The wear particles released from the polyethylene (PE) tibial insert of modular total knee replacements (TKRs) have been shown to cause wear particle induced osteolysis, which may necessitate revision surgery [1]. Wear occurs at the backside surface of the PE insert of modular TKRs, resulting from the relative movement between the PE insert and the tibial tray [2]. Wear particles generated from the backside surface of the PE insert have been shown to be smaller in size than those originating from the articular surface [1], and may therefore have increased biological activity and osteolytic potential [3-4]. The ability to predict backside micromotion and contact pressure by finite element simulation has previously been demonstrated by O'Brien et al. [6-7]. Although the effect of insert thickness on articular surface contact pressure has been investigated [5], the effects of insert thickness on backside contact pressures, backside micromotion, and wear has not received adequate attention. Brandt et al. [2] has suggested that increased insert thickness was associated with increased backside damage (Fig. 1). In the present study, finite element simulations were conducted using the Sigma - Press Fit Condylar TKR (Sigma-PFC®, DePuy Orthopedics Inc., Warsaw, IN) with inserts of different insert thickness ranging between 5, 10, 15, 20 and 25 mm. The TKRs were simulated under ISO 14343-2 [8]. A non-linear PE material model was implemented by means of the J2-plasticity theory [6] and the effects of insert thickness on backside micromotion and contact pressure were analyzed. At the peak loading of the simulated gait cycle (time=13%), the 5 mm thick PE insert showed a greater backside peak contact pressure than the 25 mm thickness PE insert. Increasing insert thickness from 5 mm to 25 mm lead to approximately 15% greater peak micromotion at the modular interface (Fig. 2). This effect may be attributed to the ability of the PE material to distribute the load more evenly through deformation at the modular interface and reduce micromotion for thinner inserts. It is suggested that increased insert thickness results in increased moments at the modular interface that could lead to increased backside wear in silico. Although an increase in PE insert thickness was only associated with a moderate increase in backside micromotion in the present study, it was deemed likely that backside micromotion could be accelerated for thicker inserts in vivo as the PE locking mechanism has been shown to degrade after extended implantation periods.
Femoral components with an oxidized zirconium-niobium (OxZr) gradient ceramic surface (Oxinium, Smith & Nephew, Memphis, TN) were introduced as an alternative to cobalt-chromium (CoCr) alloy femoral components for the purpose of PE wear reduction in total knee replacements [1]. In the present study, the surface damage and clinical performance of both CoCr alloy and OxZr femoral components were investigated. By matching CoCr alloy and OxZr femoral components for clinical factors, as done by Heyse et al. [2], the surface damage on retrieved CoCr alloy and OxZr femoral component was assessed. Twenty-six retrieved cobalt-chromium (CoCr) alloy femoral components were matched with twenty-six retrieved oxidized zirconium (OxZr) femoral components for implantation period, body-mass index, patient gender, implant type (cruciate ligament retaining/substituting), and polyethylene insert thickness. Detailed surface profilometry was performed on retrieved femoral condyles in areas that had not been damaged by gouging [3] with the specific purpose of investigating the in vivo wear behaviour of undamaged OxZr surface. In addition, the cumulative survivorships were calculated for patients who had received CoCr alloy or OxZr femoral components from our orthopaedic database. In order to identify factors that affect the clinical performance of CoCr alloy and OxZr femoral components, the findings from the retrieval analysis and the survivorship analysis were combined. The Rp, Rpm, and Rpk-values for the retrieved CoCr alloy femoral components were found significantly higher than the Rp, Rpm, and Rpk-values for the retrieved OxZr femoral components (p ≤ 0.031). The roughness parameters values (Ra, Rq, Rz, Rp, Rpm, Rpk, Rv, and Rsk) for the retrieved CoCr alloy femoral components were found significantly higher than the values of the new, never implanted CoCr alloy femoral components (p ≥ 0.001). The surface roughness was higher on the medial condyles than the lateral condyles of the retrieved CoCr alloy femoral components; such a difference was not observed on the retrieved OxZr femoral components. The OxZr bearing surface appeared to protect the femoral components from abrasive wear in vivo. At 8.5-years follow up, the cumulative survivorship for the CoCr alloy femoral components (98%) was not found to be statistically significantly different (p = 0.343, Breslow test) from the OxZr femoral components (97.5%). Therefore, OxZr femoral components appeared to possess low wear characteristics and could be particularly suitable for younger, heavier patients to ensure long-term durability.
