Repair of Total Anomalous Pulmonary Venous Connection in Early Infancy

2003 ◽  
Vol 11 (1) ◽  
pp. 18-22 ◽  
Author(s):  
Anil Kumar Dharmapuram ◽  
Raghavan Nair Suresh Kumar ◽  
Pantula Narasinga Rao ◽  
Hassan Mohamed Mahmoud ◽  
Sushil Chandran ◽  
...  

From May 1995 through October 2001, 19 infants less than 90 days old underwent surgical correction of total anomalous pulmonary venous connection. In 15 babies with isolated total anomalous pulmonary venous connection, there was one operative death. In 4 with complex anomalies, there were 2 operative deaths. The vertical vein was not ligated in 6 cases for various reasons. Two patients died during reoperation for early pulmonary venous obstruction. In the late follow-up, 2 babies required reoperation for late anastomotic stricture; one needed additional balloon dilatation. Of the 14 surviving patients, one had a small residual gradient and infrequent supraventricular tachycardia, the others were asymptomatic and without gradients. Surgical correction of total anomalous pulmonary venous connection can be carried out in early infancy with low mortality and morbidity. However, associated complex cardiac anomalies and small caliber pulmonary arteries and veins carry higher risks. Recurrent pulmonary venous obstruction and diffuse pulmonary vein stenosis are causes of early reoperation and poor surgical outcome.

2001 ◽  
Vol 122 (3) ◽  
pp. 615-617 ◽  
Author(s):  
Raghavan Nair Suresh Kumar ◽  
Anil Kumar Dharmapuram ◽  
Ivatury M. Rao ◽  
Venkitachalam C. Gopalakrishnan ◽  
Velayudhan Ramakrishna Pillai ◽  
...  

2021 ◽  
Vol 16 (1) ◽  
Author(s):  
Takahiro Ito ◽  
Ikuo Hagino ◽  
Mitsuru Aoki ◽  
Kentaro Umezu ◽  
Tomohiro Saito ◽  
...  

Abstract Background Total anomalous pulmonary venous connection accompanied by unilateral lung agenesis and Goldenhar syndrome is extremely rare. Case presentation We present a case of total anomalous pulmonary venous connection accompanied by unilateral lung agenesis and Goldenhar syndrome in a patient who was diagnosed based on transthoracic echocardiography and computed tomography. We observed complete absence of the lung, the bronchial tree, and vascular structures on the right side, with abnormal drainage of the left pulmonary veins into the innominate vein. The patient showed clear clinical evidence of pulmonary venous obstruction and underwent surgery 3 days after birth. The pulmonary venous chamber containing the vertical vein was anastomosed to the left atrium using 7–0 PDS running sutures via a median sternotomy. Echocardiography and computed tomography performed 1 year postoperatively revealed no pulmonary venous obstruction. Conclusion We report a rare case of total anomalous pulmonary venous connection accompanied by unilateral lung agenesis and Goldenhar syndrome, which was successfully repaired 3 days after birth. A median sternotomy is a safe and effective approach for surgical repair of congenital heart disease with unilateral lung agenesis. Repair of the supra cardiac total anomalous pulmonary connection using the vertical vein is feasible in patients with a small pulmonary venous chamber.


Circulation ◽  
1962 ◽  
Vol 25 (6) ◽  
pp. 916-928 ◽  
Author(s):  
ALOIS R. HASTREITER ◽  
MILTON H. PAUL ◽  
MARIAN E. MOLTHAN ◽  
ROBERT A. MILLER

ESC CardioMed ◽  
2018 ◽  
pp. 831-834
Author(s):  
Marietta Charakida ◽  
John Deanfield

Total anomalous pulmonary venous connection is repaired in childhood and the long-term results are usually excellent. Recent surgical advances have reduced further the rate of recurrent pulmonary venous obstruction.


1998 ◽  
Vol 46 (11) ◽  
pp. 1126-1132
Author(s):  
Katsunori Yoshihara ◽  
Tsukasa Ozawa ◽  
Hiroshi Sakuragawa ◽  
Takeshirou Fujii ◽  
Noritsugu Shiono ◽  
...  

2020 ◽  
pp. 1-3
Author(s):  
Yuki Kawasaki ◽  
John N. Dentel ◽  
Henry L. Walters ◽  
James M. Galas ◽  
Daisuke Kobayashi

Abstract Total anomalous pulmonary venous connection is a rare congenital heart defect. We report an infant with a mixed form of supracardiac TAPVC, in whom all pulmonary veins, except the right upper, entered a pulmonary venous confluence that is connected to a vertical vein and drained into the superior vena caval–right atrial junction. Several segmental right upper pulmonary veins entered the superior vena cava, superior to the entry of the vertical vein. Surgical repair consisted of the Warden procedure combined with direct anastomosis of the vertical vein to the left atrium. Separate pulmonary venous drainage pathways decreased the risk of post-operative pulmonary venous obstruction. Our patient had an uneventful post-operative course and encouraging 2-month follow-up echocardiography. Careful follow-up is warranted to detect post-operative complications, including obstruction of the pulmonary venous and cavoatrial anastomoses.


2012 ◽  
Vol 94 (3) ◽  
pp. 825-832 ◽  
Author(s):  
S. Adil Husain ◽  
Elaine Maldonado ◽  
Debbie Rasch ◽  
Joel Michalek ◽  
Richard Taylor ◽  
...  

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