Department of Clinical Laboratory, Peking Union Medical College Hospital, Peking Union Medical College, Chinese Academy of Medical Science, Beijing, 100730, China.
Antimicrob Resist Infect Control. 2020 Oct 27;9(1):166. doi: 10.1186/s13756-020-00829-z.
This study reports the global trends of antimicrobial susceptibility to ceftaroline and ceftazidime-avibactam using data from the Antimicrobial Testing Leadership and Surveillance (ATLAS) program between 2012 and 2016.
For the 2012-2016 ATLAS program, 205 medical centers located in Africa-Middle East (n = 12), Asia-Pacific (n = 32), Europe (n = 94), Latin America (n = 26), North America (n = 31), and Oceania (n = 10) consecutively collected the clinical isolates. The minimum inhibitory concentrations (MICs) and in vitro susceptibilities to ceftaroline and ceftazidime-avibactam were assessed using the Clinical and Laboratory Standards Institute (CLSI) 2019and European Committee on Antimicrobial Susceptibility Testing (EUCAST) 2019 guidelines.
Between 2012 and 2016, 176,345 isolates were collected from around the globe and included in the analysis. Regarding Gram-negative bacteria, ceftazidime-avibactam demonstrated high susceptibility (> 90%) against Enterobacteriaceae and Pseudomonas aeruginosa, with increased antimicrobial activity observed from the addition of avibactam (4 mg/L) to ceftazidime. Regarding Gram-positive bacteria, ceftaroline showed > 90% susceptibility against Staphylococcus aureus, Streptococcus pneumoniae, α-and β-hemolytic Streptococcus. The antimicrobial susceptibilities to ceftaroline and ceftazidime-avibactam were mostly stable from 2012 to 2016, but the susceptibilities to ceftazidime-avibactam to carbapenem-resistant (CR) Klebsiella pneumonia (88.4-81.6%) and to CR-P. aeruginosa (89.6-72.7%) decreased over time. In terms of regional difference, the susceptibilities of methicillin-resistant S. aureus to ceftaroline in Asia and of CR-K. pneumonia to ceftazidime-avibactam in Asia/Africa-Middle East were lower compared with other regions, while the susceptibility of CR-P. aeruginosa to ceftazidime-avibactam in North America was higher.
The addition of avibactam improves the activity of ceftazidime against Enterobacteriaceae and P. aeruginosa. The global antimicrobial susceptibilities to ceftaroline and ceftazidime-avibactam were, in general, stable from 2012 to 2016, but a marked reduction in the susceptibilities of specific species and CR-P. aeruginosa to ceftazidime-avibactam was observed.
本研究报告了使用 2012 年至 2016 年期间抗菌药物测试领导和监测(ATLAS)计划的数据,得出头孢洛林和头孢他啶-阿维巴坦的全球抗菌药物敏感性趋势。
在 2012-2016 年 ATLAS 计划中,来自非洲-中东(n=12)、亚太地区(n=32)、欧洲(n=94)、拉丁美洲(n=26)、北美(n=31)和大洋洲(n=10)的 205 个医疗中心连续采集临床分离株。采用临床和实验室标准协会(CLSI)2019 年和欧洲抗菌药物敏感性试验委员会(EUCAST)2019 年指南评估头孢洛林和头孢他啶-阿维巴坦的最低抑菌浓度(MIC)和体外药敏性。
2012 年至 2016 年间,从全球范围内采集了 176345 株分离株进行分析。对于革兰氏阴性菌,头孢他啶-阿维巴坦对肠杆菌科和铜绿假单胞菌表现出高度的敏感性(>90%),与头孢他啶相比,阿维巴坦(4mg/L)的加入增加了抗菌活性。对于革兰氏阳性菌,头孢洛林对金黄色葡萄球菌、肺炎链球菌、α-和β-溶血性链球菌的敏感性>90%。2012 年至 2016 年间,头孢洛林和头孢他啶-阿维巴坦的抗菌药物敏感性基本稳定,但碳青霉烯类耐药(CR)肺炎克雷伯菌(88.4-81.6%)和 CR-铜绿假单胞菌(89.6-72.7%)对头孢他啶-阿维巴坦的敏感性随时间逐渐降低。在地区差异方面,亚洲地区耐甲氧西林金黄色葡萄球菌对头孢洛林的敏感性以及亚洲/非洲-中东地区 CR-肺炎克雷伯菌对头孢他啶-阿维巴坦的敏感性低于其他地区,而北美地区 CR-铜绿假单胞菌对头孢他啶-阿维巴坦的敏感性较高。
阿维巴坦的加入提高了头孢他啶对肠杆菌科和铜绿假单胞菌的活性。2012 年至 2016 年间,头孢洛林和头孢他啶-阿维巴坦的全球抗菌药物敏感性总体稳定,但某些特定物种和 CR-铜绿假单胞菌对头孢他啶-阿维巴坦的敏感性明显降低。