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In vitro-obtained meropenem-vaborbactam resistance mechanisms among clinical Klebsiella pneumoniae carbapenemase-producing K. pneumoniae isolates.体外获得的产碳青霉烯酶肺炎克雷伯菌中黏菌素-沃巴坦耐药机制。
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1
In vitro activity of cefepime-enmetazobactam on carbapenem-resistant Gram negatives.头孢吡肟-恩美他唑巴坦对耐碳青霉烯革兰阴性菌的体外活性
Clin Microbiol Infect. 2025 Feb;31(2):240-249. doi: 10.1016/j.cmi.2024.09.031. Epub 2024 Oct 5.
2
Vaborbactam increases meropenem susceptibility in clinical isolates displaying MexXY and AmpC upregulation.沃博巴坦增加了临床分离株中对美罗培南的敏感性,这些分离株显示 MexXY 和 AmpC 的过度表达。
mSphere. 2023 Oct 24;8(5):e0016223. doi: 10.1128/msphere.00162-23. Epub 2023 Sep 28.
3
Impact of Acquired Broad Spectrum β-Lactamases on Susceptibility to Novel Combinations Made of β-Lactams (Aztreonam, Cefepime, Meropenem, and Imipenem) and Novel β-Lactamase Inhibitors in Escherichia coli and Pseudomonas aeruginosa.获得性广谱β-内酰胺酶对大肠埃希菌和铜绿假单胞菌中新型β-内酰胺类(氨曲南、头孢吡肟、美罗培南和亚胺培南)和新型β-内酰胺酶抑制剂组合药物敏感性的影响。
Antimicrob Agents Chemother. 2023 Jul 18;67(7):e0033923. doi: 10.1128/aac.00339-23. Epub 2023 May 31.
4
In Vitro Activity of Imipenem-Relebactam, Meropenem-Vaborbactam, Ceftazidime-Avibactam and Comparators on Carbapenem-Resistant Non-Carbapenemase-Producing Enterobacterales.亚胺培南-瑞来巴坦、美罗培南-巴罗沙班、头孢他啶-阿维巴坦及对照药物对耐碳青霉烯类非产碳青霉烯酶肠杆菌科细菌的体外活性
Antibiotics (Basel). 2023 Jan 6;12(1):102. doi: 10.3390/antibiotics12010102.
5
Susceptibility of OXA-48-producing Enterobacterales to imipenem/relebactam, meropenem/vaborbactam and ceftazidime/avibactam.产 OXA-48 型肠杆菌科细菌对亚胺培南/雷巴他定、美罗培南/沃巴坦和头孢他啶/阿维巴坦的敏感性。
Int J Antimicrob Agents. 2022 Oct;60(4):106660. doi: 10.1016/j.ijantimicag.2022.106660. Epub 2022 Aug 18.
6
OXA-48-Like β-Lactamases: Global Epidemiology, Treatment Options, and Development Pipeline.OXA-48 类β-内酰胺酶:全球流行病学、治疗选择和研发管道。
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7
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Front Cell Infect Microbiol. 2022 Mar 15;12:823684. doi: 10.3389/fcimb.2022.823684. eCollection 2022.
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First Report of with Enhanced Meropenem-Hydrolyzing Ability in in China.中国首次报道具有增强美罗培南水解能力的[具体对象未明确]。
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Antimicrobial activities of ceftazidime/avibactam, ceftolozane/tazobactam, imipenem/relebactam, meropenem/vaborbactam, and comparators against Pseudomonas aeruginosa from patients with skin and soft tissue infections.头孢他啶/阿维巴坦、头孢洛扎/他唑巴坦、亚胺培南/雷巴坦、美罗培南/沃巴坦和对照药物对皮肤软组织感染患者分离的铜绿假单胞菌的抗菌活性。
Int J Infect Dis. 2021 Dec;113:279-281. doi: 10.1016/j.ijid.2021.10.022. Epub 2021 Oct 17.
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美罗培南-巴坦姆同情用药全国队列研究:对……而言,其效果并不优于美罗培南

National Cohort of Compassionate Use of Meropenem-Vaborbactam: No Benefit over Meropenem for .

