Previous studies regarding modular head-neck taper corrosion were largely based on cobalt chrome (CoCr) alloy femoral heads. Less is known about head-neck taper corrosion with ceramic femoral heads. We asked (1) whether ceramic heads resulted in less taper corrosion than CoCr heads; (2) what device and patient factors influence taper fretting corrosion; and (3) whether the mechanism of taper fretting corrosion in ceramic heads differs from that in CoCr heads.Background:
Questions/purposes:
The diagnosis of periprosthetic joint infection (PJI) remains a serious challenge. Based on previous work, we believe that biomarkers will become the mainstay of diagnosing PJI in the future. We report on completion of our 8 year comprehensive biomarker program, evaluating the diagnostic profile of the 15 most promising synovial fluid biomarkers. Synovial fluid was prospectively collected from 99 patients being evaluated for infection in the setting of revision hip or knee arthroplasty. All synovial fluid samples were tested by immunoassay for 15 putative biomarkers that were developed and optimized specifically for use in synovial fluid. Sensitivity, specificity and receiver operating Characteristic (ROC) curve analysis were performed for all biomarkers.INTRODUCTION:
METHODS:
Direct anterior approach (DAA) using the Hueter interval for total hip replacement (THA) provides an inter-nervous and inter-muscular access to the hip joint. Although it is technically demanding, the learning curve has been shown to be around 40 cases and 6 months in a high-volume joint surgeon's practice. A level-one study has demonstrated that DAA provides equal or better results and an equivalent rate of complications when compared to the highly utilized direct lateral approach. Using the available evidence to perform a multi-criteria decision analysis we demonstrated that DAA can be the most efficient approach to perform THA. From our standpoint, there is no reason to speculate a surgical approach with such advantages will be abandoned in the future. The DAA is here to stay, and may become the gold standard for THA.
Total knee arthroplasty is an operation that can be performed with or without the use of tourniquet. Two systematic reviews and meta-analyses of the available literature have demonstrated that the use of tourniquet leads to a reduction in blood loss and also shortens the operative time. The opponents for use of tourniquet cite development of complications such as skin bruising, neurovascular injury, and metabolic disturbances as a deterrent for the use of tourniquet. Although the latter may be true for some patients such as those with previous vascular grafts, there is little evidence that routine use of tourniquet during TKA results in any of the above complications. The use of tourniquet on the other hand provides a bloodless field that allows the surgeon to perform the procedure with expediency and optimised visualisation. Blood conservation has gained extreme importance in recent years because of increased understanding of problems associated with blood transfusion such as increased surgical site infection (due to immunomodulation effect), increased length of hospital stay, increased cost and so on. Based on our understanding of the available evidence, we believe that routine use of tourniquet during TKA is justified and a good surgical practice.
A novel cementless tapered wedge femoral hip implant has been designed at a reduced length and with a geometry optimized to better fit a wide array of bone types (Accolade II, Stryker, Mahwah, USA). In this study, finite element analysis (FEA) is used to compare the initial stability of the new proposed hip stem to predicate tapered wedge stem designs. A fit analysis was also conducted. The novel stem was compared to a predicate standard tapered stem and a shortened version of that same predicate stem. The novel shortened tapered wedge stem geometry was designed based on a morphological study of 556 CT scans. We then selected 10 discrete femoral geometries of interest from the CT database, including champagne fluted and stove pipe femurs. The novel and the predicate stems were virtually implanted in the bones in ABAQUS CAE. A total of thirty FEA models were meshed with 4 nodes linear tetrahedral elements. Bone/implant interface properties was simulated with contact surface and a friction coefficient of 0.35. Initial stability of each stem/bone assembly was calculated using stair-climbing loading conditions. The overall initial stability of the HA coated surface was evaluated by comparing the mean rotational, vertical, gap-opening and total micromotion at the proximal bone/implant interface of the novel and predicate stem designs. To characterize the fit of the stem designs we analyzed the ratio of a distal (60 mm below lesser trochanter) and a proximal (10 mm