Scientific Affairs, International Health Management Associates (IHMA), 2122 Palmer Drive, Schaumburg, USA.
Medical Affairs, Merck & Co., Inc., 126 E. Lincoln Ave, Rahway, NJ 07065, USA.
Int J Infect Dis. 2022 Dec;125:250-257. doi: 10.1016/j.ijid.2022.10.014. Epub 2022 Oct 14.
We evaluated the activity of ceftolozane/tazobactam (C/T), and comparators against clinical Pseudomonas aeruginosa isolates collected for the global Study for Monitoring Antimicrobial Resistance Trends (SMART) surveillance program in ten countries in the Middle East and Africa to augment scarce standardized surveillance data in this region.
Minimum inhibitory concentrations (MICs) were determined using Clinical and Laboratory Standards Institute broth microdilution and interpreted with European Committee on Antimicrobial Susceptibility Testing breakpoints. P. aeruginosa isolates testing with C/T MIC >4 mg/l or imipenem MIC >2 mg/l were screened for β-lactamase genes.
C/T was active against 91.4% and 87.0% of P. aeruginosa isolates from the Middle East and Africa, respectively (14-21 and 7-16 percentage points higher than most β-lactam comparators, respectively). Considerable variation in susceptibility was seen across countries, which largely correlated with the observed prevalence of carbapenemases and/or extended-spectrum β-lactamases. Differences across countries were smaller for C/T than for the β-lactam comparators, ranging from 81% C/T-susceptible among isolates from Jordan to 95% for Qatar. Among subsets resistant to meropenem, ceftazidime, or piperacillin/tazobactam, C/T maintained activity against 51-73% of isolates from the Middle East and against 27-54% from Africa (where metallo-β-lactamase and GES carbapenemase rates were higher).
Given the desirability of β-lactam use among clinicians, C/T represents an important option in the treatment of infections caused by P. aeruginosa.
我们评估了头孢他啶/他唑巴坦(C/T)与比较药物对中东和非洲 10 个国家全球监测抗菌药物耐药性趋势(SMART)监测项目中收集的临床铜绿假单胞菌分离株的活性,以补充该地区稀缺的标准化监测数据。
使用临床和实验室标准协会肉汤微量稀释法测定最小抑菌浓度(MIC),并根据欧洲抗菌药物敏感性试验委员会的折点进行解释。C/T MIC 值>4mg/L 或亚胺培南 MIC 值>2mg/L 的铜绿假单胞菌分离株进行β-内酰胺酶基因筛选。
C/T 对来自中东和非洲的铜绿假单胞菌分离株的活性分别为 91.4%和 87.0%(分别比大多数β-内酰胺类比较药物高 14-21 和 7-16 个百分点)。不同国家之间的敏感性存在很大差异,这主要与碳青霉烯酶和/或超广谱β-内酰胺酶的观察到的流行率相关。C/T 与β-内酰胺类比较药物相比,各国之间的差异较小,约旦分离株的 C/T 敏感率为 81%,卡塔尔为 95%。在对美罗培南、头孢他啶或哌拉西林/他唑巴坦耐药的亚群中,C/T 对来自中东的 51-73%的分离株和来自非洲的 27-54%的分离株保持活性(那里金属β-内酰胺酶和 GES 碳青霉烯酶的发生率更高)。
鉴于临床医生对β-内酰胺类药物的需求,C/T 是治疗铜绿假单胞菌感染的重要选择。