Introduction

It is still controversial whether one or two-stage revision should be indicated for deeply infected hip prosthesis, and there are no scoring systems for the decision of them. An assessment system for the treatment of deeply infected hip prosthesis was evaluated for the patients who had undergone one or two-stage revision total hip arthroplasty (THA).

The accuracy of pedicle screw placement is essential for successful spinal reconstructive surgery. The authors of several previous studies have described the use of image-based navigational templates for pedicle screw placement. These are designed based on a pre-operative computed tomographic (CT) image that fits into a unique position on an individual's bone, and holes are carefully designed to guide the drill or the pedicle probe through a pre-planned trajectory. The current study was conducted to optimise navigational template design and establish its designing method for safe and accurate pedicle screw placement.

Thin-section CT scans were obtained from 10 spine surgery patients including 7 patients with adolescent idiopathic scoliosis (AIS) and three with thoracic ossification of the posterior longitudinal ligament (OPLL). The CT image data were transferred to the commercially available image-processing software and were used to reconstruct a three-dimensional (3D) model of the bony structures and plan pedicle screw placement. These data were transferred to the 3D-CAD software for the design of the template. Care was taken in designing the template so that the best intraoperative handling would be achieved by choosing several round contact surfaces on the visualised posterior vertebral bony structure, such as transverse process, spinous process and lamina. These contact surfaces and holes to guide the drill or the pedicle probe were then connected by a curved pipe. STL format files for the bony models with planned pedicle screw holes and individual templates were prepared for rapid prototype fabrication of the physical models. The bony models were made using gypsum-based 3D printer and individual templates were fabricated by a selective laser melting machine using commercially pure titanium powder. Pedicle screw trajectory of the bony model, adaptation and stability of the template on the bony model, and screw hole orientation of the template were evaluated using physical models. Custom-made titanium templates with adequate adaptation and stability in addition to proper orientation of the screw holes were sterilised by autoclave and evaluated during surgery.

During segmentation, reproducibility of transverse and spinous processes were inferior to the lamina and considered inadequate to select as contact surfaces. A template design with more bone contact area might enhance the stability of the template on the bone but it is susceptible to intervening soft tissue and geometric inaccuracy of the template. In the bony model evaluation, the stability and adaptation of the templates were sufficient with few small round contact surfaces on each lamina; thus, a large contact surface was not necessary. In clinical patients, proper fit for positioning the template was easily found manually during the operation and 141/142 screws were inserted accurately with 1 insignificant pedicle wall breach in AIS patient.

This study provides a useful design concept for the development and introduction of custom-fit navigational template for placing pedicle screws easily and safely.

Although optimal alignment is essential for improved function and implant longevity after TKA, we have less bony landmarks of tibia relative to femur. Trans-malleolar axis (TMA) is a reference line of distal tibia in the axial plane, which externally rotated relative to a ML axis of proximal tibia. We originally defined another reference axis associated with the orientation of tibial plafond, and then measured tibial torsion in the 3D-coordinate system.

Three-dimensional CAD models of 20 tibiae were reconstructed based on pre-operative CT data from OA patients (16 females and 4 males, 73.8 ± 6.9 years old). TMA was a line connecting each apex of medial and lateral malleolus. The plafond axis (PLA) that we originally defined in this study was a line connecting each midpoint of medial and lateral margin of talocrural facet. In terms of interobserver correlation coefficiency and mean errors of the designated points to define those axes, TMA was found out to be 0.982, 3.14 ± 0.47 mm (medial), and 0.988, 4.88 ± 0.59 mm (lateral). Those of PLA were 0.997, 1.97 ± 0.53 mm (medial), and 0.995, 2.02 ± 0.44 mm (lateral). The tibial torsion was 16.3 ± 6.3°with reference to TMA, and 10.2 ± 8.4°to PLA.

Based on these results, as for the rotational reference axis in the axial plain of distal tibia, we consider the plafond axis to be another reliable and reproducible axis, which is expected to be applicable in preoperative planning in TKA to reduce outliers of coronal alignment.

