Coons James C, Iasella Carlo J, Chanas Tyler, Wang Nan, Williams Kiersten, Boyd Anthony, Lyons John, Eckardt Jamie, Rihtarchik Lindsey, Merkel Alison, Chambers Alexandra, Lemon Lara S, Smith Randall, Ensor Christopher R
1 University of Pittsburgh School of Pharmacy, Pittsburgh, PA, USA.
2 University of Pittsburgh, Pittsburgh, PA, USA.
Ann Pharmacother. 2017 Aug;51(8):649-655. doi: 10.1177/1060028017706977. Epub 2017 Apr 24.
Dual antiplatelet therapy is a mainstay of care for percutaneous coronary intervention (PCI) patients; however, uncertainty exists in real-world practice about comparative effectiveness and safety outcomes.
To evaluate outcomes of different oral P2Y12 inhibitors in PCI patients.
We retrospectively studied patients treated between July 1, 2010, and December 31, 2013. Patients received clopidogrel, prasugrel, ticagrelor, or more than 1 antiplatelet (switch) during PCI. Outcomes were evaluated for major adverse cardiovascular events (MACE) and bleeding at 1 year. Propensity score matching with Cox proportional hazards analysis was used to determine predictors of MACE and bleeding.
A total of 8127 patients were included: clopidogrel (n = 6872), prasugrel (n = 605), ticagrelor (n = 181), and switch (n = 469). Treatment with prasugrel was associated with the lowest risk of MACE using multivariate regression (odds ratio [OR] = 0.57; 95% CI = 0.36-0.92; P = 0.02). In the propensity score-matched analysis, only the prasugrel group was associated with a lower risk of MACE compared with the clopidogrel group. Clopidogrel was associated with the lowest risk of major bleeding using multivariate regression (OR = 0.64; 95% CI = 0.42-0.98; P = 0.042). Both ticagrelor (hazard ratio [HR] = 2.00; 95% CI = 1.11-3.59) and the switch groups (HR = 1.65; 95% CI = 1.09-2.50) were associated with a greater risk of major bleeding compared with clopidogrel. However, no differences were found in the propensity score-matched analysis.
Dual antiplatelet therapies differed in both MACE and bleeds in a real-world setting of PCI. Prasugrel was associated with fewer MACE, whereas clopidogrel had fewer major bleeding events.
双联抗血小板治疗是经皮冠状动脉介入治疗(PCI)患者治疗的主要手段;然而,在实际临床实践中,关于其相对有效性和安全性结果仍存在不确定性。
评估不同口服P2Y12抑制剂在PCI患者中的治疗效果。
我们回顾性研究了2010年7月1日至2013年12月31日期间接受治疗的患者。患者在PCI期间接受氯吡格雷、普拉格雷、替格瑞洛或超过1种抗血小板药物(转换治疗)。评估1年时主要不良心血管事件(MACE)和出血情况。采用倾向评分匹配及Cox比例风险分析来确定MACE和出血的预测因素。
共纳入8127例患者:氯吡格雷组(n = 6872)、普拉格雷组(n = 605)、替格瑞洛组(n = 181)和转换治疗组(n = 469)。多因素回归分析显示,使用普拉格雷治疗的MACE风险最低(比值比[OR]=0.57;95%可信区间[CI]=0.36 - 0.92;P = 0.02)。在倾向评分匹配分析中,与氯吡格雷组相比,只有普拉格雷组的MACE风险较低。多因素回归分析显示,氯吡格雷的严重出血风险最低(OR = 0.64;95% CI = 0.42 - 0.98;P = 0.042)。与氯吡格雷相比,替格瑞洛组(风险比[HR]=2.00;95% CI = 1.11 - 3.59)和转换治疗组(HR = 1.65;95% CI = 1.09 - 2.50)的严重出血风险更高。然而,在倾向评分匹配分析中未发现差异。
在PCI的实际临床环境中,双联抗血小板治疗在MACE和出血方面存在差异。普拉格雷与较少的MACE相关,而氯吡格雷的严重出血事件较少。