23 research outputs found

    Pseudo-outbreak of Brevundimonas diminuta

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    Brevundimonas diminuta is a lactose non-fermenting Gram-negative rod associated with infection in immunocompromised patients. In three patients from two general wards, B. diminuta was isolated in blood culture sample. The clinical features of the patients did not coincide with the blood culture result, and pseudo-outbreak was suspected. These isolated were biochemically identified as Brevundimonas diminuta, and 16S rRNA sequencing confirmed their identification. The PFGE result showed a single pattern, and their clonality was assumed.ope

    Evaluation of Rapid Assay (Toc A/B Quik Chek) for the Detection of Clostridium difficile Toxins A and B

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    Background: Toxin immunoassay is widely used for rapid diagnosis of Clostridium difficile-associated diarrhea. The aim of this study was to evaluate the performance of Tox A/B Quik Chek test (TECHLAB, Blacksburg, VA, USA) compared to toxigenic culture. Methods: From September 2006 to August 2007, 959 stools were examined by Tox A/B Quik Chek test and toxigenic culture (C. difficile culture plus tcdB PCR using colonies obtained from culture). Results: Compared to the results of toxigenic culture, the sensitivity and specificity of Tox A/B Quik Chek test were 47.5% and 97.5%, respectively. Conclusion: The sensitivity of Tox A/B Quik Chek test was not high, but the specificity was high. Although Tox A/B Quik Chek test alone is not sufficient to diagnose Clostridium difficile-associated diarrhea, it may aid rapid diagnosis, early treatment and prevention of nosocomial spread of the infection, if supplemented by C. difficile culture or tissue culture cytotoxin assay.ope

    Two Cases of Clostridium citroniae Bacteremia in Cancer Patients

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    Clostridium citroniae is a novel species reclassified from C. clostridioforme. Clostridium species are obligate anaerobes and spore-forming gram-positive rods. However, C. citroniae stains gram negative and does not consistently produce spores, making it difficult to identify. We isolated C. citroniae from the blood and peritoneal fluid of one patient, and from the blood of another patient, both of whom were undergoing cancer chemotherapy.ope

    ๊น€์น˜์˜ ethyl carbamate ์ธก์ •

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    ํ•™์œ„๋…ผ๋ฌธ(์„์‚ฌ)--์„œ์šธ๋Œ€ํ•™๊ต ๋Œ€ํ•™์› :์‹ํ’ˆ์˜์–‘ํ•™๊ณผ,1995.Maste

    Ca2+ influx through the carbachol-activated nonselective cation channel in guinea-pig gastric myocyte

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    ํ•™์œ„๋…ผ๋ฌธ(๋ฐ•์‚ฌ)--์„œ์šธ๋Œ€ํ•™๊ต ๋Œ€ํ•™์› :์˜ํ•™๊ณผ ์ƒ๋ฆฌํ•™์ „๊ณต,1998.Docto

    Climatic and chemical factors on ethyl carbamate formation in Korean soysauce

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    ํ•™์œ„๋…ผ๋ฌธ(๋ฐ•์‚ฌ)--์„œ์šธ๋Œ€ํ•™๊ต ๋Œ€ํ•™์› :์‹ํ’ˆ์˜์–‘ํ•™๊ณผ,2003.Docto

