Evaluation of the in vitro activity of cefepime compared to other broad-spectrum cephalosporins against clinical isolates from eighteen Brazilian hospitals by using the Etest

被引:18
作者
Sader, HS
Mimica, I
Rossi, F
Zoccoli, C
Montelli, AC
Sampaio, JLM
Segura, AJA
Magalhaes, M
Nowakonski, A
Mendes, CMF
机构
[1] SANTA CASA MISERICORDIA SAO PAULO,SAO PAULO,BRAZIL
[2] EMILIO RIBAS HOSP,SAO PAULO,BRAZIL
[3] SANTA LUZIA LAB,FLORIANOPOLIS,SC,BRAZIL
[4] UNIV ESTADUAL PAULISTA JULIO MESQUITA FILHO,FAC MED,BOTUCATU,SP,BRAZIL
[5] LAMINA LAB,RIO JANEIRO,BRAZIL
[6] HOSP BASE BRASILIA,FHDF,BRASILIA,DF,BRAZIL
[7] MARCELO MAGALHAES LAB,RECIFE,PE,BRAZIL
[8] UNICAMP,HOSP CLIN,CAMPINAS,SP,BRAZIL
[9] UNIV SAO PAULO,COLL MED,HC,FM,CMFM,SAO PAULO,BRAZIL
关键词
D O I
10.1016/S0732-8893(97)00015-1
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
The in vitro activity of cefepime was compared to that of ceftazidime, ceftriaxone, and cefotaxime in a multicenter study involving 10 clinical microbiology laboratories and clinical isolates from 18 Brazilian hospitals from 7 cities (4 states). A total of 982 isolates consecutively collected between December 1995 and March 1996 were susceptibility tested by using Etest and following the NCCLS procedures for agar diffusion tests. The cefepime spectrum was broader than that of the other broad-spectrum cephalosporins against both Gram-negative rods and Gram-positive cocci. Cefepime tons particularly move active against Enterobacter sp. (MIC90, 2 mu g/ml), Serratia sp. (MIC90, 2 mu g/ml) and oxacillin-susceptible Staphylococcus aureus (MIC90, 3 mu g/ml). Against Pseudomonas aeruginosa, cefepime (MIC90 16 mu g/ml) was slightly more active than ceftazidime (MIC90 32 mu g/ml) and 8- to 16-fold more active than ceftriaxone or cefotaxime (MIC90 >256 mu g/ml). Our results show that nosocomial bacteria, especially Gram-negative rods, have a high rate of cephalosporin resistance in Brazil. However, part of these resistant bacteria remains susceptible to cefepime. The Etest was shown to be an excellent method for multicenter studies of the in vitro evaluation of new antimicrobial agents. (C) 1997 Elsevier Science Inc.
引用
收藏
页码:87 / 92
页数:6
相关论文
共 15 条
[1]   CEFEPIME - A REVIEW OF ITS ANTIBACTERIAL ACTIVITY, PHARMACOKINETIC PROPERTIES AND THERAPEUTIC USE [J].
BARRADELL, LB ;
BRYSON, HM .
DRUGS, 1994, 47 (03) :471-505
[2]   ANTIMICROBIAL ACTIVITY OF FK-037, A NEW BROAD-SPECTRUM CEPHALOSPORIN - INTERNATIONAL IN-VITRO COMPARISON WITH CEFEPIME AND CEFTAZIDIME [J].
FREI, R ;
JONES, RN ;
PIGNATARI, AC ;
YAMANE, N ;
MARCO, F ;
HOBAN, DJ .
DIAGNOSTIC MICROBIOLOGY AND INFECTIOUS DISEASE, 1994, 18 (03) :167-173
[3]   EVALUATION OF THE INVITRO ACTIVITY OF BMY-28142, A NEW BROAD-SPECTRUM CEPHALOSPORIN [J].
FUCHS, PC ;
JONES, RN ;
BARRY, AL ;
THORNSBERRY, C .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1985, 27 (05) :679-682
[4]  
GALES AC, 1995, J BRAS PATOL, V31, P55
[5]   Detection of extended-spectrum beta-lactamases in clinical isolates of Klebsiella pneumoniae and Escherichia coli [J].
Jacoby, GA ;
Han, P .
JOURNAL OF CLINICAL MICROBIOLOGY, 1996, 34 (04) :908-911
[6]   PREVALENCE OF IMPORTANT PATHOGENS AND ANTIMICROBIAL ACTIVITY OF PARENTERAL DRUGS AT NUMEROUS MEDICAL-CENTERS IN THE UNITED-STATES .1. STUDY ON THE THREAT OF EMERGING RESISTANCES - REAL OR PERCEIVED [J].
JONES, RN ;
KEHRBERG, EN ;
ERWIN, ME ;
ANDERSON, SC ;
BEAVIS, K ;
BERMAN, M ;
BOURBEAU, P ;
SINNOTT, J ;
CANAWATI, H ;
CAVALIERI, S ;
COCKERILL, F ;
DELLALATTA, P ;
DENYS, G ;
DOERN, G ;
FORBES, B ;
GAMBLE, S ;
GOODMAN, N ;
HAUGEN, T ;
HINDLER, J ;
HUMPHRIES, J ;
JOSEPHSON, S ;
KAUFFMAN, C ;
LIBERTINE, C ;
MAUNEY, C ;
METCHOCK, B ;
MICHELSON, P ;
MURRAY, P ;
NEEDHAM, C ;
OELSCHDAEGER, R ;
PRICE, M ;
SACEANU, C ;
SCHWALBE, R ;
SEGRETI, J ;
SEWELL, D ;
SIERRA, M ;
SLIFKIN, M ;
SNYDMAN, D ;
SOUTHERN, P ;
SPIEGEL, C ;
STEELEMOORE, L ;
STEIN, G ;
STRATTON, C ;
WANGER, A ;
WASHINGTON, J ;
WASILAUSKAS, B ;
WEINSTEIN, M .
DIAGNOSTIC MICROBIOLOGY AND INFECTIOUS DISEASE, 1994, 19 (04) :203-215
[7]   In vivo selection of porin-deficient mutants of Klebsiella pneumoniae with increased resistance to cefoxitin and expanded-spectrum cephalosporins [J].
MartinezMartinez, L ;
HernandezAlles, S ;
Alberti, S ;
Tomas, JM ;
Benedi, VJ ;
Jacoby, GA .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1996, 40 (02) :342-348
[8]  
*NCCLS, 1993, PERF STAND ANT DISK
[9]  
NOVAK SM, 1994, CLIN MICROBIOLOGY PR, V1
[10]   AFFINITY OF CEPHALOSPORINS FOR BETA-LACTAMASES AS A FACTOR IN ANTIBACTERIAL EFFICACY [J].
PHELPS, DJ ;
CARLTON, DD ;
FARRELL, CA ;
KESSLER, RE .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1986, 29 (05) :845-848