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1.
Orthop Traumatol Surg Res ; 106(5): 907-913, 2020 Sep.
Article in English | MEDLINE | ID: mdl-32631712

ABSTRACT

INTRODUCTION: Isolated lateral compartment osteoarthritis of the knee (LCOA) is 10 times less frequent than medial compartment involvement. Long-term assessments of unicompartmental knee arthroplasty (UKA) in this indication are rare, with small series. HYPOTHESIS: Survival and functional outcome of lateral UKA in a large series are quite acceptable; the strategy is suited for isolated LCOA. MATERIAL AND METHOD: A multicenter retrospective study in 6 French health establishments included all lateral UKAs performed between January 1988 and September 2014. Clinical data (range of motion, International Knee Society (IKS) knee and function scores, satisfaction), paraclinical data (radiologic angles) and complications were prospectively entered in medical files during follow-up and analyzed retrospectively at end of follow-up. RESULTS: During the study period, 311 lateral UKAs were performed in 295 patients, using 5 fixed-bearing implant models. Twenty-eight patients died within 5 years, and 15 (4.8%) were lost to follow-up. The series thus comprised 268 lateral UKAs in 63 male and 205 female patients, with a mean age of 68.8±10.5 years, including 7 cases of post-traumatic osteoarthritis and 4 of aseptic osteonecrosis. Mean follow-up was 9.1 years (range, 5-23 years), implant survivorship with failure defined as all-cause revision surgery was 85.4% at 10 years and 79.4% at 20 years. At last follow-up, IKS knee score was 87.0 and IKS function score 80.2. Maximal flexion was 125°. 94.3% of patients were satisfied or very satisfied. The main cause of revision surgery was osteoarthritis in another knee compartment (66,7%, n=26). CONCLUSION: Lateral UKA showed good survivorship, comparable to medial UKA, with good functional results and excellent long-term satisfaction. LEVEL OF EVIDENCE: IV, retrospective cohort study.


Subject(s)
Arthroplasty, Replacement, Knee , Knee Prosthesis , Osteoarthritis, Knee , Aged , Female , Follow-Up Studies , Humans , Knee Joint/surgery , Male , Middle Aged , Osteoarthritis, Knee/diagnostic imaging , Osteoarthritis, Knee/surgery , Range of Motion, Articular , Reoperation , Retrospective Studies , Treatment Outcome
2.
Foot Ankle Surg ; 15(4): 179-82, 2009.
Article in English | MEDLINE | ID: mdl-19840748

ABSTRACT

BACKGROUND: The public health cost impact of complex regional pain syndrome type I (CRPS I) is considerable in both emergency and scheduled orthopaedic surgery. We proposed to assess the effectiveness of vitamin C in prevention of CRPS I in foot and ankle surgery. METHODS: We carried out a "before-after" quasi-experimental study comparing two chronologically successive groups without (Group I: July 2002-June 2003) and with (Group II: July 2003-June 2004) preventive 1g daily vitamin C treatment. All patients having surgery on the foot or ankle were enrolled, with the exception of diabetic foot cases. Several factors were analysed: sex, age, type of pathology, history of CRPS I, psychological context, tourniquet time, and cast immobilisation time. RESULTS: 420 feet (392 patients) were included in the study: 185 in Group I, 235 in Group II. CRPS I occurred in 18 cases in Group I (9.6%) and 4 cases in Group II (1.7%) (p<10(-4)), with history of CRPS I as a significantly correlated factor (relative risk=10.4). The psychological context (anxio-depressive state) showed a (sub-significant) tendency to increase the risk of CRPS I (relative risk=2.6). CONCLUSION: Vitamin C has been shown to be effective in preventing CRPS I secondary to wrist fracture, but few data are available with respect to foot and ankle cases. The present study demonstrates the effectiveness of vitamin C in preventing CRPS I of the foot and ankle-a frequent complication in our control group (9.6%). The authors recommend preventive management by vitamin C.


