JMI Laboratories, Inc., 345 Beaver Kreek Center, Suite A, North Liberty, IA 52317, USA.
AstraZeneca Pharmaceuticals L.P., Waltham, MA 02451, USA.
Int J Antimicrob Agents. 2016 Mar;47(3):235-42. doi: 10.1016/j.ijantimicag.2016.01.004. Epub 2016 Feb 3.
The activities of the novel β-lactam/non-β-lactam β-lactamase inhibitor combination ceftazidime/avibactam and comparators were evaluated against isolates from pneumonia in hospitalised patients including ventilated patients (PHP, pneumonia not designated as VABP; VABP, pneumonia in ventilated patients). Isolates were from the European-Mediterranean region (EuM), China and the USA collected in the SENTRY Antimicrobial Surveillance Program between 2009 and 2011 inclusive. A total of 2393 organisms from PHP were from the EuM, 888 from China and 3213 from the USA; from VABP patients there were 918, 97 and 692 organisms collected, respectively. Among Enterobacteriaceae from PHP, ceftazidime/avibactam MIC90 values against Escherichia coli ranged from 0.25-0.5mg/L and Klebsiella spp. MIC90 values were 0.5mg/L in each region. Among VABP isolates, MIC90 values for ceftazidime/avibactam against E. coli were 0.25mg/L; for Klebsiella spp. from VABP patients, MIC90 values were similar to those obtained against PHP isolates. The MIC of ceftazidime/avibactam was ≤8mg/L against 92-96% of Pseudomonas aeruginosa isolated from PHP patients. Isolates of P. aeruginosa from VABP patients were of lower susceptibility to all antibacterial agents (e.g. depending on region, meropenem susceptibilities were 51.2-69.4% in contrast to 68.3-76.7% among PHP patients). However, ceftazidime/avibactam inhibited 79.2-95.4% of VABP isolates at an MIC of ≤8mg/L. Acinetobacter spp. were resistant to many agents and only rates of susceptibility to colistin were >90% across all regions both for PHP and VABP isolates. Ceftazidime/avibactam was generally active against a high proportion of isolates resistant to ceftazidime from PHP and VAPB patients.
新型β-内酰胺/非β-内酰胺β-内酰胺酶抑制剂组合头孢他啶/阿维巴坦与对照药物对住院肺炎患者(包括呼吸机相关肺炎患者[VAPB])分离株的活性进行了评估。分离株来自欧洲-地中海地区(EuM)、中国和美国,收集于 2009 年至 2011 年期间的 SENTRY 抗菌监测计划。来自 PHP 的 2393 株病原体来自 EuM,888 株来自中国,3213 株来自美国;来自 VABP 患者的病原体分别有 918、97 和 692 株。在来自 PHP 的肠杆菌科中,头孢他啶/阿维巴坦对大肠杆菌的 MIC90 值范围为 0.25-0.5mg/L,在每个地区对克雷伯菌属的 MIC90 值均为 0.5mg/L。在 VABP 分离株中,头孢他啶/阿维巴坦对大肠杆菌的 MIC90 值为 0.25mg/L;对来自 VABP 患者的克雷伯菌属的 MIC90 值与来自 PHP 分离株的 MIC90 值相似。对来自 PHP 患者的 92-96%铜绿假单胞菌分离株,头孢他啶/阿维巴坦的 MIC 为≤8mg/L。来自 VABP 患者的铜绿假单胞菌分离株对所有抗菌药物的敏感性较低(例如,根据地区的不同,美罗培南的敏感性分别为 51.2-69.4%,而来自 PHP 患者的敏感性分别为 68.3-76.7%)。然而,头孢他啶/阿维巴坦在 MIC≤8mg/L 时抑制 79.2-95.4%的 VABP 分离株。不动杆菌属对许多药物均具有耐药性,在所有地区,来自 PHP 和 VABP 患者的分离株对黏菌素的敏感性均>90%。头孢他啶/阿维巴坦对来自 PHP 和 VAPB 患者的大多数对头孢他啶耐药的分离株均具有较高的活性。