Association of right aortic arch and agenesis of ductus arteriosus in prenatal tetralogy of Fallot spectrum and its clinical implications

Author:

Walter Adeline1,Herberg Ulrike2,Calite Elina1,Geipel Annegret1,Recker Florian1ORCID,Strizek Brigitte1,Berg Christoph13,Gembruch Ulrich1

Affiliation:

1. Department of Obstetrics and Prenatal Medicine University Hospital Bonn Bonn Germany

2. Department of Pediatric Cardiology University Hospital RWTH Aachen Aachen Germany

3. Division of Prenatal Medicine Gynecological Ultrasound and Fetal Surgery Department of Obstetrics and Gynecology University of Cologne Cologne Germany

Abstract

AbstractObjectiveIn our center, we observed an increased frequency of right aortic arch (RAA) with an agenesis of the ductus arteriosus (ADA) in prenatally diagnosed tetralogy of Fallot (ToF) and its variations. This study aimed to determine whether there is an association of RAA and ADA in fetuses with ToF. Distribution of genetic anomalies and impact on postnatal outcome were further evaluated.MethodSingle‐center retrospective observational study including pregnancies with prenatal diagnosis of ToF from 2010 to 2023. All cases were subdivided into ToF with pulmonary stenosis (PS) and pulmonary atresia (PA). Clinical and echocardiographic databases were reviewed for pregnancy outcome, genetic anomalies, and postnatal course.ResultsThe cohort included 169 cases, 124 (73.4%) with ToF/PS and 45(26.6%) with ToF/PA. Agenesis of the ductus arteriosus was significantly associated with RAA in both subtypes of ToF (p = 0.001) compared to left aortic arch and found in 82.5% (33/40) versus 10.7% (9/84) of fetuses with ToF/PS and in 57.1% (8/14) versus 12.9% (4/31) of fetuses with ToF/PA. In both ToF/PS and ToF/PA, RAA/ADA versus RAA/patent DA revealed a significantly higher risk for the presence of genetic abnormalities, especially microdeletion 22q11.2, major aorto‐pulmonary collateral arteries and a shorter time to complete surgical repair.ConclusionWe demonstrated a significantly increased frequency of RAA/ADA in patients with prenatally diagnosed ToF. Although this association revealed no significant impact on overall survival, the prenatal detection of RAA/ADA has implications for counseling, genetic evaluation and postnatal management.

Publisher

Wiley

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