Clark Richard A, Marler Adam T, Lin Charles K, McDonough Ryan J, Prentice Ryan L, Malik Jamil A, Villines Todd C, Hulten Edward A, Thomas Dustin M, Slim Ahmad M
Cardiology Service, San Antonio Military Medical Center, San Antonio, TX, USA.
Cardiology Service, Walter Reed National Military Medical Center, Bethesda, MD, USA.
Ther Adv Cardiovasc Dis. 2014 Dec;8(6):237-41. doi: 10.1177/1753944714546482. Epub 2014 Aug 10.
Anomalous origination of a coronary artery from an opposite sinus of Valsalva (ACAOS) is a rare finding that is typically found on autopsy in a person with sudden cardiac death or during routine cardiovascular testing. The true prevalence is unknown for this reason. There is also question to the specific anatomy of the anomalies themselves and how best to correct them.
We performed a retrospective chart review of all coronary computed tomography angiography (CCTA) studies to evaluate the incidence of all-cause mortality, nonfatal myocardial infarction, stroke and late revascularization (>90 days following CCTA) from January 2005 until July 2012. We describe the origin of the artery, its course, slit-like appearance and treatment in this population.
We reviewed 1518 CCTA reports and identified 22 patients with ACAOS with an incidence of 1.4% of our original study population over a review period of 6 years with a resultant median follow-up period of 25 months [interquartile range (IQR)25,75 12-34 months]. The indication for CCTA was for chest pain in the majority of patients (73%). We had one patient undergo surgical repair and one with coronary bypass grafting for unrelated symptomatic coronary artery disease.
ACAOS continues to be a rare but presumed fatal condition in subsets identified to carry high risk features. As the characteristics of the anomalous vessels that increase risk are still debated, over an intermediate to long follow up in a single large center, none of the different anomalous findings with varying degrees of high risk findings were associated with sudden death.
冠状动脉起源于对侧瓦尔萨尔瓦窦(ACAOS)是一种罕见的发现,通常在心脏性猝死患者的尸检中或常规心血管检查时发现。因此,其真实患病率尚不清楚。对于这些异常本身的具体解剖结构以及如何进行最佳矫正也存在疑问。
我们对2005年1月至2012年7月期间所有冠状动脉计算机断层扫描血管造影(CCTA)研究进行了回顾性图表审查,以评估全因死亡率、非致命性心肌梗死、中风和晚期血运重建(CCTA后>90天)的发生率。我们描述了该人群中动脉的起源、走行、裂隙样外观及治疗情况。
我们回顾了1518份CCTA报告,确定了22例ACAOS患者,在6年的回顾期内,其发生率占我们原始研究人群的1.4%,中位随访期为25个月[四分位间距(IQR)25,75 12 - 34个月]。大多数患者(73%)进行CCTA的指征是胸痛。我们有1例患者接受了手术修复,1例因无关的有症状冠状动脉疾病接受了冠状动脉搭桥术。
在被确定具有高风险特征的亚组中,ACAOS仍然是一种罕见但可能致命的疾病。由于增加风险的异常血管特征仍存在争议,在一个大型中心进行的中长期随访中,不同程度的高风险异常发现均与猝死无关。