It is very important to fix implant to bone. Bioactive materials as hydroxyapatite or glass-ceramics have bone-bonding ability. Hydroxyapatite-coating is applied to cementless THA or TKA. I and coworkers investigated bone-bonding mechanism of bioactive material and found that bone-like apatite formation play key role for bonding. If the surface of metal is changed to form apatite on it in body, the inert metal changes into bone-bonding material. We developed alkaline and heat treatment of titanium to change titanium to bone –bonding material as follows. At first, titanium is dipped in 5N NaOH solution for 24 hours, at second the metal is washed in pure water and finally it is sintered in 500 degree C for 2 hours. The treated surface has bioactivity, bone bonding ability like hydroxyapatite. The advantage of this treatment over hydroxyapatite-coating procedure is to treat the porous surface without any change of pore figures. As to hydroxyapatite-coating procedure, pore of the small diameter is filled with hydroxyapatite and pore figures are change. We applied this alkaline and heat treatment to cementless THA and its good results of more than ten years was reported.

Porous titanium can be changed to bioactive material by alkaline and heat treatment. This bioactive porous titanium was found to have a property of material-induced osteoinduction, that is, the bone formation in pore of porous titanium implanted in canine back muscle. They can be used for bone substitute for big bone defect. We used two procedures to make porous titanium, sintering of titanium powder with spacer particle of ammonium sulfate and selective lazar melting. The latter procedure can produce any type of pore structure of titanium. Selective laser melting was employed to fabricate porous Ti implants (diameter 3.3 mm, length 15 mm) with a channel structure comprising four longitudinal square channels, representing pores, of different diagonal widths, 500, 600, 900, and 1200 micrometer. These were then subjected to chemical and heat treatments to induce bioactivity. Significant osteoinduction was observed in widths 500 and 600 micrometer, with the highest observed osteoinduction occurring at 5 mm from the end of the implants. A distance of 5 mm probably provides a favorable balance between blood circulation and fluid movement.

New bioactive bone cement is another topic of the application of bioactive titanium in this lecture. The bone cement contains barium sulphate for radiocontrast. We developed a procedure to replace barium sulphate with bioactive titanium powder. This new bone cement has not only better biocompatibility than conventional cement but also bone bonding ability. It is potent material for the fixation of implant to bone. I will speak the evaluation of this cement using canine model of THA.

Introduction

Achieving high flexion after total knee arthroplasty is very important for patients in Asian countries where deep flexion activities are an important part of daily life. The Bi-Surface Total Knee System (Japan Medical Material, Kyoto, Japan), which has a unique ball-and-socket mechanism in the mid-posterior portion of the femoral and tibial components, was designed to improve deep knee flexion and long-term durability after total knee arthroplasty (Figure 1). The purpose of this study was to determine the in vivo three dimensional kinematics of Bi-Surface Total Knee System in order to evaluate and analyze the performance of this system with other conventional TKA designs currently available in the market today.

Aims

Recently, total knee arthroplasty (TKA) has been generalized as an operation that achieves excellent clinical results. However, younger and Asian patients require even greater implant longevity and functional performance. We hypothesized a novel posterior cruciate-retaining TKA design that restores the anatomical jointline in both sagittal and coronal planes, maintains the femoral posterior condylar offset, and provides low contact stress would provide enhanced patient function with the potential for greater implant longevity.

One cementless cup which had porous outer surface with Apatite-Wollastonite glass ceramic (AWGC) coating, was revised 13 years after primary THA because of massive osteolysis expanded to medial iliac wall along the screws. While many retrieved studies of hydroxyapatite-coated cup have been reported, there has been no report on the retrieved cup with AWGC coating. The purpose of this study was to describe this rare case in detail, confirm the bone ingrowth to the porous cup, and discuss on the effectiveness of porous surface with AWGC coating.

In the light of the increasing popularity of femoral resurfacing implants, there has been growing concern regarding femoral neck fracture. This paper presents a detailed investigation of femoral neck anatomy, the knowledge of which is essential to optimise the surgical outcome of hip resurfacing as well as short hip stem implantation.

Three-dimensional lower limb models were reconstructed from the CT-scan data by using the Mimics (Materialise NV, Leuven, Belgium). We included the CT data for 22 females and nine males with average age of 60.7 years [standard deviation: 16.4]. A local coordinate system based on anatomical landmarks was defined and the measurements were made on the unaffected side of the models.

