Repairing the tricuspid valve in congenital heart diseases other than Ebstein's

Cardiol Young. 2014 Dec;24(6):1077-87. doi: 10.1017/S104795111400198X.

Abstract

The tricuspid valve is being increasingly recognised as an important safeguard to the heart with congenital heart disease. Both structural anomalies of the valve and functional burdens from other malformations of the right heart can lead to major haemodynamic consequences both upstream and downstream. The indications to surgically intervene on the tricuspid valve are evolving and vary depending on the malformation. The extant surgical techniques and their applications to corresponding frequent congenital anomalies of the tricuspid valve are reviewed.

Keywords: hypoplastic left heart syndrome.

Publication types

  • Review

MeSH terms

  • Cardiac Surgical Procedures / adverse effects
  • Cardiac Surgical Procedures / methods*
  • Cardiomyopathy, Dilated / complications
  • Cardiomyopathy, Dilated / surgery
  • Defibrillators, Implantable / adverse effects
  • Heart Defects, Congenital / complications
  • Heart Defects, Congenital / surgery*
  • Heart Septal Defects / complications
  • Heart Septal Defects / surgery
  • Heart Valve Diseases / complications
  • Heart Valve Diseases / surgery*
  • Humans
  • Hypoplastic Left Heart Syndrome / complications
  • Hypoplastic Left Heart Syndrome / surgery
  • Infant
  • Infant, Newborn
  • Marfan Syndrome / complications
  • Marfan Syndrome / surgery
  • Pacemaker, Artificial / adverse effects
  • Tetralogy of Fallot / complications
  • Tetralogy of Fallot / surgery
  • Tricuspid Valve / abnormalities
  • Tricuspid Valve / injuries
  • Tricuspid Valve / surgery*

Supplementary concepts

  • Atrioventricular Septal Defect
  • Uhl anomaly