1.The Short Time Antibacterial Effect of Tetracaine Hydrochloride(Pontocaine(R)): in vitro study.
Journal of the Korean Ophthalmological Society 1989;30(3):331-334
The short time antibacterial effect of tetracaine hydrochloride was studied. S. aureus, Coagulase Negative Staphylococcus and P. aeruginosa were each incubated with tetracaine hydrochloride(preservative free) for 18 hours or for 2 minutes and then diluted and cultured on nutrient agar plate. Colony counts were done after 18 hours. In cases of 18 hours incubation, there was no growth of microbials in 0.5%, 0.1% tetracaine hydrochloride, but there was no inhibitory effect of 0.02% of tetracaine hydrochloride on growth of microbials, irrespective of inoculum amount. In cases of 2 minutes incubation with 0.5% tetracaine hydrochloride, there was no difference between the amount of microbial inoculum and colony count. Above in vitro study indicates that tetracaine hydrochloride has no inhibitory effect on bacterial growth in short time exposure less than 2 minutes.
Agar
;
Coagulase
;
Staphylococcus
;
Tetracaine*
2.The Short Time Antibacterial Effect of Tetracaine Hydrochloride(Pontocaine(R)): in vitro study.
Journal of the Korean Ophthalmological Society 1989;30(3):331-334
The short time antibacterial effect of tetracaine hydrochloride was studied. S. aureus, Coagulase Negative Staphylococcus and P. aeruginosa were each incubated with tetracaine hydrochloride(preservative free) for 18 hours or for 2 minutes and then diluted and cultured on nutrient agar plate. Colony counts were done after 18 hours. In cases of 18 hours incubation, there was no growth of microbials in 0.5%, 0.1% tetracaine hydrochloride, but there was no inhibitory effect of 0.02% of tetracaine hydrochloride on growth of microbials, irrespective of inoculum amount. In cases of 2 minutes incubation with 0.5% tetracaine hydrochloride, there was no difference between the amount of microbial inoculum and colony count. Above in vitro study indicates that tetracaine hydrochloride has no inhibitory effect on bacterial growth in short time exposure less than 2 minutes.
Agar
;
Coagulase
;
Staphylococcus
;
Tetracaine*
3.Some Bacteriological Problems of Skin Flora.
Korean Journal of Dermatology 1985;23(5):563-580
The bacterial group which we usually consider as resident flora sometimes changes into opportuniistic pathogen which produces oppartunistic infection, so that attention to resident flora remarkably increased. The main topics of bacterioloical problems of skin flora are as follows: (1) selective localization of resident flora, (2) members of resident flora and their changes by age and area, (3) the role of action of resident flora, (4j the problems of Micrococcus, (5) coagulase negative Staphylococci, (6) coagulase positive Staphylococci, (7) the problerns of Propionilbacterium(P) acnes, (8) typing of propionibacteria existing on human skin, (9) antibiotic sensitivities of P. acnes, (10) effect of tetracycline on lipase productivity oi P. acnes.
Coagulase
;
Efficiency
;
Humans
;
Lipase
;
Micrococcus
;
Skin*
;
Tetracycline
4.Prevalence of Teicoplanin-resistant Staphylococci and Evaluation of the Disk Diffusion Test for Testing the Susceptibility of Staphylococci to Teicoplanin.
Myungshin KIM ; Yeon Joon PARK ; Byung Kee KIM ; Sun Moo KIM ; Sang In SHIM
Korean Journal of Infectious Diseases 1998;30(2):151-155
BACKGROUND: Teicoplanin is a glycopeptide antimicrobial agent effective against methicillin-resistant staphylococci. Decreased susceptibility of staphylococci to glycopeptides has been increasing. Teicoplanin diffuses poorly in agar and therefore the correlation between the inhibition zone diameter and the minimal inhibitory concentration(MIC) is rather poor. The purpose of this study was to evaluate the prevalence of teicoplanin-resistant staphylococci and to assess the reliability of inhibition zone diameters for determining the susceptibility of staphylococci to teicoplanin by comparing the results of the agar dilution MICs. METHODS: From June to August 1997, 290 clinical isolates of staphylococci(77 coagulase negative staphylococci(CNS), 213 Staphylococcus aureus) were collected. The antimicrobial susceptibilities to teicoplanin were determined by inhibition zone diameter and the results were compared with the MICs determined by the agar dilution method. RESULTS: Among 77 CNS strains, 75(97.4%) were susceptible and 2(2.6%) were intermediate by agar dilution method and all 213 strains of S. aureus were susceptible to teicoplanin. There was a poor correlation(r=0.50) between the zone diameters of inhibition and agar dilution MICs. In comparison with the results of disk diffusion test and agar dilution MIC, eight (2.8%) out of 290 isolates showed discrepancies (major error rates : 0.3%, minor error rates: 2.4%). CONCLUSIONS: Two(2.6%) out of 77 strains of CNS and none of 213 S. aureus strains revealed decreased susceptibility to teicoplanin. And the inhibition zone diameter was less reliable in determining the susceptibility of staphylococci than MICs. Therefore, the more effective and convenient method is needed.
