Department of Occupational and Environmental Medicine, College of Medicine, Dong-A University, Busan, Korea.
Division of Cardiology, Department of Internal Medicine, Hallym University Sacred Heart Hospital, Anyang-si, Gyeonggi-do, Korea.
Sci Rep. 2019 Nov 28;9(1):17783. doi: 10.1038/s41598-019-54390-w.
Anti-platelet agents are commonly used in vasospastic angina (VA) patients with comorbidity like coronary artery disease. However, long-term clinical outcomes in the use of aspirin, clopidogrel or the two agents together have rarely been investigated in VA patients. In a prospective study, we enrolled 2960 patients who received coronary angiography and ergonovine provocation test at 11 university hospitals in Korea. Among them, 1838 patients were diagnosed either with definite (n = 680) or intermediate (n = 1212) VA, using the criteria of chest pain, ECG changes and ergonovine provocation test results. They were analyzed according to their use of aspirin, clopidogrel or both, or no anti-platelet agent at all. The primary outcome was time to composite events of death from any cause, acute coronary syndrome (ACS) and symptomatic arrhythmia during a 3-year follow-up. A primary composite outcome was significantly more common in the aspirin plus clopidogrel group, at 10.8% (14/130), as compared with the non-antiplatelet group, at 4.4% (44/1011), (hazard ratio [HR] 2.41, 95% confidence interval [CI], 1.32-4.40, p = 0.004). With regard to the person-time event rate, similar results were shown, with the highest rate in the aspirin plus clopidogrel user at 4.72/1000 person months (95% CI, 2.79-7.96, log-rank test for primary outcome p = 0.016). The person-time event of the ACS rate was also highest in that group, at 2.81 (95% CI, 1.46-5.40, log-rank test for ACS p = 0.116). Kaplan-Meier survival analysis demonstrated poor prognosis in primary outcomes and ACS in aspirin plus clopidogrel users (log-rank test, p = 0.005 and p = 0.0392, respectively). Cox-proportional hazard regression analysis, adjusting for age, sex, history of coronary heart disease, hypertension, diabetes, presence or not of definite spasm, use of calcium channel blocker, demonstrated that the use of aspirin plus clopidogrel is an independent risk for the primary outcome (HR 2.01, CI: 1.07-3.81, p = 0.031). The aspirin-alone group had a similar primary and individual event rate compared to the no-antiplatelet agent group (HR 0.96, CI, 0.59-1.55, p = 0.872). Smokers using aspirin plus clopidogrel had poorer outcomes than non-smokers, with HR 6.36 (CI 2.31-17.54, p = 0.045 for interaction). In conclusion, among VA patients, aspirin plus clopidogrel use is associated with a poor clinical outcome at 3 years, especially in ACS. Aspirin alone appears to be safe for use in those patients.
抗血小板药物常用于伴有冠状动脉疾病等合并症的血管痉挛性心绞痛(VA)患者。然而,VA 患者长期使用阿司匹林、氯吡格雷或两者联合的临床结局很少被研究。在一项前瞻性研究中,我们纳入了在韩国 11 所大学医院接受冠状动脉造影和麦角新碱激发试验的 2960 名患者。其中,1838 名患者被诊断为明确(n=680)或中间(n=1212)VA,其诊断依据为胸痛、心电图改变和麦角新碱激发试验结果。根据他们使用阿司匹林、氯吡格雷或两者联合,或根本不使用抗血小板药物,对他们进行了分析。主要结局是 3 年随访期间任何原因死亡、急性冠状动脉综合征(ACS)和有症状心律失常的复合事件。阿司匹林加氯吡格雷组的主要复合结局明显更常见,为 10.8%(14/130),而非抗血小板组为 4.4%(44/1011)(风险比[HR]2.41,95%置信区间[CI]1.32-4.40,p=0.004)。就个体时间事件发生率而言,也显示出类似的结果,阿司匹林加氯吡格雷使用者的发生率最高,为 4.72/1000人月(95%CI2.79-7.96,主要结局对数秩检验p=0.016)。该组 ACS 发生率也最高,为 2.81(95%CI1.46-5.40,ACS 对数秩检验 p=0.116)。Kaplan-Meier 生存分析表明,阿司匹林加氯吡格雷使用者的主要结局和 ACS 预后较差(对数秩检验,p=0.005 和 p=0.0392,分别)。对年龄、性别、冠心病史、高血压、糖尿病、是否存在明确痉挛、钙通道阻滞剂使用情况进行 Cox 比例风险回归分析后,结果表明,使用阿司匹林加氯吡格雷是主要结局的独立危险因素(HR2.01,CI:1.07-3.81,p=0.031)。与不使用抗血小板药物组相比,阿司匹林单药组的主要和个体事件发生率相似(HR0.96,CI0.59-1.55,p=0.872)。与非吸烟者相比,使用阿司匹林加氯吡格雷的吸烟者结局较差,HR6.36(CI2.31-17.54,p=0.045 交互作用)。总之,在 VA 患者中,阿司匹林加氯吡格雷的使用与 3 年时的不良临床结局相关,尤其是 ACS。单独使用阿司匹林似乎对这些患者是安全的。