Seo Suk-Min, Kim Tae-Hoon, Koh Yoon-Seok, Her Sung-Ho, Shin Dong Il, Park Hun-Jun, Kim Pum-Joon, Park Chul Soo, Lee Jong Min, Kim Dong-Bin, Kim Hee-Yeol, Chang Kiyuk, Yoo Ki-Dong, Jeon Doo Soo, Chung Wook-Sung, Seung Ki-Bae
aCardiovascular Center and Cardiology Division, Incheon St. Mary's Hospital, College of Medicine, The Catholic University of Korea, Incheon bCardiovascular Center and Cardiology Division, Uijeongbu St. Mary's Hospital, College of Medicine, The Catholic University of Korea, Uijeongbu cCardiovascular Center and Cardiology Division, Seoul St. Mary's Hospital, College of Medicine, The Catholic University of Korea dCardiovascular Center and Cardiology Division, Yeouido St. Mary's Hospital, College of Medicine, The Catholic University of Korea eCardiovascular Center and Cardiology Division, St. Paul's Hospital, College of Medicine, The Catholic University of Korea, Seoul fCardiovascular Center and Cardiology Division, Daejeon St. Mary's Hospital, College of Medicine, The Catholic University of Korea, Daejeon gCardiovascular Center and Cardiology Division, Bucheon St. Mary's Hospital, College of Medicine, The Catholic University of Korea, Bucheon hCardiovascular Center and Cardiology Division, St Vincent's Hospital, College of Medicine, The Catholic University of Korea, Suwon, Republic of Korea.
Coron Artery Dis. 2016 Mar;27(2):143-50. doi: 10.1097/MCA.0000000000000338.
Although randomized clinical trials are valuable tools to compare treatment effects, the results of randomized clinical trials cannot usually be extrapolated to the real-world setting because of selected patient subsets. To categorize the risk of future cardiovascular events in drug-eluting stent (DES)-treated patients, we analyzed demographic, clinical, and procedural data in all-comers who underwent a percutaneous coronary intervention (PCI).
Patients who underwent PCI using DES from January 2004 were prospectively enrolled in the Catholic University of Korea-PCI registry and were followed up for a median of 2 years. We analyzed the risk of clinical outcomes in the all-patient cohort and in subsets of patients with angina and acute myocardial infarction (AMI).
The patients were categorized into two groups: those with angina (angina group, n=6183, 67.7%) and those with AMI (AMI group, n=2944, 32.3%). The AMI group had greater occurrence of major adverse cardiac events (MACE) during long-term follow-up than the angina group (23.8 vs. 20.1%, P<0.001). However, in the landmark analysis of data beyond 1 year, there was no significant difference in the occurrence of MACE between the two groups (P=0.44). In multivariable modeling, age, renal function, left ventricular ejection fraction, and multivessel disease were associated significantly with increasing MACE in the study population, angina or AMI groups.
We found that higher MACE in patients with AMI during long-term follow-up after PCI was mainly because of higher mortality in the first year. Some demographic, clinical, and angiographic factors still significantly influence the long-term occurrence of MACE in the era of DES.
尽管随机临床试验是比较治疗效果的重要工具,但由于患者选择的局限性,随机临床试验的结果通常不能外推至真实世界环境。为了对接受药物洗脱支架(DES)治疗的患者未来发生心血管事件的风险进行分类,我们分析了所有接受经皮冠状动脉介入治疗(PCI)患者的人口统计学、临床和手术数据。
2004年1月接受DES PCI治疗的患者前瞻性纳入韩国天主教大学PCI注册研究,并进行了中位时间为2年的随访。我们分析了全患者队列以及心绞痛和急性心肌梗死(AMI)患者亚组的临床结局风险。
患者分为两组:心绞痛患者(心绞痛组,n = 6183,67.7%)和AMI患者(AMI组,n = 2944,32.3%)。AMI组在长期随访期间主要不良心脏事件(MACE)的发生率高于心绞痛组(23.8%对20.1%,P<0.001)。然而,在1年以上数据的标志性分析中,两组之间MACE的发生率没有显著差异(P = 0.44)。在多变量模型中年龄、肾功能、左心室射血分数和多支血管病变与研究人群、心绞痛或AMI组中MACE的增加显著相关。
我们发现PCI术后长期随访中AMI患者较高的MACE主要是由于第一年较高的死亡率。在DES时代,一些人口统计学、临床和血管造影因素仍然显著影响MACE的长期发生。