• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

相似文献

1
Pharmacokinetic/Pharmacodynamic Index Linked to Efficacy of the Ampicillin-Ceftriaxone Combination against Enterococcus faecalis.药代动力学/药效学指数与氨苄西林-头孢曲松联合治疗粪肠球菌的疗效相关。
Antimicrob Agents Chemother. 2023 Feb 16;67(2):e0096622. doi: 10.1128/aac.00966-22. Epub 2023 Jan 25.
2
A new pharmacodynamic approach to study antibiotic combinations against enterococci in vivo: Application to ampicillin plus ceftriaxone.一种新的研究体内肠球菌抗生素组合的药效学方法:氨苄西林联合头孢曲松的应用。
PLoS One. 2020 Dec 8;15(12):e0243365. doi: 10.1371/journal.pone.0243365. eCollection 2020.
3
Pharmacodynamics of Ceftaroline plus Ampicillin against Enterococcus faecalis in an Pharmacokinetic/Pharmacodynamic Model of Simulated Endocardial Vegetations.头孢洛林联合氨苄西林在模拟心内膜赘生物药代动力学/药效学模型中对粪肠球菌的药效学研究
Antimicrob Agents Chemother. 2017 Mar 24;61(4). doi: 10.1128/AAC.02235-16. Print 2017 Apr.
4
Efficacy of Telavancin Alone and in Combination with Ampicillin in a Rat Model of Enterococcus faecalis Endocarditis.替考拉宁单独及与氨苄西林联合治疗粪肠球菌心内膜炎大鼠模型的疗效
Antimicrob Agents Chemother. 2017 May 24;61(6). doi: 10.1128/AAC.02489-16. Print 2017 Jun.
5
Meropenem plus Ceftaroline Is Active against Enterococcus faecalis in an Pharmacodynamic Model Using Humanized Dosing Simulations.美罗培南联合头孢洛林在使用人群剂量模拟的药效动力学模型中对粪肠球菌有效。
Antimicrob Agents Chemother. 2022 Oct 18;66(10):e0042622. doi: 10.1128/aac.00426-22. Epub 2022 Sep 26.
6
Efficacy of ampicillin plus ceftriaxone in treatment of experimental endocarditis due to Enterococcus faecalis strains highly resistant to aminoglycosides.氨苄西林联合头孢曲松治疗对氨基糖苷类高度耐药的粪肠球菌所致实验性心内膜炎的疗效
Antimicrob Agents Chemother. 1999 Mar;43(3):639-46. doi: 10.1128/AAC.43.3.639.
7
Differential in vitro susceptibility to ampicillin/ceftriaxone combination therapy among Enterococcus faecalis infective endocarditis clinical isolates.屎肠球菌感染性心内膜炎临床分离株对氨苄西林/头孢曲松联合治疗的体外药敏差异。
J Antimicrob Chemother. 2024 Apr 2;79(4):801-809. doi: 10.1093/jac/dkae032.
8
β-Lactams enhance daptomycin activity against vancomycin-resistant Enterococcus faecalis and Enterococcus faecium in in vitro pharmacokinetic/pharmacodynamic models.在体外药代动力学/药效学模型中,β-内酰胺类药物可增强达托霉素对耐万古霉素粪肠球菌和屎肠球菌的活性。
Antimicrob Agents Chemother. 2015 May;59(5):2842-8. doi: 10.1128/AAC.00053-15. Epub 2015 Mar 9.
9
Evaluation of the novel combination of daptomycin plus ceftriaxone against vancomycin-resistant enterococci in an in vitro pharmacokinetic/pharmacodynamic simulated endocardial vegetation model.在体外药代动力学/药效学模拟心内膜赘生物模型中评估达托霉素联合头孢曲松对耐万古霉素肠球菌的新组合疗效。
J Antimicrob Chemother. 2014 Aug;69(8):2148-54. doi: 10.1093/jac/dku113. Epub 2014 Apr 28.
10
Penicillin plus Ceftriaxone versus Ampicillin plus Ceftriaxone Synergistic Potential against Clinical Enterococcus faecalis Blood Isolates.青霉素联合头孢曲松与氨苄西林联合头孢曲松对临床粪肠球菌血分离株的协同作用潜力。
Microbiol Spectr. 2022 Aug 31;10(4):e0062122. doi: 10.1128/spectrum.00621-22. Epub 2022 Jun 15.

