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Erschienen in: Pediatric Cardiology 8/2014

01.12.2014 | Images in Pediatric Cardiology

Hepatic Vein to Atrial Fistula: Rare Cause of Cyanosis in a Post-operative Case of Fontan Surgery

verfasst von: Gaurav Garg, Himanshu Tyagi, Gaurav Agrawal, Anil Sivadasan Radha

Erschienen in: Pediatric Cardiology | Ausgabe 8/2014

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Excerpt

This is regarding a 10-year-old boy with a diagnosis of common atrium, single ventricle, common atrio ventricular (AV) canal, severe pulmonary stenosis, no AV valve regurgitation, and good biventricular function. He underwent bidirectional Glenn shunt with MPA ligation at age of 1 year in 2005. In July 2011, extra cardiac fenestrated Fontan operation was done. His saturation after surgery was 92 % on room air and child was doing well after 3 months follow up. He did not come for follow-up for 2 years. After 2 years, he came to us with dyspnoea on exertion and room air saturation of 70 %. After detailed evaluation, we found that his lungs were fairly normal with good sized branch pulmonary arteries (PA), cardiac function was good, and there was no AV valve regurgitation and no signs of Fontan failure. Confused about the cause of cyanosis, we took the patient for cardiac catheterization. We found that Fontan circuit (Fig. 1) was flowing well with no decompressing veins. Mean PA pressure was 12 mm Hg. We decided to balloon occlude the fenestration (Fig. 2), but there was only 2 % increase in saturation with no effect on PA pressures. So, it was concluded that fenestaration was not the cause of this severe cyanosis.
Metadaten
Titel
Hepatic Vein to Atrial Fistula: Rare Cause of Cyanosis in a Post-operative Case of Fontan Surgery
verfasst von
Gaurav Garg
Himanshu Tyagi
Gaurav Agrawal
Anil Sivadasan Radha
Publikationsdatum
01.12.2014
Verlag
Springer US
Erschienen in
Pediatric Cardiology / Ausgabe 8/2014
Print ISSN: 0172-0643
Elektronische ISSN: 1432-1971
DOI
https://doi.org/10.1007/s00246-014-1025-0

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