The accurate differentiation of aseptic loosening from periprosthetic infection in the painful hip prosthesis is a major clinical challenge. FDG-PET imaging has shown great promise in various clinical settings for detection of infection. This prospective study was designed to determine the efficacy of FDG-PET imaging in the assessment of patients with painful hip prosthesis.

One hundred and thirteen patients with 127 painful hip prostheses were evaluated by FDG-PET. Approximately 60 minutes after the intravenous administration of FDG images of the lower extremities were acquired using a dedicated PET machine. FDG-PET images were interpreted by experienced nuclear medicine physicians. Images were considered positive for infection if PET demonstrated increased FDG activity at the bone-prosthesis interface of the femoral component of the prosthesis. Surgical findings, histopathology, and clinical follow-up served as the “gold standard”.

FDG-PET was positive for infection in 35 hips and negative in 92 hips. Among 35 positive PET studies, 28 were proven to be infected by surgical and histopathology findings as well as follow-up tests. Of 92 hip prostheses with negative FDG-PET findings, 87 were proven to be aseptic. The sensitivity, specificity, positive and negative predictive values for FDG-PET were 0.85 (28/33), 0.93 (87/94), 0.80 (28/35), and 0.95 (87/92), respectively. The overall accuracy of FDG-PET in this clinical setting was 90.5% (115/127).

The results demonstrate that FDG-PET is a highly accurate diagnostic test for differentiating infected from non-infected painful hip prosthesis. Therefore, FDG-PET imaging is considered the study of choice in the evaluation of patients with suspected hip prosthesis infection.

The accurate diagnosis of periprosthetic infection poses a challenge to the clinician and the imaging specialist alike. In recent years, FDG-PET imaging has shown great promise in the evaluation of occult infection at various anatomic sites. The purpose of this investigation was to determine the accuracy of FDG-PET imaging in diagnosing periprosthetic infection associated with total knee arthroplasty.

Sixty eight painful knee prostheses were referred for further evaluation with FDG-PET imaging. Approximately 60 minutes after the intravenous administration of FDG, PET images of both knees were acquired and interpreted by experienced nuclear medicine physicians. PET images demonstrating increased FDG activity at the bone-prosthesis interface were considered infected. Final diagnosis was made on the basis of surgical findings, histopathology, and clinical follow-up.

FDG-PET correctly diagnosed 19 of the 22 infected cases for a calculated sensitivity of 86.4% (19/22). FDG-PET correctly predicted the absence of infection in 38 of 46 aseptic knee prostheses for a calculated specificity of 82.6% (38/46). The negative and positive predictive values for FDG-PET imaging in this setting were 92.7% (38/41) and 70.4% (19/27), respectively. The overall accuracy of FDG-PET imaging was 83.8% (57/68). FDG-PET was indeterminate in three cases which were not included in this analysis.

These results demonstrate that FDG-PET is a useful diagnostic tool for the evaluation of possible infection associated with knee arthroplasty. Considering the large number of subjects who undergo total knee arthroplasty and the sizable fraction who develop complications following surgery, the impact of FDG-PET imaging could be substantial. Examination of a larger number of patients with painful knee prostheses will further clarify the merit of this powerful technique in this clinical setting.

Currently two-stage resection arthroplasty is the preferred method for surgical treatment of periprosthetic infection in North America. However, the success of this treatment strategy has varied from 54% to 98% based on previous reports. The exact reason for this variation in outcome is not known. The purpose of this study was to determine the efficacy of this treatment modality and delineate patient risk factors that result in recurrent infection and failure.

During the period of this study (2000–2005) 77 patients with an infected THA were treated at our institution. Fifty-four patients underwent two-stage exchange arthroplasty while the remaining 22 failed to have the second stage reimplantation due to ill health. The latter 22 were excluded from the analysis. All patients were followed up prospectively for at least two years after reimplantation. Detailed data including demographics, comorbidities, surgical history, and medication intake was collected. Intraoperative data, organism profile, and complications were also documented. Failure was defined as patient requiring additional surgical procedure for control of infection or loosening.

