Walker Mikaela M, Roberts Jason A, Rogers Benjamin A, Harris Patrick N A, Sime Fekade B
UQ Centre for Clinical Research, Faculty of Medicine, University of Queensland, Brisbane, QLD 4029, Australia.
Departments of Pharmacy and Intensive Care Medicine, Royal Brisbane and Women's Hospital, Brisbane, QLD 4029, Australia.
Antibiotics (Basel). 2022 Dec 15;11(12):1821. doi: 10.3390/antibiotics11121821.
is a versatile commensal and pathogenic member of the human microflora. As the primary causative pathogen in urosepsis, places an immense burden on healthcare systems worldwide. To further exacerbate the issue, multi drug resistance (MDR) has spread rapidly through populations, making infections more troublesome and costlier to treat. This paper aimed to review the literature concerning the development of MDR in uropathogenic (UPEC) and explore the existing evidence of current and emerging treatment strategies. While some MDR strains maybe treated with β-lactam-β-lactamase inhibitor combinations as well as cephalosporins, cephamycin, temocillin and fosfomycin, current treatment strategies for many MDR UPEC strains are reliant on carbapenems. Carbapenem overreliance may contribute to the alarming dissemination of carbapenem-resistance amongst some UPEC communities, which has ushered in a new age of difficult to treat infections. Alternative treatment options for carbapenem resistant UPEC may include novel β-lactam-β-lactamase or carbapenemase inhibitor combinations, cefiderocol, polymyxins, tigecycline, aminoglycosides or fosfomycin. For metallo-β-lactamase producing strains (e.g., NDM, IMP-4), combinations of cefazidime-avibacam with aztreonam have been used. Additionally, the emergence of new antimicrobials brings new hope to the treatment of such infections. However, continued research is required to successfully bring these into the clinic for the treatment of MDR urosepsis.
是人类微生物群中一种具有多种共生和致病特性的成员。作为泌尿道感染败血症的主要致病病原体,给全球医疗系统带来了巨大负担。更糟糕的是,多重耐药性(MDR)已在其菌群中迅速传播,使得感染的治疗更加棘手且成本更高。本文旨在综述有关尿路致病性大肠杆菌(UPEC)中多重耐药性发展的文献,并探讨当前及新兴治疗策略的现有证据。虽然一些多重耐药菌株可用β-内酰胺-β-内酰胺酶抑制剂组合以及头孢菌素、头孢霉素、替莫西林和磷霉素治疗,但许多多重耐药UPEC菌株目前的治疗策略依赖于碳青霉烯类药物。过度依赖碳青霉烯类药物可能导致碳青霉烯耐药性在一些UPEC群体中惊人地传播,从而开启了难以治疗的感染的新时代。对碳青霉烯耐药UPEC的替代治疗选择可能包括新型β-内酰胺-β-内酰胺酶或碳青霉烯酶抑制剂组合、头孢地尔、多粘菌素、替加环素、氨基糖苷类药物或磷霉素。对于产金属β-内酰胺酶的菌株(如NDM、IMP-4),已使用头孢他啶-阿维巴坦与氨曲南的组合。此外,新型抗菌药物的出现为这类感染的治疗带来了新希望。然而,需要持续研究以成功地将这些药物引入临床用于治疗多重耐药性泌尿道感染败血症。