    Analysis of blood culture results at the Severance Hospital during 1994-2003

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    ์˜ํ•™๊ณผ/์„์‚ฌ[ํ•œ๊ธ€]๊ท ํ˜ˆ์ฆ์€ ๊ฐ€์žฅ ์œ„์ค‘ํ•œ ๊ฐ์—ผ์ฆ ์ค‘์˜ ํ•œ๊ฐ€์ง€์ด๋ฏ€๋กœ ํ˜ˆ์•ก์—์„œ ๋ณ‘์›์ฒด๋ฅผ ์‹ ์†ํ•˜๊ฒŒ ๊ฒ€์ถœํ•˜๋Š” ์ผ์€ ์งˆ๋ณ‘์˜ ์ง„๋‹จ, ์˜ˆํ›„ํŒ๋‹จ ๋ฐ ์น˜๋ฃŒ์ง€์นจ์„ ์„ธ์šฐ๋Š”๋ฐ ๋งค์šฐ ์ค‘์š”ํ•˜๋‹ค. ํ˜ˆ์•ก๋ฐฐ์–‘์—์„œ ๋ถ„๋ฆฌ๋˜๋Š” ๊ท ์ข…๊ณผ ํ•ญ๊ท ์ œ ๊ฐ์ˆ˜์„ฑ ์–‘์ƒ์€ ์‹œ๊ธฐ, ์ง€์—ญ ๋ฐ ๋Œ€์ƒํ™˜์ž ๋“ฑ์— ๋”ฐ๋ผ ๋‹ค๋ฅด๋ฏ€๋กœ ์ด๋ฅผ ๋ถ„์„ํ•˜๋Š” ์ผ์€ ํ™˜์ž์˜ ๊ฒฝํ—˜์  ์น˜๋ฃŒ๋ฅผ ์œ„ํ•œ ์ค‘์š”ํ•œ ์ž๋ฃŒ๊ฐ€ ๋œ๋‹ค. ๋ณธ ์—ฐ๊ตฌ์—์„œ๋Š” 1994-2003๋…„๊ฐ„์˜ ์„ธ๋ธŒ๋ž€์Šค ๋ณ‘์› ์ž…์› ๋ฐ ์™ธ๋ž˜ํ™˜์ž์˜ ํ˜ˆ์•ก๋ฐฐ์–‘ ๊ฒฐ๊ณผ์™€ ํ•ญ๊ท ์ œ ๊ฐ์ˆ˜์„ฑ ๊ฒฐ๊ณผ๋ฅผ ํ›„ํ–ฅ์ ์œผ๋กœ ๋ถ„์„ํ•˜์˜€๋‹ค.์ด ๊ธฐ๊ฐ„ ๋™์•ˆ 535,916 ๊ฒ€์ฒด์˜ ํ˜ˆ์•ก์ด ๋ฐฐ์–‘๋˜์–ด 24,877 ๊ฒ€์ฒด (4.6%)๊ฐ€ ๋ฐฐ์–‘ ์–‘์„ฑ์ด์—ˆ์œผ๋ฉฐ ์–‘์„ฑ ํ™˜์ž์ˆ˜๋Š” 13,102๋ช…์ด์—ˆ๋‹ค. ๋ถ„๋ฆฌ๋œ ๊ท ์ข… ์ค‘ ํ˜ธ๊ธฐ์„ฑ ์„ธ๊ท ์ด 93.1%, ํ˜๊ธฐ์„ฑ ์„ธ๊ท ์ด 3.3%, ์ง„๊ท ์ด 3.6%์ด์—ˆ๋‹ค. ํ”ํžˆ ๋ถ„๋ฆฌ๋œ ๊ท ์ข…์œผ๋กœ๋Š” Escherichia coli, Staphylococcus aureus, -hemolytic Streptococcus, Enterococcus, Klebsiella pneumoniae, Enterobacter, Pseudomonas aeruginosa ์ˆœ์ด์—ˆ๋‹ค.์—ฐ๋„๋ณ„ ๋ถ„๋ฆฌ์œจ์€ E. faecium์ด 3.6%์—์„œ 10.1%๋กœ ์ฆ๊ฐ€ํ•˜์˜€๊ณ , K. pneumoniae๋Š” 7.5%์—์„œ 13.0%๋กœ ์ฆ๊ฐ€ํ•˜์˜€๋‹ค. -hemolytic Streptococcus์™€ E. coli๋Š” ๋ถ„๋ฆฌ์ˆ˜๊ฐ€ ์ฆ๊ฐ€ํ•˜์˜€์œผ๋‚˜ ๋ถ„๋ฆฌ์œจ์€ ๋น„์Šทํ•˜์˜€๋‹ค. ์—ฐ๋ น๊ตฐ๋ณ„๋กœ๋Š” 50์„ธ ์ด์ƒ ๊ตฐ์—์„œ ๊ท ํ˜ˆ์ฆ์ด ๋งŽ์•˜์œผ๋ฉฐ 2์„ธ ๋ฏธ๋งŒ ๊ตฐ์—์„œ๋Š” Enterococcus์™€ ฮฑ-hemolytic Streptococcus์˜ ๋ถ„๋ฆฌ๊ฐ€ ๋งŽ์•˜๋‹ค. 50์„ธ ์ด์ƒ ๊ตฐ์—์„œ๋Š” Enterobacteriaceae์™€ ํฌ๋„๋‹น ๋น„๋ฐœํšจ ๊ทธ๋žŒ์Œ์„ฑ ๊ฐ„๊ท ์˜ ๋ถ„๋ฆฌ๊ฐ€ ๋งŽ์•˜๋‹ค. ๋‹ค๊ท ์„ฑ ๊ท ํ˜ˆ์ฆ์€ ์ „์ฒด ์„ธ๊ท ๋ฐฐ์–‘ ์–‘์„ฑ ํ™˜์ž ์ค‘ 2.6%๋ฅผ ์ฐจ์ง€ํ•˜์˜€๋‹ค.ํ•ญ๊ท ์ œ ๊ฐ์ˆ˜์„ฑ ์‹œํ—˜ ๊ฒฐ๊ณผ์—์„œ S. pneumoniae์˜ penicillin G ๋น„๊ฐ์ˆ˜์„ฑ์œจ์€ ํ˜„์ €ํžˆ ์ฆ๊ฐ€ํ•œ ๋ฐ˜๋ฉด S. aureus์˜ oxacillin ๋‚ด์„ฑ์€ ๊ฐ์†Œํ•˜์˜€๊ณ , vancomycin์— ๋‚ด์„ฑ์ธ S. aureus๋Š” ์—†์—ˆ์œผ๋‚˜, vancomycin์— ๋‚ด์„ฑ์ธ E. faecium์ด ํ˜„์ €ํžˆ ์ฆ๊ฐ€ํ•˜์˜€๋‹ค. ์ œ3์„ธ๋Œ€ cephalosporin์ œ์— ๋‚ด์„ฑ์ธ E. coli์™€ K. pneumoniae๋Š” ๊ฐ๊ฐ 10%์™€ 30% ๋‚ด์™ธ์ด์—ˆ์œผ๋ฉฐ, imipenem์— ๋‚ด์„ฑ์ธ P. aeruginosa์™€ A. baumannii ๋Š” ํ˜„์ €ํžˆ ์ฆ๊ฐ€ํ•˜์˜€๋‹ค.