Two-stage exchange arthroplasty successfully eradicated infection in 36 patients (67%) without need for further treatment. Seven patients (13%) had recurrent infection that necessitated resection arthroplasty. Eleven (20%) patients required irrigation and debridement for postoperative purulent drainage which successfully treated infection in 8 of the cases. The remaining 3 patients failed and required resection arthroplasty. Three additional patients had early loosening of components and required revision arthroplasty. The exact cause of loosening in these patients could not be determined and despite lack of isolation of organisms infection was suspected. Multivariate analysis identified previous medical comorbidity and postoperative allogenic transfusion as risk factors for failure.

Current strategies to treat periprosthetic infection remain imperfect. Two-stage exchange arthroplasty with all its inherent problems and inconveniences imparted a modest success in treatment of PPI at our high volume specialized center. With the increase in the number of virulent and resistant organisms, and the rise in arthroplasties being performed in infirm patients with medical comorbidities the success of this procedure is likely to be jeopardized. Novel treatment modalities to combat this dreaded condition is needed.

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 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 the diagnosis of PPI and their ability to clench diagnosis in the majority of cases should not be underestimated. When combined, those simple serological tests have improved sensitivity and negative predictive value to rule out infection.

Debridement of an infected total joint arthroplasty with retention of mechanically stable components is often performed for acute cases of periprosthetic infection (PPI). However, the reported success of such a procedure to fully eradicate infection has varied widely. The objective of this study was to elucidate the efficacy of debridement in both infected THA and TKA and attempt to identify risk factors responsible for failure.

During the years 2000–2005, 71 TKA and 69 THA underwent irrigation and debridement for acute PPI (< 4 weeks). All patients were followed up prospectively for at least two years. Detailed data including demographics, comorbidities, surgical history, and medication intake was collected. Intraoperative data, organism profile, and complications were also documented. Failure was defined as patient requiring additional surgical procedure for control of infection or loosening.

Of the 140 patients, 24% required repeat irrigation and debridement for postoperative drainage, hema-toma formation, or systemic symptoms. One third of these revision debridement patients underwent multiple consecutive debridements. Two-stage resection arthroplasty was required in 65 patients (46%) of the entire cohort. Fifty-eight percent of the patients with resection required revision of their cement spacer block due to continuous drainage and systemic symptoms indicative of persistent infection. We noted a total of 86 failures (61%) that required either an additional debridement or resection arthroplasty after the first debridement procedure. The failure rates of THA (62%) and TKA (55%) individually were similar (p=0.253).

Although the concept of conservative management of PPI with debridement and retention of components is an attractive alternative to resection arthroplasty, we have found that 60% of patients undergoing this procedure will inevitably undergo two-stage arthroplasty. Furthermore, more than half of the patients that required resection arthroplasty developed infection of their spacer that entailed revision of the cement block. Therefore, we can conclude that this procedure has a high failure rate and should be implemented in only a select group of patients.

Periprosthetic infection (PPI) is one of the most devastating complications of total knee arthroplasty (TKA). It is widely accepted that resection arthroplasty supplemented with intravenous antibiotics and delayed exchange arthroplasty is the treatment modality of choice for infected TKA. However, the outcome after reimplantation has varied and unpredictable results have been reported. This study evaluates the outcome of this treatment strategy in a single high volume specialised center. Furthermore, our study aims to identify the factors that lead to failure of this treatment.

A thorough review of our joint registry database revealed that 80 patients with an infected TKA underwent resection arthroplasty at our institution during 2000–2005. Sixty-five patients underwent two-stage exchange arthroplasty while the remaining 15 failed to have the second stage reimplantation due to ill health or underwent arthrodesis or amputation. The latter 15 were excluded from the analysis. All patients were followed up prospectively for at least two years. Detailed data including demographics, comorbidities, surgical history, and medication intake was collected. Intraoperative data, organism profile, and complications were also documented. Failure was defined as patient requiring additional surgical procedure for control of infection or loosening.

Two-stage exchange arthroplasty successfully eradicated infection in 45 patients (31%) without need for further treatment. Twelve patients (18%) had recurrent infection that necessitated another resection arthroplasty. Eleven (17%) patients required irrigation and debridement for postoperative purulent drainage which successfully treated infection in 5 cases (46%). The remaining 6 patients failed and required resection arthroplasty. Three additional patients had early loosening of components and required revision arthroplasty. The exact cause of loosening in these patients could not be determined, and despite lack of isolation of organisms infection was suspected. Our analysis identified that irrigation and debridement prior to resection arthroplasty are major risk factors for failure.

