Knee-joint arthroplasty according to Stanmore

Summary Of a total of 56 knee arthroplasties according to Stanmore, a clinical and radiographic follow-up was performed on 38, with mean follow-ups of 36 months for rheumatoid arthritis and 34 months for osteoarthritis. Early complications occurred in nine of 56 cases. Clinically satisfactory results were obtained in 71 %. Radiolucent zones of 3 mm or more were found to be associated with clinically verified loosening.

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Zusammenfassung Im Zeitraum von 1975 bis 1980 wurden 56 Knicarthroplastiken nach Stanmore durchgeführt. Nach 7 bis 71 Monaten konnten 38 Prothesen nachuntersucht werden. Frühkomplikationen traten in 9 von 56 Fällen auf. Klinisch gute Ergebnisse fanden sich bei 30 von den schließlich 38 nachuntersuchten Arthroplastiken. Röntgenologische Aufhellungszonen von 3 mm oder mehr konnten klinisch zu verifizierenden Lockerungen zugeordnet werden.

     

Stanmore total hip replacement. A nine- to ten-year follow-up

Between February 1975 and August 1976, 195 total hip replacements using Stanmore components were performed; of these, 146 were in 135 patients who had not had previous hip surgery. At review 52 had died, but none of the others was lost to follow-up. Of the 52, two had had a second operation, one for infection and one for recurrent dislocation. In the remaining 83 patients (92 hips) five revisions were necessary: four for aseptic loosening, and one for stem fracture. The remaining 78 patients had little or no pain and little restriction of activity. After a follow-up period of at least nine years, the survival rate of the prosthesis was 95%. There had been migration of the femoral component in five cases and migration of the acetabular cup in one case, but no wear of the acetabular component could be demonstrated.     

The Stanmore total hip replacement. A 22-year follow-up

From a series of 135 patients (146 prostheses) who had had primary hip replacement in 1975 and 1976 we reported the outcome at ten years in 83 surviving patients in 1988 and that at 15 years in 44 surviving patients in 1994. Now, 22 years after the operation, we have reviewed the 21 patients who are still alive. Nineteen (20 hips) of these 21 patients (22 hips) with a mean age of 85.7 years still had their original prosthesis. Most patients were satisfied with the result, although the level of activity in many was reduced because of increasing age and other medical problems. The stem was stable in all 20 hips. Only one cup was definitely loose. Wear was observed in 40% of the cups but this was not a clinical problem. At the 22-year follow-up the cumulative survival rate of the prosthesis was 85%, of the stem 91% and of the cup 88%. Since 1975, 11 (7.5%) of the original 146 prostheses have been revised.     

Homograft bone in revision acetabular arthroplasty. A clinical and radiographic study

Thirty-seven patients with extensive acetabular defects due to loose implants had revisions with uncemented components, the acetabulum being augmented with homograft bone. In six of these, a histological study of graft incorporation was made. At a mean follow-up of 1.5 years 34 patients were free of pain and 35 could walk for 30 minutes or longer. No graft had obviously sequestrated. Two components had radiological evidence of migration but remain asymptomatic. We conclude that cementless revision surgery with homograft supplementation of the acetabulum is clinically successful in the short-term. The long-term outcome is unknown.     

Five-Year clinical and radiographic follow-up of the uncemented long-term stable fixation total hip arthroplasty

