Risk of Periprosthetic Joint Infection After Intra-Articular Corticosteroid Injection Following Unicompartmental Knee Arthroplasty.

BACKGROUND: Perioperative intra-articular joint injection is a known risk factor for developing prosthetic joint infection (PJI) in the immediate preoperative and postoperative periods for total knee arthroplasty, but is less defined in unicompartmental knee arthroplasty (UKA). The goal of this study was to elucidate the risk of developing PJI after intra-articular corticosteroid injection (IACI) into a post UKA knee. METHODS: A retrospective review of a nationwide administrative claims database was performed from January 2015 to October 2020. Patients who underwent UKA and had an ipsilateral IACI were identified and matched 2:1 to a control group of primary UKA patients who did not receive IACI. Multivariate logistic analyses were conducted to assess differences in PJI rates at 6 months, 1 year, and 2 years. RESULTS: A total of 47,903 cases were identified, of which 2,656 (5.5%) cases received IACI. The mean time from UKA to IACI was 355 days. The incidence of PJI in the IACI group was 2.7%, compared to 1.3% in the control group. The rate of PJI after IACI was significantly higher than the rate in the control group at 6 months, 1 year, and 2 years (all P < .05). The majority of PJI occurred within the first 6 months following IACI (75%). CONCLUSION: In this study, IACI in a UKA doubled the risk of PJI compared to patients who did not receive an injection. Surgeons should be aware of this increased risk to aid in their decision-making about injecting into a UKA. LEVEL OF EVIDENCE: III, retrospective comparative study.

Incidence of heterotopic ossification in direct anterior total hip arthroplasty: a retrospective radiographic review.

Heterotopic ossification (HO) is a complication following total hip arthroplasty (THA) with traditional approaches. The direct anterior approach (DAA) has become a popular approach for THA; however, no study has evaluated HO formation following DAA THA. We examined the incidence of HO in a consecutive series of THA using the DAA in two separate hospitals. Standard preoperative radiographs were examined to determine the type of degenerative arthritis, and follow-up radiographs of at least 6 months after surgery were evaluated for the presence and classification of HO. The overall incidence of HO after DAA THA in this study was 98/236, or 41.5%, which falls within the reported range from recent studies involving more traditional approaches to the hip.

Midterm radiographic comparison of cementless acetabular shells containing lateralized and nonlateralized liners.

This retrospective study assessed the effect of lateralized acetabular inserts on polyethylene wear rates, radiographic loosening, and hip stability. Fifty-six 4-mm lateralized liners and 39 neutral liners were compared at a mean follow-up of 7.1 years. Multivariate regression analysis demonstrated a significant increase of 0.04 mm/y in polyethylene wear rate with use of lateralized liners. However, predictable cementless fixation was obtained without screws in both liner groups with no migration or radiographic signs of loosening observed for any cup. The dislocation rate for hips with lateralized liners (3.6%) was less than that for hip with neutral liners (10.3%), although the difference was not significant with the numbers available. Despite the increase in wear rate, hips with lateralized liners performed as well as those with neutral liners with regard to loosening and stability.

Isolated revision of failed metal-backed patellar components: outcome with minimum 4-year follow-up.

Several reports document high failure rates of metal-backed patellar components, but few report the outcome of revising these components to all-polyethylene, cemented implants. At a mean 87.2-month follow-up, we describe a series of 36 patients (40 knees) who underwent isolated metal-backed patellar revision to a cemented, all-polyethylene patellar component. After the patellar revision, 5 patients (6 knees) underwent additional surgery, but no patellar components required revision. The additional surgeries were performed at an average of 77.6 months after patellar revision and included 3 tibial insert exchanges for polyethylene wear, 2 revisions of femoral and tibial components for osteolysis, and 1 realignment procedure for recurrent subluxation of the patella. We conclude that revision of a failed metal-backed patellar component to a cemented, all-polyethylene patella is a durable, successful procedure.