First, the centre of the femoral head was identified by fitting an optimal sphere to the femoral head surface. Then, two reference points, one each on the superior and the inferior surface of the base of femoral neck were marked to define the neck resection line, to which an initial temporary neck axis was set perpendicular. Cross-sectional contours of the cancellous/cortical border were defined along the initial neck axis. For each cross-sectional contour, a least-square fitted ellipse was determined. The line that connects the centre of the ellipse at the base of the femoral neck and the centre of the femoral head was defined as the new neck axis. The above process was repeated to reduce variances in the estimation of the initial neck axis. The neck isthmus was identified according to the axial distributions of the cross-sectional ellipse parameters.

The short axis of the ellipse decreased monotonically since it was calculated from the center of the femoral head to the neck resection level (base of neck), whereas the long axis changed with the local minima. The cross section at which the long axis of the fitted ellipse had the local minima was determined as the neck isthmus.

The following measurements were made on the proximal part of the femur. The neck axis length measured from the center of the femoral head to the lateral endosteal border of the proximal femur was 67.3 mm [6.4]. The length between the center of the femoral head and the neck isthmus was 22.5 mm [2.7]. The diameter of the ellipse long axis at the neck isthmus was 27.6 mm [3.5] and was 23.6 mm [3.3] for the short axis.

The center of the neck isthmus did not align with the neck axis. The deviation of the isthmus from the neck axis which we defined as the isthmus offset was 0.7 mm [0.4].

If an alternative neck axis was defined between the center of the femoral head and the center of the neck isthmus, there would be a certain degree of angular shift with respect to the original neck axis. An angular shift of 1.8 degrees between the two axes can be expected for a 0.7-mm isthmus offset. In the worst case, an angular shift of 4.59 degrees was estimated for a subject with the largest isthmus offset of 1.93 mm.

Further investigations would be necessary to determine the axis configuration that represents the clinically relevant centre of the femoral neck. In order to reduce the deviations in the three-dimensional determination of the femoral neck axis, the reference anatomical landmarks and methods of evaluation should be carefully selected.

In Far East, including Japan and the Middle East, daily activities are frequently carried out on the floor. Deep flexion of the knee joint is therefore very important in these societies. Some patients who underwent total knee arthroplasty (TKA) in these countries often perform deep flexion activity, such as squatting, cross-leg sitting and kneeling. However it is still unknown that deep flexion activity affects long term durability after TKA. The purpose of this study was to examine the correlation between deep flexion and long term durability.

Between December 1989 and May 1997, 507 total knee arthroplasties were carried out in 371 patients using the Bi-Surface Knee System (Japan Medical Material, Osaka, Japan) at two institutions and routine rehabilitation program continued for one to two months after TKA. One patient who underwent simultaneous bilateral TKA was excluded because of pulmonary embolism within one month. The other 505 knees (370 patients) were divided into two groups according to the range of flexion after our routine rehabilitation program; one group (Group A: 207 knees) consisted of more than 135 degrees flexion knees and the other group (Group B: 298 knees) consists of less than 135 degrees flexion knees. Patients whose follow-up period was less than 10 years were excluded from this clinical evaluation. Range of flexion was measured preoperatively, at the time after routine rehabilitation program, and at the latest follow-up. Knee function was evaluated on the basis of Knee Society knee score and functional score preoperatively and at the latest follow-up. Kaplan-Meier survivorship analysis was performed with revision for any operation as the end point.

In Group A, the mean preoperative range of flexion was 133.0±16.3 degrees, and at the time after routine rehabilitation program, this improved to 139.7±5.1 degrees. This angle maintained to 136.2±14.3 at the latest follow-up. In Group B, the mean preoperative range of flexion was 111.6±20.4 degrees, and at the time after routine rehabilitation program, this improved to 114.5±13.6 degrees. This angle maintained to 118.2±17.8 at the latest follow-up. The Knee Society knee score and functional score was improved from 43.0±16.9 points and 39.0±20.2 points preoperatively to 95.1±5.8 points and 51.8±21.2 points at the latest follow-up, respectively in Group A. The Knee Society knee score and functional score was improved from 37.1±16.7 points and 31.9±18.4 points preoperatively to 92.5±8.7 points and 53.1±26.1 points at the latest follow-up, respectively in Group B. Kaplan-Meier survivorship at 10-year was 95.5% in Group A and 96.2% in Group B with any operation as the end point. The survivorship between Group A and Group B was not statistically significant.

Good range of flexion was maintained and Knee society score was excellent after a long time follow-up for the patients who achieved deep flexion after TKA. Deep flexion was proved not to affect long term durability in this Bi-Surface Knee System.

