Palliation of Cardiac Malformations Associated with Right Isomerism (Asplenia Syndrome) in Infancy
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Impact of Total Anomalous Pulmonary Venous Connection in Staged Single Ventricle Palliation
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2021, American Journal of the Medical SciencesCitation Excerpt :Prostaglandin E1 may facilitate such flow.62 Patients may then be treated surgically with staged palliative procedures including initial placement of a temporary shunt from the systemic circulation (usually the right superior vena cava) to the right pulmonary artery to reduce hypoxia.62–66 This is followed by a placement of a bidirectional systemic vein-pulmonary artery anastomosis.62–66,73
Visceral Heterotaxy in the Developing World
2012, Heart Lung and CirculationCitation Excerpt :The relative lack of obstructed TAPVC in our series could again be attributed to the late age at presentation, the more sick neonatal forms having succumbed earlier on. Other authors have reported adverse surgical outcomes in heterotaxy with TAPVC particularly in neonatal period [12,17]. AV septal defect is a common substrate in visceral heterotaxy, more so in RI.
Improving outcomes of the surgical management of right atrial isomerism
2012, Annals of Thoracic SurgeryIsomerism of the atrial appendages
2010, Paediatric Cardiology
Address reprint requests to Dr. Marcelletti, Dipartimento Medico-Chirurgico di Cardiologia Pediatrica, Ospedale Pediatrico Bambino Gesé, Piazza S. Onofrio 4, 00165 Roma, Italy.
We gratefully acknowledge Mrs. Sara Swartz for editing the manuscript and Mr. Giuseppe Bolla for providing photographic assistance.