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  4. Management of infections caused by extended-spectrum β–lactamase-producing Enterobacteriaceae: current evidence and future prospects
 
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Management of infections caused by extended-spectrum β–lactamase-producing Enterobacteriaceae: current evidence and future prospects

Journal
Expert Review of Anti-Infective Therapy
Journal Volume
16
Journal Issue
3
Pages
205-218
Date Issued
2018
Author(s)
Sheu C.-C.
Lin S.-Y.
Chang Y.-T.
Lee C.-Y.
Chen Y.-H.
PO-REN HSUEH  
DOI
10.1080/14787210.2018.1436966
URI
https://scholars.lib.ntu.edu.tw/handle/123456789/528218
Abstract
Introduction: The spread of extended-spectrum β–lactamase (ESBL)-producing Enterobacteriaceae has become a major public health threat worldwide. Area covered: A thorough systematic literature review describing the current evidence and future prospects of therapeutic options for infections caused by ESBL-producing Enterobacteriaceae. Expert commentary: The methods of detecting ESBLs have been evolving. The Clinical and Laboratory Standards Institute and the European Committee on Antimicrobial Susceptibility Testing lowered the MIC breakpoints of cephalosporins against ESBL-producing Enterobacteriaceae in 2010. Phenotypic testing for ESBLs is no longer recommended. Instead, the selection of appropriate antimicrobial agents largely depends on the report of minimum inhibitory concentrations (MICs). To date, therapeutic options for these multidrug-resistant organisms remain limited. The clinical efficacy of piperacillin/tazobactam and cefepime on in vitro-susceptible ESBL-producing Enterobacteriaceae remains a concern. Many studies found an in vitro-in vivo discordance based on current breakpoints. Carbapenems are the most reliable antibiotics for severe infections caused by ESBL-producing Enterobacteriaceae. However, their overuse has led to a serious problem of increasing drug resistance. Recently, ceftolozane/tazobactam and ceftazidime/avibactam have been approved for the treatment of complicated urinary tract infections and complicated intra-abdominal infections. The introduction of these new β-lactam/β-lactamase inhibitor combinations offers new carbapenem-sparing options for the treatment of ESBL infections. ? 2018 Informa UK Limited, trading as Taylor & Francis Group.
SDGs

[SDGs]SDG3

Other Subjects
amoxicillin plus clavulanic acid; avibactam plus ceftazidime; aztreonam; beta lactamase inhibitor; carbapenem; carbapenem derivative; cefepime; cefmetazole; cefoperazone plus sulbactam; ceftazidime; ceftolozane plus tazobactam; ceftriaxone; cephalosporin derivative; cephamycin; cloxacillin; doripenem; flomoxef; fosfomycin; levofloxacin; meropenem; metronidazole; penicillin derivative; piperacillin plus tazobactam; antiinfective agent; beta lactamase; beta lactamase inhibitor; abdominal infection; acute pyelonephritis; antibiotic sensitivity; antibiotic therapy; bacteremia; bacterial clearance; bacterial gene; bacterial strain; bactericidal activity; bacterium isolation; blaSHV 1 gene; blaTEM 1 gene; concentration response; disease severity; drug approval; drug efficacy; drug treatment failure; Enterobacteriaceae infection; Escherichia coli; extended spectrum beta lactamase producing Enterobacteriaceae; Gram negative infection; hospital infection; human; in vitro study; infection; Klebsiella pneumoniae; Klebsiella pneumoniae infection; minimum inhibitory concentration; multidrug resistance; nonhuman; phenotype; pneumonia; point mutation; prevalence; Review; septic shock; survival rate; urinary tract infection; animal; beta-lactam resistance; drug effect; Enterobacteriaceae; Enterobacteriaceae infection; isolation and purification; metabolism; microbial sensitivity test; microbiology; Animals; Anti-Bacterial Agents; beta-Lactam Resistance; beta-Lactamase Inhibitors; beta-Lactamases; Drug Resistance, Multiple, Bacterial; Enterobacteriaceae; Enterobacteriaceae Infections; Humans; Microbial Sensitivity Tests
Type
review

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