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新型抗革兰氏阴性菌抗生素的微生物学、临床及药代动力学/药效学特征:β-内酰胺/β-内酰胺酶抑制剂联合制剂及头孢地尔——临床医生综合指南

Microbiological, Clinical, and PK/PD Features of the New Anti-Gram-Negative Antibiotics: β-Lactam/β-Lactamase Inhibitors in Combination and Cefiderocol-An All-Inclusive Guide for Clinicians.

作者信息

Principe Luigi, Lupia Tommaso, Andriani Lilia, Campanile Floriana, Carcione Davide, Corcione Silvia, De Rosa Francesco Giuseppe, Luzzati Roberto, Stroffolini Giacomo, Steyde Marina, Decorti Giuliana, Di Bella Stefano

机构信息

Clinical Pathology and Microbiology Unit, "San Giovanni di Dio" Hospital, I-88900 Crotone, Italy.

Unit of Infectious Diseases, Cardinal Massaia Hospital, I-14100 Asti, Italy.

出版信息

Pharmaceuticals (Basel). 2022 Apr 12;15(4):463. doi: 10.3390/ph15040463.

Abstract

Bacterial resistance mechanisms are continuously and rapidly evolving. This is particularly true for Gram-negative bacteria. Over the last decade, the strategy to develop new β-lactam/β-lactamase inhibitors (BLs/BLIs) combinations has paid off and results from phase 3 and real-world studies are becoming available for several compounds. Cefiderocol warrants a separate discussion for its peculiar mechanism of action. Considering the complexity of summarizing and integrating the emerging literature data of clinical outcomes, microbiological mechanisms, and pharmacokinetic/pharmacodynamic properties of the new BL/BLI and cefiderocol, we aimed to provide an overview of data on the following compounds: aztreonam/avibactam, cefepime/enmetazobactam, cefepime/taniborbactam, cefepime/zidebactam, cefiderocol, ceftaroline/avibactam, ceftolozane/tazobactam, ceftazidime/avibactam, imipenem/relebactam, meropenem/nacubactam and meropenem/vaborbactam. Each compound is described in a dedicated section by experts in infectious diseases, microbiology, and pharmacology, with tables providing at-a-glance information.

摘要

细菌耐药机制在持续且快速地演变。革兰氏阴性菌尤其如此。在过去十年中,开发新型β-内酰胺/β-内酰胺酶抑制剂(BLs/BLIs)组合的策略已取得成效,几种化合物的3期研究和真实世界研究结果也已可得。头孢地尔因其独特的作用机制值得单独讨论。鉴于总结和整合新型BL/BLI以及头孢地尔的临床结局、微生物学机制和药代动力学/药效学特性等新出现的文献数据十分复杂,我们旨在概述以下化合物的数据:氨曲南/阿维巴坦、头孢吡肟/恩美他唑巴坦、头孢吡肟/他尼硼巴坦、头孢吡肟/齐德巴坦、头孢地尔、头孢托罗/阿维巴坦、头孢他啶/阿维巴坦、亚胺培南/瑞来巴坦、美罗培南/那库巴坦和美罗培南/瓦博巴坦。传染病、微生物学和药理学领域的专家在专门的章节中对每种化合物进行了描述,并配有表格提供一目了然的信息。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6792/9028825/be8759a0acce/pharmaceuticals-15-00463-g001.jpg

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