High incidence of ductal closure or narrowing at birth in patients with right ventricular outflow tract obstruction with normal orientation of the ductus arteriosus

2018 ◽  
Vol 29 (1) ◽  
pp. 54-58
Author(s):  
Hazumu Nagata ◽  
Eiko Terashi ◽  
Mamoru Muraoka ◽  
Kiyoshi Uike ◽  
Yuichiro Hirata ◽  
...  

AbstractBackgroundDuctal patency is mandatory to manage patients with ductal-dependent pulmonary circulation. The aim of this study is to elucidate the morphological and haemodynamic features of ductus arteriosus with right ventricular outflow tract obstruction, and investigate the appropriate perinatal management.Patients and methodsPatients with prenatal diagnosis of right ventricular outflow tract obstruction at our institution between 2010 and 2015 were included in the study. Reverse orientation of the ductus arteriosus is defined as an inferior angle of <90° at the aortic junction, and normal orientation of the ductus arteriosus as an angle of >90°. We retrospectively reviewed the shape and flow pattern of ductus arteriosus and the clinical characteristics of the cases.ResultsA total of 39 patients were enrolled. The shape was divided into normal orientation (n=15) and reverse orientation (n=24) of the ductus arteriosus. There was no significant difference in the type of oxygen saturation at birth and age at shunt operation between both the groups. However, the median narrowest diameter of ductus arteriosus in the normal orientation group was significantly smaller than that in the reverse orientation group (2.0 [1.0–5.4] versus 3.0 [1.3–4.4] mm, p<0.05). In two patients of the normal orientation group, ductus arteriosus had closed at birth, and one of whom died because of severe cyanosis.ConclusionsNormal orientation pattern might have high incidence of an early narrowing or closure of ductus arteriosus at birth. The critical patients need careful evaluation by repeated foetal echocardiography and further maternal interventions.

Circulation ◽  
1980 ◽  
Vol 62 (4) ◽  
pp. 818-822 ◽  
Author(s):  
M A Santos ◽  
J N Moll ◽  
C Drumond ◽  
W B Araujo ◽  
N Romao ◽  
...  

2020 ◽  
Vol 65 (No. 7) ◽  
pp. 320-326
Author(s):  
S Park ◽  
MJC Ang ◽  
MD Kittleson ◽  
KO Cho ◽  
J Choi

In this study we describe the echocardiographic features of a complex cardiac defect with a right to left shunt through tetralogy of Fallot and also a left to right shunt through a patent ductus arteriosus (PDA) in a 3-year-old dog. The echocardiography revealed a tetralogy of Fallot with a severely hypertrophied right ventricular outflow tract (RVOT), and a left to right shunting PDA. A contrast echocardiogram showed microbubbles moving from the right ventricle to the aorta through the ventricular septal defect. They then reached the main pulmonary artery through the PDA rather than through the RVOT. The necropsy confirmed tetralogy of Fallot with an RVOT obstruction and a PDA. This patient could have maintained the pulmonary circulation through the PDA in the spite of the right ventricular outflow tract obstruction and survive a long period. Not only the echocardiography, but also the contrast echocardiogram using agitated saline and trans-sectional images in CT enhanced the comprehensive understanding of the anatomic defects in this complex cardiac defect.


2021 ◽  
pp. 1-4
Author(s):  
Baher M. Hanna ◽  
Wesam E. El-Mozy ◽  
Sonia A. El-Saiedi

Abstract Isolated sub-pulmonary membrane is a rare condition, the origin of which has been debatable. Transcatheter treatment of pulmonary valve atresia with intact interventricular septum by radiofrequency perforation and balloon dilatation to restore biventricular circulation is gaining more popularity, with improving results over time. We report in our experience of 79 cases in 10 years the development of a sub-pulmonary membrane in 4 cases: causing significant obstruction requiring surgical excision in one case that revealed a fibrous membrane on pathology; causing mild right ventricular outflow tract obstruction in another and not yet causing obstruction in 2. On cardiac MRI, the right ventricular outflow tract and the right ventricular outflow tract/pulmonary atresia angle showed no morphological abnormalities.


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