Zena and Michael Weiner Cardiovascular Institute, Icahn School of Medicine at Mount Sinai, New York, New York.
TIMI Study Group, Division of Cardiovascular Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts.
J Am Coll Cardiol. 2018 Feb 6;71(5):489-496. doi: 10.1016/j.jacc.2017.11.050.
Patients with prior myocardial infarction (MI) and multivessel coronary disease (MVD) are at high risk for recurrent coronary events.
The authors investigated the efficacy and safety of ticagrelor versus placebo in patients with MVD in the PEGASUS-TIMI 54 (Prevention of Cardiovascular Events in Patients With Prior Heart Attack Using Ticagrelor Compared to Placebo on a Background of Aspirin-Thrombolysis In Myocardial Infarction 54) trial.
Patients with a history of MI 1 to 3 years before inclusion in the PEGASUS-TIMI 54 trial were stratified in a pre-specified analysis based on the presence of MVD. The effect of ticagrelor (60 mg and 90 mg) on the composite of cardiovascular death, MI, or stroke (major adverse cardiovascular events [MACE]), as well as the composite of coronary death, MI, or stent thrombosis (coronary events), and on TIMI major bleeding, intracranial hemorrhage (ICH), and fatal bleeding were evaluated over a median of 33 months.
A total of 12,558 patients (59.4%) had MVD. In the placebo arm, compared with patients without MVD, those with MVD were at higher risk for MACE (9.37% vs. 8.57%, adjusted hazard ratio [HR]: 1.24; p = 0.026) and for coronary events (7.67% vs. 5.34%, HR: 1.49; p = 0.0005). In patients with MVD, ticagrelor reduced the risk of MACE (7.94% vs. 9.37%, HR: 0.82; p = 0.004) and coronary events (6.02% vs. 7.67%, HR: 0.76; p < 0.0001), including a 36% reduction in coronary death (HR: 0.64; 95% confidence interval: 0.48 to 0.85; p = 0.002). In this subgroup, ticagrelor increased the risk of TIMI major bleeding (2.52% vs. 1.08%, HR: 2.67; p < 0.0001), but not ICH or fatal bleeds.
Patients with prior MI and MVD are at increased risk of MACE and coronary events, and experience substantial relative and absolute risk reductions in both outcomes with long-term ticagrelor treatment relative to those without MVD. Ticagrelor increases the risk of TIMI major bleeding, but not ICH or fatal bleeding. For patients with prior MI and MVD, ticagrelor is an effective option for long-term antiplatelet therapy. (Prevention of Cardiovascular Events [e.g., Death From Heart or Vascular Disease, Heart Attack, or Stroke] in Patients With Prior Heart Attack Using Ticagrelor Compared to Placebo on a Background of Aspirin [PEGASUS]; NCT01225562).
有心肌梗死(MI)和多血管性冠状动脉疾病(MVD)病史的患者,其发生复发性冠状动脉事件的风险很高。
作者研究了替格瑞洛在 PEGASUS-TIMI 54(在阿司匹林-溶栓治疗心肌梗死 54 背景下,与安慰剂相比,用于既往心肌梗死患者的替格瑞洛预防心血管事件)试验中对 MVD 患者的疗效和安全性。
在 PEGASUS-TIMI 54 试验中纳入的患者中,有 1 至 3 年前有 MI 病史的患者,根据是否存在 MVD 进行了预先指定的分层分析。评估替格瑞洛(60 毫克和 90 毫克)对心血管死亡、MI 或卒中(主要不良心血管事件 [MACE])的复合终点,以及对冠状动脉死亡、MI 或支架血栓形成(冠状动脉事件)的复合终点,以及对 TIMI 大出血、颅内出血(ICH)和致死性出血的影响,中位随访时间为 33 个月。
共有 12558 名患者(59.4%)存在 MVD。在安慰剂组中,与无 MVD 的患者相比,MVD 患者发生 MACE 的风险更高(9.37% vs. 8.57%,调整后的风险比 [HR]:1.24;p=0.026)和冠状动脉事件(7.67% vs. 5.34%,HR:1.49;p=0.0005)。在 MVD 患者中,替格瑞洛降低了 MACE(7.94% vs. 9.37%,HR:0.82;p=0.004)和冠状动脉事件(6.02% vs. 7.67%,HR:0.76;p<0.0001)的风险,包括冠状动脉死亡风险降低 36%(HR:0.64;95%置信区间:0.48 至 0.85;p=0.002)。在该亚组中,替格瑞洛增加了 TIMI 大出血的风险(2.52% vs. 1.08%,HR:2.67;p<0.0001),但不增加 ICH 或致死性出血的风险。
既往有 MI 和 MVD 的患者发生 MACE 和冠状动脉事件的风险增加,与无 MVD 的患者相比,长期接受替格瑞洛治疗可显著降低这两种结局的风险。替格瑞洛增加了 TIMI 大出血的风险,但不增加 ICH 或致死性出血的风险。对于既往有 MI 和 MVD 的患者,替格瑞洛是一种有效的长期抗血小板治疗选择。