Current and Emerging Treatment Options for Multidrug Resistant Escherichia coli Urosepsis: A Review

被引:19
|
作者
Walker, Mikaela M. [1 ]
Roberts, Jason A. [1 ,2 ,3 ,4 ]
Rogers, Benjamin A. [5 ,6 ]
Harris, Patrick N. A. [1 ,7 ]
Sime, Fekade B. [1 ]
机构
[1] Univ Queensland, Fac Med, UQ Ctr Clin Res, Brisbane, Qld 4029, Australia
[2] Royal Brisbane & Womens Hosp, Dept Pharm, Brisbane, Qld 4029, Australia
[3] Royal Brisbane & Womens Hosp, Dept Intens Care Med, Brisbane, Qld 4029, Australia
[4] Univ Montpellier, Nimes Univ Hosp, Div Anaesthesiol Crit Care Emergency & Pain Med, F-30029 Nimes, France
[5] Monash Hlth, Monash Infect Dis, Melbourne, Vic 3168, Australia
[6] Monash Univ, Ctr Inflammatory Dis, Melbourne, Vic 3168, Australia
[7] Hlth Support Queensland, Pathol Queensland, Herston, Qld 4006, Australia
来源
ANTIBIOTICS-BASEL | 2022年 / 11卷 / 12期
关键词
multidrug resistance; urosepsis; Escherichia coli; MRE; URINARY-TRACT-INFECTIONS; AMPC BETA-LACTAMASES; KLEBSIELLA-PNEUMONIAE; POLYMYXIN-B; PIPERACILLIN-TAZOBACTAM; INHIBITOR COMBINATIONS; CEFTAZIDIME-AVIBACTAM; PANDRUG-RESISTANT; RISK-FACTORS; TIGECYCLINE;
D O I
10.3390/antibiotics11121821
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Escherichia coli is a versatile commensal and pathogenic member of the human microflora. As the primary causative pathogen in urosepsis, E. coli places an immense burden on healthcare systems worldwide. To further exacerbate the issue, multi drug resistance (MDR) has spread rapidly through E. coli populations, making infections more troublesome and costlier to treat. This paper aimed to review the literature concerning the development of MDR in uropathogenic E. coli (UPEC) and explore the existing evidence of current and emerging treatment strategies. While some MDR strains maybe treated with beta-lactam-beta-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 beta-lactam-beta-lactamase or carbapenemase inhibitor combinations, cefiderocol, polymyxins, tigecycline, aminoglycosides or fosfomycin. For metallo-beta-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 E. coli urosepsis.
引用
收藏
页数:20
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