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Articles by Howard Weber
Percutaneous Amplatzer Septal Occluder Device Occlusion Of A Large Portal Vein To Pulmonary Venous Atrium Collateral Resulting In Severe Systemic Hypoxemia Post Fontan
By Howard S. Weber, MD, FSCAI; Farrah Munir, MD; Bryan P. Stefek, MD; Frank C. Lynch, MD Introduction The development of decompressing veno-venous collaterals is common following the bidirectional Glenn shunt and Fontan operations which can result in varying degrees of systemic desaturation. This phenomenon is thought to be a biologic reaction to the increased systemic venous pressure changes associated with this type of circulation.
January 2020 Issue - North American Edition
Percutaneous Amplatzer Septal Occluder Device Occlusion Of A Large Portal Vein To Pulmonary Venous Atrium Collateral Resulting In Severe Systemic Hypoxemia Post Fontan By Howard S. Weber, MD, FSCAI; Farrah Munir, MD; Bryan P. Stefek, MD; Frank C. Lynch, MD Introduction The development of decompressing veno-venous collaterals is common following the bidirectional Glenn shunt and Fontan operations which can result in varying degrees of systemic desaturation.
January 2020 Issue - International Edition
Percutaneous Amplatzer Septal Occluder Device Occlusion Of A Large Portal Vein To Pulmonary Venous Atrium Collateral Resulting In Severe Systemic Hypoxemia Post Fontan By Howard S. Weber, MD, FSCAI; Farrah Munir, MD; Bryan P. Stefek, MD; Frank C. Lynch, MD Introduction The development of decompressing veno-venous collaterals is common following the bidirectional Glenn shunt and Fontan operations which can result in varying degrees of systemic desaturation.
Percutaneous Amplatzer Septal Occluder Device Occlusion Of A Large Portal Vein To Pulmonary Venous Atrium Collateral Resulting In Severe Systemic Hypoxemia Post Fontan
By Howard S. Weber, MD, FSCAI; Farrah Munir, MD; Bryan P. Stefek, MD; Frank C. Lynch, MD Introduction The development of decompressing veno-venous collaterals is common following the bidirectional Glenn shunt and Fontan operations which can result in varying degrees of systemic desaturation. This phenomenon is thought to be a biologic reaction to the increased systemic venous pressure changes associated with this type of circulation.
Scimitar Syndrome in a 3-Month-Old Infant
Scimitar Syndrome is a rare congenital cardiac anomaly characterized by partial or complete anomalous pulmonary venous drainage of the right lung to the Inferior Vena Cava (IVC), either above or below the diaphragm.1, 2 It accounts for 3%–6% of all the partial anomalous pulmonary venous returns.3 Scimitar Syndrome is frequently associated with hypoplasia of the right lung, dextroposition of the heart, hypoplasia or malformations of the right pulmonary artery, anomalous systemic supply of the...
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