Bacterial resistance: Origins, epidemiology, and impact

被引:367
作者
Livermore, DM [1 ]
机构
[1] Cent Publ Hlth Lab, Antibiot Resistance Monitoring & Reference Lab, London NW9 5HT, England
关键词
D O I
10.1086/344654
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The basic mechanisms of antibacterial resistance are well known, but critical new aspects continue to be discovered. Recently discovered factors with major implications for the emergence, dissemination, and maintenance of resistance include multidrug efflux, hypermutability, integrons, and plasmid addiction. Some resistances are widespread and others local, with prevalence rates often worst in newly prosperous countries and in those specialist units where antibacterial use is heaviest. Multidrug-resistant epidemic strains are critical to the total accumulation of resistance (e. g., among Streptococcus pneumoniae, methicillin-resistant Staphylococcus aureus, Klebsiella pneumoniae), but it remains unclear why some bacterial lineages achieve epidemic spread whereas others that are equally resistant do not. The correlation between in vitro resistance and treatment failure is imperfect, but resistance undoubtedly increases mortality, morbidity, and costs in many settings. Recent concern has led to a plethora of governmental and agency reports advocating less antibacterial use, better antibacterial use, better infection control, and the development of new antibacterials. The evidence that better prescribing can reduce resistance rates is mixed, and although changes to hospital regimens may reduce one resistance problem, other opportunistic bacteria may fill the vacant niche. Overall, the best that can reasonably be anticipated is an improved balance between the accumulation of resistance and new antibacterial development.
引用
收藏
页码:S11 / S23
页数:13
相关论文
共 106 条
[1]  
[Anonymous], 2002, MMWR MORB MORTAL WKL, V51, P565
[2]   Antimicrobial resistance in isolates from inpatients and outpatients in the united states: Increasing importance of the intensive care unit [J].
Archibald, L ;
Phillips, L ;
Monnet, D ;
McGowan, JE ;
Tenover, F ;
Gaynes, R .
CLINICAL INFECTIOUS DISEASES, 1997, 24 (02) :211-215
[3]   MOLECULAR EPIDEMIOLOGY OF KLEBSIELLA-PNEUMONIAE STRAINS THAT PRODUCE SHV-4 BETA-LACTAMASE AND WHICH WERE ISOLATED IN 14 FRENCH HOSPITALS [J].
ARLET, G ;
ROUVEAU, M ;
CASIN, I ;
BOUVET, PJM ;
LAGRANGE, PH ;
PHILIPPON, A .
JOURNAL OF CLINICAL MICROBIOLOGY, 1994, 32 (10) :2553-2558
[4]   Studies of antibiotic resistance within the patient, hospitals and the community using simple mathematical models [J].
Austin, DJ ;
Anderson, RM .
PHILOSOPHICAL TRANSACTIONS OF THE ROYAL SOCIETY B-BIOLOGICAL SCIENCES, 1999, 354 (1384) :721-738
[5]   Antimicrobial resistance amongst Klebsiella spp. collected from intensive care units in Southern and Western Europe in 1997-1998 [J].
Babini, GS ;
Livermore, DM .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 2000, 45 (02) :183-189
[6]   Pneumococcal resistance to beta-lactam antibiotics: A global geographic overview [J].
Baquero, F .
MICROBIAL DRUG RESISTANCE, 1995, 1 (02) :115-120
[7]   Differential expression of over 60 chromosomal genes in Escherichia coli by constitutive expression of MarA [J].
Barbosa, TM ;
Levy, SB .
JOURNAL OF BACTERIOLOGY, 2000, 182 (12) :3467-3474
[8]   Plasmid-encoded AmpC β-lactamases:: How far have we gone 10 years after the discovery? [J].
Bauernfeind, A ;
Chong, Y ;
Lee, K .
YONSEI MEDICAL JOURNAL, 1998, 39 (06) :520-525
[9]   5-YEAR SURVEILLANCE OF AMINOGLYCOSIDE USAGE IN A UNIVERSITY HOSPITAL [J].
BETTS, RF ;
VALENTI, WM ;
CHAPMAN, SW ;
CHONMAITREE, T ;
MOWRER, G ;
PINCUS, P ;
MESSNER, M ;
ROBERTSON, R .
ANNALS OF INTERNAL MEDICINE, 1984, 100 (02) :219-222
[10]   Most Enterobacter aerogenes strains in France belong to a prevalent clone [J].
Bosi, C ;
Davin-Regli, A ;
Bornet, C ;
Mallea, M ;
Pages, JM ;
Bollet, C .
JOURNAL OF CLINICAL MICROBIOLOGY, 1999, 37 (07) :2165-2169