above lesser trochanter) cross section. A constant implantation height of 20 mm above the lesser trochanter was used. The fit of the stems was classified as Type 1 (proximal and distal engagement), Type 2 (proximal engagement only) and Type 3 (distal engagement only). The mean % micromotion of the HA coated surface greater than 50 mm was lowest at 40.2% (SD 11.5%) for the novel tapered wedge stem compared to the clinically successful predicate stem design (Accolade TMAZ, Stryker, Mahwah, USA) at 44.9% (SD 13.2%) and its shortened version at 48.5% (SD 9.0%) as shown in Figure 1. Improved initial stability of the new stem was also confirmed for rotational, vertical and gap-opening micromotion. However, there was no statistically significant difference. The novel tapered stem design showed a well balanced proximal to distal ratio throughout the complete size range. The novel tapered stem design showed a reduced percentage of distal engagements (2.8%) compared to the predicate standard stem (17.2%). In the 40 to 60 year old male group the distal engagement for the standard stem increases (28.2%), whereas the distal engagements for the novel stem remains unchanged (1.3%).Methods
Results
Sequentially annealed highly crosslinked polyethylenes (HXLPEs) were introduced in total knee replacement (TKR) starting in 2005 to reduce wear and particle-induced osteolysis. Few studies have reported on the clinical performance of HXLPE knees. In this study, we hypothesized that due to the reduced free radicals, sequentially annealed HXLPE would have lower oxidation levels than gamma inert-sterilized controls. 145 tibial components were retrieved at consecutive revision surgeries at 7 different surgical centers. 74 components were identified as sequentially annealed HXLPE (X3, Stryker) while the remainder (n = 71) were conventional gamma inert sterilized polyethylene. The sterilization method was confirmed by tracing the lot numbers by the manufacturer. The conventional inserts were implanted for 1.7 years (Range: 0.0–9.3 years), while the X3 components were implanted 1.1 years (Range: 0.0–4.5 years). Surface damage was assessed using the Hood method. Oxidation analysis was performed in accordance with ASTM 2102 following submersion in boiling heptane for 6 hours to remove absorbed lipids. 30 of the conventional and 29 of the HXLPE inserts were available for oxidation analysis.Introduction
Methods
Wear debris generation in metal-on-metal (MOM) total hip arthroplasty (THA) has emerged as a compelling issue. In the UK, clinically significant fretting corrosion was reported at head-taper junctions of MOM hip prostheses from a single manufacturer (Langton 2011). This study characterizes the prevalence of fretting and corrosion at various modular interfaces in retrieved MOM THA systems used in the United States. 106 MOM bearing systems were collected between 2003 and 2012 in an NIH-supported, multi-institutional retrieval program. From this collection, 88 modular MOM THA devices were identified, yielding 76 heads and 31 stems (22 modular necks) of 7 different bearing designs (5 manufacturers) for analysis. 10 modular CoCr acetabular liners and 5 corresponding acetabular shells were also examined. Mean age at implantation was 58 years (range, 30–85 years) and implantation time averaged 2.2 ± 1.8 years (range, 0–11.0 years). The predominant revision reason was loosening (n=52). Explants were cleaned and scored at the head taper, stem taper, proximal and distal neck tapers (for modular necks), liner, and shell interfaces in accordance with the semi-quantitative method of Goldberg et al. (2002).Introduction
Methods and Materials
The purpose of this multicenter study was to assess the oxidative stability, mechanical behavior, wear and reasons for revision of 2nd generation sequentially annealed HXLPE, X3, and compare it to 1st generation XLPE, Crossfire. We hypothesized that X3 would exhibit similar wear rates but lower oxidation than Crossfire. 182 hip liners were consecutively retrieved during revision surgeries at 7 surgical centers and continuously analyzed over the past 12 years in a prospective, multicenter study. 90 were highly crosslinked and annealed (Crossfire; Implanted 4.2±3.4 years, max: 11 years), and 92 were highly crosslinked and annealed in 3 sequential steps (X3; Implanted 1.2±1.5 years; max: 5 years). Oxidation was characterized in accordance with ASTM 2102 using transmission FTIR performed on thin sections (∼200μm) from the superior/inferior axis. Mechanical behavior was assessed via the small punch test (ASTM 2183).Introduction
Methods