Ceramic-on-ceramic (C-C) total hip replacements (THRs) are an attractive option for young, active patients [1, 2]. However, more clinical data is necessary to establish the reasons of failure of contemporary C-C THRs in vivo. The objective of the present study was to assess the surface damage on retrieved C-C THRs and determine possible influential factors that may explain their in vivo performance. Thirty-five C-C retrievals of material type Biolox® forte (n=28) and Biolox® delta (n=7) (CeramTec AG, Plochingen, Germany) were collected after a mean of 3.7 ± 3.2 years in vivo. Semi-quantitative surface damage assessment [3] was performed on all retrievals to obtain both a damage score (DS) (Fig. 1). Contact profilometry was performed on the retrieved femoral heads to characterize the type of surface damage (metal transfer, stripe wear). Scanning electron microscope (SEM) images were obtained from two femoral heads displaying areas of typical surface damage. The implantation period correlated with the damage score (DS) of the femoral heads (R=0.573, p<0.001) and the acetabular cups (R=0.592, p<0.001). However, the metal transfer DS of the femoral heads did not correlate with implantation period (R=0.185, p=0.29). Surface roughness of metal-transfer areas were positively skewed (additive metal transfer) while the stripe damage areas were negatively skewed (grain removal), as evidenced by SEM analysis. Stripe damage was observed on both the Biolox® forte and Biolox® delta retrieved femoral heads; however, the extent of grain removal appeared less severe on the Biolox® delta retrieved femoral heads due to their overall smaller grain size (Fig. 2). Inclination angles > 45° was associated with a greater DS rate [DS/time of implantation], which had also been suggested elsewhere [4]. Four patients reported squeaking in their C-C THRs; one of which was a 54 yr-old male patient who completed three full marathons with his implant. In this his case, the DS for this retrieval was below average, with metal-transfer being the only macroscopic damage feature. Fracture of the acetabular liner occurred in three patients, all of which had malpositioned components. Metal-transfer on the ceramic surface could possibly cause a local break down of the fluid film and may facilitate, in addition to an increased inclination angle, stripe damage via an adhesive wear mechanism. Therefore, direct contact between the Ti-alloy acetabular shell and the ceramic femoral head should be avoided at primary surgery. C-C THRs remain an attractive option for young, active patients, but care must be taken during implantation to appropriately position the acetabular cup and to avoid unwanted metal-transfer as such alteration at the bearing interface may change implant tribology.
Radiostereometric Analysis (RSA) is a well developed imaging technique used to estimate implant fixation of orthopaedic implants in randomized clinical trials. The precision of RSA depends on a number of factors including image quality related to the individual modality properties. This study assesses the precision of RSA with a novel Digital Radiography (DR) system compared to a CR imaging system using different imaging techniques. Additionally, the study assesses the precision of locating beads embedded in a modified spine pedicle screw. A modified titanium spinal pedicle screw 4.5 mm diameter, 35 mm length, marked with two 1.0 mm tantalum beads, one inside the head and one near the screw tip was inserted into a bovine tibia segment. Six additional 1.0 mm tantalum beads were inserted into the bone segment – superiorly, distally and adjacent to the pedicle screw. The phantom was placed on a standard clinical diagnostic imaging bed above a custom RSA carbon fiber calibration cage (Halifax Biomedical Inc.). A pair of DR or CR imaging plates were placed below the calibration cage and irradiated 15 times at 100, 125 kV at 2.5 mAs. To determine precision, the standard deviation of 3D vector distances between beads was determined using RSA for each of the different imaging parameters.Purpose
Method
Dislocation after revision total hip is a common complication. The purpose of this study was to assess whether a large femoral head (36/40mm) would result in a decreased dislocation rate compared to a standard head (32mm). A randomized clinical trial was undertaken to assess the effect of large femoral heads on dislocation after revision total hip. Patients undergoing revision hip arthroplasty at seven centers were randomized to 32mm head or 36/40mm head. Patients were stratified according to surgeon. Primary endpoint was dislocation. Rates were compared with Fishers exact test. Secondary outcome measures were quality of life: WOMAC, SF-36 and satisfaction. One hundred eighty four patients were randomized: 92 in the 32mm head group and 92 in the large head group. Baseline demographics were similar in the two groups. Patients were followed from two to five years postoperativelyPurpose
Method
The purpose of this study was to compare the clinical outcomes and complications following bilateral simultaneous total knee arthroplasty in high body mass index (BMI) patients(>30kg/m2) to those of patients with a BMI<30 kg/m2. Using data from an academic arthroplasty database and review of clinic charts we obtained health related quality of life (SF-12), and disease specific functional outcome scores (WOMAC or Oxford Knee Score). We also assessed length of hospital stay, ASA grade and transfusion requirements. Sixty six patients had a BMI<30 and 151 patients had a BMI>30.Introduction
Materials and Methods
Current practice requires all post-operative hip and knee arthroplasty patients complete a series of clinical questionnaires at each visit. The patients responses to these questionnaires are used as a clinical evaluation tool for the surgeons to assess functionality, satisfaction and pain at routine pre and post-operative visits. The recent installation of 4 touch screen computer terminals, located in the patient waiting area, has created the opportunity to have the patients complete these questionnaires by using only the touch screen entry system. This eliminates the need for clinic staff to manually enter the patients responses into the clinics database, eliminate potential data entry errors, and will significantly reduce the amount of time and paper required to prepare questionnaires for each patient. In addition to possibly increasing the volume of data we can collect in our clinic, this also allows the surgeon to have immediate access to the patients responses which can be reviewed prior to seeing the patient in the office. Our goal was to determine the overall level of patient satisfaction with using the new touch screen direct entry system, the efficiency of completion and the quality of data entry occurring from the direct entry system. During the month of April, 2010, a consecutive series of 100 patients entering the orthopaedic clinic, were directed to the touch screen kiosks to complete the required questionnaires (SF-12, Oxford Knee/Hip, Harris Hip/Knee Society Score, and the Patient Satisfaction Survey). Once the patients completed the touch screen questionnaires they were asked to complete a paper copy of the Touch Screen Satisfaction Questionnaire. This questionnaire asked 6 questions regarding their satisfaction with the touch-screen system, the ease/difficulty of use, and which method they would prefer to complete such questionnaires if given a choice.Purpose
Method
Radiostereometric Analysis (RSA) is an imaging method that is increasingly being utilized for monitoring fixation of orthopaedic implants in randomized clinical trials. Extensive RSA research has been conducted over the last 35+ years using standard clinical x-ray acquisition modalities that irradiate screen/film media or Computed Radiography (CR) plates. The precision of RSA can depend on a number of factors including modality image quality. This study assesses the precision of RSA with a novel Digital Radiography (DR) system compared to a CR imaging system using different imaging techniques. Additionally, the study assesses the precision of locating beads embedded in a modified spine pedicle screw.Introduction
Objective
Image guided navigation systems for total knee replacement surgery (TKR) are gaining popularity in an effort to improve both alignment and functional outcome. This trial was undertaken to compare one year functional outcome and radiological alignment of TKRs inserted with and without an image guided navigation system. Patients were randomised to undergo surgery using either an image guided navigation system or traditional instrumentation. Pre and post-operative Knee Society (KSS), WOMAC and SF-36 scores were collected. Postoperatively, limb and implant alignment &
rotation were assessed using both full-length films and CT scans. One hundred and twenty-three patients (one hundred and forty-five knees) were enrolled: eighty-one females, forty-two males, mean age sixty-seven years. Age, gender and pre-operative range of motion, KSS WOMAC and SF-36 scores did not differ between the groups. While there was no statistically significant difference in postoperative KSS, WOMAC and seven of eight SF-36 subscales, the navigated group demonstrated better post-operative SF-36 General Health Scores. Mean postoperative flexion in all patients was 115°, and did not differ between groups. Mean post-operative leg alignment demonstrated more varus in the navigated group (2.1°) versus the non-navigated group (0.9°, p=0.02), however there was a trend towards a smaller standard deviation in the navigated group. Rotational alignment of the femoral component relative to the femur, tibial component relative to the tibia, and tibial component relative to the femoral component were not statistically different between groups; however, there were larger standard deviations of these measures in the non-navigated group. Pre-operative alignment appeared to affect tibial component placement; varus knees had a mean of 3° of tibial component internal rotation while valgus knees had a mean of 12° external rotation. Imaged guided navigation systems appear to reduce the variability in TKR component placement and limb alignment. However, this may not necessarily translate into better mean limb alignment or early functional outcome.
