We have investigated the long-term (minimum follow-up period; 10 years) clinical results of the total hip arthroplasty (THA) using K-MAX HS-3 tapered stem. In K-MAX HS-3 THA (Kyocera Medical, Kyoto, Japan), cemented titanium alloy stem and all polyethylene cemented socket are used. This stem has the double tapered symmetrical stem design, allowing the rotational stability and uniform stress distribution. The features of this stem are; 1. Vanadium-free high-strength titanium alloy (Ti-15Mo-5Zr-3Al), 2. Double-tapered design, 3. Smooth surface (Ra 0.4µm), 4. Broad proximal profile, 5. Small collar. Previous type stem, which was made of the same smooth-surface titanium alloy, has the design with cylindrical stem tip, allowing the maximum filling of the femoral canal. Osteolysis at the distal end of the stem had been reported in a few cases in previous type with cylindrical stem tip, probably due to the local stress concentration. Therefore the tapered stem was designed, expecting better clinical results. 157 THAs using HS-3 taper type stem were performed at Kitano Hospital between March 2004 and March 2008. And 101 THAs, followed for more than 10 years, were investigated (follow-up rate; 64.3%). The average age of the patients followed at the operation was 61.7 years and the average follow-up period was 10.9 years. The all-polyethylene socket was fixed by bone cement, and the femoral head material was CoCr (22mm; 5 hips, 26 mm; 96 hips).Introduction
Materials and Methods
We have compared the middle-term (average follow-up period; 10 years) clinical results of the K-MAX HS-3 tapered stem with those of the previous type having cylindrical tip. In K-MAX HS-3 THA (Kyocera Medical, Kyoto, Japan), cemented titanium alloy stem and all polyethylene cemented socket are used. This stem has the double tapered symmetrical stem design, allowing the rotational stability and uniform stress distribution (Type T) (Fig. 1). The features of this stem are; 1. Vanadium-free high-strength titanium alloy (Ti-15Mo-5Zr-3Al), 2. Double-tapered design, 3. Smooth surface (Ra 0.4μm), 4. Broad proximal profile, 5. Small collar. In contrast, previous type stem, which was made of the same smooth-surface titanium alloy, has the design with cylindrical stem tip, allowing the maximum filling of the femoral canal (Type C) (Fig. 2). Osteolysis at the distal end of the stem had been reported in a few cases in Type C, probably due to the local stress concentration. Therefore the tapered stem was designed, expecting better clinical results. All surgery was performed at Kitano Hospital between September 2003 and June 2006. 72 THA were performed (Type T; 52 hips, Type C; 20 hips). The average age of the patients at the operation was 61 and 69 years and the average follow-up period was 10.1 and 10.4 years for the Type T and C, respectively. The all-polyethylene socket was fixed by bone cement, and the femoral head material was alumina or CoCr (22 or 26 mm).Introduction
Materials and Methods
IBBC (interfacial bioactive bone cement method, Oonishi) (1) is an excellent technique for augmenting cement-bone fixation in the long term. However, the technique is difficult and there are concerns over some points, such as bleeding control, disturbance of cement intrusion to anchoring holes by granules, difficulty of the uniform granular dispersion to the acetabular bone (Zone 1 in particular). To improve this technique, we have modified IBBC (M-IBBC), and investigated the short-term clinical results and radiographic changes. K-MAX HS-3 THA (Kyocera Medical, Japan), with cemented stem and all polyethylene cemented socket, was used for THA implants. Basically the third generation cementing technique was used for THA using bone cement. The socket fixation was performed with bone cement (Endurance, DePuy) and hydroxyapatite (HA) granules (Ca10(PO4)6(OH)2, Boneceram P; G-2, Olympus, Japan). In original IBBC technique, HA granules were dispersed on reamed acetabulum before cementing. In M-IBBC technique, HA granules were attached to bone cement on plastic plate, then inserted to reamed acetabulum and pressurized. HA granules (G-2) are 0.3–0.6mm in size, with 35–38% porosity and sintered at 1150Introduction
Materials and Methods
We have compared the short-term clinical results of total hip arthroplasty (THA) using PMMA bone cement and hydroxyapatite (HA) granules (interfacial bioactive bone cement method; IBBC) with the results of conventional method using PMMA bone cement. K-MAX HS-3 THA (JMM, Japan), with cemented titanium alloy stem and all polyethylene cemented socket, was used for THA implants. The third generation cement technique was used for the conventional THA (Group C) using bone cement (Endurance, DePuy). In the IBBC group (Group BC), the socket fixation was performed by the third generation cement technique with HA granules (Boneceram P; G-2, Olympus, Japan) according to the Ohnishi's method. In both groups, the stems were fixed by conventional cementing technique using cement gun. 76 hip joins (69 cases) were operated between April 2005 and August 2007, and followed. The group C (22 hips, 19 cases, average follow-up; 5.6 years, average age at operation; 64 years) and the group BC (54 hips, 50 cases, 5.4 years, 65 years) were investigatedPurpose
