Prenatal Diagnosis of Isolated Right Aortic Arch: A Collaborative Approach to Management of Postnatal Aerodigestive Symptoms
Jonathan N. Flyer, Kelly J. Knight, Erika M. Edwards, Caitlin S. Haxel, Thomas Lahiri

TL;DR
This study explores how to best manage infants diagnosed with a specific heart condition before birth, focusing on whether surgery or medical care is more effective.
Contribution
The study introduces a collaborative cardiopulmonary approach for managing postnatal symptoms in infants with prenatally diagnosed isolated right aortic arch.
Findings
Most infants with isolated right aortic arch managed medically showed no or intermittent symptoms.
Surgical referral was associated with specific combinations of digestive and respiratory symptoms.
Weight outcomes were similar between medically and surgically managed infants.
Abstract
Although prenatal imaging advancements have increased isolated right aortic arch (iRAA) detection, optimal postnatal vascular ring management remains uncertain. Whereas early postnatal imaging and surgical management may be clinically warranted for some infants, long‐term data are not yet available to justify an identical approach for all prenatal iRAA diagnoses. Children with prenatally diagnosed iRAA and left ductus arteriosus were included in a retrospective cohort study at a rural academic center. Fetal echocardiograms (2014–2024) were reviewed to exclude complex congenital heart disease. Joint postnatal cardiopulmonary care was standardized. Clinical data were ascertained using aerodigestive symptom checklists. Fisher's exact test was used to examine associations between symptoms and surgical referral. Growth was assessed by z‐score rates of change from birth weight until last…
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Taxonomy
TopicsTracheal and airway disorders · Congenital Heart Disease Studies · Cardiovascular Conditions and Treatments