Thirty-nine uncemented porous-coated long-term stable fixation total hip prostheses with a minimum 5-year follow-up, were retrospectively reviewed for clinical and radiographic outcome. Clinical evaluation was performed using the modified Harris Hip Score. Additionally, all patients completed a satisfaction questionnaire. Anteroposterior view and lateral view radiographs were obtained and compared with immediate postoperative films utilizing the Hip Society radiographic evaluation form for uncemented implants. The follow-up period averaged 69 months (range, 60–87 months). At the most recent follow-up visit Harris Hip Scores averaged 88 points (range, 68–100 points), with 79% good or excellent results. Of the 8 hips (6 patients) with fair or poor results, 5 patients (6 hips) were Charnley category C patients. All patients were satisfied with their surgery and all, but 2 stated that their function had significantly improved. The incidence of significant thigh pain was 13%. Calcar osteolysis was present in 13 of 39 femurs with the majority of cases being minimal. All but one femoral component demonstrated bone ingrowth. There was no distal femoral osteolysis present and no femoral revisions have been performed or are planned. Acetabular osteolysis was present in 7 of 39 hips, with 4 of the 7 centered around acetabular fixation screws. All patients who had acetabular bone loss had some degree of femoral osteolysis. Thus far, one patient has required acetabular revision secondary to osteolysis. Acetabular osteolysis in this series was more profound than on the femoral side and two other patients are being considered for revision due to pelvic side osteolysis. In conclusion, the uncemented long-term stable fixation femoral component proved to be durable in this series of patients. The circumferential porous coating on the femoral implant may protect against distal osteolysis. A concerning rate of severe pelvic osteolysis and impending failure was noted and may lead to a greater need for revision surgery with longer follow-up.     

Patellofemoral arthroplasty. A three- to nine-year follow-up study

Twenty-two patients with 25 patellofemoral arthroplasties (resurfacing of the patella and femoral groove) were evaluated to assess long-term results. A past history of patellofemoral malalignment or instability was obtained from 14 patients. Preoperative roentgenograms demonstrated patellofemoral osteoarthritis in all 25 knees; five patients had both tibiofemoral and patellofemoral osteoarthritis. The average age at the time of surgery was 62 years and follow-up time averaged 5.3 years. Results were determined using a modified Hungerford knee rating scale. Follow-up roentgenograms were evaluated for mechanical failure and progressive deterioration of the tibiofemoral joint. Eighteen of 25 (72%) patellofemoral arthroplasties were rated excellent or good. However, 15 of 17 patellofemoral arthroplasties (88%), all performed on women, had satisfactory results. There were seven failures. The presence of tibiofemoral osteoarthritis adversely affected the outcome; excluding the five patients with tibiofemoral osteoarthritis, 17 of 20 patellofemoral arthroplasties (85%) had satisfactory results. Other reasons for failure were malposition of the components and persistent patellofemoral malalignment. Mechanical failure was not observed. Patellofemoral arthroplasty may be indicated for patients with osteoarthritis limited to the patellofemoral compartment.     

Clinical and radiographic reports following cervical arthroplasty: a 24-month follow-up

We reviewed patients with cervical disc prosthesis replacement for single-level cervical disc disease to evaluate its clinical effect and maintenance of cervical spine motion. Fifteen patients underwent Bryan artificial cervical disc replacement and were followed-up for at least 24 months. No neurological or vascular complications were observed during or after operation. JOA, VAS, and NDI scores showed statistical significant improvement in our follow-up. The procedure achieved an 87% (13/15) satisfactory rate at 24-month evaluations according to Odom's criteria. The range of motion (ROM) of the cervical spine, treated segment, adjacent segment, and functional spinal unit (FSU) decreased at early follow-up, but they recovered to the preoperative level at 12- and 24-month follow-up. Also, preoperative lordosis of the cervical spine and FSU were not only maintained but also even improved during the 24-month follow-up. No obvious degeneration of adjacent discs were found at MRI. There were no cases of prosthesis subsidence or extrusion. The cervical disc prosthesis showed a good clinical outcome; it also restored ROM of the cervical spine and reestablished cervical curvature in our 24-month follow-up. But to be sure of its long term effect, a longer follow-up is needed.     

Charnley low-friction arthroplasty. A fifteen- to seventeen-year follow-up study

One hundred Charnley low-friction arthroplasties have been reviewed at 15 to 17 years. Thirty-five of the patients have died. A revision rate of 16 per cent has been recorded. Only two cases demonstrated cavitation and cortical destruction of the femur, and these cases were revised successfully. One of the major causes for revision was fracture of the femoral component. With modern alloys, this should not be a long-term problem. Our data would suggest that the cemented arthroplasty can be used with confidence in patients 65 and older. It is our hope that modern cement technology and component design will increase the longevity of the cemented arthroplasty.     