The diagnosis of Periprosthetic Joint Infection (PJI) is a considerable challenge in total joint arthroplasty. The mainstay for diagnosis of PJI is a combination of serological markers, including C-reactive protein (CRP), along with joint aspirate for white cell count, differential and culture. The aim of this study was to examine the use of synovial fluid CRP in the diagnosis of PJI. Synovial fluid samples were collected prospectively from patients undergoing primary and revision knee arthroplasty. Samples were assessed for CRP, cell count and differential. Three groups were analyzed; those undergoing primary knee arthroplasty, aseptic knee arthroplasties and infected arthroplasties. Demographic data, along with associated medical co-morbidities, were collected,. Statistical analysis was performed. Synovial fluid CRP was correlated with serum CRP values. Sensitivity and specificity were calculated.Background
Material & Methods
The origins of the uncemented tapered wedge hip stem design currently offered by several orthopaedic device companies can be linked back to the cemented Straight Mueller type stem design first used in 1977. The design, a wedge shape with a taper angle of 6 degrees, maintains a single medial curvature for all sizes and increases laterally in the width to accommodate different size femurs. Although evolutionary improvements have been made over the years the basic body geometry of the stem has stayed mainly unchanged with excellent clinical survivorship. Over the past decade, the demographics of hip replacement have changed, with a large increase in younger male patients in the age range of 40 to 60 years. In this study the femoral fit of a novel tapered stem, designed to fit a wide array of patient types, is compared to a standard predicate tapered stem design. A bone morphology study was performed on a patient population of 556 patients using three dimensional digital data from CT-scans. To characterize the fit of the stem designs we analyzed the ratio of a distal (60mm below lesser trochanter) and a proximal (10mm above lesser trochanter) cross section. The same measurements were taken with the standard tapered stem design and the novel tapered stem design, with a given constant implantation height of 20mm above the lesser trochanter. The fit of the stems was classified as Type 1, where there was both proximal and distal engagement, Type 2, proximal engagement only, Type 3, distal engagement only. The distal and proximal engagement, Type 1, was specified with a maximum engagement difference of 2mm proximal to distal.Introduction
Methods
Infection poses one of the greatest medical challenges, one further complicated by bacterial biofilm formation that renders the infection antibiotic insensitive. The goal of this investigation was to covalently link the antibiotic vancomycin (VAN) to a bone allograft so as to render the tissue inhospitable to bacterial colonization and the subsequent establishment of infection. We could achieve uniform tethering of the antibiotic to the allograft with minimal disruption of the underlying bone structure. The tethered VAN remained active against gram-positive organisms with no detectable S.aureus colonization. Additionally, the grafted VAN prevented biofilm formation, even in protected topographical niches. Attachment of the antibiotic to the allograft surface was robust-the stabilized VAN remained active for long time periods. Osteoblasts cultured on the VAN-allograft evidenced no changes in cellular phenotype. We opine that this new chimeric construct represents a superior transplantable substrate with a plethora of applications in medicine, dentistry and surgery.
Use of allograft bone has become standard for bridging defects unlikely to heal by simple fixation and routinely used in revision arthroplasties for implant stabilization. Unfortunately, this decellularized allograft provides an ideal surface for bacterial colonization, necessitating repeated surgeries, extensive debridement and lengthy antibiotic treatments. With up to 18% infection rate following allograft surgeries, a need for more effective means to prevent this process is evident. We describe a novel modification of native bone allografts that renders their surface bactericidal while increasing the effectiveness of systemic antibiotic treatments. Allograft modification: Morselized human bone was washed extensively and sequentially coupled: 2X with Fmoc-aminoethoxyethoxyacetate (Fmoc-AEEA); deprotected with 20% piperidine in Dimethylformamide (DMF); and then coupled with vancomycin (VAN) for 12–16 hours. The VAN-bone was washed extensively with DMF and PBS for at least 1 day. VAN immuno-fluorescence: Control or VAN-bone was washed 5X with PBS, blocked with 10% FBS (1hr), incubated with rabbit anti-VAN IgG (4oC, 12h) followed by an Alexa-Fluor 488-coupled goat anti-rabbit IgG (1hr), and visualized by confocal laser microscopy. Antibiotic Activity. Equal dry weights of control and VANbone were sterilized with 70% ethanol, rinsed with PBS, and incubated with either Staphylococcus aureus (S. aureus) or Escherichia Coli (Ci=104 