Many types of bioactive bone cement have been developed to overcome the disadvantages of polymethyl-methacrylate (PMMA) bone cement, especially its lack of bone-bonding ability, which occasionally leads to aseptic loosening of prostheses used for arthroplasty. Earlier, we showed that bioactive bone cements containing either nano-sized or micron-sized titania (TiO2) particles had excellent in vivo osteoconductivity.

However, anatase phase titania particles contained in these bioactive bone cements raise concerns about their safety in vivo. We developed pure rutile micron-sized titania particles. because rutile is the only stable phase, whereas anatase is metastable.

In this study, polymethylmethacrylate (PMMA)-based bone cement containing pure rutile micron-sized titania (TiO2) particles were developed, and their mechanical properties and osteoconductivity are evaluated. The three types of bioactive bone cement were T10, T20, and T30, which contained 10, 20, and 30wt% TiO2, respectively.

Commercially available PMMA cement (PMMAc) was used as a control. Hardened cylindrical cement sample (φ2.5mm*10mm) was inserted manually on rabbit femur vertically. Push out test was performed for evaluation of bonding strength. For mechanical testing, the flexural strength, flexural modulus, and compressive strength were measured.

Results of this study revealed that polymethylmeth-acrylate (PMMA)-based bone cement containing pure rutile micron-sized titania particles has outstanding osteoconductivity in vivo, and their mechanical properties were exceeded that of commercially available PMMA cement. Interfacial shear strength of T10, T20 and T30 were 17.1~24.0MPa each at 12 weeks, and were significantly higher than PMMAc. In general, the interfacial bonding strength of bone cement depends mainly on its interdigitation with cancellous tissue, which is accomplished by the pressurized injection of the cement in paste form. On the other hand, we inserted the hardened specimens into oversized holes on rabbit femur in this study, because we intended to examine the osteoconductive and bone-bonding potentials of each material. The flexural strength, flexural modulus, and compressive strength were equivalent to or exceeded that of PMMAc.

These results show that bone cement containing pure rutile micron-sized titania particles is a promising material applied to prosthesis fixation as well as vertebroplasty.

Poly-L-lactic acid (PLLA) is characterized by its biocompatibility and biodegradability, and is used clinically. In our hospital, we started to use PLLA screws instead of metallic or ceramic screws in the fixation of acetabular bone grafts in total hip arthroplasty (THA) in 1990, because there were concerns about the use of rigid and nonbioabsorble screws, which might contribute to the absorption of the grafted bone and induce metallosis or third-body wear when breakage of the screws occurs. The purpose of this study was to review a series of cemented THA for dysplasia, with structural autograft fixed with PLLA screws. We focused on the survival rate of the acetabular component and radiological change of the grafted bone–socket interface.

This study included 104 consecutive cemented total hip arthroplasties (80 patients) performed between July 1990 and December 1995 in our hospital. All patients were followed over 10 years and reviewed retrospectively. The grafted bone trimmed from the excised femoral head was fixed rigidly with 1 or 2 PLLA screws (cancellous lag screws 6.5 mm in bore diameter and 4.1 mm in grove diameter) (Fixsorb; Takiron Co., Ltd., Osaka, Japan).

X-ray photographs taken just after the primary operation showed an obscure but still visible radiolu-cent region corresponding to the inserted PLLA screws in many cases.

However, X-ray photographs at the final follow-up showed an unclear radiolucent zone at the sites of the PLLA screws, and the osteosclerotic line surrounding the site where the radiolucent zone had been found was confirmed in only 4 cases. Bone union was confirmed radiologically at the grafted site in every case, and there were no cases of early collapse or extravasation of the grafted bone. No positive resorption of the grafted bone was observed in any case. Kaplan–Meier survivorship analysis of socket revision, radiological loosening of the socket, and the appearance of a radiolucent line > 1 mm in the graft–socket interface as the endpoints indicated survival rates of 99%, 97.1%, and 63.5% at 10 years, and 96.6%, 90.2%, and 56.1% at 15 years, respectively.

The results of this study indicated that PLLA screws are safe and useful for the fixation of acetabular bone graft concomitant to cemented THA with a careful rehabilitation program. However, because of concern about the mechanical insufficiency of the PLLA screws for THA with an early weight-bearing rehabilitation program, we have used mechanically stronger and bioabsorbable screws made of forged composites of hydroxyapatite and PLLA since 2003.