Current strategies to treat periprosthetic infection remain imperfect. Two-stage exchange arthroplasty with all its inherent problems and inconveniences imparted a modest success in treatment of PPI at our high volume specialised center. The rise in the number of resistant and virulent organisms, increase in the number of patients with severe medical comorbidities who develop infection may account for the decline in the success of two-stage resection arthroplasty. Novel strategies for treatment of PPI are desperately needed.

One of the routinely used intraoperative tests for diagnosis of periprosthetic infection (PPI) is Gram stain that is reported to carry a very high specificity and a poor sensitivity. However, it is not known if the result of this test can vary according to the type of joint affected or the number of specimen samples collected. This study intended to examine the role of this diagnostic test in a large cohort of patients from single institution.

A review of our joint registry database revealed that 453 total knee arthroplasty (TKA) and 551 total hip arthroplasty (THA) of which 171 and 150 cases were respectively infected underwent revision surgery during 2000–2005 and had intraoperative cultures available for interpretation. A positive gram stain was defined as the visualisation of bacterial cells or ‘many leukocytes’ (> 5 per high power field) under the smear. The sensitivity, specificity, and predictive values of each individual diagnostic arm of Gram stain were determined. Combinations were performed in series that require both tests to be positive to confirm infection and in parallel that necessitate both tests to be negative to rule out infection. This analysis was performed for THA and TKA separately and later compared for each joint type.

The presence of organism cells and ‘many’ neutrophils on a Gram smear had high specificity (98%–100%) and positive predictive value (89%–100%) in both THA and TKA. The sensitivities (30%–50%) and negative predictive values (70%–79%) of the two tests were low as expected among both joint types. When the two tests were combined in series the specificity and positive predictive value were absolute (100%). The sensitivity (43%–64%) and the negative predictive value (82%) improved among both THA and TKA.

The presence of organisms or ‘many’ leukocytes on the Gram smear can confirm PPI in TJA. As expected, the sensitivity and negative predictive value of the two tests were low, and therefore infection could not be safely ruled out. Although the two diagnostic arms of Gram stain can be combined to achieve improved negative predictive value (82%), Gram stain continues to have poor value in ruling out PPI. With the advances in the field of molecular biology, novel diagnostic modalities need to be designed that can replace these traditional and poor tests.

Introduction: Pulmonary embolism (PE) is a potentially fatal complication of total joint arthroplasty (TJA). Therefore, reliable means for diagnosis and evaluation of severity is essential. This study evaluates the reliability of common clinical signs and symptoms in the diagnosis of PE. In addition, clinical presentation is correlated with size and location of emboli within the pulmonary vasculature (segmental, lobar, or main).

Methods: The clinical and imaging records of all patients with confirmed diagnosis of PE following TJA performed between 2000 and 2004 were reviewed in detail. The mode of presentation and the subsequent imaging findings were noted.

Results: A total of 132 confirmed PE cases were studied. Clinical presentation included dyspnea (19.7%), chest pain (7.6%), change of mental status (6.8%0, hypotension (6.1%), and diaphoresis (3.8%). Mean room air pulse-oximetry was 85.5%. Arterial sampling showed mean O2 saturation of 88.1% and pO2 of 58.7. There was not a direct correlation between the size of the PE and the clinical presentation. However, there was a correlation between the severity of oxygen desaturation and the size and location of the embolus.

Conclusions: The presentation of PE can be non-specific and highly variable ranging from mild dyspnea to catastrophic hemodynamic collapse. Common clinical signs have a low sensitivity for diagnosis and do not correlate with severity of disease. The only correlation seemed to be measured arterial O2 saturation and pressure. Thresholds for the diagnosis of clinically significant pulmonary embolisms need to be established to improve management of this important condition.

Introduction: The use of coumadin for prophylaxis against thromboembolism (TE) following total joint arthroplasty is the standard of care. In light of recent publication of the American College of Chest Physicians (ACCP), we altered our anticoagulation protocol to be compliant with the recommendations. This study evaluates the incidence of TE and bleeding complications following TJA when low dose coumadin vs. regular dose coumadin was administered.

