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新型AVE微型冠状动脉支架在补救治疗中的急性临床和血管造影结果。

Acute clinical and angiographic results with the new AVE Micro coronary stent in bailout management.

作者信息

Ozaki Y, Keane D, Ruygrok P, de Feyter P, Stertzer S, Serruys P W

机构信息

Catheterization Laboratory, Thoraxcenter, Erasmus University, Rotterdam, The Netherlands.

出版信息

Am J Cardiol. 1995 Jul 15;76(3):112-6. doi: 10.1016/s0002-9149(99)80040-x.

DOI:10.1016/s0002-9149(99)80040-x
PMID:7611142
Abstract

To determine the feasibility and safety of development of this new stent, we deployed 28 AVE Micro stents in 23 native coronary artery lesions in 20 patients who developed acute or threatened closure after balloon angioplasty (BA). Ten stents were deployed in the left anterior descending artery, 10 in the circumflex, and 8 in the right coronary artery. Luminal dimensions were measured using a computer-based quantitative coronary angiographic analysis system (CAAS II). Stent deployment was successful in 27 of 28 attempts (96%). In 1 patient with a threatened closure of the left anterior descending artery associated with proximal vessel tortuosity, attempted stent deployment was unsuccessful. The clinical course of the other 19 patients in whom stent deployment was successful was free of coronary reintervention, bypass surgery, and death. A myocardial infarction was observed in 2 patients (10%), in 1 of whom the stent was implanted within 24 hours after the onset of acute myocardial infarction, and in the other acute vessel occlusion was present for 58 minutes before stent implantation. No subacute occlusion was observed. Event-free survival at 30 days after stent implantation was 85% (17 of 20 patients). Minimal luminal diameter was 0.85 +/- 0.57 mm before and 1.19 +/- 0.66 mm after BA, 2.61 +/- 0.39 mm during balloon inflation, 3.26 +/- 0.46 mm during and 2.74 +/- 0.51 mm after stenting, 3.43 +/- 0.52 mm during balloon inflation after stenting (Swiss Kiss), and 2.85 +/- 0.48 mm after Swiss Kiss.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

为确定这种新型支架研发的可行性与安全性,我们在20例球囊血管成形术(BA)后发生急性闭塞或有闭塞风险的患者的23处天然冠状动脉病变中植入了28枚AVE微型支架。10枚支架植入左前降支,10枚植入回旋支,8枚植入右冠状动脉。使用基于计算机的定量冠状动脉造影分析系统(CAAS II)测量管腔尺寸。28次尝试中有27次成功植入支架(96%)。1例左前降支有闭塞风险且近端血管迂曲的患者,支架植入尝试未成功。其他19例支架植入成功的患者临床过程中未进行冠状动脉再次干预、搭桥手术及死亡。2例患者(10%)发生心肌梗死,其中1例在急性心肌梗死发病后24小时内植入支架,另1例在支架植入前急性血管闭塞达58分钟。未观察到亚急性闭塞。支架植入后30天无事件生存率为85%(20例患者中的17例)。BA前最小管腔直径为0.85±0.57mm,BA后为1.19±0.66mm,球囊扩张时为2.61±0.39mm,支架植入时及植入后分别为3.26±0.46mm和2.74±0.51mm,支架植入后球囊扩张(瑞士吻合法)时为3.43±0.52mm,瑞士吻合法后为2.85±0.48mm。(摘要截断于250字)

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Int J Card Imaging. 1997 Feb;13(1):3-13. doi: 10.1023/a:1005703106724.