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美罗培南/威拉巴坦:一种新一代的β-内酰胺类-β-内酰胺酶抑制剂复方制剂。

Meropenem/vaborbactam: a next generation β-lactam β-lactamase inhibitor combination.

机构信息

Department of Health Sciences, Clinical Pharmacology and Oncology Section, University of Florence , Florence, Italy.

UOC Malattie Infettive, Fondazione Policlinico Universitario A. Gemelli IRCCS , Rome, Italy.

出版信息

Expert Rev Anti Infect Ther. 2020 Jul;18(7):643-655. doi: 10.1080/14787210.2020.1756775. Epub 2020 May 3.

Abstract

INTRODUCTION

infections due to carbapenem-resistant (CRE) constitute a worldwide threat and are associated with significant mortality, especially in fragile patients, and costs. Meropenem-vaborbactam (M/V) is a combination of a group 2 carbapenem with a novel cyclic boronic acid-based β-lactamase inhibitor which has shown good efficacy against KPC carbapenemase-producing , which are amongst the most prevalent types of CRE.

AREAS COVERED

This article reviews the microbiological and pharmacological profile and current clinical experience and safety of M/V in the treatment of infections caused by CRE.

EXPERT OPINION

M/V is a promising drug for the treatment of infections due to KPC-producing CRE (KPC-CRE). It exhibited an almost complete coverage of KPC-CRE isolates from large surveillance studies and a low propensity for resistance selection, retaining activity also against strains producing KPC mutants resistant to ceftazidime-avibactam. Both meropenem and vaborbactam have a favorable pharmacokinetic profile, with similar kinetic properties, a good intrapulmonary penetration, and are efficiently cleared during continuous venovenous hemofiltration (CVVH). According to available data, M/V monotherapy is associated with higher clinical cure rates and lower rates of adverse events, especially in terms of nephrotoxicity, if compared to 'older' combination therapies.

摘要

简介

耐碳青霉烯肠杆菌科(CRE)感染构成了全球性威胁,与高死亡率相关,尤其是在脆弱患者中,还会导致高昂的医疗费用。美罗培南-法硼巴坦(M/V)是一种新型的环状硼酸β-内酰胺酶抑制剂与 2 组碳青霉烯类药物的组合,对产 KPC 碳青霉烯酶的菌株具有良好的疗效,而产 KPC 碳青霉烯酶的菌株是 CRE 中最常见的类型之一。

涵盖领域

本文综述了 M/V 治疗 CRE 感染的微生物学和药理学特性、临床应用经验及安全性。

专家意见

M/V 是治疗产 KPC 耐碳青霉烯肠杆菌科(KPC-CRE)感染的一种很有前景的药物。它对大型监测研究中的 KPC-CRE 分离株具有几乎完全的覆盖,而且不易产生耐药性,对产 KPC 突变体的菌株(对头孢他啶-阿维巴坦耐药)也保持活性。美罗培南和法硼巴坦均具有良好的药代动力学特性,其动力学特性相似,在肺部有良好的穿透性,并且在连续静脉-静脉血液滤过(CVVH)中能被有效清除。根据现有数据,与“旧”联合疗法相比,M/V 单药治疗的临床治愈率更高,不良反应发生率更低,尤其是在肾毒性方面。

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