Department of Cardiovascular Diseases, Mayo Clinic College of Medicine, 200 1st St SW, Rochester, MN, 55905, USA.
Department of Cardiovascular Disease, Confluence Health, Wenatchee, WA, USA.
Curr Cardiol Rep. 2024 Mar;26(3):91-96. doi: 10.1007/s11886-023-02019-w. Epub 2024 Jan 18.
Spontaneous coronary artery dissection (SCAD) is an increasingly recognized cause of acute coronary syndrome (ACS), particularly among women < 50 years of age. Here, we aim to review the pathogenesis of SCAD, discuss SCAD as an initial manifestation of systemic arterial disease, and highlight invasive strategies as well as unique challenges in the care of women with SCAD.
A paradigm shift has occurred in the care of SCAD patients in the past decade as recommendations for conservative management have become widespread. Invasive interventions are reserved for patients with hemodynamic compromise or active ischemia due to increased periprocedural complications and failure rates. Certain patient populations have been identified for larger territory infarcts and proximal disease including patients with known connective tissue disease, premenopausal women, and patients with pregnancy-associated SCAD (P-SCAD). Current recommended management of SCAD is conservative. Despite a growing awareness of SCAD and its known association with systemic arteriopathies in women, evidence-based data remains scarce. Future studies focused on identifying genetic factors, optimal medical therapy after SCAD, and techniques to minimize interventional complications are needed.
自发性冠状动脉夹层(SCAD)是急性冠状动脉综合征(ACS)的一个日益被认识的病因,尤其在 50 岁以下的女性中。在此,我们旨在回顾 SCAD 的发病机制,讨论 SCAD 作为系统性动脉疾病的初始表现,并强调 SCAD 女性的侵入性策略和独特的护理挑战。
过去十年中,SCAD 患者的治疗观念发生了转变,因为广泛推荐保守治疗。由于围手术期并发症和失败率增加,侵入性干预仅保留用于存在血流动力学障碍或因活动缺血的患者。某些特定的患者人群包括已知结缔组织疾病、绝经前女性和妊娠相关 SCAD(P-SCAD)患者出现大的梗死和近端病变。目前 SCAD 的推荐治疗是保守的。尽管人们对 SCAD 及其与女性系统性动脉疾病的已知关联有了更多的认识,但循证数据仍然很少。需要未来的研究来确定遗传因素、SCAD 后的最佳药物治疗以及最大限度减少介入并发症的技术。