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Cost-effectiveness of bivalirudin versus heparin plus glycoprotein IIb/IIIa inhibitor in the treatment of non-ST-segment elevation acute coronary syndromes

机译:比伐卢定与肝素加糖蛋白IIb / IIIa抑制剂在非ST段抬高急性冠状动脉综合征治疗中的成本效益

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摘要

OBJECTIVES: This study sought to assess the cost-effectiveness of bivalirudin versus heparin plus glycoprotein IIb/IIIa inhibitor (GPI) in thienopyridine-treated non-ST-segment elevation acute coronary syndrome (NSTE-ACS) patients undergoing early or urgent invasive management, from a United Kingdom National Health Service perspective.\ud\udMETHODS: A decision-analytic model with lifelong time horizon was populated with event risks and resource use parameters derived from the Acute Catheterization and Urgent Intervention Triage Strategy (ACUITY) trial raw data. In a parallel analysis, key comparator strategy inputs came from Global Registry of Acute Coronary Events (GRACE) patients enrolled in the United Kingdom. Upstream and catheter laboratory-initiated GPI were assumed to be tirofiban and abciximab, respectively. Life expectancy of first-year survivors, unit costs, and health-state utilities came from United Kingdom sources. Costs and effects were discounted at 3.5%. Incremental cost-effectiveness ratios (ICERs) were expressed as cost per quality-adjusted life year (QALY) gained.\ud\udRESULTS: Higher acquisition costs for bivalirudin were partially offset by lower hospitalization and bleeding costs. In the ACUITY-based analysis, per-patient lifetime costs in the bivalirudin and heparin plus GPI strategies were £10,903 and £10,653, respectively. Patients survived 10.87 and 10.82 years on average, corresponding to 5.96 and 5.93 QALYs and resulting in an ICER of £9,906 per QALY gained. The GRACE-based ICER was £12,276 per QALY gained. In probabilistic sensitivity analysis, 72.1% and 67.0% of simulation results were more cost-effective than £20,000 per QALY gained, in the ACUITY-based and GRACE-based analyses, respectively. Additional scenario analyses implied that greater cost-effectiveness may be achieved in actual clinical practice.\ud\udCONCLUSIONS: Treating NSTE-ACS patients undergoing invasive management with bivalirudin is likely to represent a cost-effective option for the United Kingdom, when compared with the current practice of using heparin and a GPI
机译:目的:本研究旨在评估比伐卢定与肝素加糖蛋白IIb / IIIa抑制剂(GPI)在噻吩吡啶治疗的非ST段抬高急性冠状动脉综合征(NSTE-ACS)患者中进行早期或紧急侵入性治疗的成本效益,方法:从生命周期和从急性导管插入和紧急干预分类策略(ACUITY)试验原始数据得出的资源使用参数中,填充了具有终生视野的决策分析模型。在平行分析中,主要比较策略的输入来自英国的急性冠脉事件全球登记系统(GRACE)患者。上游和导管实验室启动的GPI分别假定为替罗非班和abciximab。第一年幸存者的预期寿命,单位成本和国家医疗卫生设施来自英国。成本和效果折现为3.5%。成本效益比(ICER)的增量表示为每质量调整生命年(QALY)的成本。\ ud \ ud结果:比伐卢定的较高购置成本部分被较低的住院和出血成本所抵消。在基于ACUITY的分析中,比伐卢定和肝素加GPI策略的每位患者终生成本分别为10,903英镑和10,653英镑。患者平均存活10.87年和10.82年,对应于5.96和5.93 QALYs,每获得的QALY ICER为9,906英镑。基于GRACE的ICER为每QALY获得12,276英镑。在概率敏感性分析中,分别在基于ACUITY和GRACE的分析中,模拟结果的72.1%和67.0%比获得的每QALY 20,000英镑更具成本效益。其他情景分析表明,在实际的临床实践中可能会实现更高的成本效益。使用肝素和GPI的当前实践

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