Oueslati Saoussen, Bogaerts Pierre, Dortet Laurent, Bernabeu Sandrine, Ben Lakhal Hend, Longshaw Christopher, Glupczynski Youri, Naas Thierry
Team ReSIST, LabEx LERMIT, INSERM U1184, School of Medicine, Université Paris-Saclay, 94270 Le Kremlin-Bicêtre, France.
Bacteriology-Hygiene Unit, Assistance Publique/Hôpitaux de Paris, Bicêtre Hospital, 94270 Le Kremlin-Bicêtre, France.
Antibiotics (Basel). 2022 Oct 4;11(10):1352. doi: 10.3390/antibiotics11101352.
Infections with carbapenem-resistant (CR) Gram-negative (GN) pathogens have increased in many countries worldwide, leaving only few therapeutic options. Cefiderocol (CFDC) is approved in Europe for the treatment of aerobic GN infections in adults with limited treatment options. This study evaluated the in vitro activity of cefiderocol and comparators against multidrug-resistant (MDR) bacteria including meropenem-resistant (MR) or pandrug-resistant (PR) GN clinical isolates from France and Belgium. The minimum inhibitory concentrations (MICs) of CFDC were determined by broth microdilution, using iron-depleted cation-adjusted Mueller-Hinton broth, and were compared to those of 10 last-line antibiotics. The MICs were interpreted according to EUCAST and CLSI breakpoints, and in the absence of species-specific breakpoints, non-species-related pharmacokinetic/pharmacodynamic breakpoints were used. Among the 476 isolates tested, 322 were carbapenemase producers (CP), 58 non-CP-CRs, 52 intrinsically CR, 41 expanded-spectrum cephalosporin resistant and 5 were multi-susceptible. Susceptibility to CFDC was high using EUCAST breakpoints 81%, 99% and 84%, and was even higher using CLSI breakpoints to 93%, 100% and 88% for Enterobacterales, and , respectively. Susceptibility to cefiderocol using non-species-related breakpoints for , and , was 100%, 100% and 92.3%, respectively. The susceptibility rates were lower with the NDM producers, with values of 48% and 30% using EUCAST breakpoints and 81% and 50% using CLSI breakpoints for Enterobacterales and spp, respectively. CFDC demonstrated high in vitro susceptibility rates against a wide range of MDR GN pathogens, including MR and PR isolates.
耐碳青霉烯类(CR)革兰氏阴性(GN)病原体感染在全球许多国家呈上升趋势,治疗选择极为有限。头孢地尔(CFDC)在欧洲被批准用于治疗治疗选择有限的成人需氧GN感染。本研究评估了头孢地尔及对照药物对多药耐药(MDR)细菌的体外活性,这些细菌包括来自法国和比利时的耐美罗培南(MR)或泛耐药(PR)GN临床分离株。CFDC的最低抑菌浓度(MIC)通过肉汤微量稀释法测定,使用缺铁阳离子调整的 Mueller-Hinton 肉汤,并与 10 种最后一线抗生素的 MIC 进行比较。MIC 根据 EUCAST 和 CLSI 断点进行解释,在没有物种特异性断点的情况下,使用非物种相关的药代动力学/药效学断点。在测试的 476 株分离株中,322 株是碳青霉烯酶产生菌(CP),58 株是非 CP-CR,52 株为固有CR,41 株对超广谱头孢菌素耐药,5 株对多种药物敏感。使用 EUCAST 断点时,对 CFDC 的敏感性较高,肠杆菌科细菌、铜绿假单胞菌和鲍曼不动杆菌的敏感性分别为 81%、99%和 84%;使用 CLSI 断点时,敏感性更高,分别为 93%、100%和 88%。使用非物种相关断点时,CFDC 对肺炎克雷伯菌、铜绿假单胞菌和鲍曼不动杆菌的敏感性分别为 100%、100%和 92.3%。NDM 产生菌的敏感性率较低,使用 EUCAST 断点时,肠杆菌科细菌和鲍曼不动杆菌的敏感性值分别为 48%和 30%;使用 CLSI 断点时,分别为 81%和 50%。CFDC 对多种 MDR GN 病原体,包括 MR 和 PR 分离株,表现出较高的体外敏感性率。