์ด ์—ฐ๊ตฌ์—์„œ ๊ท ํ˜ˆ์ฆ ํ™˜์ž์—์„œ ๊ฐ€์žฅ ํ”ํžˆ ๋ถ„๋ฆฌ๋˜๋Š” ๊ฒƒ์€ E. coli์ด๋ฉฐ S. aureus, -hemolytic Streptococcus, Enterococcus, Klebsiella pneumoniae๊ฐ€ ๋ณ€ํ•จ์—†์ด ํ”ํžˆ ๋ถ„๋ฆฌ๋˜๋Š” ์›์ธ๊ท ์ด๋ฉฐ, Enterococcus์— ์˜ํ•œ ๊ท ํ˜ˆ์ฆ๊ณผ ์ง„๊ท ์— ์˜ํ•œ ๊ท ํ˜ˆ์ฆ ํŠนํžˆ C. albicans ๊ฐ€ ์•„๋‹Œ Candida ๊ท ์ข…์— ์˜ํ•œ ๊ท ํ˜ˆ์ฆ์ด ์ฆ๊ฐ€ํ•˜๊ณ  ์žˆ์œผ๋ฉฐ vancomycin์— ๋‚ด์„ฑ์ธ E. faecium๊ณผ imipenem์— ๋‚ด์„ฑ์ธ P. aeruginosa์™€ A. baumannii ๊ฐ€ ์ฆ๊ฐ€ํ•˜๊ณ  ์žˆ๋‹ค๋Š” ๊ฒฐ๋ก ์„ ์–ป์—ˆ๋‹ค. [์˜๋ฌธ]Blood culture is an important procedure for the determination of the etiologic agent of bacteremia. Analysis of blood culture results and antimicrobial susceptibility trend can provide the clinicians with relevant information for the empirical treatment of patients. In this study, the results of both the species and antimicrobial susceptibility of the isolates at the Severance Hospital during the years 1994-2003 were analyzed.During the study period, a total of 536,916 blood specimens were cultured, and 24,877 positive specimens were obtained from 13,102 patients. Among the isolates, 93.1% were aerobic or facultative anaerobic bacteria, 3.3% anaerobes, and 3.6% fungi.E. coli was isolated most frequently, followed by Staphylococcus aureus, -hemolytic Streptococcus, Enterococcus, Klebsiella pneumoniae, Enterobacter and Pseudomonas aeruginosa.The proportion of patients with E. faecium increased from 3.6% in 1994 to 10.1% in 2003, and those with K. pneumoniae increased from 7.5% in 1994 to 13.0% in 2003.-hemolytic Streptococcus was frequently isolated from the age group of less than 2 years, Enterobacteriaceae and glucose-nonfermenting gram-negative bacilli from the age group of more than 50 years.Polyclonal bacteremia was found in 2.6% of patients with positive blood cultures. The organisms frequently involved were E. coli, S. aureus, K. pneumoniae and Enterococcus.Penicillin-nonsusceptible S. pneumoniae, vancomycin-resistant E. faecium, imipenem-resistant P. aeruginosa and A. baumannii increased, but oxacillin-resistant S. aureus decreased significantly during the study period.It is concluded from the study that E. coli is the most common cause of bacteremia and that S. aureus, -hemolytic Streptococcus and Klebsiella pneumoniae remains to be frequently isolated pathogens. The bacteremia due to Enterococcus and fungi has increased. The proportion of non-albicans Candida species among Candida species increased. More frequent resistance of S. pneumoniae, E. faecium, P. aeruginosa and A. baumannii become problems in the selection of antimicrobial agent.ope

