Decreased vancomycin susceptibility of coagulase-negative staphylococci in a neonatal intensive care unit:: Evidence of spread of Staphylococcus warneri

被引:55
作者
Center, KJ
Reboli, AC
Hubler, R
Rodgers, GL
Long, SS
机构
[1] Drexel Univ, St Christophers Hosp Children, Coll Med, Infect Dis Sect, Philadelphia, PA 19134 USA
[2] Univ Med & Dent New Jersey, Robert Wood Johnson Med Sch, Camden, NJ 08103 USA
关键词
D O I
10.1128/JCM.41.10.4660-4665.2003
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Coagulase-negative staphylococci (CoNS) are important pathogens in premature neonates; decreasing glycopeptide susceptibility has been observed among these isolates. The epidemiology of colonization with CoNS, the organisms' vancomycin susceptibilities, and genetic relatedness were studied over 6 months in a tertiary-care neonatal unit. A total of 321 isolates of CoNS were isolated. Seventy-five percent of the infants were colonized at admission, and virtually all were colonized thereafter. Common species were Staphylococcus epidermidis (69%), S. warneri (12%), S. haemolyticus (9.7%), and S. hominis (5.6%). A total of 3.9% of CoNS isolates had decreased vancomycin susceptibility (DVS) (MICs > 2.0 mug/ml); isolate recovery was associated with a stay in a neonatal intensive care unit for >28 days (P = 0.039), vancomycin exposure (P = 0.021), and S. warneri colonization (P < 0.0001). Nine of 12 (75%) CoNS with DVS were S. warneri, had enhanceable high-level resistance in vitro, were indistinguishable or closely related by pulsed-field gel electrophoresis, and were different from 29 vancomycin-susceptible S. warneri isolates. Epidemiological analysis suggested unsuspected nosocomial spread. Species determination in certain settings may aid in the understanding of emerging nosocomial problems.
引用
收藏
页码:4660 / 4665
页数:6
相关论文
共 43 条
[1]  
[Anonymous], 2002, MMWR MORB MORTAL WKL, V51, P902
[2]  
[Anonymous], 2002, MMWR MORB MORTAL WKL, V51, P565
[3]   PULSED-FIELD GEL-ELECTROPHORESIS AS A REPLACEMENT FOR BACTERIOPHAGE-TYPING OF STAPHYLOCOCCUS-AUREUS [J].
BANNERMAN, TL ;
HANCOCK, GA ;
TENOVER, FC ;
MILLER, JM .
JOURNAL OF CLINICAL MICROBIOLOGY, 1995, 33 (03) :551-555
[4]   SEPSIS WITH COAGULASE-NEGATIVE STAPHYLOCOCCI IN CRITICALLY ILL NEWBORNS [J].
BAUMGART, S ;
HALL, SE ;
CAMPOS, JM ;
POLIN, RA .
AMERICAN JOURNAL OF DISEASES OF CHILDREN, 1983, 137 (05) :461-463
[5]   Occurrence of nosocomial bloodstream infections in six neonatal intensive care units [J].
Brodie, SB ;
Sands, KE ;
Gray, JE ;
Parker, RA ;
Goldmann, DA ;
Davis, RB ;
Richardson, DK .
PEDIATRIC INFECTIOUS DISEASE JOURNAL, 2000, 19 (01) :56-65
[6]   NATIVE VALVE ENDOCARDITIS DUE TO COAGULASE-NEGATIVE STAPHYLOCOCCI - CLINICAL AND MICROBIOLOGIC FEATURES [J].
CAPUTO, GM ;
ARCHER, GL ;
CALDERWOOD, SB ;
DINUBILE, MJ ;
KARCHMER, AW .
AMERICAN JOURNAL OF MEDICINE, 1987, 83 (04) :619-625
[7]   STAPHYLOCOCCAL COLONIZATION IN A NEWBORN NURSERY, 1971-1976 [J].
CZARLINSKY, DK ;
HALL, RT ;
BARNES, WG ;
JENKINS, DC ;
RHODES, PG ;
HARRIS, DJ .
AMERICAN JOURNAL OF EPIDEMIOLOGY, 1979, 109 (02) :218-225
[8]   Genetic population structure of coagulase-negative staphylococci associated with carriage and disease in preterm infants [J].
de Silva, GDI ;
Justice, A ;
Wilkinson, AR ;
Buttery, J ;
Herbert, M ;
Day, NPJ ;
Peacock, SJ .
CLINICAL INFECTIOUS DISEASES, 2001, 33 (09) :1520-1528
[9]  
Dunne WM, 2001, CLIN INFECT DIS, V33, P135, DOI 10.1086/320890
[10]  
ETIENNE J, 1990, BRIT HEART J, V64, P831