Methods: 987 consecutive patients undergoing total joint arthroplasty by a single surgeon between the years of 2004–2005 were included. 446 patients operated on during the 2004 received low dose coumadin (intended INR 1.5–1.7) whilst 541 patients undergoing TJA during 2005 were given regular dose coumadin (intended INR 2–2.5).

Results: The mean INR for patients operated during the year 2005 was significantly higher than the INR for patients receiving TJA in 2004. There were more complications in 2005. There were 13 PE, 44 wound drainage, 4 DVT, and 11 hematoma formation (requiring surgical evacuation) during the year 2005 compared to 10 PE, 26 wound drainage, 6 DVT, and 5 hematoma formation in 2004. The difference for all complications except DVT was significant.

Conclusion: This study confirms the commonly held belief that aggressive anticoagulation does carry a higher incidence of complications such as wound drainage and bleeding. It appears that administering higher dose coumadin increased the bleeding complications without conferring additional protection against thromboembolic disease.

Background: Vascular injuries associated with total joint arthroplasty are the most feared complication. The arterial and venous injury can occur due to direct or indirect trauma. A high index of suspicion, recognition of the injury and prompt treatment, with the immediate availability of a vascular surgeon is vital for good outcome.

Methods: Using prospectively collected data on 13624 patients undergoing total joint arthroplasty at our institution, all incidences of vascular injury were identified. Detailed data regarding the mode of presentation, the type and the outcome of intervention delivered, and the eventual functional outcome of the total joint arthroplasty were determined.

Results: There were a total of 17 vascular injuries (0.1%). Majority (16/17) of these vascular injuries were detected in the postoperative recovery area. 9 injuries occurred after TKA and 8 occurred after THA. Indirect injury was the mechanism in TKA patients with popliteal artery thrombosis being the mechanism. In contrast direct injury was the mechanism in THA patients. Fasciotomy was performed in all TKA patients and none were needed in the THA patients. One patient died of complications related to vascular injury. 12 of 17 patients (70%) had launched a legal suit against the operating surgeon.

Conclusions: After more than 80 years of accumulated experience and more than 35000 joint replacements performed by 5 surgeons in our center, the vascular complication still continues to occur. Patient awareness regarding this real problem may play a role in defraying the extremely high likelihood of legal suits associated with this complication.

INTRODUCTION: We have previously demonstrated the efficacy of a modified Ti-surface tethered with antibiotics in preventing bacterial colonization. It is not known if coverage of this surface with serum or other physiological material may hinder the bactericidal properties of such a surface.. The in vitro activity and efficacy of such a surface against S. aureus and S. epidermidis was tested following coverage of the surface with serum.

METHODS: Vancomycin was coupled to Ti6Al4V pins by aminopropylation, linker addition, and vancomycin coupling (VancTi). Bactericidal activity was tested in solutions of bacteria (Ci=1×104cfu/ml) incubated with pins±pre-incubation with fetal bovine serum (FBS). Anti fibronectin and anti-vancomycin antibodies were used to detect surface coating or modification. Bacteria were detected by fluorescent labeling (Syto9) or by direct counting after solubilization.

RESULTS: By immunofluorescence, pins were extensively covered with serum fibronectin which did not interfere with the diffuse, intense vancomycin staining. When incubated with S. epidermidis or S. aureus, VancTi showed little colonization compared to control pins (> 95% reduction in cfu).

DISCUSSION: In a physiological environment, implants will be coated with serum proteins. Activity of the VancTi was unaffected by this coating and maintained potent inhibition of bacterial colonization. We have described a surface modification that allows Ti implants to resist colonization and subsequent periprosthetic infection. Such surfaces hold great promise for the prevention and treatment of periprosthetic infections.

Introduction: Many patients with DJD of the hip may have co-existent spinal arthritis. This prospective study sought to determine: how hip arthritis commonly presents, the incidence of low back pain- as identified by patients- before and after THA and the correlation between LBP and hip arthritis.

Methods: 344 consecutive patients undergoing THA were recruited prospectively at a single institution. A detailed questionnaire containing diagrams on which the patient could draw out the site of their pain was administered to all patients preoperatively and postoperatively. Detailed clinical, radiographic, and cross sectional imaging of all the patients were reviewed in detail by a hip surgeon, a spine surgeon, and a neurologist.

