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The Use of Noncarbapenem β-Lactams for the Treatment of Extended-Spectrum β-Lactamase Infections
Author(s) -
Pranita D. Tamma,
Jesús RodríguezBaño
Publication year - 2017
Publication title -
clinical infectious diseases
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.44
H-Index - 336
eISSN - 1537-6591
pISSN - 1058-4838
DOI - 10.1093/cid/cix034
Subject(s) - cefepime , medicine , tazobactam , piperacillin , piperacillin/tazobactam , carbapenem , ceftazidime , antibiotics , ceftazidime/avibactam , cephalosporin , intensive care medicine , beta lactamase inhibitors , beta lactamase , microbiology and biotechnology , imipenem , biology , antibiotic resistance , escherichia coli , pseudomonas aeruginosa , bacteria , biochemistry , gene , genetics
The continued rise in infections caused by extended-spectrum β-lactamase (ESBL)-producing pathogens is recognized globally as one of the most pressing concerns facing the healthcare community. Carbapenems are widely regarded as the antibiotics of choice for the treatment of ESBL-producing infections, even when in vitro activity to other β-lactams has been demonstrated. However, indiscriminant carbapenem use is not without consequence, and carbapenem overuse has contributed to the emergence of carbapenem-resistant Enterobacteriaceae. The use of non-carbapenem β-lactams for the treatment of ESBL infections has yielded conflicting results. In this review, we discuss the available data for the use of cephamycins, cefepime, piperacillin-tazobactam, ceftolozane-tazobactam, and ceftazidime-avibactam for the treatment of ESBL infections.

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