KILLING OF NONGROWING AND ADHERENT ESCHERICHIA-COLI DETERMINES DRUG EFFICACY IN DEVICE-RELATED INFECTIONS

被引:109
作者
WIDMER, AF
WIESTNER, A
FREI, R
ZIMMERLI, W
机构
[1] UNIV HOSP BASEL,DEPT INTERNAL MED,CH-4031 BASEL,SWITZERLAND
[2] UNIV HOSP BASEL,CENT LAB BACTERIOL,CH-4031 BASEL,SWITZERLAND
[3] UNIV HOSP BASEL,DEPT RES,CH-4031 BASEL,SWITZERLAND
关键词
D O I
10.1128/AAC.35.4.741
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Antimicrobial therapy of device-related infections often fails, despite the in vitro susceptibility of the infecting strain. Therefore, alternative laboratory-based in vitro tests are required to predict the outcome. Fleroxacin, ciprofloxacin, azteronam, and co-trimoxazole were tested against Escherichia coli ATCC 25922 in vitro and in the tissue-cage animal model. The importance of early treatment was evaluated by starting the drugs either 30 min before or 4, 12, and 24 h after bacterial challenge. Results were compared with the in vitro drug efficacy against nongrowing and adherent Escherichia coli ATCC 25922. The alternative in vitro tests correlated highly with the outcome in the tissue-cage animal model. In the prophylaxis group (drug given 30 min before bacterial challenge), co-trimoxazole was less efficacious than the other three drugs (P < 0.001). In delayed treatment, ciprofloxacin showed the highest cure rate. It was also more potent than the other drugs against nongrowing and adherent E. coli ATCC 25922. The efficacies of azteronam, fleroxacin, and ciprofloxacin dropped significantly (P < 0.01) when the time interval between bacterial challenge and the start of treatment was delayed to > 4 h. These data emphasize (i) the need for proper timing of prophylaxis in patients undergoing implant surgery, and (ii) the possibility of successful treatment of established device-related infections with drugs which kill not only growing but also nongrowing and adherent bacteria.
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页码:741 / 746
页数:6
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