Efficacy of Cefepime in the Treatment of Infections Due to Multiply Resistant Enterobacter Species
Cefepime is a new cephalosporin with an enhanced antibacterial potency and spectrum. More rapid penetration into many gram-negative bacilli, targeting of multiple penicillin-binding proteins, and resistance to inactivation by many β-lactamases account for its activity against organisms that have dev...
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Published in | Clinical infectious diseases Vol. 23; no. 3; pp. 454 - 461 |
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Main Authors | , , |
Format | Journal Article |
Language | English |
Published |
Chicago, IL
University of Chicago Press
01.09.1996
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Subjects | |
Online Access | Get full text |
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Summary: | Cefepime is a new cephalosporin with an enhanced antibacterial potency and spectrum. More rapid penetration into many gram-negative bacilli, targeting of multiple penicillin-binding proteins, and resistance to inactivation by many β-lactamases account for its activity against organisms that have developed resistance to agents such as ceftazidime, cefotaxime, or ceftriaxone. This study identified 16 patients with 17 infections due to Enterobacter species organisms with reduced susceptibility or resistance to ceftazidime. Most isolates were multiply resistant to other β-lactam drugs as well, but all were susceptible to cefepime. All 17 infections, which included pneumonia, urinary tract infection, intraabdominal infection, and bacteremia, responded clinically to intravenous cefepime. In particular, cefepime was successfully used in the management of cases of chronic infection that had responded poorly to repeated therapy with imipenem, aminoglycosides, or ciprofloxacin. Eradication of Enterobacter species organisms occurred at 15 (88.2%) of the 17 sites of infection. No emergence of resistance to cefepime was noted. |
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Bibliography: | Reprints or correspondence: Dr. W. Eugene Sanders, Jr., Department of Medical Microbiology and Immunology, Creighton University School of Medicine, 2500 California Plaza, Omaha, Nebraska 68178. ark:/67375/HXZ-LMNX2GG2-Q istex:54D626CD051CD8810785B062512B4BEF28548AC6 ObjectType-Article-2 SourceType-Scholarly Journals-1 ObjectType-Feature-1 content type line 23 ObjectType-Article-1 ObjectType-Feature-2 |
ISSN: | 1058-4838 1537-6591 |
DOI: | 10.1093/clinids/23.3.454 |