Comparative in vitro study in new cephalosporins
Author(s) -
Gerald P. Bodey,
Victor Fainstein,
A M Hinkle
Publication year - 1981
Publication title -
antimicrobial agents and chemotherapy
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.07
H-Index - 259
eISSN - 1070-6283
pISSN - 0066-4804
DOI - 10.1128/aac.20.2.226
Subject(s) - ceftazidime , microbiology and biotechnology , ceftizoxime , cephalosporin , cefotiam , cefotaxime , proteus mirabilis , enterobacter , mezlocillin , biology , proteus , cefadroxil , pseudomonas aeruginosa , antibiotics , piperacillin , escherichia coli , bacteria , biochemistry , genetics , gene
Three new cephalosporins, ceftazidime, ceftizoxime, and cefotiam, were evaluated in vitro against clinical isolates, and their activities were compared with those of other cephalosporins, mezlocillin, and tobramycin. All three new cephalosporins were very active against gram-positive cocci (except enterococci), but mezlocillin was more active against Streptococcus ssp. Cefotiam and cefamandole were the most active antibiotics against Streptococcus aureus. Ceftazidime had broad-spectrum activity against all gram-negative bacilli tested, except Enterobacter spp. Ceftizoxime was active against all, except Enterobacter spp. and Pseudomonas aeruginosa. Although cefotiam was quite active against Escherichia coli, Klebsiella pneumoniae, and Proteus mirabilis, it was inactive against indole-positive Proteus spp., Serratia spp, and P. aeruginosa. The in vitro activity suggests that ceftazidime should prove useful as a broad-spectrum antibiotic, in those settings in which the most likely pathogens are gram-negative bacilli.
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