A retrospective case-control study was performed to examine modifiable medical co-morbidities in patients who develop deep infection after primary total hip or knee replacement. To reduce bias, matching was undertaken using age, gender, and procedure. Co-morbidities were classified by system: cardiovascular, respiratory, gastrointestinal, genitourinary, metabolic, haematological and neurological. Initial analyses demonstrate that patients with infected primary hip or knee replacements are more likely to suffer from medical conditions than patients who did not develop infections. Since many of these co-morbidities are preventable or treatable, early screening and intervention may play a role in reducing prosthetic joint infection. Deep infection of total hip (THA) and knee replacements (TKA) causes significant patient morbidity and requires considerable health care resources to treat. In order to identify preventable or modifiable medical conditions associated with prosthetic joint infection, a retrospective case-control study was undertaken. Fifty patients who developed a culture proven deep infection after primary THA or TKA were studied. To reduce bias, a control group of arthroplasty patients was selected using one to one matching based on age, gender, and procedure. Co-morbidities in each group were recorded, and classified by system. Analysis revealed that patients with joint infections are more likely to suffer from an increased number of co-morbidities than the matched control group. The odds ratios and 95% confidence intervals were determined as: cardiovascular 2.3 (1.0–5.0), respiratory 2.3 (0.8–6.7), gastrointestinal 0.8 (0.4–1.9), genitourinary 3.1 (1.1–8.9), metabolic 1.8 (0.7–4.9), haematological 2.9 (1.1–7.8), neurological 2.9 (0.8–9.9) and diabetes 4.0 (1.2–13.4). The case group had a higher mean BMI than the control group: 33.7 versus 30.9, p=0.00. Since many of the co-morbidities associated with infection are preventable or readily treatable, early screening and intervention may play a role in reducing the burden of prosthetic joint infection.
A retrospective case-control study was performed to examine modifiable medical co-morbidities in patients who develop deep infection after primary total hip or knee replacement. To reduce bias, matching was undertaken using age, gender, and procedure. Co-morbidities were classified by system: cardiovascular, respiratory, gastrointestinal, genitourinary, metabolic, haematological and neurological. Initial analyses demonstrate that patients with infected primary hip or knee replacements are more likely to suffer from medical conditions than patients who did not develop infections. Since many of these co-morbidities are preventable or treatable, early screening and intervention may play a role in reducing prosthetic joint infection. Deep infection of total hip (THA) and knee replacements (TKA) causes significant patient morbidity and requires considerable health care resources to treat. In order to identify preventable or modifiable medical conditions associated with prosthetic joint infection, a retrospective case-control study was undertaken. Fifty patients who developed a culture proven deep infection after primary THA or TKA were studied. To reduce bias, a control group of arthroplasty patients was selected using one to one matching based on age, gender, and procedure. Co-morbidities in each group were recorded, and classified by system. Analysis revealed that patients with joint infections are more likely to suffer from an increased number of co-morbidities than the matched control group. The odds ratios and 95% confidence intervals were determined as: cardiovascular 2.3 (1.0 – 5.0), respiratory 2.3 (0.8 – 6.7), gastrointestinal 0.8 (0.4–1.9), genitourinary 3.1 (1.1–8.9), metabolic 1.8 (0.7 – 4.9), haematological 2.9 (1.1–7.8), neurological 2.9 (0.8–9.9) and diabetes 4.0 (1.2–13.4). The case group had a higher mean BMI than the control group: 33.7 versus 30.9, p=0.00. Since many of the co-morbidities associated with infection are preventable or readily treatable, early screening and intervention may play a role in reducing the burden of prosthetic joint infection.
We undertook a prospective, single blinded, randomized, controlled trial of one hundred children treated with either an above or below elbow cast for treatment of closed, distal third forearm fractures requiring reduction. The re-manipulation rate in the below elbow group was 2% (95%CI: 0–11%) compared to 6% (95%CI: 2–15%) in the above elbow group, p=0.62. Above elbow casts do not appear to improve fracture immobilization nor reduce the requirement for re-manipulation in pediatric distal third forearm fractures. Debate exists regarding the benefits of using below elbow casts instead of above elbow casts for maintaining reduction in pediatric distal third forearm fractures. The literature indicates a loss of reduction rate of 14.6% of children treated in an above elbow cast and 2.5% in those treated with a below elbow cast. We undertook a prospective, single blinded, randomized, controlled trial of one hundred children treated with either an above or below elbow cast for treatment of closed, distal third forearm fractures requiring reduction. Outcome measures included re-manipulation rate, fracture displacement during cast wear, and cast complications. One hundred patients were suitably enrolled; fifty-four received an above elbow cast, forty-six received a below elbow cast. The two groups were similar in terms of age and gender. The above elbow group contained a higher proportion of both bone fractures (41/54) than the below elbow group (27/46). There were no significant differences between the two cast groups in initial, post-reduction or cast-off fracture angulation; nor any difference in the amount of fracture displacement during cast wear. The number of cast complications was similar between the two groups. The re-manipulation rate in the below elbow group was 2% (95%CI: 0–11%) compared to 6% (95%CI: 2–15%) in the above elbow group, p=0.62. Above elbow casts do not appear to improve fracture immobilization nor reduce the requirement for re-manipulation in pediatric distal third forearm fractures.