Potential of high-dose cefepime/tazobactam against multiresistant Gram-negative pathogens
Author(s) -
David M. Livermore,
Shazad Mushtaq,
Marina Warner,
Simon Turner,
Neil Woodford
Publication year - 2017
Publication title -
journal of antimicrobial chemotherapy
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.124
H-Index - 194
eISSN - 1460-2091
pISSN - 0305-7453
DOI - 10.1093/jac/dkx360
Subject(s) - cefepime , tazobactam , cephalosporin , microbiology and biotechnology , acinetobacter , enterobacteriaceae , antibiotics , medicine , carbapenem , biology , imipenem , antibiotic resistance , escherichia coli , biochemistry , gene
Early β-lactamase inhibitors were combined with established penicillins, but different combinations may be more appropriate to counter current β-lactamase threats, with development facilitated by the US Generating Antibiotic Incentives Now (GAIN) Act. Cefepime/tazobactam is especially attractive, combining an AmpC-stable cephalosporin with a clinically established inhibitor, active against ESBLs and suitable for high-dose administration.
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom