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产金属β-内酰胺酶革兰阴性菌所致严重感染的治疗。

Treatment of severe infections due to metallo-β-lactamases-producing Gram-negative bacteria.

作者信息

Bassetti Matteo, Di Pilato Vincenzo, Giani Tommaso, Vena Antonio, Rossolini Gian Maria, Marchese Anna, Giacobbe Daniele R

机构信息

Infectious Diseases Unit, Ospedale Policlinico San Martino - IRCCS, Genoa, Italy.

Department of Health Sciences, University of Genoa, Genoa, Italy.

出版信息

Future Microbiol. 2020;15(15):1489-1505. doi: 10.2217/fmb-2020-0210. Epub 2020 Nov 3.

Abstract

In the last decades, there was an important paucity of agents for adequately treating infections due to metallo-β-lactamases-producing Gram-negative bacteria (MBL-GNB). Cefiderocol, a novel siderophore cephalosporin showing activity against MBL-GNB, has been recently marketed, and a combination of aztreonam and ceftazidime/avibactam has shown a possible favorable effect on survival of patients with severe MBL-GNB infections in observational studies. Other agents showing activity against MBL-GNB are currently in clinical development (e.g., cefepime/taniborbactam, LYS228, cefepime/zidebactam) that could be an important addition to our future armamentarium for severe MBL-GNB infections. Nonetheless, we should not discontinue our efforts to optimize the use of non-β-lactams agents, since they could remain an essential last-resort or alternative option in selected cases.

摘要

在过去几十年中,用于充分治疗产金属β-内酰胺酶革兰氏阴性菌(MBL-GNB)感染的药物严重匮乏。头孢地尔是一种新型铁载体头孢菌素,对MBL-GNB具有活性,最近已上市,在观察性研究中,氨曲南与头孢他啶/阿维巴坦联合使用已显示出对严重MBL-GNB感染患者的生存可能产生有利影响。目前还有其他对MBL-GNB具有活性的药物正在临床开发中(例如头孢吡肟/他尼硼巴坦、LYS228、头孢吡肟/齐德巴坦),这些药物可能会成为我们未来治疗严重MBL-GNB感染的重要武器库补充。尽管如此,我们不应停止优化非β-内酰胺类药物使用的努力,因为在某些特定情况下,它们可能仍然是至关重要的最后手段或替代选择。

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