Mogabgab Owen, Wiviott Stephen D, Cannon Christopher P, Sloan Sarah, Sabatine Marc S, Antman Elliott M, Braunwald Eugene, Giugliano Robert P
1Cardiology Division, University of Texas Southwestern Medical School, Dallas, TX, USA.
J Cardiovasc Pharmacol Ther. 2013 Nov;18(6):555-9. doi: 10.1177/1074248413497534. Epub 2013 Sep 24.
The well-described morning peak in the onset of acute coronary syndromes has been partly attributed to increased platelet activity upon arising. It has been suggested that stent thrombosis (ST) exhibits a similar pattern. We assessed whether a diurnal variation in ST occurs, and whether more robust antiplatelet therapy with prasugrel (vs clopidogrel) can attenuate a morning excess.
Patients from the Trial to Assess Improvement in Therapeutic Outcomes by Optimizing Platelet Inhibition with Prasugrel-Thrombolysis in Myocardial Infarction (TRITON-TIMI) 38 trial (N = 13 608) with adjudicated ST classified per the Academic Research Consortium definitions of definite (N = 135) and probable (N = 27) were grouped into prespecified 8-hour intervals by time of onset: early (6 am-2 pm), late-day (2 pm-10 pm), and overnight (10 pm-6 am). We compared the rates per 1000 patients of ST across time intervals and stratified by treatment and stent type.
A diurnal variation in definite/probable ST was observed with rates of 6.5, 3.7, and 2.1 for early, late-day, and overnight intervals, respectively (P < .001), per 1000 patients treated. A sensitivity analysis excluding periprocedural acute-ST (<24 hours after index percutaneous coronary intervention [PCI]) resulted in similar findings (5.2, 2.5, and 1.8 per 1000, P < .001). The circadian variation in ST was observed in patients on clopidogrel (9.7, 4.8, and 3.1 per 1000, P < .001) with the highest rate of ST early in the day. Patients on prasugrel also demonstrated a circadian variation with particularly low rates of overnight ST (3.4, 3.0, and 1.1 per 1000, P = .020).
In TRITON-TIMI 38 trial, the timing of ST exhibited a significant diurnal variation similar to that seen with onset of other acute coronary syndromes. ST occurred less frequently among patients randomized to prasugrel compared to clopidogrel with the greatest absolute reduction (6.2 per 1000 patients) in events earlier in the day when platelet activity is known to be highest.
急性冠脉综合征发病存在着众所周知的早晨高峰,这部分归因于起床后血小板活性增加。有人提出支架血栓形成(ST)也呈现类似模式。我们评估了ST是否存在日变化,以及与氯吡格雷相比,普拉格雷更有效的抗血小板治疗能否减轻早晨的过量风险。
来自心肌梗死溶栓治疗中普拉格雷优化血小板抑制评估治疗结果改善试验(TRITON-TIMI)38试验(N = 13608)的患者,根据学术研究联盟对明确(N = 135)和可能(N = 27)ST的定义进行判定,并按发病时间分为预先设定的8小时间隔:上午(上午6点至下午2点)、下午晚些时候(下午2点至晚上10点)和夜间(晚上10点至上午6点)。我们比较了不同时间间隔每1000例患者的ST发生率,并按治疗和支架类型进行分层。
观察到明确/可能ST的日变化,上午、下午晚些时候和夜间间隔每1000例接受治疗患者的发生率分别为6.5、3.7和2.1(P < 0.001)。排除围手术期急性ST(在首次经皮冠状动脉介入治疗[PCI]后<24小时)的敏感性分析得出了类似结果(每1000例分别为5.2、2.5和1.8,P < 0.001)。氯吡格雷治疗的患者中观察到ST的昼夜变化(每1000例分别为9.7、4.8和3.1,P < 0.001),ST发生率在一天中较早时最高。普拉格雷治疗的患者也表现出昼夜变化,夜间ST发生率特别低(每1000例分别为3.4、3.0和1.1,P = 0.020)。
在TRITON-TIMI 38试验中,ST的发生时间呈现出与其他急性冠脉综合征发病类似的显著日变化。与氯吡格雷相比,随机接受普拉格雷治疗的患者中ST发生频率较低,在已知血小板活性最高的一天中较早时段,事件的绝对减少量最大(每1000例患者减少6.2例)。