Dowzicky Michael J, Park Choong H
Wyeth Pharmaceuticals, Collegeville, Pennsylvania 19426, USA.
Clin Ther. 2008 Nov;30(11):2040-50. doi: 10.1016/j.clinthera.2008.11.006.
The Tigecycline Evaluation and Surveillance Trial (TTEST) is a global surveillance study initiated in 2004.Its goal is to assess the in vitro activity of the glycylcycline, tigecycline, and comparator antimicrobials.
The aim of this study was to measure the in vitro activity of a panel of antimicrobial agents against gram-negative and gram-positive organisms collected in the United States in 2005, 2006, and 2007.
Isolates were collected from 172 centers across the United States.In vitro activity was assessed using Clinical and Laboratory Standards Institute (CLSI) guidelines and CLSI or US Food and Drug Administration interpretive criteria.
Overall, data on 20,897 gram-negative and 8949 gram-positive isolates were collected. For the majority of organisms, percentage susceptibilities were unchanged over the 3 years of collection. One exception was Acinetobacter baumannii; rates of susceptibility to the majority of agents in the panel decreased by approximately 10% over the 3 years. Rates of resistant phenotypes were relatively unchanged with mean percentages over the 3 years of: 8.9% (337/3787) for extended beta-spectrum beta-lactamase (ESBL)-producing Klebsiella pneumoniae; 2.1% (17/801) for ESBL-producing Klebsiella oxytoca; 2.3% (111/4861) for ESBL-pproducing Escherichia coli; 56.2% (2564/4560) for methicillin-resistant Staphylococcus aureus; 5.1% (97/1903) for vancomycin-resistant Enterococcus faecalis; and 67.2% (487/725) for vancomycin-resistant Enterococcus faecium. The minimum inhibitory concentration required to inhibit the growth of 90% of organisms (MIC(90)) for tigecycline was stable over the 3 years and was < or = 22 mg/L against non-ESBL-producing K pneumoniae, K oxytoca, E coli, Enterobacter aerogenes, Enterobacter cloacae, Serratia marcescens, and A baumannii. Against methicillin susceptible and -resistant S aureus, E faecalis, E faecium, and Streptococcus agalactiae tigecycline MIC(90)s were < or = 0.25 mg/L.
This report of 3 years of data from the TEST study suggests stable susceptibility rates among gram-negative and gram-positive organisms, with the exception of decreased susceptibility rates for A baumannii. Tigecycline continued to have good activity against Enterobacteriaceae, A baumannii, S aureus, E faecalis, E faecium, and S agalactiae.
替加环素评估与监测试验(TTEST)是一项于2004年启动的全球监测研究。其目的是评估甘氨酰环素、替加环素及对照抗菌药物的体外活性。
本研究旨在测定一组抗菌药物对2005年、2006年和2007年在美国收集的革兰阴性菌和革兰阳性菌的体外活性。
从美国各地的172个中心收集分离株。使用临床和实验室标准协会(CLSI)指南以及CLSI或美国食品药品监督管理局的解释标准评估体外活性。
总体而言,收集了20897株革兰阴性菌和8949株革兰阳性菌的相关数据。在3年的收集期内,大多数菌株的药敏率没有变化。一个例外是鲍曼不动杆菌;在这3年中,该菌对大多数受试药物的药敏率下降了约10%。耐药表型的发生率相对稳定,3年的平均发生率分别为:产超广谱β-内酰胺酶(ESBL)的肺炎克雷伯菌为8.9%(337/3787);产ESBL的产酸克雷伯菌为2.1%(17/801);产ESBL的大肠埃希菌为2.3%(111/4861);耐甲氧西林金黄色葡萄球菌为56.2%(2564/4560);耐万古霉素粪肠球菌为5.1%(97/1903);耐万古霉素屎肠球菌为67.2%(487/725)。替加环素抑制90%菌株生长所需的最低抑菌浓度(MIC90)在3年内保持稳定,对非产ESBL的肺炎克雷伯菌、产酸克雷伯菌、大肠埃希菌、产气肠杆菌、阴沟肠杆菌、粘质沙雷菌和鲍曼不动杆菌,MIC90≤22mg/L。对甲氧西林敏感和耐药的金黄色葡萄球菌、粪肠球菌、屎肠球菌和无乳链球菌,替加环素的MIC90≤0.25mg/L。
这份来自TTEST研究的3年数据报告表明,革兰阴性菌和革兰阳性菌的药敏率总体稳定,但鲍曼不动杆菌的药敏率有所下降。替加环素对肠杆菌科细菌、鲍曼不动杆菌、金黄色葡萄球菌、粪肠球菌、屎肠球菌和无乳链球菌仍具有良好的活性。