Team "Resist", INSERM Unit 1184, Faculty of Medicine, Université Paris-Saclay, Service de Bactériologie-Hygiène, Hôpital Bicêtre, 78 rue du Général Leclerc, 94275, Le Kremlin-Bicêtre, France.
Bacteriology-Hygiene Unit, Assistance Publique-Hôpitaux de Paris, AP-HP Paris-Saclay, Bicêtre Hospital, Le Kremlin-Bicêtre, France.
J Antimicrob Chemother. 2023 Jul 5;78(7):1672-1676. doi: 10.1093/jac/dkad149.
Cefiderocol is a catechol-substituted cephalosporin with potent in vitro activity against carbapenem-resistant (CR) Gram-negative bacteria (GNB). Cefiderocol susceptibility testing is complex because iron concentrations need to be taken into consideration. Here, we assessed the clinical performance of Bruker's UMIC® Cefiderocol and corresponding iron-depleted CAMHB to determine MIC by broth microdilution (BMD) for clinically relevant GNB.
MICs of cefiderocol for 283 GN clinical isolates were determined by BMD using iron-depleted CAMHB. Frozen panels were used as a reference. The concentration range of cefiderocol was 0.03-32 mg/L. The isolates, with different degrees of susceptibility to cefiderocol, included Enterobacterales (n = 180), Pseudomonas aeruginosa (n = 49), Acinetobacter baumannii (n = 44) and Stenotrophomonas maltophilia (n = 10).
The rates of categorical agreement (CA), essential agreement (EA) and bias were calculated to evaluate the performance of the UMIC® Cefiderocol, as compared with the reference method. Overall, the UMIC® Cefiderocol showed 90.8% EA (95% CI: 86.9%-93.7%) with a bias of -14.5% and a CA of 90.1% (95% CI: 86.1%-93.1%). For Enterobacterales, the UMIC® Cefiderocol showed 91.7% EA (95% CI: 86.7%-94.9%) with a bias of -25.0% and a CA of 87.8% (95% CI: 82.2%-91.8%). For non-fermenters, the UMIC® Cefiderocol showed 89.3% EA (95% CI: 81.9%-93.9%) (not significantly different from 90.0%, Student t-test) with a bias of -3.9% and a CA of 94.2% (95% CI: 87.7%-97.3%).
UMIC® Cefiderocol is a valid method for the determination of cefiderocol MICs even if higher than expected discrepancies were observed with NDM-producing Enterobacterales, which presented in most cases MIC values close to the breakpoint.
头孢他啶是一种儿茶酚取代的头孢菌素,对碳青霉烯类耐药(CR)革兰氏阴性菌(GNB)具有很强的体外活性。头孢他啶药敏试验较为复杂,因为需要考虑铁浓度。在此,我们评估了布鲁克公司的 UMIC®头孢他啶和相应的缺铁 CAMHB 的临床性能,以通过肉汤微量稀释(BMD)确定临床相关 GNB 的 MIC。
使用缺铁 CAMHB 通过 BMD 测定 283 种 GN 临床分离物的头孢他啶 MIC。冷冻板用作参考。头孢他啶的浓度范围为 0.03-32 mg/L。具有不同程度头孢他啶敏感性的分离株包括肠杆菌科(n=180)、铜绿假单胞菌(n=49)、鲍曼不动杆菌(n=44)和嗜麦芽窄食单胞菌(n=10)。
计算分类一致率(CA)、基本一致率(EA)和偏差率以评估 UMIC®头孢他啶与参考方法的性能。总体而言,UMIC®头孢他啶的 EA 率为 90.8%(95%CI:86.9%-93.7%),偏差率为-14.5%,CA 率为 90.1%(95%CI:86.1%-93.1%)。对于肠杆菌科,UMIC®头孢他啶的 EA 率为 91.7%(95%CI:86.7%-94.9%),偏差率为-25.0%,CA 率为 87.8%(95%CI:82.2%-91.8%)。对于非发酵菌,UMIC®头孢他啶的 EA 率为 89.3%(95%CI:81.9%-93.9%)(与 90.0%无显著差异,Student t 检验),偏差率为-3.9%,CA 率为 94.2%(95%CI:87.7%-97.3%)。
UMIC®头孢他啶是一种测定头孢他啶 MIC 的有效方法,即使与产 NDM 的肠杆菌科观察到高于预期的差异,这些差异在大多数情况下接近折点的 MIC 值。