Purpose of the study: The aim of this work was to determine whether erythrocyte sedimentation rate (ESR), C-reactive protein (CRP) and alpha-1-antitrypsin (A1AT) levels are correlated significantly with early postoperative infectious complications after hip
Purpose: The indication for humeral or total shoulder prosthesis in patients with avascular osteonecrosis of the shoulder depends on the radiographic stage of the necrosis. The purpose of this study was to analyse the prognostic radiographic features enabling proper identification of the indications for humeral or total prostheses. Material and methods: This retrospective multicentric study included 53 shoulders operated on for prosthetic repair of avascular osteonecrosis. There were 20 men and 29 women, mean age 57 years. A humeral prosthesis was used in 34 cases and a total prosthesis in 19. Clinical assessment was based on the Constant score and the radiographic analysis used the Arlet and Ficat classification. Staging was II (n=4), III (n=16), IV (n=21) and V (n=12). Independently of the radiographic stage of necrosis, three characteristic groups were defined. Group 1 (19 shoulders) included necrosis without bony collapse of the humeral head. Group 2 (20 shoulders) included necrosis with bony collapse of the humeral head with preservation of the anatomic relations with the glenoid cavity. Group 3 (14 shoulders) included necrosis with bony collapse and impaction of the humeral head in the glenoid with medialisation of the humerus. Results: Preoperatively, presence of bony collapse was associated with decreased pain and motion score. Major joint stiffness was noted in group 3 (8). The humeral prosthesis gave similar results for groups 1 and 2 (Constant score 73 and 75.3). Less satisfactory results was the rule in group 3 (Constant score 51.6). There was a postoperative erosion of the glenoid cavity in 83% of the shoulders in group 3 versus 12.5% in group 1 and 17% in group 2. The total prosthesis optimised results despite persistence of a difference between groups 2 and 3 (Constant score 83 and 64 respectively). Discussion: Destabilisation of the glenohumeral joint by impaction of the humeral head against the glenoid cavity has an effect on the clinical result of the
The aim is: to point out, in respect of Italian case law trends, the concept and the boundaries of surgeon malpractice liability in evaluating and implanting new prosthesic materials. The surgeon is liable for damages caused by fraudulent intention or fault during his clinical and operating activity. In a civil perspective, it could be the result of either a breach of a contract or a tort, depending on the existing relationship between the surgeon and the patient; but in both case there might be a serious inexperience or a light imprudence or negligence to admit a fair compensation for damages. While in a criminal perspective, the personal injuries might be the result of a serious fault also in the area of imprudence and negligence to admit the application of criminal sanctions. Of course, personal liability of surgeon stands by vicarious liability of health unit. Civil sanctions are more effective than criminal sanctions, not only because they have a wider area of application, but also because they are more incisive in quantitative terms, considering the new guidelines on pecuniary and biological damages that make out, at the same time, a compensatory and punitive function. The surgeon, to be sure not to be affected by civil and criminal actions, might inform the patient about the operating features and the consequences of non operating, follow standardized protocols, use products and materials tested and certified by the most influential scientific literature, be care of post-operating effects and adopt all remedies and treatments that can eliminate or reduce post-operating risks, use the best and up-to-date techniques available. In any case he is not liable for unforeseeable events, even if they are in a causative relationship with surgical activity.
To assess the reliability of a biomimetic osteochondral scaffold Maioregen (Finceramica Faenza SpA, Faenza, Italt) as a salvage and joint-preserving procedure in the treatment of late stages of osteonecrosis of the knee. Nine active patients aged under 65 year presenting with clinical and radiological signs of SPONK were treated with a biomimetic osteochondral scaffold. All patients were clinically evaluated preoperatively and yearly with a minimum follow-up of 2 years. Subjective IKDC and Lysholm Knee Scale were used to assess clinical outcome. Pre-operative and post-operative pain was quantified with VAS scale. Activity level were evaluated pre-operatively and at follow-up according to Tegner Activity Scale.Purpose
Methods
Total temporomandibular joint (TMJ) replacements reduce pain and improve quality of life in patients suffering from end-stage TMJ disorders, such as osteoarthritis and trauma. Jaw kinematics measurements following TMJ arthroplasty provide a basis for evaluating implant performance and jaw function. The aim of this study is to provide the first measurements of three-dimensional kinematics of the jaw in patients following unilateral and bilateral
Despite the fact that uncemented cup and stems are specifically designed for dysplasia to recover the true acetabular region in Crowe IV and sometimes Crowe III additional surgical procedure are required. Purpose of the study is to analize surgical procedure and then reconstruction options on severe hip dysplasia.
