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药物涂层球囊(DCB)联合临时药物洗脱支架(DES)植入治疗初发 Medina 0,1,0 或 0,0,1 左主干冠状动脉分叉病变:一项概念验证研究。

DCB combined with provisional DES implantation in the treatment of De Novo Medina 0,1,0 or 0,0,1 left main coronary bifurcation lesions: A proof-of-concept study.

机构信息

Department of Cardiology, Barts Heart Centre, Barts Health NHS Trust; London-UK; Centre for Cardiovascular Medicine and Devices, William Harvey Research Institute, Queen Mary University of London; London-UK; Department of Cardiology, Faculty of Medicine, Yüzüncü Yıl University; Van-Turkey.

Department of Cardiology, Xuzhou Third People's Hospital, Xuzhou Hospital Affiliated to Jiangsu University; Xuzhou-China.

出版信息

Anatol J Cardiol. 2022 Mar;26(3):218-225. doi: 10.5152/AnatolJCardiol.2021.1157.

Abstract

OBJECTIVE

To investigate the safety and efficacy of a percutaneous revascularization strategy that is based on the use of drug-coated balloon for the treatment of patients with acute coronary syndrome and de novo Medina type 0,1,0 or 0,0,1 left main stem bifurcation lesions.

METHODS

In this multicenter, prospective, proof-of-concept study, patients fulfilling the above criteria were enrolled and received treatment with drug-coated balloon combined with provisional drug-eluting stent implantation in the proximal major branches of the left main stem. Patients who declined this revascularization approach were treated with drug-eluting stent implantation 1-2 mm distally to the left anterior descending or left circumflex artery ostium followed by drug-coated balloon therapy for the ostial disease. The primary endpoint of the study was the calculation of percent diameter stenosis on quantitative coronary angiography post-procedure as well as event rate at 8 months follow-up.

RESULTS

A total of 30 patients were enrolled in the study; their mean age was 60.3 ± 7.8 years, while 22 (73.3%) were male. Twenty-two patients were treated only with drugcoated balloon and provisional drug-eluting stent implantation and 8 had drug-eluting stent implantation followed by drug-coated balloon therapy of the ostium of the left main stem major branch. All the procedures were successful with no immediate complications. The percent diameter stenosis of lesion decreased significantly post-procedure from 87.5% (80.0-90.0) to 20% (17.5-30.0), P <.001. During the follow-up period, no major adverse cardiac events were reported.

CONCLUSIONS

This proof-of-concept study indicates that ostial drug-coated balloon therapy of the left main stem major branches is safe and effective. Larger clinical data and longer follow-up are needed before advocating its regular use in clinical practice.

摘要

目的

研究一种基于药物涂层球囊的经皮血运重建策略的安全性和有效性,该策略用于治疗急性冠状动脉综合征和新发 Medina 0、1、0 或 0、0、1 型左主干分叉病变患者。

方法

在这项多中心、前瞻性、概念验证研究中,符合上述标准的患者被纳入研究,并接受药物涂层球囊联合左主干近端大分支临时药物洗脱支架置入术治疗。拒绝这种血运重建方法的患者在左前降支或左回旋支开口处 1-2mm 处接受药物洗脱支架置入术,然后对开口病变进行药物涂层球囊治疗。研究的主要终点是计算术后定量冠状动脉造影的直径狭窄百分比以及 8 个月随访时的事件发生率。

结果

共纳入 30 例患者,平均年龄为 60.3±7.8 岁,其中 22 例(73.3%)为男性。22 例患者仅接受药物涂层球囊和临时药物洗脱支架置入术治疗,8 例患者接受药物洗脱支架置入术,随后对左主干大分支开口进行药物涂层球囊治疗。所有手术均成功,无即刻并发症。术后病变的直径狭窄百分比从 87.5%(80.0-90.0)显著下降至 20%(17.5-30.0),P<0.001。在随访期间,未报告重大不良心脏事件。

结论

这项概念验证研究表明,左主干大分支开口药物涂层球囊治疗是安全有效的。在倡导其在临床实践中的常规应用之前,需要更多的临床数据和更长的随访时间。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8388/9366374/5791be0cf323/ajc-26-3-218_f001.jpg

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