Results: 170 patients (49.4%) had true LBP which resolved in 63 patients (37%). Of the remaining 107 patients the back pain was of the same intensity following THA in 33 patients (30%) and had decreased in 74 (70%) patients. 22 of the 33 patients with continued LBP were known to have spine pathology. 35 patients developed LBP after THA.18 patients in the latter group were investigated further and 12 were found to have severe previously unrecognized spine pathology.

Discussion: Hip and spine arthritis often co-exist. Majority of patients with ‘back’ pain experience a complete resolution of their pain following THA so long as prior spine pathology did not exist. THA seems to be beneficial in reducing the symptoms even for those with a pre-existent LBP and spine pathology. A number of patients may develop LBP following THA that may relate to unidentified spine pathology. Patients with true LBP may benefit form evaluation of their spine prior to THA.

Introduction: The potential benefits of Minimally invasive total hip arthroplasty (MIS THA) continues to be heavily debated. We hypothesized that the potential benefits of MIS THA may relate to factors such as patient selection, patient preconditioning, improvements in anesthesia technique, pain management, and not the incision size. This randomized, prospective study was designed to investigate the role of these confounding factors in general and aggressive rehabilitation in particular on the outcome of THA.

Methods: 100 patients undergoing THA at our institution were randomized into one of four groups. Group A was patients who had standard THA (incision length> 10 cm) and received standard preoperative and postoperative care. Group B patients had THA using small incision (< 10 cm) and standard protocols. Group C patients had regular incision THA, but received aggressive rehabilitation and pain control regimen. Group D patients had THA through small incision and received aggressive regimen.

Results: The demographic distribution amongst all the groups was similar. There was a significant improvement in function as measured by Harris Hip Score, LASA (validated rehabilitation score), SF-36, and lower extremity function test in all groups. The extent of functional improvement, home discharge, patient satisfaction, and analgesia requirement was better in patients who received aggressive preoperative and postoperative care regimen regardless of the size of their incision. There was no difference in estimated blood loss, mean operative time, transfusion needs, and complications between the groups.

Discussion: This study highlights the importance of family education, patient conditioning, pre-emptive analgesia, and aggressive preoperative and postoperative rehabilitation in influencing the outcome of THA. The aforementioned factors, and perhaps not the surgical technique per se, may play a major role in imparting advantageous outcome to MIS THA that is reported by various investigators.

Purpose: Periprosthetic infection (PPI) is a devastating complication. Surgical intervention to treat PPI is often required. The objective of this prospective study is to determine if there is any difference in functional improvement following revision TKA in patients with infected and non-infected failures.

Methods: 123 consecutive patients undergoing revision TKA at our institution were prospectively recruited into this study. The indication for revision TKA was PPI in 37 cases and aseptic failure in 86 cases. Detailed patient demographics and functional outcome using SF-36, KSS, Womac, lower extremity functional outcome score were collected at base line and at various time points after revision TKA. The baseline and two year follow up functional scores were calculated and compared. The functional score at the time of diagnosis of PPI (prosthesis in place) were used for baseline comparisons

Results: All baseline functional scores, and their individual elements, for the infected cases were worse than the non-infected cases. The functional scores at the two-year follow-up were not different between the infected and non-infected cases. Hence, there was a more impressive improvement (Δ) in functional outcome for the infected cases following revision TKA compared to non-infected cases. However, the general health perception as determined by the patients themselves appeared to deteriorate after revision TKA in both groups.

Discussion: It appears that patients with PPI are markedly more disabled at base line than the non-infected cases. These patients, however, benefit the most from surgical intervention compared to the non-infected cases. It appears that the patients’ perception of improvement in functional scores is less optimistic than physician measured parameters.

Introduction: Intraoperative tissue culture remains the “gold standard” in diagnosing periprosthetic infection (PPI). However, an organism is not always cultured and this has been attributed to the fact that preoperative antibiotics were administered. This study intends to examine if preoperative antibiotics prevent isolation of intraoperative organisms.

Methods: 91 total joint arthroplasty patients diagnosed with PPI during (1999–2005) and who had positive aspiration culture were included in the study. All intravenous antibiotics that were given to the patient within seven days of surgery were documented. The total number of positive intraoperative fluid and tissue samples of patients who did and did not receive antibiotics was calculated. Susceptibility of the organism(s) to antibiotics was determined by antibiogram of the preoperative and intraoperative culture.

