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替罗非班对血小板糖蛋白IIb/IIIa受体的阻断作用对不稳定型心绞痛/非ST段抬高型心肌梗死女性患者不良心脏事件的影响(PRISM-PLUS研究)

Effect of platelet glycoprotein IIb/IIIa receptor blockade with tirofiban on adverse cardiac events in women with unstable angina/non-ST-elevation myocardial infarction (PRISM-PLUS Study).

作者信息

Huynh Thao, Theroux Pierre, Snapinn Steven, Wan Ying

机构信息

PRISM-PLUS Investigators

出版信息

Am Heart J. 2003 Oct;146(4):668-73. doi: 10.1016/S0002-8703(03)00255-2.

Abstract

BACKGROUND

Previous trials demonstrated the efficacy of platelet glycoprotein IIb/IIIa receptors blockade with tirofiban in reducing acute ischemic events in patients with unstable angina/non-ST-elevation myocardial infarction. Little is known about the effect of tirofiban among women with acute coronary syndromes.

OBJECTIVE

We aimed to determine the benefit and safety of tirofiban plus heparin versus heparin alone on cardiac ischemic events among women with unstable angina/non-ST-elevation myocardial infarction.

METHODS AND RESULTS

We performed a post hoc analysis of all women enrolled in the PRISM-PLUS trial. At early time points, there appeared to be a reduction of the primary composite end point of death, myocardial infarction, or refractory ischemia among women treated with tirofiban plus heparin (RR, 0.78 and 0.67) compared with women treated with heparin alone. However, at 30 and 180 days, there was no significant reduction of events with the combination therapy of tirofiban plus heparin (treatment-by-sex interaction, P =.05). Death or myocardial infarction was not significantly reduced by the combination therapy among women at all time points.

CONCLUSIONS

Although the effects of tirofiban in reducing the primary composite outcome were similar among men and women early in the study, there appeared to be a difference at the later time points. In particular, tirofiban was effective among men, but there was no clear effect among women at 30 and 180 days.

摘要

背景

既往试验证明,替罗非班阻断血小板糖蛋白IIb/IIIa受体可减少不稳定型心绞痛/非ST段抬高型心肌梗死患者的急性缺血事件。关于替罗非班在急性冠状动脉综合征女性患者中的作用知之甚少。

目的

我们旨在确定替罗非班联合肝素与单用肝素相比,对不稳定型心绞痛/非ST段抬高型心肌梗死女性患者心脏缺血事件的益处及安全性。

方法与结果

我们对参加PRISM-PLUS试验的所有女性进行了一项事后分析。在早期时间点,与单用肝素治疗的女性相比,接受替罗非班联合肝素治疗的女性的主要复合终点(死亡、心肌梗死或难治性缺血)似乎有所降低(相对危险度分别为0.78和0.67)。然而,在30天和180天时,替罗非班联合肝素治疗并未显著降低事件发生率(治疗与性别的交互作用,P = 0.05)。在所有时间点,联合治疗均未显著降低女性患者的死亡或心肌梗死发生率。

结论

尽管在研究早期替罗非班降低主要复合结局的效果在男性和女性中相似,但在后期时间点似乎存在差异。特别是,替罗非班在男性中有效,但在30天和180天时对女性没有明显效果。

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