Cho Sungsoo, Kang Do-Yoon, Kim Jung-Sun, Park Duk-Woo, Kim In-Soo, Kang Tae Soo, Ahn Jung-Min, Lee Pil Hyung, Kang Soo-Jin, Lee Seung-Whan, Kim Young-Hak, Lee Cheol Whan, Park Seong-Wook, Lee Seung-Jun, Hong Sung-Jin, Ahn Chul-Min, Kim Byeong-Keuk, Ko Young-Guk, Choi Donghoon, Jang Yangsoo, Hong Myeong-Ki, Park Seung-Jung
Department of Cardiology, Heart and Brain Hospital, Chung-Ang University Gwangmyeong Hospital, Chung-Ang University College of Medicine, Gwangmyeong, Gyeonggi-do, Republic of Korea.
Division of Cardiology, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Republic of Korea.
Rev Esp Cardiol (Engl Ed). 2023 Apr;76(4):245-252. doi: 10.1016/j.rec.2022.07.007. Epub 2022 Jul 27.
There are scarce data on the optimal duration and prognostic impact of dual antiplatelet therapy (DAPT) after percutaneous coronary intervention (PCI) with second-generation drug-eluting stents for left main coronary artery (LMCA) disease. The aim of this study was to investigate the practice pattern and long-term prognostic effect of DAPT duration in patients undergoing PCI with second-generation drug-eluting stents for LMCA disease.
Using individual patient-level data from the IRIS-MAIN and KOMATE registries, 1827 patients undergoing PCI with second-generation drug-eluting stents for LMCA disease with valid information on DAPT duration were included. The efficacy outcome was major adverse cardiovascular events (MACE, a composite of cardiac death, myocardial infarction, and stent thrombosis) and the safety outcome was TIMI major bleeding.
DAPT duration was <6 months (n=273), 6 to 12 months (n=477), 12 to 24 months (n=637), and ≥ 24 months (n=440). The median follow-up duration was 3.9 [interquartile range, 3.01-5.00] years. Prolonged DAPT duration was associated with lower incidences of MACE. In multigroup propensity score analysis, adjusted HR for MACE were significantly higher for DAPT <6 months and DAPT 6 to 12 months than for DAPT 12 to 24 months (HR, 4.51; 95%CI, 2.96-6.88 and HR 1.92; 95%CI, 1.23-3.00). There was no difference in HR for major bleeding among the assessed groups.
DAPT duration following PCI for LMCA disease is highly variable. Although the duration of DAPT should be considered in the context of the clinical situation of each patient, <12 months of DAPT was associated with higher incidence of MACE. Registration identifiers: NCT01341327; NCT03908463.
关于第二代药物洗脱支架治疗左主干冠状动脉(LMCA)疾病后双联抗血小板治疗(DAPT)的最佳持续时间及其对预后的影响,相关数据较少。本研究的目的是调查接受第二代药物洗脱支架治疗LMCA疾病的患者中DAPT持续时间的实际模式及其长期预后效果。
利用IRIS-MAIN和KOMATE注册研究中的个体患者水平数据,纳入1827例接受第二代药物洗脱支架治疗LMCA疾病且有DAPT持续时间有效信息的患者。疗效结局为主要不良心血管事件(MACE,包括心源性死亡、心肌梗死和支架血栓形成的复合事件),安全性结局为TIMI大出血。
DAPT持续时间<6个月(n=273)、6至12个月(n=477)、12至24个月(n=637)和≥24个月(n=440)。中位随访时间为3.9[四分位间距,3.01 - 5.00]年。DAPT持续时间延长与MACE发生率较低相关。在多组倾向评分分析中,DAPT<6个月和DAPT 6至12个月时MACE的调整后HR显著高于DAPT 12至24个月(HR,4.51;95%CI,2.96 - 6.88和HR 1.92;95%CI,1.23 - 3.00)。评估组之间大出血的HR无差异。
LMCA疾病PCI术后DAPT持续时间差异很大。虽然应根据每位患者的临床情况考虑DAPT的持续时间,但DAPT<12个月与MACE发生率较高相关。注册标识符:NCT01341327;NCT03908463。