选择性经皮腔内冠状动脉成形术后至少1周可检测到凝血酶生成增加

D. Prisco , E. Antonucci , M. Capanni , L. Chiarugi , V. Boddi , C. Giglioli , M. Comeglio , S. Fedi , G.F. Gensini , R. Abbate
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引用次数: 1

摘要

目的:本前瞻性研究旨在调查:(1)PTCA后早期止血变化持续多久;(2)PTCA术后第一个月评估的一些凝血和/或纤溶参数是否可以预测随后的临床复发。背景:意大利佛罗伦萨大学心内科临床研究所。材料和方法:72例PTCA患者在术前(T1)、术后2天(T2)、术前7天(T7)和术后30天(T30)分别测定纤维蛋白原、F1+2、TAT、D-二聚体和ELT;PAI-1和t-PA在PTCA前、7天和30天后进行评估。随访血管造影术仅在缺血复发或测力计测试呈阳性的患者中进行。结果:F1+2、TAT和纤维蛋白原在T2时显著升高(P<0.005);一周后,与基线值相比,F1+2和纤维蛋白原仍然显著升高(P<;0.005)。在T30时,这些参数显示出与T1相比显著更低的水平(P<!0.005)。血浆D-二聚体浓度在T2和T7时显著增加(P<;0.001),但基线值与T30时没有发现差异。PAI-1活性在T7时显著降低(P<0.001),而在T30时与基线相似。在不同时间没有观察到t-PA水平的显著变化。最后,ELT在T2时显著增加(P<;0.001),但在T7和T30时,这些值与基线值相似。临床复发19例。在任何时候,研究的各种参数的值在有和没有后续临床复发的患者之间都没有差异。肝素治疗对不同时间的凝血酶生成没有显著影响,而对纤维蛋白原、PAI-1和t-PA抗原水平的影响很小。结论:选择性经皮冠状动脉成形术后2天和7天,止血发生了许多改变并持续存在,肝素治疗不能阻断凝血激活。PTCA后第一个月评估的止血参数似乎不能预测随后的临床复发。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
An increased thrombin generation is detectable for at least 1 week following elective percutaneous transluminal coronary angioplasty

Objective: The present prospective study was planned to investigate: (1) how long the early haemostatic changes after PTCA last and (2) if some coagulation and/or fibrinolytic parameters assessed during the first month after PTCA may be predictive of subsequent clinical recurrence.

Setting: Istituto di Clinica Medica Generale e Cardiologia, University of Florence, Florence, Italy.

Material and Methods: In 72 patients undergoing PTCA fibrinogen, F1+2, TAT, D-dimer and ELT were evaluated before the procedure (T1) and 2 (T2), 7 (T7) and 30 days (T30) after PTCA; PAI-1 and t-PA were assessed before PTCA and after 7 and 30 days. Follow-up angiography was performed only in patients with recurrence of ischaemia or positive ergometric tests.

Results: F1+2, TAT and fibrinogen were significantly increased at T2 (P<0.005); after a week, F1+2 and fibrinogen were still significantly higher in comparison to baseline values (P<0.005). At T30 these parameters showed significantly lower levels if compared to T1 (P<0.005). Plasma D-dimer concentration significantly increased at T2 and T7 (P<0.001), but no difference was found between baseline values and those at T30. PAI-1 activity significantly decreased at T7 (P<0.001), whereas it was similar to baseline at T30. No significant variations of t-PA levels were observed at the different times. Finally, ELT significantly increased at T2 (P<0.001), but at T7 and T30 the values were similar to baseline values. Clinical recurrence occurred in 19 patients. The values of various parameters investigated were not different at any time considered between the patients with and without subsequent clinical recurrence. Heparin treatment had no significant influence on thrombin generation at different times whereas it had marginal influences on fibrinogen, PAI-1 and t-PA antigen levels.

Conclusion: A number of alterations in haemostasis takes place and persists 2 and 7 days after elective PTCA and heparin treatment is not able to blunt clotting activation. The haemostatic parameters assessed during the first month after PTCA seem not to be predictive of subsequent clinical recurrence.

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