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.

Purpose: Problem : Infection in TKA is a devastating yet common complication. 2-stage reimplant procedures are performed in the treatment of this condition. Purpose:To evaluate the clinical, radiographic, complications, and patient satisfaction results of 2nd stage reimplantation revision TKA with the use of a TTO. Technical aspects of TTO length, fixation, bypass, and complications are reported.

Methods: From 1996–2004 our database identified 25 revision TKA (12% of 206 revision TKA) performed using a TTO. In 20/25 cases the procedure was a 2nd stage reimplant. Demographics, infecting organism, Gustillo grade, clinical, radiographic, AORI defects, complications, patient satisfaction were evaluated prospectively. All patients were followed until radiographic union of the TTO.

Results: At a mean follow up of 22 mo(range,6–84) no patients were lost to follow-up. 24 (96%)TTO’s healed - 1 requiring revision ORIF. Prior to reimplantation, patients had undergone a mean of 3.3 prior knee surgeries(range,2–8). Prior extensor mechanism procedures had been performed in 43% of knees. Methicillin resistant staphylococcus was the infecting organism in > 50% of knees. 19 knees had a static cement spacer removed at revision. Time to 2nd stage reimplant was 39 weeks(range,15–68). Poor preop range of motion and stiffness (mean arc 430 , range 10–950) improved significantly postop (mean flexion 880 p< .05). 13 (56%) knees required an adjunctive extensor procedure at the time of TTO. TTO length averaged 8.8cm(range,8–10). Screws(15 knees), 2mm cables(6), wires(4) were used for TTO fixation. Mean stem bypass of the TTO was 63mm (−20 to 100). 21 (84%) patients were satisfied with the procedure, despite 8 knees(32%) requiring further surgery. 6 (24%) TTO complications occurred; 1 escape requiring fixation. All TTO’s had healed at recent follow up.

Conclusions: TTO is a useful procedure for exposure in 2nd stage revision TKA. TTO union is predictable(96%), despite technical complications. Recurrence of infection requiring further surgery did not compromise TTO results. Prior/concurrent extensor mechanism procedures were noted frequently.

Funding : Other Education Grant

Funding Parties : Wright Medical Technologies

Introduction and Aims: The use of porous coated femoral stems in revision hip arthroplasty has been associated with a high rate of complications including femoral fracture, femoral perforation and eccentric reaming. The purpose is to determine if using a distally slotted-fluted femoral stem is associated with lower incidence of the above three intra-operative complications.

Method: The intra-operative complications of 175 cementless revision total hip arthropasties (THA) using a distally slotted-fluted femoral stem were reviewed. Three categories of complications were recorded: femoral fracture, femoral perforation and eccentric reaming. Radiographic evaluation was based on standard antero-posterior and lateral views of the hip joint performed in the intra-operative or immediate post-operative period. Statistical analysis for factors associated with complications was performed using the chi-square test.

Results: Intra-operative complications occurred in 16 patients (9.1%). There was no statistically significant association between complication rate and type of surgical approach, stem length, stem diameter, or host bone quality. The complication rate was significantly lower than the 44% total complication rate previously reported utilising a long, solid, extensively coated revision stem without a slot or flute (p< .01). These results are consistent with laboratory testing, which revealed significantly lower bone strains at the isthmus when inserting a long cementless revision stem with a slot and flute compared to a solid fully coated stem of identical geometry.

Conclusion: The use of a distally slotted fluted porous coated femoral stem in revision hip arthroplasty results in a dramatically lower complication rate compared to rates previously reported for solid porous stems. These results strongly support the continued use of such a prosthesis for revision THA.

We examined 108 uncemented femoral stems with modular femoral heads which had been retrieved for reasons other than loosening. There were detectable amounts of wear and corrosion in 10 of 29 (34.5%) mixed-alloy components and 7 of 79 (9%) single-alloy components after a mean implantation time of 25 months. We found no correlation between the presence or extent of corrosion or surface damage and any of time in situ, initial diagnosis, reason for removal, age, or weight. Stems with wear and corrosion were less likely to show histological bony ingrowth. The interface between the head and stem of modular total hip components is a possible source of ion release and wear debris, but wear and corrosion were totally absent in most specimens. This suggests that this problem could be avoided, and that further research is required to develop manufacturing methods which would minimise such changes.

We report complications from the use of modular components in 20 hip replacements in 18 patients. Fifteen complications (in 13 patients) were related to failure of a modular interface after operation. Femoral head detachment from its trunnion was seen in 6 hips from trauma (3), reduction of a dislocation (2), and normal activity (1). In one case the base of the trunnion fractured below an extra-long modular head. In seven other hips the modular polyethylene liner dislodged from its shell, causing severe damage to the shell in four cases with extensive metallosis. In one other hip an asymmetrical polyethylene liner rotated, resulting in impingement of the femoral component and recurrent dislocation. Operative errors were seen in five cases: implantation of a trial acetabular component in one; and mismatching between the size of the femoral head and the acetabular component in the others. Surgeons who use hip replacements with modular components should be aware of the potential for operative error and of the importance of early treatment for postoperative mechanical failure.

Six porous-coated, uncemented femoral components were revised at a mean of 34.5 months for persistent thigh pain. At operation the stems were rigidly stable, difficult to extract, and showed good bony ingrowth. The four men and two women, with an average age of 59 years, all had thigh pain starting within the first year, progressive over time and unresponsive to conservative measures. These cases show that rigid fixation with good bony ingrowth does not guarantee the clinical success of a porous-coated uncemented femoral stem.

To assess the effect of improved methods of femoral cementing on the loosening rates in young patients, we reviewed 50 'second-generation' cemented hip arthroplasties in 44 patients aged 50 years or less. The femoral stems were all collared and rectangular in cross-section with rounded corners. The cement was delivered by a gun into a medullary canal occluded distally with a cement plug. A clinical and radiographic review was undertaken at an average of 12 years (10 to 14.8) and no patient was lost to follow-up. No femoral component was revised for aseptic loosening, and only one stem was definitely loose by radiographic criteria. By contrast, 11 patients had undergone revision for symptomatic aseptic loosening of the acetabular component and 11 more had radiographic signs of acetabular loosening.

A study was undertaken to determine whether a significantly different clinical outcome could be expected following nonoperative treatment of acute partial anterior cruciate ligament (ACL) tears from that of complete tears. A detailed follow-up of 107 patients with arthroscopically confirmed tears was obtained; 72 were complete tears and 35 partial. The overall results in those with partial tears were 23% excellent, 29% good, 17% fair, and 31% poor; with complete tears the results were 11% excellent, 20% good, 15% fair, and 54% poor. The patients with partial tears had a lower incidence of associated meniscal tears, needed fewer reconstructions and more of them returned to sport than those with complete tears.

Recent clinical studies have suggested that a neurological lesion may be a cause of adolescent idiopathic scoliosis and animal experiments have implicated the posterior column pathway. We have tried to determine if differences in neurological response could be detected and measured clinically, and have compared the threshold of detection of vibratory sensation in 20 girls with adolescent idiopathic scoliosis with that in 20 clinically normal age-matched controls. A highly significant reduction of the threshold of detection of vibration was seen in the scoliotic group compared to the controls (p less than 0.001). Curve magnitude did not correlate with this threshold for either the upper (r = 0.172) or lower extremity (r = 0.126). Significant asymmetry between right- and left-sided thresholds to vibration was demonstrated in the scoliotic group. Our study supports the concept that an aberration in the function of the posterior column pathway of the cord may be of primary importance in the aetiology of idiopathic scoliosis. A clinically practical test to measure this function is presented.