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抗菌药物组合对嗜麦芽窄食单胞菌(嗜麦芽黄单胞菌)的体外活性。

In vitro activities of antimicrobial combinations against Stenotrophomonas (Xanthomonas) maltophilia.

作者信息

Poulos C D, Matsumura S O, Willey B M, Low D E, McGeer A

机构信息

Department of Microbiology, Princess Margaret Hospital, Toronto, Ontario, Canada.

出版信息

Antimicrob Agents Chemother. 1995 Oct;39(10):2220-3. doi: 10.1128/AAC.39.10.2220.

Abstract

Stenotrophomonas (Xanthomonas) maltophilia is inherently resistant to multiple antimicrobial agents. In order to investigate the in vitro potential of combinations of antimicrobial agents, we obtained 230 epidemiologically unrelated clinical isolates from seven hospitals across Canada and from Northwestern Memorial Hospital in Chicago. Ticarcillin-clavulanate combined with ciprofloxacin or trimethoprim-sulfamethoxazole were assayed for synergy against 31 ticarcillin-resistant strains of S. maltophilia by using microtiter checkerboard panels and against 20 strains by using time-kill methodology. The combination of ciprofloxacin with ceftazidime was also evaluated by time-kill studies. Ticarcillin-clavulanate plus trimethoprim-sulfamethoxazole demonstrated synergy by checkerboard panels, with fractional inhibitory concentration indices ranging from 0.033 to 0.49, and by time-kill studies for all 20 strains tested. Synergy between ticarcillin-clavulanate plus ciprofloxacin was found by the checkerboard method for 24 of 31 strains (77%), with fractional inhibitory concentration indices ranging from 0.188 to 0.75. A correlation between synergy by the checkerboard method and the reference time-kill study method was not observed for ticarcillin-clavulanate plus ciprofloxacin, with results for 3 of 10 strains being nonconcordant. Synergy with both ticarcillin-clavulanate plus ciprofloxacin and ceftazidime plus ciprofloxacin by the time-kill method was found to correlate with ciprofloxacin MICs of <32 micrograms/ml and zone diameters of >15 mm on Mueller-Hinton agar. Evaluation of these combinations in vivo may be warranted.

摘要

嗜麦芽窄食单胞菌(嗜麦芽黄单胞菌)对多种抗菌药物具有内在抗性。为了研究抗菌药物联合使用的体外潜力,我们从加拿大的七家医院以及芝加哥的西北纪念医院获取了230株无流行病学关联的临床分离株。通过微量滴定棋盘法检测替卡西林 - 克拉维酸联合环丙沙星或甲氧苄啶 - 磺胺甲恶唑对31株耐替卡西林嗜麦芽窄食单胞菌的协同作用,并通过时间 - 杀菌方法检测对20株菌的协同作用。还通过时间 - 杀菌研究评估了环丙沙星与头孢他啶的联合作用。替卡西林 - 克拉维酸加甲氧苄啶 - 磺胺甲恶唑通过棋盘法显示出协同作用,部分抑菌浓度指数范围为0.033至0.49,并且通过时间 - 杀菌研究对所有20株受试菌株均显示协同作用。替卡西林 - 克拉维酸加环丙沙星通过棋盘法在31株菌中的24株(77%)中发现有协同作用,部分抑菌浓度指数范围为0.188至0.75。对于替卡西林 - 克拉维酸加环丙沙星,未观察到棋盘法与参考时间 - 杀菌研究方法之间的协同作用相关性,10株菌中有3株结果不一致。通过时间 - 杀菌法发现,替卡西林 - 克拉维酸加环丙沙星以及头孢他啶加环丙沙星的协同作用与环丙沙星在穆勒 - 欣顿琼脂上的最低抑菌浓度<32微克/毫升和抑菌圈直径>15毫米相关。可能有必要对这些联合用药进行体内评估。

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