JMI Laboratories, North Liberty, Iowa, USA.
Antimicrob Agents Chemother. 2013 Dec;57(12):6305-10. doi: 10.1128/AAC.01802-13. Epub 2013 Oct 7.
Ceftolozane/tazobactam, a novel antimicrobial agent with activity against Pseudomonas aeruginosa (including drug-resistant strains) and other common Gram-negative pathogens (including most extended-spectrum-β-lactamase [ESBL]-producing Enterobacteriaceae strains), and comparator agents were susceptibility tested by a reference broth microdilution method against 7,071 Enterobacteriaceae and 1,971 P. aeruginosa isolates. Isolates were collected consecutively from patients in 32 medical centers across the United States during 2011 to 2012. Overall, 15.7% and 8.9% of P. aeruginosa isolates were classified as multidrug resistant (MDR) and extensively drug resistant (XDR), and 8.4% and 1.2% of Enterobacteriaceae were classified as MDR and XDR. No pandrug-resistant (PDR) Enterobacteriaceae isolates and only one PDR P. aeruginosa isolate were detected. Ceftolozane/tazobactam was the most potent (MIC50/90, 0.5/2 μg/ml) agent tested against P. aeruginosa and demonstrated good activity against 310 MDR strains (MIC50/90, 2/8 μg/ml) and 175 XDR strains (MIC50/90, 4/16 μg/ml). Ceftolozane/tazobactam exhibited high overall activity (MIC50/90, 0.25/1 μg/ml) against Enterobacteriaceae and retained activity (MIC50/90, 4/>32 μg/ml) against many 601 MDR strains but not against the 86 XDR strains (MIC50, >32 μg/ml). Ceftolozane/tazobactam was highly potent (MIC50/90, 0.25/0.5 μg/ml) against 2,691 Escherichia coli isolates and retained good activity against most ESBL-phenotype E. coli isolates (MIC50/90, 0.5/4 μg/ml), but activity was low against ESBL-phenotype Klebsiella pneumoniae isolates (MIC50/90, 32/>32 μg/ml), explained by the high rate (39.8%) of meropenem coresistance observed in this species phenotype. In summary, ceftolozane/tazobactam demonstrated high potency and broad-spectrum activity against many contemporary Enterobacteriaceae and P. aeruginosa isolates collected in U.S. medical centers. Importantly, ceftolozane/tazobactam retained potency against many MDR and XDR strains.
头孢洛扎他唑巴坦是一种新型抗菌药物,对铜绿假单胞菌(包括耐药菌株)和其他常见革兰氏阴性病原体(包括大多数产生超广谱β-内酰胺酶[ESBL]的肠杆菌科菌株)具有活性,以及比较剂通过参考肉汤微量稀释法对 7071 株肠杆菌科和 1971 株铜绿假单胞菌分离株进行了药敏试验。分离株于 2011 年至 2012 年期间连续从美国 32 家医疗中心的患者中采集。总体而言,15.7%和 8.9%的铜绿假单胞菌分离株被归类为多药耐药(MDR)和广泛耐药(XDR),8.4%和 1.2%的肠杆菌科被归类为 MDR 和 XDR。未检测到泛耐药(PDR)肠杆菌科分离株,仅检测到一株 PDR 铜绿假单胞菌分离株。头孢洛扎他唑巴坦对铜绿假单胞菌的作用最有效(MIC50/90,0.5/2μg/ml),并对 310 株 MDR 株(MIC50/90,2/8μg/ml)和 175 株 XDR 株(MIC50/90,4/16μg/ml)表现出良好的活性。头孢洛扎他唑巴坦对肠杆菌科具有很高的总体活性(MIC50/90,0.25/1μg/ml),并保留了对许多 601 株 MDR 株的活性(MIC50/90,4/>32μg/ml),但对 86 株 XDR 株没有活性(MIC50,>32μg/ml)。头孢洛扎他唑巴坦对 2691 株大肠埃希菌分离株具有高度活性(MIC50/90,0.25/0.5μg/ml),并对大多数 ESBL 表型大肠埃希菌分离株保持良好的活性(MIC50/90,0.5/4μg/ml),但对 ESBL 表型肺炎克雷伯菌分离株的活性较低(MIC50/90,32/>32μg/ml),这归因于该种表型中观察到的美罗培南核心耐药率很高(39.8%)。总之,头孢洛扎他唑巴坦对美国医疗中心采集的许多当代肠杆菌科和铜绿假单胞菌分离株表现出高活性和广谱活性。重要的是,头孢洛扎他唑巴坦对许多 MDR 和 XDR 株仍保持活性。