Outcomes Following Aortic Valve Replacement in Children With Conotruncal Anomalies

Medicine and Dentistry

• Reoperation 100%
• Aortic Valve Replacement 100%
• Pediatrics 66%
• Transplantation 66%
• Hazard Ratio 66%
• Organ Transplantation 66%
• Aortic Valve Disease 66%
• Surgical Mortality 66%
• Cardiac Care 66%
• Disease 33%
• Allograft 33%
• Infant Survival 33%
• Long Term Survival 33%
• Odds Ratio 33%
• Pathophysiology 33%
• Stenosis 33%
• Persistent Truncus Arteriosus 33%
• Ventricular Septal Defect 33%
• Tetralogy of Fallot 33%
• Double Outlet Right Ventricle 33%
• Aortic Valve 33%
• Pulmonary Atresia 33%
• Aortic Valvuloplasty 33%
• Aortopathy 33%

Keyphrases

• Aortic Valve Replacement 100%
• Conotruncal Anomaly 100%
• Confidence Interval 50%
• Reoperation 50%
• Transplantation 33%
• Risk Factors 33%
• Infant Age 33%
• Hazard Ratio 33%
• Postoperative Mortality 33%
• Pediatric Cardiac 33%
• Cardiac Care 33%
• Competing Risk Analysis 33%
• Transplant-free Survival 33%
• Non-associated 16%
• Regression Analysis 16%
• Odds Ratio 16%
• Long-term Survival 16%
• Regurgitation 16%
• Pathophysiology 16%
• Stenosis 16%
• Congenital Heart Disease 16%
• Hospital Discharge 16%
• Tetralogy of Fallot 16%
• Cardiac Defects 16%
• Organ Transplantation 16%
• Attrition 16%
• Double Outlet Right Ventricle 16%
• Conotruncal 16%
• Aortic Valve Disease 16%
• Aortic Valve 16%
• National Death Index 16%
• Pulmonary Atresia with Intact Ventricular Septum 16%
• Organ Procurement 16%
• Valve Type 16%
• Aortic Valvuloplasty 16%
• Mitral Surgery 16%
• Homograft 16%
• Congenital Aortic Valve Disease 16%
• Corrected Transposition 16%
• Truncus 16%
• Aortopathy 16%