Postnatal Outcomes in Prenatally Detected Vascular Rings.

IF 1.5 4区 医学 Q3 CARDIAC & CARDIOVASCULAR SYSTEMS
Nikkan Das, Havisha Pedamallu, Kristen Young, Laura H Rosenthal, Taher Valika, Andrada R Popescu, Allison B Davila, Osama M Eltayeb, Stefani M Samples, Michael R Carr, Angira Patel, Sheetal R Patel
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Abstract

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.

产前检测血管环的产后结局。
血管环是一种罕见的先天性缺陷,可引起气管和/或食管压迫。由于筛查和胎儿超声心动图的进步,产前检测正在增加。产后结果仍然是可变的。我们描述了我们在产前检测血管环的产后结局的单中心经验,并评估了与手术相关的因素。我们对2016年至2023年间评估的所有胎儿诊断的可能血管环进行了回顾性回顾。有明显心内异常、没有产后资料或没有确诊的产后诊断的患者被排除在产后分析之外。结果变量包括症状、气管/食管压迫和手术修复。产前队列包括109例右主动脉弓(RAA)占80%,双主动脉弓(DAA)占20%。在72名出生后队列患者中,85%的患者在中位年龄为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 mSv。在CTA上,69%有憩室。在RAA患者中,95%的患者有左锁骨下异常。大多数(79%)患者在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%是由于症状。在单因素分析中,DAA与CTA上的气道异常和手术修复有关。在30个月的随访中,99%的患者仍无症状。产前血管环的诊断与气道异常的高发率相关,即使在没有症状的情况下也是如此。对于无症状的DAA和气道异常患者,我们都进行了手术修复。由于DAA与气道异常有关,这些患者可能需要密切监测未来症状的发展。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Pediatric Cardiology
Pediatric Cardiology 医学-小儿科
CiteScore
3.30
自引率
6.20%
发文量
258
审稿时长
12 months
期刊介绍: The editor of Pediatric Cardiology welcomes original manuscripts concerning all aspects of heart disease in infants, children, and adolescents, including embryology and anatomy, physiology and pharmacology, biochemistry, pathology, genetics, radiology, clinical aspects, investigative cardiology, electrophysiology and echocardiography, and cardiac surgery. Articles which may include original articles, review articles, letters to the editor etc., must be written in English and must be submitted solely to Pediatric Cardiology.
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