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亚胺培南-瑞来巴坦的临床综述与批判性评价:迄今的证据

A Clinical Review and Critical Evaluation of Imipenem-Relebactam: Evidence to Date.

作者信息

Campanella Toni A, Gallagher Jason C

机构信息

Department of Pharmacy, Jefferson Health Northeast, Philadelphia, PA, USA.

Department of Pharmacy Practice, Temple University, Philadelphia, PA, USA.

出版信息

Infect Drug Resist. 2020 Nov 25;13:4297-4308. doi: 10.2147/IDR.S224228. eCollection 2020.

DOI:10.2147/IDR.S224228
PMID:33268997
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7701153/
Abstract

Imipenem-relebactam (I-R) is a novel beta-lactam/beta-lactamase inhibitor combination given with cilastatin. It is indicated for the treatment of complicated urinary tract infections, complicated intra-abdominal infections, and hospital-acquired or ventilator-associated bacterial pneumonia. A literature search was completed to evaluate the evidence to date of I-R. I-R has in vitro activity against multidrug-resistant organisms including carbapenem-resistant and extended-spectrum beta-lactamase and carbapenem-resistant Enterobacterales. It was granted FDA approval following the promising results of two phase II clinical trials in patients with complicated urinary tract infections and complicated intra-abdominal infections. The most common adverse drug events associated with I-R were nausea (6%), diarrhea (6%), and headache (4%). I-R is a new beta-lactam/beta-lactamase inhibitor combination that will be most likely used for patients with multidrug-resistant gram-negative infections in which there are limited or no available alternative treatment options.

摘要

亚胺培南-瑞来巴坦(I-R)是一种与西司他丁联用的新型β-内酰胺类/β-内酰胺酶抑制剂组合。它适用于治疗复杂性尿路感染、复杂性腹腔内感染以及医院获得性或呼吸机相关性细菌性肺炎。已完成一项文献检索以评估迄今为止关于I-R的证据。I-R对包括耐碳青霉烯类、产超广谱β-内酰胺酶以及耐碳青霉烯类肠杆菌科细菌在内的多重耐药菌具有体外活性。在两项针对复杂性尿路感染和复杂性腹腔内感染患者的II期临床试验取得有前景的结果后,它获得了美国食品药品监督管理局(FDA)的批准。与I-R相关的最常见不良药物事件为恶心(6%)、腹泻(6%)和头痛(4%)。I-R是一种新型β-内酰胺类/β-内酰胺酶抑制剂组合,极有可能用于多重耐药革兰氏阴性菌感染且可供选择的治疗方案有限或没有的患者。

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Clin Infect Dis. 2021 Dec 6;73(11):e4599-e4606. doi: 10.1093/cid/ciaa1306.
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Impact of Intrinsic Resistance Mechanisms on Potency of QPX7728, a New Ultrabroad-Spectrum Beta-Lactamase Inhibitor of Serine and Metallo-Beta-Lactamases in , Pseudomonas aeruginosa, and Acinetobacter baumannii.内在耐药机制对QPX7728效力的影响,QPX7728是一种新型超广谱β-内酰胺酶抑制剂,可抑制铜绿假单胞菌和鲍曼不动杆菌中的丝氨酸和金属β-内酰胺酶。
Antimicrob Agents Chemother. 2020 May 21;64(6). doi: 10.1128/AAC.00552-20.
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Aloe-emodin plus TIENAM ameliorate cecal ligation and puncture-induced sepsis in mice by attenuating inflammation and modulating microbiota.
芦荟大黄素联合亚胺培南通过减轻炎症和调节微生物群改善小鼠盲肠结扎和穿刺诱导的脓毒症。
Front Microbiol. 2024 Dec 12;15:1491169. doi: 10.3389/fmicb.2024.1491169. eCollection 2024.
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Activity of imipenem/relebactam and comparators against KPC-producing Klebsiella pneumoniae and imipenem-resistant Pseudomonas aeruginosa.产 KPC 肺炎克雷伯菌和耐碳青霉烯类铜绿假单胞菌中亚胺培南/雷巴他定与其他药物的活性比较。
Eur J Clin Microbiol Infect Dis. 2024 Mar;43(3):445-457. doi: 10.1007/s10096-023-04735-1. Epub 2023 Dec 29.
5
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6
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: Infections, Animal Modeling, and Therapeutics.感染、动物模型与治疗学
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Antibiotics (Basel). 2022 Nov 14;11(11):1621. doi: 10.3390/antibiotics11111621.
In vitro activity of the novel β-lactamase inhibitor taniborbactam (VNRX-5133), in combination with cefepime or meropenem, against MDR Gram-negative bacterial isolates from China.
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Antimicrob Agents Chemother. 2020 May 21;64(6). doi: 10.1128/AAC.00130-20.
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Antimicrob Agents Chemother. 2020 Mar 24;64(4). doi: 10.1128/AAC.02255-19.
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VNRX-5133 (Taniborbactam), a Broad-Spectrum Inhibitor of Serine- and Metallo-β-Lactamases, Restores Activity of Cefepime in and Pseudomonas aeruginosa.VNRX-5133(替拉贝肟),一种广谱丝氨酸和金属β-内酰胺酶抑制剂,可恢复头孢吡肟在 和铜绿假单胞菌中的活性。
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Clin Infect Dis. 2020 Aug 14;71(4):1099-1101. doi: 10.1093/cid/ciz1159.