Aim of this prospective, randomized study is to introduce and compare a new technique of reduction of the anterior dislocation of the shoulder with the “Hippocrates” and “Kocher” methods, as far as its efficacy, safety and intensity of the pain felt by the patient during the reduction, are concerned. This is the first reported prospective, randomized comparative study of three reduction techniques of anterior dislocations of the shoulder. 154 patients suffering from acute anterior shoulder dislocation participated in the study. Patients were randomly assigned to one of the three study groups (New, “Hippocrates” and “Kocher”) and underwent reduction of their dislocation performed by residents orthopaedic surgeons. The groups were statistically comparable (age, male/ female ratio, mechanism of dislocation, mean time interval between injury and first attempt of reduction). Reduction was achieved with the “Fares” method in 88.6%, with the “Hippocrates” in 72.5% and with the “Kocher” in 68% of the patients. This difference was statistically significant, favoring the new method (p=0.033). The mean duration of the reduction (p=0.000) and the mean reported by the patients VAS with the new method (p=0.000) were also statistically significantly lower than those of the other methods. No complications were noted in any group. The new method seems to be more effective, faster and less painful method of reduction of the anterior shoulder dislocation, when compared with the “Hippocrates” and the “Kocher” methods. It is easily performed by only one physician and it is not more morbid that the other two methods.
The aim of this study is the presentation of the midterm results of the radial head replacement with pyrocarbon head prosthesis (MoPyc). Thirty two patients (20 males and 12 females) with a mean age of 54 y.o. (32–68 y.o.) were subjected to replacement of the radial head with a pyrocarbon head prosthesis. Twenty of them had a comminuted radial head fracture(15 Mason IV type and 5 Mason III), two had a malunion and ten had a complex elbow injury (ligamentous rupture and comminuted radial head fracture with/without coronoid process fracture). In 22 patients the fracture was on the dominant side. The mean follow up time was 27 months (21 – 46 months). The post-operative results were:
The mean range of motion in flexion-extension was 130° (105° to 150°), while in pronation and supination was 74° (60°–80°). The mean grip strength was 96% of the contralateral side. There was no clinical laxity in the varus or valgus stress test. According to the Broberg-Morrey score the good and excellent result were 77%, while according to the Mayo Clinic Elbow Performance Score (MEPS) good and excellent results were up to 97% of the total. Pain was evaluated with a visual analogue scale. Finally there was also a radiographic evaluation of the patients (that yielded six cases of loosening or osteolysis without any clinical manifestation) Replacement of the radial head with the specific prosthesis leads to very satisfactory results when performed under specific indications.
To determine the effectiveness of Ilizarov external fixator in the treatment of complex fractures of the tibial plateau. From July 2006 to April 2009, we treated 10 patients with the Ilizarov fixator. Six men and four women ranging in age from 31 to 70 (mean age 56.3 years) were evaluated. All patients were preoperatively evaluated with Computed Tomography scans for better preoperative planning. Eight cases had fractures type VI according to Schatzker Classification and 2 cases type V. In all patients fixation included pushing olive wires or simple wires and 2 to 4 frames. In 4 patients minimal invasive open reduction was performed with use of bone allograft. In 2 fractures, we combined the treatment with minimal internal fixation There was no major complication trans- or postoperatively. The mean follow-up was 16 months (4–30). The mean hospitalization was 8 days and there were no cases of blood transfusion. Mobilization with no weight-bearing was immediately allowed, with partial weight bearing after 2 months and full weight bearing after 3 months. Three patients had minor pin tract complications. The average duration of external fixation was 120 days. All the fractures united and patients achieved full extension with more than 110 degrees of flexion. Ilizarov circular fixation is an alternative method of treatment for these fractures when internal fixation is contraindicated due to trauma to the soft tissue, deficiency of bone stock, and bony comminution
Aggrecan is a major constituent of joint cartilage. A prominent feature in joint disease is loss of Aggrecan. The aim of this study was to assess the relation between the concentration of Aggrecan in the synovial fluid of knee joint and this of the peripheral blood in patients suffering from end stage knee osteoarthritis 37 postmenopausal women suffering from end-stage idiopathic knee osteoarthritis, scheduled to undergo Total Knee Arthroplasty (TKA), were enrolled in this study. Their mean age was 69.8 years (range: 49–81 years). The serum levels of Aggrecan were evaluated one day pre-operatively whether synovial fluid levels from fluid taken during the operation day. Patients suffering from any endocrine disorder, rheumatoid or other secondary arthritis or any other disease that could interfere with the cartilage homeostasis were excluded from the study. Concentrations of aggrecan turnover were measured with appropriate assays. Moderate correlation between serum and synovial fluid concentrations of aggrecan was revealed (r= 0, 337, p=0,197) Serum levels of aggrecan may be related to the synovial concentration of Aggrecan in patients suffering from end stage knee osteoarthritis. The possible significant relationship between these markers may be of value in assessing cartilage degradation in patients with involvement of a single joint with a blood sample. However this correlation needs to be further investigated
The purpose of this study was to correlate the bone mineral density measured by DXA with the mechanical properties of the femoral neck.
