Antimicrobial Focus, Sawbridgeworth, UK.
IHMA Europe Sàrl, Monthey, Switzerland.
J Glob Antimicrob Resist. 2024 Sep;38:71-82. doi: 10.1016/j.jgar.2024.04.014. Epub 2024 May 8.
This study was performed to investigate the activity of the novel ß-lactam/ß-lactamase inhibitor combination cefepime/enmetazobactam, against recently circulating Enterobacterales isolates from Europe from 2019 to 2021.
A total of 2627 isolates were collected, and antimicrobial susceptibility was determined according to the European Committee on Antimicrobial Susceptibility Testing guidelines. Isolates with phenotypic resistance to ceftriaxone and ceftazidime (but susceptible to meropenem) and isolates nonsusceptible to meropenem were screened for the presence of ß-lactamases.
Overall, susceptibility to third-generation cephalosporins was 77%, and 97.3% were susceptible to meropenem. Cefepime/enmetazobactam susceptibility was 97.9% (72% of these isolates were Klebsiella pneumoniae from Italy), compared with 80.0% susceptibility to piperacillin/tazobactam and 99.4% to ceftazidime/avibactam. A total of 320 isolates (12.2%) were resistant to third-generation cephalosporins but susceptible to meropenem, and virtually all (96.3%) carried an extended-spectrum ß-lactamase with or without an AmpC and these were all susceptible to cefepime/enmetazobactam. Most meropenem-nonsusceptible isolates carried a KPC (68%), which were not inhibited by cefepime/enmetazobactam but were inhibited by ceftazidime/avibactam. Additionally, most meropenem-nonsusceptible isolates carrying OXA-48 (9/12 isolates) were susceptible to cefepime/enmetazobactam.
Cefepime/enmetazobactam was highly active against Enterobacterales isolates, especially those resistant to third-generation cephalosporins. These data suggest that cefepime/enmetazobactam could be used as a carbapenem-sparing agent to replace piperacillin/tazobactam.
本研究旨在调查新型β-内酰胺/β-内酰胺酶抑制剂组合头孢吡肟/恩他培南对 2019 年至 2021 年期间来自欧洲的流行肠杆菌科分离株的活性。
共收集了 2627 株分离株,并根据欧洲抗菌药物敏感性试验委员会指南测定了抗菌药物敏感性。对表型上对头孢曲松和头孢他啶耐药(但对美罗培南敏感)的分离株以及对美罗培南不敏感的分离株进行了β-内酰胺酶的筛选。
总体而言,第三代头孢菌素的敏感性为 77%,97.3%对美罗培南敏感。头孢吡肟/恩他培南的敏感性为 97.9%(其中 72%为来自意大利的肺炎克雷伯菌),而哌拉西林/他唑巴坦的敏感性为 80.0%,头孢他啶/阿维巴坦的敏感性为 99.4%。共有 320 株(12.2%)对第三代头孢菌素耐药但对美罗培南敏感,几乎所有(96.3%)均携带扩展谱β-内酰胺酶,无论是否带有 AmpC,且均对头孢吡肟/恩他培南敏感。大多数美罗培南不敏感的分离株携带 KPC(68%),该酶不能被头孢吡肟/恩他培南抑制,但可被头孢他啶/阿维巴坦抑制。此外,携带 OXA-48(12 株中的 9 株)的大多数美罗培南不敏感的分离株对头孢吡肟/恩他培南敏感。
头孢吡肟/恩他培南对肠杆菌科分离株高度有效,特别是对第三代头孢菌素耐药的分离株。这些数据表明,头孢吡肟/恩他培南可作为碳青霉烯类药物的节约剂,替代哌拉西林/他唑巴坦。