Das Nikkan, Pedamallu Havisha, Young Kristen, Rosenthal Laura H, Valika Taher, Popescu Andrada R, Davila Allison B, Eltayeb Osama M, Samples Stefani M, Carr Michael R, Patel Angira, Patel Sheetal R
Division of Pediatric Cardiology, Ann and Robert H. Lurie Children's Hospital of Chicago, Chicago, IL, USA.
Feinberg School of Medicine, Northwestern University, Chicago, IL, USA.
Pediatr Cardiol. 2025 Feb 24. doi: 10.1007/s00246-025-03803-x.
Vascular rings are rare congenital defects that can cause tracheal and/or esophageal compression. Prenatal detection is increasing due to advances in screening and fetal echocardiography. Postnatal outcomes remain variable. We describe our single-center experience of postnatal outcomes in prenatally detected vascular rings and evaluate factors associated with surgery. We performed a retrospective review of all fetal diagnoses of possible vascular ring evaluated between 2016 and 2023. Patients with significant intracardiac abnormalities, without postnatal data, or without confirmed postnatal diagnosis were excluded from postnatal analysis. Outcome variables included symptoms, tracheal/esophageal compression, and surgical repair. The prenatal cohort included 109 patients with 80% right aortic arch (RAA) and 20% double aortic arch (DAA). Of 72 patients in the postnatal cohort, 85% underwent computed tomography angiography (CTA) at median age of 2 months with 0.84 ± 0.34 mSv of radiation. On CTA, 69% had a diverticulum. Of those with RAA, 95% had an aberrant left subclavian. Most (79%) had airway abnormalities on CTA. Fifteen (21%) developed symptoms at median age of 5 months. Fifty-eight percent of patients underwent surgery at median age of 10 months, of which 33% were due to symptoms. On univariate analysis, DAA was associated with airway abnormalities on CTA and surgical repair. At 30-month follow up, 99% of patients remained asymptomatic. Prenatal diagnosis of vascular rings is associated with high rates of airway abnormalities, even in those without symptoms. Surgical repair was pursued in asymptomatic patients with DAA and airway abnormalities in our institution. As DAA is associated with airway abnormalities, these patients may require closer monitoring for future symptom development.
血管环是一种罕见的先天性缺陷,可导致气管和/或食管受压。由于筛查和胎儿超声心动图技术的进步,产前检测率正在上升。产后结局仍存在差异。我们描述了我们单中心对产前检测出的血管环的产后结局的经验,并评估了与手术相关的因素。我们对2016年至2023年间评估的所有可能血管环的胎儿诊断进行了回顾性研究。有严重心脏内异常、无产后数据或未确诊产后诊断的患者被排除在产后分析之外。结局变量包括症状、气管/食管受压情况和手术修复情况。产前队列包括109例患者,其中80%为右位主动脉弓(RAA),20%为双主动脉弓(DAA)。产后队列中的72例患者中,85%在中位年龄2个月时接受了计算机断层血管造影(CTA),辐射剂量为0.84±0.34毫希沃特。在CTA上,69%有憩室。在RAA患者中,95%有迷走左锁骨下动脉。大多数(79%)在CTA上有气道异常。15例(21%)在中位年龄5个月时出现症状。58%的患者在中位年龄10个月时接受了手术,其中33%是因为症状。单因素分析显示,DAA与CTA上的气道异常和手术修复相关。在30个月的随访中,99%的患者仍无症状。血管环的产前诊断与气道异常的高发生率相关,即使是无症状的患者。在我们机构,对于无症状的DAA和气道异常患者进行了手术修复。由于DAA与气道异常相关,这些患者可能需要更密切的监测以观察未来症状的发展。