Prenatal diagnosis of vascular ring: evaluation of fetal diagnosis and postnatal outcomes
Autor: | K Papneja, W Mawad, Shi-Joon Yoo, E Jaeggi, S Aly |
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Rok vydání: | 2021 |
Předmět: |
Down syndrome
medicine.medical_specialty Fetus Double aortic arch business.industry Obstetrics Vascular ring Gestational age Prenatal diagnosis General Medicine Prenatal care medicine.disease medicine.anatomical_structure Ductus arteriosus medicine Radiology Nuclear Medicine and imaging Cardiology and Cardiovascular Medicine business |
Zdroj: | European Heart Journal - Cardiovascular Imaging. 22 |
ISSN: | 2047-2412 2047-2404 |
Popis: | Funding Acknowledgements Type of funding sources: None. Background The performance of fetal echocardiogram in diagnosing vascular ring (VR) and its impact on postnatal outcomes has not been well examined. Methods We reviewed all patients with VR diagnosis from 2000-2020. Results 50 patients with antenatal diagnosis of VR; 42(84%) with right aortic arch aberrant left subclavian artery and left-sided ductus arteriosus ((RAA-ALS) and 8(16%) with double aortic arch (DAA) were compared to 120 patients with postnatal diagnosis; 90(75%) with DAA, 22(18%) with RAA-ALS (Table 1). Prenatal diagnosis of VR increased over study period; 4 vs 31, 10 vs 29, 14 vs 25, 22 vs 35 between 2000-2005, 2005-2010, 2010-2015, and 2015-2020 respectively, p< 0.01. Prenatal diagnosis of VR was associated with less symptoms [26(52%) vs 72(60%), p Conclusion Prenatal diagnosis of VR has evolved over time. RAA-ALS versus DAA were dominant in the prenatally and postnatally diagnosed cohorts respectively. Prenatal diagnosis of VR was associated less symptoms, less cross-sectional imaging, earlier age of surgical intervention and less residual symptoms. Table 1 Prenatal Diagnosis (N = 50) Postnatal Diagnosis (N = 120) p-value Gestational Age (weeks) 39 ± 3 38 ± 2 0.9 Male (%) 31 (62%) 69(58%) 0.8 Subtype of vascular ring: Double aortic arch RAA-ALSA Others 8 (16%) 42 (80 %) 0 (0 %) 90 (72%) 22 (17%) 8 (11%) 0.002 0.01 Associated intracardiac CHD: VSD TOF DORV AVSD Coarctation of aorta Others 11 (22%) 1 1 3 0 3 3 24 (20%) 5 7 2 2 3 5 0.8 Associated genetic diagnosis: 22q11 deletion Trisomy 21 Others 9 (18%) 6 3 0 32 (26%) 29 3 0 0.1 Symptomatic presentation: Respiratory Gastrointestinal 26 (52 %) 15 11 72 (60 %) 57 15 |
Databáze: | OpenAIRE |
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