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口服抗凝药物在心房颤动中的药代动力学和药效学。

Pharmacokinetics and pharmacodynamics of oral anticoagulants used in atrial fibrillation.

机构信息

a Institute of Applied Health Research, University of Birmingham , UK.

b Liverpool Centre for Cardiovascular Science , University of Liverpool and Liverpool Heart & Chest Hospital , Liverpool , UK.

出版信息

Expert Opin Drug Metab Toxicol. 2019 May;15(5):381-398. doi: 10.1080/17425255.2019.1604686. Epub 2019 Apr 19.

Abstract

The availability of non-vitamin K antagonist oral anti-coagulants alongside vitamin K antagonists has offered a variety of options for anti-coagulation, but has also necessitated a good understanding of the pharmacological properties of each of these drugs prior to their use, to maximise the therapeutic benefit and minimise patient harm Areas covered: This review article outlines the pharmacokinetic and pharmacodynamic profiles of the currently licensed VKAs and NOACs that are most commonly used in clinical practice, with the aim of demonstrating how variations in these characteristics influence their use in clinical practice. A literature search was conducted on PubMed using keywords and relevant articles published by the 31 of December 2018 were included. Expert opinion: The effect of a drug is determined by a combination of elements which include patient characteristics and external factors, in addition to its pharmacokinetic and pharmacodynamic properties. A good understanding of these is essential. Despite the wealth of information available, particularly on VKAs, our knowledge on the pharmacology responsible for certain drug effects and inter-individual variations is still limited. Increasing efforts are being made to understand these and include focus on pharmacogenomics and drug transporter proteins.

摘要

非维生素 K 拮抗剂口服抗凝剂与维生素 K 拮抗剂的可用性为抗凝治疗提供了多种选择,但在使用这些药物之前,还需要充分了解每种药物的药理学特性,以最大限度地提高治疗效果并最大程度地减少患者伤害。

涵盖领域

本文综述了目前在临床实践中最常用的已获许可的 VKA 和新型口服抗凝剂的药代动力学和药效学特征,旨在展示这些特征的变化如何影响它们在临床实践中的应用。使用 PubMed 上的关键词进行了文献检索,并纳入了截至 2018 年 12 月 31 日发表的相关文章。

专家意见

药物的作用是由多种因素决定的,包括患者特征和外部因素,以及其药代动力学和药效学特性。充分了解这些因素至关重要。尽管有大量的信息,特别是关于 VKA 的信息,但我们对导致某些药物作用和个体间差异的药理学的了解仍然有限。目前正在做出更多努力来理解这些因素,并包括对药物基因组学和药物转运蛋白的关注。

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