Pharmacoeconomics. 2013 Nov;31(11):959-70. doi: 10.1007/s40273-013-0088-8.
Percutaneous coronary intervention (PCI) is one of the most common medical procedures performed for treatment of coronary artery disease. Antiplatelet medications as adjunctive therapy for PCI are used routinely, with indications for specific agents or their combinations varying depending on the clinical scenario. While the cost-effectiveness of well-established agents has been extensively studied, newer drugs have not been evaluated as thoroughly. In addition, the clinical application of some antiplatelet drugs has recently changed, thus making older studies of cost effectiveness less applicable to the current landscape of clinical practice. This article reviews cost-effectiveness considerations of antiplatelet therapies in the treatment of coronary artery disease in patients undergoing PCI. Aspirin, P2Y12 inhibitors including clopidogrel and the newer agents prasugrel and ticagrelor, as well as glycoprotein (GP) IIb/IIIa inhibitors, are discussed. Overall, the use of dual antiplatelet therapy with aspirin and a P2Y12 inhibitor in patients undergoing PCI improves ischaemic outcomes and appears to be cost effective. The few available studies suggest that the recently approved medications prasugrel and ticagrelor are cost-effective alternatives to clopidogrel. However, no direct comparison between these two newer agents is available. The indications for GP IIb/IIIa inhibitors have changed in the current PCI era, and there is a paucity of cost-effectiveness data for their use in contemporary care.
经皮冠状动脉介入治疗(PCI)是治疗冠状动脉疾病最常见的医疗程序之一。抗血小板药物作为 PCI 的辅助治疗常规使用,具体药物或其组合的适应证因临床情况而异。虽然已广泛研究了确立的抗血小板药物的成本效益,但尚未对新药进行如此全面的评估。此外,一些抗血小板药物的临床应用最近发生了变化,因此, older studies of cost effectiveness 对当前临床实践的现状适用性较低。本文综述了在接受 PCI 的冠状动脉疾病患者中抗血小板治疗的成本效益考虑因素。讨论了阿司匹林、包括氯吡格雷在内的 P2Y12 抑制剂以及较新的普拉格雷和替格瑞洛、以及糖蛋白(GP)IIb/IIIa 抑制剂。总体而言,在接受 PCI 的患者中使用阿司匹林和 P2Y12 抑制剂的双联抗血小板治疗可改善缺血性结局,并且似乎具有成本效益。为数不多的可用研究表明,最近批准的药物普拉格雷和替格瑞洛是氯吡格雷的具有成本效益的替代品。然而,这两种较新药物之间没有直接比较。在当前的 PCI 时代,GP IIb/IIIa 抑制剂的适应证发生了变化,并且缺乏其在当代治疗中的成本效益数据。