VA North Texas Healthcare System and UT Southwestern Medical Center, Dallas, TX.
Am Heart J. 2013 Sep;166(3):474-80. doi: 10.1016/j.ahj.2013.06.019. Epub 2013 Jul 26.
Patients with prior coronary artery bypass graft surgery (CABG) who present with an acute coronary syndrome have a high risk for recurrent events. Whether intensive antiplatelet therapy with ticagrelor might be beneficial compared with clopidogrel is unknown. In this substudy of the PLATO trial, we studied the effects of randomized treatment dependent on history of CABG.
Patients participating in PLATO were classified according to whether they had undergone prior CABG. The trial's primary and secondary end points were compared using Cox proportional hazards regression.
Of the 18,613 study patients, 1,133 (6.1%) had prior CABG. Prior-CABG patients had more high-risk characteristics at study entry and a 2-fold increase in clinical events during follow-up, but less major bleeding. The primary end point (composite of cardiovascular death, myocardial infarction, and stroke) was reduced to a similar extent by ticagrelor among patients with (19.6% vs 21.4%; adjusted hazard ratio [HR], 0.91 [0.67, 1.24]) and without (9.2% vs 11.0%; adjusted HR, 0.86 [0.77, 0.96]; P(interaction) = .73) prior CABG. Major bleeding was similar with ticagrelor versus clopidogrel among patients with (8.1% vs 8.7%; adjusted HR, 0.89 [0.55, 1.47]) and without (11.8% vs 11.4%; HR, 1.08 [0.98, 1.20]; P(interaction) = .46) prior CABG.
Prior-CABG patients presenting with acute coronary syndrome are a high-risk cohort for death and recurrent cardiovascular events but have a lower risk for major bleeding. Similar to the results in no-prior-CABG patients, ticagrelor was associated with a reduction in ischemic events without an increase in major bleeding.
曾接受过冠状动脉旁路移植术(CABG)的急性冠状动脉综合征患者再次发生事件的风险较高。与氯吡格雷相比,替格瑞洛强化抗血小板治疗是否有益尚不清楚。在 PLATO 试验的这项亚研究中,我们研究了根据 CABG 史进行随机治疗的影响。
根据是否接受过 CABG 将参与 PLATO 的患者进行分类。使用 Cox 比例风险回归比较试验的主要和次要终点。
在 18613 名研究患者中,有 1133 名(6.1%)有 CABG 史。CABG 史患者在研究入组时具有更多的高危特征,且随访期间临床事件发生率增加了两倍,但大出血减少。在有(19.6%比 21.4%;调整后的危险比[HR],0.91[0.67,1.24])和无(9.2%比 11.0%;调整后的 HR,0.86[0.77,0.96];P(交互作用)=0.73)CABG 史的患者中,替格瑞洛对主要终点(心血管死亡、心肌梗死和中风的复合终点)的降低程度相似。在有(8.1%比 8.7%;调整后的 HR,0.89[0.55,1.47])和无(11.8%比 11.4%;HR,1.08[0.98,1.20];P(交互作用)=0.46)CABG 史的患者中,替格瑞洛与氯吡格雷的大出血发生率相似。
急性冠状动脉综合征伴 CABG 史的患者死亡和再发心血管事件的风险较高,但大出血风险较低。与无 CABG 史患者的结果相似,替格瑞洛可减少缺血事件而不增加大出血。