In vitro activity of 15 antimicrobial agents against clinical isolates of Clostridium difficile in Kuwait

被引:32
作者
Jamal, WY
Mokaddas, EM
Verghese, TL
Rotimi, VO
机构
[1] Kuwait Univ, Fac Med, Dept Microbiol, Safat 13110, Kuwait
[2] Mubarak Al Kabeer Teaching Hosp, Safat 13110, Kuwait
关键词
Clostridium difficile; clinical isolates; antibiotic susceptibility;
D O I
10.1016/S0924-8579(02)00180-2
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
A total of 73 clinical isolates of Clostridium difficile isolated from stool/rectal swabs of patients admitted to the intensive care units at Mubarak Hospital, Ibn Sina Hospital Burn unit and Haematology wards at the Kuwait Cancer Control Centre, were investigated for their susceptibility to 15 antibiotics using the Etest. Amoxycillin-clavulanic acid, ampicillin, meropenem, metronidazole, penicillin, piperacillin, piperacillin/tazobactain, teicoplanin and vancomycin had excellent activities with MIC(90)s of 0.38, 0.5, 1, 0.19, 1.5, 2, 3, 0.25 and 0.75 mg/l, respectively. Of the 73 C difficile isolates, 86% were resistant to imipenem (MIC90 > 32 mg/l) and almost 97% were resistant to trovafloxacin (MIC90 > 256 mg/l). Forty eight percent of the isolates were resistant to clindamycin. A total of 18 isolates were highly clindamycin-resistant with an MIC of > 256 mg/l; 10 of these were toxin producers. Multiple antibiotic resistance (two or more antibiotics) was noted in 63 isolates. These were more common among the toxigenic strains than the non-toxigenic strains by a ratio of 2.5:1. (C) 2002 Elsevier Science B.V. and International Society of Chemotherapy. All rights reserved.
引用
收藏
页码:270 / 274
页数:5
相关论文
共 35 条
[1]   SUSCEPTIBILITY PATTERNS AND RESISTANCE TO IMIPENEM IN THE BACTEROIDES-FRAGILIS GROUP SPECIES IN JAPAN - A 4-YEAR STUDY [J].
BANDOH, K ;
UENO, K ;
WATANABE, K ;
KATO, N .
CLINICAL INFECTIOUS DISEASES, 1993, 16 :S382-S386
[2]   Antimicrobial susceptibilities and serogroups of clinical strains of Clostridium difficile isolated in France in 1991 and 1997 [J].
Barbut, F ;
Decré, D ;
Burghoffer, B ;
Lesage, D ;
Delisle, F ;
Lalande, V ;
Delmée, M ;
Avesani, V ;
Sano, N ;
Coudert, C ;
Petit, JC .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1999, 43 (11) :2607-2611
[3]   ANTIBIOTIC-ASSOCIATED PSEUDOMEMBRANOUS COLITIS DUE TO TOXIN-PRODUCING CLOSTRIDIA [J].
BARTLETT, JG ;
CHANG, TW ;
GURWITH, M ;
GORBACH, SL ;
ONDERDONK, AB .
NEW ENGLAND JOURNAL OF MEDICINE, 1978, 298 (10) :531-534
[4]   INVITRO ACTIVITY OF VANCOMYCIN, TEICOPLANIN, DAPTOMYCIN, RAMOPLANIN, MDL 62873 AND OTHER AGENTS AGAINST STAPHYLOCOCCI, ENTEROCOCCI AND CLOSTRIDIUM-DIFFICILE [J].
BARTOLONI, A ;
COLAO, MG ;
ORSI, A ;
DEI, R ;
GIGANTI, E ;
PARENTI, F .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 1990, 26 (05) :627-633
[5]   INVITRO ACTIVITIES OF RAMOPLANIN AND 4 GLYCOPEPTIDE ANTIBIOTICS AGAINST CLINICAL ISOLATES OF CLOSTRIDIUM-DIFFICILE [J].
BIAVASCO, F ;
MANSO, E ;
VARALDO, PE .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1991, 35 (01) :195-197
[6]  
Chang T. W., 1985, BOCKUS GASTROENTEROL, P2583
[7]   INVITRO SUSCEPTIBILITY OF CLOSTRIDIUM-DIFFICILE TO NEW BETA-LACTAM AND QUINOLONE ANTIBIOTICS [J].
CHOW, AW ;
CHENG, N ;
BARTLETT, KH .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1985, 28 (06) :842-844
[8]   PROSPECTIVE-STUDY OF ORAL TEICOPLANIN VERSUS ORAL VANCOMYCIN FOR THERAPY OF PSEUDOMEMBRANOUS COLITIS AND CLOSTRIDIUM-DIFFICILE-ASSOCIATED DIARRHEA [J].
DELALLA, F ;
NICOLIN, R ;
RINALDI, E ;
SCARPELLINI, P ;
RIGOLI, R ;
MANFRIN, V ;
TRAMARIN, A .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1992, 36 (10) :2192-2196
[9]  
Fekety R, 1997, AM J GASTROENTEROL, V92, P739
[10]  
GERDING DN, 1995, INFECT CONT HOSP EP, V16, P459