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Evaluation of uncemented total hip arthroplasty in patients with avascular necrosis of the femoral head.

Thirty-seven uncemented primary porous coated anatomic (PCA) total hip arthroplasties (THA) that were performed in 33 patients for the diagnosis of avascular necrosis (AVN) between June 1984 and December 1986 were reexamined at four- to six-year follow-up periods. Final clinical evaluation showed an 86-point average Harris hip rating (range, 47-100 points), which had improved from an average preoperative rating of 42 points (range, 20-61 points). Thigh pain, which was usually not functionally limiting, occurred in 11 patients (25%), and seven patients (16%) had a moderate or severe limp. Nine patients (20%) required the use of a cane. Long-term radiographic evaluation in 37 hips demonstrated acetabular cup migration in one hip, acetabular lucencies in four hips (11%), and acetabular bead loosening in ten hips (27%). Femoral subsidence occurred in five hips (14%) and femoral bead loosening in 11 hips (30%). Thirty hips (81%) demonstrated radiographic evidence of stable bony ingrowth. No revisions were performed for aseptic loosening, but two prostheses were removed for infection. These results of uncemented THA in patients with AVN appear to be as good or better than the results reported for cemented arthroplasty in AVN at this interval of a follow-up period. This study supports the use of uncemented devices, especially with the newer designs and increasing surgical experience in this difficult patient population.

Acetabulum↗

Noncemented stem tibial component in total knee replacement: the 2- to 6-year results.

OBJECTIVE: To determine if the addition of a stem to the tibial component in noncemented total knee replacement affects sinkage of that component or micromotion. DESIGN: A cohort of 176 consecutive cases with no exclusions. Follow-up ranged from 2 to 6 years. SETTING: A university-affiliated institution specializing in elective orthopedic surgery. PARTICIPANTS: All 176 patients had arthritis of the knee, mainly osteoarthritis. All agreed preoperatively to prolonged postoperative follow-up. INTERVENTION: Noncemented total knee replacement with the Tricon M long-stem tibial component. MAIN OUTCOME MEASURES: Hospital for Special Surgery rating system for clinical results and degree of tibial sinkage and stem lucency seen radiologically. RESULTS: Eight (4.5%) of the 176 prostheses required revision, none for sinkage. Of the remaining 168 knees, 156 (92.9%) scored good or excellent, 6% fair and 1.2% poor. Sinkage occurred in 3%, but was not of sufficient severity to require revision. No lucency was visible in 33.8% of stems, partial lucency in 62%, complete lucency with the lines being parallel to the stem in 3.5% and complete lucency with divergent lines, indicating a loose implant, in 1.7%. Lucency, when present, was seen mainly in the lateral view, seldom in the anteroposterior view. There was no correlation between radiologic results and clinical results. CONCLUSIONS: The addition of a metaphyseal stem reduces the incidence of sinkage of the tibial component in total knee replacement. The stem largely solves the problem of mediolateral micromotion but does not completely prevent anteroposterior micromotion.

Aged↗

[Informed consent in orthopedic surgery].

Twenty-eight patients who had total joint replacement (TJR) and twenty-eight patients who sustained open reduction for fracture within or close to the joint were studied to determine their recall of the informed consent procedure. The questionnaire covered a postoperative time range of more than 5 months and less than 6 years (average: 2 years and 4 months). The patient's recall and the doctor's document of informed consent were scored 4 points for diagnosis and treatment, 1 point for prognosis, 3 points for benefits, 4 points for complications and 1 point for alternatives with a total of 13 points. In TJR, the average recall and document score were 8.6 points and 6.5 points respectively; and in fracture, 6.6 points and 4.9 points. Fifty-seven per cent of the patients with TJR recalled the risk of infection; and 54 per cent recalled the problem of loosening. Twenty-nine per cent of the patients with fracture recalled the risk of infection, and 29 per cent the risk of nonunion. In TJR, the recall score was related to the patient's age and the document score. There was significant difference in document scores among doctors. As a result of this study, standard documents for informed consent in each operation have been compiled with the aid of a word-processor to improve the quality of informed consent.