Purpose: There is no report concerning about long-term comparison result of high placed cementless cup stability with or without screws for developmental dysplasia of the hip. The aim of this study was to ascertain whether or not there are any differences in high placed cementless cup stability with or without screws at the mean 10-year (6–14) follow-up period.

Method: We divided 109 hip-cases who underwent identical cementless total hip arthoplasty system (Mallory – Head : Biomet Inc.) to two groups: 57 cups with screw (screw group) and 52 cups without screw (no screw group). No case in both group underwent bulk bone graft for acetabular roof. Radiographic signs of cup instability were defined as the development of radiolucent line (> 2mm) or migration (> 4mm). Degree of subluxation by Crowe classification, cup size and cup abduction angle were also measured.

Results: In both groups, there was no significant difference in terms of degree of subluxation (each grade’s %) (screw vs no screw = I (68, 73), II (21, 25), III (11,0), IV (0, 2)), age (yrs) (58, 60), cup size (mm) (46, 47) and cup abduction angle (49, 47). In screw group, one case was revised by replacing only polyethylene insert due to excessive ware. No case in both group showed any sign of component instability.

Conclusion: High placed Mallory-Head type cementless cup without screws showed stable radiographic fixation as well as cup with screws at mean 10 years follow-up period.

Removal of femoral bone cement is required for preparation of proper implant bed for reimplantation of a new femoral component in revision total hip arthroplasty. Several devices and procedures have been developed for cement removal, including an extracorporal shock-wave lithotripter and YAG laser, as well as a high-powered drill or burr under the control of conventional fluoroscopic images and an intrafemoral endoscopy. Ultrasonic tools are efficient for removal of bone cement with minimal damage to bone. We use a high-powered burr to remove the deep femoral bone cement under the control of conventional fluoroscopic images, although the problem of this procedure is large exposure of X-ray and two dimensional viewing of burr position which can result in perforation in the third plane.

Computer-assisted fluoroscopic navigation system allows the surgeons to provide positional information about surgical instrument to target bones during operations. Two-dimensional image data are obtained using the fluoroscope with a reference frame and stored on a computer workstation. A camera interfaced with the computer then tracks the position of the patient and registered surgical instruments during the procedure. Taking advantage of the real-time guidance of computer-assisted fluoroscopic navigation system, we introduce a valuable technique using computer-assisted fluoroscopic navigation system for performing removal of the cement of the femoral canal in revision cemented total hip arthroplasty.

Titanium alloys such as Ti-6Al-4V and Ti-6Al-7Nb have been widely used as orthopedic implants such as artificial hip joint, because of their high mechanical strengths and good biocompatibilities. Recently, new kinds of titanium-based alloys free from elements such as V and Al, which are suspicious for cytotoxicities, are being developed. Ti-15Zr-4Ta-4Nb (Ti-15-4-4) is one of such alloys and shows high mechanical strength and corrosion resistance which are comparable to those of the Ti-6Al-4V alloy. In the present study, chemical treatments for providing bone-bonding ability to this alloy were investigated. Apatite-forming ability in a simulated body fluid (SBF) was used as an indication of the bone-bonding ability.

Ti-15-4-4 alloy plates 10×10×1 mm3 in size were soaked in 5M-NaOH solution at 60 °C for 24 h, soaked in 100mM-CaCl2 solution at 40 °C for 24 h, heated at 600 °C for 1 h and then soaked in hot water at 80 °C for 24 h. Surface structural changes of the alloy with these treatments were analyzed by a field emission scanning electron microscope (FE-SEM) attached with an energy-dispersive X-ray spectrometer (EDX), Thin-film X-ray diffraction (TF-XRD) and Fourier transform confocal laser Raman spectroscopy (FT-Raman). Scratch resistance of surface layer of the alloy was measured by a thin-film scratch tester. Apatite-forming ability of the specimens was examined by soaking them in SBF for 3 days. Long-term stability of the apatite-forming ability was examined after keeping the specimens in an incubator with relative humidity of 95 % at 80 °C for 1 week.

A sodium hydrogen titanate layer about 500 nm in thickness was formed on the surface of the alloy by the NaOH treatment. This specimen formed some amounts of apatite in SBF within 3 days, but its scratch resistance was as low as less than 10 mN. When the NaOH-treated specimen was subsequently heat treated, the sodium hydrogen titanate transformed into sodium titanate to give scratch resistance as high as 92 mN, but lost its apatite-forming ability.

