10:00 – 12:00 PAH: Pulmonary Arterial Hypertension (PAH)-CHD | |
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10:00 – 10:20 | Pathophysiology of pulmonary hypertension in congenital heart disease |
10:20 – 10:40 | Operability in PAH-CHD |
10:40 – 11:00 | Management of Eisenmenger syndrome |
11:00 – 11:20 | Evaluation and management of pulmonary hypertension in children with end stage left heart failure |
11:20 – 11:40 | PAH in the child with Down Syndrome |
11:40 – 12:00 | Persistent postoperative PAH |
13:30 – 15:30 PAH: Treatment of Pulmonary Arterial Hypertension (PAH) | |
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13:30 – 13:50 | General measures |
13:50 – 14:10 | cGMP Treatment |
14:10 – 14:30 | Prostacyclin Treatment |
14:30 – 14:50 | Endothelin Receptor Antagonist Treatment |
14:50 – 15:10 | Interventional Approaches in Pulmonary Hypertension (BAS/Cath Potts) |
15:10 – 15:30 | Surgical Approaches in PAH (Potts/Transplant) |