Ventricular outflow tract obstruction
Condition involving obstruction of blood flow from the ventricles of the heart
Ventricular outflow tract obstruction (VOTO) is a condition characterized by a blockage or narrowing in the pathways through which blood exits the ventricles of the heart. This obstruction can occur in either the left or right ventricular outflow tract, leading to various clinical manifestations depending on the severity and location of the obstruction.
Types[edit | edit source]
Ventricular outflow tract obstruction can be classified based on the affected ventricle:
Left Ventricular Outflow Tract Obstruction (LVOTO)[edit | edit source]
LVOTO involves obstruction in the pathway from the left ventricle to the aorta. Common causes include:
Right Ventricular Outflow Tract Obstruction (RVOTO)[edit | edit source]
RVOTO involves obstruction in the pathway from the right ventricle to the pulmonary artery. Common causes include:
Causes[edit | edit source]
The causes of ventricular outflow tract obstruction can be congenital or acquired. Congenital causes are often due to structural heart defects present at birth, while acquired causes may develop later in life due to conditions such as rheumatic heart disease or degenerative changes.
Symptoms[edit | edit source]
Symptoms of ventricular outflow tract obstruction vary depending on the severity of the obstruction and the ventricle involved. Common symptoms include:
- Shortness of breath
- Chest pain
- Fatigue
- Syncope (fainting)
- Heart murmur
Diagnosis[edit | edit source]
Diagnosis of ventricular outflow tract obstruction typically involves:
Treatment[edit | edit source]
Treatment options depend on the severity and cause of the obstruction. They may include:
- Medications to manage symptoms
- Surgical intervention, such as valve repair or replacement
- Balloon valvuloplasty
Prognosis[edit | edit source]
The prognosis for individuals with ventricular outflow tract obstruction varies. Early detection and appropriate management can improve outcomes, but severe cases may lead to complications such as heart failure or arrhythmias.
Related pages[edit | edit source]
References[edit | edit source]
- Maron, B. J., & Maron, M. S. (2013). Hypertrophic cardiomyopathy. The Lancet, 381(9862), 242-255.
- Bonow, R. O., & Carabello, B. A. (2008). Aortic valve disease. Circulation, 118(8), 841-852.
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