CEFDINIR (FK482), AN ORALLY-ADMINISTERED CEPHALOSPORIN INVITRO ACTIVITY COMPARISON AGAINST RECENT CLINICAL ISOLATES FROM 5 MEDICAL-CENTERS AND DETERMINATION OF MIC QUALITY-CONTROL GUIDELINES

被引:16
作者
GERLACH, EH
JONES, RN
ALLEN, SD
KOONTZ, FP
MURRAY, PR
PFALLER, MA
WASHINGTON, JA
ERWIN, ME
机构
[1] UNIV IOWA HOSP & CLIN,IOWA CITY,IA 52242
[2] VET AFFAIRS MED CTR,IOWA CITY,IA
[3] INDIANA UNIV,MED CTR,INDIANAPOLIS,IN 46204
[4] WASHINGTON UNIV,SCH MED,ST LOUIS,MO 63110
[5] CLEVELAND CLIN,CLEVELAND,OH 44106
关键词
D O I
10.1016/0732-8893(92)90105-3
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Cefdinir, a new oral cephalosporin, was compared to cefaclor, cefadroxil, cefixime, and cefuroxime against >5000 recent aerobic clinical isolates. This multicenter study revealed broad-spectrum cefdinir activity against all Enterobacteriaceae (MIC50s, 0.06-2-mu-g/ml) except Enterobacter cloacae, Morganella morganii, Proteus vulgaris, and Serratia marcescens (MIC50s, greater-than-or-equal-to 4-mu-g/ml). Oxacillin-susceptible staphylococci (MIC90s, 0.5-2-mu-g/ml), beta-hemolytic Streptococcus group B (MIC90, 0.06-mu-g/ml), and Acinetobacter lwoffii were also susceptible to cefdinir. The activity of cefdinir was similar to that of cefixime and cefuroxime against Gram-negative organisms and superior to all tested oral cephems when tested against Gram-positive cocci. None of the cephalosporins were active against oxacillin-resistant Staphylococcus spp., enterococci, Pseudomonas spp., or Xanthomonas maltophilia. MIC quality control range guidelines were established for the strains recommended by the National Committee for Clinical Laboratory Standards documents.
引用
收藏
页码:537 / 543
页数:7
相关论文
共 12 条
[1]   INVITRO ACTIVITY EVALUATIONS OF CEFDINIR (FK482, CI-983, AND PD134393) - A NOVEL ORALLY-ADMINISTERED CEPHALOSPORIN [J].
BRIGGS, BM ;
JONES, RN ;
ERWIN, ME ;
BARRETT, MS ;
JOHNSON, DM .
DIAGNOSTIC MICROBIOLOGY AND INFECTIOUS DISEASE, 1991, 14 (05) :425-434
[2]   FK-482, A NEW ORALLY ACTIVE CEPHALOSPORIN SYNTHESIS AND BIOLOGICAL PROPERTIES [J].
INAMOTO, Y ;
CHIBA, T ;
KAMIMURA, T ;
TAKAYA, T .
JOURNAL OF ANTIBIOTICS, 1988, 41 (06) :828-830
[3]  
Jones R. N., 1988, Antimicrobic Newsletter, V5, P1, DOI 10.1016/0738-1751(88)90015-9
[4]   INTERPRETIVE CRITERIA FOR DISK DIFFUSION TESTS USING 5-MICROGRAM CEFDINIR DISKS WITH RAPIDLY GROWING CLINICAL ISOLATES [J].
JONES, RN ;
ERWIN, ME ;
GOODING, BB .
JOURNAL OF CLINICAL MICROBIOLOGY, 1992, 30 (04) :1022-1023
[5]  
MINE Y, 1988, J ANTIBIOT, V41, P1873, DOI 10.7164/antibiotics.41.1873
[6]  
Neu H.C., 1986, REV INFECT DIS S3, V8, P237
[7]   COMPARATIVE INVITRO ACTIVITY AND BETA-LACTAMASE STABILITY OF FK482, A NEW ORAL CEPHALOSPORIN [J].
NEU, HC ;
SAHA, G ;
CHIN, NX .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1989, 33 (10) :1795-1800
[8]   COMPARATIVE INVITRO ACTIVITY AND BETA-LACTAMASE STABILITY OF FR-17027, A NEW ORALLY ACTIVE CEPHALOSPORIN [J].
NEU, HC ;
CHIN, NX ;
LABTHAVIKUL, P .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1984, 26 (02) :174-180
[9]   PHARMACOKINETICS OF FK482, A NEW ORALLY ACTIVE CEPHALOSPORIN, IN ANIMALS [J].
SAKAMOTO, H ;
HIROSE, T ;
NAKAMOTO, S ;
HATANO, K ;
SHIBAYAMA, F ;
KIKUCHI, H ;
MINE, Y ;
KUWAHARA, S .
JOURNAL OF ANTIBIOTICS, 1988, 41 (12) :1896-1905
[10]  
SHIMADA K, 1987, 27TH INT C ANT AG CH