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Prenatal ultrasound diagnosis and management of fetal aortopulmonary septal defects: a case series
BACKGROUND: To investigate the prenatal ultrasound diagnosis and management of patients with aortopulmonary septal defects (APSDs). METHODS: A total of 8 fetuses with APSDs who underwent fetal echocardiography at our hospital from January 2015 to January 2019 were retrospectively included in this st...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
AME Publishing Company
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8649606/ https://www.ncbi.nlm.nih.gov/pubmed/34976772 http://dx.doi.org/10.21037/tp-21-488 |
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author | Yu, Junjian Liu, Kang Xu, Weichang Xiong, Jianxian Zhong, Xuehong Hu, Shuo Li, Wentong |
author_facet | Yu, Junjian Liu, Kang Xu, Weichang Xiong, Jianxian Zhong, Xuehong Hu, Shuo Li, Wentong |
author_sort | Yu, Junjian |
collection | PubMed |
description | BACKGROUND: To investigate the prenatal ultrasound diagnosis and management of patients with aortopulmonary septal defects (APSDs). METHODS: A total of 8 fetuses with APSDs who underwent fetal echocardiography at our hospital from January 2015 to January 2019 were retrospectively included in this study. RESULTS: Among the 8 fetuses, there were 4 cases of type I APSD, 3 cases were type II, and 1 case was type III. Among the 8 cases, there were 2 cases of simple APSD. There were echocardiographic characteristics that were common to all 3 types of APSD. This included defects between the ascending aorta and the trunk of the pulmonary artery in the short-axis section of the aorta, and in the three vessels and the three-vessel trachea section. Furthermore, the “V”-shaped structure confluence point of all APSD cases was positioned more forward than normal in the three-vessel trachea section. Type I APSD can be better characterized by the cross-section of the double outflow tract of the aorta and the pulmonary artery, which is close to the aortic valve and pulmonary valve. Type II APSD can be clearly diagnosed by the short-axis view of the aorta. Since the defect between the aorta and the pulmonary artery is distant from the aortic valve and pulmonary valve, the defect does not involve the bifurcation of the pulmonary artery and may be associated with an ectopic origin of the right pulmonary artery. Type III APSD is similar to a permanent arterial trunk, and the space between the ascending aorta and the trunk of the pulmonary artery is completely missing. Color and pulse Doppler showed shunt flow in the defects. CONCLUSIONS: APSD can be diagnosed and classified by fetal echocardiography. This, together with the presence or absence of fetal intracardiac and extracardiac deformities, can provide valuable prenatal information to pregnant women and their families, which may facilitate timely diagnosis and timely surgical treatment after birth. |
format | Online Article Text |
id | pubmed-8649606 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | AME Publishing Company |
record_format | MEDLINE/PubMed |
spelling | pubmed-86496062021-12-30 Prenatal ultrasound diagnosis and management of fetal aortopulmonary septal defects: a case series Yu, Junjian Liu, Kang Xu, Weichang Xiong, Jianxian Zhong, Xuehong Hu, Shuo Li, Wentong Transl Pediatr Original Article BACKGROUND: To investigate the prenatal ultrasound diagnosis and management of patients with aortopulmonary septal defects (APSDs). METHODS: A total of 8 fetuses with APSDs who underwent fetal echocardiography at our hospital from January 2015 to January 2019 were retrospectively included in this study. RESULTS: Among the 8 fetuses, there were 4 cases of type I APSD, 3 cases were type II, and 1 case was type III. Among the 8 cases, there were 2 cases of simple APSD. There were echocardiographic characteristics that were common to all 3 types of APSD. This included defects between the ascending aorta and the trunk of the pulmonary artery in the short-axis section of the aorta, and in the three vessels and the three-vessel trachea section. Furthermore, the “V”-shaped structure confluence point of all APSD cases was positioned more forward than normal in the three-vessel trachea section. Type I APSD can be better characterized by the cross-section of the double outflow tract of the aorta and the pulmonary artery, which is close to the aortic valve and pulmonary valve. Type II APSD can be clearly diagnosed by the short-axis view of the aorta. Since the defect between the aorta and the pulmonary artery is distant from the aortic valve and pulmonary valve, the defect does not involve the bifurcation of the pulmonary artery and may be associated with an ectopic origin of the right pulmonary artery. Type III APSD is similar to a permanent arterial trunk, and the space between the ascending aorta and the trunk of the pulmonary artery is completely missing. Color and pulse Doppler showed shunt flow in the defects. CONCLUSIONS: APSD can be diagnosed and classified by fetal echocardiography. This, together with the presence or absence of fetal intracardiac and extracardiac deformities, can provide valuable prenatal information to pregnant women and their families, which may facilitate timely diagnosis and timely surgical treatment after birth. AME Publishing Company 2021-11 /pmc/articles/PMC8649606/ /pubmed/34976772 http://dx.doi.org/10.21037/tp-21-488 Text en 2021 Translational Pediatrics. All rights reserved. https://creativecommons.org/licenses/by-nc-nd/4.0/Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) . |
spellingShingle | Original Article Yu, Junjian Liu, Kang Xu, Weichang Xiong, Jianxian Zhong, Xuehong Hu, Shuo Li, Wentong Prenatal ultrasound diagnosis and management of fetal aortopulmonary septal defects: a case series |
title | Prenatal ultrasound diagnosis and management of fetal aortopulmonary septal defects: a case series |
title_full | Prenatal ultrasound diagnosis and management of fetal aortopulmonary septal defects: a case series |
title_fullStr | Prenatal ultrasound diagnosis and management of fetal aortopulmonary septal defects: a case series |
title_full_unstemmed | Prenatal ultrasound diagnosis and management of fetal aortopulmonary septal defects: a case series |
title_short | Prenatal ultrasound diagnosis and management of fetal aortopulmonary septal defects: a case series |
title_sort | prenatal ultrasound diagnosis and management of fetal aortopulmonary septal defects: a case series |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8649606/ https://www.ncbi.nlm.nih.gov/pubmed/34976772 http://dx.doi.org/10.21037/tp-21-488 |
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