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新出现的耐碳青霉烯类感染、其流行病学及新的治疗选择:综述

Emerging Carbapenem-Resistant Infection, Its Epidemiology and Novel Treatment Options: A Review.

作者信息

Tilahun Mihret, Kassa Yeshimebet, Gedefie Alemu, Ashagire Melaku

机构信息

Department of Medical Laboratory Sciences, College of Medicine and Health Science, Wollo University, Dessie, Ethiopia.

出版信息

Infect Drug Resist. 2021 Oct 21;14:4363-4374. doi: 10.2147/IDR.S337611. eCollection 2021.

Abstract

Infections due to multidrug-resistant have become major international public health problem due to the inadequate treatment options and the historically lagged pace of development of novel antimicrobial drugs. Inappropriate antimicrobial use in humans and animals coupled with increased global connectivity aided to the transmission of drug-resistant infections. Carbapenems are the medications of choice for extended-spectrum beta-lactamase and AmpC producers, but alternatives are currently needed because carbapenem resistance is increasing globally. This review pointed to discuss emerging drug-resistant , its epidemiology and novel treatment options for infections, which date back from 2010 to 2019 by searching Google Scholar, PubMed, PMC, Hinari and other different websites. The occurrence of carbapenem-resistant is reported worldwide with great regional variability. The rise of carbapenem-resistant poses a threat to all nations. Enzyme synthesis, efflux pumps, and porin mutations are the main methods by which acquire resistance to carbapenems. The major resistance mechanism among these is enzyme synthesis. Most carbapenem resistance is caused by three enzyme groups: carbapenemase (Ambler class A), metallo-ß-lactamases (Ambler class B), and oxacillinase-48 (Ambler class D). Ceftazidime-avibactam, which was newly licensed for carbapenemase producers, is the most common treatment option for infections. Meropenem-vaborbactam, imipenem-relebactam, plazomicin, cefiderocol, eravacycline, and aztreonam-avibactam are recently reported to be active against carbapenem-resistant ; and are also in ongoing trials for different populations and combinations with other antibacterial agents. Overall, treatment must be tailored to the patient's susceptibility profile, type and degree of infection, and personal characteristics.

摘要

由于治疗选择有限以及新型抗菌药物研发长期滞后,耐多药感染已成为重大的国际公共卫生问题。人类和动物中抗菌药物的不当使用,再加上全球连通性增加,助长了耐药感染的传播。碳青霉烯类药物是治疗产超广谱β-内酰胺酶和AmpC酶菌株感染的首选药物,但由于全球范围内碳青霉烯耐药性不断增加,目前需要其他替代药物。本综述旨在通过检索谷歌学术、PubMed、PMC、Hinari和其他不同网站,讨论2010年至2019年期间出现的耐药感染、其流行病学及新型治疗方案。全球范围内均有碳青霉烯耐药感染的报道,且存在很大的地区差异。碳青霉烯耐药感染的增加对所有国家都构成威胁。酶合成、外排泵和孔蛋白突变是细菌对碳青霉烯类药物产生耐药性的主要方式。其中主要的耐药机制是酶合成。大多数碳青霉烯耐药是由三类酶引起的:A类碳青霉烯酶(安布勒A类)、金属β-内酰胺酶(安布勒B类)和氧头孢烯酶-48(安布勒D类)。新获批用于治疗产碳青霉烯酶菌株感染的头孢他啶-阿维巴坦是最常用的治疗方案。最近有报道称,美罗培南-巴坦、亚胺培南-瑞巴坦、普拉佐米星、头孢地尔、依拉环素和氨曲南-阿维巴坦对碳青霉烯耐药菌有活性;并且它们也正在针对不同人群以及与其他抗菌药物联合使用进行临床试验。总体而言,治疗必须根据患者的药敏情况、感染类型和程度以及个人特征进行调整。

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