非st段抬高型心肌梗死患者的止血特点

M. Popovici, L. Ciobanu, I. Popovici, V. Ivanov, M. Ivanov, Ion Ion Popovici, Tatiana Dănilă, V. Cobet
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引用次数: 0

摘要

背景:冠状动脉血栓形成是急性心脏病发作的关键致病机制,包括非st段抬高(NSTEMI)。因此,在优化NSTEMI的诊断过程中,检测可靠的止血障碍标志物非常重要。材料与方法:研究对象为54例非stemi患者(平均年龄69.7±1.5岁)。60%的病例有三支血管病变;56%的患者有射血分数bbb50 %, 78%的患者有Killip I级心力衰竭。在STA-Liatest(法国)设备的帮助下,血液测试确定了以下止血标志物:纤维蛋白单体(FM),凝血因子II, VII和x的复合物活性。其他标志物如Procoag,依赖于循环磷脂或SPA的凝血指标,d -二聚体,以及因子C, S和抗凝血酶III。20例健康人(对照组)以同样方法测定的各项指标为正常值。结果:入院时循环FM水平较对照组升高2倍,而Procoag和SPA值较对照组显著降低35.3%。因子C、S、抗凝血酶III在控制值范围的54 ~ 80%,d -二聚体在允许范围内。在心脏病发作的急性期,除d -二聚体外,止血指标均出现恶化。与对照组相比,血运重建后24和72小时测定的FM水平持续升高(高达3.8倍),而Procoag和SPA下降了54-57%。C、S因子和抗凝血酶III进一步降低占正常指标的42-54%。5天后,止血指标有所改善,但与对照组相比仍有显著差异。结论:在NSTEMI患者中发现的止血特点表明其血栓形成前状态处于活化状态,FM与正常值(>100%)偏差最大,可作为NSTEMI的重要诊断指标。它能可靠地反映凝血酶水平,从而触发血栓形成的最后一个酶促阶段。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Features of hemostasis in patients with non-ST-elevation myocardial infarction
Background: Coronary thrombosis is the key pathogenic mechanism of acute heart attack, including non-ST segment elevation (NSTEMI). Given that, the detection of reliable markers of hemostasis disorders is important in the process of optimizing the diagnosis of NSTEMI. Material and methods: The study was conducted on 54 patients with NSTEMI (average age 69.7±1.5 years). In 60% of cases, 3-vessel disease was noted; 56% of patients had ejection fraction >50%, and Killip class I of heart failure was revealed in 78% of patients. With the help of the STA-Liatest (France) equipment, the blood tests determined the following hemostasis markers: fibrin monomers (FM), thrombotic complex activity of factors II, VII and X. Additional markers like Procoag, the coagulation indicator dependent on circulating phospholipids or SPA, D-dimers, as well as factors C, S and antithrombin III were appreciated. The values of these markers determined by the same method in 20 healthy persons (control group) were used as normal values. Results: Circulating level of FM on admission was increased twice, while the values of Procoag and SPA were significantly decreased by 35.3% compared to the control. Factors C, S and antithrombin III were 54-80% of the control value range, and D-dimers were within the permissible values. In the acute phase of the heart attack, a deterioration of hemostasis indicators was noted, excepting the D-dimers. The levels of FM determined 24 and 72 hours after revascularization were consistently increased (up to 3.8 times) compared to the control, while Procoag and SPA decreased by 54-57%. Further reduction of factors C, S and antithrombin III accounted for 42-54% of normal indicators. After 5 days, an improvement in hemostasis markers was observed, but a significant difference still remained comparing to the control group. Conclusions: The hemostasis particularities discovered in patients with NSTEMI indicate the features of an activated prothrombotic status, and FM could be an important diagnostic marker of NSTEMI, due to its most significant deviation from the normal value (>100%). It can reliably reflect the thrombin level, which triggers the last enzymatic phase of thrombus formation.
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