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1
Meropenem-Vaborbactam as Salvage Therapy for Ceftazidime-Avibactam-Resistant Bacteremia and Abscess in a Liver Transplant Recipient.美罗培南-法硼巴坦作为肝移植受者中头孢他啶-阿维巴坦耐药菌血症和脓肿的挽救疗法。
Antimicrob Agents Chemother. 2018 Dec 21;63(1). doi: 10.1128/AAC.01551-18. Print 2019 Jan.
2
Cefiderocol versus imipenem-cilastatin for the treatment of complicated urinary tract infections caused by Gram-negative uropathogens: a phase 2, randomised, double-blind, non-inferiority trial.头孢地尔优于亚胺培南西司他丁钠治疗革兰氏阴性尿路病原体引起的复杂性尿路感染:一项 2 期、随机、双盲、非劣效性试验。
Lancet Infect Dis. 2018 Dec;18(12):1319-1328. doi: 10.1016/S1473-3099(18)30554-1. Epub 2018 Oct 25.
3
Ceftolozane-Tazobactam for the Treatment of Multidrug-Resistant Infections: A Multicenter Study.头孢洛扎-他唑巴坦治疗多重耐药感染:一项多中心研究。
Open Forum Infect Dis. 2018 Oct 31;5(11):ofy280. doi: 10.1093/ofid/ofy280. eCollection 2018 Nov.
4
Effect and Safety of Meropenem-Vaborbactam versus Best-Available Therapy in Patients with Carbapenem-Resistant Enterobacteriaceae Infections: The TANGO II Randomized Clinical Trial.美罗培南-巴坦与最佳可用疗法治疗耐碳青霉烯类肠杆菌科细菌感染患者的疗效和安全性:TANGO II随机临床试验
Infect Dis Ther. 2018 Dec;7(4):439-455. doi: 10.1007/s40121-018-0214-1. Epub 2018 Oct 1.
5
Analyses of a Ceftazidime-Avibactam-Resistant Isolate Carrying Reveals a Heterogenous Population and Reversible Genotype.携带 blaOXA-23 基因的头孢他啶-阿维巴坦耐药分离株的分析揭示了一个异质群体和可逆转的基因型。
mSphere. 2018 Sep 26;3(5):e00408-18. doi: 10.1128/mSphere.00408-18.
6
Phenotypic Detection of Carbapenemase-Producing Organisms from Clinical Isolates.从临床分离株中表型检测碳青霉烯酶产生菌。
J Clin Microbiol. 2018 Oct 25;56(11). doi: 10.1128/JCM.01140-18. Print 2018 Nov.
7
Activity of imipenem/relebactam against Pseudomonas aeruginosa with antimicrobial-resistant phenotypes from seven global regions: SMART 2015-2016.来自全球七个地区具有抗微生物耐药表型的铜绿假单胞菌对亚胺培南/雷巴他定的活性:SMART 2015-2016。
J Glob Antimicrob Resist. 2018 Dec;15:140-147. doi: 10.1016/j.jgar.2018.07.012. Epub 2018 Jul 30.
8
In Vitro Activity of Ceftolozane/Tazobactam vs Nonfermenting, Gram-Negative Cystic Fibrosis Isolates.头孢洛扎/他唑巴坦对非发酵革兰阴性囊性纤维化分离株的体外活性
Open Forum Infect Dis. 2018 Jul 2;5(7):ofy158. doi: 10.1093/ofid/ofy158. eCollection 2018 Jul.
9
Ceftazidime/Avibactam, Meropenem/Vaborbactam, or Both? Clinical and Formulary Considerations.头孢他啶/阿维巴坦、美罗培南/维巴坦还是两者皆有?临床和处方考虑。
Clin Infect Dis. 2019 Jan 18;68(3):519-524. doi: 10.1093/cid/ciy576.
10
Ceftolozane/tazobactam sensitivity patterns in Pseudomonas aeruginosa isolates recovered from sputum of cystic fibrosis patients.从囊性纤维化患者痰液中分离出的铜绿假单胞菌菌株对头孢洛赞/他唑巴坦的敏感性模式。
Diagn Microbiol Infect Dis. 2018 Sep;92(1):75-77. doi: 10.1016/j.diagmicrobio.2018.05.002. Epub 2018 May 12.

定义新型针对碳青霉烯类耐药革兰氏阴性菌的β-内酰胺类药物的作用。

Defining the Role of Novel β-Lactam Agents That Target Carbapenem-Resistant Gram-Negative Organisms.

机构信息

Departments of Pediatrics, Johns Hopkins University School of Medicine, Baltimore, Maryland.

Departments of Pharmacy, Johns Hopkins University School of Medicine, Baltimore, Maryland.

出版信息

J Pediatric Infect Dis Soc. 2019 Jul 1;8(3):251-260. doi: 10.1093/jpids/piz002.

DOI:10.1093/jpids/piz002
PMID:30793757
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6601385/
Abstract

With the current carbapenem-resistant organism crisis, conventional approaches to optimizing pharmacokinetic-pharmacodynamic parameters are frequently inadequate, and traditional salvage agents (eg, colistin, tigecycline, etc) confer high toxicity and/or have low efficacy. However, several β-lactam agents with activity against carbapenem-resistant organisms were approved recently by the US Food and Drug Administration, and more are anticipated to be approved in the near future. The primary goal of this review is to assist infectious disease practitioners with preferentially selecting 1 agent over another when treating patients infected with a carbapenem-resistant organism. However, resistance to some of these antibiotics has already developed. Antibiotic stewardship programs can ensure that they are reserved for situations in which other options are lacking and are paramount for the survival of these agents.

摘要

随着当前碳青霉烯类耐药菌危机的出现,优化药代动力学-药效学参数的常规方法往往不够充分,传统的挽救性药物(如多粘菌素、替加环素等)具有高毒性和/或低疗效。然而,最近美国食品和药物管理局批准了几种对碳青霉烯类耐药菌有活性的β-内酰胺类药物,预计在不久的将来还会有更多的药物获得批准。本综述的主要目的是帮助传染病医生在治疗感染碳青霉烯类耐药菌的患者时,优先选择一种药物而不是另一种药物。然而,这些抗生素中的一些已经产生了耐药性。抗生素管理计划可以确保这些药物仅在缺乏其他选择的情况下使用,并且对于这些药物的生存至关重要。