Ziegler S, Maca T, Alt E, Speiser W, Schneider B, Minar E
Department of Angiology, University Hospital School of Medicine, Vienna, Austria.
Platelets. 2002 Dec;13(8):493-7. doi: 10.1080/0953710021000057866.
In patients suffering from peripheral arterial occlusive disease (PAOD) the risk of restenosis after percutaneous transluminal angioplasty (PTA) might be influenced by platelet mediated factors.
To look for a correlation between the effect of antiplatelet therapy and recurrence of disease after PTA by monitoring platelet function in 3-month intervals by the platelet function analyzer system, PFA-100, over a period of 1 year.
A group of 98 patients (43 females, 55 males) with PAOD, treated with aspirin (n = 52), thienopyridine (n = 34) or combination therapy of both (n = 12) were followed over a period of 12 months after elective PTA of the lower extremities with regard to occurrence of restenosis or reocclusion at the site of angioplasty, to demonstrate inhibitory effects on platelets, induced by antiplatelet therapy.
PFA-100 proved suitable to identify 'non-responders' to antiplatelet therapy, in a 12-month follow-up period. In 'non-responders' to clopidogrel therapy, a higher incidence of restenosis or reocclusion after PTA of the lower limbs was detected compared with 'responders'.
PFA-100, upon stimulation with ADP, might predict patients under clopidogrel therapy with elevated risk for the development of complications following PTA of the lower limbs. This could offer the chance to switch to an alternative therapy or adapt the dose.
在患有外周动脉闭塞性疾病(PAOD)的患者中,经皮腔内血管成形术(PTA)后再狭窄的风险可能受血小板介导的因素影响。
通过使用血小板功能分析仪系统PFA-100每隔3个月监测血小板功能,为期1年,来寻找抗血小板治疗效果与PTA后疾病复发之间的相关性。
一组98例PAOD患者(43例女性,55例男性),接受阿司匹林治疗(n = 52)、噻吩吡啶治疗(n = 34)或两者联合治疗(n = 12),在接受下肢选择性PTA后随访12个月,观察血管成形术部位再狭窄或再闭塞的发生情况,以证明抗血小板治疗对血小板的抑制作用。
在12个月的随访期内,PFA-100被证明适用于识别对抗血小板治疗“无反应者”。与“有反应者”相比,在接受氯吡格雷治疗的“无反应者”中,下肢PTA后再狭窄或再闭塞的发生率更高。
在用ADP刺激时,PFA-100可能预测接受氯吡格雷治疗的患者在下肢PTA后发生并发症的风险升高。这可能提供改用替代治疗或调整剂量的机会。