64 cases were subjected to a greater trochanteric osteotomy. In 12 cases proximal femural shortening was associated. In 9 cases rotational abnormality and shortening were controlled with a distal femur osteotomy. 55 cases were treated by a shortening subtrochanteric osteotomy that allows corrections of any deformity. Only uncemented stems were used and in the majority of cases a specific device for displastic hip (Wagner Conus produced by Zimmer).
Despite this, the more promising outcomes are concerning shortening subtrochanteric osteotomy with uncemented stem but only early and mid-term data are available.
The primary etiology necessitating revision is aseptic loosening. According to the SOFCOT classification, the acetabular deficiency was grade IV 9 times, grade III 47 times, grade I or II 107 times. All the implanted acetabular components are SERF dual-mobility implants. This system consists of a metal back which can be HA-coated and Press Fit or cemented in a Kerboull cross or in a Novae Arm. The mobile-bearing insert which allows a dual articulation between the head and the metal back is of polyethylene. We implanted 119 HA-coated press-fit cups and cemented 44 dual-mobility cups in a support ring or in a Kerboull cross.
We reported 8 complications: 6 early dislocations and 2 acetabular revisions for secondary mobilisation of the cup.
With 4% dislocations at a mean follow-up of 56 months, the dual-mobility cup seems to provide high stability in revision hip surgery when other factors such as muscular deficiency, extended synovectomies, difficult implant placement, encourage an uncertain postoperative prosthetic stability. These results have to be compared to those of other systems such as constrained acetabular cups or tripolar cups.
From 1998 to July 2003 admissions for elective arthroplasty surgery in Derriford Hospital were nursed alongside other orthopaedic and general medical patients. Since August 2003 a policy of pre-operative MRSA screening and a unit reserved exclusively for MRSA-free joint replacement patients have been used. No transfers from other wards were allowed. Patients positive on screening underwent eradication and were admitted to a different ward where they received teicoplanin on induction (in addition to standard policy cephradine). All post-operative wound infections following THR & TKR were monitored (NINSS surveillance system). Infections within 3 months were recorded. A control of non-screened hip hemi-arthroplasty patients was used to ensure a departmental wide reduction in MRSA was not occurring. 1.9% MRSA carriage rate was detected over the study. Before screening, 0.59% of 3386 cases were acutely infected with MRSA. After institution of screening and a dedicated MRSA free unit, 0.10% of 1034 were acutely infected. This was a 6-fold decrease (p<0.05). The infection noted was in a patient treated outside the ringfenced unit on High Dependency. In fact the infection rate on the ringfenced unit was zero. MRSA infection in the control was statistically unchanged during this period. A policy of MRSA screening and an MRSA free joint replacement ward reduces the incidence of acute MRSA infections.Conclusion
Since Aug‘03 pre-operative MRSA screening &
a ward reserved exclusively for MRSA free joint replacement patients has been used. All postoperative wound infections within 3 months following THR &
TKR were monitored. Before screening, 0.59% of 3386 were acutely infected with MRSA. After institution of study policy, 0.10% of 1034, were infected with MRSA.. This was a 6 fold decrease (p<
0.05). The rate of MRSA infection in a control of hemiarthroplasties was unchanged during this period. A policy of MRSA screening &
an MRSA free joint replacement ward reduces the incidence of acute MRSA infections.
The use of implant biomaterials for
The surgical treatment of a secondary gonarthrosis caused by haemophilic arthropathy needs high quality in soft tissue balancing and accurate alignment in total knee arthroplasty (TKA), which are essential for good long-term results. Due to the early-onset severe arthropathy, haemophiliacs undergo
Post-surgical infections are still one of the most frequent adverse events in the
Introduction and Objectives: In this study we assessed the usefulness of preoperative urine cultures as a tool to prevent infections due to Gram negative microorganisms in patients undergoing
Aim. Prosthetic joint infections (PJI) due to Enterobacter cloacae are rare and often severe. The aim of this study is to describe cases with E. cloacae PJI. Method. We conducted a retrospective and a monocentric study in an orthopedic unit where complex bone and joint infections are managed. From 2012 to 2016, we included patients with PJI which perioperative samples were positive with E. cloacae. We collected background, clinical, biological and microbiological data of the current infection, surgical and medical treatment, and the outcome of these patients. Results. A total of twenty patients were included which 8 were male. Location was hip in 14 cases, knee in 5 cases and ankle in one case. The median time between arthroplasty and revision for infection was 3 years. Fourteen patients had at least two surgeries for previous PJI. The median time between the last surgery and the revision for E. cloacae infection was 31 days. Eleven patients were infected by extended-spectrum beta-lactamases (ESBL) strains. Most frequently, the antibiotics used were carbapenem in 9 cases, cefepim in 7 cases, a quinolone in 7 cases and fosfomycin in 4 cases. Infection was cured in 10 cases (50%) with a median time of follow-up of 24 months. Five patients had a recurrent infection, three due to Staphylococcus epidermidis, one to Staphylococcus epidermidis and Propionibacterium acnes and one to Escherichia coli. Four patients had a relapse of E. cloacae infection. One patient died from non-infectious cause (stroke). Conclusions. PJI infections due to E.cloacae usually occur early after the last