A plane bone slice with 6mm thickness was sawed of femoral neck using a double cutting saw. The exact specimen dimensions were measured using a sliding calliper with high accuracy. All bone specimens were destructively tested on a material testing machine, in order to determine the material properties (Young’s modulus and yield stress) of the samples. The maximum available compression load was 100 kN with a load rate of 10 kN/min. The operational parameters and experimental data were fully controlled and handled by a graphical software package. Finally all data were evaluated and statistically analyzed.
The aim of this study was to extend the evaluation of the course of bone turnover markers over a longer period (12 postoperative months) following a TJA, and to assess the postoperative course for two of them (RANKL and Osteoprotegerin) for the first time.
The adolescents were divided in two groups. In the first group (n=47) were included adolescents wearing the brace for over two years (mean time of application 3, 3 years) and the second group (n=44) included adolescents, which have been treated with Boston brace for less than two years (mean time of application 1, 2 years). Every child completed a detailed questionnaire (SRS-22) concerning the evaluation of function, pain, self image, mental health and satisfaction with management. Both groups were comparable according to age and degrees of scoliotic curve.
Patients were divided into two groups according to the type of hip fracture. Group 1 included 299 patients with subcapital fractures, 61 men and 238 women and the second group 353 patients with intertrochanteric fractures, 98 men and 298 women. Patients’ demographics concerning age, sex, weight, height on admission at the hospital were compared between groups.
The use of polymethylmethacrylate (PMMA) bone cement loaded with antibiotics has become increasingly common in orthopaedic surgery. However, bacterial resistance in antibiotics is an increasing and emerging problem. PMMA bone cements containing different antibiotics, such as gentamicin plus vancomycin may be effective in prevention and treatment of infections (particularly from MRSA and MRSE). The purpose of this study was to determine the in vitro elution characteristics of gentamicin and vancomycin when combined in acrylic cement. Three groups of ten cement disks were prepared. Group I (control group) contained 0.5g of gentamicin per 40-g packet of Palacos-R+G powder. Group II contained 0.5g of gentamicin and 1g of powdered vancomycin and group III contained 0.5g of gentamicin and aqueous solution of vancomycin. Each cement disc (25mm x 20mm) was immersed in a 50-mL bath of normal saline at 37oC. Samples were taken at specific sampling intervals (1, 3, 7, 15, 30, 60, 90, 120, 150, 180 days). Antibiotic concentrations were measured using fluorescence polarisation immunoassay. With regards to gentamicin release, high but rapidly decreasing antibiotic levels were detected within the first week and low concentration after the first month. Samples from Group II eluted significantly more gentamicin (120%–20% during the first month). The influence on the gentamicin release was significant but minor when aqueous solution of vancomycin (Group III) was added. With regards to vancomycin release, high antibiotic levels were detected within the first 3 days and low concentrations after the first week. Cement samples from Group II eluted significantly more antibiotic in comparison with samples from Group III. Bone cements loaded with combinations of gentamicin and vancomycin are more effective in releasing gentamicin than bone cements with gentamicin as a single drug. Powdered vancomycin in cement samples has better elution characteristics in comparison with aqueous solution of vancomycin.
With regards to vancomycin release, high antibiotic levels were detected within the first 3 days and low concentrations after the first week. Cement samples from Group II eluted significantly more antibiotic (80%–100%) in comparison with samples from Group III during the first days. Gentamicin and vancomycin are detectable in measurements at 150 and 180 days samples.
i) powdered vancomycin or teicoplanin, ii) aqueous solution of vancomycin or teicoplanin.
With regards to samples from Groups IV and V (aqueous solutions of antibiotics) mechanical properties were significant deteriorated in comparison with cement samples from the other groups.
Aqueous solutions of antibiotics must not be added to the bone cement because they dramatically impair mechanical properties of the cement.
Patients were divided into two groups according to the injected drug. Group 1 or the injected group (n=91) received a caudal extradural injection (CEI) that consists of 12 to 15 ml of 2% xylocaine together with 1 ml of Betamethasone Dipropionate and Betamethasone phosphate. Group 2 or the placebo group (n=52), received a caudal extradural injection that consists of 6–8 ml of 2% xylocaine mixed with 6–8 ml of water for injection. The mean duration of symptoms was comparable between the two groups. In order to estimate the degree of recovery from symptoms, all patients answered a specific questionnaire. The Oswestry Disability Index Questionnaire (ODI) was answered by all patients on the first day of clinical examination, and on different follow-up periods after caudal injection. The straight leg-raising test was evaluated in all patients at the same follow – up periods.