Abstract

Mobile knee spacers can be utilized in the first stage of atwo-stage exchange in periprosthetic joint infection or septic arthritis of the knee to prevent soft tissue contraction, enable local antibiotic elution, and improve patient mobility. Commercially made moulds enable the surgeon to prepare areproducible spacer design and match the preparation of the arthroplasty, which will be carried out in a second step. Periprosthetic joint infection of the knee and severe cases of septic arthritis of the knee with advanced destruction/infiltration of the cartilage. Antibiotic resistance of the microbiological pathogen to available antibiotic agents, incompliant patient, large osseous defect preventing proper fixation, known allergy to polymethylmethacrylate (PMMA) or antibiotic, severe soft tissue damage with high ligament instability, especially deterioration of extensor mechanism and insufficient patella/quadricep tendon. After thorough debridement and removal of all foreign material, cutting blocks are used to shape femur and tibia to the implant design required. Using asilicone mould, PMMA with suitable antibiotics is moulded into the shape of the future implant. After polymerization, the implants are fixed onto the bone with additional PMMA without pressurize for the sake of easy removal. Partial weight bearing with no restriction of flexion/extension while spacer is in place; second stage reimplantation as soon as infection is controlled. In all, 22cases were treated, mostly with aPMMA spacer containing gentamicin and vancomycin. Pathogens were detected in13 of 22cases (59%). We observed two complications (9%). Twentyof 22patients (86%) were reimplanted with anew arthroplasty; 16of the 20patients remained revision-free and infection-free at the last follow-up (average time to follow-up 13months, range 1-46months). Average range of motion in flexion and extension at follow-up was98°.

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