Palmar shelf arthroplasty. A follow-up note

Palmar shelf arthroplasty was described by Albright and Chase as a successful, so-called conservative surgical alternative for the treatment of subluxation of a wrist that is affected by advanced rheumatoid arthritis. Subsequent to their report, seven wrists in six patients who had been treated with a palmar shelf arthroplasty by Albright and Chase or by their trainees were studied, after an average follow-up of nine years. All of the patients had long-term relief of pain and improved motion of the wrist, and all were satisfied with the result of the procedure. All but one patient had increased function.     

Duofit total hip arthroplasty: a medium- to long-term clinical and radiographic evaluation

We report the retrospective analysis of 716 cases of Duofit total hip arthroplasty performed from 1994 to 2005. Since 2004, both standard and lateralized stems were used, while previously only the standard type was available. The results show a low occurrence of complications and a good medium-to long-term survival. The good functional outcome, measured with the Harris hip score, confirms the validity of the prosthetic design and materials.     

初次全髋关节置换术后6年以上随访的临床疗效分析

目的评价初次全髋关节置换（THA）术后6年以上的临床疗效及术后的各种并发症。方法自2001年1月至2005年1月,本中心共对北京地区210例225侧髋关节进行初次THA。其中单侧髋关节置换术195例,双髋同时置换术15例。半髋置换10例,全髋关节置换术215例。骨水泥固定假体18例,非骨水泥固定假体207例。围手术期及术后处理基本一致。术后定期随访,最新的随访时间平均为6.5年（5.5~8.5年）。结果围手术期并发症包括：术中股骨干骨折6例;下肢深静脉血栓28例,无肺栓塞病例;术后伤口感染4例;术后4周内脱位3例;术后出现一过性意识障碍3例。术后平均6.5年时176例183髋得到随访,34例42髋失访。远期感染病例1例,脱位2例,股骨干骨折4例。Harris评分由术前平均40.6分（-12~59分）提高到术后平均80.4分（75~94分）。其中152例评分〉80分,19例评分位于70~80分之间,5例评分〈70分。影像学检查3例髋臼假体、4例6髋股骨假体周围出现小范围的透亮线,2例3髋发现位于髋关节周围的异位骨化。其余X线片示髋臼和股骨柄假体位置满意,无松动和感染征象。结论 THA是治疗各种晚期重度髋关节疾病很好的方法,6年以上的临床效果良好,并发症少。     

Failed Christiansen total hip arthroplasty. A radiographic and histologic study

Twenty-two consecutive cases of the Christiansen total hip arthroplasty revised because of aseptic loosening were analyzed with regard to radiographic changes and operative and histopathologic findings. This prosthesis was designed with a socket and a trunnion sleeve made of polyoxymethylene or Delrin. In 18 cases there was isolated socket loosening, in all cases there was obvious bone resorption beneath the collar of the stem, and in 20 cases the socket had migrated. The radiographic socket wear rate averaged 0.4 mm/year. In 18 cases a significant amount of debris material was found in the joint cavity. Light microscopy revealed a severe foreign body reaction with numerous plastic particles, most often engulfed by macrophages. Taken together, these findings indicate that socket wear leading to a foreign body reaction with bone resorption is the main cause of the poor results noted with this particular total hip prosthesis.     

Minimum ten-year follow-up clinical and radiographic results of Mark I and Mark II Lord type femoral component in total hip arthroplasty

The purpose of this study was to evaluate the clinical and radiographic results in 103 hips in 88 patients who had cementless primary Lord type femoral component (stem), with a mean follow-up of 11.8 years (range, 10 to 16 years). The original diagnoses were: osteoarthritis in 77 hips, rheumatoid arthritis in 15, and osteonecrosis of the femoral head in 11. Clinical results were assessed using the Harris hip score. Biological fixation, stem full-fit ratio in the intramedullary canal, and bone remodeling were evaluated by X-ray findings. The average clinical hip scores were: 47.1 points preoperatively, 81.7 points at 1 year, 86.6 points at 5 years, 79.0 points at 10 years, and 76.8 points at 15 years. By setting the endpoint at the time when loosening was radiologically confirmed, the 10-year survivorship of the femoral component was 96.9%, and the 16-year survivorship was 95.9%. The full-fit ratio between the bone implant interface just after surgery showed a significant relationship to stability of the femoral component. The decrease in the hip score at 10 years was caused by aseptic loosening of the acetabular threaded cup. However, the femoral component was stable for more than 10 years after the operation. In conclusion, long-term acceptable durability can be expected with the Lord type femoral component. Received: July, 27, 2000 / Accepted: February 14, 2001     