Subject(s)
Ankle Injuries/surgery , Antioxidants/administration & dosage , Ascorbic Acid/administration & dosage , Foot Injuries/surgery , Orthopedic Procedures/adverse effects , Pain, Postoperative/prevention & control , Reflex Sympathetic Dystrophy/prevention & control , Adolescent , Adult , Aged , Dose-Response Relationship, Drug , Female , Follow-Up Studies , Humans , Male , Middle Aged , Prospective Studies , Reflex Sympathetic Dystrophy/etiology , Syndrome , Treatment Outcome , Young Adult
3.
J Pediatr Orthop ; 28(5): 534-7, 2008.
Article in English | MEDLINE | ID: mdl-18580368

ABSTRACT

Although there are many publications concerning the mechanical behavior of adult bone, there are few data about mechanical properties of children's bone. In vivo bone stiffness measurement with Orthometer device has been validated and extensively used in adults to assess bone healing after fracture or lengthening. We hypothesized that in vivo stiffness measurement with Orthometer was applicable in children and was correlated with age, height, body weight, and corpulence index. The purpose was to establish baseline stiffness values for femur and tibia in growing children.Sixteen bone measurements (7 femurs and 9 tibias) were obtained during application of an external fixator for leg lengthening in 11 children aged between 5.5 and 16.7 years. A 3-point bending test with an Orthometer was carried out on the intact bone (before osteotomy) under general anesthesia. The anteroposterior stiffness measurement was successful in all children of the series, aged from 5.5 to 16.7 years. A wide variation of femoral and tibial bone stiffness values were observed. The use of a unique value as in adults as the end point of bending stiffness during bone healing process is not possible for children. The anteroposterior bone stiffness was found to have linear correlation with children's height and body weight, but not with age and corpulence indexes. The original data obtained by this study will give a stiffness reference for height and weight and could be useful as reference values for monitoring of healing process after fracture or limb lengthening.


Subject(s)
Bone Lengthening/methods , Femur/physiopathology , Tibia/physiopathology , Age Factors , Biomechanical Phenomena , Body Height , Body Weight , Child , Female , Femur/abnormalities , Femur/surgery , Humans , Leg Length Inequality/surgery , Male , Reference Values , Regression Analysis , Tibia/abnormalities , Tibia/surgery
4.
J Pediatr Orthop ; 28(5): 538-43, 2008.
Article in English | MEDLINE | ID: mdl-18580369

ABSTRACT

BACKGROUND: The decision when to remove the frame after limb lengthening through standard distraction osteogenesis remains a challenge. Multiple studies have attempted to find objective criteria to assess bone healing after fracture or bone lengthening. However, there is a paucity of such data for the pediatric population. The purpose of this study was to correlate data obtained after dual-energy x-ray absorptiometry (DXA) measurement and bending stiffness in children to find an end-point value for the safe removal of an external fixation device. METHODS: We investigated 16 consecutive children aged between 5.5 and 16.7 years who had 22 lengthenings by callotasis. Twelve femurs and 10 tibiae were lengthened with a monoplane Orthofix external fixator. Fifty simultaneous measurements of bending bone stiffness measured with an Orthometer and DXA scans (bone mineral content [BMC], bone mineral density, volumetric bone mineral density, BMC/1 cm, Area/1 cm, BMC/1 cm, Area) were obtained during healing process. Four femoral fractures were reported after the removal of the external fixation device. Linear regression analysis was used to calculate the squared correlation coefficients for the relation between the DXA scans and the mechanical tests measuring bone stiffness. RESULTS: The bone stiffness measurement of the intact bone was compared with consecutive measurements of the bone stiffness of the regenerate, and it was expressed as a percentage (coefficient). We compared the BMC of the regenerate with the same bone area of the opposite limb. The best correlation was observed for anteroposterior (AP) bone stiffness coefficient and BMC coefficient (R = 0.82). The linear equation was BMC coefficient = 0.5 x AP stiffness coefficient + 30. The end point of 75% of BMC of the regenerate corresponds to 75% of the AP stiffness on DXA scanning; this is the time when we should consider safe removal of the fixator. CONCLUSIONS: Our method of comparing bone stiffness and DXA measurements gives an objective healing end point for every patient irrespective of his or her size. This method could allow noninvasive measurement of the end point and identified at-risk population of children, reducing regenerate fracture after bone lengthening.


Subject(s)
Bone Lengthening/methods , Femur/physiopathology , Tibia/physiopathology , Absorptiometry, Photon , Adolescent , Biomechanical Phenomena , Bone Density , Child , Child, Preschool , Female , Femur/abnormalities , Femur/diagnostic imaging , Femur/surgery , Humans , Leg Length Inequality/surgery , Linear Models , Male , Prospective Studies , Tibia/abnormalities , Tibia/diagnostic imaging , Tibia/surgery , Wound Healing/physiology
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