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回顾针对耐碳青霉烯类药物的新型治疗选择。

Reviewing novel treatment options for carbapenem-resistant .

作者信息

Mackow Natalie A, van Duin David

机构信息

Division of Infectious Diseases, University of North Carolina School of Medicine, Chapel Hill, NC, USA.

出版信息

Expert Rev Anti Infect Ther. 2024 Jan-Jun;22(1-3):71-85. doi: 10.1080/14787210.2024.2303028. Epub 2024 Feb 12.

Abstract

INTRODUCTION

Carbapenem resistant (CRE) are a major threat to global health and hospital-onset CRE infections have risen during the COVID-19 pandemic. Novel antimicrobials are now available for the treatment of CRE infections. There remains an urgent need for new antimicrobials for CRE, especially for those producing metallo-β-lactamases.

AREAS COVERED

This article discusses previously published research supporting currently available novel antimicrobials for the treatment of CRE infections. Newer compounds currently being evaluated in clinical trials are covered. A literature search was conducted in PubMed over all available dates for relevant published papers and conference abstracts with the search terms, 'CRE,' 'carbapenem-resistant Enterobacterales,' 'β-lactam-β-lactamase inhibitor,' 'KPC,' 'NDM,' 'metallo-β-lactamase,' 'ceftazidime-avibactam,' 'meropenem-vaborbactam,' 'imipenem-cilastatin-relebactam,' 'cefiderocol,' 'eravacycline,' 'plazomicin,' 'taniborbactam,' 'zidebactam,' and 'nacubactam.'

EXPERT OPINION

Novel antimicrobials for CRE infections have been developed, most notably the β-lactam-β-lactamase inhibitor combinations, though treatment options for infections with metallo-β-lactamase producing Enterobacterales remain few and have limitations. Development of antibiotics with activity against metallo-β-lactamase producing Enterobacterales is eagerly awaited, and there are promising new compounds in clinical trials. Finally, more clinical research is needed to optimize and individualize treatment approaches, which will help guide antimicrobial stewardship initiatives aimed at reducing the spread of CRE and development of further resistance.

摘要

引言

耐碳青霉烯类肠杆菌科细菌(CRE)是对全球健康的重大威胁,且在新冠疫情期间医院获得性CRE感染有所增加。目前已有新型抗菌药物可用于治疗CRE感染。对于CRE,尤其是产金属β-内酰胺酶的CRE,仍然迫切需要新的抗菌药物。

涵盖领域

本文讨论了先前发表的支持目前可用于治疗CRE感染的新型抗菌药物的研究。还涵盖了目前正在临床试验中评估的更新的化合物。在PubMed上对所有可用日期进行了文献检索,以搜索词“CRE”、“耐碳青霉烯类肠杆菌科细菌”、“β-内酰胺-β-内酰胺酶抑制剂”、“KPC”、“NDM”、“金属β-内酰胺酶”、“头孢他啶-阿维巴坦”、“美罗培南-巴罗巴坦”、“亚胺培南-西司他丁-瑞来巴坦”、“头孢地尔”、“依拉环素”、“普拉唑米星”、“他尼硼巴坦”、“齐德巴坦”和“那库巴坦”搜索相关发表的论文和会议摘要。

专家意见

已开发出用于治疗CRE感染的新型抗菌药物,最显著的是β-内酰胺-β-内酰胺酶抑制剂组合,不过对于产金属β-内酰胺酶的肠杆菌科细菌感染的治疗选择仍然很少且有局限性。急切期待开发出对产金属β-内酰胺酶的肠杆菌科细菌有活性的抗生素,并且在临床试验中有一些有前景的新化合物。最后,需要更多的临床研究来优化和个体化治疗方法,这将有助于指导旨在减少CRE传播和进一步耐药性发展的抗菌药物管理举措。

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