Results: 60 out of 91 patients received preoperative antibiotics within seven days of surgery. Antibiotics prevented isolation of an intraoperative organism in 6 out of the 60 (10%) cases. All of the 31 patients who did not receive any preoperative antibiotics had positive intraoperative cultures. Chi-square analysis revealed no significant difference between giving preoperative antibiotics within 7 days and isolating an intraoperative organism (p=0.068). Giving antibiotics that specifically targets the culprit organism did not significantly affect the fluid (p=0.585) or tissue culture yield (p=0.152) either.

Discussion: Although, giving preoperative antibiotics can prevent isolation of intraoperative organisms in 10% of cases, this is not statistically or clinically significant in patients with positive aspiration cultures because the organism is known beforehand. However, it is clinically and medicolegally relevant to withhold antibiotics in patients with negative aspiration cultures since the postoperative treatment antibiotic is tailored according to the organism cultured.

INTRODUCTION: Range of motion following TKA is a commonly assessed and important outcome parameter. The reported knee ROM is often measured using manual goniometers. The accuracy of goniometer in measuring ROM of the knee is not known. We compared the knee ROM measured with a manual goniometer and compared that to measurements obtained from computer assisted navigation system.

METHODS: This prospective ongoing study has so far recruited 60 patients (71 knees) undergoing TKA by a single surgeon. Measurements of the ROM were performed intraoperatively using a 14 inch 360° Nexgen Baseline® goniometer, validated by physical therapists, and the Stryker knee navigation system^™. Consistent anatomical landmarks were used to obtain flexion and extension measurements. Each goniometer and navigation measurement was performed twice by the same reader.

RESULTS: Goniometer was more inaccurate in measuring the knee ROM than the navigation. There was a 5.07° difference between two measurements obtained with the goniometer compared to a mean discrepancy of 1.15° using the navigation system. Further, the ROM measured by navigation was on average 13.9° larger than that measured by the goniometer. BMI affected the ROM recording obtained by both the goniometer and the navigation system.

DISCUSSION AND CONCLUSION: This study indicates that goniometer is not an accurate tool for measurements of knee ROM as there is a marked discrepancy between two goniometer readings. The navigation system seemed to produce more consistent, but markedly higher, readings than a manual goniometer. Reported results on knee ROM in the literature need to be interpreted with caution and scrutinized for potential inaccuracy of the measuring tool.

Introduction: The safety of simultaneous bilateral knee replacement (BTKA) remains controversial. Some studies have proposed a higher incidence of serious complications, even death, following BTKA whilst others refute the latter. The objective of this meta-analysis was to evaluate the safety of BTKA.

Methods: A computerized literature search was conducted to identify all citations, between 1966 to 2005, concerning BTKA. All the English-language abstracts were obtained. A multistage assessment was then used to identify articles fulfilling the inclusion criteria for the study. All randomized, prospective studies reporting the outcome of BTKA were included. Details of any reported data were extracted and extensive analysis of relevant variables carried out.

Results: 150 published articles pertaining to BTKA were identified of which 18 papers on 27,807 patients (44,684 knees) were included in the meta-analysis.10,734 cases were unilateral TKA, 16,378 were simultaneous BTKA and 458 were staged bilateral TKA with at least 3 months time duration between the surgical procedures. The complications analyzed were DVT, PE, cardiac events and mortality. The incidence of PE (OR=1.8), cardiac complications (OR=2.4), and mortality (OR=2.24) were higher after simultaneous BTKA. The incidence of DVT was LOWER in the group with simultaneous BTKA.

Discussion: Based on the findings of this meta-analysis, simultanous BTKA seems to carry a higher risk of serious cardiac complications, pulmonary complications, and mortality. This procedure should be reserved for the healthy and young patients.

Introduction: A small, yet not uncommon, problem following total joint arthroplasty (TJA) is post-operative ileus (POI). The purpose of this study was two-fold. First the study sought to determine the incidence of POI after TJA in a consecutive series of patients receiving regional anesthesia and an aggressive postoperative rehabilitation protocol. Second, the influence of narcotic medications, including intrathecal medications, in the incidence of POI was examined.

Methods: 5,262 patients underwent total joint replacements, including primary and revision surgery, at our institution from 2004 to 2005. All surgeries were performed at a university-affiliated institution where complications, if any, are prospectively recorded in a comprehensive database. Demographic, clinical, surgical, and radiographic details were obtained and examined.