引用本文的文献

1
High-Dose Ceftriaxone in Elderly Patients with Enterococcal Infective Endocarditis: Population Pharmacokinetics of Free Ceftriaxone and Dose Optimization.大剂量头孢曲松治疗老年肠球菌感染性心内膜炎:游离头孢曲松的群体药代动力学及剂量优化
Antibiotics (Basel). 2025 May 15;14(5):508. doi: 10.3390/antibiotics14050508.
2
Pharmacokinetics-Pharmacodynamics Modeling for Evaluating Drug-Drug Interactions in Polypharmacy: Development and Challenges.多药治疗中药物-药物相互作用的药代动力学-药效学建模:开发与挑战。
Clin Pharmacokinet. 2024 Jul;63(7):919-944. doi: 10.1007/s40262-024-01391-2. Epub 2024 Jun 18.
3
Treatment of Infective Endocarditis: A Continuing Challenge.感染性心内膜炎的治疗:一项持续的挑战。
Antibiotics (Basel). 2023 Apr 4;12(4):704. doi: 10.3390/antibiotics12040704.

本文引用的文献

1
A new pharmacodynamic approach to study antibiotic combinations against enterococci in vivo: Application to ampicillin plus ceftriaxone.一种新的研究体内肠球菌抗生素组合的药效学方法:氨苄西林联合头孢曲松的应用。
PLoS One. 2020 Dec 8;15(12):e0243365. doi: 10.1371/journal.pone.0243365. eCollection 2020.
2
MIC profiling of ceftazidime/avibactam against two carbapenemase-producing Klebsiella pneumoniae isolates.头孢他啶/阿维巴坦对两株产碳青霉烯酶肺炎克雷伯菌分离株的MIC分析
J Glob Antimicrob Resist. 2020 Dec;23:385-387. doi: 10.1016/j.jgar.2020.10.014. Epub 2020 Nov 6.
3
In vivo synergism of ampicillin, gentamicin, ceftaroline and ceftriaxone against Enterococcus faecalis assessed in the Galleria mellonella infection model.在大蜡螟感染模型中评估氨苄西林、庆大霉素、头孢洛林和头孢曲松对粪肠球菌的体内协同作用。
J Antimicrob Chemother. 2020 Aug 1;75(8):2173-2181. doi: 10.1093/jac/dkaa129.
4
[Effectiveness of the antibiotic combinations for enterococcal infections treatment: a critical review].[抗生素联合用药治疗肠球菌感染的有效性:一项批判性综述]
Rev Chilena Infectol. 2019 Oct;36(5):556-564. doi: 10.4067/S0716-10182019000500556.
5
Optimal Piperacillin-Tazobactam Dosing Strategies against Extended-Spectrum-β-Lactamase-Producing .优化哌拉西林-他唑巴坦治疗产超广谱β-内酰胺酶的剂量策略。
Antimicrob Agents Chemother. 2019 Jan 29;63(2). doi: 10.1128/AAC.01906-18. Print 2019 Feb.
6
Pharmacokinetics/pharmacodynamics characterization of combined antimicrobial agents: a real challenge and an urgent need.联合抗菌药物的药代动力学/药效学特征:一项真正的挑战和迫切需求。
Clin Microbiol Infect. 2018 Jul;24(7):687-688. doi: 10.1016/j.cmi.2018.03.047. Epub 2018 Apr 9.
7
A Review of Combination Antimicrobial Therapy for Enterococcus faecalis Bloodstream Infections and Infective Endocarditis.肠球菌属血流感染和感染性心内膜炎的联合抗菌治疗综述
Clin Infect Dis. 2018 Jul 2;67(2):303-309. doi: 10.1093/cid/ciy064.
8
Semi-mechanistic pharmacokinetic-pharmacodynamic modelling of antibiotic drug combinations.抗生素药物组合的半机械药代动力学-药效学建模。
Clin Microbiol Infect. 2018 Jul;24(7):697-706. doi: 10.1016/j.cmi.2017.11.023. Epub 2017 Dec 8.
9
In vivo infection models in the pre-clinical pharmacokinetic/pharmacodynamic evaluation of antimicrobial agents.在抗菌药物临床前药代动力学/药效学评价中的体内感染模型。
Curr Opin Pharmacol. 2017 Oct;36:94-99. doi: 10.1016/j.coph.2017.09.004. Epub 2017 Sep 29.
10
Experimental design and modelling approach to evaluate efficacy of β-lactam/β-lactamase inhibitor combinations.评估β-内酰胺/β-内酰胺酶抑制剂联合制剂疗效的实验设计和建模方法。
Clin Microbiol Infect. 2018 Jul;24(7):707-715. doi: 10.1016/j.cmi.2017.07.020. Epub 2017 Jul 29.

