Evaluation of Ultrathin Strut Biodegradable Polymer-Coated Sirolimus-Eluting Stents in an All-Comers Patient Population: 1-Year Results of the S-FLEX Slovakia Registry.

IF 1.4 4区 医学 Q3 CARDIAC & CARDIOVASCULAR SYSTEMS
Martin Hudec, Andrej Kupec, Pavol Gazdic
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引用次数: 0

Abstract

Background: Supraflex (Sahajanand Medical Technologies Limited, Surat, India) is a new-generation, biodegradable polymer-coated sirolimus-eluting stent (SES) designed on an ultrathin (60 µm) cobalt-chromium platform with a flexible 'S-link.' The S-FLEX Slovakia registry aimed to assess the safety and effectiveness of Supraflex SES in an all-comers population, with a subgroup of diabetic patients.

Methods: This was a prospective, observational, multi-center, post-market registry conducted between February 2018 and May 2019. All consecutive patients with symptomatic coronary artery disease scheduled for percutaneous coronary intervention with Supraflex SES were enrolled. The primary endpoint was target lesion failure (TLF), defined as a composite of cardiac death, target vessel myocardial infarction (TV-MI), or clinically indicated target lesion revascularization (CI-TLR) by percutaneous or surgical methods at 1-year follow-up. Stent thrombosis was a safety endpoint.

Results: A total of 413 patients was assessed (145 diabetics and 268 nondiabetics). At 1-year follow-up, the primary endpoint of TLF occurred in 5.1% patients, comprised of 3.9% cardiac deaths, 0.5% TV-MI, and 0.7% CI-TLR. Overall stent thrombosis occurred in 0.5% patients at 1-year follow-up. In the subgroup analysis, TLF occurred in 6.2% diabetics and 4.5% nondiabetics (P =.433) and comprised 4.8% and 3.4% cardiac deaths (P =.447), 0.7% and 0.4% TV-MI (P =.653), and 0.7%, and 0.7% CI-TLR (P =.952) in diabetics and non-diabetics, respectively. Overall stent thrombosis occurred in 0.7% diabetic and 0.4% non-diabetic patient (P =.659).

Conclusion: This registry demonstrates favourable clinical outcomes after the implantation of the ultrathin biodegradable polymer coated Supraflex SES in an all-comers population, with event rates that were similar in diabetic and nondiabetic patients.

超薄支柱生物可降解聚合物涂层西罗莫司洗脱支架在全科患者中的评估:斯洛伐克 S-FLEX 注册的 1 年结果。
背景:Supraflex(Sahajanand医疗技术有限公司,印度苏拉特)是新一代生物可降解聚合物涂层西罗莫司洗脱支架(SES),设计基于超薄(60微米)钴铬平台,具有灵活的 "S-链接"。S-FLEX 斯洛伐克登记旨在评估 Supraflex SES 在所有患者中的安全性和有效性,其中包括糖尿病患者:这是一项前瞻性、观察性、多中心、上市后登记项目,在 2018 年 2 月至 2019 年 5 月期间进行。所有计划使用 Supraflex SES 进行经皮冠状动脉介入治疗的无症状冠状动脉疾病连续患者均被纳入。主要终点是靶病变失败(TLF),定义为随访 1 年时心脏死亡、靶血管心肌梗死(TV-MI)或经皮或手术方法临床指示靶病变血运重建(CI-TLR)的综合结果。支架血栓是安全性终点:共评估了 413 名患者(145 名糖尿病患者和 268 名非糖尿病患者)。随访1年时,5.1%的患者出现了TLF这一主要终点,其中3.9%的患者出现心脏死亡,0.5%的患者出现TV-MI,0.7%的患者出现CI-TLR。1年随访期间,0.5%的患者发生了支架血栓。在亚组分析中,6.2%的糖尿病患者和4.5%的非糖尿病患者发生了TLF(P =.433),糖尿病患者和非糖尿病患者分别有4.8%和3.4%的心脏死亡(P =.447)、0.7%和0.4%的TV-MI(P =.653)、0.7%和0.7%的CI-TLR(P =.952)。总体而言,0.7%的糖尿病患者和0.4%的非糖尿病患者发生了支架血栓(P =.659):该登记结果表明,在所有患者中植入涂有超薄生物可降解聚合物的 Supraflex SES 后,临床疗效良好,糖尿病患者和非糖尿病患者的事件发生率相似。
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来源期刊
Anatolian Journal of Cardiology
Anatolian Journal of Cardiology CARDIAC & CARDIOVASCULAR SYSTEMS-
CiteScore
2.30
自引率
7.70%
发文量
270
审稿时长
12 weeks
期刊介绍: The Anatolian Journal of Cardiology is an international monthly periodical on cardiology published on independent, unbiased, double-blinded and peer-review principles. The journal’s publication language is English. The Anatolian Journal of Cardiology aims to publish qualified and original clinical, experimental and basic research on cardiology at the international level. The journal’s scope also covers editorial comments, reviews of innovations in medical education and practice, case reports, original images, scientific letters, educational articles, letters to the editor, articles on publication ethics, diagnostic puzzles, and issues in social cardiology. The target readership includes academic members, specialists, residents, and general practitioners working in the fields of adult cardiology, pediatric cardiology, cardiovascular surgery and internal medicine.
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