Outcome of Systemic-to-Pulmonary Shunts in Cyanotic Congenital Heart Disease- A 9-year Experience

The aim of this study is to evaluate early and late results of surgery in children with congenital heart disease and decreased pulmonary blood flow, who underwent a palliative systemic-to-pulmonary shunt. during the past 9 years, 157 systemic-to-pulmonary artery shunts were performed in 130 patients (69 males, 61 females) with ages from 1 day to 31 years old. they had been evaluated for their clinical effectiveness, the need for a repeat operation and the mortality and morbidity. there were 101 (77.7%) modified blalock- tausig (bt) shunts, 19 (14.6%) modified waterston shunts, 8 (6.2%) central shunts, 1 waterston shunt, and 1 glenn shunt created throughout the study. tetralogy of fallot comprised the majority of cases (113; 86.9%) while the remaining 17 (13.1%) included transposition of the great arteries with pulmonary stenosis, tricuspid atresia, pulmonary atresia, atrioventricular septal defect (canal) with pulmonary stenosis, and univentricular heart complex. early mortality was 12.3% (16 patients). second shunts were created in 25 (19.2%) patients. forty patients (30.8%) have undergone subsequent intracardiac repair 37.7 ± 17.8 months after original shunt procedure. there were four (3%) late deaths. follow-up was achieved in 105 of 114 early survivors for a period of 3 to 117 months (mean 31.7 ± 19.4 months). modified bt shunt was performed most frequently in our service; it was associated with less closure and mortality than other types of shunt and had excellent clinical palliation and patency rates.