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Tetralogy of Fallot TOF with pulmonary atresia Pulmonary atresia with intact interventricular septum Tricuspid atresia Double outlet right ventricle Transposition of great arteries with ventricular septal defect and pulmonary stenosis Ebstein’s anomaly of tricuspid valve In DORV and tricuspid atresia, there are also variants with increased pulmonary (..)
Pulmonary arterial hypertension related to congenital heart disease as a paradigm of complexity Pulmonary arterial hypertension related to congenital heart disease (PAH-CHD) really represents a paradigm of complexity.
Transcript of the video: Ebstein’s Anomaly is one of the cyanotic congenital heart disease in which survival to adult life is common. In Ebstein’s anomaly, there is downward or apical displacement of posterior and septal tricuspid leaflets. Anterior leaflet is elongated and sail like.
Objective This study assessed the long-term effects of triple therapy with prostanoids on patients with pulmonary arterial hypertension associated with congenital heart disease (PAH-CHD), as there is limited information on the safety and efficacy of this treatment approach.
Introduction Isolated tricuspid valve surgery (TVS) may be associated with high morbidity and mortality. Patients with congenital heart disease, infective endocarditis and those who underwent concomitant valve or pericardial surgery were excluded. We only included those who had all three tests before surgery: ECHO, CMR and RHC.
Crochetage sign on ECG in ASD ECG in ASD with severe pulmonary hypertension: Tall R’ in V1, ST depression in inferior leads and V2-V5, and T inversion in inferior leads and V1-V6 are seen. All these features together in a cyanotic congenital heart disease is characteristic of tricuspid atresia.
D-Transposition of the great arteries (TGA) is a rare congenital heart defect where the pulmonary artery originates from the left ventricle (LV) and the aorta from the right ventricle (RV).
And that will be the approximate level of the tricuspid valve, the reference point for measuring right atrial pressure. In right atrial tracing, this occurs at the time of right ventricular contraction, with bulging upwards of the tricuspid valve. The Y descent is shallow in tricuspid stenosis, and absent in cardiac tamponade.
ET – Congenital Cardiac Q&A 6:00 p.m. The program also focuses on reimbursement issues affecting the specialty as a whole. Live Q&A and Discussion Schedule Friday, February 10 4:00 p.m. Live Q&A and Discussion Schedule Friday, February 10 4:00 p.m. ET – 4:15 p.m. ET – Welcome/Introductions 4:15 p.m. ET – 5:15 p.m.
This becomes more difficult in complex congenital heart diseases where the cardiac chamber positions and size may vary. The aorta, right ventricular outflow tract and pulmonary artery up to its bifurcation is imaged in the upward angulation shown in the left panel. Colour flow shows the flow in pulmonary artery.
We are blessed with 4 heart valves – 2 on the left side which are known as the mitral and aortic valves and 2 on the right side – the tricuspid and pulmonary valves.
BACKGROUND:Right ventricular-arterial coupling (RVAC) describes the relationship between right ventricular contractility and pulmonary vascular afterload. In a retrospective analysis, hybrid (echo and invasive) RVAC metrics included TAPSE/pulmonary vascular resistance (PVRi) and RVFW-LS/PVRi.
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