ABSTRACT
Bacterial resistance is usually a serious problem in tertiary care hospitals. The aim of this in vitro study was to evaluate the beta-lactamase inhibitor combination piperacillin/tazobactam in a hospital environment with high bacterial resistance rates and compare it with other beta-lactam agents. Three hundred and sixty-two isolates from various clinical materials were studied during the period March-August 1996. Material for culture was collected from patients of all the wards of our hospital, with the majority being from the Intensive Care Unit (45%). Pathogenic Gram-positive and Gram-negative bacteria with high resistance rates and beta-lactamase production were studied (staphylococci, enterococci, Enterobacteriaceae, Pseudomonas). Significant bacterial resistance rates were identified for ceftazidime (50% for Klebsiellae, 60% for Enterobacter spp, 60% for Proteus spp, 33% for Pseudomonas spp, 75% for Acinetobacter spp) and ciprofloxacin (33% for both Klebsiellae and Enterobacter spp, 67% for Pseudomonas spp, 50% Acinetobacter spp). Fifty percent of Enterococcus isolates were resistance to ciprofloxacin but all of them were susceptible to piperacillin/tazobactam, amoxicillin/clavulanate and imipenem. The antibacterial activity of piperacillin/tazobactam (susceptibility rates 83 to 100% for Enterobacteriaceae, 83% for Pseudomonas spp and 75% for Acinetobacter spp) was higher than that of ceftazidime, piperacillin and ciprofloxacin. Imipenem, being mostly a reserve product, showed higher activity against Acinetobacter, Klebsiella and Enterobacter species.
Subject(s)
Cephalosporins/pharmacology , Gram-Negative Bacteria/drug effects , Gram-Negative Bacteria/isolation & purification , Gram-Positive Bacteria/drug effects , Gram-Positive Bacteria/isolation & purification , Penicillanic Acid/analogs & derivatives , Penicillins/pharmacology , Piperacillin/pharmacology , Amoxicillin/pharmacology , Ceftazidime/pharmacology , Cephalosporin Resistance , Ciprofloxacin/pharmacology , Clavulanic Acid/pharmacology , Enzyme Inhibitors/pharmacology , Gram-Negative Bacteria/enzymology , Gram-Positive Bacteria/enzymology , Humans , Intensive Care Units , Microbial Sensitivity Tests , Penicillanic Acid/pharmacology , Penicillin Resistance , TazobactamSubject(s)
Bacteria/drug effects , Cephalosporins/pharmacology , Humans , Microbial Sensitivity Tests , CefpiromeSubject(s)
Anti-Bacterial Agents/pharmacology , Respiratory Tract Infections/microbiology , Administration, Oral , Haemophilus influenzae/drug effects , Humans , Klebsiella pneumoniae/drug effects , Microbial Sensitivity Tests , Moraxella catarrhalis/drug effects , Streptococcus pneumoniae/drug effectsABSTRACT
The in vitro activity of cefodizime and two comparative cephalosporins, cefuroxime and ceftriaxone were studied against respiratory pathogens. MIC90s of cefodizime were 0.06-0.512 microgram/ml for Streptococcus pneumoniae, Moraxella catarrhalis and Haemophilus influenzae. MIC50s of cefodizime for Klebsiella pneumoniae and Staphylococcus aureus isolates were 2 micrograms/ml and 8 micrograms/ml respectively. Cefuroxime and ceftriaxone at a concentration of 2 micrograms/ml and 1 microgram/ml inhibited 50% of Klebsiella pneumoniae and 50% of Staphylococcus aureus strains studied respectively. Cefodizime inhibited many of the important respiratory pathogens and can be suggested as an active antimicrobial agent for respiratory tract infections.
