Bach Jürgen, Kammerer Inna, Isgro Frank, Haubelt Hannelore, Vogt Anette, Saggau Werner, Hellstern Peter
Institute of Hemostaseology and Transfusion Medicine, Academic City Hospital, Ludwigshafen/Germany.
Platelets. 2009 May;20(3):150-7. doi: 10.1080/09537100902780650.
Aspirin resistance continues to be a major challenge in patients after coronary artery bypass grafting (CABG). We investigated the impact of intravenous aspirin on platelet function in this clinical setting. Forty-two patients received 100 mg of oral aspirin once daily, beginning on day 1 after the operation. Between day 6 and 8 post operation one oral dose was replaced by an intravenous dose of 300 mg. Platelet function analyzer (PFA-100) closure times (CT), turbidimetric platelet aggregation (TPA) and impedance platelet aggregation (IPA) induced by arachidonic acid (AA), collagen and ADP were measured prior to and 1 h and 24 h after intravenous aspirin. Results obtained prior to the intravenous aspirin were compared with respective values from 120 healthy individuals. Despite the postoperative oral aspirin that was given once daily, ADP-induced TPA (ADPTPA) and IPA values induced by AA, ADP or collagen were significantly greater in patients than in controls, while PFA-100 CT were significantly shorter. Intravenous aspirin induced a significant reduction of platelet aggregability as measured by collagen/epinephrine (CEPI) CT, TPA and IPA induced by AA and collagen 1 h and 24 h after administration. Intravenous aspirin was not found to influence collagen/ADP (CADP) CT and IPA induced by ADP. Concomitantly, the number of patients with laboratory aspirin resistance as measured by CEPI-CT and TPA but not by IPA induced by AA or collagen dropped significantly. Agreement in the detection of aspirin responders and non-responders among platelet function tests was poor. Our findings indicate that the intravenous aspirin appears to be a promising approach for reducing laboratory aspirin resistance during the postoperative phase of CABG.
阿司匹林抵抗仍然是冠状动脉旁路移植术(CABG)后患者面临的主要挑战。我们在这种临床情况下研究了静脉注射阿司匹林对血小板功能的影响。42例患者术后第1天开始每天口服100mg阿司匹林。术后第6至8天,将一次口服剂量替换为300mg静脉注射剂量。在静脉注射阿司匹林前、注射后1小时和24小时,测量血小板功能分析仪(PFA-100)的封闭时间(CT)、花生四烯酸(AA)、胶原和二磷酸腺苷(ADP)诱导的比浊法血小板聚集(TPA)和阻抗法血小板聚集(IPA)。将静脉注射阿司匹林前获得的结果与120名健康个体的相应值进行比较。尽管术后每天口服阿司匹林,但患者中由ADP诱导的TPA(ADPTPA)以及由AA、ADP或胶原诱导的IPA值显著高于对照组,而PFA-100 CT显著缩短。静脉注射阿司匹林后1小时和24小时,通过胶原/肾上腺素(CEPI)CT、AA和胶原诱导的TPA和IPA测量,血小板聚集性显著降低。未发现静脉注射阿司匹林会影响胶原/ADP(CADP)CT和ADP诱导的IPA。同时,通过CEPI-CT和TPA而非AA或胶原诱导的IPA测量的实验室阿司匹林抵抗患者数量显著下降。血小板功能测试在检测阿司匹林反应者和无反应者方面的一致性较差。我们的研究结果表明,静脉注射阿司匹林似乎是一种在CABG术后阶段降低实验室阿司匹林抵抗的有前景的方法。