Flamm Robert K, Sader Helio S, Farrell David J, Jones Ronald N
JMI Laboratories, North Liberty, IA 52317 USA.
JMI Laboratories, North Liberty, IA 52317 USA.
Diagn Microbiol Infect Dis. 2014 Nov;80(3):233-8. doi: 10.1016/j.diagmicrobio.2014.07.005. Epub 2014 Jul 24.
Ceftazidime-avibactam, a combination of ceftazidime and the non-β-lactam β-lactamase inhibitor avibactam, is in advanced clinical development. In this study, we report results of in vitro testing of ceftazidime-avibactam and comparator agents against a collection of urinary tract infection (UTI) isolates from the United States (USA), Europe and Mediterranean region (EMR), Latin America (LATAM), and the Asia-Pacific/South Africa regions (APAC). Clinical isolates (1 per patient episode) were collected from patients with a UTI during 2011. A total of 1797 isolates were collected from 159 medical centers. Isolates were processed at the medical centers and forwarded to a central monitoring laboratory for confirmatory identification and reference susceptibility testing. Ceftazidime-avibactam was highly active against Enterobacteriaceae and Pseudomonas aeruginosa. The MIC90 values for ceftazidime-avibactam against Enterobacteriaceae in the USA, EMR, and LATAM regions ranged from 0.25 to 0.5μg/mL. The MIC90 in the APAC was slightly elevated at 1μg/mL. A total of 6.1% (8/131) of Escherichia coli in the USA, 23.5% (43/183) in the EMR, 61.2% (30/49) in LATAM, and 75.0% (9/12) in APAC exhibited an extended-spectrum β-lactamase (ESBL) screen-positive phenotype. A total of 1.6% (2/129) of Klebsiella pneumoniae isolates in the USA were meropenem-non-susceptible (MIC ≥2μg/mL), but a rate of 10.3% (10/97) was observed in the EMR. All ESBL screen-positive phenotype and meropenem-non-susceptible E. coli and K. pneumoniae isolates exhibited a ceftazidime-avibactam MIC ≤4μg/mL. All isolates of P. aeruginosa in the USA and 80.9% (38/47) in the EMR were inhibited at a ceftazidime-avibactam MIC of ≤8μg/mL compared to 88.2% (15/17) and 61.7% (29/47) for ceftazidime alone. Ceftazidime-avibactam demonstrated wide in vitro activity against Gram-negative bacteria from patients with UTI including high potencies against multidrug-resistant organisms.
头孢他啶-阿维巴坦是头孢他啶与非β-内酰胺类β-内酰胺酶抑制剂阿维巴坦的组合,正处于临床开发后期。在本研究中,我们报告了头孢他啶-阿维巴坦及对照药物针对从美国、欧洲和地中海地区(EMR)、拉丁美洲(LATAM)以及亚太/南非地区(APAC)收集的一系列尿路感染(UTI)分离株的体外测试结果。临床分离株(每位患者发作期1株)于2011年从UTI患者中收集。共从159个医疗中心收集了1797株分离株。分离株在各医疗中心进行处理,然后送至中央监测实验室进行确证鉴定和参考药敏试验。头孢他啶-阿维巴坦对肠杆菌科细菌和铜绿假单胞菌具有高度活性。在美国、EMR和LATAM地区,头孢他啶-阿维巴坦针对肠杆菌科细菌的MIC90值范围为0.25至0.5μg/mL。APAC地区的MIC90略高,为1μg/mL。美国6.1%(8/131)的大肠杆菌、EMR地区23.5%(43/183)的大肠杆菌、LATAM地区61.2%(30/49)的大肠杆菌以及APAC地区75.0%(9/12)的大肠杆菌表现出超广谱β-内酰胺酶(ESBL)筛选阳性表型。美国1.6%(2/129)的肺炎克雷伯菌分离株对美罗培南不敏感(MIC≥2μg/mL),但在EMR地区这一比例为10.3%(10/97)。所有ESBL筛选阳性表型以及对美罗培南不敏感的大肠杆菌和肺炎克雷伯菌分离株的头孢他啶-阿维巴坦MIC≤4μg/mL。美国所有铜绿假单胞菌分离株以及EMR地区80.9%(38/47)的铜绿假单胞菌分离株在头孢他啶-阿维巴坦MIC≤8μg/mL时被抑制,而单独使用头孢他啶时这一比例分别为88.2%(15/17)和61.7%(29/47)。头孢他啶-阿维巴坦对UTI患者的革兰阴性菌表现出广泛的体外活性,包括对多重耐药菌的高效活性。