Three-Year Clinical Outcomes With the Cilotax Dual Drug-Eluting Stent vs Everolimus-Eluting Stents in Patients With Acute Myocardial Infarctionopen access
- Authors
- Yu, HyeYon; Ahn, Jihun; Choi, Byoung Geol; Park, Soohyung; Kang, Dong Oh; Choi, Cheol Ung; Rha, Seung-Woon; Jeong, Myung Ho
- Issue Date
- Jan-2024
- Publisher
- TEXAS HEART INST
- Keywords
- Myocardial infarction; drug-eluting stents; percutaneous coronary intervention
- Citation
- TEXAS HEART INSTITUTE JOURNAL, v.51, no.1
- Journal Title
- TEXAS HEART INSTITUTE JOURNAL
- Volume
- 51
- Number
- 1
- URI
- https://scholarworks.bwise.kr/sch/handle/2021.sw.sch/26297
- DOI
- 10.14503/THIJ-23-8271
- ISSN
- 0730-2347
1526-6702
- Abstract
- Background: This study compared the safety and effectiveness of paclitaxel/cilostazol-eluting Cilotax stents with those of everolimus-eluting stents in patients with acute myocardial infarction. Real-world data from the Korea Acute Myocardial Infarction Registry were examined. Methods: A total of 5,472 patients with acute myocardial infarction underwent percutaneous coronary intervention with Cilotax stents (n = 212) or everolimus-eluting stents (n = 5,260). The primary end point was the 3-year rate of target lesion failure. The other end points were major adverse cardiovascular events (a composite of cardiac death, target vessel myocardial infarction, and ischemia-driven target lesion revascularization), target vessel revascularization, and stent thrombosis. A propensity score matching analysis was performed to adjust for potential confounders by using a logistic regression model; propensity score matching generated 2 well-balanced groups (Cilotax group, n = 180; everolimus-eluting stents group, n = 170; N = 350). After propensity score matching, baseline clinical characteristics were similar between the groups. Results: After percutaneous coronary intervention, compared with the everolimus-eluting stents group, the Cilotax group more often had major adverse cardiovascular events (24.1% vs 18.5%; P =.042), myocardial infarction (8.0% vs 3.2%; P <.001), target lesion revascularization (8.0% vs 2.6%; P <.001), target vessel revascularization (11.3% vs 4.5%; P <.001), and stent thrombosis (4.7% vs 0.5%; P <.001) before matching. Even after matching, the Cilotax group had more frequent target lesion revascularization (9.4% vs 2.9%; P =.22) and stent thrombosis (5.6% vs 1.2%; P =.34). Conclusion: In patients with acute myocardial infarction who underwent percutaneous coronary intervention, use of the Cilotax stent was associated with higher rates of target lesion revascularization, target vessel revascularization, and stent thrombosis than were everolimus-eluting stents. Use of the Cilotax dual drugeluting stent should be avoided in the treatment of myocardial infarction.
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