cfu) in TSB, 37oC, for 2, 5, 8 and 12 hrs. Antibiotic treatment: Clinical grade vancomycin was added to the solution with bacteria or following infection at a final concentration of 10μg/ml. Bacterial counts: Non-adherent bacteria were removed by washing and adherent bacteria suspended by sonication in 0.3% Tween-80 for 10mins followed by plating on 3M® Petrifilms. Bacterial visualization: Non-adherent bacteria were removed by washing extensively with PBS and adherent bacteria stained with the Live/Dead BacLight Kit (20mins, RT) to cause viable bacteria to fluoresce green. Samples were visualized by confocal microscopy. In comparison to controls, VAN-bone consistently reduced the graft bacterial load by ~90% at all time points. After staining and visualization of adherent bacteria, biofilm formation was apparent on controls by 12 hrs and absent from VAN-bone. E.coli, a gramnegative organism that is not sensitive to VAN, readily colonized both control and VANbone, confirming retention of VAN specificity. We then evaluated VAN-bone activity in a system that modeled systemic antibiotic therapy and antibiotic prophylaxis. In the absence of solution antibiotics, VAN-bone exhibited a significant decrease in bacterial colonization as compared to controls. When 10 μg/ml VAN was added to the medium for the last 4 h (modeling systemic antibiotic therapy), colonization of control surfaces was reduced, while colonization of VAN-allograft was almost eliminated. When 10 μg/ml VAN was added concomitantly with S. aureus, VAN-bone colonization was undetectable, while colonization of control surfaces still occurred. We have previously described an antibiotic-tethered allograft that resists bacterial colonization. In this abstract, we test this technology with an vitro model of bone implantation in the presence of solution antibiotics. In these models, solution antibiotics failed to prevent infection of control bone while completely clearing the bacteria on VAN-bone. Furthermore, VAN bone exhibited high activity against S. aureus, a gram positive organism, whereas it was ineffective against E. coli, a gram negative organism. The specificity of the tethered antibiotic supported the view that the antibacterial properties of the allograft were related to the tethered antibiotic and not to undefined aspects of the attachment chemistry. In terms of antibacterial activity, when challenged with 104 CFU S. aureus (with concentrations reaching >
107 CFU by 24 h), the antibiotic -modified allograft consistently decreased bacterial colonization by >
90%; S. aureus inocula <
102 CFU resulted in no detectable colonization of the VAN-allograft. Thus, development of these allografts may not only combat allograft colonization but increase the effectiveness of prophylactic antibiotics to ultimately result in a new therapy for allograft-associated infection.
Persistent wound drainage after total joint arthroplasty (TJA) has been associated with a higher incidence of superficial and deep periprosthetic infection but the predictors for prolonged drainage and its outcome have not been thoroughly studied. A consecutive series of 7,153 TJA cases performed between 2000 and 2006 at our institute, were recruited into this study. There were 301 cases (4.2%) of persistent wound drainage, defined as discharge from the wound for >
48 hours. The cases were matched in a 2:1 ratio for type of surgery, joint replaced, and date of surgery. This study identified higher BMI (p<
0.005), malnutrition as defined by serum albumin<
3.4g/dl (p<
0.04), longer operative time (p<
0.01), and higher medical comorbidities, in particular diabetes (p<
0.001) as important risk factors for persistent wound drainage. In addition, patients in the drainage group were more likely to have a peak INR of >
1.5 (p<
0.001) during their hospital stay. Patients with wound drainage had a significantly lower hemoglobin postoperatively (p<
0.01) that necessitated greater number of postoperative allogenic transfusions (p=0.004). The hospital length of stay for the drainage group was also significantly higher (p<
0.005). One of the major risk factors for development of deep infection was prolonged drainage (>
7 days). In the deep hematoma and periprosthetic subgroups, the mean of delay in treatment was 6 days in those with retention of the prosthesis and successful outcome, and 9.5 days for those with failure of incision and drainage leading to resection arthroplasty (p= 0.03). 72% of the patient were successfully treated by oral or intravenous antibiotics. 27% required at least one re-operation for deep hematoma and 13% developed deep periprosthetic infection, resulting in 6% rate of resection arthroplasty. 1.5% of those with drainage remained in girdlestone status. This study suggests early surgery for persistent drainage and avoidance of aggressive anticoagulation.
