Spontaneous coronary artery dissection 'storm' in post-partum: a case report.

Pub Date : 2024-10-26 eCollection Date: 2024-11-01 DOI:10.1093/ehjcr/ytae567
Nicolas Combaret, Géraud Souteyrand, Pascal Motreff
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Abstract

Background: Spontaneous coronary artery dissection (SCAD) remains a rare form of acute coronary syndrome (ACS) in young women. It is not always easy to diagnose and its management can be complex, particularly in the case of severe forms.

Case summary: A 29-year-old Mahorese woman presented with non-ST-elevation acute coronary syndrome 72 h after vaginal delivery of an uncomplicated twin pregnancy. Coronary angiography revealed a SCAD of the left anterior descending artery (LAD) treated medically. At Day 4, urgent coronary angiography was performed due to recurrent ACS with unfavourable evolution on LAD SCAD with worsening flow and appearance of right coronary artery (RCA) dissection. Percutaneous coronary intervention (PCI) was performed with drug-eluting stent (DES) implantation in LAD under optical coherence tomography (OCT) guidance. At Day 6, the patient suffered from inferior ST segment elevation myocardial infarction due to extension of the RCA SCAD with occlusion of the posterior descending artery. Once again, under OCT guidance, PCI was performed in RCA with implantation of four DES. At Day 8, the patient presented with an intra-hospital cardiac arrest by electromechanical dissociation. Urgent coronary angiography revealed a diffuse extension of the SCAD to the circumflex artery and the left main trunk (LM). Rescue PCI of the LM was performed under OCT guidance, and a femoro-femoral extracorporeal life support was implanted because of haemodynamic instability. With no hope of left ventricular ejection fraction recovery, the patient eventually benefited from a heart transplant 12 days after the first ACS with excellent evolution.

Discussion: Although the majority of SCAD have a favourable outcome with spontaneous healing, it is important to keep in mind that certain severe forms exist and could require specific management as PCI under OCT guidance and potential transfer to surgical centres where heart transplants and mechanical circulatory support are available.

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产后自发性冠状动脉夹层 "风暴":病例报告。
背景:自发性冠状动脉夹层(SCAD自发性冠状动脉夹层(SCAD)在年轻女性中仍是一种罕见的急性冠状动脉综合征(ACS)。病例摘要:一名 29 岁的马霍雷斯妇女在无并发症的双胎妊娠经阴道分娩 72 小时后出现非 ST 段抬高的急性冠状动脉综合征。冠状动脉造影显示左前降支动脉(LAD)的 SCAD 曾接受过药物治疗。第4天,由于ACS复发,LAD SCAD病情恶化,血流恶化,出现右冠状动脉(RCA)夹层,因此紧急进行了冠状动脉造影。在光学相干断层扫描(OCT)引导下,患者接受了经皮冠状动脉介入治疗(PCI),在左冠状动脉植入了药物洗脱支架(DES)。第6天,患者因RCA SCAD扩展伴后降支动脉闭塞而发生下ST段抬高型心肌梗死。在 OCT 引导下,再次对 RCA 进行了 PCI,并植入了四个 DES。第8天,患者因机电分离出现院内心脏骤停。急诊冠状动脉造影显示,SCAD弥漫性扩展至环状动脉和左主干(LM)。由于血流动力学不稳定,在OCT引导下对左主干进行了抢救性PCI,并植入了股股体外生命支持系统。由于左心室射血分数恢复无望,患者最终在首次ACS发生12天后接受了心脏移植手术,并取得了良好的进展:讨论:尽管大多数SCAD患者的预后良好,可以自发痊愈,但必须牢记,某些严重的SCAD患者可能需要在OCT引导下进行PCI等特殊治疗,并有可能转至可进行心脏移植和机械循环支持的外科中心。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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