Charnley total hip arthroplasty. A ten- to 14-year follow-up study

The long-term results of 325 consecutive Charnley total hip arthroplasties (THAs) were assessed at an average of 62 and 140 months (five-year and ten-year follow-up examinations) postoperatively. Cases developing deep infection during the first five years were not included. Pain, walking ability, and mobility were rated as advocated by Charnley. The results were then graded as excellent, good, fair (clinically successful), and failure. At the five-year follow-up evaluation, 77 hips were excluded; 92% (228/248) of the results were successful. At the ten-year follow-up examination, interest was focused on the 228 hips graded as successful after five years. Sixty-six were excluded, one that had not been included at the five-year evaluation was traced, and 92% (150/163) were again clinically successful. The failure rate owing to mechanical causes during the first five years and between the five-year and ten-year follow-up examinations was 6.9% and 6.7%, respectively. The clinical results were considered highly satisfactory because only 50% of the hips judged successful at the ten-year examination had roentgenographically intact components. There is good reason to have great confidence in the Charnley THA.     

Anterior urethropexy according to Lapides in stress urinary incontinence. A follow-up study.

Thirty-five women with a mean age of 53 years were investigated for an average of 3 1/2 years after anterior urethropexy according to Lapides (1961). The material was divided into two groups: 23 patients with a history of pure stress urinary incontinence and 12 patients with a mixed stress and urgency incontinence. In the former group, the cure rate was nearly 100%; one patient had a remaining nonembarrassing slight stress incontinence, which could not be classified as pathologic. Another patient had a recurrence 2 years postoperatively at which time she fractured her pelvis in an accident. In the latter group, only 4 patients were cured while another 3 patients improved considerably. The operative procedure did not cause residual urine, since the urethra cannot be compressed as in other retropubic operations. The risk of recurrence is minimized, since continence is not dependent upon non-relaxation of other structures, but upon scar-fixation between the urethra and the periosteum of the pubic bone.     

Trapeziometacarpal arthroplasty. A clinical review

Silicone implants for the damaged trapeziometacarpal joint have been used for over 15 years. Relief of pain has been significant with increasing grip and pinch strengths reported for up to one year following arthroplasty. Three problems remain with the use of these implants: instability, deformation and implant failure, and more recently reported, silicone synovitis. Silicone synovitis is such a major concern that surgeons are now using allograft or autograft tendon as a spacer when resection arthroplasty of the trapezium is required.     

Primary total hip arthroplasty with use of the modular S-ROM prosthesis. Four to seven-year clinical and radiographic results

