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Safety of 3‐Month Dual Antiplatelet Therapy After Implantation of Ultrathin Sirolimus‐Eluting Stents With Biodegradable Polymer (Orsiro): Results From the SMART‐CHOICE Trial

Authors :
Kyeong Ho Yun
Seung‐Yul Lee
Byung Ryul Cho
Woo Jin Jang
Young Bin Song
Ju‐Hyeon Oh
Woo Jung Chun
Yong Hwan Park
Eul‐Soon Im
Jin‐Ok Jeong
Seok Kyu Oh
Deok‐Kyu Cho
Jong‐Young Lee
Young‐Youp Koh
Jang‐Whan Bae
Jae Woong Choi
Wang Soo Lee
Hyuck Jun Yoon
Seung Uk Lee
Jang Hyun Cho
Woong Gil Choi
Seung‐Woon Rha
Joo Myung Lee
Taek Kyu Park
Jeong Hoon Yang
Jin‐Ho Choi
Seung‐Hyuck Choi
Sang Hoon Lee
Hyeon‐Cheol Gwon
Joo‐Yong Hahn
Source :
Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease, Vol 10, Iss 1 (2021)
Publication Year :
2021
Publisher :
Wiley, 2021.

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.clinicaltrials.gov; Unique identifier: NCT02079194.

Details

Language :
English
ISSN :
20479980
Volume :
10
Issue :
1
Database :
Directory of Open Access Journals
Journal :
Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease
Publication Type :
Academic Journal
Accession number :
edsdoj.501db5b9094f39bd06fccc661e6722
Document Type :
article
Full Text :
https://doi.org/10.1161/JAHA.120.018366