1.Utility of arterial gas analysis in multiple injured patients.
Kyoung Soo LIM ; Sung Oh HWANG ; Kap Jun YOON
Korean Journal of Clinical Pathology 1991;11(1):41-47
No abstract available.
Humans
2.Analysis of platelet glycoprotein IIIa by flow cytometry and diagnosis of Glanzmann's thrombasthenia.
Myung Seo KANG ; Jae Yoon CHANG ; Kap Jun YOON ; Hwang Min KIM
Korean Journal of Clinical Pathology 1992;12(3):305-309
No abstract available.
Blood Platelets*
;
Diagnosis*
;
Flow Cytometry*
;
Integrin beta3*
;
Thrombasthenia*
3.Prevalence of hepatitis C virus in liver diseases and high risk groups in Kangwon area.
Myung Seo KANG ; Won Keun SONG ; Kap Jun YOON ; Kyung Won LEE
Korean Journal of Blood Transfusion 1991;2(2):199-204
No abstract available.
Gangwon-do*
;
Hepacivirus*
;
Hepatitis C*
;
Hepatitis*
;
Liver Diseases*
;
Liver*
;
Prevalence*
4.Detection of N-myc Gene Amplification in Neuroblastoma Using the Semiquantitative Polymerase Chain Reaction.
Dong Woo PARK ; Chang Hoon LEE ; Kap Jun YOON ; Hwang Min KIM ; Woo Ick YANG
Korean Journal of Clinical Pathology 1997;17(2):351-359
No abstract available.
Genes, myc*
;
Neuroblastoma*
;
Polymerase Chain Reaction*
5.Rapid Detection of Mycobacteria usin Mycobacteria Growith Indicator tube(MGIT)and Ogawa Media.
Oh Gun KWON ; Hyun Mi CHO ; In Ho JANG ; Young UH ; Kap Jun YOON
Korean Journal of Clinical Microbiology 2000;3(2):116-120
BACKGROUND: As many as several weeks of incubation may be necessary for the recovery of mycobacteria when conventional culture media are used. Previous studies evaluating Mycobacteria Growth Indicator Tube (MGIT) as a rapid for the growth and detection of mycobacteria from clinical specimens have been reported. We compared MGIT with Ogawa media for the recovery of mycobacteria from clinical specimens. METHODS: Ninety nine clinical specimens received in the laboratory of Wonju Christian Hospital from June to September 199 were used for this study. The specimens from nonsterile body sites were digested, decontaminated, and concentrated, for culture and Ziehl-Neelsen stain, and specimen were inoculated onto MGIT tube and 3% Ogawa egg medium, and cultured for 8 weeks. RESULTS: Of the 38 specimens culture-positive for mycobacteria, 3 grew isolates in MGIT medium only, 8 grew isolates in Ogawa media only, and 27 grew isolates in both media. Mean (median, range) times to detection of mycobacteria were 13.7 (5.5, 2-48) days with MGIT and 19.6 (18, 13-37) days with Ogawa (P>0.05). The number recovered with MGIT plus Ogawa media was 24 (63.2%) within 14 days of receipt of specimen, and 31 (81.6%) within 21 days. The contamination rates were 31 % for MGIT and 1 % for Ogawa media. CONCLUSIONS: MGIT appears useful to quickly detect and identify mycobacteria from clinical specimens. However, because the number of culture-positive specimen in MGIT was not greater than those recovered with Ogawa media, MGIT should be used in combination with solid media to reduce turnaround times and increase the isolation rate.
Culture Media
;
Gangwon-do
;
Mycobacterium
;
Ovum
6.Rapid Detection of Mycobacteria usin Mycobacteria Growith Indicator tube(MGIT)and Ogawa Media.
Oh Gun KWON ; Hyun Mi CHO ; In Ho JANG ; Young UH ; Kap Jun YOON
Korean Journal of Clinical Microbiology 2000;3(2):116-120
BACKGROUND: As many as several weeks of incubation may be necessary for the recovery of mycobacteria when conventional culture media are used. Previous studies evaluating Mycobacteria Growth Indicator Tube (MGIT) as a rapid for the growth and detection of mycobacteria from clinical specimens have been reported. We compared MGIT with Ogawa media for the recovery of mycobacteria from clinical specimens. METHODS: Ninety nine clinical specimens received in the laboratory of Wonju Christian Hospital from June to September 199 were used for this study. The specimens from nonsterile body sites were digested, decontaminated, and concentrated, for culture and Ziehl-Neelsen stain, and specimen were inoculated onto MGIT tube and 3% Ogawa egg medium, and cultured for 8 weeks. RESULTS: Of the 38 specimens culture-positive for mycobacteria, 3 grew isolates in MGIT medium only, 8 grew isolates in Ogawa media only, and 27 grew isolates in both media. Mean (median, range) times to detection of mycobacteria were 13.7 (5.5, 2-48) days with MGIT and 19.6 (18, 13-37) days with Ogawa (P>0.05). The number recovered with MGIT plus Ogawa media was 24 (63.2%) within 14 days of receipt of specimen, and 31 (81.6%) within 21 days. The contamination rates were 31 % for MGIT and 1 % for Ogawa media. CONCLUSIONS: MGIT appears useful to quickly detect and identify mycobacteria from clinical specimens. However, because the number of culture-positive specimen in MGIT was not greater than those recovered with Ogawa media, MGIT should be used in combination with solid media to reduce turnaround times and increase the isolation rate.
Culture Media
;
Gangwon-do
;
Mycobacterium
;
Ovum
7.Evaluation of aniline blue dye method for rapid identification of candida albicans.
Kap Jun YOON ; Won Keun SONG ; In Ho JANG ; Dong Hun SHIN
Korean Journal of Clinical Pathology 1993;13(2):271-274
No abstract available.