Female↗

The regenerative potential of plaque-induced peri-implant bone defects treated by a submerged membrane technique: an experimental study.

The aim of the present study was to experimentally induce peri-implant bone defects around three different types of implants by plaque accumulation and to determine whether new bone formation can occur on previously contaminated dental implants. Dental implants were placed into the mandibles of beagle dogs. Gross plaque accumulation around the implants was undisturbed for 3 months, which resulted in circumferential peri-implant bone defects. Bony defects surrounding the hydroxyapatite implants were significantly greater than those around the titanium implants. Surgical treatment consisted of granulation tissue removal, preparation of the implant surface, and the placement of an e-PTFE membrane over each test implant. Before the flap was closed to cover the implants, perforations were made into the cancellous bone. Each control implant received identical treatment, but without placement of a membrane. Surgical exposure after an uneventful submerged healing period showed evidence of closure of the peri-implant bone defects. Corresponding histologic examination of 2-month sections demonstrated large amounts of rapidly formed lamellar bone beneath the membrane. Some areas of the previously contaminated implant surface showed evidence of "re-osseointegration." These preliminary results support the hypothesis that plaque-induced peri-implant bone defects can be successfully treated by a submerged membrane technique in the dog model.

Alveolar Bone Loss↗

Developments in diagnosis of the painful total hip replacement.

There has been significant improvement in the interpretation of diagnostic tests for the evaluation of the cemented and uncemented symptomatic total hip replacement. Lucent lines around cemented implants have often been found to represent remodeling rather than loosening. Lysis without looseness has been described as a cause of hip pain in both cemented and uncemented hip replacements. Therefore, there are a number of recent developments in diagnosis that must be considered when evaluating the symptomatic cemented or cementless total hip replacement. Some of these developments are reviewed in this paper. Other developments and contemporary algorithms for treatment incorporating these recent data will be presented in next month's issue.

Arthrography↗

Knee effusion after total knee replacement.

The various causes of effusions in artificial knees can be divided into four groups: implant related, technique related, interface problems, and infection. Diagnosis can be made from the patient's history and a clinical examination. Treatment is usually surgical revision.

Clinical Protocols↗

The implant periapical lesion: etiology, prevention, and treatment.

A classification of implant periapical lesions that separates them into inactive and infected has been suggested. The inactive form is likely to be an apical scar, resulting from a residual bone cavity created by placing an implant that was shorter than the prepared drill site. The infected focus probably occurs when an implant apex is placed in proximity to an existing infection or when a contaminated implant is placed. Bone necrosis caused by overheating during preparation may also be a causative factor. Suggested preventions of implant periapical lesions include careful management of contaminants and heat generation during implant surgery. Treatment varies according to the type of lesion. The inactive type is observed and monitored. The infected type requires surgical intervention, elimination of the infection, and an implant apical resection or implant removal depending on the extent of the infection and the stability of the implant.

Bacterial Infections↗

Immediate placement of implants into extraction sockets: implant survival.

In 51 patients (21 males and 30 females) aged 16 to 72 years, a total of 109 Nobelpharma implants were placed into extraction sockets immediately following extraction. The follow-up period varied between 1 and 67 months with a mean of 30.5 months. Osseointegration was determined by clinical stability, lack of symptoms, and lack of peri-implant pathology based on radiographic examination. The implant survival rate was 93.6%. Six implants were mobile at the abutment connection stage, and one was lost when function commenced. The success rate was 92.0% for implants replacing teeth extracted because of periodontitis and 95.8% for implants replacing teeth extracted for other reasons. Two other complications occurred: 12 cover screws perforated the gingiva during healing; and infection developed in five cases. The incidence of infection was higher in the periodontitis group. It was found that immediate placement of implants into extraction sockets is a safe and predictable procedure if certain guidelines are followed.

Adolescent↗

["Circumscribed defibrillator erythema": a differential diagnostic and therapeutic problem in differential occult defibrillator infection diagnosis].

