首页> 外文期刊>Advances in Interventional Cardiology: Postepy w Kardiologii Interwencyjnej >Treatment of left main coronary artery stenosis with the STENTYS self-expandable drug-eluting stent – a pilot registry
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Treatment of left main coronary artery stenosis with the STENTYS self-expandable drug-eluting stent – a pilot registry

机译:STENTYS自膨式药物洗脱支架治疗左主干狭窄

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Percutaneous coronary intervention (PCI) of the left main coronary artery (LMCA) for revascularization after stenosis is still considered controversial therapy. Previous studies were performed with balloon-expandable drug-eluting stents (DES). Balloon-expandable stents presented a challenge because they were not able to adapt effectively to variation in the vessel lumen. There are limited data on LMCA therapy with self-expandable DES for treatment of medial and distal lesions. The advantages of a self-apposing stent are adaptation to vessel size, vessel tapering, stent sizing, and good apposition. This was a pilot study to determine safety and device success rate in patients with middle and distal LMCA stenosis treated with the STENTYS self-expanding coronary DES stent. The primary endpoints were device success, acute procedural success and in-hospital and 30-day MACE. Twenty-four patients were included. Median logistic EuroSCORE was 1.6% (1.1–2.6%). Median Syntax score was 20.0 (20.0–27.2) points. Significant stenosis according to the anatomical region was in the middle of the LMCA in 5 cases (21%) and the distal part in 19 (79%). Stent sizes used were: 3.0 × 3.5 mm in 9 (37.5%); 3.5 × 4.0 mm in 3 (12.5%); 3.5 × 4.5 mm in 12 (50%). Device success and acute procedural success were achieved in 23 patients (95.8%), with no edge dissection in any patient. In 1 patient the proximal end of the stent protruded into the aorta. In all patients during their hospitalization and 30-day follow-up there were no adverse events. The data compiled from this small, single-center pilot study suggest that the STENTYS self-expanding coronary stent may be a reasonable approach to treat lesions within the LMCA. These results warrant a larger future clinical trial.
机译:狭窄后左主冠状动脉(LMCA)的经皮冠状动脉介入治疗(PCI)用于血运重建仍被认为是有争议的治疗方法。先前的研究是使用球囊扩张式药物洗脱支架(DES)进行的。球囊扩张式支架提出了一项挑战,因为它们无法有效适应血管腔的变化。 LMCA联合可自我扩张的DES治疗内侧和远端病变的数据有限。自对置支架的优点是适应血管大小,逐渐变细,支架尺寸大小和良好的并置性。这是一项初步研究,目的是确定使用STENTYS自扩张冠状动脉DES支架治疗的中,远端LMCA狭窄患者的安全性和设备成功率。主要终点是设备成功,急性手术成功以及院内和30天MACE。包括二十四名患者。物流EuroSCORE的中位数为1.6%(1.1-2.6%)。语法中位数为20.0(20.0-27.2)分。根据解剖部位的明显狭窄在LMCA中部5例(21%),远端19例(79%)。使用的支架尺寸为:3.0 x 3.5毫米in 9(37.5%); 3.5×4.0毫米in 3(12.5%); 3.5×4.5毫米(12(50%))。 23例患者(95.8%)达到了器械成功率和急性手术成功率,任何患者均未发生边缘夹层。在1名患者中,支架的近端伸入主动脉。在住院和30天随访期间,所有患者均未发生不良事件。这项小型的单中心先导研究收集的数据表明,STENTYS自扩张式冠状动脉支架可能是治疗LMCA内病变的合理方法。这些结果值得将来进行更大的临床试验。

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