Subject(s)
Lupus Vulgaris/pathology , Nose , Osteoarthritis, Hip/pathology , Skin/pathology , Tuberculosis, Osteoarticular/pathology , Antitubercular Agents/therapeutic use , Biopsy , Female , Humans , Lupus Vulgaris/diagnosis , Lupus Vulgaris/drug therapy , Lupus Vulgaris/microbiology , Mycobacterium tuberculosis/isolation & purification , Osteoarthritis, Hip/diagnosis , Osteoarthritis, Hip/drug therapy , Osteoarthritis, Hip/microbiology , Synovial Fluid/microbiology , Treatment Outcome , Tuberculosis, Osteoarticular/diagnosis , Tuberculosis, Osteoarticular/drug therapy , Tuberculosis, Osteoarticular/microbiologyABSTRACT
PURPOSE OF THE STUDY: This prospective randomized study was conducted to analyze the anatomic and functional impact of an extra-articular lateral plasty associated with patellar tendon-bone autograft in anterior cruciate ligament reconstruction. MATERIAL AND METHODS: A consecutive series of 100 patients with grade II (Noyes classification) chronic anterior laxity confirmed on stress x-rays were included in the study. All patients had a positive Trillat-Lachman test, a direct anterior drawer at 90 degrees flexion confirmed on the lateral x-ray, and an instrumental differential laxity greater than 5 mm (manual arthrometry, Medmetric KT1000). Mean patient age was 27 years (range 16-29 years) and time from the accident to ligamentoplasty was 29 months (range 3-156 months). In the operating theater, the patients were assigned at random to two groups. Group 1 (50 patients) underwent arthroscopic free patellar tendon-bone autograft reconstruction of the anterior cruciate ligament. In the second group (50 patients) the same reconstruction was further supported by a lateral extra-articular plasty using the quadriceps tendon. All patients were followed prospectively. At 58 months follow-up (none of the patients were lost to follow-up) residual laxity (Medmetric KT1000) was noted and functional outcome was assessed using the IKDC criteria. The Aglietti method was used to assess the position of the drill holes. RESULTS: The two groups were strictly identical at inclusion. At last follow-up, the statistical analysis did not reveal any significant difference between the groups for subjective outcome, joint motion, instrumental residual laxity, meniscal stock, or radiological changes. The overall IKDC score was A or B in 80% of the patients in group 1 and 88% of the patients in group 2. Delay to resumed sports activities (about 12 months) was also equivalent in the two groups with a trend towards lower intensity and sports producing less stress on the knee. A minimally positive pivot test with no effect on stability was observed in 4 patients in group 1 (intra-articular plasty alone) and in 2 patients in group 2 (intra- and extra-articular plasty). 16% of the insufficient results (IKDC C and D) were related to repeated tears (n=8, 6 patients in group 1 and 2 patients in group 2, p=0.268), and failure (n=8, 4 in each group) due to defective motion and pain. Repeated tears were strongly correlated with incorrect drill hole position in the tibia (p=0.01) or femur (p=0.024). Despite the stabilization, radiological remodeling was observed in 31% of the patients in both groups. DISCUSSION: The results in this consecutive series of patients demonstrated the good results obtained with intra-articular ligamentoplasy using the mid third of the patellar tendon. The rate of repeated tears or minimally positive pivot tests was higher in group 1 with intra-articular plasty alone but did not reach statistical significance and was generally related to a technical error in positioning the autograft, making it difficult to draw any conclusion concerning the anatomic superiority of mixed plasty. CONCLUSION: At the current follow-up of 5 years, this study was unable to demonstrate any advantage of systematic conjunction of an extra-articular lateral support for advanced chronic anterior laxity of the knee treated by a free patellar tendon graft.
