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替加环素与其他抗菌药物联合应用:体外、动物及病例报告研究综述

Tigecycline in combination with other antimicrobials: a review of in vitro, animal and case report studies.

作者信息

Entenza J M, Moreillon P

机构信息

Department of Fundamental Microbiology, Faculty of Biology and Medicine, University of Lausanne, CH-1015 Lausanne, Switzerland.

出版信息

Int J Antimicrob Agents. 2009 Jul;34(1):8.e1-9. doi: 10.1016/j.ijantimicag.2008.11.006. Epub 2009 Jan 21.

Abstract

Tigecycline has been investigated in combination with other antibacterials against a wide range of susceptible and multiresistant Gram-positive and Gram-negative bacteria. Combinations have been analysed in vitro, in animal models and in human case reports. In vitro, tigecycline combined with other antimicrobials produces primarily an indifferent response (neither synergy nor antagonism). Nevertheless, synergy occurred when tigecycline was combined with rifampicin against 64-100% of Enterococcus spp., Streptococcus pneumoniae, Enterobacter spp. and Brucella melitensis isolates. Combinations of tigecycline with amikacin also showed synergy for 40-100% of Enterobacter spp., Klebsiella pneumoniae, Proteus spp. and Stenotrophomonas maltophilia isolates. Moreover, bactericidal synergisms occurred with tigecycline plus amikacin against problematic Acinetobacter baumannii and Proteus vulgaris, and with colistin against K. pneumoniae. Data from animal experiments and case reports, although limited, displayed consistent beneficial activity of tigecycline in combination with other antibacterials against multiresistant organisms, including vancomycin against penicillin-resistant S. pneumoniae in experimental meningitis, gentamicin against Pseudomonas aeruginosa in experimental pneumonia, daptomycin against Enterococcus faecium endocarditis, and colistin against K. pneumoniae bacteraemia and P. aeruginosa osteomyelitis. Antagonism was extremely rare in vitro and was not reported in vivo. Thus, tigecycline may be combined with a second antimicrobial as part of a combination regimen.

摘要

替加环素已与其他抗菌药物联合用于研究针对多种敏感及多重耐药的革兰氏阳性和革兰氏阴性细菌。这些联合用药已在体外、动物模型及人类病例报告中进行了分析。在体外,替加环素与其他抗菌药物联合使用主要产生无明显作用的反应(既无协同作用也无拮抗作用)。然而,当替加环素与利福平联合使用时,对64 - 100%的肠球菌属、肺炎链球菌、肠杆菌属和羊布鲁氏菌分离株有协同作用。替加环素与阿米卡星的联合用药对40 - 100%的肠杆菌属、肺炎克雷伯菌、变形杆菌属和嗜麦芽窄食单胞菌分离株也显示出协同作用。此外,替加环素加阿米卡星对鲍曼不动杆菌和普通变形杆菌有杀菌协同作用,替加环素与黏菌素联合对肺炎克雷伯菌有杀菌协同作用。动物实验和病例报告的数据虽然有限,但显示出替加环素与其他抗菌药物联合针对多重耐药菌具有一致的有益活性,包括在实验性脑膜炎中万古霉素联合针对青霉素耐药的肺炎链球菌、在实验性肺炎中庆大霉素联合针对铜绿假单胞菌、在粪肠球菌心内膜炎中达托霉素联合针对粪肠球菌以及在肺炎克雷伯菌败血症和铜绿假单胞菌骨髓炎中黏菌素联合针对肺炎克雷伯菌。体外拮抗作用极为罕见,体内未报告有拮抗作用。因此,替加环素可作为联合治疗方案的一部分与第二种抗菌药物联合使用。

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