ANTIMICROBIAL ACTIVITY OF THE NEW CARBAPENEM BIAPENEM COMPARED TO IMIPENEM, MEROPENEM AND OTHER BROAD-SPECTRUM BETA-LACTAM DRUGS

被引:18
作者
SADER, HS [1 ]
JONES, RN [1 ]
机构
[1] UNIV IOWA,COLL MED,DEPT PATHOL,5232 RCP,IOWA CITY,IA 52242
关键词
D O I
10.1007/BF01964439
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
The in vitro activity of biapenem was compared to that of imipenem, meropenem and other broad-spectrum beta-lactams. A total of 716 isolates from recent cases of clinical septicemia and an additional 137 stock strains possessing known beta-lactamases or other well-characterized resistance mechanisms were tested. The minimal concentrations inhibiting 90 % of strains (MIC90) of Enterobacteriaceae species were for biapenem 0.03 to 1 mg/l and for imipenem 0.25 to 2 mg/l. No member of the Enterobacteriaceae was found to be resistant to biapenem. Biapenem and meropenem were the most active drugs against Pseudomonas aeruginosa, with an MIC90 of 1 mg/l. Biapenem was more active than ceftazidime against most gram-negative and gram-positive bacteria tested. Biapenem was as potent as imipenem against anaerobic bacteria (including Bacteroides fragilis), with an MIC90 of 0.25 mg/l. High MICs of biapenem, were demonstrated for Xanthomonas maltophilia, oxacillin-resistant Staphylococcus spp. and Enterococcus spp. These species have demonstrated resistance to other carbapenems and to most of the newer cephalosporins. The results of this study, coupled with previously documented favorable qualities of biapenem, endorse further investigation of this broad-spectrum antibacterial agent for clinical use.
引用
收藏
页码:384 / 391
页数:8
相关论文
共 20 条
[1]  
BIRNBAUM J, 1985, AM J MED, V78, P3, DOI 10.1016/0002-9343(85)90097-X
[2]   INVITRO ACTIVITY OF L-627, A NEW CARBAPENEM [J].
CATCHPOLE, CR ;
WISE, R ;
THORNBER, D ;
ANDREWS, JM .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1992, 36 (09) :1928-1934
[3]   RENAL DEHYDROPEPTIDASE-I STABILITY OF LJC 10,627, A NEW CARBAPENEM ANTIBIOTIC [J].
HIKIDA, M ;
KAWASHIMA, K ;
NISHIKI, K ;
FURUKAWA, Y ;
NISHIZAWA, K ;
SAITO, I ;
KUWAO, S .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1992, 36 (02) :481-483
[4]   REVIEW OF THE INVITRO SPECTRUM OF ACTIVITY OF IMIPENEM [J].
JONES, RN .
AMERICAN JOURNAL OF MEDICINE, 1985, 78 (6A) :22-32
[5]   STANDARDIZATION OF DISK DIFFUSION AND AGAR DILUTION SUSCEPTIBILITY TESTS FOR NEISSERIA-GONORRHOEAE - INTERPRETIVE CRITERIA AND QUALITY-CONTROL GUIDELINES FOR CEFTRIAXONE, PENICILLIN, SPECTINOMYCIN, AND TETRACYCLINE [J].
JONES, RN ;
GAVAN, TL ;
THORNSBERRY, C ;
FUCHS, PC ;
GERLACH, EH ;
KNAPP, JS ;
MURRAY, P ;
WASHINGTON, JA .
JOURNAL OF CLINICAL MICROBIOLOGY, 1989, 27 (12) :2758-2766
[6]   USE OF HAEMOPHILUS TEST MEDIUM FOR BROTH MICRODILUTION ANTIMICROBIAL SUSCEPTIBILITY TESTING OF STREPTOCOCCUS-PNEUMONIAE [J].
JORGENSEN, JH ;
MAHER, LA ;
HOWELL, AW .
JOURNAL OF CLINICAL MICROBIOLOGY, 1990, 28 (03) :430-434
[7]   IMPROVED MEDIUM FOR ANTIMICROBIAL SUSCEPTIBILITY TESTING OF HAEMOPHILUS-INFLUENZAE [J].
JORGENSEN, JH ;
REDDING, JS ;
MAHER, LA ;
HOWELL, AW .
JOURNAL OF CLINICAL MICROBIOLOGY, 1987, 25 (11) :2105-2113
[8]  
KAHAN JS, 1979, J ANTIBIOT, V32, P1
[9]   METABOLISM OF THIENAMYCIN AND RELATED CARBAPENEM ANTIBIOTICS BY THE RENAL DIPEPTIDASE, DEHYDROPEPTIDASE-I [J].
KROPP, H ;
SUNDELOF, JG ;
HAJDU, R ;
KAHAN, FM .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1982, 22 (01) :62-70
[10]   OUTER-MEMBRANE ALTERATIONS IN MULTIRESISTANT MUTANTS OF PSEUDOMONAS-AERUGINOSA SELECTED BY CIPROFLOXACIN [J].
LEGAKIS, NJ ;
TZOUVELEKIS, LS ;
MAKRIS, A ;
KOTSIFAKI, H .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1989, 33 (01) :124-127