Your browser doesn't support javascript.
loading
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.
Afiliação
  • Yu J; Department of Cardiovascular and Thoracis Surgery, The First Affiliated Hospital of Gannan Medical University, Ganzhou, China.
  • Liu K; Department of Cardiovascular and Thoracis Surgery, The First Affiliated Hospital of Gannan Medical University, Ganzhou, China.
  • Xu W; Department of Cardiovascular and Thoracis Surgery, The First Affiliated Hospital of Gannan Medical University, Ganzhou, China.
  • Xiong J; Department of Cardiovascular and Thoracis Surgery, The First Affiliated Hospital of Gannan Medical University, Ganzhou, China.
  • Zhong X; Department of Cardiovascular and Thoracis Surgery, The First Affiliated Hospital of Gannan Medical University, Ganzhou, China.
  • Hu S; Department of Cardiovascular and Thoracis Surgery, The First Affiliated Hospital of Gannan Medical University, Ganzhou, China.
  • Li W; Department of Cardiovascular and Thoracis Surgery, The First Affiliated Hospital of Gannan Medical University, Ganzhou, China.
Transl Pediatr ; 10(11): 3068-3074, 2021 Nov.
Article em En | MEDLINE | ID: mdl-34976772
ABSTRACT

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.
Palavras-chave

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Diagnostic_studies Idioma: En Revista: Transl Pediatr Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Diagnostic_studies Idioma: En Revista: Transl Pediatr Ano de publicação: 2021 Tipo de documento: Article