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2010 年拉丁美洲导致社区获得性呼吸道和皮肤软组织感染的主要病原体的头孢洛林的光谱和效价。

Spectrum and potency of ceftaroline against leading pathogens causing community-acquired respiratory tract and skin and soft tissue infections in Latin America, 2010.

机构信息

JMI Laboratories, North Liberty, IA, USA.

出版信息

Braz J Infect Dis. 2013 Sep-Oct;17(5):564-72. doi: 10.1016/j.bjid.2013.02.008. Epub 2013 Jul 31.

Abstract

Ceftaroline, the active metabolite of the prodrug ceftaroline fosamil, is a cephalosporin with in vitro bactericidal activity against Gram-positive organisms, including methicillin-susceptible and -resistant Staphylococcus aureus, β-haemolytic and viridans group streptococci, and Streptococcus pneumoniae, as well as common Gram-negative organisms. In this study a total of 986 isolates collected in 2010 from patients in 15 medical centers in five Latin American countries from the Assessing Worldwide Antimicrobial Resistance Evaluation Program were identified as community-acquired respiratory tract or skin and soft tissue infection pathogens. Ceftaroline was the most potent agent tested against S. pneumoniae with a MIC90 value (0.12μg/mL) that was eight-fold lower than ceftriaxone, levofloxacin, and linezolid. Its spectrum of coverage (100.0% susceptible) was similar to tigecycline, linezolid, levofloxacin and vancomycin. Against Haemophilus influenzae and Moraxella catarrhalis, ceftaroline was the most active agent tested. The activity of ceftaroline against S. aureus (including MRSA) was similar to that of vancomycin and tetracycline (MIC90, 1μg/mL) and linezolid (MIC90, 2μg/mL). The β-haemolytic streptococci exhibited 100.0% susceptibility to ceftaroline. Ceftaroline activity against Escherichia coli, Klebsiella spp., and Enterobacter spp. was similar to that of ceftriaxone and ceftazidime. These parenteral cephalosporin agents have potent activity against non-extended-spectrum β-lactamase-phenotype strains, but are not active against extended-spectrum β-lactamase-phenotype strains. These results confirm the in vitro activity of ceftaroline against pathogens common in community-acquired respiratory tract and skin and soft tissue infection in Latin America, and suggest that ceftaroline fosamil could be an important therapeutic option for these infections.

摘要

头孢洛林是前体药物头孢洛林磷酸酯的活性代谢物,是一种头孢菌素,具有体外杀菌活性,可对抗革兰氏阳性菌,包括甲氧西林敏感和耐药的金黄色葡萄球菌、β-溶血性链球菌和草绿色链球菌以及肺炎链球菌,以及常见的革兰氏阴性菌。在这项研究中,从拉丁美洲五个国家的 15 个医疗中心的 2010 年收集的总共 986 株分离株被鉴定为社区获得性呼吸道或皮肤和软组织感染病原体。头孢洛林对肺炎链球菌的活性最强,其 MIC90 值(0.12μg/ml)比头孢曲松、左氧氟沙星和利奈唑胺低 8 倍。其覆盖范围(100.0%敏感)与替加环素、利奈唑胺、左氧氟沙星和万古霉素相似。对流感嗜血杆菌和卡他莫拉菌,头孢洛林是最有效的药物。头孢洛林对金黄色葡萄球菌(包括耐甲氧西林金黄色葡萄球菌)的活性与万古霉素和四环素(MIC90,1μg/ml)和利奈唑胺(MIC90,2μg/ml)相似。β-溶血性链球菌对头孢洛林 100.0%敏感。头孢洛林对大肠埃希菌、克雷伯菌属和肠杆菌属的活性与头孢曲松和头孢他啶相似。这些注射用头孢菌素对非扩展型β-内酰胺酶表型菌株具有强大的活性,但对扩展型β-内酰胺酶表型菌株没有活性。这些结果证实了头孢洛林对拉丁美洲社区获得性呼吸道和皮肤软组织感染病原体的体外活性,并表明头孢洛林磷酸酯可能是这些感染的重要治疗选择。

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Ceftaroline fosamil: a new broad-spectrum cephalosporin.头孢呋辛酯:一种新型的广谱头孢菌素。
J Antimicrob Chemother. 2011 Apr;66 Suppl 3:iii11-8. doi: 10.1093/jac/dkr095.

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