Restoration of joint line in total knee arthroplasty (TKA) is important for kinematics of knee and ligamentous balance. Especially in revision TKA, it may be difficult to identify the joint line. The aim of this study is to define the relationship between epicondyles and articular surface using CT based three-dimensional digital templating sofware $“Athena” (Soft Cube, Osaka, Japan).

137 knees with osteoarthritis, all caces were grade 2 or lower in Kellgren-Lawrence index, were investigated. Perpendicular lines were dropped from the prominences of the medial and lateral femoral epicondyles to the most distal points of articular surfaces and distances of the lines were measured on the axial and coronal planes. The femoral width was measured as the distance between medial and lateral epicondyles. Each of the distance described above was converted to a ratio by dividing by the femoral width.

On the axial plane, the average distance from epicondyles to the posterior articular surfaces were 29.4±2.2mm on the medial side and 21.2±2.3mm on the lateral side. The average of the femoral width was 75.2±4.1mm. On coronal plane, the average distance from epicondyles to the distal articular surfaces were 25.2±2.8mm on the medial side and 21.4±2.5mm on the lateral side.

The ratio for the distance from epicondyles to the distal and posterior joint line compared to femoral width was 0.39±0.02, 0.28±0.03, 0.33±0.03 and 0.28±0.03. The distance from epicondyles to the distal and posterior joint line correlates with the femoral width of the distal femur. This information can be useful in determining appropriate joint line.

Introduction: Appropriate femoral component alignment is important for long-term survival of total knee arthroplasty (TKA). Valgus angle of femoral component is recommended as the angle between mechanical axis and anatomical axis of the femur. Intramedullary guide system is widely used for determining the valgus positioning of femoral component. Entry point of intramedullary guide is one of the key factors for determining valgus angle of femoral component. Some investigators have shown appropriate entry points of intramedullary guide, however, it is still unclear. In this study, appropriate entry point of intramedullary guide system was calculated using three-dimensional digital templating software “Athena” (Soft Cube, Osaka, Japan).

Method: Forty-one knees in 34 osteoarthritis patients except valgus deformity (30 females and 4 males, mean age 75.1 years) received TKA and were simulated using “Athena” from January 2009 to March 2009. All cases were grade III or IV in Kellgren-Lawrence index. Radiograph and CT scan image were used for determination of appropriate entry point of femur using “Athena”. The anatomical axis of femur was defined as a line connecting the midpoints of femoral AP and lateral diameter, at 60 mm and 110 mm proximal to the center of intercondylar notch. Two coordinate systems were configured as representation of entry points. One was at the center of intercondylar notch defined as the point of origin in axial view of CT image and the line parallel to the clinical epicondylar axis (cTEA) defined as X-axis. Another coordinate system was the same point of origin but parallel to the line between trochlear groove and the center of intercondylar notch (AP line) defined as Y-axis.

Result: In the coordinate system that defined the cTEA as the X-axis, the average of entry point was 0.3± 0.30 mm medial (range, −4.8~ 4.7mm) and 11.6 ± 0.52mm anterior (range, 3.1~ 16.5mm) to the center of intecondylar notch. In the other coordinate system that defined AP line as the Y-axis, the average of entry point was 2.6± 0.29 mm medial (range, −1.5~ 6.3mm) and 11.2±0.52 mm anterior (range, 2.8~ 16.0mm) to the center of intercondylar notch.

Discussion: In this study, the appropriate entry point of intramdullary guide was slightly medial and about 11mm anterior to the center of intercondylar notch on average. However, individual entry point varied considerably in distance. These data indicates that it is important to simulate the appropriate entry point of intramedullary guide in preoperative planning.

Using in situ hybridisation and the terminal deoxynucleotidyl transferase-mediated biotin-dUTP nick end-labelling (TUNEL) reaction in rats with osteonecrosis of the femoral head we have studied the effect of ischaemia on the gene expression of the stress proteins oxygen-regulated protein 150 (ORP150) and haemoxygenase 1 (HO1) and the death mechanism of the cells involved in osteonecrosis. Both ORP150 and HO1 have been reported to have important roles in the successful adaptation to oxygen deprivation.

ORP150 and HO1 mRNA expression was induced by ischaemia in osteoblasts and osteocytes. In proliferative chondrocytes, these signals were detected constitutively. During the development of ischaemic osteonecrosis, the mechanism of cell death was apoptosis as indicated by DNA fragmentation and the presence of apoptotic bodies in osteocytes, chondrocytes and bone-marrow cells. After the initial ischaemic event, expression of ORP150 and HO1 mRNA, the TUNEL-positive reaction and empty lacunae were found sequentially. These findings were exclusive and may be considered to be markers for each stage in the development of osteonecrosis.

We developed a rat model of limb lengthening to study the basic mechanism of distraction osteogenesis, using a small monolateral external fixator. In 11-week-old male rats we performed a subperiosteal osteotomy in the midshaft of the femur with distraction at 0.25 mm every 12 hours from seven days after operation.

Radiological and histological examinations showed a growth zone of constant thickness in the middle of the lengthened segment, with formation of new bone at its proximal and distal ends.

Osteogenic cells were arranged longitudinally along the tension vector showing the origin and the fate of individual cells in a single section. Typical endochondral bone formation was prominent in the early stage of distraction, but intramembraneous bone formation became the predominant mechanism of ossification at later stages. We also showed a third mechanism of ossification, ‘transchondroid bone formation’. Chondroid bone, a tissue intermediate between bone and cartilage, was formed directly by chondrocyte-like cells, with transition from fibrous tissue to bone occurring gradually and consecutively without capillary invasion.

In situ hybridisation using digoxigenin-11-UTP-labelled complementary RNAs showed that the chondroid bone cells temporarily expressed type-II collagen mRNA. They did not show the classical morphological characteristics of chondrocytes, but were assumed to be young chondrocytes undergoing further differentiation into bone-forming cells.

We found at least three different modes of ossification during bone lengthening by distraction osteogenesis. We believe that this is the first report of such a rat model, and have shown the validity of in situ hybridisation techniques for the study of the cellular and molecular mechanisms involved in distraction osteogenesis.