| Literature DB >> 29544416 |
Zoel A Quinonez1, Laura Downey2, Rania K Abbasi3, Calvin Kuan4, Ritu Asija5, Doff B McElhinney6, Frank L Hanley6, Richard D Mainwaring6, Lisa Wise-Faberowski4.
Abstract
Tetralogy of Fallot with pulmonary atresia and major aortopulmonary collaterals (TOF/PA/MAPCAs) is a heterogeneous disease with varying degrees of severity, requiring complex anesthetic management. Our institution has adopted the approach of early complete repair with incorporation of all lung segments, extensive lobar and branch segmental pulmonary artery reconstruction, and ventricular septal defect closure. While the surgical management of TOF/PA/MAPCAs has been extensively described and varies depending on the institution, there is a paucity of literature on the anesthetic management for such procedures. Herein, we describe our anesthetic management based on our own institution's surgical approach at Lucile Packard Children's Hospital/Stanford University.Entities:
Keywords: MAPCAs (multiple aortopulmonary collateral arteries); anesthesia (includes agents; cardiopulmonary bypass (CPB); care and research); pharmacology; pulmonary atresia with ventricular septal defect (VSD)
Mesh:
Year: 2018 PMID: 29544416 DOI: 10.1177/2150135118754522
Source DB: PubMed Journal: World J Pediatr Congenit Heart Surg ISSN: 2150-1351