Wise Mark G, Karlowsky James A, Chen Wei-Ting, Siddiqui Fakhar, Young Katherine, Motyl Mary R, Sahm Daniel F
IHMA, Schaumburg, IL 60173, USA.
IHMA, Schaumburg, IL 60173, USA; Department of Medical Microbiology and Infectious Diseases, Max Rady College of Medicine, University of Manitoba, Winnipeg, MB R3E 0J9, Canada.
J Formos Med Assoc. 2024 Mar;123(3):400-407. doi: 10.1016/j.jfma.2023.09.006. Epub 2023 Sep 20.
Imipenem/relebactam (IMR) was approved for patient use in Taiwan in 2023. We evaluated the in vitro susceptibility of recent Gram-negative pathogens collected in Taiwan hospitals to IMR and comparators with a focus on carbapenem-resistant and KPC-carrying non-Morganellaceae Enterobacterales (NME), and carbapenem-resistant Pseudomonas aeruginosa (CRPA).
From 2018 to 2021, eight hospitals in Taiwan each collected up to 250 consecutive, aerobic or facultative, Gram-negative pathogens per year from patients with bloodstream, intraabdominal, lower respiratory tract, and urinary tract infections. MICs were determined using Clinical Laboratory Standards Institute (CLSI) broth microdilution. Most isolates that were IMR-, imipenem-, or ceftolozane/tazobactam-nonsusceptible were screened for β-lactamase genes by PCR or whole-genome sequencing.
Ninety-eight percent of NME (n = 5063) and 94% of P. aeruginosa (n = 1518) isolates were IMR-susceptible. Percent susceptible values for non-carbapenem β-lactam comparators, including piperacillin/tazobactam, were 68-79% for NME isolates, while percent susceptible values for all β-lactam comparators, including meropenem, were 73-81% for P. aeruginosa. IMR retained activity against 93% of multidrug-resistant (MDR) NME and 70% of MDR P. aeruginosa. Sixty-five percent of carbapenem-resistant NME and 81% of KPC-positive NME (n = 80) were IMR-susceptible. IMR inhibited 70% of CRPA (n = 287). Fifty percent of IMR-nonsusceptible NME tested for β-lactamase carriage had an MBL or OXA-48-like enzyme, whereas most (95%) IMR-nonsusceptible P. aeruginosa examined did not carry acquired β-lactamase genes.
Based on our in vitro data, IMR may be a useful option for the treatment of hospitalized patients in Taiwan with infections caused by common Gram-negative pathogens, including carbapenem-resistant NME, KPC-positive NME, and CRPA.
亚胺培南/瑞来巴坦(IMR)于2023年在台湾获批用于患者。我们评估了台湾医院近期收集的革兰阴性病原体对IMR及对照药物的体外敏感性,重点关注耐碳青霉烯类和携带KPC的非摩根菌属肠杆菌科细菌(NME)以及耐碳青霉烯类铜绿假单胞菌(CRPA)。
2018年至2021年,台湾的八家医院每年从血流感染、腹腔感染、下呼吸道感染和尿路感染患者中各收集多达250株连续的需氧或兼性革兰阴性病原体。采用临床实验室标准协会(CLSI)肉汤微量稀释法测定最低抑菌浓度(MIC)。对大多数对IMR、亚胺培南或头孢洛扎/他唑巴坦不敏感的分离株,通过聚合酶链反应(PCR)或全基因组测序筛查β-内酰胺酶基因。
98%的NME分离株(n = 5063)和94%的铜绿假单胞菌分离株(n = 1518)对IMR敏感。非碳青霉烯类β-内酰胺对照药物(包括哌拉西林/他唑巴坦)对NME分离株的敏感率为68% - 79%,而所有β-内酰胺对照药物(包括美罗培南)对铜绿假单胞菌的敏感率为73% - 81%。IMR对93%的多重耐药(MDR)NME和70%的MDR铜绿假单胞菌仍有活性。65%的耐碳青霉烯类NME和81%的KPC阳性NME(n = 80)对IMR敏感。IMR抑制了70%的CRPA(n =
287)。检测β-内酰胺酶携带情况的IMR不敏感NME中,50%携带金属β-内酰胺酶(MBL)或OXA - 48样酶,而检测的大多数(95%)IMR不敏感铜绿假单胞菌未携带获得性β-内酰胺酶基因。
根据我们的体外数据,IMR可能是治疗台湾住院患者由常见革兰阴性病原体引起的感染的有用选择,这些病原体包括耐碳青霉烯类NME、KPC阳性NME和CRPA。