Division of Cardiology, Department of Medicine, Verona University Hospital, Verona, Italy; The Lambe Institute for Translational Medicine, Smart Sensors Laboratory and Curam, University of Galway, Galway, Ireland.
Division of Cardiology, Department of Medicine, Verona University Hospital, Verona, Italy.
Int J Cardiol. 2024 Jan 1;394:131341. doi: 10.1016/j.ijcard.2023.131341. Epub 2023 Sep 9.
Bioresorbable scaffolds (BRS) provide the prospect of restoring the anatomic and physiologic characteristics of the vascular wall.
This study sought to examine the long-term outcomes of BRS-based coronary intervention in a young population with diffuse and severe coronary atherosclerotic disease (CAD) and to compare the long-term evolution of treated segments versus the natural progression of untreated non-flow limiting stenoses.
Observational, single-center cohort study that prospectively included patients that underwent percutaneous coronary intervention with implantation of ABSORB BRS (Abbott Vascular). The clinical endpoint was the incidence of device-oriented composite endpoint (DoCE) up to 5 years follow-up. A subgroup of patients with baseline intracoronary imaging assessment of long lesions and/or multivessel disease underwent elective angiographic (70 patients, 129 lesions) and intracoronary imaging (55 patients, 102 lesions) follow-up. Paired intravascular ultrasound (IVUS) and quantitative flow reserve (QFR) were analyzed.
Between 2012 and 2017, 159 patients (mean age 54.0 ± 11.1) with native CAD were treated with BRS on 247 lesions. Patients were mainly at their first cardiac event, mostly acute coronary syndromes (86.5%). At the median follow-up time of 56 months [41-65], DoCE occurred in 15/159 (9.4%) patients, while non-target vessel-oriented composite endpoint occurred in 16 patients (10.4%). A significant atherosclerotic progression was detected on residual non-flow limiting plaques as per IVUS and QFR assessment, while no significant change was detected in the treated segment.
Mild-to-moderate asymptomatic CAD progressed significantly at 5-year despite OMT. BRS-treated segments had a less aggressive progression at 5-year despite more severe and symptomatic CAD at baseline.
生物可吸收支架(BRS)提供了恢复血管壁解剖和生理特征的前景。
本研究旨在检查在弥漫性和严重冠状动脉粥样硬化性疾病(CAD)的年轻人群中基于 BRS 的冠状动脉介入治疗的长期结果,并比较治疗节段与未治疗的非血流限制狭窄的自然进展的长期演变。
观察性、单中心队列研究,前瞻性纳入接受经皮冠状动脉介入治疗并植入 ABSORB BRS(雅培血管)的患者。临床终点是 5 年随访时设备导向的复合终点(DoCE)的发生率。基线时进行冠状动脉内影像学评估的长病变和/或多血管病变的亚组患者进行选择性血管造影(70 例患者,129 处病变)和冠状动脉内影像学(55 例患者,102 处病变)随访。分析配对血管内超声(IVUS)和定量血流储备(QFR)。
2012 年至 2017 年,159 名(平均年龄 54.0±11.1)患有原发性 CAD 的患者在 247 处病变中接受了 BRS 治疗。患者主要处于首次心脏事件中,主要为急性冠状动脉综合征(86.5%)。在中位数 56 个月(41-65)的随访中,15/159(9.4%)名患者发生了 DoCE,而 16 名患者发生了非靶血管导向的复合终点事件(10.4%)。IVUS 和 QFR 评估显示,残留非血流限制斑块的动脉粥样硬化进展明显,而治疗节段未发生明显变化。
尽管接受了 OMT,5 年内轻度至中度无症状 CAD 仍显著进展。尽管基线时 CAD 更严重和症状更明显,但 BRS 治疗节段在 5 年内的进展程度较轻。