Molecular correlation for the treatment outcomes in bloodstream infections caused by Escherichia coli and Klebsiella pneumoniae with reduced susceptibility to ceftazidime

被引:97
作者
Wong-Beringer, A
Hindler, J
Loeloff, M
Queenan, AM
Lee, N
Pegues, DA
Quinn, JP
Bush, K
机构
[1] Western Univ Hlth Sci, Coll Pharm, Pomona, CA 91766 USA
[2] Univ Calif Los Angeles, Med Ctr, Dept Clin Microbiol, Los Angeles, CA 90024 USA
[3] Univ Calif Los Angeles, Med Ctr, Dept Pharmaceut Serv, Los Angeles, CA 90024 USA
[4] Univ Calif Los Angeles, Med Ctr, Dept Med, Los Angeles, CA 90024 USA
[5] RW Johnson Pharmaceut Res Inst, Raritan, NJ 08869 USA
[6] Univ Illinois, Chicago, IL USA
关键词
D O I
10.1086/324742
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Data are limited on outcomes of treatment with extended-spectrum cephalosporins (ESCs) for infections caused by Enterobacteriaceae that produce extended-spectrum beta -lactamases (ESBLs). This study describes the largest treatment experience of a nonoutbreak series of bloodstream infections caused by strains of Escherichia coli (23 episodes) and Klebsiella pneumoniae (13 episodes) with a ceftazidime minimal inhibitory concentration of greater than or equal to2 mug/mL. E. coli isolates produced a greater variety of beta -lactamase types than did K. pneumoniae isolates, among which ESBL production was predominant. Five ESBL types were identified: TEM-12, TEM-71, TEM-6, SHV-12, and SHV-5. Most patients were treated empirically with an ESC-based regimen. A favorable response to treatment with a nonceftazidime ESC was observed when the causative pathogen produced either TEM-6 or TEM-12; ceftazidime treatment was associated with failure of therapy in all patients. Despite the limited clinical success, ESCs are currently not recommended for the treatment of serious infections caused by ESBL-producing strains.
引用
收藏
页码:135 / 146
页数:12
相关论文
共 29 条
[1]  
ARLET G, 1995, FEMS MICROBIOL LETT, V134, P203, DOI 10.1111/j.1574-6968.1995.tb07938.x
[2]   MOLECULAR EPIDEMIOLOGY OF PLASMID SPREAD AMONG EXTENDED BROAD-SPECTRUM BETA-LACTAMASE-PRODUCING KLEBSIELLA-PNEUMONIAE ISOLATES IN A PEDIATRIC HOSPITAL [J].
BINGEN, EH ;
DESJARDINS, P ;
ARLET, G ;
BOURGEOIS, F ;
MARIANIKURKDJIAN, P ;
LAMBERTZECHOVSKY, NY ;
DENAMUR, E ;
PHILIPPON, A ;
ELION, J .
JOURNAL OF CLINICAL MICROBIOLOGY, 1993, 31 (02) :179-184
[3]  
BRUNBUISSON C, 1987, LANCET, V2, P302
[5]   A FUNCTIONAL CLASSIFICATION SCHEME FOR BETA-LACTAMASES AND ITS CORRELATION WITH MOLECULAR-STRUCTURE [J].
BUSH, K ;
JACOBY, GA ;
MEDEIROS, AA .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1995, 39 (06) :1211-1233
[6]  
*CDCP, 2000, MMWR-MORBID MORTAL W, V48, P1167
[7]   TREATMENT OF A MENINGITIS DUE TO AN ENTEROBACTER-AEROGENES PRODUCING A DEREPRESSED CEPHALOSPORINASE AND A KLEBSIELLA PNEUMONIAE PRODUCING AN EXTENDED-SPECTRUM BETA-LACTAMASE [J].
DECHAMPS, C ;
GUELON, D ;
JOYON, D ;
SIROT, D ;
CHANAL, M ;
SIROT, J .
INFECTION, 1991, 19 (03) :181-183
[8]   Detection and clinical significance of extended-spectrum beta-lactamases in a tertiary-care medical center [J].
Emery, CL ;
Weymouth, LA .
JOURNAL OF CLINICAL MICROBIOLOGY, 1997, 35 (08) :2061-2067
[9]   Hospital outbreak of Klebsiella pneumoniae resistant to broad-spectrum cephalosporins and beta-lactam-beta-lactamase inhibitor combinations by hyperproduction of SHV-5 beta-lactamase [J].
French, GL ;
Shannon, KP ;
Simmons, N .
JOURNAL OF CLINICAL MICROBIOLOGY, 1996, 34 (02) :358-363
[10]   CDC DEFINITIONS FOR NOSOCOMIAL INFECTIONS, 1988 [J].
GARNER, JS ;
JARVIS, WR ;
EMORI, TG ;
HORAN, TC ;
HUGHES, JM .
AMERICAN JOURNAL OF INFECTION CONTROL, 1988, 16 (03) :128-140