Materials and Methods
This study reports the comparison of the clinical use of a new tourniquet system for total knee arthroplasty that can determine its pressure in synchrony with systolic blood pressure (SBP) with the conventional that keeps the initial setting pressure. We prospectively applied the additional pressure of 100 mmHg based on the SBP recorded prior to skin incision to consecutive 72 procedures (conventional; initial 36, new; following 36). Six knees with the conventional and none of 5 with the new showed oozing blood in surgical field after sharp rise in SBP. According to statistically no difference of the perioperative blood loss without any tourniquet-related postoperative complications in both groups, the new system seemed to be much practical device especially for controlling a bloodless surgical field.
Suggestions for improved wear performance of total knee replacements have included replacement of standard CoCr femoral components with ceramic. Yttria-stabilized zirconia (y-TZP) was introduced as high-strength and high toughness ceramic as an alternative to alumina ceramic. Since the introduction of zirconia in 1985, the clinical outcomes and successes for hip joint have been controversial. Y-TZP ceramics have been studied both experimentally and clinically. Magnesia-stabilized zirconia (Mg-PSZ) also appears promising for total knee replacements (TKR). Mg-ZrO2 and CoCr femoral condyles were compared in the VanguardTM knee configuration (Biomet Inc, IN). Molded tibial inserts (GUR1050) were gamma-irradiation sterilization to 3.2-Mrad under argon. Knee simulation was conducted on a 6 station simulator (Shore Western Manufacturing, Monrovia, CA). Motion included 20 degrees of flexion/extension, 5 degrees of internal/external rotation and 5 mm of AP-translation. All knee components were subjected to 6 million cycles of normal walking (2.9 kN max, freq 1.4 Hz). Lubricant was 50% alfa-calf serum diluted to 20 mg/ml protein and using EDTA additive. Test duration was 6 million cycles (6-Mc), and wear was measured by weight-loss techniques. For wear trending of CoCr/PE and MGZ/PE, linear wear trends were apparent from 1 to 6 Mc test duration. The control implants (CoCr/PE) showed excellent linear trending (regression coeff r>
0.99) with wears rate averaging 6.3 mm3/Mc. These data showed good control of experimental variance (<
10%). The ZrO2/PE combination showed good linear trending (r >
0.86) with wear rate averaging only 0.8 mm3/Mc. This set also showed good control of experimental variance (<
15%. The MGZ/PE wear was 8-fold reduced from that of CoCr/PE. The laboratory knee wear simulation appeared very supportive of femoral condyles of Mg-stabilized zirconia. Such implants may provide excellent performance for active patients who may risk high wear rates over many years of use.
A randomized, prospective stress arthrometric study was done on 60 knees in 60 patients, using a Telos arthrometer to determine the changes of varus-valgus laxity with time and to evaluate the relationship between laxity and retention of posterior cruciate ligament (PCL) using mobile bearing prostheses. Thirty knees had PCL -retaining (PCLR) with an average 75 months follow-up (range; 60–106 months) and 30 had PCL-sacrificing (PCLS) prostheses with an average 78 months (range; 60–109 months). In all patients, the preoperative diagnosis was osteoarthritis. The coronal conformity of the PCLR and PCLS designs was similar. All of the TKA procedures were judged clinically successful (Hospital for Special Surgery scores: PCLR 92 ±4 points, PCLS 92 ±3 points). The patients had no clinical complications. Varus-valgus laxity was measured with the knee in extension at 6 months, 1 year, 2 year and 5 year after surgery. The intrasubject error was less than 1 degree. Laxity with PCLR at 6 months, 1, 2 and 5 years was 3.7, 4.0, 4.1, 4.2 degrees with varus, 3.5, 3.5, 3.5, 3.6 degrees with valgus laxity. Laxity with PCLS was 4.3, 4.3, 4.3, 4.4 degrees with varus, 3.7, 3.4, 3.5, 3.6 degrees with valgus laxity. The changes of the varus and valgus laxity had no significant differences in both PCLR and PCLS groups using a repeated measure ANOVA methods (p>
0.05). The coronal laxity has proved to be no changes with time for the patients who have clinical good results. The changes of the varus-valgus laxity for long timehad no significant differences in both PCLR and PCLS groups. Therefore, we conclude that the PCL doesn’t affect coronal stability in Extension and that the characteristics of the component geometry may act as a resistance factor. We surgeons should have a new understanding of the importance to obtain the balanced coronal laxity for successful mobile-bearing TKA for long period.
