In vitro activities of three carbapenems against recent bacterial isolates from severely ill patients at Swedish hospitals

被引:14
作者
Fraenkel, Carl-Johan
Ullberg, Mans
Bernander, Sverker
Ericson, Evalena
Larsson, Peter
Rydberg, Johan
Tornqvist, Eva
Melhus, Asa
机构
[1] Blekinge Hosp, Dept Clin Microbiol, S-37180 Karlskrona, Sweden
[2] Univ Uppsala Hosp, Dept Med Sci, Sect Clin Bacteriol, Uppsala, Sweden
[3] Karolinska Univ Hosp, Dept Clin Microbiol, Solna, Sweden
[4] Huddinge Hosp, Dept Immunol Microbiol Pathol & Infect Dis, S-14186 Huddinge, Sweden
[5] Sahlgrens Univ Hosp, Dept Clin Bacteriol, S-41345 Gothenburg, Sweden
[6] Univ Lund Hosp, Dept Med Microbiol, S-22185 Lund, Sweden
[7] Orebro Univ Hosp, Dept Clin Microbiol & Immunol, Orebro, Sweden
[8] Malmo Univ Hosp, Dept Lab Med, Div Med Microbiol, Malmo, Sweden
关键词
D O I
10.1080/00365540600684371
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
To study the in vitro activity of imipenem, meropenem and ertapenem against common pathogens isolated from patients in intensive care, haematology and dialysis/nephrology units at 7 Swedish university hospitals, a total of 788 isolates were collected during 2002-2003. The distribution of the isolates was as follows: Escherichia coli (n = 140), Klebsiella spp. (n = 132), Proteus spp. (n = 97), Enterobacter spp. (n = 113), Pseudomonas aeruginosa (n = 126), Acinetobacter spp. (n = 53) and Enterococcus faecalis (n = 127). The susceptibility to the 3 carbapenems was determined by E-test, and the MICs were interpreted according to SRGA criteria. All 3 carbapenems were highly active against Enterobacteriaceae. The overall susceptibility to imipenem, meropenem and ertapenem was 90%, 98% and 93%, respectively. Against Enterobacteriaceae, Enterobacter spp. excluded, ertapenem had an equal or lower MIC90 than meropenem. Apart from being the most active carbapenem against Enterobacteriaceae, meropenem was also the most active carbapenem against P. aeruginosa, whereas imipenem was the most active drug against Acinetobacter spp. The carbapenems are still potent antibiotics. With the introduction of ertapenem, and an expected increase in the carbapenem consumption due to an increased prevalence of strains with extended-spectrum beta-lactamases, continuous surveillance of carbapenem resistance appears to be warranted, with special attention to P. aeruginosa, Enterobacter and Proteus spp.
引用
收藏
页码:853 / 859
页数:7
相关论文
共 25 条
[1]   Imipenem resistance of Enterobacter aerogenes mediated by outer membrane permeability [J].
Bornet, C ;
Davin-Regli, A ;
Bosi, C ;
Pages, JM ;
Bollet, C .
JOURNAL OF CLINICAL MICROBIOLOGY, 2000, 38 (03) :1048-1052
[2]   Carbapenems in clinical practice: a guide to their use in serious infection [J].
Bradley, JS ;
Garau, J ;
Lode, H ;
Rolston, KVI ;
Wilson, SE ;
Quinn, JP .
INTERNATIONAL JOURNAL OF ANTIMICROBIAL AGENTS, 1999, 11 (02) :93-100
[3]  
Fluit AC, 2001, EUR J CLIN MICROBIOL, V20, P617
[4]   Use of surrogate antimicrobial agents to predict susceptibility to ertapenem [J].
Friedland, IR ;
Isaacs, R ;
Mixson, LA ;
Motyl, M ;
Woods, GL .
DIAGNOSTIC MICROBIOLOGY AND INFECTIOUS DISEASE, 2002, 43 (01) :61-64
[5]   In-vitro antimicrobial activity of a carbapenem, MK-0826 (L-749,345) and provisional interpretive criteria for disc tests [J].
Fuchs, PC ;
Barry, AL ;
Brown, SD .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 1999, 43 (05) :703-706
[6]   In vitro activities of ertapenem (MK-0826) against clinical bacterial isolates from 11 North American medical centers [J].
Fuchs, PC ;
Barry, AL ;
Brown, SD .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2001, 45 (06) :1915-1918
[7]  
GOOSSENS H, 1997, DIAGN MICROBIOL INFE, V41, P183
[8]   New species-related MIC breakpoints for early detection of development of resistance among Gram-negative bacteria in Swedish intensive care units [J].
Hanberger, H ;
Nilsson, LE ;
Claesson, B ;
Kärnell, A ;
Larsson, P ;
Rylander, M ;
Svensson, E ;
Sörberg, M ;
Sörén, L .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 1999, 44 (05) :611-619
[9]   Surveillance of antibiotic resistance in European ICUs [J].
Hanberger, H ;
Diekema, D ;
Fluit, A ;
Jones, R ;
Struelens, M ;
Spencer, R ;
Wolff, M .
JOURNAL OF HOSPITAL INFECTION, 2001, 48 (03) :161-176
[10]   Resistance mechanisms in Pseudomonas aeruginosa and other nonfermentative gram-negative bacteria [J].
Hancock, REW .
CLINICAL INFECTIOUS DISEASES, 1998, 27 :S93-S99