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直接凝血酶抑制剂依非加群在不稳定型心绞痛患者中的抗凝特性、临床疗效及安全性

Anticoagulant properties, clinical efficacy and safety of efegatran, a direct thrombin inhibitor, in patients with unstable angina.

作者信息

Klootwijk P, Lenderink T, Meij S, Boersma H, Melkert R, Umans V A, Stibbe J, Müller E J, Poortermans K J, Deckers J W, Simoons M L

机构信息

Department of Cardiology, Rotterdam Heart Centre, Division Thoraxcentre, The Netherlands.

出版信息

Eur Heart J. 1999 Aug;20(15):1101-11. doi: 10.1053/euhj.1999.1477.

Abstract

AIMS

Thrombin plays a key role in the clinical syndrome of unstable angina. We investigated the safety and efficacy of five dose levels of efegatran sulphate, a direct thrombin inhibitor, compared to heparin in patients with unstable angina.

METHODS

Four hundred and thirty-two patients with unstable angina were enrolled. Five dose levels of efegatran were studied sequentially, ranging from 0.105 mg. kg(-1). h(-1)to 1.2 mg. kg(-1). h(-1)over 48 h. Safety was assessed clinically, with reference to bleeding and by measuring clinical laboratory parameters. Efficacy was assessed by the number of patients experiencing any episode of recurrent ischaemia as measured by computer-assisted continuous ECG ischaemia monitoring. Clinical end-points were: episodes of recurrent angina, myocardial infarction, coronary intervention (PTCA or CABG), and death.

RESULTS

Efegatran demonstrated dose dependent ex-vivo anticoagulant activity with the highest dose level of 1.2 mg. kg(-1). h(-1)resulting in steady state mean activated partial thromboplastin time values of approximately three times baseline. Thrombin time was also increased. Neither of the efegatran doses studied were able to suppress myocardial ischaemia during continuous ECG ischaemia monitoring to a greater extent than that seen with heparin. There were no statistically significant differences in clinical outcome or major bleeding between the efegatran and heparin groups. Minor bleeding and thrombophlebitis occurred more frequently in the efegatran treated patients.

CONCLUSION

Administration of efegatran sulphate at levels of at least 0.63 mg. kg(-1). h(-1)provided an anti-thrombotic effect which is at least comparable to an activated partial thromboplastin time adjusted heparin infusion. There was no excess of major bleeding. The level of thrombin inhibition by efegatran, as measured by activated partial thromboplastin time, appeared to be more stable than with heparin. Thus, like other thrombin inhibitors, efegatran sulphate is easier to administer than heparin. However, no clinical benefits of efegatran over heparin were apparent.

摘要

目的

凝血酶在不稳定型心绞痛的临床综合征中起关键作用。我们研究了与肝素相比,直接凝血酶抑制剂硫酸艾非加群五个剂量水平在不稳定型心绞痛患者中的安全性和有效性。

方法

纳入432例不稳定型心绞痛患者。依次研究了硫酸艾非加群的五个剂量水平,在48小时内从0.105毫克·千克-1·小时-1到1.2毫克·千克-1·小时-1。通过临床评估安全性,参考出血情况并测量临床实验室参数。通过计算机辅助连续心电图缺血监测测量经历任何复发性缺血发作的患者数量来评估疗效。临床终点包括:复发性心绞痛发作、心肌梗死、冠状动脉介入治疗(PTCA或CABG)和死亡。

结果

硫酸艾非加群表现出剂量依赖性的体外抗凝活性,最高剂量水平1.2毫克·千克-1·小时-1导致稳态平均活化部分凝血活酶时间值约为基线的三倍。凝血酶时间也增加。在连续心电图缺血监测期间,所研究的硫酸艾非加群剂量均未能比肝素更有效地抑制心肌缺血。硫酸艾非加群组和肝素组在临床结局或大出血方面无统计学显著差异。在接受硫酸艾非加群治疗的患者中,轻微出血和血栓性静脉炎更频繁发生。

结论

至少以0.63毫克·千克-1·小时-1的水平给予硫酸艾非加群可提供一种抗血栓形成作用,其至少与活化部分凝血活酶时间调整的肝素输注相当。没有大出血过多的情况。通过活化部分凝血活酶时间测量,硫酸艾非加群的凝血酶抑制水平似乎比肝素更稳定。因此,与其他凝血酶抑制剂一样,硫酸艾非加群比肝素更易于给药。然而,硫酸艾非加群相对于肝素没有明显的临床益处。

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