Karaiskos Ilias, Galani Irene, Daikos George L, Giamarellou Helen
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.
Antibiotics (Basel). 2025 May 21;14(5):528. doi: 10.3390/antibiotics14050528.
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.
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。