Smoking and outcomes following personalized antiplatelet therapy in chronic coronary syndrome patients: A substudy from the randomized PATH-PCI trial

IF 4.6 Q2 MATERIALS SCIENCE, BIOMATERIALS
Ying Pan MD, Ting-Ting Wu MD, PhD, Chang-Jiang Deng MD, Yi Yang MD, Xian-Geng Hou MD, Tuo Yan BS, Shun Wang BS, Ying-Ying Zheng MD, PhD, FACC, Xiang Xie MD, PhD, FACC
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Abstract

Background

This is a sub-analysis of the Personalized Antithrombotic Therapy for Coronary Heart Disease after PCI (PATH-PCI) trial in China to explore the relationship between smoking and outcomes following personalized antiplatelet therapy (PAT) in chronic coronary syndrome (CCS) patients undergoing percutaneous coronary intervention (PCI).

Methods

As a single-center, prospective, randomized controlled and open-label trial, the PATH-PCI trial randomized CCS patients undergoing PCI into standard group or personalized group guided by a novel platelet function test (PFT), from December 2016 to February 2018. All patients were divided into smokers and nonsmokers according to their smoking status. Subsequently, we underwent a 180-day follow-up evaluation. The primary endpoint was the net adverse clinical events (NACE).

Results

Regardless of smoking status, in the incidence of NACE, there was a reduction with PAT but that the reductions are not statistically significant. In the incidence of bleeding events, we found no statistically significant difference between two groups (smokers: 2.0% vs. 1.4%, HR = 1.455, 95% confidence interval [CI]: 0.595−3.559, p = .412; nonsmokers: 2.2% vs. 1.8%, HR = 1.228, 95% CI: 0.530−2.842, p = .632). In smokers, PAT reduced major adverse cardiac and cerebrovascular events (MACCE) by 48.7% (3.0% vs. 5.9%, HR = 0.513, 95% CI: 0.290−0.908, p = .022), compared with standard antiplatelet therapy (SAT). PAT also reduced the major adverse cardiovascular events (MACE) but there was no statistically difference in the reductions (p > .05). In nonsmokers, PAT reduced MACCE and MACE by 51.5% (3.3% vs. 6.7%, HR = 0.485, 95% CI: 0.277−0.849, p = .011) and 63.5% (1.8% vs. 4.9%, HR = 0.365, 95% CI: 0.178−0.752, p = .006), respectively. When testing p-values for interaction, we found there was no significant interaction of smoking status with treatment effects of PAT (pint-NACE = .184, pint-bleeding = .660).

Conclusion

Regardless of smoking, PAT reduced the MACE and MACCE, with no significant difference in bleeding. This suggests that PAT was an recommendable regimen to CCS patients after PCI, taking into consideration both ischemic and bleeding risk.

Abstract Image

吸烟与慢性冠状动脉综合征患者个性化抗血小板治疗后的预后:随机 PATH-PCI 试验的子研究。
研究背景这是中国PCI术后冠心病个性化抗栓治疗(PATH-PCI)试验的一项子分析,旨在探讨接受经皮冠状动脉介入治疗(PCI)的慢性冠状动脉综合征(CCS)患者在接受个性化抗血小板治疗(PAT)后吸烟与预后之间的关系:作为一项单中心、前瞻性、随机对照和开放标签试验,PATH-PCI试验于2016年12月至2018年2月将接受PCI治疗的慢性冠脉综合征患者随机分为标准组和以新型血小板功能检测(PFT)为指导的个性化组。所有患者根据吸烟状况分为吸烟者和非吸烟者。随后,我们进行了为期 180 天的随访评估。主要终点为净不良临床事件(NACE):无论吸烟与否,NACE的发生率都随着PAT的使用而降低,但降低幅度在统计学上并不显著。在出血事件的发生率方面,我们发现两组之间的差异没有统计学意义(吸烟者:2.0% 对 1.4%,HR = 1.455,95% 置信区间 [CI]:0.595-3.559):0.595-3.559, p = .412;非吸烟者:2.2% vs. 1.8%,HR = 1.228, 95% CI: 0.530-2.842, p = .632)。与标准抗血小板疗法(SAT)相比,PAT可将吸烟者的主要不良心脑血管事件(MACCE)减少48.7%(3.0% vs. 5.9%,HR = 0.513,95% CI:0.290-0.908,p = .022)。PAT 还能减少主要心血管不良事件 (MACE),但在减少幅度上没有统计学差异(P > .05)。在非吸烟者中,PAT 可使 MACCE 和 MACE 分别减少 51.5%(3.3% 对 6.7%,HR = 0.485,95% CI:0.277-0.849,p = .011)和 63.5%(1.8% 对 4.9%,HR = 0.365,95% CI:0.178-0.752,p = .006)。在检测交互作用的 P 值时,我们发现吸烟状况与 PAT 的治疗效果之间没有显著的交互作用(pint-NACE = .184,pint-出血 = .660):结论:无论吸烟与否,PAT 均能降低 MACE 和 MACCE,而出血量无明显差异。这表明,考虑到缺血和出血风险,PAT 是一种值得推荐的方案。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
ACS Applied Bio Materials
ACS Applied Bio Materials Chemistry-Chemistry (all)
CiteScore
9.40
自引率
2.10%
发文量
464
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