When the NaOH-treated specimen was soaked in CaCl2 solution, the sodium hydrogen titanate was isomorphously transformed into calcium hydrogen titanate. Thus treated specimen increased its apatite-forming ability, but its scratch resistance was still low. When the NaOH- and CaCl2-treated specimen was subsequently heat treated, the calcium hydrogen titanate transformed into calcium titanate to give scratch resistance as high as 169 mN. However, its apatite-forming ability was lost. Thus treated specimen was then soaked in hot water. As a result, its apatite-forming ability remarkably increased without decreasing scratch resistance. It showed high apatite-forming ability even after a long-term-stability test.

The NaOH-, CaCl2-, heat- and hot-water-treated Ti-15-4-4 alloy is believed to be promising materials for artificial joints, because of its high apatite-forming ability with long-term stability as well as high scratch resistance.

Kokubo and one of the present authors (T.N) have developed a new technique of bioactive coating using alkaline and heat treatment, which induces the formation of a thin HA layer on the surface of titanium after implantation in the body. This new coating technique is not associated with degradation or separation of the HA coating, because a bone-like apatite layer of 1 μm in width begins to form in the body tissue after implantation.

Chemically and thermally treated titanium possesses bone-bonding ability, which has been confirmed by detachment tests. Bone ingrowth into bioactive titanium continues to increase throughout the 26 weeks of implantation, whereas bone ingrowth into non-treated or HA plasma coating implants tends to decrease between 6 and 12 weeks. These findings suggest the long-term stability and osteoconduction of the bioactive layer of chemically and thermally treated titanium.

We carried out a series of 70 cementless primary total hip arthroplasties using this coating technique on a porous titanium surface, and followed up the patients for a mean period of 4.8 years. There were no instances of loosening or revision, or formation of a reactive line on the porous coating. Although radiography just after surgery showed a gap between the host bone and the socket in 70% of cases, all the gaps disappeared within a year, indicating the good osteoconduction provided by the coating. Alkaline-heat treatment of titanium to provide a HA coating has several advantages over plasma-spraying, including no degeneration or absorption of the HA coating, simplicity of the manufacturing process, and cost effectiveness. In addition, this method allows homogeneous deposition of bone-like apatite within a porous implant.

Although this was a relatively short-term study, treatment that creates a bioactive surface on titanium and titanium alloy implants has considerable promise for clinical application.

Thigh pain appears often after THA used of the cement-less femoral components, but the appearance mechanism of thigh pain does not have been elucidated. As one factor of manifestation of thigh pain, it has been guessed that the pressure from the inside of medullary cavity of bone by the stem. The purpose of this study is confirming whether the flexor reflex is caused, by using the femur of a rabbit that applied the pressure from the inside of medullary cavity of bone.

Japanese white rabbits with weight of about 3kg were used. Evaluation of the appearance of the pain by the pressure was performed by measurement of the hind leg flexor activity produced by the flexor reflex. After confirming that appearance of the muscles activity by the pain reflex from adding the pain stimulus to the hind leg skin of rabbits, we loaded of the pressure into the inside of medullary cavity of bone and observed whether the muscles activity appears. As the laboratory animals model, we prepared two kinds of rabbits by the difference in the amount of reaming. And we tested how the differences show up between these two kinds of rabbits.

In the rabbits with few amounts of reaming, the flexor reflex appeared in low pressure. But, in the rabbits with many amounts of reaming, the flexor reflex did not appear in high pressure, either.

It is known that the somatic sensory nerves are distributed in the bone, and it is known that the sensory nerve ends exist in the medullary cavity of bone. It was suggested that the pain is induced, when the sensory nerve ends remained in the inside of medullary cavity of bone and the pressure in whicha reaction is possible was carried out there.

We evaluated intermediate-term results of primary cementless Omniflex prostheses.

Forty-nine patients (57 hips) with a mean age of 44 years were observed for an average of 8.6 years.

These results were inferior to those using other recent cementless total hip systems. The increasing prevalence of loosening and osteolysis with time are problems related to this Omniflex femoral component. Although the implant design is unique, the authors no longer use this system.

