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The Last Generation or the First Enhanced-Potency Broad Spectrum Cephalosporin?

Christine C. Sanders, Ellen Smith Moland

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Abstract

Summary Cefepime and 8 other ~-lactam antibiotics were compared with regard to in vitro activity against 134 clinical isolates of Gram-negative bacteria resistant to ~-lactam antibiotics by a variety of mechanisms. Overall, cefepime was the most active cephalosporin tested, inhibiting 104 of 112 (93%) strains of Enterobacteriaceae and 12 of 22 (55%) strains of Pseudomonas aeruginosa at concentrations of 8 mg/L or less. In contrast, ceftazidime inhibited only 64 (57%) of the Enterobacteriaceae and 11 (50%) of the P. aeruginosa strains . Imipenem was the most active ~-Iactam agent tested, although some strains resistant to the carbapenem were susceptible to cefepime. Cefepime was less likely than ceftazidime to select mutants from organisms possessing inducible Bush Group I ~-lactamases. Of 19 mutants selected by various cephalosporins, 18 (95%) re­ mained susceptible to cefepime, whereas only 6 (32%) were susceptible to ceftazidime. These findings suggest that cefepime possesses enhanced activity compared with other cephalosporins, and this may result from its improved penetration into the Gram-negative cell and the lower affinity of ~-lactamases for the drug.

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Summary Cefepime and 8 other ~-lactam antibiotics were compared with regard to in vitro activity against 134 clinical isolates of Gram-negative bacteria resistant to ~-lactam antibiotics by a variety of mechanisms. Overall, cefepime was the most active cephalosporin tested, inhibiting 104 of 112 (93%) strains of Enterobacteriaceae and 12 of 22 (55%) strains of Pseudomonas aeruginosa at concentrations of 8 mg/L or less. In contrast, ceftazidime inhibited only 64 (57%) of the Enterobacteriaceae and 11 (50%) of the P. aeruginosa strains . Imipenem was the most active ~-Iactam agent tested, although some strains resistant to the carbapenem were susceptible to cefepime. Cefepime was less likely than ceftazidime to select mutants from organisms possessing inducible Bush Group I ~-lactamases. Of 19 mutants selected by various cephalosporins, 18 (95%) re­ mained susceptible to cefepime, whereas only 6 (32%) were susceptible to ceftazidime. These findings suggest that cefepime possesses enhanced activity compared with other cephalosporins, and this may result from its improved penetration into the Gram-negative cell and the lower affinity of ~-lactamases for the drug.

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Available abstract

Summary Cefepime and 8 other ~-lactam antibiotics were compared with regard to in vitro activity against 134 clinical isolates of Gram-negative bacteria resistant to ~-lactam antibiotics by a variety of mechanisms. Overall, cefepime was the most active cephalosporin tested, inhibiting 104 of 112 (93%) strains of Enterobacteriaceae and 12 of 22 (55%) strains of Pseudomonas aeruginosa at concentrations of 8 mg/L or less. In contrast, ceftazidime inhibited only 64 (57%) of the Enterobacteriaceae and 11 (50%) of the P. aeruginosa strains . Imipenem was the most active ~-Iactam agent tested, although some strains resistant to the carbapenem were susceptible to cefepime. Cefepime was less likely than ceftazidime to select mutants from organisms possessing inducible Bush Group I ~-lactamases. Of 19 mutants selected by various cephalosporins, 18 (95%) re­ mained susceptible to cefepime, whereas only 6 (32%) were susceptible to ceftazidime. These findings suggest that cefepime possesses enhanced activity compared with other cephalosporins, and this may result from its improved penetration into the Gram-negative cell and the lower affinity of ~-lactamases for the drug.

Key concepts: Cefepime, Cephalosporin, Ceftazidime, Microbiology, Imipenem, Antibiotics, Enterobacteriaceae, Pseudomonas aeruginosa

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