作者信息

Dinh Aurélien, Bleibtreu Alexandre, Duran Clara, Bouchand Frédérique, Bosch Alexie, Crozon-Clauzel Jullien, Roncato-Saberan Mariam, Matt Morgan, Boibieux André, Fanton Annlyse, Wille Heidi, Fiaux Elise, Pilmis Benoît, Lacoste Marie, Saint-Genis Quentin, Thumerelle Caroline, Pavese Patricia, Vuotto Fanny, Senneville Eric, Potron Anaïs, Corvec Stéphane, Boutoille David, Jeannot Katy, Dortet Laurent

机构信息

Infectious Disease Unit, Raymond-Poincaré University Hospital, AP-HP Paris Saclay University, 92380 Garches, France.

Infectious Disease Unit, La Pitié-Salpétrière University Hospital, AP-HP University of Paris, 75013 Paris, France.

出版信息

Antibiotics (Basel). 2024 Dec 1;13(12):1152. doi: 10.3390/antibiotics13121152.

DOI:
10.3390/antibiotics13121152
PMID:39766541
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11672642/
Abstract

BACKGROUND

Meropenem-vaborbactam (MEM-VAB) is a novel carbapenem-beta-lactamase-inhibitor combination that demonstrates activity against carbapenem-resistant (CR) Gram-negative bacteria, and more specifically KPC-producers, since vaborbactam is an effective inhibitor of KPC enzymes in vitro. This study aimed to describe the initial uses and efficacy of MEM-VAB for compassionate treatment during the first 21 months following its early access in France.

METHOD

A national multicenter retrospective study was conducted, including all patients who received at least one dose of MEM-VAB between 20 July 2020, and 5 April 2022. Clinical characteristics and outcomes were collected using a standardized questionnaire. The minimum inhibitory concentration (MIC) of antimicrobials, and complete genome sequencing of bacteria were performed when bacterial isolates were available.

RESULTS

Ultimately, 21 patients from 15 French hospitals were included in the study. The main indication for MEM-VAB treatment was respiratory tract infections ( = 9). The targeted bacteria included ( = 12), ( = 3), ( = 3), ( = 1), ( = 1), and ( = 1). Overall, no significant advantage of vaborbactam over meropenem alone was observed across all strains of in terms of in vitro susceptibility. However, MEM-VAB demonstrated a notable impact, compared to carbapenem alone, on the MIC for the two KPC-3-producing and .

CONCLUSIONS

MEM-VAB seems effective as a salvage treatment in compassionate use, but vaborbactam was shown to lack benefits compared to meropenem in treating -related infections. Therefore, it is crucial to compare meropenem to MEM-VAB MICs, particularly for , before prescribing MEM-VAB.

摘要

背景

美罗培南-巴波巴坦(MEM-VAB)是一种新型碳青霉烯类-β-内酰胺酶抑制剂组合,对耐碳青霉烯类(CR)革兰氏阴性菌具有活性,更具体地说,对产KPC酶的细菌有活性,因为巴波巴坦在体外是KPC酶的有效抑制剂。本研究旨在描述MEM-VAB在法国早期准入后的前21个月内用于同情用药的初始用途和疗效。

方法

进行了一项全国多中心回顾性研究,纳入了2020年7月20日至2022年4月5日期间接受至少一剂MEM-VAB的所有患者。使用标准化问卷收集临床特征和结局。当有细菌分离株时,进行抗菌药物的最低抑菌浓度(MIC)测定和细菌全基因组测序。

结果

最终,来自15家法国医院的21名患者纳入研究。MEM-VAB治疗的主要适应证是呼吸道感染(n = 9)。目标细菌包括肺炎克雷伯菌(n = 12)、鲍曼不动杆菌(n = 3)、铜绿假单胞菌(n = 3)、阴沟肠杆菌(n = 1)、嗜麦芽窄食单胞菌(n = 1)和产气肠杆菌(n = 1)。总体而言,就体外敏感性而言,在所有肺炎克雷伯菌菌株中,未观察到巴波巴坦比单独使用美罗培南有显著优势。然而,与单独使用碳青霉烯类药物相比,MEM-VAB对两种产KPC-3酶的肺炎克雷伯菌和鲍曼不动杆菌的MIC有显著影响。

结论

MEM-VAB在同情用药中作为挽救治疗似乎有效,但在治疗肺炎克雷伯菌相关感染方面,与美罗培南相比,巴波巴坦未显示出益处。因此,在开具MEM-VAB之前,比较美罗培南与MEM-VAB的MIC至关重要,尤其是对于肺炎克雷伯菌。