Abstract

Objectives. Total anomalous pulmonary venous connection (TAPVC) is a rare congenital heart disease. This study aimed to evaluate the outcomes of TAPVC repair in neonates, controlling for anatomic subtypes and surgical techniques. Methods. Between 1997 and 2013, 88 patients (median age: 16 days) underwent repair for supracardiac (31), cardiac (18), infracardiac (36), or mixed (3) TAPVC. All the patients underwent emergency operation due to obstructed drainage. Supracardiac and infracardiac TAPVC repair included a side-to-side anastomosis between the pulmonary venous confluence and left atrium. Coronary sinus unroofing was preferred for cardiac TAPVC repair. Results. The early mortality rate was 2.3% (2/88 patients). The echocardiogram showed no obstruction in the pulmonary vein anastomosis, and flow rate was 1.1–1.42 m/s in the 3-year follow-up period. Conclusions. The accurate preoperative diagnosis, improved protection of heart function, use of pulmonary vein tissue to anastomose and avoid damage of the pulmonary vein, and delayed sternum closure can reduce the risk of mortality. The preoperative severity of pulmonary vein obstruction, the timing of the emergency operation, and infracardiac or mixed-type TAPVC can affect prognosis. Using our surgical technique, the TAPVC mortality among our patients was gradually reduced with remarkable results. However, careful monitoring of the patient with pulmonary vein restenosis and the timing and method of reoperation should also be given importance.

Highlights

  • Total anomalous pulmonary venous connection (TAPVC) is a rare congenital heart disease, accounting for only approximately 2% of congenital heart diseases

  • The current remarkable results of TAPVC repair reflect the general improvements in preoperative diagnostic techniques, intraoperative techniques, and postoperative management strategies that have occurred over the last decade [1]

  • 2 patients (2.9%) with infracardiac TAPVC died after the operation because of low cardiac output syndrome and bleeding, respectively

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Summary

Introduction

Total anomalous pulmonary venous connection (TAPVC) is a rare congenital heart disease, accounting for only approximately 2% of congenital heart diseases. The current remarkable results of TAPVC repair reflect the general improvements in preoperative diagnostic techniques, intraoperative techniques, and postoperative management strategies that have occurred over the last decade [1]. Symptoms of TAPVC occur early among infants, often causing deaths within 1 month after birth. Infants should undergo emergency surgical correction within the first month of life [2]. The aim of this study was to review and summarize the outcomes of emergency surgery for TAPVC and evaluate the postoperative risk factors

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