Weintraub William S, Mahoney Elizabeth M, Lamy Andre, Culler Steven, Yuan Yong, Caro Jaime, Gabriel Sylvie, Yusuf Salim
Emory University, Atlanta, Georgia, USA.
J Am Coll Cardiol. 2005 Mar 15;45(6):838-45. doi: 10.1016/j.jacc.2004.11.051.
We sought to evaluate the long-term cost-effectiveness of clopidogrel for up to one year after an acute coronary syndrome (ACS) without ST-segment elevation.
The efficacy of platelet inhibition with clopidogrel for up to one year after ACS was demonstrated in the Clopidogrel in Unstable angina to prevent Recurrent Events (CURE) trial, a randomized trial of 12,562 patients in 28 countries that was conducted between 1998 and 2000. Patients were given clopidogrel (300-mg load followed by 75 mg/day) versus placebo, both in addition to aspirin, for a mean of nine months.
We used patient-level clinical outcomes and resource use from the CURE trial and estimates of life expectancy gains as a result of the prevention of the clinical events of death, stroke, and myocardial infarction on the basis of data from external sources.
Excluding clopidogrel costs, average costs of hospitalizations alone were 325 dollars less for the clopidogrel arm (95% confidence interval -722 dollars to 45 dollars) using diagnosis-related group-based Medicare reimbursement rates. When including clopidogrel costs (766 dollars greater for the clopidogrel arm), average total costs were 442 dollars higher for the clopidogrel arm (95% confidence interval 62 dollars to 820 dollars). The incremental cost-effectiveness ratio (ICER) on the basis of the Framingham Heart Study was 6,318 dollars per life-year gained (LYG) with clopidogrel, with 94% of bootstrap-derived ICER estimates <50,000 dollars/LYG; based on Saskatchewan, the ICER was 6,475 dollars/LYG with 98% of estimates <50,000 dollars.
Platelet inhibition with clopidogrel in patients for up to one year after presentation with an acute coronary syndrome is both effective and cost-effective.
我们旨在评估氯吡格雷在非ST段抬高型急性冠脉综合征(ACS)后长达一年的长期成本效益。
氯吡格雷在不稳定型心绞痛中预防复发性事件(CURE)试验证明了氯吡格雷在ACS后长达一年的血小板抑制疗效,该试验是一项在1998年至2000年间对28个国家的12,562例患者进行的随机试验。患者除服用阿司匹林外,还接受氯吡格雷(300毫克负荷剂量,随后每日75毫克)或安慰剂治疗,平均治疗九个月。
我们使用了CURE试验中的患者层面临床结局和资源使用情况,并根据外部来源的数据,估计了因预防死亡、中风和心肌梗死等临床事件而获得的预期寿命增加情况。
不包括氯吡格雷成本,使用基于诊断相关组的医疗保险报销率,氯吡格雷组的仅住院平均成本比安慰剂组少325美元(95%置信区间为-722美元至45美元)。当包括氯吡格雷成本(氯吡格雷组高766美元)时,氯吡格雷组的平均总成本高442美元(95%置信区间为62美元至820美元)。根据弗雷明汉心脏研究,氯吡格雷每获得一个生命年(LYG)的增量成本效益比(ICER)为6318美元,94%的自举法得出的ICER估计值<50,000美元/LYG;基于萨斯喀彻温省的数据,ICER为6475美元/LYG,98%的估计值<50,000美元。
急性冠脉综合征患者使用氯吡格雷进行长达一年的血小板抑制既有效又具有成本效益。