Suppr超能文献

突破耐药性:新型β-内酰胺酶抑制剂(阿维巴坦、瓦博巴坦、瑞来巴坦)抗多重耐药超级细菌的比较综述

Breaking Through Resistance: A Comparative Review of New Beta-Lactamase Inhibitors (Avibactam, Vaborbactam, Relebactam) Against Multidrug-Resistant Superbugs.

作者信息

Karaiskos Ilias, Galani Irene, Daikos George L, Giamarellou Helen

机构信息

First Department of Internal Medicine-Infectious Diseases, Hygeia General Hospital, 15123 Athens, Greece.

Infectious Diseases Laboratory, Fourth Department of Internal Medicine, National and Kapodistrian University of Athens, 12462 Athens, Greece.

出版信息

Antibiotics (Basel). 2025 May 21;14(5):528. doi: 10.3390/antibiotics14050528.

Abstract

The introduction of new β-lactam-β-lactamase inhibitors (BLBLIs), such as ceftazidime/avibactam, meropenem/vaborbactam, and imipenem/cilastatin/relebactam, expands our therapeutic options against carbapenem-resistant Gram-negative bacteria, including those pathogens for which therapeutic options are limited. These new combinations are active against ESBL-, AmpC-, and KPC-producing Enterobacterales, with the exception of ceftazidime/avibactam, which is active in vitro against OXA-48. However, one drawback that must be taken seriously by the clinician is that they are ineffective against metallo-β-lactamases as well as . The recent introduction of aztreonam/avibactam marks a significant advancement in our therapeutic armamentarium against metallo-β-lactamase-producing pathogens. The question to be answered is whether there is a preferred, newer BLBLI combination for the treatment of KPC-producing Enterobacterales infections. This review provides a thorough analysis of the similarities and differences between these new combinations to identify the most effective treatment options. The present review aims to provide clinicians with a detailed understanding of each BLBLI treatment option to guide the optimal use of these new agents for the effective treatment of difficult infections caused by carbapenemase-producing Enterobacterales infections. This review is based on literature retrieved from PubMed, Scopus, Web of Science, and the Cochrane Library.

摘要

新型β-内酰胺-β-内酰胺酶抑制剂(BLBLIs)的引入,如头孢他啶/阿维巴坦、美罗培南/伏巴拉坦和亚胺培南/西司他丁/瑞来巴坦,拓宽了我们针对耐碳青霉烯革兰氏阴性菌的治疗选择,包括那些治疗选择有限的病原体。这些新组合对产ESBL、AmpC和KPC的肠杆菌科细菌有活性,但头孢他啶/阿维巴坦除外,它在体外对OXA-48有活性。然而,临床医生必须认真对待的一个缺点是,它们对金属β-内酰胺酶无效。氨曲南/阿维巴坦的近期引入标志着我们针对产金属β-内酰胺酶病原体的治疗武器库有了重大进展。有待回答的问题是,对于治疗产KPC的肠杆菌科细菌感染,是否有一种更优的新型BLBLI组合。本综述对这些新组合之间的异同进行了全面分析,以确定最有效的治疗选择。本综述旨在让临床医生详细了解每种BLBLI治疗选择,以指导这些新药的最佳使用,有效治疗由产碳青霉烯酶的肠杆菌科细菌感染引起的疑难感染。本综述基于从PubMed、Scopus、科学网和考克兰图书馆检索到的文献。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/778e/12108312/662a08b07e23/antibiotics-14-00528-g001.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验