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急性心肌梗死患者溶栓及联合肝素治疗期间的凝血酶生成与活性

Thrombin generation and activity during thrombolysis and concomitant heparin therapy in patients with acute myocardial infarction.

作者信息

Merlini P A, Bauer K A, Oltrona L, Ardissino D, Spinola A, Cattaneo M, Broccolino M, Mannucci P M, Rosenberg R D

机构信息

Second Division of Cardiology, Ca' Granada Niguarda Hospital, Milan, Italy.

出版信息

J Am Coll Cardiol. 1995 Jan;25(1):203-9. doi: 10.1016/0735-1097(94)00360-3.

Abstract

OBJECTIVES

This prospective study investigated the behavior of thrombin generation and activity during thrombolysis and concomitant heparin administration.

BACKGROUND

It has been shown that during thrombolytic therapy there is an increase in thrombin generation and activity. Increased thrombin activity is suppressed by concomitant intravenous heparin, but it is unknown whether thrombin generation is also affected.

METHODS

Thrombin generation was assessed by measuring prothrombin fragment 1 + 2 and thrombin-antithrombin complex plasma levels and thrombin activity by measuring fibrinopeptide A plasma levels. Serial blood samples were obtained before and at 90 min and 24 and 48 h after the administration of streptokinase (15 patients), recombinant tissue-type plasminogen activator (15 patients) or anistreplase (13 patients). An intravenous bolus of heparin (5,000 IU) was administered before the start of thrombolytic therapy, followed by an infusion of 1,000 U/h to maintain an activated partial thromboplastin time > 1.5 times baseline.

RESULTS

During thrombolytic and concomitant heparin therapy, there was an increase in the plasma levels of prothrombin fragment 1 + 2 (baseline 1.08 vs. 2.73 nmol/liter, p < 0.001) and thrombin-antithrombin complex (baseline 6.5 vs. 17.1 micrograms/ml, p < 0.01) at 90 min, whereas no change was observed in fibrinopeptide A at 90 min (baseline 2.8 vs. 3.0 nmol/liter, p = NS).

CONCLUSIONS

During thrombolytic therapy with both fibrin-specific and non-fibrin-specific drugs, there is an increase in thrombin generation despite concomitant administration of intravenous heparin.

摘要

目的

本前瞻性研究调查了溶栓及同时给予肝素治疗期间凝血酶生成及活性的变化情况。

背景

研究表明,溶栓治疗期间凝血酶生成及活性会增加。静脉给予肝素可抑制凝血酶活性增加,但凝血酶生成是否也受影响尚不清楚。

方法

通过检测凝血酶原片段1+2及凝血酶-抗凝血酶复合物血浆水平评估凝血酶生成,通过检测纤维蛋白肽A血浆水平评估凝血酶活性。在给予链激酶(15例患者)、重组组织型纤溶酶原激活剂(15例患者)或茴香酰化纤溶酶原链激酶激活剂复合物(13例患者)之前及给药后90分钟、24小时和48小时采集系列血样。在溶栓治疗开始前静脉推注肝素(5000IU),随后以1000U/小时的速度输注以维持活化部分凝血活酶时间>基线的1.5倍。

结果

在溶栓及同时给予肝素治疗期间,90分钟时凝血酶原片段1+2血浆水平升高(基线1.08 vs. 2.73nmol/升,p<0.001),凝血酶-抗凝血酶复合物血浆水平升高(基线6.5 vs. 17.1μg/ml,p<0.01),而90分钟时纤维蛋白肽A未观察到变化(基线2.8 vs. 3.0nmol/升,p=无统计学意义)。

结论

在使用纤维蛋白特异性和非纤维蛋白特异性药物进行溶栓治疗期间,尽管同时静脉给予肝素,凝血酶生成仍会增加。

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