In vitro susceptibility of Stenotrophomonas maltophilia to various antimicrobial combinations

被引:56
作者
Krueger, TS [1 ]
Clark, EA [1 ]
Nix, DE [1 ]
机构
[1] Univ Arizona, Coll Pharm, Dept Pharm Practice & Sci, Tucson, AZ 85721 USA
关键词
D O I
10.1016/S0732-8893(01)00281-4
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Stenotrophomonas maltophilia has emerged as a significant pathogen in compromised patients, causing infections which are difficult to treat. Clinical isolates from patients in the Tucson area were tested against single and combination antibiotics using three testing methods. Ticarcillin/clavulanate, trimethoprim/sulfamethoxazole and trovafloxacin provided comparable inhibitory activity, in vitro. Ciprofloxacin, imipenem and ticarcillin were active less often. Agreements between disk diffusion and broth microdilution results were poor for ciprofloxacin and trimethoprim/sulfamethoxazole; however, agreement was greater than or equal to 90% for the other drugs tested. Major or very major errors were observed with ticarcillin, ticarcillin/clavulanate, and trovafloxacin. The addition of aztreonam to ticarcillin/clavulanate enhanced the activity compared to ticarcillin/clavulanate alone using the double-disk diffusion, broth microdilution (checkerboard), and time-kill testing methods. Trovafloxacin exhibited good activity by all three methods, with bactericidal activity at greater than or equal to 2 x MIC. These results indicate that the newer fluoroquinolones or the triple combination of ticarcillin/clavulanate plus aztreonam may be potential options for treatment of infection caused by S. maltophilia in patients who are intolerant to or fail trimethoprim/sulfamethoxazole therapy. (C) 2001 Elsevier Science Inc. All rights reserved.
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页码:71 / 78
页数:8
相关论文
共 17 条
[1]  
Acar JF, 1991, ANTIBIOTICS LAB MED, P17
[2]   In vitro activities of beta-lactam-beta-lactamase inhibitor combinations against Stenotrophomonas maltophilia: Correlation between methods for testing inhibitory activity, time-kill curves, and bactericidal activity [J].
Bellido, JLM ;
Criado, SM ;
Garcia, IG ;
Manzanares, MAA ;
Zufiaurre, MNG ;
GarciaRodriguez, JA .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1997, 41 (12) :2612-2615
[3]   A FUNCTIONAL CLASSIFICATION SCHEME FOR BETA-LACTAMASES AND ITS CORRELATION WITH MOLECULAR-STRUCTURE [J].
BUSH, K ;
JACOBY, GA ;
MEDEIROS, AA .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1995, 39 (06) :1211-1233
[4]   Comparison of various in vitro susceptibility methods for testing Stenotrophomonas maltophilia [J].
Carroll, KC ;
Cohen, S ;
Nelson, R ;
Campbell, DM ;
Claridge, JD ;
Garrison, MW ;
Kramp, J ;
Malone, C ;
Hoffmann, M ;
Anderson, DE .
DIAGNOSTIC MICROBIOLOGY AND INFECTIOUS DISEASE, 1998, 32 (03) :229-235
[5]  
Fang F C, 1996, Curr Clin Top Infect Dis, V16, P52
[6]   ANTIBIOTIC SUSCEPTIBILITY PROFILE OF XANTHOMONAS-MALTOPHILIA - INVITRO ACTIVITY OF BETA-LACTAM BETA-LACTAMASE INHIBITOR COMBINATIONS [J].
GARCIARODRIGUEZ, JA ;
SANCHEZ, JEG ;
GARCIA, MIG ;
SANCHEZ, EG ;
BELLIDO, JLM .
DIAGNOSTIC MICROBIOLOGY AND INFECTIOUS DISEASE, 1991, 14 (03) :239-243
[7]   Stenotrophomonas maltophilia: Emergence of multidrug-resistant strains during therapy and in an in vitro pharmacodynamic chamber model [J].
Garrison, MW ;
Anderson, DE ;
Campbell, DM ;
Carroll, KC ;
Malone, CL ;
Anderson, JD ;
Hollis, RJ ;
Pfaller, MA .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1996, 40 (12) :2859-2864
[8]   Resistance mechanisms in Pseudomonas aeruginosa and other nonfermentative gram-negative bacteria [J].
Hancock, REW .
CLINICAL INFECTIOUS DISEASES, 1998, 27 :S93-S99
[9]   INVITRO SUSCEPTIBILITY OF 33 CLINICAL CASE ISOLATES OF XANTHOMONAS-MALTOPHILIA - INCONSISTENT CORRELATION OF AGAR DILUTION AND OF DISK DIFFUSION TEST-RESULTS [J].
HOHL, P ;
FREI, R ;
AUBRY, P .
DIAGNOSTIC MICROBIOLOGY AND INFECTIOUS DISEASE, 1991, 14 (05) :447-450
[10]   Bacteremia due to Stenotrophomonas (Xanthomonas) maltophilia: A prospective, multicenter study of 91 episodes [J].
Muder, RR ;
Harris, AP ;
Muller, S ;
Edmond, M ;
Chow, JW ;
Papadakis, K ;
Wagener, MW ;
Bodey, GP ;
Steckelberg, JM .
CLINICAL INFECTIOUS DISEASES, 1996, 22 (03) :508-512