Full metadata record
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | 신상훈 | * |
| dc.date.accessioned | 2024-05-20T16:31:08Z | - |
| dc.date.available | 2024-05-20T16:31:08Z | - |
| dc.date.issued | 2024 | * |
| dc.identifier.issn | 0009-7322 | * |
| dc.identifier.issn | 1524-4539 | * |
| dc.identifier.other | OAK-34906 | * |
| dc.identifier.uri | https://dspace.ewha.ac.kr/handle/2015.oak/268434 | - |
| dc.description.abstract | BACKGROUND: Stopping aspirin within 1 month after implantation of a drug-eluting stent for ticagrelor monotherapy has not been exclusively evaluated for patients with acute coronary syndrome. The aim of this study was to investigate whether ticagrelor monotherapy after <1 month of dual antiplatelet therapy (DAPT) is noninferior to 12 months of ticagrelor-based DAPT for adverse cardiovascular and bleeding events in patients with acute coronary syndrome.METHODS: In this randomized, open-label, noninferiority trial, 2850 patients with acute coronary syndrome who underwent drug-eluting stent implantation at 24 centers in South Korea were randomly assigned (1:1) to receive either ticagrelor monotherapy (90 mg twice daily) after <1 month of DAPT (n=1426) or 12 months of ticagrelor-based DAPT (n=1424) between April 24, 2019, and May 31, 2022. The primary end point was the net clinical benefit as a composite of all-cause death, myocardial infarction, definite or probable stent thrombosis, stroke, and major bleeding at 1 year after the index procedure in the intention-to-treat population. Key secondary end points were the individual components of the primary end point.RESULTS: Among 2850 patients who were randomized (mean age, 61 years; 40% ST-segment-elevation myocardial infarction), 2823 (99.0%) completed the trial. Aspirin was discontinued at a median of 16 days (interquartile range, 12-25 days) in the group receiving ticagrelor monotherapy after <1 month of DAPT. The primary end point occurred in 40 patients (2.8%) in the group receiving ticagrelor monotherapy after <1-month DAPT, and in 73 patients (5.2%) in the ticagrelor-based 12-month DAPT group (hazard ratio, 0.54 [95% CI, 0.37-0.80]; P<0.001 for noninferiority; P=0.002 for superiority). This finding was consistent in the per-protocol population as a sensitivity analysis. The occurrence of major bleeding was significantly lower in the ticagrelor monotherapy after <1-month DAPT group compared with the 12-month DAPT group (1.2% versus 3.4%; hazard ratio, 0.35 [95% CI, 0.20-0.61]; P<0.001).CONCLUSIONS: This study provides evidence that stopping aspirin within 1 month for ticagrelor monotherapy is both noninferior and superior to 12-month DAPT for the 1-year composite outcome of death, myocardial infarction, stent thrombosis, stroke, and major bleeding, primarily because of a significant reduction in major bleeding, among patients with acute coronary syndrome receiving drug-eluting stent implantation. Low event rates, which may suggest enrollment of relatively non-high-risk patients, should be considered in interpreting the trial.REGISTRATION: URL: https://www.clinicaltrials.gov; Unique identifier: NCT03797651. | * |
| dc.language | English | * |
| dc.publisher | LIPPINCOTT WILLIAMS & | * |
| dc.publisher | WILKINS | * |
| dc.subject | acute coronary syndrome | * |
| dc.subject | antiplatelet agent | * |
| dc.subject | aspirin | * |
| dc.subject | drug-eluting stents | * |
| dc.title | Stopping Aspirin Within 1 Month After Stenting for Ticagrelor Monotherapy in Acute Coronary Syndrome: The T-PASS Randomized Noninferiority Trial | * |
| dc.type | Article | * |
| dc.relation.issue | 8 | * |
| dc.relation.volume | 149 | * |
| dc.relation.index | SCIE | * |
| dc.relation.index | SCOPUS | * |
| dc.relation.startpage | 562 | * |
| dc.relation.lastpage | 573 | * |
| dc.relation.journaltitle | CIRCULATION | * |
| dc.identifier.doi | 10.1161/CIRCULATIONAHA.123.066943 | * |
| dc.identifier.wosid | WOS:001273411700006 | * |
| dc.identifier.scopusid | 2-s2.0-85179695121 | * |
| dc.author.google | Hong, Sung-Jin | * |
| dc.author.google | Lee, Seung-Jun | * |
| dc.author.google | Suh, Yongsung | * |
| dc.author.google | Yun, Kyeong Ho | * |
| dc.author.google | Kang, Tae Soo | * |
| dc.author.google | Shin, Sanghoon | * |
| dc.author.google | Kwon, Sung Woo | * |
| dc.author.google | Lee, Jun-Won | * |
| dc.author.google | Cho, Deok-Kyu | * |
| dc.author.google | Park, Jong-Kwan | * |
| dc.author.google | Bae, Jang-Whan | * |
| dc.author.google | Kang, Woong Cheol | * |
| dc.author.google | Kim, Seunghwan | * |
| dc.author.google | Lee, Yong-Joon | * |
| dc.author.google | Ahn, Chul-Min | * |
| dc.author.google | Kim, Jung-Sun | * |
| dc.author.google | Kim, Byeong-Keuk | * |
| dc.author.google | Ko, Young-Guk | * |
| dc.author.google | Choi, Donghoon | * |
| dc.author.google | Jang, Yangsoo | * |
| dc.author.google | Hong, Myeong-Ki|T-PASS Ticagrelor Monotherapy Patients Treated New-Generation | * |
| dc.contributor.scopusid | 신상훈(7403646689) | * |
| dc.date.modifydate | 20260820133701 | * |