Abstract
Pulmonary atresia with restrictive ventricular septal defect is a rare congenital cardiac anomaly. A Blalock-Taussig shunt and surgical perforation of the atretic pulmonary valve is often performed as the initial palliation. We present our experience of utilizing both transesophageal and epicardial echocardiography during surgical pulmonary valvuloplasty in a 22-day-old neonate with pulmonary atresia with restrictive ventricular septal defect. The atretic pulmonary valve was perforated using a sheath introduced through the pulmonary artery.
Keywords:
Heart septal defects; heart ventricles; infant; newborn; pulmonary atresia; pulmonary valve; tricuspid valve; ventricular.
© The Author(s) 2014.
Publication types
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Case Reports
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Video-Audio Media
MeSH terms
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Abnormalities, Multiple*
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Balloon Valvuloplasty*
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Coronary Circulation
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Echocardiography, Doppler, Color
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Echocardiography, Transesophageal
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Heart Septal Defects / diagnosis
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Heart Septal Defects / physiopathology
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Heart Septal Defects / therapy*
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Humans
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Infant, Newborn
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Male
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Pulmonary Artery / abnormalities*
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Pulmonary Artery / diagnostic imaging
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Pulmonary Artery / physiopathology
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Pulmonary Atresia / diagnosis
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Pulmonary Atresia / physiopathology
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Pulmonary Atresia / therapy*
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Pulmonary Circulation
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Pulmonary Valve / abnormalities*
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Pulmonary Valve / diagnostic imaging
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Pulmonary Valve / physiopathology
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Punctures
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Treatment Outcome
Supplementary concepts
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Pulmonary Atresia With Ventricular Septal Defect