首页> 外文期刊>Clinical therapeutics >Update on antimicrobial susceptibility rates among gram-negative and gram-positive organisms in the United States: results from the Tigecycline Evaluation and Surveillance Trial (TEST) 2005 to 2007.
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Update on antimicrobial susceptibility rates among gram-negative and gram-positive organisms in the United States: results from the Tigecycline Evaluation and Surveillance Trial (TEST) 2005 to 2007.

机译:美国革兰氏阴性和革兰氏阳性生物之间的抗菌药敏感性最新情况:2005年至2007年的Tigecycline评价和监视试验(TEST)的结果。

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BACKGROUND: 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. Objective: 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. METHODS: 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. RESULTS: 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. CONCLUSIONS: 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.
机译:背景:替加环素评估和监测试验(TTEST)是一项始于2004年的全球监测研究,其目的是评估甘氨酰环素,替加环素和比较抗菌素的体外活性。目的:本研究的目的是测量2005年,2006年和2007年在美国收集的一组抗菌药物对革兰氏阴性和革兰氏阳性生物的体外活性。方法:从172个中心收集了分离株使用临床和实验室标准协会(CLSI)指南以及CLSI或美国食品和药物管理局的解释性标准评估了体外活性。结果:总体上,收集了20897克阴性和8949克阳性菌株的数据。对于大多数生物来说,在收集的三年中,药敏百分比没有变化。鲍曼不动杆菌是一个例外。在过去的三年中,小组中大多数药物的敏感性下降了大约10%。耐药表型的发生率相对不变,在过去三年中的平均百分比为:产生扩大的β光谱的β-内酰胺酶(ESBL)肺炎克雷伯菌的8.9%(337/3787);产生ESBL的产酸克雷伯菌占2.1%(17/801);生产ESBL的大肠杆菌为2.3%(111/4861);耐甲氧西林的金黄色葡萄球菌为56.2%(2564/4560);耐万古霉素的粪肠球菌为5.1%(97/1903);对万古霉素耐药的粪肠球菌为67.2%(487/725)。抑制替加环素90%的微生物(MIC(90))的生长所需的最小抑制浓度在3年内保持稳定,并且对不产生ESBL的肺炎克雷伯氏菌,产氧克雷伯氏菌,大肠杆菌E≤22 mg / L大肠杆菌,产气肠杆菌,阴沟肠杆菌,粘质沙雷氏菌和鲍曼不动杆菌。对于耐甲氧西林的金黄色葡萄球菌,粪便中的大肠杆菌,粪便中的粪便和无乳链球菌tigecycline MIC(90)s≤0.25 mg / L。结论:该TEST研究的3年数据报告表明,革兰氏阴性和革兰氏阳性菌之间的药敏率稳定,但鲍曼不动杆菌的药敏率降低。 Tigecycline继续对肠杆菌科,鲍曼不动杆菌,金黄色葡萄球菌,粪肠球菌,粪肠球菌和无乳链球菌具有良好的活性。

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