Clinical and bacteriological characteristics of IMP-type metallo-β-lactamase-producing Pseudomonas aeruginosa

被引:70
作者
Hirakata, Y
Yamaguchi, T
Nakano, M
Izumikawa, K
Mine, M
Aoki, S
Kondoh, A
Matsuda, J
Hirayama, M
Yanagihara, K
Miyazaki, Y
Tomono, K
Yamada, Y
Kamihira, S
Kohno, S
机构
[1] Nagasaki Univ, Sch Med, Dept Lab Med, Nagasaki 8528501, Japan
[2] Nagasaki Univ, Sch Med, Dept Internal Med 2, Nagasaki 8528501, Japan
[3] Nagasaki Univ, Sch Med, Atom Bomb Dis Inst, Div Sci Data Registry, Nagasaki 8528501, Japan
关键词
D O I
10.1086/375594
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
IMP-type metallo-beta-lactamase-producing bacteria have recently emerged worldwide. We conducted a case-control study in which 69 inpatients harboring bla(IMP)-positive Pseudomonas aeruginosa and 247 control subjects with bla(IMP)-negative pathogens were investigated. Prolonged hospitalization, antineoplastic chemotherapy, corticosteroid therapy (P=.001), and indwelling urinary catheters (P=.04) were risk factors for isolation of bla(IMP)-positive pathogens. The predominant source was urine (P=.001). The duration of antibiotic treatment and the total dose ( including of carbapenems) were significantly greater among case patients than among control subjects (P<.01). bla(IMP)-positive P. aeruginosa isolates were more frequently resistant to multiple drugs (P=.001) and caused more infections (P=.001) than bla(IMP)-negative pathogens. There were no significant differences in bacteriological outcome (P=.94); however, infection-related death was more frequent among case patients than among control subjects (P=.023). These results suggest that precautionary measures against the spread of bla(IMP)-positive isolates are needed, because, for most of such pathogens, no antibiotic is potent enough to be used as a single agent in treatment of infection.
引用
收藏
页码:26 / 32
页数:7
相关论文
共 30 条
[2]   A NOVEL INTEGRON-LIKE ELEMENT CARRYING THE METALLO-BETA-LACTAMASE GENE BLA(IMP) [J].
ARAKAWA, Y ;
MURAKAMI, M ;
SUZUKI, K ;
ITO, H ;
WACHAROTAYANKUN, R ;
OHSUKA, S ;
KATO, N ;
OHTA, M .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1995, 39 (07) :1612-1615
[3]   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
[4]  
Bush K, 2001, CLIN INFECT DIS, V32, P1085, DOI 10.1086/319610
[5]   IMP-4, a novel metallo-β-lactamase from nosocomial Acinetobacter spp. collected in Hong Kong between 1994 and 1998 [J].
Chu, YW ;
Afzal-Shah, M ;
Houang, ETS ;
Palepou, MFI ;
Lyon, DJ ;
Woodford, N ;
Livermore, DM .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2001, 45 (03) :710-714
[6]   Appearance of IMP-1 metallo-β-lactamase in Europe [J].
Cornaglia, G ;
Riccio, ML ;
Mazzariol, A ;
Lauretti, L ;
Fontana, R ;
Rossolini, GM .
LANCET, 1999, 353 (9156) :899-900
[7]   Nosocomial outbreak of carbapenem-resistant Pseudomonas aeruginosa with a new blaIMP allele, blaIMP-7 [J].
Gibb, AP ;
Tribuddharat, C ;
Moore, RA ;
Louie, TJ ;
Krulicki, W ;
Livermore, DM ;
Palepou, MFI .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2002, 46 (01) :255-258
[8]   Rapid detection and evaluation of clinical characteristics of emerging multiple-drug-resistant gram-negative rods carrying the metallo-β-lactamase gene blaIMP [J].
Hirakata, Y ;
Izumikawa, K ;
Yamaguchi, T ;
Takemura, H ;
Tanaka, H ;
Yoshida, R ;
Matsuda, J ;
Nakano, M ;
Tomono, K ;
Maesaki, S ;
Kaku, M ;
Yamada, Y ;
Kamihira, S ;
Kohno, S .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1998, 42 (08) :2006-2011
[9]   PLASMID-MEDIATED DISSEMINATION OF THE METALLO-BETA-LACTAMASE GENE BLA(IMP) AMONG CLINICALLY ISOLATED STRAINS OF SERRATIA-MARCESCENS [J].
ITO, H ;
ARAKAWA, Y ;
OHSUKA, S ;
WACHAROTAYANKUN, R ;
KATO, N ;
OHTA, M .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1995, 39 (04) :824-829
[10]   Amino acid substitutions in a variant of IMP-1 metallo-β-lactamase [J].
Iyobe, S ;
Kusadokoro, H ;
Ozaki, J ;
Matsumura, N ;
Minami, S ;
Haruta, S ;
Sawai, T ;
O'Hara, K .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2000, 44 (08) :2023-2027