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重新审视未分级肝素的药理学。

Revisiting the Pharmacology of Unfractionated Heparin.

机构信息

School of Pharmacy, University of Otago, Dunedin, New Zealand.

Department of Nursing, The University of Melbourne, Parkville, VIC, Australia.

出版信息

Clin Pharmacokinet. 2019 Aug;58(8):1015-1028. doi: 10.1007/s40262-019-00751-7.

Abstract

Unfractionated heparin (UFH) is a commonly used anticoagulant therapy for the acute treatment and prevention of thrombosis. Its short duration of action, reversibility of effect by protamine sulfate, and extensive clinical experience are some of the advantages that support its use. However, the choice of dose and dosing regimen of UFH remains challenging for several reasons. First, UFH has a narrow therapeutic window and wide variability in the dose-response relationship. Second, its pharmacodynamic (PD) properties are difficult to characterise owing to the complex multidimensional mechanisms of interaction with the haemostatic system. Third, the complex heterogeneous chemical composition of UFH precludes precise characterisation of its pharmacokinetic (PK) properties. This review provides a comprehensive mechanistic approach to the interaction of UFH with the haemostatic system. The effect of chemical structure on its PK and PD properties is quantitatively described, and a framework for characterisation of the dose-response relationship of UFH for the purpose of dose optimisation is proposed.

摘要

未分级肝素(UFH)是一种常用的抗凝治疗药物,用于急性治疗和预防血栓形成。其作用时间短、硫酸鱼精蛋白可逆转其作用效果以及广泛的临床经验是支持其使用的一些优点。然而,由于多种原因,UFH 的剂量选择和给药方案仍然具有挑战性。首先,UFH 的治疗窗较窄,剂量反应关系的变异性较大。其次,由于与止血系统相互作用的复杂多维机制,其药效学(PD)特性难以描述。第三,UFH 复杂的异质化学组成排除了对其药代动力学(PK)特性的精确描述。本综述提供了一种全面的机制方法来研究 UFH 与止血系统的相互作用。定量描述了化学结构对其 PK 和 PD 特性的影响,并提出了一个用于描述 UFH 剂量反应关系以实现剂量优化的框架。

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