    1999~2008๋…„ ๋ช…๋ฌธ๋Œ€-๋น„๋ช…๋ฌธ๋Œ€ ์ž„๊ธˆ๊ฒฉ์ฐจ์˜ ๋ณ€ํ™”

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    ํ•™์œ„๋…ผ๋ฌธ(์„์‚ฌ)--์„œ์šธ๋Œ€ํ•™๊ต ๋Œ€ํ•™์› :๊ฒฝ์ œํ•™๋ถ€,2011.2. ์ด์ฒ ํฌ.Maste

    ์š” ๊ฒ€์ฒด์—์„œ ๋ถ„๋ฆฌ๋œ ๋Œ€์žฅ๊ท ์˜ ํ•ญ๊ท ์ œ ๋‚ด์„ฑ ๊ธฐ์ „

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    BACKGROUND: This study was designed to characterize urinary isolates of Escherichia coli that produce extended-spectrum beta-lactamases (ESBLs) and to determine the prevalence of other antimicrobial resistance genes. METHODS: A total of 264 non-duplicate clinical isolates of E. coli were recovered from urine specimens in a tertiary-care hospital in Busan in 2005. Antimicrobial susceptibility was determined by disk diffusion and agar dilution methods, ESBL production was confirmed using the double-disk synergy (DDS) test, and antimicrobial resistance genes were detected by direct sequencing of PCR amplification products. E. coli isolates were classified into four phylogenetic biotypes according to the presence of chuA, yjaA, and TSPE4. RESULTS: DDS testing detected ESBLs in 27 (10.2%) of the 264 isolates. The most common type of ESBL was CTX-M-15 (N=14), followed by CTX-M-3 (N=8) and CTX-M-14 (N=6). All of the ESBL-producing isolates were resistant to ciprofloxacin. PCR experiments detected genes encoding DHA-1 and CMY-10 AmpC beta-lactamases in one and two isolates, respectively. Also isolated were 5 isolates harboring 16S rRNA methylases, 2 isolates harboring Qnr, and 19 isolates harboring AAC(6')-Ib-cr. Most ESBL-producing isolates clustered within phylogenetic groups B2 (N=14) and D (N=7). CONCLUSION: CTX-M enzymes were the dominant type of ESBLs in urinary isolates of E. coli, and ESBL-producing isolates frequently contained other antimicrobial resistance genes. More than half of the urinary E. coli isolates harboring CTX-M enzymes were within the phylogenetic group B2ope
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