Agar
;
Coagulase
;
Diffusion*
;
Glycopeptides
;
Methicillin Resistance
;
Prevalence*
;
Staphylococcus
;
Teicoplanin*
5.Epidemiology of Early and Late Onset Neonatal Sepsis.
Journal of the Korean Society of Neonatology 2012;19(3):115-120
Sepsis is a significant cause of mortality and morbidity in the neonates. This article reviews the studies which analyzed the causative pathogens of neonatal sepsis in Korea. The changes of bacterial pathogens in other countries are reviewed. This review also introduces the recent updates of preventive and immunotherapy in neonatal sepsis. Coagulase negative staphylococci and Staphylococcus aureus were the most commonly isolated organisms in the early and late onset neonatal sepsis in Korea. Group B streptococcus was a rare cause of the early onset disease in Korea. To obtain a more accurate data, prospective nationwide surveillance will be warranted.
Coagulase
;
Humans
;
Immunotherapy
;
Infant, Newborn
;
Korea
;
Sepsis
;
Staphylococcus aureus
;
Streptococcus
6.Clinical Results of Bacterial Endophthalmitis: Bacterial Culture and Visual Acuity Outcomes.
Journal of the Korean Ophthalmological Society 2011;52(10):1173-1181
PURPOSE: To evaluate the clinical characteristics of bacterial culture, and visual outcome in patients with acute endophthalmitis. METHODS: Clinical records of patients treated for acute endophthalmitis in GNUH from 2000 to 2009 were reviewed. The specimens for culture were obtained from the anterior chamber or vitreous. Clinical outcome measures were bacterial culture, culture rate, and final visual acuity. RESULTS: Cultures (total 59 cases) showed bacterial growth in 37 cases (63%). Among 35 cases vitreous specimens, bacteria growth was found in 22 cases (63%), and from the 27 anterior chamber specimens, 12 cases (44%) were culture positive. From these 37 bacterial-positive cultures, 11 (30%) were coagulase negative Staphylococcus species, 16 (43.0%) were other Gram-positive species, 9 (24%) were Gram-negative species, and 1 (3%) produced a polymicrobial culture. Final visual acuity above 0.5 was achieved in 16 of 59 (27%) cases and coagulase negative Staphylococcus species had the greatest proportion being 5 of 11 (45%). CONCLUSIONS: The bacterial culture positivity rate in bacterial endophthalmitis was 63%, and the culture yield rate from the vitreous was higher than the anterior chamber aqueous samples. Coagulase negative Staphylococcus species were the most common causative organisms and showed the best final visual outcome in endophthalmitis.
Anterior Chamber
;
Bacteria
;
Coagulase
;
Endophthalmitis
;
Humans
;
Outcome Assessment (Health Care)
;
Staphylococcus
;
Visual Acuity
7.Evaluation of Effectiveness and Safety of Pazeron Treatment of Infection in Obstetric and Gynecology; Phase IV Clinical Study.
Jae Wook KIM ; Eun Kyoung CHOI ; Yong Won PARK ; Young Tae KIM
Korean Journal of Obstetrics and Gynecology 1999;42(9):2071-2077
OBJECTIVES: This study was planned to evaluate the clinical efficacy and safety of cefazedone in the treatment of patients with infectious disease in the field of obstetrics and gynecology. METHOD: Cefazedone was used in 20 patients with infectious disease in obstetrics and gynecology, who visited the department of obstetrics and gynecology, Yonsei university college of medicine, from June 1998 through July 1999. RESULTS: The mean age of the patients was 42.5 years(range of 18 to 68 years) and 17 of patients were diagnosed as pelvic inflammatory disease(PID), 2 were urinary tract infection due to huge ovarian tumor, and 1 was Bartholin's gland abscess. Cefazedone was proven its efficacy in treating infections of obstetrics and gynecology so as to reach 100% of response rate. The cefazedone was sensitive to all isolated organisms - G. vaginalis, E. coli, Staphylococcus, coagulase (+), etc. In the course of treatment, 1 patient experienced mild nausea, another 1 patient complained mild diarrhea, and another 1 patient showed transient leukopenia but their symptoms and signs were disappeared with only conservative management. There was no significant renal and hepatic function changes. CONCLUSION: Our results suggest that cefazedone is relatively effective in treating infections of obstetrics and gynecology to show excellent antibacterial effects and low incidence of complications.
Abscess
;
Coagulase
;
Communicable Diseases
;
Diarrhea
;
Gynecology*
;
Humans
;
Incidence
;
Leukopenia
;
Nausea
;
Obstetrics
;
Staphylococcus
;
Urinary Tract Infections
8.Experimental Studies on the Sterilization of The Soft Contact Lens.
