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吗啡降低氯吡格雷的浓度和效果:一项随机、双盲、安慰剂对照试验。

Morphine decreases clopidogrel concentrations and effects: a randomized, double-blind, placebo-controlled trial.

机构信息

Department of Clinical Pharmacology, Medical University of Vienna, Vienna, Austria.

Department of Laboratory Medicine, Medical University of Vienna, Vienna, Austria.

出版信息

J Am Coll Cardiol. 2014 Feb 25;63(7):630-635. doi: 10.1016/j.jacc.2013.10.068. Epub 2013 Dec 4.

DOI:10.1016/j.jacc.2013.10.068
PMID:24315907
Abstract

OBJECTIVES

This study sought to examine the possible drug-drug interactions between clopidogrel and morphine.

BACKGROUND

Because morphine-the recommended treatment for pain of myocardial infarction-is associated with poor clinical outcome, we hypothesized that morphine lowers the plasma levels of clopidogrel active metabolite as well as its effects on platelets.

METHODS

Twenty-four healthy subjects received a loading dose of 600 mg clopidogrel together with placebo or 5 mg morphine intravenously in a randomized, double-blind, placebo-controlled, cross-over trial. Pharmacokinetics was determined by liquid chromatography tandem mass spectrometry, and clopidogrel effects were measured by platelet function tests.

RESULTS

Morphine injection delayed clopidogrel absorption (p = 0.025) and reduced the area under the curve levels of its active metabolite by 34% (p = 0.001). Morphine delayed the maximal inhibition of platelet aggregation on average by 2 h (n = 24; p < 0.001). Residual platelet aggregation was higher 1 to 4 h after morphine injection (n = 24; p < 0.005). Furthermore, morphine delayed the inhibition of platelet plug formation under high shear rates (P2Y-Innovance; n = 21; p < 0.004) and abolished the 3-fold prolongation in collagen adenosine diphosphate-induced closure times seen in extensive and rapid metabolizers (n = 16; p = 0.001).

CONCLUSIONS

Morphine delays clopidogrel absorption, decreases plasma levels of clopidogrel active metabolite, and retards and diminishes its effects, which can lead to treatment failure in susceptible individuals. (Drug/Drug Interactions of Aspirin and P2Y12-inhibitors; NCT01369186).

摘要

目的

本研究旨在探讨氯吡格雷与吗啡之间可能存在的药物相互作用。

背景

由于吗啡(推荐用于治疗心肌梗死疼痛)与不良临床结局相关,我们假设吗啡会降低氯吡格雷活性代谢物的血浆水平及其对血小板的作用。

方法

24 名健康受试者随机、双盲、安慰剂对照、交叉试验中接受 600mg 氯吡格雷负荷剂量加安慰剂或 5mg 吗啡静脉注射。通过液相色谱串联质谱法测定药代动力学,通过血小板功能试验测定氯吡格雷的作用。

结果

吗啡注射延迟了氯吡格雷的吸收(p = 0.025),并使活性代谢物的曲线下面积水平降低了 34%(p = 0.001)。吗啡平均延迟了血小板聚集的最大抑制作用 2 小时(n = 24;p < 0.001)。吗啡注射后 1 至 4 小时,残留血小板聚集率更高(n = 24;p < 0.005)。此外,吗啡延迟了高剪切率下血小板栓子形成的抑制作用(P2Y-Innovance;n = 21;p < 0.004),并消除了广泛和快速代谢者中胶原二磷酸腺苷诱导的闭合时间延长 3 倍的现象(n = 16;p = 0.001)。

结论

吗啡延迟了氯吡格雷的吸收,降低了氯吡格雷活性代谢物的血浆水平,并延缓和减弱了其作用,这可能导致易感性个体的治疗失败。(阿司匹林和 P2Y12 抑制剂的药物相互作用;NCT01369186)。

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