23 research outputs found
Pseudo-outbreak of Brevundimonas diminuta
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
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
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
๊น์น์ ethyl carbamate ์ธก์
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ผ๋ฌธ(์์ฌ)--์์ธ๋ํ๊ต ๋ํ์ :์ํ์์ํ๊ณผ,1995.Maste
Ca2+ influx through the carbachol-activated nonselective cation channel in guinea-pig gastric myocyte
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ผ๋ฌธ(๋ฐ์ฌ)--์์ธ๋ํ๊ต ๋ํ์ :์ํ๊ณผ ์๋ฆฌํ์ ๊ณต,1998.Docto
Climatic and chemical factors on ethyl carbamate formation in Korean soysauce
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ผ๋ฌธ(๋ฐ์ฌ)--์์ธ๋ํ๊ต ๋ํ์ :์ํ์์ํ๊ณผ,2003.Docto
Analysis of blood culture results at the Severance Hospital during 1994-2003
์ํ๊ณผ/์์ฌ[ํ๊ธ]๊ท ํ์ฆ์ ๊ฐ์ฅ ์์คํ ๊ฐ์ผ์ฆ ์ค์ ํ๊ฐ์ง์ด๋ฏ๋ก ํ์ก์์ ๋ณ์์ฒด๋ฅผ ์ ์ํ๊ฒ ๊ฒ์ถํ๋ ์ผ์ ์ง๋ณ์ ์ง๋จ, ์ํํ๋จ ๋ฐ ์น๋ฃ์ง์นจ์ ์ธ์ฐ๋๋ฐ ๋งค์ฐ ์ค์ํ๋ค. ํ์ก๋ฐฐ์์์ ๋ถ๋ฆฌ๋๋ ๊ท ์ข
๊ณผ ํญ๊ท ์ ๊ฐ์์ฑ ์์์ ์๊ธฐ, ์ง์ญ ๋ฐ ๋์ํ์ ๋ฑ์ ๋ฐ๋ผ ๋ค๋ฅด๋ฏ๋ก ์ด๋ฅผ ๋ถ์ํ๋ ์ผ์ ํ์์ ๊ฒฝํ์ ์น๋ฃ๋ฅผ ์ํ ์ค์ํ ์๋ฃ๊ฐ ๋๋ค. ๋ณธ ์ฐ๊ตฌ์์๋ 1994-2003๋
๊ฐ์ ์ธ๋ธ๋์ค ๋ณ์ ์
์ ๋ฐ ์ธ๋ํ์์ ํ์ก๋ฐฐ์ ๊ฒฐ๊ณผ์ ํญ๊ท ์ ๊ฐ์์ฑ ๊ฒฐ๊ณผ๋ฅผ ํํฅ์ ์ผ๋ก ๋ถ์ํ์๋ค.์ด ๊ธฐ๊ฐ ๋์ 535,916 ๊ฒ์ฒด์ ํ์ก์ด ๋ฐฐ์๋์ด 24,877 ๊ฒ์ฒด (4.6%)๊ฐ ๋ฐฐ์ ์์ฑ์ด์์ผ๋ฉฐ ์์ฑ ํ์์๋ 13,102๋ช
์ด์๋ค. ๋ถ๋ฆฌ๋ ๊ท ์ข
์ค ํธ๊ธฐ์ฑ ์ธ๊ท ์ด 93.1%, ํ๊ธฐ์ฑ ์ธ๊ท ์ด 3.3%, ์ง๊ท ์ด 3.6%์ด์๋ค. ํํ ๋ถ๋ฆฌ๋ ๊ท ์ข