Journal of the Korean Ophthalmological Society 1974;15(1):9-15
Mycon-soft lenses (made by Tokyo contact lens Co., Japan) were contaminated experimentally with coagulase positive staphylococcus aureus and pseudomonas aeruginosa and sterilizing effects of some disinfectants (3% H2O2, 6% H2O2, 0.1% Benzalkonium and 1:1000 Merthiolate solutions) on those contaminated lenses were studied. The following results were obtained: 1. SCL contaminated with staphylcoccus were sterilized by soaking in 3% H2O2, 6% H2O2, or 1:1000 Merthiolate solution over 15 minutes, and in 0.1 Benzalkonium over 60 minutes. 2. SCL contaminated with pseudomonas aeruginosa were sterilizd by soaking in 6% H2O2 over 15 minutes, in 1:1000 MerthioJate solution over 60 minutes, in 3% H2O2 over 60 minutes, but no sterilization was obtained by soaking in 0.1 % Benzalkonium solution for less than 180 minutes. 3. No signs of irritation were noted on rabbit corneas fitted with SCL after soaking in 3% H2O2 or 6% H2O2 for 15 minutes followed by soaking in 20cc of normal saline for 15 minutes.
Benzalkonium Compounds
;
Coagulase
;
Contact Lenses, Hydrophilic*
;
Cornea
;
Disinfectants
;
Pseudomonas aeruginosa
;
Staphylococcus aureus
;
Sterilization*
;
Thimerosal
9.Pathogens of Corneal Ulcer (II).
Journal of the Korean Ophthalmological Society 1987;28(1):31-36
One hundred and thirty-two cases(132 eyes) of corneal ulcer were analysed on the clinical and etiologic basis. The history of evident ocular trauma was found in 28.8% of the cases and ocular disease was found in 7.6% of the cases. Positive results were 16/55 in smear and 33/61 in culture, and the most common isolate was coagulase negative staphylococcus in bacteriologic studies. In fungal studies, positive results were 1/42 in smear and 5/42 in culture, and Aspergillus was the most common isolate. Cephalexin was the most sensitive antibiotics for Gram positive organism and carbenicillin and gentamicin were the most sensitive antibiotics for Gram negative orgamsm. These results indicate that gentamicin and cephalexin in combination would be recommended as the initial treatment of wide-spectrum antibiotics coverage for bacterial corneal ulcer until the final culture results and senitivity are available.
Anti-Bacterial Agents
;
Aspergillus
;
Carbenicillin
;
Cephalexin
;
Coagulase
;
Corneal Ulcer*
;
Gentamicins
;
Staphylococcus
10.Storage of the split-thickness skin piece using proper antibiotics.
Journal of the Korean Society of Plastic and Reconstructive Surgeons 1998;25(6):997-1002
Todays, remnant split-thickness skin graft is stored for graft failure or for delayed grafting. Refrigerated skin is usually stored for 3 weeks, after which, cellular respiration ceaces. Even though the refrigerated skin can be used before 3 weeks after harvest, the success rate of the skin graft is usually lower than in case of fresh skin. One of the most reliable explanations is multiplication of microorganisms on the stored skin, that is, the more microorganisms on the refrigerated skin, the less the success rate of grafts. For this reasons, some kind of antibiotics have been used for storage of the split-thickness skin piece. But there is no report about the effect of antibiotics on stored skin. We want to know the effect of the antibiotics on stored skin. For this purpose, we did three experiments for qualititative bacteriology of refrigerated skin. Experiment 1 was qualititative identification of microorganisms colonizing split-thickness skin after 2 weeks storage in low temperature, and sensitivity tests for identified microorganisms. On the basis of experiment 1, the proper antibiotics were selected and samples of split-thickness skin were stored using this antibiotics. At 2 weeks after storage in low temperature, samples of split-thickness skin were cultured for identification of bacterial growth. This is experiment 2. Experiment 3 is histologic examination of the split-thickness skin involved in experiment 1 and 2.In the experiment 1, we found five kinds of microorganisms in 9 out of 30 split-thickness skin samples. The most common microorganism was coagulase negative Staphylococcus which was found in 4 samples. Through the antibiotics sensitivity test, teicoplanin was selected as the most proper antibiotics. In experiment 2, we could not find any microorganisms in 30 split-thickness skin samples. In experiment 3, there were no histologic differences in the split-thickness skin samples whether antibiotics were used or not. Through these results, we have confirms that split-thickness skin pieces are more safely stored using proper antibiotics.
Anti-Bacterial Agents*
;
Bacteriology
;
Cell Respiration
;
Coagulase
;
Colon
;
Skin*
;
Staphylococcus
;
Teicoplanin
;
Transplants