Graidis Christos, Dimitriadis Dimokritos, Karasavvidis Vasileios, Dimitriadis Georgios, Argyropoulou Efstathia, Economou Fotios, George Dadoush, Antoniou Antonios, Karakostas Georgios
Department of Interventional Cardiology, Kyanous Stavros Hospital, Vizyis-Vyzantos 1 Street, Thessaloniki, 54636, Greece.
BMC Cardiovasc Disord. 2015 Oct 2;15:112. doi: 10.1186/s12872-015-0098-x.
Congenital coronary anomalies are uncommon with an incidence ranging from 0.17 % in autopsy cases to 1.2 % in angiographically evaluated cases. The recent development of ECG-gated multi-detector row computed tomography (MDCT) coronary angiography allows accurate and noninvasive depiction of coronary artery anomalies.
This retrospective study included 2572 patients who underwent coronary 64-slice MDCT coronary angiography from January 2008 to March 2012. Coronary angiographic scans were obtained with injection of 80 ml nonionic contrast medium. Retrospective gating technique was used to synchronize data reconstruction with the ECG signal. Maximum intensity projection, multi-planar reformatted, and volume rendering images were derived from axial scans.
Of the 2572 patients, sixty (2.33 %) were diagnosed with coronary artery anomalies (CAAs), with a mean age of 53.6 ± 11.8 years (range 29-80 years). High take-off of the RCA was seen in 16 patients (0.62 %), of the left main coronary artery (LMCA) in 2 patients (0.08 %) and both of them in 2 patients (0.08 %). Separate origin of the left anterior descending artery (LAD) and left circumflex artery (LCx) from left sinus of Valsalva (LSV) was found in 15 patients (an incidence of 0.58 %). In 9 patients (0.35 %) the right coronary artery (RCA) arose from the opposite sinus of Valsalva with a separate ostium. In 6 patients (0.23 %) an abnormal origin of LCX from the right sinus of Valsalva (RSV) was found with a further posterior course within the atrioventricular groove. A single coronary artery was seen in 3 patients (0.12 %). It originated from the right sinus of Valsalva in one patient and from LSV in two patients. In two other patients (0.08 %) the left coronary trunk originated from the RSV with separate ostium from the RCA. LCA originating from the pulmonary artery was found in one patient (0.04 %). A coronary artery fistula, which is a termination anomaly, was detected in 4 patients (0.15 %).
Although these anomalies, which are remarkably different from the normal structure, exist as early as birth, they are incidentally encountered during selective angiography or at autopsy. The incidence in reported angiographic series ranges from 0.6 % to 1.3 %. Variations in the frequency of primary congenital coronary anomalies may possibly have a genetic background. The largest angiographic series of 126595 patients, by Yamanaka and Hobbs, reported a 1.3 % incidence of anomalous coronary artery.
The results of this study support the use MDCT coronary angiography as a safe and effective noninvasive imaging modality for defining CAAs in an appropriate clinical setting, providing detailed three-dimensional anatomic information that may be difficult to obtain with invasive angiography.
先天性冠状动脉异常并不常见,其发生率在尸检病例中为0.17%,在血管造影评估病例中为1.2%。心电图门控多层螺旋计算机断层扫描(MDCT)冠状动脉造影技术的最新发展使得能够准确且无创地描绘冠状动脉异常。
这项回顾性研究纳入了2008年1月至2012年3月期间接受64层MDCT冠状动脉造影的2572例患者。注入80毫升非离子型造影剂后进行冠状动脉造影扫描。采用回顾性门控技术使数据重建与心电图信号同步。最大密度投影、多平面重组和容积再现图像均由轴位扫描获得。
在2572例患者中,60例(2.33%)被诊断为冠状动脉异常(CAA),平均年龄为53.6±11.8岁(范围29 - 80岁)。16例患者(0.62%)出现右冠状动脉高位起源,2例患者(0.08%)出现左主干冠状动脉(LMCA)高位起源,2例患者(0.08%)两者均有高位起源。15例患者(发生率0.58%)发现左前降支动脉(LAD)和左旋支动脉(LCx)分别起自主动脉窦(LSV)。9例患者(0.35%)右冠状动脉(RCA)起自对侧主动脉窦且开口独立。6例患者(0.23%)发现左旋支动脉(LCX)起自右主动脉窦(RSV)且在房室沟内走行更靠后。3例患者(0.12%)发现单支冠状动脉。其中1例起自右主动脉窦,2例起自左主动脉窦。另外2例患者(0.08%)左冠状动脉主干起自右主动脉窦且开口与右冠状动脉独立。1例患者(0.04%)发现左冠状动脉起自肺动脉。4例患者(0.15%)检测到冠状动脉瘘,这是一种终末异常。
尽管这些与正常结构显著不同的异常在出生时就已存在,但它们是在选择性血管造影或尸检时偶然发现的。在已报道的血管造影系列研究中,其发生率为0.6%至1.3%。原发性先天性冠状动脉异常频率的差异可能具有遗传背景。Yamanaka和Hobbs对126595例患者进行的最大规模血管造影系列研究报告冠状动脉异常发生率为1.3%。
本研究结果支持在适当的临床环境中,将MDCT冠状动脉造影作为一种安全有效的无创成像方式来定义冠状动脉异常,它能提供侵入性血管造影可能难以获得的详细三维解剖信息。