1. Periprosthetic acetabular radiolucency progression in mid-term follow-up of the articular surface replacement hip system
- Author
-
Henrik Malchau, Janus Christiansen, James W. Connelly, Orhun K. Muratoglu, Sean J. Matuszak, and Vincent P. Galea
- Subjects
musculoskeletal diseases ,Adult ,Chromium ,Male ,medicine.medical_specialty ,Osteolysis ,genetic structures ,Radiodensity ,Radiography ,medicine.medical_treatment ,Arthroplasty, Replacement, Hip ,Periprosthetic ,Prosthesis Design ,Lesion ,03 medical and health sciences ,Young Adult ,0302 clinical medicine ,Postoperative Complications ,Risk Factors ,medicine ,Humans ,Orthopedics and Sports Medicine ,030212 general & internal medicine ,Prospective Studies ,Registries ,Aged ,Aged, 80 and over ,030222 orthopedics ,business.industry ,Acetabulum ,General Medicine ,Middle Aged ,medicine.disease ,Hip resurfacing ,Arthroplasty ,Surgery ,Prosthesis Failure ,Metals ,Orthopedic surgery ,Disease Progression ,Female ,Hip Joint ,Hip Prosthesis ,medicine.symptom ,business ,Follow-Up Studies - Abstract
Recent registry studies show that aseptic loosening secondary to osteolysis is the second leading cause of hip implant failure in patients implanted with metal-on-metal (MoM) bearings. The primary aim of our study was to report on the progression of acetabular osteolysis during mid-term follow-up in patients treated with MoM hip resurfacing arthroplasty (HRA) and MoM total hip arthroplasty (THA). The secondary aim was to identify independent predictors of osteolytic lesion progression. A total of 805 patients (805 hips) were included in this study (541 MoM HRA, 264 MoM THA) from a prospective, international clinical registry of the Articular Surface Replacement Hip System. Patients were enrolled a median of 6.6 years from surgery. Osteolytic lesion progression was defined either as any lesion developing de novo, or as an existing lesion progressing from radiolucency to osteolysis during the study period (range 0.5–4.3 years). The number of cases with any osteolysis or radiolucency was 21 (3.9%) for ASR HRA and 29 (11.0%) for ASR XL THA at enrollment and increased to 69 (12.8%) for ASR HRA and 41 (15.5%) for ASR XL THA after follow-up. Osteolytic lesion progression was found in 66 (12.2%) ASR HRA patients and 31 (11.7%) ASR XL THA patients. Multivariate models determined that lower acetabular version angle (OR 0.963, p = 0.011) and elevated whole blood chromium (OR 1.110, p = 0.044) were independent predictors of osteolytic lesion progression in ASR HRA. We suggest that physicians of patients implanted with ASR HRA implants closely monitor patients with higher chromium levels and lower version angles, as they are at increased risk for osteolytic lesion progression, and we recommend annual radiographic follow-up on all patients with ASR implants.
- Published
- 2018