National Institute of Infectious Diseases and Vaccinology, National Health Research Institutes, Zhunan, Taiwan.
Division of Infectious Disease, Department of Internal Medicine, Changhua Christian Hospital, Changhua, Taiwan.
Int J Antimicrob Agents. 2020 Mar;55(3):105883. doi: 10.1016/j.ijantimicag.2020.105883. Epub 2020 Jan 8.
The aim of this study was to investigate the susceptibility of respiratory Gram-negative bacteria to ceftolozane/tazobactam and other antibiotics in the Asia-Pacific region during 2015-2016. MICs were determined using the CLSI standard broth microdilution method and interpreted accordingly. Pseudomonas aeruginosa (1574 isolates), Klebsiella pneumoniae (1226), Acinetobacter baumannii (627) and Escherichia coli (476) accounted for 73.1% of 5342 Gram-negative respiratory pathogens. Susceptibility to ceftolozane/tazobactam of individual Enterobacteriaceae was >80%, except for Enterobacter cloacae (76.6%). Ceftolozane/tazobactam inhibited 81.9% of K. pneumoniae and 91.9% of E. coli, with respective MIC/MIC values of 0.5/>32 and 0.25/2 mg/L. For carbapenem-susceptible, ESBL-producing K. pneumoniae and E. coli, susceptibility was 65.5% and 93.3%, respectively, and respective MIC/MIC values were 2/>32 and 0.5/2 mg/L. Bla was most prevalent in selected ESBL-producing K. pneumoniae (40 of 54 isolates) and E. coli (15 of 22 isolates), with ceftolozane/tazobactam susceptibility rates of 50% and 80%, respectively. Bla was the second most prevalent, and ceftolozane/tazobactam inhibited 20% of 20 K. pneumoniae isolates with bla. The only effective antibiotics for carbapenem-non-susceptible K. pneumoniae (111 isolates) and E. coli (24 isolates) were amikacin and colistin. Ceftolozane/tazobactam was effective against almost all tested P. aeruginosa and carbapenem-non-susceptible strains, with susceptibility of 92.3% and 72.8%, respectively; the respective MIC/MIC values were 1/4 and 2/>32 mg/L. The high susceptibility of ceftolozane/tazobactam remained in different age groups, patient locations, recovery times and countries, except Vietnam. In conclusion, ceftolozane/tazobactam was effective against most respiratory Gram-negative pathogens in the Asia-Pacific region; however, the emergence of carbapenem resistance mandates ongoing surveillance.
本研究旨在调查 2015-2016 年亚太地区呼吸革兰氏阴性菌对头孢洛扎他巴坦和其他抗生素的敏感性。使用 CLSI 标准肉汤微量稀释法测定 MICs,并进行相应的解释。铜绿假单胞菌(1574 株)、肺炎克雷伯菌(1226 株)、鲍曼不动杆菌(627 株)和大肠埃希菌(476 株)占 5342 株呼吸道革兰氏阴性病原体的 73.1%。除阴沟肠杆菌(76.6%)外,个别肠杆菌科对头孢洛扎他巴坦的敏感性>80%。头孢洛扎他巴坦抑制肺炎克雷伯菌和大肠埃希菌分别为 81.9%和 91.9%,MIC/MIC 值分别为 0.5/>32 和 0.25/2mg/L。对碳青霉烯类敏感、产 ESBL 的肺炎克雷伯菌和大肠埃希菌,敏感性分别为 65.5%和 93.3%,MIC/MIC 值分别为 2/>32 和 0.5/2mg/L。bla 在选定的产 ESBL 肺炎克雷伯菌(54 株中的 40 株)和大肠埃希菌(22 株中的 15 株)中最为普遍,头孢洛扎他巴坦的敏感性分别为 50%和 80%。bla 是第二常见的,头孢洛扎他巴坦抑制了 20 株 bla 阳性的肺炎克雷伯菌的 20%。对所有测试的耐碳青霉烯类肺炎克雷伯菌(111 株)和大肠埃希菌(24 株)唯一有效的抗生素是阿米卡星和黏菌素。头孢洛扎他巴坦对几乎所有测试的铜绿假单胞菌和耐碳青霉烯类的菌株均有效,敏感性分别为 92.3%和 72.8%;MIC/MIC 值分别为 1/4 和 2/>32mg/L。头孢洛扎他巴坦在亚太地区不同年龄组、患者位置、恢复时间和国家的敏感性仍然很高,除越南外。总之,头孢洛扎他巴坦对亚太地区大多数呼吸道革兰氏阴性病原体有效;然而,碳青霉烯类耐药的出现需要持续监测。