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COMPARATIVE ACTIVITIES OF NEWER BETA-LACTAM AGENTS AGAINST MEMBERS OF THE BACTEROIDES-FRAGILIS GROUP

被引：55
作者：
CUCHURAL, GJ
TALLY, FP
JACOBUS, NV
CLEARY, T
FINEGOLD, SM
HILL, G
IANNINI, P
OKEEFE, JP
PIERSON, C
机构：
[1] TUFTS UNIV,NEW ENGLAND MED CTR HOSP,DEPT PATHOL,BOSTON,MA 02111
[2] UNIV MIAMI,JACKSON MEM MED CTR,MIAMI,FL 33136
[3] VET ADM WADSWORTH MED CTR,LOS ANGELES,CA 90073
[4] DUKE UNIV,MED CTR,DURHAM,NC 27710
[5] DANBURY HOSP,DANBURY,CT 06810
[6] LOYOLA UNIV,MED CTR,MAYWOOD,IL 60153
[7] UNIV MICHIGAN,HOSP MED,ANN ARBOR,MI 48104
来源：
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY | 1990年 / 34卷 / 03期
关键词：
D O I：
10.1128/AAC.34.3.479
中图分类号：
Q93 [微生物学];
学科分类号：
071005 ; 100705 ;
摘要：
A nationwide susceptibility survey of 557 isolates of the Bacteroides fragilis group was continued in 1986. The most active β-lactam drugs were imipenem and ticarcillin-clavulanic acid, which had 0.2 and 1.7% resistance, respectively. The rank order of activity of β-lactam drugs was imipenem, tricarcillin-clavulanic acid, cefoxitin, piperacillin, moxalactam, ceftizoxime, cefotetan, cefotaxime, cefoperazone, and ceftazadime.
引用
收藏
页码：479 / 480
页数：2
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