利福平(利福平)是治疗马驹马红球菌感染的必要药物吗?利福平作用的综述。

IF 1.5 4区 农林科学 Q3 PHARMACOLOGY & PHARMACY
Keith Edward Baptiste, Niels Christian Kyvsgaard, Mohamed Omar Ahmed, Peter Damborg, Patricia M Dowling
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引用次数: 0

摘要

利福平是抗菌剂中的一个谜。由于体内复杂的药效学相互作用,血液和组织间室浓度在治疗过程中是一个“移动目标”。利福平联合治疗马驹马红球菌感染已有近40年的历史。利福平联合治疗的必要性是基于这样一种信念,即两种抗菌素(例如,利福平加大环内酯)均能穿透肺脓肿和细胞内腔,其最低抑菌浓度(mic)高于等量链球菌,而且与其他方法相比,疗效更好,并且限制了对任何一种单一药物的抗菌素耐药率。然而,利福平是许多联合用药的肇事者。这篇重要的综述评估了利福平在马驹中使用的现有证据,包括利福平在马驹中的药代动力学/药效学特征、体外微生物学研究和抗菌药物耐药性的选择,以及随机临床试验的分析。利福平是一种核孕烷X受体激活剂,通过上调全身前消除机制(如肠道和肝脏CYP3A4),或功能性药物吸收载体(如肠道p -糖蛋白)和/或抑制肠道和/或肝脏药物摄取载体(如OATP1B1、OATP2B1、MRP2),对自身和其他药物产生强烈的负相互作用。长期给予利福平可导致许多母体药物的血清和靶位点/s浓度降低,包括利福平本身。无论初始肺脓肿评分如何,在随机对照盲法和双盲法临床试验中,利福平联合治疗与大环内酯类单药治疗相比,并未显示出明显的优势。利福平联合治疗严重马红球菌肺炎的疗效尚未得到充分调查,但在马驹中积累了足够的证据,引起了对在马药中不正确使用利福平的主要关注。这些问题包括利福平作为一种针对马链球菌的抑菌抗生素,在治疗过程中改变药代动力学,降低亲本/亲本浓度,以及选择多重耐药马链球菌的风险。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Is Rifampin (Rifampicin) Essential for the Treatment of Rhodococcus equi Infections in Foals? A Critical Review of the Role of Rifampin.

Rifampin is an enigma among antimicrobials. Blood and tissue compartment concentrations are a "moving target" along the treatment course due to the complex pharmacodynamic interactions within the body. Rifampin concomitant therapies are for the prevention and treatment of Rhodococcus equi infection in foals, for nearly 40 years. The necessity of rifampin concomitant therapies is based on beliefs that both antimicrobials (e.g., rifampin plus macrolide) penetrate into pulmonary abscesses and intracellular compartments above R. equi minimum inhibitory concentrations (MICs), as well as better efficacy, compared with other approaches, and limiting the rate of antimicrobial resistance to either single agent. However, rifampin acts as a perpetrator drug for many co-administered drugs. This critical review evaluates the available evidence for rifampin use in foals with R. equi, concerning pharmacokinetic/pharmacodynamic characteristics of rifampin in foals, in vitro microbiological studies and selection of antimicrobial resistance, as well as an analysis of randomized clinical trials. Rifampin is a nuclear pregnane X receptor activator, which results in strong negative drug interactions towards itself and other drugs, for drug-absorption routes either by upregulation of presystemic elimination mechanisms (e.g., intestinal and hepatic CYP3A4), or functional drug-absorption carriers (e.g., intestinal P-glycoprotein) and/or inhibition of intestinal and/or hepatic drug-uptake carriers (e.g., OATP1B1, OATP2B1, MRP2). Chronic rifampin administration results in decreases in the serum and target site/s concentrations of many parent drugs, including itself. Rifampin concomitant therapies do not demonstrate a significant advantage over monotherapy with macrolides, in randomized controlled blinded and double-blinded clinical trials for subclinical, and mild-to-moderate bronchopneumonia in foals with pulmonary abscesses, regardless of initial pulmonary abscess score. Efficacy of rifampin concomitant therapies for severe Rhodococcus equi pneumonia has not been fully investigated, but there is sufficient accumulated evidence in foals to raise major concerns about the incorrect use of rifampin in equine medicine. These concerns include rifampin as a bacteriostatic antibiotic against R. equi, with changing pharmacokinetics during treatment that decreases parent/coparent concentrations as well as the risk of selecting for multi-resistant R. equi.

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来源期刊
CiteScore
3.10
自引率
15.40%
发文量
69
审稿时长
8-16 weeks
期刊介绍: The Journal of Veterinary Pharmacology and Therapeutics (JVPT) is an international journal devoted to the publication of scientific papers in the basic and clinical aspects of veterinary pharmacology and toxicology, whether the study is in vitro, in vivo, ex vivo or in silico. The Journal is a forum for recent scientific information and developments in the discipline of veterinary pharmacology, including toxicology and therapeutics. Studies that are entirely in vitro will not be considered within the scope of JVPT unless the study has direct relevance to the use of the drug (including toxicants and feed additives) in veterinary species, or that it can be clearly demonstrated that a similar outcome would be expected in vivo. These studies should consider approved or widely used veterinary drugs and/or drugs with broad applicability to veterinary species.
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