@article{29472feaa16847998e51920f132606c6,
title = "Safety of 3-month dual antiplatelet therapy after implantation of ultrathin sirolimus-eluting stents with biodegradable polymer (Orsiro): Results from the SMART-CHOICE trial",
abstract = "BACKGROUND: This study sought to investigate the safety of 3-month dual antiplatelet therapy (DAPT) in patients receiving ultrathin sirolimus-eluting stents with biodegradable polymer (Orsiro). METHODS AND RESULTS: The SMART-CHOICE (Smart Angioplasty Research Team: Comparison Between P2Y12 Antagonist Monotherapy vs Dual Anti- platelet Therapy in Patients Undergoing Implantation of Coronary Drug-Eluting Stents) randomized trial compared 3-month DAPT followed by P2Y12 inhibitor monotherapy with 12-month DAPT in 2993 patients undergoing percutaneous coronary intervention. The present analysis was a prespecified subgroup analysis for patients receiving Orsiro stents. As a post hoc analysis, comparisons between Orsiro and everolimus-eluting stents were also done among patients receiving 3-month DAPT. Of 972 patients receiving Orsiro stents, 481 patients were randomly assigned to 3-month DAPT and 491 to 12-month DAPT. At 12 months, the target vessel failure, defined as a composite of cardiac death, target vessel-related myocardial infarction, or target vessel revascularization, occurred in 8 patients (1.7%) in the 3-month DAPT group and in 14 patients (2.9%) in the 12-month DAPT group (hazard ratio [HR], 0.58; 95% CI, 0.24-1.39; P=0.22). In whole population who were randomly assigned to receive 3-month DAPT (n=1495), there was no significant difference in the target vessel failure between the Orsiro group and the everolimus-eluting stent group (n=1014) (1.7% versus 1.8%; HR, 0.96; 95% CI, 0.41-2.22; P=0.92). CONCLUSIONS: In patients receiving Orsiro stents, clinical outcomes at 1 year were similar between the 3-month DAPT followed by P2Y12 inhibitor monotherapy and 12-month DAPT strategies. With 3-month DAPT, there was no significant difference in target vessel failure between Orsiro and everolimus-eluting stents. REGISTRATION: URL: https://www.clini caltr ials.gov; Unique identifier: NCT02079194.",
keywords = "Antiplatelet therapy, Coronary artery disease, Percutaneous coronary intervention",
author = "{SMART-CHOICE Investigators} and {Ho Yun}, Kyeong and Lee, {Seung Yul} and Cho, {Byung Ryul} and Jang, {Woo Jin} and {Bin Song}, Young and Oh, {Ju Hyeon} and Chun, {Woo Jung} and Park, {Yong Hwan} and Im, {Eul Soon} and Jeong, {Jin Ok} and {Kyu Oh}, Seok and Cho, {Deok Kyu} and Lee, {Jong Young} and Koh, {Young Youp} and Bae, {Jang Whan} and Choi, {Jae Woong} and {Soo Lee}, Wang and {Jun Yoon}, Hyuck and {Uk Lee}, Seung and Cho, {Jang Hyun} and {Gil Choi}, Woong and Rha, {Seung Woon} and Lee, {Joo Myung} and {Kyu Park}, Taek and Yang, {Jeong Hoon} and Choi, {Jin Ho} and Choi, {Seung Hyuck} and Lee, {Sang Hoon} and Gwon, {Hyeon Cheol} and Hahn, {Joo Yong} and Cho, {Sang Cheol} and Hwang, {Sun Ho} and Kim, {Dong Bin} and Jeon, {Dong Woon} and Ryu, {Jae Kean} and Kim, {Moo Hyun} and Chae, {In Ho} and Kim, {Sang Hyun} and Kim, {Hack Lyoung} and {Kyu Jin}, Dong and {Woo Suh}, Il and Park, {Jong Seon} and Shin, {Eun Seok} and Kim, {Shin Jae} and Cheong, {Sang Sig} and {Yun Lee}, Sung and Chae, {Jei Keon} and {Mo Yang}, Yong",
note = "Funding Information: This study was supported by the Korean Society of Interventional Cardiology, Abbott Vascular Korea, Biotronik Korea, and Boston Scientific Korea. The sponsors had no role in the design and conduct of the study; collection, management, analysis, and interpretation of the data; preparation, review, or approval of the manuscript; and decision to submit the manuscript for publication. Funding Information: This study was supported by the Korean Society of Interventional Cardiology, Abbott Vascular Korea, Biotronik Korea, and Boston Scientific Korea. The sponsors had no role in the design and conduct of the study; collection, management, analysis, and interpretation of the data; preparation, review, or approval of the manuscript; and decision to submit the manuscript for publication. Dr Hahn has received grants from Abbott Vascular, Boston Scientific, Biotronik, Daiichi Sankyo, and Medtronic; and speaker?s fees from AstraZeneca, Daiichi Sankyo, and Sanofi-Aventis. Dr Gwon has received research grants from Abbott Vascular, Boston Scientific, and Medtronic; and speaker?s fees from Abbott Vascular, Boston Scientific, and Medtronic. The remaining authors have no disclosures to report. Publisher Copyright: {\textcopyright} 2020 The Authors.",
year = "2021",
doi = "10.1161/JAHA.120.018366",
language = "English",
volume = "10",
pages = "1--9",
journal = "Journal of the American Heart Association",
issn = "2047-9980",
publisher = "Wiley-Blackwell",
number = "1",
}