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Malformation where the heart lacks the tricuspid valve From Wikipedia, the free encyclopedia
Tricuspid atresia is a form of congenital heart disease whereby there is a complete absence of the tricuspid valve.[2] Therefore, there is an absence of right atrioventricular connection.[2] This leads to a hypoplastic (undersized) or absent right ventricle. This defect occurs during prenatal development, when the heart does not finish developing. It causes the systemic circulation to be filled with relatively deoxygenated blood. The causes of tricuspid atresia are unknown.[3]
| Tricuspid atresia | |
|---|---|
| Other names | Tri atresia[1] |
| |
| Anterior (frontal) view of the opened heart in tricuspid atresia with ASD+VSD. White arrows indicate blood flow. (Atresic tricuspid valve labeled at bottom left.) | |
| Specialty | Medical genetics  |
In most cases of tricuspid atresia, additional defects exist to allow exchange of blood between the loops of systematic circulation and pulmonary circulation, filling in the role of the missing atrioventricular connection. An atrial septal defect (ASD) must be present to fill the left atrium and the left ventricle with blood.[4] Since there is a lack of connection to the right ventricle, there must also be a way to pump blood into the pulmonary artery. This can be accomplished by a ventricular septal defect (VSD) connecting the left ventricle to the pulmonary artery or by a patent ductus arteriosus (PDA) connecting the aorta to the pulmonary artery. In the latter case, prostaglandin E1 is used to maintain the PDA connection until emergency corrective surgery can be completed. As oxygenated blood is mixed with deoxygenated blood in both cases, there is a reduction in the oxygen-carrying capacity.[4]
It is also possible for tricuspid atresia to appear without the life-saving defects. In this case, the systemic and pulmonary circulations would be cut off from each other and no useful breathing can occur. An experimental procedure called fetal balloon atrial septostomy can be used to artificially create the required defect in utero.[5]
Tricuspid atresia is caused by complete absence of the tricuspid valve.[2] The underlying cause of this absence remains unknown.[3] This prevents direct blood flow between the right atrium and the right ventricle.[2] This usually causes the foramen ovale to remain open after birth, leading to atrial septal defect.[4]
As there is no communication between the right atrium and the right ventricle, there must be an atrial septal defect to allow blood to flow into the left cardiac chambers. Due to the lack of blood flow into the right ventricle, it will be hypoplastic. In most cases, there will also be a ventricular septal defect allowing some blood into the pulmonary circulation. Due to the lack of blood flow into the pulmonary circulation, there is poor oxygenation of blood, leading to progressively worsening cyanosis.[6]
The majority of cases can be diagnosed prenatally during a routine anomaly scan. If evidence of a congenital heart disease is found, the diagnosis can be confirmed by a foetal echocardiogram.
If it is not diagnosed prenatally, it may be diagnosed shortly after birth with physical examination, which would reveal cyanosis and murmur. Further evidence for the diagnosis can be obtained with an electrocardiogram and a chest radiograph. ECG will typically show a left axis deviation, while the chest X-ray may show pulmonary oligaemia or hyperaemia. The definitive investigation is, as in all congenital heart diseases, an echocardiogram, although the aforementioned tests along with clinical features might be sufficient for most cases.[6]
Treatment is based on:
Tricuspid atresia is the third most common critical congenital heart defect.[2] It is estimated to cause between 1% and 3% of all congenital heart defects.[8]
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