TY - JOUR
T1 - Bactericidal Activity of Meropenem and Interactions With Other Antibiotics
AU - Ferrara, A.
AU - Grassi, G.
AU - Grass, F. A.
AU - Picdoni, P. D.
AU - Giamroni Grassi, G.
PY - 1989
Y1 - 1989
N2 - MICs of meropenem for selected clinical isolates of bacteria were determined. Killing curves were performed on strains of methicillin-sensitive Staphylococcus aureus, methiciilin-resistant Staph. aureus (MRSA), methidllin-resistant Staph. epidermidis, Escherichia coli, Klebsiella spp., Enterobacter cloacae, Pseudomonas aeruginosa, Citrobacter freundii and Acinetobacter spp. A reduction of ≥3 x log10, in viable cells was observed at 4 and 6 h of exposure to 4 and 8 x MIC, and this was usually maintained at 24 h (with a few exceptions for methicillin-resistant Staph. Epidermidis and Ent. cloacae). At the MIC and twice the MIC regrowth tended to occur at 24 h although this varied from strain to strain. The interaction with other antibiotics was determined by the chequerboard technique. Usually an additive or synergistic effect was observed when meropenem or imipenem was used in combination with βan aminoglycoside against Gramnegative species, while in a few cases antagonism occurred in combination with filactams. Against Staph. aureus, MRSA and Staph. epidermidis synergism was usually obtained with combinations with teicoplanin or vancomycin and either synergism or addition with combinations with rifampicin, co-trimoxazole or ciprofloxacin.
AB - MICs of meropenem for selected clinical isolates of bacteria were determined. Killing curves were performed on strains of methicillin-sensitive Staphylococcus aureus, methiciilin-resistant Staph. aureus (MRSA), methidllin-resistant Staph. epidermidis, Escherichia coli, Klebsiella spp., Enterobacter cloacae, Pseudomonas aeruginosa, Citrobacter freundii and Acinetobacter spp. A reduction of ≥3 x log10, in viable cells was observed at 4 and 6 h of exposure to 4 and 8 x MIC, and this was usually maintained at 24 h (with a few exceptions for methicillin-resistant Staph. Epidermidis and Ent. cloacae). At the MIC and twice the MIC regrowth tended to occur at 24 h although this varied from strain to strain. The interaction with other antibiotics was determined by the chequerboard technique. Usually an additive or synergistic effect was observed when meropenem or imipenem was used in combination with βan aminoglycoside against Gramnegative species, while in a few cases antagonism occurred in combination with filactams. Against Staph. aureus, MRSA and Staph. epidermidis synergism was usually obtained with combinations with teicoplanin or vancomycin and either synergism or addition with combinations with rifampicin, co-trimoxazole or ciprofloxacin.
UR - http://www.scopus.com/inward/record.url?scp=0024469759&partnerID=8YFLogxK
U2 - 10.1093/jac/24.suppl_A.239
DO - 10.1093/jac/24.suppl_A.239
M3 - Article
SN - 0305-7453
VL - 24
SP - 239
EP - 250
JO - Journal of Antimicrobial Chemotherapy
JF - Journal of Antimicrobial Chemotherapy
ER -