We report about three out of 452 patients (pts) (< 1 %) with circumscribed erythema (E) after implantation of an automatic cardioverter defibrillator (ICD). ICD-E occurred in two pts after pulse generator replacements and in one pt after initial ICD implantation. There were no clinical signs of inflammation and laboratory and technical finding were completely normal. Allergic reactions could be ruled out in all pts. Local or systemic drug treatment did not influence the ICD-E. During a follow-up of 28, 10 or 9 months, the ICD-E is still present in two patients and much improved in one pt without any treatment. We did not observe an infection in any of the pts. Our data show that the ICD-E occur rarely after ICD implantation and no special treatment is necessary if an infection or allergic reaction has been excluded. Nevertheless, it is sometimes difficult to exclude in those pts an atypical infection.

Adult↗

[An original procedure for cement diaphyseal extraction. The segmental cement extraction system or SEG-CES].

PURPOSE OF THE STUDY: We report our first eleven uses of a new cement mantle extraction system. The basis of this technique relies on a cement bone interface with a lower strength compared to the old cement-new cement interface. MATERIAL AND METHODS: The first stage of the procedure consists in a specific preparation of the inner surface of the old cement, mantle. It should be clean and dry after being abraded with a stainless steel wire brush. Then a thin cement syringe filled with low Viscosity PMMA cement, is injected in the old mantle in a retrograde fashion. A threaded rod with nuts is centered within the cement sheath to the bottom and held until the injected cement has fully polymerised. Then the threaded rod is unscrewed from the femur; nuts are established along the entire length of the cement column. To prevent trochanteric fracture occurring upon cement extraction, its is important to clear away sufficient bone from the lateral aspect of the canal. A series of extraction rods are then used to sequentially remove the cement mantle. The removal rod is screwed back into the threaded channel at a distance of every one to three nuts, and then attached to the slap hammer via a quick release connection. Cement extraction is performed using deliberate slaps of the slap hammer. The last segment is drilled with the use of a distal plug drill centering sleeve. After having inserted the plug removal rod, the last segment is extracted. We used this technique eleven times in 8 hips for 5 loosening of femoral component and 3 revisions hip arthroplasties without loosening and 2 revisions knee arthroplasties without loosening (an extraction system for the femur and the tibia). RESULTS: For the 5 loosening cases extraction was easy. In 2 cases, cement mantle was removed as a single "en bloc" piece. In the 3 other cases, the extraction was segmental only in the distal third of the cement mantle. Without loosening, the extraction was completely segmental. In all cases, cement mantles were successfully removed. There was no fracture and no loss of bone stock. There was only one "fissuration" alpha the great trochanter and we only made one distal window. All hip arthroplasties were replaced and arthrodesis were performed after removal of the knee arthroplasties. DISCUSSION: The cement-assisted mantle removal technique appears to be a simple, quick and effective methods for cement mantle removal. Perforation and diaphyseal window can be avoided by the technique even when loosening does not exist. However, it is necessary to establish a thorough preoperating plan in order to eliminate contraindications such as too narrow or too curved sheath. CONCLUSION: It appears that this new procedure will facilitate future reoperations which are reputed to be difficult and dangerous.

Bone Cements↗

Charnley total hip arthroplasty with use of improved techniques of cementing. The results after a minimum of fifteen years of follow-up.

