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In vitro activity of ertapenem (MK-0826) against multi-drug resistant Streptococcus pneumoniae compared with 13 other antimicrobials

机译:厄他培南(MK-0826)对多种药物耐药的肺炎链球菌的体外活性与其他13种抗菌药物的比较

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We tested ertapenem (MK-0826), a new carbapenem, and 13 other antimicrobials by microbroth dilution against 102 isolates of Streptococcus pneumoniae, selected to include organisms resistant to a variety of drug classes. Ertapenem MICs ranged from less than or equal to 0.008 to 4 mg/l, MIC50 = 0.5 mg/l, and MIC90 = 2 mg/l. Based on MIC90, ertapenem potency was 4-fold greater than cefuroxime, 2-fold greater than amoxycillin/clavulanate, = penicillin, 2-fold less than meropenem and ceftriaxone, and 4-fold less than imipenem. Other drug classes including macrolides, tetracycline and fluoroquinolones were less potent overall than the carbapenems. Linezolid (MIC90 = 1 mg/l) was the only agent tested for which all isolates were fully susceptible. Activity of ertapenem decreased as MICs to penicillins, cephalosporins, other carbapenems and macrolides increased. Isolates resistant to clindamycin, tetracycline or fluoroquinolones showed no obvious decrease in ertapenem activity when compared with susceptible isolates with the majority of isolates resistant to these drug classes inhibited by ertapenem at concentrations less than I mg/l. Ertapenem may prove useful as an alternative to ceftriaxone and other agents in the treatment of community-acquired pneumonia (CAP) due to S. pneumoniae, including infections caused by organisms with reduced susceptibilities to other antimicrobial agents. (C) 2002 Elsevier Science B.V. and International Society of Chemotherapy. All rights reserved. [References: 13]
机译:我们通过微肉汤稀释对102株肺炎链球菌分离株(包括对多种药物有抗药性的微生物)进行了测试,测试了厄他培南(MK-0826),一种新的碳青霉烯和其他13种抗微生物药。厄他培南的MIC范围小于或等于0.008至4 mg / l,MIC50 = 0.5 mg / l,MIC90 = 2 mg / l。根据MIC90,厄他培南的效力比头孢呋辛大4倍,比阿莫西林/克拉维酸盐大2倍,=青霉素,比美罗培南和头孢曲松低2倍,比亚胺培南小4倍。总的来说,包括大环内酯类,四环素和氟喹诺酮类在内的其他药物的效力不及碳青霉烯类药物。利奈唑胺(MIC90 = 1 mg / l)是所有分离株均完全易感的唯一测试药物。随着MICs对青霉素,头孢菌素,其他碳青霉烯和大环内酯类药物的增加,厄他培南的活性降低。与易感分离株相比,对克林霉素,四环素或氟喹诺酮类耐药的分离株未显示出厄他培南活性的明显降低,大多数对这些药物类型具有耐药性的分离株在浓度低于1 mg / l时被厄他培南抑制。厄他培南可能被证明是头孢曲松和其他药物的替代品,可用于治疗由肺炎链球菌引起的社区获得性肺炎(CAP),包括由对其他抗菌药物敏感性降低的生物体引起的感染。 (C)2002 Elsevier Science B.V.和国际化学疗法学会。版权所有。 [参考:13]

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