新型β-内酰胺/β-内酰胺酶抑制剂联合用药的临床疗效、安全性及药代动力学:一项系统评价

Clinical efficacy, safety and pharmacokinetics of novel β-lactam/β-lactamase inhibitor combinations: a systematic review.

作者信息

Alarcia-Lacalle Ana, Canut-Blasco Andrés, Solinís María Ángeles, Isla Arantxa, Rodríguez-Gascón Alicia

机构信息

Microbiology, Infectious Disease, Antimicrobial Agents, and Gene Therapy, Bioaraba Health Research Institute, Vitoria-Gasteiz, Spain.

Microbiology Service, Osakidetza Basque Health Service, Araba University Hospital, Vitoria-Gasteiz, Spain.

出版信息

JAC Antimicrob Resist. 2025 Jun 19;7(3):dlaf096. doi: 10.1093/jacamr/dlaf096. eCollection 2025 Jun.

Abstract

BACKGROUND

Antimicrobial resistance is a global public health threat that requires urgent solutions. One strategy to decrease resistance of Gram-negative bacteria (GNB) to β-lactam antibiotics (BL) is their combination with β-lactamase inhibitors (BLI).

OBJECTIVES

This systematic review analyses the outcomes, safety and pharmacokinetics (PK) of recently approved or under clinical development BLI and BL/BLI combinations.

METHODS

The systematic review was conducted following the Preferred Reporting Items for Systematic Reviews and Meta-analyses (PRISMA) guidelines. PubMed, Embase, and Cochrane electronic databases were used to search for articles from January 2010 to November 2024. The studies were retrieved and screened on the basis of predefined exclusion and inclusion criteria. A quality assessment of the included studies was conducted following the New Castle-Ottawa Scale.

RESULTS

A total of 191 articles addressing clinical research regarding the efficacy, safety, tolerability, and PK of new BL/BLI combinations with avibactam, durlobactam, enmetazobactam, nacubactam, relebactam, taniborbactam, tazobactam, vaborbactam and zidebactam were included. According to the published literature, clinical research supports the novel BL/BLI combinations for the treatment of complicated urinary tract infections, complicated intra-abdominal infections, and hospital-acquired and ventilator-associated pneumonia (HAP/VAP) caused by GNB. In spite of that, the development of new BLI effective for class B metallo-β-lactamases (MBL) is still challenging, being aztreonam/avibactam the only approved combination active against MBL-producing bacteria.

CONCLUSIONS

Although there has been extensive research to develop new BLI and BL/BLI combinations, only a few have reached the market. More evidence of its usefulness in the real world is still needed.

摘要

背景

抗菌药物耐药性是一个全球性的公共卫生威胁,需要迫切解决。降低革兰氏阴性菌(GNB)对β-内酰胺类抗生素(BL)耐药性的一种策略是将其与β-内酰胺酶抑制剂(BLI)联合使用。

目的

本系统评价分析了最近获批或正在临床开发的BLI以及BL/BLI联合制剂的疗效、安全性和药代动力学(PK)。

方法

本系统评价按照系统评价和Meta分析的首选报告项目(PRISMA)指南进行。使用PubMed、Embase和Cochrane电子数据库检索2010年1月至2024年11月的文章。根据预先定义的排除和纳入标准检索并筛选研究。按照纽卡斯尔-渥太华量表对纳入研究进行质量评估。

结果

共纳入191篇关于新的BL/BLI联合制剂(含阿维巴坦、杜洛巴坦、恩美他唑巴坦、那库巴坦、雷利巴坦、他尼硼巴坦、他唑巴坦、瓦博巴坦和齐德巴坦)的疗效、安全性、耐受性和PK的临床研究文章。根据已发表的文献,临床研究支持新型BL/BLI联合制剂用于治疗由GNB引起的复杂性尿路感染、复杂性腹腔内感染以及医院获得性肺炎和呼吸机相关性肺炎(HAP/VAP)。尽管如此,开发对B类金属β-内酰胺酶(MBL)有效的新型BLI仍然具有挑战性,氨曲南/阿维巴坦是唯一获批的对产MBL细菌有效的联合制剂。

结论

尽管为开发新型BLI和BL/BLI联合制剂进行了广泛研究,但只有少数进入市场。仍需要更多其在现实世界中有用性的证据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f636/12204647/9a76544c085c/dlaf096f1.jpg

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