Subject(s)
Anterior Cruciate Ligament Injuries , Anterior Cruciate Ligament/surgery , Bone Transplantation , Joint Instability/surgery , Orthopedic Procedures/methods , Plastic Surgery Procedures/methods , Tendons/transplantation , Adolescent , Adult , Female , Humans , Male , Pain , Prospective Studies , Range of Motion, Articular , Transplantation, Autologous , Treatment OutcomeABSTRACT
PURPOSE OF THE STUDY: Clinical outcome and technical difficulties observed after total hip arthroplasty subsequent to osteotomy of the proximal femur were studied in 75 total hip arthroplasties. MATERIAL AND METHOD: Sixty-four patients underwent 75 total hip arthroplasty procedures at the Caen University Hospital between 1978 and 1995. These patients were reviewed at least two years after implantation. The Postel Merle d'Aubigné (PMA) score was used to assess clinical outcome and the Lequesne criteria to determine acetabular and femoral parameters on the weight-bearing AP radiograph. Off-set of the femoral epiphysis was determined by measuring the relation between the femoral shaft axis and the digital fossa. The population was composed of young active subjects who had had several operations. The main underlying diseases were: congenital dislocation of the hip (32%), dysplasia (23%), and primary degenerative hip disease (34%). Two-thirds of the hips were stiff and more than three-quarters were unstable. There were 28 osteotomies for varisation, 19 medial translations, 20 osteotomies for valgisation, and 7 subtrochanteric osteotomies. All femoral pieces except one were cemented. Implantation required 39 trochanterotomies, 39 Hardinge approaches, and 5 deosteotomies. RESULTS: The medial offset of the digital fossa compared with the diaphysis led to operative difficulties and femoral complications: Their were eight femoral fractures: 7 of these occurred with a digital fossa situated medially to the diaphysis. The Postel-Merle-d'Aubigné score at last follow-up was satisfactory in 57 cases (76%). Among the 18 non-satisfactory results, there was 7 failures requiring surgical revision, 5 potential loosenings, and 6 stiff hips in patients with congenital dislocation. For the 7 revisions (9.3%), 3 were for infection (2 late hematogenous), 1 for early dislocation, 2 for aseptic acetabular loosening, and 1 for aseptic femoral loosening. Medial translation of the digital fossa led to a larger number of varus positions (44%). For femoral cementing, 10 hips showed a non-progressive secondary lucent line; these prostheses were considered as potentially loose. Among them, varisation osteotomies has been performed in 5 cases, and in 8 the digital fossa was medial to the diaphyseal axis. There was only one aseptic femoral loosening requiring surgical revision. Implant survival, established according to the actuarial method, was 94.9% at 10 years. DISCUSSION: The almost 95% implant survival at 10 years observed in our patients is comparable with most reports in the literature and slightly better than those reported at the 1997 SOFCOT symposium on total hip arthroplasty after 50 years (84%). The most important factor determining surgical difficulty and operative complications at the femoral level was the position of the digital fossa, more than the type of initial osteotomy. CONCLUSION: Indications for osteotomy must account for subsequent total hip arthoplasty. Implantation is difficult after subtrochanteric osteotomy which can cause important technical problems. The rate of failure is very high. The risk of femoral complications and misalignment of the femoral stem, irrespective of the type of initial osteotomy, is greater when the digital fossa lies medially to the diaphyseal axis. We prefer trochanterotomy or desosteotomy for such cases. Osteotomy did not rule out arthroplasty for any of the femurs. There were however important operative difficulties and the frequency of complications suggest we should be most prudent about careful preoperative planning in the frontal plane.
Subject(s)
Arthroplasty, Replacement, Hip , Femur/surgery , Osteotomy , Adult , Femur/diagnostic imaging , Follow-Up Studies , Humans , Middle Aged , Radiography , Retrospective Studies , Time FactorsABSTRACT
PURPOSE OF THE STUDY: The purpose of this retrospective analysis was to study clinical and radiological outcome of 95 stable meniscal tears left in place after arthroscopic reconstruction of the anterior cruciate ligament with a free patellar autograft (with or without a lateral component). MATERIAL AND METHODS: We reviewed 86 patients who had undergone arthroscopic treatment for chronic anterior laxity (56% solely anterior laxity) with at least one meniscal lesion left in place after ligamentoplasty. IKDC criteria and ARPEGE scores were recorded. A total of 95 stable meniscal lesions had been left in place: 35 lateral lesions (80% longitudinal tears and 77% posterior lesions) and 60 medial lesions (55% peripheral disinsertions and 90% posterior lesions). The lesions measured a mean 10 mm (range 5-20 mm) for the lateral and medial menisci. Mean follow-up was 4 years (range 3-9 years). These patients were young (mean age 26 years), and predominantly men (75%). The right knee was involved in 53% of the cases. RESULTS: At last follow-up, 26% of the patients were grade A, 65% B, 7% C and 2% D according to the IKDC criteria. No revision procedure was required for lateral menisci despite the large size of the lesions left in place in certain cases. Among the 60 medial lesions left in place, 10 (17%) had become symptomatic (8 bucket-handle, 1 longitudinal tear, 1 posterior fragment) and required surgery a mean 3 years (range 1-6 years) after ligamentoplasty. There was no statistical difference between functional score, residual laxity, or type of stabilization in patients who had revision surgery for symptomatic meniscal lesions and the others. Inversely, these lesions were statistically larger (p=0.038) than the others (mean 13 mm versus 9.8 mm). CONCLUSION: Outcome of stable meniscal lesions left in place after treatment for anterior laxity depends on the meniscus involved. For the lateral meniscus, irrespective of the size of the lesion, therapeutic abstention has no clinical impact at 4 years. Inversely, for the medial meniscus, 37.5% of the lesions measuring more than 10 mm that were left in place required revision while only 9% of those measuring less than 10 mm necessitated subsequent surgery. Beyond 10 mm, therapeutic abstention led to a revision procedure in 17% of the cases, suggesting the usefulness of a discussion on other indications. Stable lesions of the medial meniscus should not be left in place if they measure more than 10 mm.