Three hundred and fifty-seven consecutive Charnley total hip arthroplasties were performed in 320 patients with use of a so-called second-generation technique of cementing between July 1976 and June 1978. This technique includes use of a distal femoral intramedullary cement plug, hand-mixing of the cement, and use of a cement gun to deliver the cement into the femoral canal in a retrograde fashion. At the time of the latest follow-up evaluation, a minimum of fifteen years after the arthroplasty, 130 patients (142 hips) were still alive, 189 patients (214 hips) had died, and one patient (one hip) had been lost to follow-up. A radiograph was made for 116 (82 per cent) of the 142 hips in the 130 surviving patients. Of the 356 hips that had not been lost to follow-up, thirty-three (9 per cent) had had a revision and two (1 per cent), a Girdlestone resection arthroplasty during the follow-up period. Nineteen hips (5 per cent) were revised because of aseptic loosening of the femoral or acetabular component, or both (two hips); seven (2 per cent), because of loosening with infection; and seven (2 per cent), because of dislocation. The two resection arthroplasties were performed because of loosening with infection; both were done in patients who died before the time of the latest follow-up evaluation. Of the 142 hips in the 130 patients who were alive at a minimum of fifteen years, twenty-two (15 per cent) had been revised: fifteen (11 per cent), because of aseptic loosening; three (2 per cent), because of loosening with infection; and four (3 per cent), because of dislocation. Revision of the femoral component because of aseptic loosening (excluding components that were revised because of dislocation or infection) was performed in four (1 per cent) of the entire series of 356 hips and in three (2 per cent) of the 142 hips in the 130 patients who survived for at least fifteen years. Two of the 356 hips and two of the 142 hips had aseptic loosening of the acetabular as well as the femoral component at the time of the revision. Loosening of the femoral component, defined as aseptic loosening leading to revision or as definite or probable radiographic loosening, occurred in ten (3 per cent) of the 356 hips and in six (5 per cent) of the 116 hips for which radiographs were made at a minimum of fifteen years. The acetabular component was revised because of aseptic loosening in seventeen (5 per cent) of the entire series of 356 hips and in fourteen (10 per cent) of the 142 hips in the 130 patients who survived for at least fifteen years. The acetabular component loosened without infection in forty-one (12 per cent) of the 356 hips and in twenty-six (22 per cent) of the 116 hips for which radiographs were made at a minimum of fifteen years. In two of these patients, the femoral component was also revised. Thus, of the entire series of 356 hips, two had a revision of the femoral component alone because of aseptic loosening; fifteen, a revision of the acetabular component alone; and two, a revision of both components. Of the 142 hips in the 130 patients who survived for at least fifteen years, one was revised for loosening of the femoral component alone; twelve, for loosening of the acetabular component alone; and two, for loosening of both components. These findings demonstrate long-term durability of fixation of the femoral component but less reliable fixation of the acetabular component, even when the surgeon is experienced and improved techniques of cementing are used.

Activities of Daily Living↗

[Clinical experience with a new antimicrobially coated InterGard-IgK/AM vascular prosthesis in surgical treatment of deep wound infection with involvement of the synthetic bypass: report of 2 cases].

We report 2 cases of infected vascular prosthesis, where the infected alloplastic material was removed and the revascularisation of the lower extremity was done by implantation of the new antimicrobial surface-coated InterGard prosthesis in the area of the former infected graft. An extra-anatomical bypass was not promising in these cases. Clinical, bacteriological and granulocyte-scintigraphic examinations have provided no evidence for persisting infection 12 and 11 months after implantation of this prosthesis. We are aware that the postoperative observation periods are too short to allow definitive assessment. Nevertheless we still consider that this prosthesis means a new and promising option in the treatment of infected vascular graft.

Angiography↗

Reimplantation of infected hip arthroplasties using bone allografts.

Twenty-two patients with deep infection of an hip prosthesis received delayed reimplantation using bone allografts. Sixteen were done using noncemented components and 6 using femoral components that were fixed with antibiotic impregnated cement. Bulk allografts were used at the acetabular site in 2 patients and at the femoral site in 4 patients. Morselized allografts were used at the acetabular site in 20 patients and at the femoral site in 10 patients. The causative organisms were virulent in 10 hips and low virulent in 12 hips. At an average followup of 4 years (range, 2-7 years), 91% of patients were free of infection and 73% had a successful functional result. Two had a recurrent infection; 1 of them had a pseudomonas infection and another had a methicillin resistant Staphylococcal infection. The recurrence of infection tended to be higher if the causative organism was virulent. The use of bone allografts at the staged reimplantation of the infected hip arthroplasty did not increase the incidence of recurrent infection. Both cemented and noncemented reimplantations had a successful result in eradicating the infection. However, hybrid reimplantation with a cemented femoral component and fixed porous acetabular component had a better functional outcome than noncemented reimplantation using porous femoral component and nonfixed acetabular component.

Adult↗