1.Trends of Viral Respiratory Pathogens Detected in Pediatric Patients, 1996 Through 2001.
Kyutaeg YI ; Jung Oak KANG ; Jae Won OH ; Si Young HAM ; Tae Yeal CHOI
Korean Journal of Clinical Microbiology 2002;5(2):77-83
BACKGROUND: Acute lower respiratory tract infections are common causes of hospitalization in children and viruses are major causative agents. The causative viruses are known to be variable by age, region, or year. We investigated the recent 5-year epidemics of respiratory viruses for pediatric patients in two university hospitals in Korea. MATERIALS AND METHODS: From July 1996 through June 2001, viral agents were detected for the 2,317 pediatric patients who were hospitalized with acute respiratory tract infection in Hanyang University Hospital and Hanyang University Guri Hospital. We obtained nasopharyngeal aspirates on the day of admission and detected the viruses by indirect immunofluorescent staining method (Respiratory panel I viral Screening & Identification Kit, Light Diagnostics, Chemicon, Temecula, CA, USA). RESULTS: The causative viral agents were detected in 737(31.76%) patients. They were respiratory syncytial virus of 53.6%, influenza A virus 38.6%, adenovirus 5.5%, influenza B virus 1.9%, and parainfluenzavirus 0.4%. The epidemics of RSV were found during winter, but the epidemics of influenza A were found more frequently in spring, which had tendency of following the epidemic of RSV. Adenovirus was detected sporadically throughout year. RSV was found more frequently in patient with bronchiolitis and pneumonia and also found more frequently in patient less than 6 month of age. Influenza A and adenovirus were in patients of pneumonia and in more frequently in patient one to two year of age. CONCLUSION: Viruses were the leading causative agents of acute lower respiratory tract infections in pediatric patients. RSV was the most important causative agent. Influenza A virus was the second frequent viral agent and detection rate was higher than other reports. The detection rate of parainfluenza virus was lower than other reports from Korea or from abroad.
Adenoviridae
;
Bronchiolitis
;
Child
;
Hospitalization
;
Hospitals, University
;
Humans
;
Influenza A virus
;
Influenza B virus
;
Influenza, Human
;
Korea
;
Mass Screening
;
Orthomyxoviridae
;
Paramyxoviridae Infections
;
Pneumonia
;
Respiratory Syncytial Viruses
;
Respiratory Tract Infections
2.Evaluation of the VITEK 2 Advanced Expert System to Detect Extended- Spectrum beta-Lactamase Production in Klebsiella Pneumoniae and Escherichia Coli.
Kyutaeg YI ; Jung Oak KANG ; Kyung Suk KIM ; Tae Yeal CHOI
Korean Journal of Clinical Microbiology 2002;5(1):15-20
BACKGROUND: Extended-spectrum beta-lactamase (ESBL) producing Enterobacteriaceae are a serious problem worldwide because of their resistance to all beta-lactam antibiotics, except carbapenem or cephamycin. To prevent erroneous selection of antibiotics for ESBL producers, the role of clinical microbiology laboratory in accurate detection of this organism is important. Several ESBL detection methods has been proposed, and recently ESBL detection could become possible without additional test using automated microbiology system was developed for used in which detect ESBL by comparing obtained AST results with the pooled data about species-resistance mechanisms. This study was designed to evaluate the abilities of VITEK 2 system (bioMerieux, Marcy l'Etoile, France) and it's computer program, Advanced Expert System (AES) to detect ESBL-producing Escherichia coli (E. coli) and Klebsiella pneumoniae (K. pneumoniae). METHODS: A total 54 isolates of ESBL-positive (12 strains of E. coli, 42 strains of K. pneumoniae) and 33 ESBL-negative gram-negative isolates (21 of E. coli, 12 of K. pneumoniae) from hopitalized patients of Hanyang university Kuri hospital were evaluated. ESBL detection was done first by screening and confirmatory disk diffusion method recommended by NCCLS. Next, double disk synergy (DDS) test was performed. And also antimicrobial susceptibility of each isolate was determined with the VITEK 2 system and the results were analyzed with the expert system, AES. RESULTS: All the 54 ESBL-positive isolates by the NCCLS confirmatory test, demonstrated ESBL positive by both DDS test and VITEK 2 AES. Also all the 33 ESBL-negatives by the NCCLS confirmatory test, demonstrated ESBL negative by ESBL-negative isolates were confirmed as ESBL negative both DDS test and VITEK 2 AES. The sensitivities of ceftazidime and cefotaxime disks used in disk diffusion confirmatory test recommended by NCCLS were 92.6%, 81.5% respectively. The specificities were 100% in both disks. VITEK 2 AES predicted ESBLs as "ESBL"phenotype of 85.2% and as "ESBL+impermeability"phenotype of 14.8% according to resistance mechanisms.The 6 strains of K. pneumoniae revealing "ESBL+impermeability"phenotype were all resistant to cefoxitin, but 2 strains of E. coli demonstrating "ESBL+impermeability"phenotype was susceptible to cefoxitin. CONCLUSION: These results suggest that the VITEK 2 AES can identify ESBL accurately at least for K. pneumoniae and E. coli without additional confirmatory test. Also, AES can predict resistance mechanisms of ESBL, which is difficult to detect by routine AST results. Additional study is needed to reveal the molecular mechanism of the "ESBL+impermeability"phenotype.
