Nørskov-Lauritsen Niels, Marchandin Hélène, Dowzicky Michael J
Department of Clinical Microbiology, Aarhus University Hospital, Skejby DK-8200 Aarhus N, Denmark.
Int J Antimicrob Agents. 2009 Aug;34(2):121-30. doi: 10.1016/j.ijantimicag.2009.02.003. Epub 2009 Apr 1.
Tigecycline is a broad-spectrum antimicrobial agent that has been approved for the treatment of skin and soft-tissue infections as well as intra-abdominal infections. The Tigecycline Evaluation and Surveillance Trial (TEST) is a global, longitudinal surveillance study established in 2004 to monitor the in vitro activity of tigecycline and comparator agents against key Gram-negative and Gram-positive pathogens. This report examines data obtained for 24748 isolates collected across 24 European countries between 2004 and 2007. Tigecycline, meropenem and imipenem were the most active antimicrobial agents against most Gram-negative isolates including multidrug-resistant Acinetobacter baumannii (15.7% of the A. baumannii isolates in this study), extended-spectrum beta-lactamase (ESBL)-producing Escherichia coli (8.5% of E. coli) and ESBL-producing Klebsiella pneumoniae (13.6% of K. pneumoniae). Only amikacin was active against >90% of Pseudomonas aeruginosa isolates (92.8% susceptible). Tigecycline, linezolid and vancomycin were the most active agents against Gram-positive agents across Europe between 2004 and 2007, with tigecycline displaying the lowest MIC(90) values (minimum inhibitory concentration for 90% of the organisms) against meticillin-resistant Staphylococcus aureus (26.5% of the collected S. aureus isolates), vancomycin-resistant Enterococcus faecium (15.7% of the E. faecium strains) and penicillin-resistant Streptococcus pneumoniae (9.3% of the S. pneumoniae strains). Longitudinal analysis showed no increase in tigecycline MIC values over the 4-year study period, whilst increased resistance was noted for several comparator agents.
替加环素是一种广谱抗菌药物,已被批准用于治疗皮肤和软组织感染以及腹腔内感染。替加环素评估与监测试验(TEST)是一项于2004年设立的全球纵向监测研究,旨在监测替加环素及对照药物对关键革兰氏阴性和革兰氏阳性病原体的体外活性。本报告分析了2004年至2007年间在24个欧洲国家收集的24748株分离菌的数据。替加环素、美罗培南和亚胺培南是对大多数革兰氏阴性分离菌最具活性的抗菌药物,包括多重耐药鲍曼不动杆菌(本研究中鲍曼不动杆菌分离菌的15.7%)、产超广谱β-内酰胺酶(ESBL)的大肠埃希菌(大肠埃希菌的8.5%)和产ESBL的肺炎克雷伯菌(肺炎克雷伯菌的13.6%)。只有阿米卡星对>90%的铜绿假单胞菌分离菌有活性(92.8%敏感)。2004年至2007年间,替加环素、利奈唑胺和万古霉素是欧洲对革兰氏阳性菌最具活性的药物,替加环素对耐甲氧西林金黄色葡萄球菌(所收集金黄色葡萄球菌分离菌的26.5%)、耐万古霉素粪肠球菌(粪肠球菌菌株的15.7%)和耐青霉素肺炎链球菌(肺炎链球菌菌株的9.3%)显示出最低的MIC(90)值(90%菌株的最低抑菌浓度)。纵向分析显示,在4年的研究期间,替加环素的MIC值没有增加,而几种对照药物的耐药性有所增加。