药代动力学/药效学指数与氨苄西林-头孢曲松联合治疗粪肠球菌的疗效相关。

Pharmacokinetic/Pharmacodynamic Index Linked to Efficacy of the Ampicillin-Ceftriaxone Combination against Enterococcus faecalis.

机构信息

GRIPE, School of Medicine, University of Antioquia, Medellin, Colombia.

Laboratorio Integrado de Medicina Especializada, School of Medicine, IPS Universitaria, University of Antioquia, Medellín, Colombia.

出版信息

Antimicrob Agents Chemother. 2023 Feb 16;67(2):e0096622. doi: 10.1128/aac.00966-22. Epub 2023 Jan 25.

DOI:10.1128/aac.00966-22
PMID:36695584
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9933695/
Abstract

Combination therapy with ampicillin plus ceftriaxone (AMP+CRO) is the first-line therapy for treating severe infections due to Enterococcus faecalis. However, the pharmacokinetic/pharmacodynamic (PK/PD) index linked to the efficacy of the combination is not yet defined, hindering dose optimization in the clinic. Because classical PK/PD indices are not directly applicable to antimicrobial combinations, two novel indices were tested in the optimized murine model of infection by E. faecalis to delineate the potentiation of AMP by CRO: the time above the CRO threshold (T) and the time above the AMP instantaneous MIC (T). The potential clinical relevance was evaluated by simulating human doses of AMP and CRO. Hill's equation fitted well the exposure-response data in terms of T, with a CRO threshold of 1 mg/L. The required exposures were 46%, 49%, and 52% for stasis and 1- and 2-log killing, respectively. Human ceftriaxone doses of 2 g every 12 h (q12h) would reach the target in >90% of strains with thresholds ≤64 mg/L. The AMP T index also fitted well, and the required exposures were 37%, 41%, and 46% for stasis and 1- and 2-log killing, respectively. In humans, the addition of CRO would allow use of lower AMP doses to reach the same T and to treat strains with higher MICs. This is the first report of the PK/PD indices and required magnitudes linked to AMP+CRO against E. faecalis; these results can be used as the basis to guide the design of clinical trials to improve combined therapy against enterococci.

摘要

氨苄西林联合头孢曲松(AMP+CRO)联合治疗是治疗粪肠球菌引起的严重感染的一线治疗方法。然而,与联合疗效相关的药代动力学/药效学(PK/PD)指标尚未确定,这阻碍了临床优化剂量。由于经典的 PK/PD 指标不能直接应用于抗菌药物联合治疗,因此在优化的粪肠球菌感染小鼠模型中测试了两种新的指标来描述 CRO 对 AMP 的增效作用:CRO 阈值以上时间(T)和 AMP 瞬时 MIC 以上时间(T)。通过模拟人类 AMP 和 CRO 剂量来评估潜在的临床相关性。Hill 方程在 T 方面很好地拟合了暴露-反应数据,CRO 阈值为 1mg/L。对于停滞和 1-和 2-对数杀伤,分别需要 46%、49%和 52%的暴露。每 12 小时(q12h)给予 2g 的头孢曲松将达到阈值≤64mg/L 的>90%菌株的目标。AMP T 指数也很好地拟合,对于停滞和 1-和 2-对数杀伤,分别需要 37%、41%和 46%的暴露。在人类中,添加 CRO 可以降低 AMP 剂量以达到相同的 T,并治疗 MIC 更高的菌株。这是首次报道与粪肠球菌相关的 AMP+CRO 的 PK/PD 指标和所需强度,这些结果可用于指导临床试验设计,以改善针对肠球菌的联合治疗。