Almost any kind of bacteria can be involved in prosthetic joint infections (PJI). In 2014 we collected data on 3 patients presenting with hip or knee pain and radiological signs of prosthetic joint mobilization without any other clinical or biochemical suspect of infection. Interestingly, in all cases we isolated bacteria very rarely involved in human infections: Cupriavidus pauculus, Ralstonia paucula and Neisseria flavescens. Both Cupriavidus pauculus and Ralstonia paucula are Gram negative environmental bacteria which can contaminate water (tap, pool and mineral) and have been isolated from a variety of human clinical sources including blood, wounds, sputum, urine, eye, throat and peritoneal fluid, as non pathogenic flora. In such two patients we were able to cure the infection with quinolones (both strains were sensible). Neisseria species are Gram-negative bacteria included among the proteobacteria. Neisseria flavescens is often found in the upper respiratory tract and oropharynx of humans, rarely associated with infectious process (necrotizing pneumonia and empyema). In this last patient we successfully used piperacillin-tazobactam i.v. during hospitalization and shifted to amoxicillin-clavulanate per os at discharge. In conclusion, any bacteria can induce PJI: in some cases pre-operative blood tests are normal and therefore useless. We need new tests to overcome this diagnostic problem (such as alpha-defensin) and we must check on rare bacteria prolonging incubation to a more extended period of time (as in Propionebacterium acnes or Mycobacterium spp) and/or sending samples to specialized laboratories. We thank all the medical and nurse staff of Prosthetic Joint Replacement Unit of Orthopaedic Center, Humanitas Research Hospital
The objective of the present study was to assess the efficacy and tolerability of antibiotic prophylaxis for THR at S. Corona Hospital Pietra Ligure SV (Italy). In our hospital the majority of prostethic device infections are due to MRSA, but recently we have described increment of infection due to Pseudomonas spp and other gram-. For this reason we used association of vancomycin plus pefloxacin in primary prophylaxis.
Positron emission tomography (PET) with 2-deoxy-2-[18F]fluoro-D-glucose (FDG) has evolved from a research imaging modality to a clinical practice for the assessment of malignancies. FDG, a nonspecific tracer of increased intracellular glucose metabolism, has been found to accumulate not only in malignant cells but also in infection and inflammation foci. Aim of the study was to evaluate the usefulness of FDG PET scan in patients with joint replacement.
Adolescent idiopathic scoliosis is known to aggregate within families; however, the pattern of inherited susceptibility is unclear. A genomic screen and statistical linkage analysis of a genetic isolate including individuals with idiopathic scoliosis is being performed to identify variants responsible for this disease. Scoliosis does not demonstrate a characteristic pattern of classical genetic (inherited) disorders. The severity of the disease within families can change and sometimes generations are skipped. However, the role of hereditary or genetic factors in the development of this condition is widely accepted. Numerous investigators are currently attempting to locate these genes. Studies based on a wide variety of populations have suggested an autosomal dominant mode of inheritance or sex-linked inheritance pattern. Other authors state that the “genetics link” may be complex, with an interaction of several genes rather than just one. To identify chromosomal loci encoding genes involved in susceptibility to idiopathic scoliosis and the trasmission way of scoliosis we are studing a genetic isolate. We have generated a 10,600 individual pedigree of the village of Campora, in the Cilento area, starting from the beginning of the 17th century connecting all the 1200 living inhabitants. The actual population of Campora derives from a few founders; therefore, the living inhabitants are all related to each other. The population will undergo clinical and radiographic evaluation for the presence and degree of scoliosis. A genomic screen and statistical linkage analysis of the families with individuals having idiopathic scoliosis will be performed. With this approach we can identify variants responsible for this complex disease and genetic links of scoliosis.