BACKGROUND: A multicenter retrospective study was conducted to determine the clinical and radiographic results of primary total hip arthroplasty with insertion of the S-ROM modular femoral stem without cement in a series of patients who had been followed for four to seven years. Four centers participated in the study, with one contributing surgeon at each center. METHODS: Two hundred and eight consecutive patients who had a total hip arthroplasty with implantation of the S-ROM femoral prosthesis at one of the four centers during the study period were identified. Twenty-nine patients were lost to follow-up or had incomplete radiographic data, and twenty patients died from causes unrelated to the index arthroplasty. The remaining 159 patients formed the basis of this study. Sixteen of these patients had a bilateral procedure, resulting in 175 hips with complete clinical and radiographic data. The average age of the patients at the time of the index operation was fifty-nine years (range, twenty-two to ninety-three years). The duration of clinical follow-up averaged 5.3 years (range, four to 7.8 years), and the duration of radiographic follow-up averaged 4.9 years (range, four to 7.3 years). RESULTS: One patient (0.6 percent) had a failed femoral component, which was evidenced by progressive subsidence and lack of bone ingrowth. In addition, two patients (1 percent) had a revision of the acetabular component. The average Harris hip score increased from 35 points (range, 10 to 76 points) preoperatively to 91 points (range, 52 to 100 points) at the most recent follow-up examination. The radiographic evaluation revealed that 172 hips (98 percent) had stable bone ingrowth, two hips (1 percent) had stable fibrous ingrowth, and one hip (0.6 percent) had unstable fibrous ingrowth. Periprosthetic osteolytic lesions were noted in twelve hips (7 percent). The lesions were observed in the femur in eight hips, in the acetabulum in two hips, and in both the femur and the acetabulum in two hips. All femoral osteolytic lesions were localized within the greater trochanter or the proximal-medial portion of the femoral neck. No osteolytic lesions were evident distal to the stem-sleeve junction. CONCLUSIONS: Use of the modular S-ROM femoral prosthesis yielded excellent intermediate-term outcomes with respect to standard radiographic and clinical criteria. The issue regarding the theoretical increase in the rate of osteolysis due to metal debris generated at the modular femoral stem-sleeve junction was specifically addressed. We found that the rate of osteolysis in this series was not notably higher than that in other series reported in the orthopaedic literature. Although many possible factors may influence the rate of osteolysis in total hip arthroplasty, this finding suggests that the potential increase in osteolysis theoretically associated with this modular femoral implant was not observed at intermediate-term follow-up. Although longer follow-up is warranted so that the potential for osteolysis can be evaluated fully, no osteolytic lesions were evident distal to the stem-sleeve interface at the time of intermediate-term follow-up. This finding suggests that there is a circumferential seal at the modular junction of the stem that prevents the distal egress of wear debris.     

Polycentric total knee arthroplasty. A ten-year follow-up study

After review of the first 209 polycentric total knee arthroplasties (in 159 patients) performed at the Mayo Clinic between July 1970 and November 1971, we found that the calculated probability of the arthroplasty remaining successful ten years postoperatively was 66 per cent. Actual results showed 42 per cent of the arthroplasties to be successful in patients who were still alive at review; another 24 per cent were successful but were in patients who had died or were lost to follow-up before ten years postoperatively. In 34 per cent failure occurred, which we defined as reoperation for any reason, unacceptable pain, or loss of function. The most common causes of failure were instability or ligament laxity (13 per cent), loosening of a component (7 per cent), infection (3 per cent), and patellofemoral joint pain (4 per cent). Prior knee surgery significantly decreased the probability of success, as did axial malalignment of the prosthetic components at operation.     

Effect of age on clinical and radiographic outcomes and adverse events following 1-level lumbar arthroplasty after a minimum 2-year follow-up

OBJECT: Lumbar arthroplasty is approved in the US for the treatment of degenerative disc disease at 1 level in skeletally mature patients. However, a bias toward older patients (> 45 years of age) who are otherwise indicated for the procedure may exist. In this study, the clinical outcomes of patients from the Charité Investigational Device Exemption (IDE) study were analyzed on the basis of patient age. METHODS: There were 276 patients enrolled in the IDE study of the Charité Artificial Disc who underwent 1-level arthroplasty at either L4-5 or L5-S1, including 71 nonrandomized and 205 randomized individuals. Patient data were analyzed based on age (18-45 years [217 patients, Group 1] compared with 46-60 years [59 patients, Group 2]). Statistical analyses were performed based on 2-year postoperative improvements in Oswestry Disability Index (ODI), 36-item Short Form Health Survey (SF-36), and visual analog scale (VAS) scores (clinical outcome), as well as range of motion (radiographic outcome), and adverse events. RESULTS: There was no significant difference between the groups with respect to level implanted, operative time, blood loss, changes in ODI and VAS scores or any of the 8 component scores of the SF-36, compared with baseline, at all time points throughout the 24-month follow-up period (p > 0.10). Patient satisfaction was equivalent at 24 months, with 87% satisfaction in Group 1 and 85% satisfaction in Group 2 (no statistical difference). In addition, no significant differences were identified with respect to adverse events including approach related, neurological, technique related, or reoperation. CONCLUSIONS: Although patients > 45 years of age may have comorbidities or contraindications for arthroplasty for a number of reasons, particularly osteopenia, this analysis demonstrates that patients who are indicated for 1-level arthroplasty experience similar clinical outcome, satisfaction, or adverse events compared with their younger counterparts.