide and custom rasp for the selected stem(versys fibermetal midcoat, zimmer co.)were developed and tested with 4 synthetic femurs (model 1130, Sawbones co.). After rasping, a plastic copy of the stem was inserted into the femur and sliced at 5 mm thickness. From obtained cross sections, percentages of the gap larger than 0.3mm between the stem and the bone was measured. 6_C_Results: In average, 79% of bone-implant interface was close contact. Valgus/varus deviations of the stem were 0.40±0.45 degree, which means the angle of axis of straight reamer and axis of final cut. In average, 79% of bone-implant interface was close contact. Valgus/varus deviations of the stem were 0.40±0.45 degree, which means the angle of axis of straight reamer and axis of final cut. The conformity of femoral canal with the femoral stem in this approach was higher than the conventional hip surgery and comparable to those in the robotic surgery. The alignment of the stem within the femur is also as good as those in the robotic surgery(0.34±0.67 approach does require neither expensive system nor CT scan. Also this approach can be executed swiftly without extra time and unnecessary large incision compared with the robotic surgery.
Patellofemoral complications after TKA are mostly avoided with appropriate operative technique. Although most orthopedic surgeons performed using a medial parapatellar approach at TKA, but a large amount of the patellar blood flow is blocked by this procedure. A certain surgical exposure, including the midvastus and subvastus approach, has resulted in good clinical results. It is important to maintain the integrity of the extensor mechanism. But the southern or subvastus approach has inadequate exposure in some patients. And then we have had the primary total knee Arthroplasty using midvastus approach in 98 cases, 68 patients. Mean follow up is 30 months, between from 20 months to 43 months. We estimated parameters of total blood loss, surgical time, difficulty of exposure, number of lateral releases. The clinical parameters of range of motion, ability to perform a straight leg raise, and the number of operative or postoperative complications were evaluated. The patients who had the midvastus approach had minor blood loss, resonable surgical time, no difficulty of exposure even in patients with severe varus or valgus deformities, required lateral retinacular releases only 5% of the cases. The range of motion was all above 120 degrees flexion, no extension loss, had a higher incidence of ability to straight leg raise and fewer complications as like superficial wound infection. The midvastus surgical approach have some more advantages with less pain and earlier control of the operative leg, and may be discharged from the hospital earlier. Because preserving the integrity of the vastus medialis insertion into the medial border of the quadriceps tendon and limited disruption of the extensor mechanism improves the rapid control of quadriceps muscle and improves the more stable patellofemoral articulation, and then evidenced a marked reduction in the need for lateral retinacular releases. We recommend the mid-vastus surgical approach for total knee arthroplasty. The Midvastus approach is an efficacious alternative to the medial parapatellar approach for primary total knee arthroplasties in selected patients who are not obese and who have not had previous arthrotomy. And if needed more additional exposure, the muscle can be safely split by further dissection.
The purpose of this study was to investigate the efficacy of oral alendronate for the older children with osteogenesis imperfecta. Eight boys and 6 girls with average age of 9.7 years were given oral alendronate, 10mg everyday for those >
35kg, 10mg every other day for those 20 – 35 kg, and 10mg every three days for those <
20 kg. Treatment period averaged 3.3 years (range, 2.1 to 3.6). The number of fractures decreased by 39% in the lower extremity, although not statistically significant. Ten patients or their parents reported improved well-being during the treatment period. Z score for bone mineral density improved from −3.75 to −1.18 in the lumbar spine, and from −3.84 to −2.74 in the femur neck. Restoration of the collapsed vertebral bodies was observed, and the metaphyseal bands appeared on the simple radiographs. Urinary excretion of calcium and N-telopeptide of type I collagen were decreased by 64% and 47%, respectively. Abdominal discomfort was reported in five patients, one of which needed temporary switch to intravenous protocol. Iliac crest biopsy including the physis showed expanded primary spongiosa area with numeric multi-nucleated cells, which had heterogenous immunoreactivity for osteoclast markers. This study revealed beneficial effects of oral alendronate in osteogenesis imperfecta patients, supported by radiological, biochemical and histological findings. We believe that oral alendronate is a more convenient method of bisphosphonate treatment for osteogenesis imperfecta, especially in older children.
We have carried out prosthetic reconstruction in six patients with malignant or aggressively benign bone tumours of the distal tibia or fibula. The diagnoses were osteosarcoma in four patients, parosteal osteosarcoma in one and recurrent giant-cell tumour in one. Five tumours were in the distal tibia and one in the distal fibula. The mean duration of follow-up was 5.3 years (2.0 to 7.1). Reconstruction was achieved using custom-made, hinged prostheses which replaced the distal tibia and the ankle. The mean range of ankle movement after operation was 31° and the joints were stable. The average functional score according to the system of the International Society of Limb Salvage was 24.2 and five of the patients had a good outcome. Complications occurred in two with wound infection and talar collapse. All patients were free from neoplastic disease at the latest follow-up. Prosthetic reconstruction may be used for the treatment of malignant tumours of the distal tibia and fibula in selected patients.
Stable fixation after a corrective supracondylar osteotomy in adults is difficult because of the irregularity of the area of bony contact, displacement of the fragments, the predominance of cortical bone, and the need for early mobilisation. We have used the Ilizarov apparatus for fixation in 15 patients who were treated by complex osteotomies with displacement of fragments for cubitus varus or valgus. Most patients with cubitus varus required medial displacement with rotation of the distal fragment. Those with cubitus valgus required lateral shift of the distal fragment to reduce the medial prominence of the elbow that would otherwise result. All osteotomies united within the expected time without loss of correction, despite early mobilisation. Complications related to the fixation were few and had resolved at the long-term follow-up.