This study was conducted by two orthopedic surgeons (UT, AF), each with a minimum of 10 years in experiences, over the period March 2017 - January 2018 at Kırıkkale University Hospital and Atatürk Training and Research Hospital. The informed consent of the patients and approval from the local ethics committee (IRB number: 13/6) were obtained for the study. The demographic data of the patients were recorded (Table 1).
Table 1
The demographic data of the patients.
| Grup 1 (n:35) | Grup 2 (n:35) | P value |
Mean age | 68.3 ± 6.1 | 67.8 ± 6.9 | P ˃ 0.05 |
Mean body mass index (kg/m2) | 29.1 ± 5.2 | 29.4 ± 4.9 | P ˃ 0.05 |
Gender (Female/Male) | 11/24 | 13/22 | P ˃ 0.05 |
Mean preoperative flexion contracture | 7.6 ± 5.0 | 7.4 ± 4.9 | P ˃ 0.05 |
Mean preoperative varus angle | 13.4 ± 5.2 | 12.5 ± 5.1 | P ˃ 0.05 |
Table 2
| Grup 1 | Grup 2 | P value |
Extra tibial bone resection(%) | n:2 (5.7%) (2 mm) | n:10 (28.6%) (2–6 mm) | 0.018 |
Insert size (8, 10, 12,14,16) | 8 (n:29) (82.9%) 10 (n:6) (17.1%) | 8 (n:22) (62.9%) 10 (n:9) (25.7%) 12 (n:4) (11.4%) | 0.024 |
Mean resection of the medial femoral bone | 10.5 ± 1.2 (8–14 mm) | 10.5 ± 1.1 (8–12 mm) | 0.841 |
Mean resection of the medial tibial bone | 4.0 ± 1.8 (2–8 mm) | 3.6 ± 1.8 (2–8 mm) | 0.298 |
Table 3
Data of the articles related with parameters of bone spesific recuts in TKA.
Author/s | Patients | Additional tibial bone resection | Additional femoral bone resection | Procedure |
Kawano T. et al.(14) | n:30 | n:3(10%) | - | Conventional measured resection technique |
Gregory C. et al.(20) | n:116 | n:18(16%) | n:20(21%) | Patient-specific cutting guides |
Pietsch M. et al.(21) | n:50 | n:17(34%) | n:31(62%) | Patient-specific cutting guides |
Seong et al.(22) | n:59 | - | n:16(27%) | Navigated total knee arthroplasy |
Group 1 Current study Group 2 | n:35 n:35 | n:2 (5.7%) n:10(28.6%) | - - | Measuring the medial gap with measured resection technique Conventional measured resection technique |
The research was conducted with patients undergoing total knee arthroplasty on the basis of a diagnosis of varus knee osteoarthritis. Including criteria were: patients undergoing total knee arthroplasty due to varus knee osteoarthritis, a tibiofemoral angle of ≤ 20°. Exclusion criteria were: posttraumatic osteoarthritis, rheumatoid arthritis, hemophilic arthropathy, postseptic arthritis, tibiofemoral varus of more than 20°, flexion contracture of more than 10°, patients with extraarticular deformities, those that had undergone deformity surgery and patients with valgus gonarthrosis. Seventy patients meeting the inclusion criteria were taken into the study. Patients were separated into two groups, Group 1 being those whose medial joint gap were measured prior to bone resection during surgery and Group 2 comprising those who underwent standard surgical bone resection without measuring. Each group comprised 35 patients. For randomization, the first group of patients (Group 1) was selected by drawing lots while the participants in the other group (Group 2) were recruited in order of their admittance. A posterior cruciate sacrificing implant (Scorpio® NRG PS, Stryker Howmedica Osteonics, Allendale, NJ, USA) was used on all the patients.
Specifications of the Prosthesis
The technical specifications of this knee prosthesis include a femoral component thickness of 8 mm, tibial component thickness of 6 mm and an insert of 8-16 mm. A minimum gap distance of 22 mm, 2 cm cement (1 mm for the femoral, 1 mm for the tibial component), and an allowance of 2 mm. for joint movement, comprising in total, a gap distance of 26 mm are required for this implant.
Technique of measuring the medial joint gap
This measurement is taken with a custom-designed gap measuring device that starts from a measurement of 6 mm to 16 m with 2 mm intervals in between (Figure 1). Since knee prosthesis cutting systems are designed for 2 mm intervals, the device was manufactured in matching specifications. The medial joint gap was measured with the device positioned between the most distal medial femoral condyle and the central medial tibial plateau with the knee in extension. While applying varus stress on the knee, the device was placed in the smallest gap and using the cable technique, the size was increased until the mechanical axis of the knee was corrected. The last gap thickness measurement was recorded.
Determining the amount of tibial resection
The distal femoral cutting block was positioned with the femoral intramedullar guide. The distal femoral bone resection was performed using the “sulcus cut” method [5,6]. The thickest part of the medial distal bone fragment removed from the femur was measured with the help of a compass. The following formula was used to calculate the amount of tibial bone to be resected: Tibial bone resection amount = 26 - (Measured medial joint gap + Femoral bone resection amount) (Figure 2). Then an amount from the medial proximal part of the tibia equal to the amount in the tibial cutting block was measured and resected.
Surgical technique for Group 1
Surgery was performed with a standard anterior longitudinal incision and a parapatellar approach. Anterior and posterior cruciate ligament excision, meniscectomy, tibial and femoral osteophyte excision and the standard medial release of the anteromedial tibial periosteum and deep medial ligament were performed. Then the medial joint gap was measured. With the help of a guide, the distal femoral cut was first performed and the piece of medial bone excised was measured. The amount of tibial resection was calculated according to the formula. The tibial extramedullary cutting guide was placed. Then with the tibial stylus matching the value obtained from the formula touching the medial central tibial plateau, this was fixed with a block pin and the bone resection was performed. Subsequently, using the femoral Chamfer guide, notch block guide, and tibial baseplate trial guide, the tibia was prepared. A gap block was used to measure the extension gap and this was recorded (Figure 3a, 3b). An additional tibial cut was made for those with tight extension gaps and this was recorded. The trial implants were then placed. At this stage, flexion and extension ranges of motion (ROM), patellar tracking, medial and lateral balance were evaluated. The suitable trial insert size was recorded. In cases that required it, extra medial soft tissue release was performed. In this group, the insert thickness determined with the gap measuring device and the trial insert were compatible in all patients. Irrigation was performed and the implants were affixed with cement.
Surgical technique for Group 2
Surgery was performed using the same approach that was implemented in the case of Group 1 patients. Femoral bone resection was performed using the technique of the sulcus cut. Then a 8 mm tibial stylus was placed at the highest point of the lateral tibial central plateau and the tibial bone was cut. The other stages of the surgery were performed as in Group 1. Again, patients for whom an additional bone cutting was performed, their gap intervals and insert thicknesses were recorded.
Assessment criteria
Medial joint gap distances, distal medial femoral bone cut thicknesses, amounts of tibial resection calculated, gap internal distances measured after cutting, and the thicknesses of the trial inserts were recorded. A comparison was made between the groups in terms of the number of patients requiring an additional tibial bone cut and the distribution of insert thicknesses.
Statistics
SPSS v.16.0 software (SPSS Inc., Chicago, USA) was used in the statistical analysis. The analyses were performed at a confidence interval (CI) of 95% and two-tailed testing determined that P<0.05 could be accepted as statistically significant. The Shapiro-Wilk test was used to evaluate the numerical data to determine whether they were parametric. The Wilcoxon Signed Rank Test was performed to make a statistical evaluation of differences in each of the groups.