We have developed bioactive bone cements manufactured from bioactive glass-ceramic powder and BIS-GMA resin, which has the bone-bonding ability. In the present clinical trial, this bioactive bone cement was used for fixation of total hip arthroplasty (THA) and the clinical results were investigated

Two types of bioactive bone cements (high- and low- viscosity type cements) were prepared (Nippon Electric Glass Co. Ltd.). Inorganic filler contained 72.0 wt% AW-GC (apatite and wollastonite containing glass-ceramic) and 27.0 wt% SiO2 powder. All surgery was performed at Kyoto University Hospital between February and October 1996. 20primary THA (20 patients) were performed using bioactive bone cement as a clinical trial. The average age of the patients was 58 years. The average follow-up period was 6 years, 9 months. The diagnosis for 18 hips at the operation was osteoarthritis and 2 hips were rheumatoid arthritis. All sockets and one stem were fixed by bioactive cement, and all but one stem were fixed by PMMA cement. In all cases all polyethylene socket and titanium stem were used (14 KC type THA and 8 KMAX type THA). For the femoral head 22 mm diameter alumina head was used in all cases.

If the bone cement is bioactive and shows direct bonding with the bone, wear particles can’t enter the interface and thus prevention of loosening due to bone resorption would be expected. This cement demonstrated satisfactory clinical results, proving to be a promising material for implant fixation.

Zirconia ceramic femoral head has better mechanical properties than those alumina head has. However, it is concerning whether the wear of UHMWPE against zirconia head is as low as that of alumina head. We compared polyethylene wears against 22.225mm alumina and zirconia heads in total hip arthroplasties (THA) occupied in our hospital.

Kobelco hip prostheses (Kobelco, Kobe, Japan) were used. Titanium alloy stem was cement-fixed and all-polyethylene acetabular components were articulated with alumina or zirconia femoral heads. In the cases from February 1996 to December 1998, 96 primary cemented total hip arthroplasties (THA) in 87 patients of osteoarthritis were observed with a minimum follow-up of five years. The clinical results were evaluated using JOA hip score (100 in normal hip). There were 46 hips with alumina heads and mean follow-up of 6.2 years, and 51 hips with zirconiaheads and mean follow-up of 5.2 years. Mean ages at operation were 58 years. For each patient, the initial postoperative and the latest anterior-posterior radiographs of the pelvis were selected. With the custom software Image-Pro Plus version 4.0, linear wear and volumetric wear were measured.

Clinical results of both heads showed no difference. Linear wear rate of alumina is 0.080±0.047mm/year, while it is 0.147±0.069mm/year for zirconia, significantly higher than alumina (p?0.0001). Volumetric wear rate of zirconia (42.499±20.233mm3/year) is also significantly higher than alumina (27.049±17.216mm3/year) (p?0.0001).

The low thermal conductivity of zirconia is thought to cause local high temperature, leading to the phase transformation and lower-temperature aging degeneration (LTAD) of zirconia head surface. In order to solve this problem, alumina-adding zirconia compound ceramics with lower phase transformation were developed. Hip simulator test revealed much lower wear rate of improved zirconia. This will be discussed.

Prosthetic impingement after THA is to different for the angle and shape of the implant. Purpose of this study is examine the range of motion(ROM) on a computer when angle and shape of the implant are changed.

The 3D implant models were created on a computer. The angle was measured in the flexion, extension, adduction direction byevery 0.1 degrees. There are three kinds of acetabular abduction angle, two kinds of acetabular anteversion angle and two kinds of femoral anteversion angle. There are three kinds of the radius of neck and the neck shaft angle. All 324 patterns of the above model were measured.

When the radius of neck decreased, the ROM increased in all cases. When the neck shaft angle decreased, the ROM increased by almost all cases. When the acetabular anteversion angle increased, the ROM of flexion direction increased and adduction direction decreased, and as for the extension direction, all the factors had influenced the change in the ROM. When the acetabular angle increased, the ROM of the extension direction increased and the flexion directions decreased. As for adduction direction, femoral anteversion angle, acetabular anteversion angles, and the radius of neck had influenced the ROM. When the femoral anteversion angle increased, the ROM of flexion direction increased and extension, adduction direction decreased.

The clinical ROM is affected by the impingement of non-implant and the strain of the soft tissue. Therefore, It’ s considered that the clinical ROM is smaller than the ROM which was investigated in this study in many cases. When the radius of neck and the neck shaft angle decrease, the increase of the ROM expected. However the radius of the neck should not be decreased too much to avoid the decrease of the neck strength.