Journal article

Fetal and Neonatal Diagnosis of Interrupted Aortic Arch: Associations and Outcomes


Authors listAxt-Fliedner, Roland; Kawecki, Andrea; Enzensberger, Christian; Wienhard, Julia; Degenhardt, Jan; Schranz, Dietmar; Vogel, Melanie

Publication year2011

Pages299-305

JournalFetal Diagnosis and Therapy

Volume number30

Issue number4

ISSN1015-3837

DOI Linkhttps://doi.org/10.1159/000332982

PublisherKarger Publishers


Abstract
Objective: Interrupted aortic arch (IAA) is a rare but serious anomaly. Prenatal diagnosis is challenging and published data are limited. The aim of the study was to review the data of fetuses and neonates diagnosed with IAA during a 16-year period at Children's Hospital Giessen. Methods: Retrospective ascertainment of 8 fetuses and 20 neonates with a confirmed diagnosis of IAA from 1994 to 2010 by reviewing the hospital database of the cardiovascular program of the prenatal and pediatric cardiology clinics at the University Hospital Giessen. Results: Eighteen cases with IAA type B and 10 cases with IAA type A were found. After 2005, prenatal diagnosis was achieved in 8 cases and postnatal imaging confirmed IAA in all 8 neonates. Twenty-nine percent of individuals had a chromosomal anomaly, with microdeletion 22q11.2 being the most common abnormality (n = 6, 21%). In 46% (13/28) other complex cardiac anomalies were present. Mortality after surgery was 18%. Long-term morbidity and mortality was due to neurological impairment in the presence of microdeletion 22q11.2 and the need of surgical or catheter re-intervention. Conclusion: Despite the difficulties and challenges in diagnosis, the prenatal detection rate of IAA is increasing. Associated complex cardiac and chromosomal abnormalities influence the outcome of patients with IAA and are important issues of parental counseling. Copyright (C) 2011 S. Karger AG, Basel



Citation Styles

Harvard Citation styleAxt-Fliedner, R., Kawecki, A., Enzensberger, C., Wienhard, J., Degenhardt, J., Schranz, D., et al. (2011) Fetal and Neonatal Diagnosis of Interrupted Aortic Arch: Associations and Outcomes, Fetal Diagnosis and Therapy, 30(4), pp. 299-305. https://doi.org/10.1159/000332982

APA Citation styleAxt-Fliedner, R., Kawecki, A., Enzensberger, C., Wienhard, J., Degenhardt, J., Schranz, D., & Vogel, M. (2011). Fetal and Neonatal Diagnosis of Interrupted Aortic Arch: Associations and Outcomes. Fetal Diagnosis and Therapy. 30(4), 299-305. https://doi.org/10.1159/000332982



Keywords


22Q11ANOMALIEScongenital heart diseaseCONGENITAL HEART-DISEASEDIGEORGE-SYNDROMEInterrupted aortic archMicrodeletion 22q11.2prenatal diagnosisREPAIRTBX1

Last updated on 2025-21-05 at 18:42