近乎灾难性的冠状动脉穿孔:第二个药物洗脱支架有效吗?

Narra J Pub Date : 2024-03-19 DOI:10.52225/narra.v4i1.637
Haris Munirwan, T. F. Hadi, Adi Purnawarman, Muhammad H. Latief, Wittawat Wattanasiriporn, T. Yusrizal
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引用次数: 0

摘要

冠状动脉穿孔(CAP)是一种不常见的严重并发症。虽然严重穿孔(Ellis III)的发生率越来越高,但近年来与穿孔相关的总死亡率(7.5%)却有所下降。遗憾的是,我们的医疗机构并不总能获得覆盖支架。本病例报告旨在展示在一名 CAP 患者身上使用第二个药物洗脱支架作为替代治疗方法的有效性和成功率。这是一例 67 岁女性患者的病例,她患有稳定型心绞痛加拿大心血管协会分类 III(CCS III)、三血管冠状动脉疾病(CAD),拒绝接受 CABG(Syntax 评分 44 分),并患有 II 型糖尿病。患者接受了选择性经皮冠状动脉介入治疗(PCI),我们发现患者的左前降支动脉(LAD)近端至远端存在弥漫性狭窄,并伴有广泛钙化。此外,钝缘(OM)2处有慢性全闭塞(CTO),OM3处有临界狭窄,右冠状动脉(RCA)近端有80%的狭窄,RCA中部有90%的狭窄,RCA远端有90-95%的狭窄,远端后外侧有70-80%的弥漫性狭窄。在缓解左侧环状动脉(LCx)狭窄的手术过程中,我们在使用 2.5/20 毫米 NC 球囊充气至 12 个大气压并持续 12 秒时,遇到了被归类为 Ellis III 型的冠状动脉穿孔。为此,我们使用 2.5/28 毫米的 Xience Xpedition 药物洗脱支架 (DES) 从 LCx 近端到 OM2 进行了支架置入。随后,我们进行了长达五分钟的球囊充气(间歇式)。尽管做了这些努力,冠状动脉穿孔依然存在,仍被归类为 Ellis III 型。我们决定使用 2.5/28 毫米的 Coroflex Isar DES 进行腔内支架植入(第二种 DES 策略),然后进行长时间球囊充气。结果显示,48 小时监测后未发现穿孔残留、心肌梗死溶栓(TIMI)III 级血流,也未出现心包积液等并发症。事实证明,植入第二个 DES 是处理重大 CAP 的实用方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Nearly catastrophe coronary perforation: Is it second drug-eluting stent effective?
Coronary artery perforation (CAP) is an uncommon yet serious complication. Although severe perforations (Ellis III) have become more frequent, the overall mortality rate associated with perforations (7.5%) has decreased in recent years. Unfortunately, our medical facility cannot always access a cover stent. The aim of this case report was to demonstrate the effectiveness of using a second drug-eluting stent as an alternative and successful treatment approach in a CAP patient. This is the case of a 67-year-old female with stable angina pectoris Canadian Cardiovascular Society classification III (CCS III), three-vessel coronary artery disease (CAD), who declined CABG (Syntax score of 44) and had type II diabetes mellitus. The patient underwent elective percutaneous coronary intervention (PCI), and we identified diffuse stenosis in the proximal to distal portions of the left anterior descending artery (LAD) with extensive calcification. Furthermore, there was a chronic total occlusion (CTO) in obtuse marginal (OM) 2, as well as critical stenosis in OM3, 80% stenosis in the proximal part of right coronary artery (RCA), 90% stenosis in the middle of the RCA, 90–95% in the distal RCA, and diffuse stenosis ranging from 70–80% in the distal posterolateral. During the procedure to alleviate the stenosis in the left circumflex artery (LCx), we encountered a coronary perforation classified as Ellis type III while using a 2.5/20 mm NC balloon inflated to 12 atm for 12 seconds. In response, we performed stent placement from the proximal LCx to OM2 using the Xience Xpedition drug-eluting stent (DES) measuring 2.5/28 mm. Subsequently, we conducted extended balloon inflation (intermittent) for five minutes. Despite these efforts, the coronary perforation, still classified as Ellis type III, persisted. We decided to employ intrastent stenting (a second DES strategy) with the Coroflex Isar DES measuring 2.5/28 mm, followed by prolonged balloon inflation. The outcome revealed no remaining perforation, Thrombolysis in Myocardial Infarction (TIMI) III flow, and no complications such as pericardial effusion after 48 hours of monitoring. The implantation of a second DES proved to be a practical approach for managing a significant CAP.
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