Chakrabarti Anjan K, Patel Shalin J, Kohli Payal, Udell Jacob A, Singh Priyamvada, Gopalakrishnan Lakshmi, Kumar Varun, Gibson C Michael
Cardiovascular Division, Department of Medicine, Beth Israel Deaconess Medical Center (AKC, SJP, LG, VK, CMG), Harvard Medical School, Boston, MA; TIMI Study Group, Cardiovascular Division, Department of Medicine, Brigham and Women?s Hospital (PK, JAU), Harvard Medical School, Boston, MA; and the PERFUSE Angiographic Core Laboratories and Data Coordinating Center, Beth Israel Deaconess Medical Center (PS) in Boston, MA.
J Atr Fibrillation. 2012 Jun 15;5(1):470. doi: 10.4022/jafib.470. eCollection 2012 Jun-Jul.
Non-valvular atrial fibrillation is the most common arrhythmia encountered in clinical practice and is associated with substantial healthcare costs. The risk of thromboembolic stroke is 3-5 times higher in patients with atrial fibrillation compared with the general population. Until the recent emergence of direct thrombin (factor IIa) and factor Xa inhibitors, antithrombotic therapy for atrial fibrillation was achieved with antiplatelet agents or vitamin K antagonists, which are considered cost-effective strategies when compared to no treatment. Now newer agents, such as the direct thrombin inhibitor dabigatran, can lower thromboembolic events and reduce the risk of fatal and intracerebral hemorrhage compared with warfarin, in addition to eliminating the need for costly therapeutic monitoring. Multiple analyses have shown that dabigatran, when compared with warfarin therapy that achieves a time in therapeutic range (TTR) consistent with previous large-scale trials, is a cost-effective approach to antithrombotic therapy in atrial fibrillation, ranging from $16,385 to $86,000 per quality-adjust life-year (QALY) gained. It has been shown to be especially cost-effective (QALY < $50,000) for high stroke-risk patients, those with a CHADS score of > 3 (barring excellent INR control) and for lower-risk patients with a CHADS of 2 but concomitant high risk of hemorrhage. In addition, factor Xa inhibitors, such as rivaroxaban (recently approved by the Federal Drug Administration [FDA]) and apixaban, may exhibit the same cost savings as dabigatran in terms of reduction of bleeding and elimination of therapeutic level monitoring costs. Going forward, the use of these agents and their role in thromboembolic stroke prophylaxis will need to be evaluated on a patient-by-patient basis, balancing consideration of the patient?s stroke and bleeding risks, as well as quality of life post-therapy.
非瓣膜性心房颤动是临床实践中最常见的心律失常,且涉及高昂的医疗费用。与普通人群相比,心房颤动患者发生血栓栓塞性卒中的风险要高出3至5倍。在直接凝血酶(因子IIa)和因子Xa抑制剂出现之前,心房颤动的抗栓治疗采用抗血小板药物或维生素K拮抗剂,与不进行治疗相比,这些方法被认为具有成本效益。现在,新型药物如直接凝血酶抑制剂达比加群,与华法林相比,除了无需进行昂贵的治疗监测外,还能降低血栓栓塞事件的发生,并减少致命性和脑出血的风险。多项分析表明,与华法林治疗相比,达比加群在达到与既往大规模试验一致的治疗时间范围(TTR)时,是一种成本效益高的心房颤动抗栓治疗方法,每获得一个质量调整生命年(QALY)的成本在16,385美元至86,000美元之间。对于中风高风险患者(CHADS评分>3,不包括国际标准化比值[INR]控制良好的情况)以及CHADS评分为2但伴有高出血风险的低风险患者,达比加群已被证明具有特别的成本效益(QALY<50,000美元)。此外,因子Xa抑制剂,如利伐沙班(最近已获美国食品药品监督管理局[FDA]批准)和阿哌沙班,在减少出血和消除治疗水平监测成本方面可能与达比加群具有相同的成本节约效果。展望未来,需要根据患者个体情况评估这些药物的使用及其在预防血栓栓塞性卒中中的作用,平衡考虑患者的中风和出血风险以及治疗后的生活质量。