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临时支架置入术中边支血管的药物涂层球囊血管成形术:多中心随机DCB-BIF试验

Drug-Coated Balloon Angioplasty of the Side Branch During Provisional Stenting: The Multicenter Randomized DCB-BIF Trial.

作者信息

Gao Xiaofei, Tian Nailiang, Kan Jing, Li Ping, Wang Mian, Sheiban Imad, Figini Filippo, Deng Jianping, Chen Xiang, Santoso Teguh, Shin Eun-Seok, Munawar Muhammad, Wen Shangyu, Wang Zhengzhong, Nie Shaoping, Li Yue, Xu Tan, Wang Bin, Ye Fei, Zhang Junjie, Shou Xiling, Chen Shao-Liang

机构信息

Nanjing First Hospital, Nanjing Medical University, Nanjing, China.

Yulin First People's Hospital, Yulin, China.

出版信息

J Am Coll Cardiol. 2025 Jan 7;85(1):1-15. doi: 10.1016/j.jacc.2024.08.067. Epub 2024 Oct 28.

Abstract

BACKGROUND

Side branch stenting is often required during provisional stenting, leading to suboptimal results. Drug-coated balloons (DCB) for the compromised side branch have emerged as an attractive strategy. However, the benefit of DCB for coronary bifurcations remains unclear.

OBJECTIVES

This study aimed to investigate whether DCB, compared with a noncompliant balloon (NCB), for the pinched side branch improves the outcomes of provisional stenting in patients with simple, true coronary bifurcations.

METHODS

In this multicenter, randomized controlled trial, patients with true coronary bifurcations who had side branch diameter stenosis of ≥70% after main vessel stenting at 22 centers in China, Indonesia, Italy, and Korea were randomly assigned to either DCB or NCB intervention. The primary endpoint was major adverse cardiac events, a composite of cardiac death, target vessel myocardial infarction, or clinically driven target-lesion revascularization at the 1-year follow-up.

RESULTS

Between September 8, 2020, and June 2, 2023, 784 patients with true coronary bifurcation lesions undergoing main vessel stenting and having a severely compromised side branch were randomly assigned to the DCB (n = 391) or NCB (n = 393) group. One-year follow-up was completed in all patients. The primary endpoint occurred in 28 patients in the DCB group and 49 patients in the NCB group (Kaplan-Meier rate: 7.2% vs 12.5%; HR: 0.56; 95% CI: 0.35-0.88; P = 0.013), driven by a reduction in myocardial infarction. There were no significant differences between groups in procedural success, crossover to a 2-stent approach, all-cause death, revascularization, or stent thrombosis.

CONCLUSIONS

In patients with simple and true coronary bifurcation lesions undergoing provisional stenting, main vessel stenting with a DCB for the compromised side branch resulted in a lower 1-year rate of the composite outcome compared with an NCB intervention for the side branch. The high rates of periprocedural myocardial infarction, which occurred early and did not lead to revascularization, are of unclear clinical significance.

摘要

背景

临时支架置入过程中常常需要对分支血管进行支架置入,但其效果往往不尽人意。药物涂层球囊(DCB)用于处理受损分支血管已成为一种颇具吸引力的策略。然而,DCB用于冠状动脉分叉病变的益处仍不明确。

目的

本研究旨在探讨在单纯真性冠状动脉分叉病变患者中,相较于非顺应性球囊(NCB),使用DCB处理受压分支血管是否能改善临时支架置入的效果。

方法

在这项多中心随机对照试验中,在中国、印度尼西亚、意大利和韩国的22个中心,对真性冠状动脉分叉病变且主血管支架置入后分支血管直径狭窄≥70%的患者,随机分配至DCB组或NCB组进行干预。主要终点是1年随访时的主要不良心脏事件,包括心源性死亡、靶血管心肌梗死或因临床因素导致的靶病变血运重建。

结果

在2020年9月8日至2023年6月2日期间,784例接受主血管支架置入且分支血管严重受损的真性冠状动脉分叉病变患者被随机分配至DCB组(n = 391)或NCB组(n = 393)。所有患者均完成了1年随访。DCB组有28例患者发生主要终点事件,NCB组有49例患者发生主要终点事件(Kaplan-Meier率:7.2%对12.5%;HR:0.56;95%CI:0.35 - 0.88;P = 0.013),主要是由于心肌梗死发生率降低。两组在手术成功率、转为双支架置入术、全因死亡、血运重建或支架血栓形成方面无显著差异。

结论

在接受临时支架置入的单纯真性冠状动脉分叉病变患者中,使用DCB对受损分支血管进行主血管支架置入,与使用NCB对分支血管进行干预相比,1年时复合结局发生率更低。围手术期心肌梗死发生率较高,且发生较早,未导致血运重建,其临床意义尚不清楚。

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