Periprosthetic infection (PPI) remains the most dreaded and difficult complication of total joint arthroplasty. Although there is no definite diagnostic test for PPI, synovial leukocyte count and neutrophil percentage have been reported to have high sensitivity and specificity. However, leukocytes and neutrophils introduced into the joint during a traumatic aspiration can skew results and undermine the predictive value of this diagnostic test. This study intends to determine the diagnostic value of implementing a corrective formula frequently used in traumatic spinal taps to adjust for serum leukocytes introduced into the joint fluid during a bloody tap. We conducted a review of all TKA aspirations of infected and non-infected patients performed at our institute from 2000 to 2005. The following inclusion criteria were used:
(a) a red cell count (RBC) was performed on the aspirate, and (b) a blood white cell count with differential was done within one week of aspiration. Patients with inflammatory arthropathy or those who underwent reimplantation after PPI were excluded. Strict criteria for diagnosis of PPI were used. We previously determined at our institute the cut-off values for fluid leukocyte count (>
1760 cells/μl) and neutrophil percentage (>
73%). The adjusted fluid leukocyte counts were calculated using the following formula: Wadjusted = WBCobserved – [(WBCblood * RBC-fluid/RBCblood)] predicted. A similar formula was implemented to calculate the adjusted absolute neutrophil counts. Our cohort included 73 infected and 32 aseptic total knee arthroplasties that fulfilled the above criteria. After correcting for introduced red blood cells, cell counts of 3 infected patients dropped below the cut-off value, while the remaining 70 maintained a high cell count. However, the 3 infected patients had initial cell counts below our reported cut-offs. Of the 32 non-infected patients, 10 patients had false positive cell counts due to the presence of extremely high numbers of blood RBC. Five of the 10 false positive aspirates successfully corrected to levels below the thresholds used to diagnose infection. The aspirates that corrected had a greater number of introduced RBCs, an initial higher cell count, and 20 times more fluid WBC deducted from the initial cell count. The corrective formula can safely adjust for RBC found in a traumatic tap and detect false positive results among non-infected TKA without compromising the diagnosis of infection. Adjusted aspirates of non-infected TKA can be expected to decrease below zero due to one of the following: adherence of the introduced systemic WBC to the joint synovium, greater rate of lysis of the introduced systemic WBC compared to the systemic RBC, laboratory errors in performing fluid cell counts.
The differential diagnosis of pain after total knee arthroplasty (TKA) should always include periprosthetic infection (PPI). The current diagnostic tools vary in sensitivity, specificity, and predictive value. Currently there is no test with an absolute accuracy for diagnosis of PPI. Furthermore, cost effectiveness of investigations has become an important issue in recent years as increased expenses can place an unnecessary heavy burden on the medical system. We retrospectively evaluated 296 patients who underwent revision TKA at our institution during 2000–2005 and had preoperative erythrocyte sedimentation rate (ESR) and C-reactive protein (CRP) performed. The criteria used for diagnosing infection were a positive intraoperative culture on solid media, presence of an abscess or sinus tract that communicated with the joint, positive preoperative aspiration culture, and/or elevated fluid cell count and neutrophil differential of the aspirated fluid. The sensitivity, specificity, and predictive values of ESR and CRP were determined. Combinations were performed in parallel that necessitate both tests to be negative to rule out infection. The cost of each serological test was compared to that of other commonly used screening modalities. One hundred and sixteen patients (39%) were classified as infected and 180 patients (61%) were considered non-infected. The sensitivity, specificity, positive predictive value, and negative predictive value for the ESR were: 91%, 72%, 68%, and 93%. The sensitivity, specificity, positive predictive value, and negative predictive value for the CRP were: 94%, 74%, 70%, and 95%. The sensitivity and negative predictive value for the combined studies were 96% and 95%, respectively. However, five infected patients (4%) had a normal ESR and CRP. An organism was cultured on solid media in 4 of the 5 cases. ESR and CRP were the least costly of all the preoperative tests including radionuclide imaging and joint fluid analysis. ESR and CRP are important preoperative tests in diagnosis of PPI and their ability to clench the diagnosis in the majority of cases should not be underestimated. When combined, these simple serological tests have improved sensitivity and negative predictive value to rule out infection.