Early clinical experience with the Multi-Link coronary stent.

P Wong, C M Wong, C H Cheng, P Ko, J Chow, Y T Tai, C Barnes
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引用次数: 24

Abstract

The Multi-Link coronary stent (Advanced Cardiovascular Systems, Santa Clara, CA) is a balloon expandable stent carved from a stainless steel cylinder and is composed of 12 corrugated rings connected by multiple links. This design gives the stent great flexibility and conformity as well as radial strength. For the 3 month period from November 1995 to January 1996, all patients undergoing stent implantation in our institution were treated with this device, except for vessels smaller than 2.7 mm or larger than 3.7 mm in diameter, left main disease, or those who could not tolerate anticoagulation therapy. Forty patients, with a total of 42 arteries or 44 lesions, were treated with 56 stents, or 1.33 stents per artery. Clinical presentation included stable angina in 13 (32.5%), unstable angina in 24 (60%), acute myocardial infarction in 2 (5%), of whom 1 was in cardiogenic shock, and atypical symptoms with an abnormal thallium stress test in 1 (2.5%). According to the American College of Cardiology/ American Heart Association (ACC/AHA) classification, 8 lesions (18%) were type A, 14 (32%) type B1, 11 (25%) type B2, and 11 (25%) type C. Forty-three lesions (97.7%) were de novo and 1 (2.3%) restenotic. Stent delivery was successful in all patients. Complications included 1 balloon rupture at 7 atm but without sequelae, and 2 patients in whom the coronary guide wire became kinked and locked inside the catheter shaft of the stent delivery system but stent delivery was eventually successful. Mean diameter stenosis was reduced from 76 +/- 13% presenting to 2 +/- 9% poststenting and minimal lumen diameter increased from 0.87 +/- 0.38 to 2.82 +/- 0.34 mm. There were no acute-subacute stent thromboses, bleeding/vascular complications, or major cardiac events such as myocardial infarction, coronary artery bypass surgery, or death during a follow-up period of 2-5 months (mean 3.6 months). In conclusion, our early clinical experience with the Multi-Link stent is very encouraging, with a very high rate of successful delivery and minimal complications.

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多节段冠状动脉支架的早期临床经验。
多链接冠状动脉支架(Advanced Cardiovascular Systems, Santa Clara, CA)是一个由不锈钢圆柱体雕刻而成的气球式可膨胀支架,由12个波纹环由多个链接连接而成。这种设计使支架具有很大的灵活性和一致性以及径向强度。1995年11月至1996年1月3个月期间,除血管直径小于2.7 mm或大于3.7 mm、左主干病变或抗凝治疗不能耐受者外,所有在我院行支架植入术的患者均使用本装置治疗。40例患者共42条动脉或44个病变,接受56个支架治疗,每条动脉1.33个支架。临床表现包括稳定型心绞痛13例(32.5%),不稳定型心绞痛24例(60%),急性心肌梗死2例(5%),其中心源性休克1例,非典型症状伴铊应激试验异常1例(2.5%)。根据美国心脏病学会/美国心脏协会(ACC/AHA)的分类,A型病变8例(18%),B1型14例(32%),B2型11例(25%),c型11例(25%),新发病变43例(97.7%),再狭窄1例(2.3%)。所有患者的支架置入均成功。并发症包括1例7atm球囊破裂,但无后遗症,2例冠状动脉导丝在支架输送系统导管轴内扭结锁定,但最终支架输送成功。平均直径狭窄从支架置入前的76 +/- 13%减少到支架置入后的2 +/- 9%,最小管腔直径从0.87 +/- 0.38 mm增加到2.82 +/- 0.34 mm。在2-5个月(平均3.6个月)的随访期间,无急性-亚急性支架血栓形成、出血/血管并发症、心肌梗死、冠状动脉搭桥手术等主要心脏事件或死亡。总之,我们使用Multi-Link支架的早期临床经验是非常令人鼓舞的,它具有非常高的成功率和最小的并发症。
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