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环丙沙星与利福平在实验性嗜肺军团菌肺炎中的比较。

Comparison of ciprofloxacin and rifampicin in experimental Legionella pneumophila pneumonia.

作者信息

Havlichek D, Pohlod D, Saravolatz L

机构信息

Division of Infectious Diseases, Henry Ford Hospital, Detroit, Michigan 48202.

出版信息

J Antimicrob Chemother. 1987 Dec;20(6):875-81. doi: 10.1093/jac/20.6.875.

Abstract

We evaluated intraperitoneal ciprofloxacin and rifampicin alone and as combination therapy in experimentally induced Legionella pneumophila pneumonia in guinea pigs. Intraperitoneal treatment began 48 h after intratracheal inoculation of 3 X 10(6) L. pneumophila and consisted of sterile saline (0.3 ml bid), ciprofloxacin (30 mg/kg bid), rifampicin (10 mg/kg/bid), or ciprofloxacin plus rifampicin (same doses). Animals were treated for five days and survivors killed after 11 days. Quantitative lung cultures were done post mortem. Respective mean and median days of animal survival were increased by treatment with ciprofloxacin plus rifampicin (8.4 and 9.5 days), ciprofloxacin (8.2 and 7.5 days), or rifampicin (8.3 and 7.5 days), compared with controls (5.5 and 5.0 days). Compared with control animals (log rank test) survival was improved by treatment with ciprofloxacin plus rifampicin (P less than or equal to 0.047) ciprofloxacin (P less than or equal to 0.047) or rifampicin (P less than or equal to 0.047). Quantitative lung cultures (cfu/g) were also decreased by treatment with ciprofloxacin plus rifampicin (2.0 X 10(4)), ciprofloxacin (5.4 X 10(4)), or rifampicin (1.7 X 10(4)) compared with controls (3.2 X 10(8)). No differences in survival, quantitative lung cultures, or animal weights were noted between treatment groups. This study demonstrates that ciprofloxacin is as effective as rifampicin in the treatment of experimentally induced L. pneumophila pneumonia and that the combination of ciprofloxacin plus rifampicin has no advantages over single agent therapy in this model.

摘要

我们评估了腹腔注射环丙沙星和利福平单独用药以及联合用药,对豚鼠实验性诱导的嗜肺军团菌肺炎的治疗效果。在气管内接种3×10⁶嗜肺军团菌48小时后开始腹腔内治疗,治疗药物包括无菌生理盐水(0.3毫升,每日两次)、环丙沙星(30毫克/千克,每日两次)、利福平(10毫克/千克,每日两次)或环丙沙星加利福平(相同剂量)。动物接受治疗五天,存活者在11天后处死。死后进行肺脏定量培养。与对照组(平均存活5.5天,中位数存活5.0天)相比,环丙沙星加利福平治疗组(平均存活8.4天,中位数存活9.5天)、环丙沙星治疗组(平均存活8.2天,中位数存活7.5天)或利福平治疗组(平均存活8.3天,中位数存活7.5天)的动物存活天数的均值和中位数均增加。与对照动物相比(对数秩检验),环丙沙星加利福平治疗组(P≤0.047)、环丙沙星治疗组(P≤0.047)或利福平治疗组(P≤0.047)的存活率均有所提高。与对照组(3.2×10⁸菌落形成单位/克)相比,环丙沙星加利福平治疗组(2.0×10⁴菌落形成单位/克)、环丙沙星治疗组(5.4×10⁴菌落形成单位/克)或利福平治疗组(1.7×10⁴菌落形成单位/克)的肺脏定量培养菌落形成单位数也减少。各治疗组之间在存活率、肺脏定量培养或动物体重方面未观察到差异。本研究表明,在治疗实验性诱导的嗜肺军团菌肺炎方面,环丙沙星与利福平效果相当,且在该模型中环丙沙星加利福平联合治疗并不比单药治疗更具优势。

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