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厄他培南对主要腹腔内病原体的杀菌活性。

Bactericidal activity of ertapenem against major intra-abdominal pathogens.

作者信息

Borbone Sonia, Cascone Carmela, Santagati Maria, Mezzatesta Maria Lina, Stefani Stefania

机构信息

Department of Microbiological and Gynaecological Science, University of Catania, Via Androne 81, 95124 Catania, Italy.

出版信息

Int J Antimicrob Agents. 2006 Nov;28(5):396-401. doi: 10.1016/j.ijantimicag.2006.07.018. Epub 2006 Oct 11.

Abstract

Treatment of intra-abdominal infections remains a challenge owing to their polymicrobial nature and associated mortality risk. Treatment regimens must provide broad-spectrum coverage, including Gram-positive and Gram-negative aerobic and anaerobic bacteria of gastrointestinal origin. Ertapenem is a long-acting 1-beta-methyl parenteral group 1 carbapenem antibiotic that has a broad antibacterial spectrum and once-daily dosing supported by clinical studies. It is active against Gram-positive and Gram-negative bacteria, including Enterobacteriaceae, Streptococcus pneumoniae and most species of anaerobic bacteria. The aim of this study was to measure the killing effects of ertapenem against a selected group of strains responsible for intra-abdominal infections. Gram-negative isolates comprised the following species: Escherichia coli, Klebsiella pneumoniae, Klebsiella oxytoca, Klebsiella ozaenae, Enterobacter cloacae and Proteus mirabilis (extended-spectrum beta-lactamase (ESBL) producers and non-producers). Gram-positive isolates comprised methicillin-susceptible Staphylococcus aureus (MSSA), Enterococcus faecalis and anaerobic Bacteroides fragilis. Ertapenem activity was tested by determination of minimal inhibitory concentrations (MICs) and minimal bactericidal concentrations (MBCs). Killing curves were performed in monocultures and co-cultures at selected antibiotic concentrations. Ertapenem showed a rapid and potent bactericidal activity in the first few hours of the kinetic curves against E. coli (6 log(10) colony-forming unit (CFU) reduction in the first 2h), B. fragilis (4 log(10) CFU reduction in 4h), MSSA (3 log(10) CFU reduction in 4-6h), K. ozaenae (ESBL+), K. pneumoniae (ESBL+ and -), E. cloacae (ESBL-) in 1h and P. mirabilis (ESBL+) in the first 2h. The potent bactericidal activity of ertapenem compared with ceftriaxone and piperacillin/tazobactam was well demonstrated in the co-cultures of E. coli-B. fragilis and E. coli-B. fragilis-E. faecalis, whilst ertapenem was shown to be bactericidal at 24h in the mixed culture of S. aureus-P. mirabilis. These results support the potent in vitro bactericidal activity of ertapenem against all multiresistant strains selected in this study and the use of this drug in the treatment of intra-abdominal infections.

摘要

由于腹腔内感染具有多种微生物的特性以及相关的死亡风险,其治疗仍然是一项挑战。治疗方案必须提供广谱覆盖,包括革兰氏阳性和革兰氏阴性需氧菌及厌氧菌,这些细菌源自胃肠道。厄他培南是一种长效的1-β-甲基肠外1类碳青霉烯类抗生素,具有广谱抗菌谱,临床研究支持每日一次给药。它对革兰氏阳性和革兰氏阴性细菌均有活性,包括肠杆菌科细菌、肺炎链球菌和大多数厌氧菌。本研究的目的是测定厄他培南对一组引起腹腔内感染的菌株的杀菌效果。革兰氏阴性分离株包括以下菌种:大肠埃希菌、肺炎克雷伯菌、产酸克雷伯菌、臭鼻克雷伯菌、阴沟肠杆菌和奇异变形杆菌(产超广谱β-内酰胺酶(ESBL)和不产ESBL的菌株)。革兰氏阳性分离株包括甲氧西林敏感金黄色葡萄球菌(MSSA)、粪肠球菌和厌氧脆弱拟杆菌。通过测定最低抑菌浓度(MIC)和最低杀菌浓度(MBC)来测试厄他培南的活性。在选定的抗生素浓度下,在单培养物和共培养物中绘制杀菌曲线。厄他培南在动力学曲线的最初几个小时内对大肠埃希菌(前2小时菌落形成单位(CFU)减少6 log(10))、脆弱拟杆菌(4小时内CFU减少4 log(10))、MSSA(4 - 6小时内CFU减少3 log(10))、臭鼻克雷伯菌(产ESBL+)、肺炎克雷伯菌(产ESBL+和 -)、阴沟肠杆菌(产ESBL-)在1小时内以及奇异变形杆菌(产ESBL+)在前2小时内均显示出快速且强效的杀菌活性。在大肠埃希菌 - 脆弱拟杆菌以及大肠埃希菌 - 脆弱拟杆菌 - 粪肠球菌的共培养物中,厄他培南与头孢曲松和哌拉西林/他唑巴坦相比,其强效杀菌活性得到了充分证明,而在金黄色葡萄球菌 - 奇异变形杆菌的混合培养物中,厄他培南在24小时时显示出杀菌作用。这些结果支持了厄他培南对本研究中所选的所有多重耐药菌株具有强效的体外杀菌活性,以及该药物在腹腔内感染治疗中的应用。

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