Results: 26 (0.5%) patients developed ileus. There were 17 males and 9 female patients, who had a mean age of 67.7 years (range, 52.7 to 91.2 years). The mean BMI was 30.2 kg/m2. The index procedures included 15 primary hip, 4 primary knee, 4 revision hip, and 3 revision knee procedures. Of the patients who developed ileus, intrathecal narcotics were administered in 16 patients (62%).

Discussion: There is a very low incidence of postoperative ileus and gastrointenstinal hypomobility following joint arthroplasty. Early patient ambulation, a reduction in the use of postoperative narcotics, supplementation of analgesia with non-narcotic drugs, and reduced length of hospital stay may all have an important role in reducing this complication. Based on our findings, it seems unlikely that intrathecal narcotics have an adverse effect on gastrointestinal motility.

Introduction: Diabetes mellitus type 2 (DM II) affects 18.2 million Americans and can cause several chronic and morbid complications. Furthermore, 90% of Americans have radiographic evidence of osteoarthritis by age 40. Diabetes may be an important risk factor for symptomatic osteoarthritis later in life. The aim of our study is to determine if diabetic patients are predisposed to osteoarthritis.

Methods: We conducted a review of the all total knee arthroplasty (TKA) cases performed at our institute during the past two years for end stage osteoarthritis. We excluded TKAs performed for post-traumatic arthritis and patients with inflammatory diseases. Comorbidities and demographical information including age, gender, BMI, and family history were collected from our database. A cross sectional study was performed to analyze the prevalence of DM II in our population. This prevalence was compared to that of diabetics in the general population available from various sources including the National Center for Health Statistics.

Results: Our cohort included a total of 3421 patients (1972 females, 1449 males) who had undergone TKA for end stage osteoarthritis. The average age and BMI were 66 years (range: 39–92) and 32 (range: 21–65) respectively. The prevalence of diabetes mellitus type 2 in our cohort was 12%, while the prevalence of DM II in the general US population currently ranges from 6%–7%.

Discussion: Chronic diabetes causes multiorgan failure via microvascular and macrovascular damage and may possibly lead to degeneration of articular cartilage and eventual arthritis. Based on this study, diabetes appears to be a strong predisposing factor for arthritis. Our laboratory has launched an extensive series of experiments delinating the potential cellular mechanism for such association.

Introduction: We have previously described modification of Ti that renders the implant surface bactericidal and prevents bacterial colonization in vitro. This study evaluates the efficacy of the same surface in preventing periprosthetic infection in a small mammal model.

Methods: Control or VancTi rods were incubated with S. aureus (Ci=104CFU/mL) in TSB containing 0, 5×10-3, 4, or 100 μg/mL vancomycin at 37°C for 24h. Bacteria were detected by fluorescence (Live/Dead BacLight) and imaged by confocal microscopy. Resistance was tested by incubating control or VancTi rods with S. aureus for 0–8 weeks. Adherent bacteria were tested every 7 days on vancomycin screening agar (6μg/mL).

Results: Using a percutanous approach, the intercondylar region of the knee in rats were identified. The intrameduallry canal of the femur was retrograde reamed using an 18-gauge needle. Infection was induced by injection of 103 CFU S. aureus in 150uL of saline into the femoral canal followed by insertion of a 20 mm Ti implant. Animals were harvested at various time points. At harvest, animals were euthanized with CO2.. Detailed analysis including radiographic, micro-CT, histological, bacteriological, and clinical evaluation was performed.

Results: All animals showed signs of infection within the first few post-operative days with increased soft tissue swelling and limited mobility. At 1 week 75% of the animals showed radiographic signs of periprosthetic infection including periosteal reaction, abscess formation, widened canal, bone destruction, and formation of involucrum. PPI could be prevented in 92% of cases when modified Ti-Van was used. In one animal despite the use of antibiotic-tethered implant, PPI occurred partially due to the pin insertion penetrating the bone cortex.

Discussion: Biologically modified implants with bactericidal surface can have a promising role in management of periprosthetic infection. The modified implant described herein contains a nanoscale surface of covalently linked antibiotics that can potentially confer bactericidal properties throughout the life of the implant