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Showing 4 results for Tabatabaei

S Noorbakhsh,, M Farhadi, A Tabatabaei, M Ghafari,
Volume 2, Issue 2 (Autumn – Winter 2009[PERSIAN] 2008)
Abstract

Abstract Background and objectives: Paranasal sinuses are the common place for infection in children and adults. Early and effective antibiotic treatment is necessary to reduce the infection period and mucosal injuries, and to prevent from the Involvements of orbit or CNS. This article aims to clarify the Serum immunoglobulins accompanying by Sinusitis in Children. Material and Methods: the Subjects of this Cross-Sectional study were 400 patients with paranasal sinusitis confirmed by imaging techniques. The study was conducted in infectious and ENT Clinics of Rasoul Akram hospital in 2003-2004. We measured the Levels of serum immoglobulins including IgG, IgM, IgA and IgE by standard radio-immunodiffusion test, and Compared with normal range of each age group. The data was analyzed by SPSS software (11.5) Results: The Subjects aged 4.42±2.62 are both male (70.7%) and female (29.3%). Maxilla is the most Common Sinus involved. Thirty-eight of them (95%) have increased IgG Level. Forty-four percent of children suffered from rhinosinusitis have been diagnosed with Immune-humoral disorders: the increase of IgE (N=9), Lack of IgA (N=3), decrease of Isolated IgG (N=2), decrease of both IgG and IgA (N=1) and Hyper IgM syndrome (N=3). There is Significant Correlation between different Immunoglobulins and duration of Sinusitis (P<0.05). Conclusion: The results of this study show that an increase of IgE is one of the most Common disorders in children suffering from Sinusitis and the incidence of immunity disorders is higher than the expected rate. Thus, we recommend the Immunologic assessment for Children Contracting with Sinusitis, esp. for protracted one. Key words: Rhinosinusitis, Hypogamma Globulinemia, Resistant Rhinosinusitis, Serum Immunoglobulins
Mm Soltan Dallal, M Hosseini, Tp Abedi Mohtaseb, A Tabatabaei Bafroei,
Volume 3, Issue 2 (Autumn – Winter 2010[PERSIAN] 2009)
Abstract

Abstract Background and objectives: Water-born diseases are typically caused by pathogens transmitted by orofecal way. Because it is no practical and no economical and also it is time-consuming to find water-born pathogens in water reservoirs, the laboratory studies are performed on the basis of indicator microorganism. Escherichia coli is considered as the most important indicator bacterium for water monitoring. The aim of this study was to evaluate the three methods of Pour Plate (PP), Most Probable Number (MPN) and Membrane Filter (MF) in isolation of Escherichia coli in well water of Parks. Material and Methods: One hundred and sixty five samples of well water, from five geographical zones of north, south, east, west and center of Tehran, were taken in a sterile condition and sent to microbiology department of health faculty to assess with three methods of PP, MPN and MF. The results were analyzed by chi-square. Results: The results indicate that 90 water samples (54.5%) aren’t health. The samples taken from south of Tehran are most contaminant than other zones. The highest contaminated Samples (54.5%) are related to membrane filtration method in comparison with MPN (34.5%) and PP (27.3%). Conclusion: Since the MF method can recognize the contaminants quickly and effectively, we recommend it more. Based on these results, it is essential to educate children not to drink well water in parks. Keywords: well water contamination, Escherichia coli, Tehran's parks
Roya Rafiee , Fereshte Eftekhar , Seyed Ahmad Tabatabaei , Dariush Minaee-Tehrani ,
Volume 10, Issue 3 (May-Jun 2016 2016)
Abstract

ABSTRACT

       Background and Objectives: Pseudomonas aeruginosa is the most frequent opportunistic pathogen isolated from the sputum of patients with cystic fibrosis (CF). Resistance to β -lactam antibiotics may arise from over expression of the naturally occurring AmpC cephalosporinases or acquired extended-spectrum β-lactamases (ESBL). The aim of this study was to determine the antibiotic resistance profiles as well as the prevalence of ESBL and AmpC production in clinical isolates of P. aeruginosa from CF patients in Tehran.

         Methods: Antibiotic resistance of 50 non-duplicate P. aeruginosa isolates was determined by the disc diffusion method. AmpC β-lactamase production was detected by the antagonism disc test and ESBL production was detected by the phenotypic confirmatory test. The presence of ESBL and AmpC genes was assessed by PCR, followed by sequencing the PCR products.

         Results: The antibiotic resistance rates were as follows: 22% to ceftriaxone, 20% to cefotaxime, 10% to imipenem, 8% to carbenicillin and 6% to ticarcillin, 4% each to cefepime, tobramycin, amikacin and aztreonam and 2% to each piperacilin, meropenem and ceftazidime. AmpC production was observed in 47 isolates (94%) and ESBL production was observed in one isolate (2%). PCR results showed that all isolates carried the blaAmpC β-lactamase gene. One multidrug-resistant isolate carried both blaTEM and blaPER-1 genes.

        Conclusion: The results showed that despite the low rate of antibiotic resistance in P. aeruginosa CF isolates,the  presence of multiple β-lactamases even in one isolate is alarming and can complicate the already difficult treatment of chronic infections in the lungs of CF patients.

         


Mohammad Tabatabaei, Aslam Dehvari, Bita Geramizadeh, Mohammad Hadi Niakan,
Volume 14, Issue 1 (Jan-Feb 2020)
Abstract

ABSTRACT
           Background and Objective: Bilophlia spp. are gram-negative, pleomorphic rod, obligate anaerobe, oxidase-negative, catalase-positive and non-motile bacteria. B. wadsworthia is type species of genus Bilophila with the additional characteristic of urea hydrolysis. B. wadsworthia can be found in a variety of anaerobe infections, particularly appendicitis and intra-abdominal infection that are considered as important opportunistic pathogens.
           Methods: This study was designed to identify Bilophila spp. in clinical specimens by culture and PCR. We examined 91 DNA samples extracted from infected appendix tissues with specific primers.
           Results: Data showed that Bilophila spp. DNA existence in 53.85% (n=49) provided appendiceal tissue.
           Conclusion: The pathological and molecular examination of infected appendiceal tissues revealed that B. wadsworthia is able to act as the primary cause of significant lesions in the appendicle tissues.
           Key words: Bilophila spp., Appendectomy, Appendicle specimens, PCR, Nucleotide sequencing


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