Pulmonary Artery Development Over Time in Severe Ebstein Anomaly

• Published in: Pediatric cardiology Vol. 43; no. 7; pp. 1653 - 1658
• Main Authors: Shirozu, Hiromitsu, Kodama, Yoshihiko, Kuraoka, Ayako, Ishikawa, Yuichi, Nakano, Toshihide, Kado, Hideaki, Sagawa, Koichi
• Format: Journal Article
• Language: English
• Published: New York Springer US 01-10-2022
• Subjects: Cardiac Surgery; Cardiology; Medicine; Medicine & Public Health; Original Article; Vascular Surgery; Starnes procedure; Pulmonary artery development; Ebstein anomaly
• ISSN: 0172-0643; 1432-1971
• DOI: 10.1007/s00246-022-02898-w

Recently, the outcome of severe Ebstein anomaly (EA) has improved with the prevalence of the Starnes procedure. However, time-dependent changes in the size of the central pulmonary artery (PA) have not been fully understood. A retrospective chart review of patients with EA who underwent the Starnes procedure during the neonatal period and those with pulmonary atresia with intact ventricular septum (PAIVS) was performed at Fukuoka Children’s Hospital. There were 14 patients in the severe EA group and 36 in the PAIVS group, with mean observational periods of 3.8 and 4.2 years, respectively. No significant difference in survival was observed between the groups. However, the mean size of the central PA was smaller in the severe EA group at each surgical stage (after systemic-to-pulmonary shunt, after the bidirectional Glenn procedure, and after the Fontan procedure). A significantly larger ventricular volume was observed in the severe EA group after the Fontan procedure. The growth of the central PA was poor in patients with severe EA. Patients with severe EA should be carefully monitored in this regard both before and after undergoing the Fontan procedure. Further studies regarding long-term prognosis are expected.