์ผ๋ก๋ Escherichia coli, Staphylococcus aureus, -hemolytic Streptococcus, Enterococcus, Klebsiella pneumoniae, Enterobacter, Pseudomonas aeruginosa ์์ด์๋ค.์ฐ๋๋ณ ๋ถ๋ฆฌ์จ์ E. faecium์ด 3.6%์์ 10.1%๋ก ์ฆ๊ฐํ์๊ณ , K. pneumoniae๋ 7.5%์์ 13.0%๋ก ์ฆ๊ฐํ์๋ค. -hemolytic Streptococcus์ E. coli๋ ๋ถ๋ฆฌ์๊ฐ ์ฆ๊ฐํ์์ผ๋ ๋ถ๋ฆฌ์จ์ ๋น์ทํ์๋ค. ์ฐ๋ น๊ตฐ๋ณ๋ก๋ 50์ธ ์ด์ ๊ตฐ์์ ๊ท ํ์ฆ์ด ๋ง์์ผ๋ฉฐ 2์ธ ๋ฏธ๋ง ๊ตฐ์์๋ Enterococcus์ ฮฑ-hemolytic Streptococcus์ ๋ถ๋ฆฌ๊ฐ ๋ง์๋ค. 50์ธ ์ด์ ๊ตฐ์์๋ Enterobacteriaceae์ ํฌ๋๋น ๋น๋ฐํจ ๊ทธ๋์์ฑ ๊ฐ๊ท ์ ๋ถ๋ฆฌ๊ฐ ๋ง์๋ค. ๋ค๊ท ์ฑ ๊ท ํ์ฆ์ ์ ์ฒด ์ธ๊ท ๋ฐฐ์ ์์ฑ ํ์ ์ค 2.6%๋ฅผ ์ฐจ์งํ์๋ค.ํญ๊ท ์ ๊ฐ์์ฑ ์ํ ๊ฒฐ๊ณผ์์ S. pneumoniae์ penicillin G ๋น๊ฐ์์ฑ์จ์ ํ์ ํ ์ฆ๊ฐํ ๋ฐ๋ฉด S. aureus์ oxacillin ๋ด์ฑ์ ๊ฐ์ํ์๊ณ , vancomycin์ ๋ด์ฑ์ธ S. aureus๋ ์์์ผ๋, vancomycin์ ๋ด์ฑ์ธ E. faecium์ด ํ์ ํ ์ฆ๊ฐํ์๋ค. ์ 3์ธ๋ cephalosporin์ ์ ๋ด์ฑ์ธ E. coli์ K. pneumoniae๋ ๊ฐ๊ฐ 10%์ 30% ๋ด์ธ์ด์์ผ๋ฉฐ, imipenem์ ๋ด์ฑ์ธ P. aeruginosa์ A. baumannii ๋ ํ์ ํ ์ฆ๊ฐํ์๋ค.์ด ์ฐ๊ตฌ์์ ๊ท ํ์ฆ ํ์์์ ๊ฐ์ฅ ํํ ๋ถ๋ฆฌ๋๋ ๊ฒ์ E. coli์ด๋ฉฐ S. aureus, -hemolytic Streptococcus, Enterococcus, Klebsiella pneumoniae๊ฐ ๋ณํจ์์ด ํํ ๋ถ๋ฆฌ๋๋ ์์ธ๊ท ์ด๋ฉฐ, Enterococcus์ ์ํ ๊ท ํ์ฆ๊ณผ ์ง๊ท ์ ์ํ ๊ท ํ์ฆ ํนํ C. albicans ๊ฐ ์๋ Candida ๊ท ์ข
์ ์ํ ๊ท ํ์ฆ์ด ์ฆ๊ฐํ๊ณ ์์ผ๋ฉฐ vancomycin์ ๋ด์ฑ์ธ E. faecium๊ณผ imipenem์ ๋ด์ฑ์ธ P. aeruginosa์ A. baumannii ๊ฐ ์ฆ๊ฐํ๊ณ ์๋ค๋ ๊ฒฐ๋ก ์ ์ป์๋ค.
[์๋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 ๋ฌธ๋-๋น๋ช ๋ฌธ๋ ์๊ธ๊ฒฉ์ฐจ์ ๋ณํ
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ผ๋ฌธ(์์ฌ)--์์ธ๋ํ๊ต ๋ํ์ :๊ฒฝ์ ํ๋ถ,2011.2. ์ด์ฒ ํฌ.Maste
์ ๊ฒ์ฒด์์ ๋ถ๋ฆฌ๋ ๋์ฅ๊ท ์ ํญ๊ท ์ ๋ด์ฑ ๊ธฐ์
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