Antimicrobial resistance of Acinetobacter spp. in Europe

被引:240
作者
Van Looveren, M
Goossens, H
机构
[1] Univ Antwerp Hosp, UA, Dept Med Microbiol, Antwerp, Belgium
[2] Leiden Univ, Med Ctr, Dept Med Microbiol, NL-2300 RA Leiden, Netherlands
[3] Leiden Univ, Med Ctr, ESCMID Study Grp Anitmicrobial Resistance Surveil, NL-2300 RA Leiden, Netherlands
关键词
Acinetobacter; antimicrobial resistance; carbapenems; Europe; review; surveillance;
D O I
10.1111/j.1469-0691.2004.00942.x
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Bacteria of the genus Acinetobacter are ubiquitous in nature. These organisms were invariably susceptible to many antibiotics in the 1970s. Since that time, acinetobacters have emerged as multiresistant opportunistic nosocomial pathogens. The taxonomy of the genus Acinetobacter underwent extensive revision in the mid-1980s, and at least 32 named and unnamed species have now been described. Of these, Acinetobacter baumannii and the closely related unnamed genomic species 3 and 13 sensu Tjernberg and Ursing (13TU) are the most relevant clinically. Multiresistant strains of these species causing bacteraemia, pneumonia, meningitis, urinary tract infections and surgical wound infections have been isolated from hospitalised patients worldwide. This review provides an overview of the antimicrobial susceptibilities of Acinetobacter spp. in Europe, as well as the main mechanisms of antimicrobial resistance, and summarises the remaining treatment options for multiresistant Acinetobacter infections.
引用
收藏
页码:684 / 704
页数:21
相关论文
共 146 条
  • [11] OXA-24, a novel class D β-lactamase with carbapenemase activity in an Acinetobacter baumannii clinical strain
    Bou, G
    Oliver, A
    Martínez-Beltran, J
    [J]. ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2000, 44 (06) : 1556 - 1561
  • [12] Characterization of a nosocomial outbreak caused by a multiresistant Acinetobacter baumannii strain with a carbapenem-hydrolyzing enzyme:: High-level carbapenem resistance in A. baumannii is not due solely to the presence of β-lactamases
    Bou, G
    Cerveró, G
    Domínguez, MA
    Quereda, C
    Martínez-Beltrán, J
    [J]. JOURNAL OF CLINICAL MICROBIOLOGY, 2000, 38 (09) : 3299 - 3305
  • [13] Limitation of Acinetobacter baumannii treatment by plasmid-mediated carbapenemase ARI-2
    Brown, S
    Bantar, C
    Young, HK
    Amyes, SGB
    [J]. LANCET, 1998, 351 (9097) : 186 - 187
  • [14] BUIRMA RJA, 1991, SCAND J INFECT DIS, P35
  • [15] Metallo-β-lactamases:: A class apart
    Bush, K
    [J]. CLINICAL INFECTIOUS DISEASES, 1998, 27 : S48 - S53
  • [16] A reassessment of the in-vitro activity of colistin sulphomethate sodium
    Catchpole, CR
    Andrews, JM
    Brenwald, N
    Wise, R
    [J]. JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 1997, 39 (02) : 255 - 260
  • [17] Tetracycline antibiotics: Mode of action, applications, molecular biology, and epidemiology of bacterial resistance
    Chopra, I
    Roberts, M
    [J]. MICROBIOLOGY AND MOLECULAR BIOLOGY REVIEWS, 2001, 65 (02) : 232 - +
  • [18] Skin carriage of acinetobacters in Hong Kong
    Chu, YW
    Leung, CM
    Houang, ETS
    Ng, KC
    Leung, CB
    Leung, HY
    Cheng, AFB
    [J]. JOURNAL OF CLINICAL MICROBIOLOGY, 1999, 37 (09) : 2962 - 2967
  • [19] IMP-4, a novel metallo-β-lactamase from nosocomial Acinetobacter spp. collected in Hong Kong between 1994 and 1998
    Chu, YW
    Afzal-Shah, M
    Houang, ETS
    Palepou, MFI
    Lyon, DJ
    Woodford, N
    Livermore, DM
    [J]. ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2001, 45 (03) : 710 - 714
  • [20] Bacteremia due to Acinetobacter baumannii epidemiology, clinical findings, and prognostic features
    Cisneros, JM
    Reyes, MJ
    Pachon, J
    Becerril, B
    Caballero, FJ
    GarciaGarmendia, JL
    Ortiz, C
    Cobacho, AR
    [J]. CLINICAL INFECTIOUS DISEASES, 1996, 22 (06) : 1026 - 1032