Kammerer I, Bach J, Saggau W, Isgro F
Department of Cardiac Surgery, Academic City Hospital Ludwigshafen, Ludwigshafen, Germany.
Thorac Cardiovasc Surg. 2011 Oct;59(7):425-9. doi: 10.1055/s-0030-1270711. Epub 2011 Mar 24.
The predominant mechanism of early graft failure after coronary artery bypass grafting (CABG) is associated with antiplatelet treatment using drugs such as acetylsalicylic acid (ASA). Impaired hemostasis of multiple etiologies is often present in patients undergoing on-pump cardiac surgery. We investigated the impact of intravenous ASA administration on platelet function in this setting.
Forty-two patients were enrolled in the study. Patients received 100 mg oral ASA once daily, beginning in the early postoperative period. Noncompliance was eliminated by the administration of 300 mg ASA intravenously at 6-8 days post-operation. Blood was drawn immediately before, 1 h and 24 h after ASA administration.
A platelet function analyzer (PFA-100™) was used to evaluate closure time (CT), turbidimetric platelet aggregation (TPA) and impedance platelet aggregation (IPA) induced by arachidonic acid (AA), collagen and ADP and results were compared with the respective values from 120 healthy individuals. At 1 h and 24 h after administration, we found that intravenous ASA caused CEPI-CT to be significantly prolonged with a reduction of AA and collagen-induced IPA. Despite postoperative oral ASA administration for 6-8 days, PFA-100™ CEPI and CADP-CT were significantly shorter and ADP-TPA and IPA values induced by any agonist were significantly greater in patients than in controls. Intravenous ASA had no significant influence on CADP-CT or ADP-induced IPA (ADP-IPA).
Platelet tests for diagnosing patients as aspirin responders (ASA-R) or aspirin non-responders (ASA-NR) were found to be not comparable. Patients after CABG show augmented platelet dysfunction. Intravenous ASA administration may indicate a promising approach to reduce laboratory resistance after CABG procedure. The reason for this is not clear and requires additional clinical studies.
冠状动脉旁路移植术(CABG)后早期移植失败的主要机制与使用乙酰水杨酸(ASA)等药物进行抗血小板治疗有关。在接受体外循环心脏手术的患者中,多种病因导致的止血功能受损常常存在。我们研究了在这种情况下静脉注射ASA对血小板功能的影响。
42名患者纳入本研究。患者从术后早期开始每天口服100mg ASA。术后6 - 8天静脉注射300mg ASA以消除不依从情况。在ASA给药前、给药后1小时和24小时立即采血。
使用血小板功能分析仪(PFA - 100™)评估花生四烯酸(AA)、胶原和二磷酸腺苷(ADP)诱导的封闭时间(CT)、比浊法血小板聚集(TPA)和阻抗法血小板聚集(IPA),并将结果与120名健康个体的相应值进行比较。给药后1小时和24小时,我们发现静脉注射ASA导致CEPI - CT显著延长,AA和胶原诱导的IPA降低。尽管术后口服ASA 6 - 8天,但患者的PFA - 100™ CEPI和CADP - CT明显缩短,任何激动剂诱导的ADP - TPA和IPA值均显著高于对照组。静脉注射ASA对CADP - CT或ADP诱导的IPA(ADP - IPA)无显著影响。
发现用于诊断患者为阿司匹林反应者(ASA - R)或阿司匹林无反应者(ASA - NR)的血小板检测结果不可比。CABG术后患者表现出增强的血小板功能障碍。静脉注射ASA可能是一种有前景的方法,可降低CABG术后的实验室抵抗。其原因尚不清楚,需要进一步的临床研究。