In Japan, edoxaban has been used for the prevention of venous thromboembolism (VTE) after total knee arthroplasty (TKA) since June 2011. Edoxaban is an oral direct factor Xa inhibitor, expected to be more convenient for the postoperative treatment of TKA. Enoxaparin, a II and Xa inhibitor, was approved in Japan for the prevention of VTE in patients undergoing orthopedics surgery from 2008. In this study, the effect for the prevention of VTE after TKA was compared between these two drugs in Japanese patients. We studied 42 Japanese patients who underwent TKA from May 2011 to April 2012. The operations were performed under general anesthesia, continuous femoral nerve block, an air tourniquet, and using cements for implant fixation. These patients were divided in two groups, use of 30 mg edoxaban once daily (ED group), and use of 1000 IU of enoxaparin twice daily (EN group). The initial dose was administered between 12 and 21 hours after surgery. We compared the incidence of VTE, bleeding complications, D dimer levels, and hemoglobin (Hb) loss. The screening of VTE was performed by enhanced CT scan screening from the chest to the foot on postoperative day 5 or 6 in all patients. The bleeding complication was divided into major bleeding and minor bleeding with Japanese guideline for the prevention of VTE. D dimer levels and Hb levels were preoperatively and postoperative day 1, 3, 5, 7, and 14. The loss of Hb was calculated from preoperative Hb level minus lowest postoperative Hb level.Introduction
Patients and Methods
Computer navigation system has been reported as a useful tool to obtain the proper alignment of lower leg and precise implantation in TKA. This system alsoãζζhas shown the accurate gap balancing which was lead to implants longevity and optimal knee function. The aim of this study was determine that the postoperative acquired deep knee flexion would be influenced by intraoperative kinematics on navigated TKA even under anesthesia. Forty knees from 40 patients, who underwent primary TKA (P.F.C. sigma RPF, DePuy Orhopaedic International, Leed, UK) with computer-navigation system (Ci Knee, BrainLAB / DePuy Inc, Leeds, UK), were recruited in this study. These patients were classified into two groups according to the recorded value of maximum knee flexion at three month after surgery: 15 patients who obtained more than 130 degrees of flexion in Group A, and 25 patients less than 130 degrees in Group B. We retrospectively reviewed about intraoperative kinematics in each group, to obtain the clue for post operative deep-flexion. The measurements of intraoperative kinematics were consisted of 3 points: femoral rotation angle (degree) and antero-posterior translation (mm), which were measured as the translation of the lowest points of femoral component to tibial cutting surface, and the joint gap difference between the medial and lateral components gap (mm). All joint kinematic data were recorded at every 10 degrees of flexion from maximum extension to flexion under anesthesia.Purpose
Materials & methods
The complication of patellofemoral compartment was quite often in total knee arthroplasty. One of the impotant factors in these complications would be the femoral component rotation in TKA. To determine the rotation of the femoral component, the reference of the surgical epicondylar axis (SEA), posterior condylar axis (PCA), AP axis with three dimensional model achieved from computed tomography data were considered. There are some limitations with pre-oprerative CT-based planning such as radio exposure, cost, time and detection of the depth of cartilage. We evaluate the determination of the femoral component rotation with image-free registration method to compare with three-dimensional template system. Thirty six knees were evaluated to determine the femoral component rotation. The reference points were marked to measure the PCA (posterior condylar axis), SEA (surgical transepicondylar axis), and APA (anteroposterior axis, Whiteside line) intra-operatively and calculated the angle from PCA to SEA and PCA to APA with Image free navigation system (BrainLAB). Those knees were preoperatively evaluated the angle deviation from SEA to PCA with three dimensional template system. These angle deviations, which suggested the femoral component rotation obtained from preoperative template system, were statistically compared with the femoral rotation angle in clinical situation.Purpose
Material and Methods
Biomechanical stimuli have fundamental roles in the maintenance and remodeling of ligaments including collagen gene expressions. Mechanical stretching signals are mainly transduced by cell adhesion molecules such as integrins. However, the relationships between stress-induced collagen expressions and integrin-mediated cellular behaviors are still unclear in anterior cruciate ligament cells. Human ACL cells were harvested from ligament samples donated by patients who underwent total knee arthroplasties with informed consents. Interface cells were isolated from the 5-mm-end of ACL. Midsubstance cells were cultured from the middle part of ACL. The cells were seeded onto stretch chambers (2Ä−2 cm, 50,000 cells/chamber) and uni-axial cyclic mechanical stretch (0.5 Hz, 7%) was applied for 2 h using a ST140. RNA samples were reverse-transcripted and quantitative real-time RT-PCR analysis were performed. To inhibit the function of integrin alphaVbeta3 subunit or alpha5 in stretching experiments, anti-human integrin alphaVbeta3 and alpha5 functional blocking antibodies (alphaVbeta3: 20 mg/ml, alpha5: 4 mg/ml) were used. To investigate the cellular attachments responding to mechanical stretch, we observed the distribution of integrins and stress fibers in both ACL cells. The shape of midsubstance cells showed spindle and fibroblastic cellular morphologies. On the other hand, the interface cells displayed chondroblastic appearances such as small and triangular morphologies. The expressions of COL1A1, COL2A1, and COL3A1 genes were detected in the tissue RNAs of interface zones. However, these expressions were decreased in cultured interface cells. In midsubstance cells, the expression of COL1A1 gene was equally detected in both tissues and cultured cells. COL3A1 gene expression was maintained in cultured midsubstance cells. These results indicated that the phenotypes of both ACL cells were changed by cultured conditions, especially in the interface cells. After mechanical stretch, the COL1A1 expression of midsubstance and interface cells were stimulated up to 6 and 14-fold levels of each non-stretched control, respectively. The COL3A1 expressions were also enhanced up to 1.8-fold level of controls by stretching treatment in both cells. Integrin alphaVbeta3 was shifted to the peripheral edge of cells by stretching treatment. In addition, mechanical stretch changed the integrin alphaVbeta3-dependent stress fiber formation in both ACL cells. The functional blocking of integrin alphaVbeta3 inhibited stretch-activated COL1A1 and COL3A1 expressions. However, the functional blocking of integrin alpha5 did not suppress the stretch-induced COL1A1 and COL3A1 expressions in both ACL cells. Cultured interface cells loose their phenotypes in collagen gene expressions. However, mechanical stretch reproduces the expression of COL1A1 and COL3A1 genes in cultured ACL cells. The present study demonstrated that stretch-activated collagen gene expressions depend on the integrin alphaVbeta3-mediated cellular adhesions.
