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用于监测接受支架植入术患者抗血小板药物血小板抑制情况的比浊法聚集试验与体外出血时间(PFA-100)的比较

Comparison of turbidimetric aggregation and in vitro bleeding time (PFA-100) for monitoring the platelet inhibitory profile of antiplatelet agents in patients undergoing stent implantation.

作者信息

Van der Planken Marc G, Claeys Marc J, Vertessen Francine J, Dilling Dagmara, Bosmans Johan M, Berneman Zwi N, Michiels Jan J, Vrints Christian

机构信息

Laboratory of Hematology and Hemostasis, Department of Clinical Pathology, University Hospital Antwerp, Wilrijkstraat 10, 2650, Edegem, Belgium.

出版信息

Thromb Res. 2003;111(3):159-64. doi: 10.1016/j.thromres.2003.09.002.

Abstract

The present study compared classical ADP-induced platelet aggregation vs. PFA-100 closure times using collagen/ADP membrane cartridges to monitor the degree of platelet-inhibiting effect of three drug regimens: ticlopidin, abciximab/ticlopidin and loading dose clopidogrel, each on top of aspirin (acetylsalicylic acid, ASA) during and after elective stent placement (intervention) in a total of 31 patients with acute coronary syndrome. Ticlopidin was started directly after stent implantation, abciximab was started before coronary intervention and given intravenously for 12 h, and a clopidogrel loading dose was given before intervention. The 10 patients treated with ticlopidin (500 mg daily) showed no significant prolongation of PFA closure times and a slight increase of ADP-induced platelet aggregation shortly after intervention. In 11 patients treated with abciximab/ticlopidin, the PFA closure times were significantly prolonged, and ADP-induced platelet aggregation was reduced by more than 80% during the 12-h abciximab infusion after intervention. The 10 patients pretreated with loading dose clopidogrel (450 mg followed by 75 mg daily) showed an intermediate but significant prolongation of PFA closure times and reduction of ADP-induced platelet aggregation at levels between the ticlopidin/aspirin- and the abciximab/ticlopidin/aspirin-treated groups. At 20 h after intervention, a similar degree of PFA closure time prolongation and inhibition of ADP-induced aggregation was observed in the abciximab/ticlopidin/aspirin- and the clopidogrel/aspirin-treated patient groups. Both measurement of PFA-100 closure times and inhibition of ADP-induced platelet aggregation showed a similar degree of platelet inhibition, but had rather broad SD ranges, which limit their precision for the follow-up of individual patients. In conclusion, abciximab on top of ticlopidin/aspirin showed a stronger antiplatelet effect for only less than 20 h, as compared to loading dose clopidogrel/aspirin in acute coronary syndrome patients undergoing stent implantation. Whether such a short-term superiority of abciximab, as compared to loading dose clopidogrel, translates into an overall clinical benefit of thombotic and bleeding complications remains to be established in a randomized clinical trial.

摘要

本研究比较了经典的ADP诱导的血小板聚集与使用胶原/ADP膜片盒的PFA-100封闭时间,以监测三种药物治疗方案(噻氯匹定、阿昔单抗/噻氯匹定和负荷剂量氯吡格雷)对血小板的抑制作用程度,这三种方案均在阿司匹林(乙酰水杨酸,ASA)基础上,应用于31例急性冠脉综合征患者择期支架置入术(干预)期间及术后。噻氯匹定在支架植入后直接开始使用,阿昔单抗在冠脉介入术前开始使用并静脉输注12小时,氯吡格雷负荷剂量在介入术前给予。接受噻氯匹定治疗的10例患者(每日500mg)干预后不久,PFA封闭时间无显著延长,ADP诱导的血小板聚集略有增加。11例接受阿昔单抗/噻氯匹定治疗的患者,PFA封闭时间显著延长,干预后阿昔单抗输注12小时期间,ADP诱导的血小板聚集减少超过80%。10例接受氯吡格雷负荷剂量预处理的患者(450mg,随后每日75mg),PFA封闭时间延长程度中等但显著,ADP诱导的血小板聚集减少程度介于噻氯匹定/阿司匹林治疗组和阿昔单抗/噻氯匹定/阿司匹林治疗组之间。干预后20小时,阿昔单抗/噻氯匹定/阿司匹林治疗组和氯吡格雷/阿司匹林治疗组患者的PFA封闭时间延长程度及ADP诱导聚集的抑制程度相似。PFA-100封闭时间测量及ADP诱导血小板聚集抑制均显示出相似程度的血小板抑制,但标准差范围较宽,这限制了它们对个体患者随访的精确性。总之,在接受支架植入的急性冠脉综合征患者中,与负荷剂量氯吡格雷/阿司匹林相比,阿昔单抗联合噻氯匹定/阿司匹林仅在不到20小时内显示出更强的抗血小板作用。与负荷剂量氯吡格雷相比,阿昔单抗的这种短期优势是否能转化为血栓形成和出血并发症方面的总体临床获益,仍有待在随机临床试验中确定。

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