This study compared patient-reported outcomes of three total knee arthroplasty (TKA) designs from one manufacturer: one cruciate-retaining (CR) design, and two cruciate-sacrificing designs, anterior-stabilized (AS) and posterior-stabilized (PS). Patients scheduled for primary TKA were included in a single-centre, prospective, three-armed, blinded randomized trial (n = 216; 72 per group). After intraoperative confirmation of posterior cruciate ligament (PCL) integrity, patients were randomly allocated to receive a CR, AS, or PS design from the same TKA system. Insertion of an AS or PS design required PCL resection. The primary outcome was the mean score of all five subscales of the Knee injury and Osteoarthritis Outcome Score (KOOS) at two-year follow-up. Secondary outcomes included all KOOS subscales, Oxford Knee Score, EuroQol five-dimension health questionnaire, EuroQol visual analogue scale, range of motion (ROM), and willingness to undergo the operation again. Patient satisfaction was also assessed.Aims
Methods
Early prosthetic joint infection (PJI) is a feared complication of hip arthroplasty. Debridement, antibiotics and implant retention (DAIR) is attempted to avoid removal of the implant. The aim of this retrospective cohort study was to evaluate the success rate of DAIR in early PJI. All patients who were diagnosed with early PJI and treated with DAIR at our center from 2003 to 2013 were included in the study. During the time period, 5176 primary hip arthroplasties and 555 revision hip arthroplasties were performed. Early PJI was diagnosed in 54 patients (43 primary and 11 revisions). Median follow-up was 5.6 years (range 2.0–12.1). Standard postoperative antibiotic treatment at our centre is vancomycin and rifampicin.Aim
Method
In the past it has been widely accepted that bone remodelling of the proximal femur after cementless total hip replacement is a result of the altered mechanical environment. Usually, there is are distribution of the stresses in the bone, and subsequently bone mass, from the metaphysis to the proximal part of the diaphysis. The design rationale for some cementless stems is to transmit load to the proximal femur and thus to preserve the bone mineral content in this area. The aim of the present study was to investigate the relationship between postoperative strain shielding of the proximal femur and the bone remodelling after insertion of two different cementless femoral stems.
Clinical study: In a prospective, randomized study including 80 patients, the same types of stems were inserted and the bone mineral density (BMD) was measured during the first two years postoperatively using DEXA. Then, the pattern of remodelling was compared with the gradient of strain shielding in each of the Gruen zones in the frontal plane. In Gruen zone 7 the relative cortical strain shielding was45% in the femurs with a custom stem and 87% in the femurs with an anatomic stem. In zone 6 the corresponding figures were 2% and 38%, in zone 5 0% and15% and in zone 3 0% and 20%. The DEXA measurements showed a decrease in BMD in zone 7 of 22% and 23% for the two stems, respectively. In the other zones the bone loss was smaller and there was no difference between the stems. In the proximal zones there was a highly significant difference in strain shielding between femurs receiving a customor an anatomic stem. However, there was no difference in the pattern of bone remodelling. The bone remodelling around these two stems does not seem to mirror the gradient of strain shielding.
A customised, uncemented femoral stem was introduced clinically in 1995 after several years of development and pre-clinical testing. All the patients operated in our hospital have entered a prospective clinical study. The aim of this study is to present the short-term clinical data. Furthermore, the measurement of implant migration and the periprosthetic bone remodelling at two years is also reported.
An argument against the use of canal-filling, customised femoral stems has been that such implants have a large cross-sectional area and therefore are stiffer than standard, uncemented implants, thus inducing more stress shielding and bone loss in the proximal femur. The purpose of this study was to evaluate the association between the volume of the femoral stem and the change in periprosthetic bone mineral density (BMD) measured with DEXA.
New prosthesis designs should be compared to a standard implant in randomized studies evaluated by radiostereometric analysis (RSA). The Unique customized prosthesis (UCP) is a newly developed concept for fitting uncemented prosthesis to the exact internal shape of the proximal femur [
The aim of this paper is to present our 7 years experience with the use of a custom femoral stem with proximal HA-coating (Unique SCP). This prosthesis was developed to optimise the þxation and the strain distribution to the proximal femur and also the biomechanics of the hip in uncemented femoral stems.
CT-based, customised femoral stem enables optimal reconstruction of hip mechanics and leg length. However, traditional planning and execution of cup insertion may jeopardise these biomechanical parameters. The aim of this study was to examine the agreement of the preoperative planning of cup position and the final position of the cup. Thirty total hip replacements with an uncemented acetabular cup (Duraloc, DePuy) or a cemented cup (Elite-Plus, DePuy) were included. A customised femoral stem was used in all hips. On the preoperative X-rays the planned position and orientation of the cup had been marked prior to the surgery. The pre- and postoperative X-ray images were then digitised and scaled. The planned and final positions of the cup centre in the frontal plane was then measured relative to a horizontal line defined by the tear-drops and to a vertical line through the centre of the tear-drop on the operated side. In addition the concurrence between the planned and final cup size was examined. In the horizontal direction the cups were positioned 1.4 (7.6) mm (median, ±2SD) more medial than planned on the preoperative X-rays. In the vertical direction the corresponding figures were 1.2 (6.6) mm (median, ±2SD) and the cups were usually placed more cranially than was planned. The maximum discrepancy between the planned and final position was 10,6 mm in the horizontal direction (medial) and 7.1 mm in the vertical direction (cranial). In 63% of the hips there was agreement between the size of the cup planned preoperatively and the cup that was finally inserted. In 25% of the hips the final cup was larger and in 12% the final cup was smaller. In most cases the acetabular cups were inserted within a few millimetres of the planned position. The combination of a standard uncemented or cemented cup with a custom femoral stem enables the surgeon to restore hip mechanics and leg length.