The current state of multidrug-resistant gram-negative bacilli in north America

被引:91
作者
Nicasio, Anthony M. [1 ]
Kuti, Joseph L.
Nicolau, David P. [1 ]
机构
[1] Hartford Hosp, Ctr Anti Infect Res & Dev, Hartford, CT 06102 USA
来源
PHARMACOTHERAPY | 2008年 / 28卷 / 02期
关键词
gram-negative bacilli; multidrug resistance; treatment options;
D O I
10.1592/phco.28.2.235
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Although much of today's media focuses on multidrug-resistant gram-positive bacteria such as methicillin-resistant Staphylococcus aureus and vancomycin-resistant Enterococcus, resistance within gram-negative bacilli continues to rise, occasionally creating situations in which few or no antibiotics that retain activity are available. Extended-spectrum P-lactamase (ESBL)-producing Escherichia coli and Klebsiella sp are emerging threats nationally Although carbapenems are considered the antibiotic class of choice to treat ESBL-producing Enterobacteriaceae, the ability of these organisms to produce carbapenemases has now become apparent in some regions throughout the United States. Although still rare, Klebsiella sp that produce KPC-2 retain susceptibility only to tigecycline, polymyxins, and occasionally amino,glycosides. Multidrug resistance among Pseudomonas aeruginosa and Acinetobacter sp has always been apparent across many hospitals in the United States. Recent surveillance indicates increasing resistance to all currently available antibiotics, including carbapenems, cephalosporins, penicillins, fluoroquinolones, and aminoglycosides. Against many strains, only polymyxins retain activity; however, resistance has also been reported to these agents. Fortunately, resistance mechanisms such as metallo-beta-lactamases are still rare in the United States. As no new antibiotics with novel mechanisms against many of these gram-negative bacilli are expected to be developed in the foreseeable future, careful and conservative use of agents combined with good infection control practices is required.
引用
收藏
页码:235 / 249
页数:15
相关论文
共 143 条
[1]   blaVIM-2 and blaVIM-7 carbapenemase-producing Pseudomonas aeruginosa isolates detected in a tertiary care medical center in the United States:: Report from the MYSTIC program [J].
Aboufaycal, H. ;
Sader, H. S. ;
Rolston, K. ;
Deshpande, L. M. ;
Toleman, M. ;
Bodey, G. ;
Raad, I. ;
Jones, R. N. .
JOURNAL OF CLINICAL MICROBIOLOGY, 2007, 45 (02) :614-615
[2]  
ABRAHAM EP, 1940, NATURE, V41, P848
[3]   The role of multidrug efflux pumps in the antibiotic resistance of Pseudomonas aeruginosa and other gram-negative bacteria -: Insights from the society of infectious diseases pharmacists [J].
Aeschlimann, JR .
PHARMACOTHERAPY, 2003, 23 (07) :916-924
[4]   Reemergence of gram-negative health care-associated bloodstream infections [J].
Albrecht, Svenja J. ;
Fishman, Neil O. ;
Kitchen, Jennifer ;
Nachamkin, Irving ;
Bilker, Warren B. ;
Hoegg, Cindy ;
Samel, Carol ;
Barbagallo, Stephanie ;
Arentzen, Judy ;
Lautenbach, Ebbing .
ARCHIVES OF INTERNAL MEDICINE, 2006, 166 (12) :1289-1294
[6]  
[Anonymous], BAD BUGS NO DRUGS AN
[7]   What's new in antibiotic resistance? Focus on beta-lactamases [J].
Babic, Maja ;
Hujer, Andrea M. ;
Bonomo, Robert A. .
DRUG RESISTANCE UPDATES, 2006, 9 (03) :142-156
[8]   High-dose ampicillin-sulbactam as an alternative treatment of late-onset VAP from multidrug-resistant Acinetobacter baumannii [J].
Betrosian, Alex P. ;
Frantzeskaki, Frantzeska ;
Xanthaki, Anna ;
Georgiadis, George .
SCANDINAVIAN JOURNAL OF INFECTIOUS DISEASES, 2007, 39 (01) :38-43
[9]   Growing group of extended-spectrum β-lactamases:: The CTX-M enzymes [J].
Bonnet, R .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2004, 48 (01) :1-14
[10]   Mechanisms of multidrug resistance in Acinetobacter species and Pseudomonas aeruginosa [J].
Bonomo, Robert A. ;
Szabo, Dora .
CLINICAL INFECTIOUS DISEASES, 2006, 43 :S49-S56