Suppr超能文献

美罗培南-法硼巴坦:一种碳青霉烯类和β-内酰胺酶抑制剂,对碳青霉烯类耐药的肠杆菌科具有活性。

Meropenem-vaborbactam: a carbapenem and beta-lactamase inhibitor with activity against carbapenem-resistant Enterobacteriaceae.

机构信息

School of Pharmacy, Texas Tech University Health Sciences Center, 1718 Pine Street, Abilene, TX, 79601, USA.

出版信息

Eur J Clin Microbiol Infect Dis. 2018 Aug;37(8):1411-1419. doi: 10.1007/s10096-018-3260-4. Epub 2018 Apr 19.

Abstract

Meropenem-vaborbactam is a carbapenem and β-lactamase inhibitor combination that is newly indicated for the treatment of complicated urinary tract infections (cUTI), including adult pyelonephritis. Vaborbactam was developed due to emergence of carbapenem-resistant strains of Enterobacteriaceae. In a phase I trial, patients that received meropenem-vaborbactam 2-2 g intravenously over 3 h every 8 h, C was 58.2 ± 10.8 μg/mL for meropenem and 59.0 ± 8.4 μg/mL for vaborbactam. AUC was 186 ± 33.6 μg • h/mL for meropenem and 204 ± 34.6 μg • h/mL for vaborbactam. V = 16.3 ± 2.6 L for meropenem and 17.6 ± 2.6 L for vaborbactam. Protein binding for vaborbactam averaged 33% in humans. Plasma clearance ranged from 10.42 ± 1.85 to 14.77 ± 2.84 L/h. One phase III trial evaluated efficacy for meropenem-vaborbactam 2-2 g intravenously every 8 h versus piperacillin-tazobactam 4-0.5 g intravenously every 8 h in complicated UTI. It found non-inferiority and statistical superiority for meropenem in overall success at the end of treatment primary end point. In another phase III trial evaluating efficacy in carbapenem-resistant Enterobacteriaceae (CRE) infections, meropenem-vaborbactam 2-2 g intravenously every 8 h was associated with decreased 28-day mortality and increased clinical cure compared with a best available therapy group.

摘要

美罗培南-法硼巴坦是一种碳青霉烯类和β-内酰胺酶抑制剂的复方制剂,新适应证为治疗复杂性尿路感染(cUTI),包括成人肾盂肾炎。由于肠杆菌科出现了耐碳青霉烯类菌株,因此开发了法硼巴坦。在一项 I 期临床试验中,接受美罗培南-法硼巴坦 2-2 g 静脉滴注,每 8 小时 1 次,3 小时滴注完毕,美罗培南的 C 为 58.2±10.8μg/mL,法硼巴坦的 C 为 59.0±8.4μg/mL。美罗培南的 AUC 为 186±33.6μg·h/mL,法硼巴坦的 AUC 为 204±34.6μg·h/mL。美罗培南的 V 为 16.3±2.6 L,法硼巴坦的 V 为 17.6±2.6 L。法硼巴坦在人体内的平均蛋白结合率为 33%。血浆清除率范围为 10.42±1.85-14.77±2.84 L/h。一项 III 期临床试验评估了美罗培南-法硼巴坦 2-2 g 静脉滴注,每 8 小时 1 次与哌拉西林-他唑巴坦 4-0.5 g 静脉滴注,每 8 小时 1 次在复杂性尿路感染中的疗效。该研究发现,在治疗结束时的主要终点(总体疗效)方面,美罗培南具有非劣效性和统计学优越性。在另一项评估美罗培南-法硼巴坦在耐碳青霉烯类肠杆菌科(CRE)感染中的疗效的 III 期临床试验中,与最佳可用治疗组相比,美罗培南-法硼巴坦 2-2 g 静脉滴注,每 8 小时 1 次可降低 28 天死亡率和增加临床治愈率。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验