| Literature DB >> 29515081 |
Hiroo Kinami1, Kiyozo Morita1, Yoshihiro Ko1, Gen Shinohara1, Kazuhiro Hashimoto1.
Abstract
Neonatal primary repair of tetralogy of Fallot (TOF) with absent pulmonary valve (APV) syndrome is associated with high mortality rates. Our plan involves a staged repair that avoids one-stage intracardiac repair (ICR), with a first palliation that closes the main pulmonary orifice using an expanded polytetrafluoroethylene (ePTFE) patch, pulmonary arterioplication, and an adjustable Blalock-Taussig (BT) shunt. This strategy was used for a neonatal case with TOF/APV syndrome with hypoplastic left ventricle (LV). There was evidence of subsequent progressive increase in the LV size, and bronchial compression was relieved and an ICR was performed successfully at 9 months of age.Entities:
Keywords: neonatal palliation; small left ventricle; tetralogy of Fallot with absent pulmonary valve syndrome
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Year: 2018 PMID: 29515081 PMCID: PMC6823175 DOI: 10.5761/atcs.cr.17-00085
Source DB: PubMed Journal: Ann Thorac Cardiovasc Surg ISSN: 1341-1098 Impact factor: 1.520