In this prospectively randomized study, we compared the changes in the range of motion (ROM) in posterior cruciate ligament-retaining (PCLR) (n=50) and -sacrificing (PCLS) (n=50) total knee arthroplasties during the perioperative period. The median ROM in PCLR prostheses was 122.5° preoperatively, 120.0° intraoperatively, and 100.0° at discharge, and 115.0°, 120.0°, and 95.0°, respectively, in PCLS. The designs did not differ statistically in each period (p>
0.05). Both designs showed significant correlations between the preoperative and intraoperative ROM, and between the preoperative and discharge ROM. Only the PCLS showed a significant correlation between the intraoperative and discharge ROM. Since the PCL tenses with flexion, the degree of preoperative degeneration, intraoperative recession, and postoperative tension of the PCL may have played a major role in the results. The PCLS design has an advantage in rehabilitation planning because of the predictable changes in the ROM during the perioperative period, although the acquired average ROM at discharge did not differ statistically.
We investigated clinical features and surgical outcomes for compressive cervical myelopathy in patients over 75 years of age. Twenty-one patients who underwent surgical decompression for cervical myelopathy were reviewed. The average age at the time of operation was 78.0 years and the mean follow-up period was 5.7 years. Posterior decompression in 19 patients and anterior decompression in 2 patients were performed. Neurologic deficits before and after surgery were assessed using a scoring system by the Japanese Orthopaedic Association (JOA score). Radiological features were examined with radiographs and MRI. The clinical results were compared to those of 24 control patients who were less than 65 years of age at the time of surgery. The average age was 50.2 years and the mean follow-up period was 4.5 years. In the aged patients, the preoperative mean JOA score was 6.2. Radiological examination revealed that the spinal cord was multisegmentally impinged. The postoperative maximum JOA score averaged 11.1, and the recovery rate was 45.4%. All patients became ambulatory and independent in fundamental daily activities following surgery. Maximum recovery was obtained from 1 to 3 years after the operation and function was maintained for at least 3 years. At the final follow up, the mean JOA score had been reduced to 9.5 and the recovery rate to 27.4%. Only the preoperative duration of symptoms correlated with the outcomes. The pre-operative JOA score in the control patients was 6.5. The postoperative maximum JOA score was 13.8 and the recovery rate was 69.4%. This was not significantly changed at the final follow-up. Although postoperative recovery of function was significantly inferior to that of the control patients, surgical treatment appears to be beneficial, even in patients over 75 years of age, in improving neurological function and ability of activities in daily living.
Yachting is dangerous sport due to weather conditions. But, before this study, no data was available in the medical literature on yachting injuries. We undertook this study to analyze the yachting injury mechanism and to make inquires about this prevention. The players were asked about the details of yachting injuries they had experienced, in a questionnaire. 114 players (40.6%) out of 281 responded to the questionnaire. 35 players had experienced at least one injury (30.7%). Injury incidence of 470 class (66.7%) was significantly higher of other class; snipe38%, sea hopper 23%, FJ 22% (P<
0.05). Heads and faces were involved in 30.8% of the injuries, and upper and lower extremities in 26.8%. 44% of injury mechanism is attributed to free running injuries, which occurred during a Gybing or wild Gybing predominantly. The boom was part of the yacht which most commonly caused injury, followed by the sheet, side stay, spinnaker pole. We concluded that advancement of performance level, protection equipment, and proper judgement about weather conditions were necessary to prevent these yachting injuries.