Lee Cheol Hyun, Lee Seonhwa, Hwang Jongmin, Kim In-Cheol, Cho Yun-Kyeong, Yoon Hyuck-Jun, Kim Hyungseop, Nam Chang-Wook, Hur Seung-Ho
Division of Cardiology, Department of Internal Medicine, Keimyung University Dongsan Hospital, Daegu, Republic of Korea.
Coron Artery Dis. 2025 May 27. doi: 10.1097/MCA.0000000000001536.
Although drug-eluting stents (DES) are effective, stent thrombosis (ST) remains a major concern in patients with acute myocardial infarction (AMI) who undergo DES implantation. We aimed to evaluate the incidence of late stent malapposition (SM) and uncovered struts 12 months after implantation of a bioabsorbable polymer everolimus-eluting stent (BP-EES) or a durable polymer zotarolimus-eluting stent (DP-ZES) in patients with AMI using optical coherence tomography (OCT).
Sixty-nine patients with AMI were randomly assigned 2:1 to the BP-EES (46 patients) or DP-ZES (23 patients) groups. The coprimary endpoints were the incidences of late SM and uncovered stent struts in OCT strut-level analysis at 12 months postimplantation.
The 51 patients who completed the 12-month follow-up OCT (BP-EES, 36 patients, 39 lesions; DP-ZES, 15 patients, 18 lesions) showed no intergroup differences in the incidence of acute SM (BP-EES vs. DP-ZES; 12.25 ± 14.27% vs. 12.35 ± 10.55%, P = 0.981) at the index procedure. The incidence of late SM (0.12 ± 0.42% vs. 0.14 ± 0.25%, P = 0.873) and uncovered struts (1.69 ± 3.44% vs. 2.45 ± 3.23%, P = 0.532) also did not differ between the two DES groups at 12-month postimplantation.
Twelve-month OCT measurements showed no significant differences in late SM and uncovered struts between the BP-EES and DP-ZES stents. Thus, contemporary second-generation DES show a very low rate of late SM and uncovered struts after 12 months in AMI, regardless of stent polymer type.
Late stent strut apposition and coverage after drug-eluting stent implantation by OCT in patients with AMI (APPOSITION AMI-II) (NCT02770651).
尽管药物洗脱支架(DES)有效,但支架血栓形成(ST)仍是接受DES植入的急性心肌梗死(AMI)患者的主要担忧。我们旨在使用光学相干断层扫描(OCT)评估急性心肌梗死患者植入生物可吸收聚合物依维莫司洗脱支架(BP-EES)或耐用聚合物佐他莫司洗脱支架(DP-ZES)12个月后晚期支架贴壁不良(SM)和未覆盖支架小梁的发生率。
69例AMI患者按2:1随机分为BP-EES组(46例)或DP-ZES组(23例)。共同主要终点是植入后12个月OCT支架小梁水平分析中晚期SM和未覆盖支架小梁的发生率。
完成12个月随访OCT的51例患者(BP-EES组36例,39个病变;DP-ZES组15例,18个病变)在首次手术时急性SM发生率(BP-EES组与DP-ZES组;12.25±14.27%对12.35±10.55%,P = 0.981)无组间差异。植入后12个月时,两个DES组之间晚期SM发生率(0.12±0.42%对0.14±0.25%,P = 0.873)和未覆盖支架小梁发生率(1.69±3.44%对2.45±3.23%,P = 0.532)也无差异。
12个月的OCT测量显示,BP-EES和DP-ZES支架在晚期SM和未覆盖支架小梁方面无显著差异。因此,当代第二代DES在AMI患者中12个月后晚期SM和未覆盖支架小梁的发生率非常低,与支架聚合物类型无关。
急性心肌梗死患者药物洗脱支架植入后OCT评估晚期支架小梁贴壁和覆盖情况(APPOSITION AMI-II)(NCT02770651)。