The prenatal diagnosis and prognosis of fetal right aortic arch and double aortic arch malformation: A single‐center study

Abstract

AbstractAimThis study aimed to characterize the pathological types, diagnosis, chromosomal abnormalities, and postnatal clinical manifestations of right and double aortic arch malformations in fetuses.MethodsIn this retrospective study, all fetuses diagnosed with right or double aortic arch anomalies for whom conventional two‐dimensional echocardiography combined with spatio‐temporal image correlation was performed at our tertiary referral center between December 2012 and December 2021 were included.ResultsIn total, 234 fetuses with aortic arch abnormalities were identified. Forty‐one cases lost to follow‐up. One hundred ninety‐three cases were included in this study. One hundred eighty‐seven cases with right aortic arch. Six cases with double aortic arch. Most cases of right aortic arch with aberrant left subclavian artery (77/101, 76.2%) were isolated lesions, whereas most of those with mirror‐image branching (45/75, 60%) were associated with intracardiac or extracardiac anomalies. Chromosomal abnormalities were screened prenatally in 113 fetuses with right aortic arch, among whom three with aberrant left subclavian artery (3/63, 4.8%) and eight with mirror‐image branching (8/50, 16%) had chromosome anomalies (p < 0.05). Furthermore, three cases had microdeletion 22q11.2 and these were significantly associated with intracardiac malformations.ConclusionsMost cases of isolated right aortic arch do not present with clinical symptoms except isolated left subclavian artery and isolated left brachiocephalic trunk. In addition, the risk of chromosomal abnormalities in patients with isolated right aortic arch is very low. We recommend that pregnant women should be informed of the risks and benefits of undergoing invasive prenatal chromosomal detection.