Cohen David J, Lincoff A Michael, Lavelle Tara A, Chen Huei-Ling, Bakhai Ameet, Berezin Ronna H, Jackman Daniel, Sarembock Ian J, Topol Eric J
Cardiovascular Division, Beth Israel Deaconess Medical Center, Boston, Massachusetts, USA.
J Am Coll Cardiol. 2004 Nov 2;44(9):1792-800. doi: 10.1016/j.jacc.2004.05.085.
The purpose of this study was to compare the cost of percutaneous coronary intervention (PCI) using bivalirudin with provisional platelet glycoprotein (GP) IIb/IIIa inhibition with that of heparin + routine GP IIb/IIIa inhibition.
Although GP IIb/IIIa inhibition has been shown to reduce ischemic complications in a broad range of patients undergoing PCI, many patients currently do not receive such therapy because of concerns about bleeding complications or cost. Recently, bivalirudin with provisional GP IIb/IIIa inhibition has been validated as an alternative to heparin + routine GP IIb/IIIa inhibition for patients undergoing PCI. However, the cost-effectiveness of this novel strategy is unknown.
In the Randomized Evaluation in PCI Linking Angiomax to Reduced Clinical Events (REPLACE)-2 trial, 4,651 U.S. patients undergoing non-emergent PCI were randomized to receive bivalirudin with provisional GP IIb/IIIa (n = 2,319) versus heparin + routine GP IIb/IIIa (n = 2,332). Resource utilization data were collected prospectively through 30-day follow-up on all U.S. patients. Medical care costs were estimated using standard methods including bottom-up accounting (for procedural costs), the Medicare fee schedule (for physician services), hospital billing data (for 2,821 of 4,862 admissions), and regression-based approaches for the remaining hospitalizations.
Among the bivalirudin group, 7.7% required provisional GP IIb/IIIa. Thirty-day ischemic outcomes including death or myocardial infarction were similar for the bivalirudin and GP IIb/IIIa groups, but bivalirudin resulted in lower rates of major bleeding (2.8% vs. 4.5%, p = 0.002) and minor bleeding (15.1% vs. 28.1%, p < 0.001). Compared with routine GP IIb/IIIa, in-hospital and 30-day costs were reduced by $405 (95% confidence interval [CI] $37 to $773) and $374 (95% CI $61 to $688) per patient with bivalirudin (p < 0.001 for both). Regression modeling demonstrated that, in addition to the costs of the anticoagulants themselves, hospital savings were due primarily to reductions in major bleeding (cost savings = $107/patient), minor bleeding ($52/patient), and thrombocytopenia ($47/patient).
Compared with heparin + routine GP IIb/IIIa inhibition, bivalirudin + provisional GP IIb/IIIa inhibition resulted in similar acute ischemic events and cost savings of $375 to $400/patient depending on the analytic perspective.
本研究旨在比较使用比伐卢定并临时抑制血小板糖蛋白(GP)IIb/IIIa与肝素+常规抑制GP IIb/IIIa进行经皮冠状动脉介入治疗(PCI)的成本。
尽管已证明抑制GP IIb/IIIa可减少接受PCI的广泛患者群体的缺血性并发症,但由于担心出血并发症或成本,目前许多患者未接受此类治疗。最近,对于接受PCI的患者,比伐卢定联合临时抑制GP IIb/IIIa已被证实可替代肝素+常规抑制GP IIb/IIIa。然而,这种新策略的成本效益尚不清楚。
在PCI中连接Angiomax与减少临床事件的随机评估(REPLACE)-2试验中,4651例接受非紧急PCI的美国患者被随机分为接受比伐卢定联合临时GP IIb/IIIa(n = 2319)组和肝素+常规GP IIb/IIIa(n = 2332)组。前瞻性收集所有美国患者30天随访期的资源利用数据。使用标准方法估算医疗费用,包括自下而上核算(用于手术费用)、医疗保险费用表(用于医生服务)、医院计费数据(4862例住院中的2821例)以及其余住院基于回归的方法。
在比伐卢定组中,7.7%的患者需要临时抑制GP IIb/IIIa。比伐卢定组和GP IIb/IIIa组的30天缺血性结局(包括死亡或心肌梗死)相似,但比伐卢定导致大出血发生率较低(2.8%对4.5%,p = 0.002)和小出血发生率较低(15.1%对28.1%,p < 0.001)。与常规抑制GP IIb/IIIa相比,使用比伐卢定的患者住院期间和30天成本分别降低了405美元(95%置信区间[CI] 37美元至773美元)和374美元(95% CI 61美元至688美元)(两者p均< 0.001)。回归模型表明,除了抗凝剂本身的成本外,医院节省的费用主要归因于大出血减少(成本节省 = 107美元/患者)、小出血减少(52美元/患者)和血小板减少(47美元/患者)。
与肝素+常规抑制GP IIb/IIIa相比,比伐卢定+临时抑制GP IIb/IIIa导致的急性缺血事件相似,根据分析角度,每位患者可节省375至400美元。