Coons James C, Seybert Amy L, Saul Melissa I, Kirisci Levent, Kane-Gill Sandra L
Cardiology Specialty Resident, University of Pittsburgh Medical Center, Pittsburgh, PA, USA.
Ann Pharmacother. 2005 Oct;39(10):1621-6. doi: 10.1345/aph.1G129. Epub 2005 Aug 16.
Patients undergoing percutaneous coronary intervention (PCI) with stent placement are often prescribed glycoprotein IIb/IIIa inhibitors. However, drug selection is often based on clinicians' preference and cost because few studies have directly compared abciximab and eptifibatide.
To compare clinical outcomes and total hospital costs of abciximab and eptifibatide in patients undergoing stent placement during PCI in a real-world setting.
A retrospective cohort analysis was conducted of 960 patients administered abciximab or eptifibatide for intracoronary stent placement between 1999 and 2001 at a tertiary care hospital. The primary outcome was bleeding, defined as major, moderate, or minor according to published criteria. Secondary outcomes included in-hospital death, myocardial infarction, revascularization, and the triple composite endpoint of those outcomes, thrombocytopenia, length-of-stay, and total hospital costs. Pearson's chi(2) analysis, Fisher's exact test, and ANOVA were used for statistical analysis.
The frequency of bleeding complications based on severity was similar between abciximab and eptifibatide: major (2.4% vs 2.8%), moderate (12.4% vs 10.5%), and minor (4.0% vs 3.9%), respectively (p = 0.86). Secondary clinical outcomes were also similar between groups (p > 0.05). Total costs for hospitalization were significantly greater for abciximab compared with eptifibatide ($16,383 +/- 6799 vs $14,115 +/- 6285; p < 0.001). Drug acquisition costs were also significantly greater for abciximab compared with eptifibatide ($508 +/- 159 vs $465 +/- 263; p = 0.003).
In patients undergoing stent placement during PCI, abciximab and eptifibatide are comparable in terms of safety and effectiveness despite significant differences in hospitalization and acquisition costs.
接受经皮冠状动脉介入治疗(PCI)并植入支架的患者通常会使用糖蛋白IIb/IIIa抑制剂。然而,药物选择往往基于临床医生的偏好和成本,因为很少有研究直接比较阿昔单抗和依替巴肽。
在现实环境中比较阿昔单抗和依替巴肽在接受PCI支架植入患者中的临床结局和总住院费用。
对1999年至2001年在一家三级护理医院接受冠状动脉内支架植入并使用阿昔单抗或依替巴肽的960例患者进行回顾性队列分析。主要结局是出血,根据已发表的标准分为严重、中度或轻度。次要结局包括院内死亡、心肌梗死、血运重建以及这些结局的三联复合终点、血小板减少症、住院时间和总住院费用。采用Pearson卡方分析、Fisher精确检验和方差分析进行统计分析。
阿昔单抗和依替巴肽在出血并发症的严重程度方面频率相似:严重出血(分别为2.4%对2.8%)、中度出血(12.4%对10.5%)和轻度出血(4.0%对3.9%)(p = 0.86)。两组间次要临床结局也相似(p > 0.05)。与依替巴肽相比,阿昔单抗的住院总费用显著更高(16383美元±6799美元对14115美元±6285美元;p < 0.001)。与依替巴肽相比,阿昔单抗的药物购置成本也显著更高(508美元±159美元对465美元±263美元;p = 0.003)。
在接受PCI支架植入的患者中,尽管住院和购置成本存在显著差异,但阿昔单抗和依替巴肽在安全性和有效性方面具有可比性。