TY - EJOU AU - Pang, Tong AU - Jiang, Li AU - Zhang, Yi AU - Yang, Mengxi AU - Wang, Jin AU - Li, Yuan AU - Yang, Zhigang TI - Comparison of Intracardiac and Extracardiac Malformations Associated with Single Atrium, Single Ventricle and Single Atrium-Single Ventricle Using DualSource Computed Tomography T2 - Congenital Heart Disease PY - 2022 VL - 17 IS - 4 SN - 1747-0803 AB - Background: To evaluate the qualitative and quantitative differences between intracardiac and extracardiac vascular malformations in patients with a single atrium (SA), single ventricle (SV) and single atrium-single ventricle (SA-SV) using dual-source CT (DSCT), and to compare the diagnostic performances of DSCT and transthoracic echocardiography (TTE). Methods: This retrospective study included 24 SA, 75 SV and 24 SA-SV patients who underwent both DSCT and TTE before surgery. The diagnostic values of DSCT and TTE for intracardiac and extracardiac malformations were compared according to the surgical results. The diameters of the major artery and vein were measured and calculated based on DSCT and compared among the three groups. Results: The most common malformation was pulmonary artery disease in SA (50.0%) and SA-SV (45.8%) groups and patent ductus arteriosus (33.3%) in SV group. Although there was no statistical difference, arterial development was relatively poor in the SA group. All groups showed the trend of pulmonary artery stenosis (SAvs. SVvs. SA-SV: 50.0% vs. 30.7% vs. 33.3%). There was a significant difference in mean pulmonary vein index among the groups (p = 0.017). The diagnostic sensitivity of DSCT was superior to that of TTE for extracardiac malformations. Conclusions: The most common malformation in SA and SA-SV patients is pulmonary artery stenosis. SV patients are most likely to be complicated with patent ductus arteriosus. DSCT is more advantageous than TTE for diagnosing combined extracardiac malformations and can accurately measure the diameter of arteriovenous vessels. KW - Single atrium; single ventricle; computed tomography; congenital heart disease DO - 10.32604/chd.2022.020401