Candida albicans*
;
Candida*
8.A Case of Bacteremia Caused by Vibrio parahaemolyticus.
Il Gu PARK ; Young UH ; In Ho JANG ; Kap Jun YOON ; Woo Ik JANG ; Jong In LEE
Korean Journal of Clinical Pathology 1997;17(2):303-307
Vibrio parahaemolyticus is a gram-negative halophilic organism commonly associated with outbreaks of acute gastroenteritis which also sometimes causes serious wound infection. It is an uncommon cause of bacteremia. We have experienced a case of bacteremia due to Vibrio parahaemolyticus in a 59-year old man who initially presented with edema and dyspnea. He was diagnosed as liver cirrhosis, gastric cancer, and hepatoma. On hospital day 13, Vibrio parahaemolyticus was isolated from blood culture. The isolate showed typical cultural and biochemical characteristics such as salt tolerance and did not ferment lactose. The isolate was intermediate to ampicillin but susceptible to other agents.
Ampicillin
;
Bacteremia*
;
Carcinoma, Hepatocellular
;
Disease Outbreaks
;
Dyspnea
;
Edema
;
Gastroenteritis
;
Humans
;
Lactose
;
Liver Cirrhosis
;
Middle Aged
;
Salt-Tolerance
;
Stomach Neoplasms
;
Vibrio parahaemolyticus*
;
Vibrio*
;
Wound Infection
9.Antimicrobial Susceptibilities and Serotypes of Group B Streptococci Isolated from Pregnant Women.
Young UH ; In Ho JANG ; Gyu Yel HWANG ; Kap Jun YOON ; Jang Yeon KWON ; Myeong Cheol KIM
Korean Journal of Clinical Pathology 1997;17(2):260-268
BACKGROUND: Recent data suggest that the colonization rate of group B streptococci(GBS) in pregnant women and the incidence of neonatal infections by GBS is increasing trend in Korea, but the antimicrobial susceptibilities and serotypes in pregnant women have not been reported in Korea. So, we studied to define the antimicrobial susceptibility patterns and frequency of serotypes of GBS in pregnant women. METHODS: The susceptibility and serotyping of 60 GBS isolates from 27 pregnant women and four isolates from their two neonates were tested by an agar dilution method and agglutination test, respectively. The typing sera used in this study were Ia, Ib, II, III, IV, and V. RESULTS: Minimal inhibitory concentration range of 60 GBS from pregnant women were penicillin G 0.015-0.12 microgram/ml, vancomycin 0.5-2 microgram/ml, clindamycin 0.015-4.0 microgram/ml, chloramphenicol 2-4 microgram/ml, erythromycin 0.015-2 microgram/ml, tetracycline 0.5-256 microgram/ml, cephalothin 0.12-0.25 microgram/ml, ceftriaxone 0.03-0.12 microgram/ml, respectively. The resistance rate of GBS were 6.7% to clindamycin, 0% to erythromycin, and 98.3% to tetracycline. Most of GBS serotypes from pregnant women in decreasing order were Ib(48.3%), Ia(24.1%), III(20.7%). CONCLUSION: All GBS strains isolated from pregnant women are highly susceptible to commonly used antimicrobial agents with the exception of tetracycline. The low prevalence of severe neonatal GBS infections in Korea is not due to the absence of serotype III, but probably due to a low genital carriage rate of GBS by pregnant women.
Agar
;
Agglutination Tests
;
Anti-Infective Agents
;
Ceftriaxone
;
Cephalothin
;
Chloramphenicol
;
Clindamycin
;
Colon
;
Erythromycin
;
Female
;
Humans
;
Incidence
;
Infant, Newborn
;
Korea
;
Penicillin G
;
Pregnant Women*
;
Prevalence
;
Serotyping
;
Tetracycline
;
Vancomycin
10.Microplate Identification System of Enterobacteriaceae.
Young UH ; Jeong Seog SON ; Gyu Yel HWANG ; In Ho JANG ; Kap Jun YOON ; Dong Min SEO
Korean Journal of Clinical Microbiology 1999;2(2):135-143
BACKGROUND: To access the accuracy and clinical usefulness of microplate identification (ID) system for the identification of Enterobacteriaceae, we compared microplate ID system with API 20E(bioMerieux, Etoile, France). METHODS: Ninety-two cultures of Enterobacteriaceae and one isolate of Aeromonas species were simultaneously identified by microplate ID system and the API 20E. Twenty biochemical tests used in microplate ID system were lactose, sucrose, and H2S in Kligler's iron agar media; indole, sucrose, raffinose, arabinose, trehalose, adonitol, dulcitol, sorbitol, cellibiose, methy-red, phenylalanine deaminase, ornithine decarboxylase, lysine decarboxylase, arginine dihydrolase, urease, and citrate in microplate; and oxidase test. The identification was obtained by considering percent likelihood(% ID), modal frequency and ID score method. RESULTS: Among the 92 cultures of Enterobacteriaceae and one isolate of Aeromonas species, agreement rate of identification according to the % ID between microplate ID system and API 20E were 90.3% to the species level and 97.8% to the genus level. CONCLUSIONS: For the identification of clinical Enterobacteriaceae isolates, the microplate ID system compares favorably with API 20E in identification accuracy and have the advantage of costsaving and easy to use.
Aeromonas
;
Agar
;
Arabinose
;
Arginine
;
Citric Acid
;
Enterobacteriaceae*
;
Galactitol
;
Iron
;
Lactose
;
Lysine
;
Ornithine Decarboxylase
;
Oxidoreductases
;
Phenylalanine
;
Raffinose
;
Ribitol
;
Sorbitol
;
Sucrose
;
Trehalose
;
Urease