Aim. When a prosthetic joint infection (PJI) is suspected, guidelines recommend performing periprosthetic samples, at least one for histopathological examination and 3 to 6 for microbiological culture. The diagnosis of infection is based on the presence of neutrophil granulocytes whose number and morphology can be variable, resulting in definition of “acute” inflammation. The acute inflammation of periprosthetic tissue is supportive of infection. Since 2007, in our hospital, for all patients with suspected PJI who underwent surgery, from each sample taken by the surgeon, one part has been sent to the pathologist and the other one to the microbiologist. Our aim was to compare histopathological to microbiological results from samples taken intraoperatively at the same site. Method. We conducted a retrospective study including all surgeries for which at least one couple “histopathology-culture” was found. Exclusion criterion was a history of antimicrobial treatment 2 weeks prior the surgery. Results. From July 2007 to April 2015, 309 surgeries for suspected PJI were performed in 181 patients. Median age of the study population was 70 years, 60% of patients were male, 45% had a history of joint infection. The location of arthroplasty was knee in 50% of cases and hip in 46%, ankle and shoulder in 4%. Surgery was performed within one month after the last
PJI du to Enterobacter cloacae are rare and often severe. The aim of our study is to define the history of patients with such infections and their outcome. We conducted a retrospective monocentric study in an orthopedic unit where complex bone and joint infections are supported. From 2011 to 214 we selected patients with E. cloacae PJI based on data from the microbiology laboratory. In their files we collected information on their background, their medical and surgical history, antibiotics they received in the year before infection, the suspected portal of entry, the management and the outcome. Twelve patients were included, 7 male and 5 female. PJI was located to the hip in 8 cases, the knee in 3 cases and the ankle in one case. The average time between the placing of the first prosthesis and infection was 3 years. Eleven patients had one or more surgery for previous PJI. The average time elapsed since the last surgery was 30 days. Eleven patients had been treated with antibiotic combinations for at least 6 weeks, in the year before E cloacae infection. A portal of entry was identified only two times: urinary tract infection in one patient and catheter-related infection in one patient. Antibiotics the more often prescribed were carbapenems (n = 5) and cefepime (n = 4), each combined with quinolones (n =4) or fosfomycin (n = 3). Two patients required an additional debridement within an average of 18 days. Infectious outcome was favorable in 8 cases (67%) with a median duration of follow-up of 26 months. Two patients had a recurrent infection, one due to Streptococcus oralis and one to Candida albicans. One patient had a relapse of E cloacae infection. One patient died from unknown cause. PJI infections due to E.cloacae usually occur early after
Haemophilia is a lifelong inherited bleeding disorder characterized by spontaneous bleeding resulting in painful joint deformities. Even if
Introduction and purpose: To assess the long-term results of Coventry-type tibial osteotomies performed in our center. Materials and methods: This is a retrospective study. We carried out a review of 324 histories of Coventry-type osteotomies selected from a total of 76 with a mean follow-up of 12.9 years (minimum 5, maximum 25). We reviewed the patients’ preoperative assessment, postoperative assessment and last assessment or consultation before a total knee replacement. We also looked at the clinical evaluation of the patients’ pain, degree of arthritis on x-ray (Ahlbäck) and degree of postoperative correction obtained. Results: 76 cases. Mean age 57.9 years (range: 35–72). Radiological degree of arthritis: 36.8% slight; 57.9% moderate; 5.2% severe. We found that patients with slight arthritis at the end of follow-up (mean 12.5 years) had 71% of satisfactory results. Satisfactory results were seen in 50% of patients with moderate arthritis (mean follow-up 16 years). With reference to the degree of correction, patients with mild over-correction had better results (8–12° valgus), followed by those normally corrected (0–8° valgus). A total of 30 patients (41%) required TKR at the end of their evolution (mean period of 13 years to TKR). Conclusions: In spite of the advances of
Surgical site infection (SSI) is an important outcome indicator. It is estimated that 70% of post-operative infections present after discharge. A reliable post-discharge surveillance (PDS) method is yet to be described. The aim of this prospective cohort study was to assess the reliability of patient self-diagnosis. Telephone questionnaires were used following hip and knee