TY - JOUR
T1 - Clinical study of cefluprenam, a new parenteral cephem antibiotic, in the treatment of complicated urinary tract infection
AU - Suzuki, Keizo
AU - Horiba, Masaki
AU - Ishikawa, Kiyohito
AU - Katoh, Shinobu
PY - 1995
Y1 - 1995
N2 - Cefluprenam (CFLP), a new injectable cephem antibiotic, was administered in the treatment of 16 cases with chronic complicated UTI and 1 case with acute prostatitis. The results obtained were as follows. Seventeen patients who received the drug were given at a dose of 0.5 g or 1.0 g, twice a day by drip infusion for 5 days. In complicated UTI, 15 patients out of 16 were evaluable by the Japanese UTI criteria, and its assessment was excellent or moderate in all cases treated (efficacy rate: 100%). In 1 case of acute prostatitis the effectiveness was fair. Response against clinical isolates, 25 strains out of 26, that included 16 of gram negative bacilli, 10 of gram positive cocci, were eradicated after treatment. A great potent in vitro activity on such strains as Escherichia coli, Morganella morganii, Proteus mirabilis, was proven as much as ≤0.05 μg/ml of MIC values. So far the clincal data obtained, the relationship between the in vitro study and the clinical one was considered to be detected. In the safety profile, nothing was observed for adverse drug reaction. In laboratory values, in 2 cases, mild transient elevations of S-GOT, S-GPT/S-GOT, SGPT, γ-GTP were noted. Conclusively, CFLP showed a useful strategy for complicated UTI, even though with stubborn UTI caused by Pseudomonas aeruginosa, Enterococcus faecalis. As for safety, no significant differences were observed, compared to the conventional compounds.
AB - Cefluprenam (CFLP), a new injectable cephem antibiotic, was administered in the treatment of 16 cases with chronic complicated UTI and 1 case with acute prostatitis. The results obtained were as follows. Seventeen patients who received the drug were given at a dose of 0.5 g or 1.0 g, twice a day by drip infusion for 5 days. In complicated UTI, 15 patients out of 16 were evaluable by the Japanese UTI criteria, and its assessment was excellent or moderate in all cases treated (efficacy rate: 100%). In 1 case of acute prostatitis the effectiveness was fair. Response against clinical isolates, 25 strains out of 26, that included 16 of gram negative bacilli, 10 of gram positive cocci, were eradicated after treatment. A great potent in vitro activity on such strains as Escherichia coli, Morganella morganii, Proteus mirabilis, was proven as much as ≤0.05 μg/ml of MIC values. So far the clincal data obtained, the relationship between the in vitro study and the clinical one was considered to be detected. In the safety profile, nothing was observed for adverse drug reaction. In laboratory values, in 2 cases, mild transient elevations of S-GOT, S-GPT/S-GOT, SGPT, γ-GTP were noted. Conclusively, CFLP showed a useful strategy for complicated UTI, even though with stubborn UTI caused by Pseudomonas aeruginosa, Enterococcus faecalis. As for safety, no significant differences were observed, compared to the conventional compounds.
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U2 - 10.11250/chemotherapy1995.43.Supplement4_332
DO - 10.11250/chemotherapy1995.43.Supplement4_332
M3 - Article
AN - SCOPUS:0029587384
SN - 1340-7007
VL - 43
SP - 332
EP - 337
JO - Japanese Journal of Chemotherapy
JF - Japanese Journal of Chemotherapy
ER -