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Outcomes of repair of left partial anomalous pulmonary venous connection in children.

作者信息

Naimo Phillip S, d'Udekem Yves, Brizard Christian P, Konstantinov Igor E

机构信息

Royal Children's Hospital, Melbourne, Australia University of Melbourne, Melbourne, Australia.

Royal Children's Hospital, Melbourne, Australia University of Melbourne, Melbourne, Australia Murdoch Children's Research Institute, Melbourne, Australia.

出版信息

Interact Cardiovasc Thorac Surg. 2015 Aug;21(2):254-6. doi: 10.1093/icvts/ivv133. Epub 2015 May 16.

Abstract

Herein, we report a case series of patients who underwent repair of left partial anomalous pulmonary venous connection (L-PAPVC) via anastomosing the anomalous pulmonary vein (PV) to the left atrial appendage. Fifteen children underwent repair of L-PAPVC between 1980 and 2014. The median age at surgery was 3.6 years (range: 5 days to 17.2 years). Concomitant anomalies were present in 87% (13/15). There were no early deaths. There was 1 late death occurring 63 days following surgical repair due to pneumococcal septicaemia in a patient with prior atrial septal defect closure and Ehlers-Danlos syndrome. The overall survival rate was 93.7% at 15 years. A single patient (1/15, 7%) required reoperation 1 year after L-PAPVC repair for PV stenosis due to several thrombi located throughout the PV. The rate of freedom from PV reoperation was 90% at 10 years. The follow-up was 100% complete with a median time of 11 years (range: 52 days to 20 years). To our knowledge, this is the youngest cohort of patients who have undergone surgical repair of L-PAPVC. Repair of L-PAPVC in children can be achieved via anastomosis of the anomalous vessel to the left atrial (LA) with excellent outcomes. The rate of anastomotic stenosis at the site of implantation on the LA is low.

摘要

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