Anti-Bacterial Agents
;
beta-Lactamases*
;
Cefotaxime
;
Cefoxitin
;
Ceftazidime
;
Diffusion
;
Enterobacteriaceae
;
Escherichia coli*
;
Escherichia*
;
Expert Systems*
;
Humans
;
Klebsiella pneumoniae*
;
Klebsiella*
;
Mass Screening
;
Pneumonia
3.Serotype Distribution and Antimicrobial Resistance of Invasive and Noninvasive Streptococcus pneumoniae Isolates in Korea between 2014 and 2016
Dong Chul PARK ; Si Hyun KIM ; Dongeun YONG ; In Bum SUH ; Young Ree KIM ; Jongyoun YI ; Wonkeun SONG ; Sae Am SONG ; Hee Won MOON ; Hae Kyung LEE ; Kyoung Un PARK ; Sunjoo KIM ; Seok Hoon JEONG ; Jaehyeon LEE ; Joseph JEONG ; Yu Kyung KIM ; Miae LEE ; Jihyun CHO ; Jong Wan KIM ; Kyeong Seob SHIN ; Sang Hyun HWANG ; Jae Woo CHUNG ; Hye In WOO ; Chae Hoon LEE ; Namhee RYOO ; Chulhun L CHANG ; Hyun Soo KIM ; Jayoung KIM ; Jong Hee SHIN ; Soo Hyun KIM ; Mi Kyung LEE ; Seong Gyu LEE ; Sook Jin JANG ; Kyutaeg LEE ; HunSuk SUH ; Yong Hak SOHN ; Min Jung KWON ; Hee Joo LEE ; Ki Ho HONG ; Kwang Sook WOO ; Chul Min PARK ; Jeong Hwan SHIN
Annals of Laboratory Medicine 2019;39(6):537-544
BACKGROUND: Several factors contribute to differences in Streptococcus pneumoniae serotype distribution. We investigated the serotype distribution and antimicrobial resistance of S. pneumoniae isolated between 2014 and 2016 in Korea. METHODS: We collected a total of 1,855 S. pneumoniae isolates from 44 hospitals between May 2014 and May 2016, and analyzed the serotypes by sequential multiplex PCR. We investigated the distribution of each serotype by patient age, source of the clinical specimen, and antimicrobial resistance pattern. RESULTS: The most common serotypes were 11A (10.1%), followed by 19A (8.8%), 3 (8.5%), 34 (8.1%), 23A (7.3%), and 35B (6.2%). The major invasive serotypes were 3 (12.6%), 19A (7.8%), 34 (7.8%), 10A (6.8%), and 11A (6.8%). Serotypes 10A, 15B, 19A, and 12F were more common in patients ≤5 years old, while serotype 3 was more common in patients ≥65 years old compared with the other age groups. The coverage rates of pneumococcal conjugate vaccine (PCV)7, PCV10, PCV13, and pneumococcal polysaccharide vaccine 23 were 11.8%, 12.12%, 33.3%, and 53.6%, respectively. Of the 1,855 isolates, 857 (46.2%) were multi-drug resistant (MDR), with serotypes 11A and 19A predominant among the MDR strains. The resistance rates against penicillin, cefotaxime, and levofloxacin were 22.8%, 12.5%, and 9.4%, respectively. CONCLUSIONS: There were significant changes in the major S. pneumoniae serotypes in the community. Non-PCV13 serotypes increased in patients ≤5 years old following the introduction of national immunization programs with the 10- and 13-polyvalent vaccines.
Cefotaxime
;
Humans
;
Immunization Programs
;
Korea
;
Levofloxacin
;
Multiplex Polymerase Chain Reaction
;
Penicillins
;
Pneumococcal Vaccines
;
Pneumonia
;
Serogroup
;
Streptococcus pneumoniae
;
Streptococcus
;
Vaccines