Trilogy of Fallot: Difference between revisions
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{{Short description|Congenital heart defect}} | |||
{{Use dmy dates|date=October 2023}} | |||
'''Trilogy of Fallot''' is a rare congenital heart defect characterized by three primary cardiac anomalies: [[pulmonary valve stenosis]], [[right ventricular hypertrophy]], and an [[atrial septal defect]]. This condition is related to, but distinct from, the more well-known [[Tetralogy of Fallot]]. | |||
[[ | |||
== | ==Anatomy and Pathophysiology== | ||
== | ===Pulmonary Valve Stenosis=== | ||
[[File:Pulmonary_valve_stenosis.svg|thumb|right|Diagram of pulmonary valve stenosis]] | |||
Pulmonary valve stenosis is a narrowing of the [[pulmonary valve]] opening, which restricts blood flow from the right ventricle to the [[pulmonary artery]]. This obstruction increases the workload on the right ventricle, leading to [[right ventricular hypertrophy]]. | |||
== | ===Right Ventricular Hypertrophy=== | ||
[[File:Right_Ventricular_hypertrophy.svg|thumb|right|Diagram of right ventricular hypertrophy]] | |||
Right ventricular hypertrophy refers to the thickening of the muscular walls of the right ventricle. This occurs as a compensatory mechanism in response to the increased pressure required to overcome the obstruction caused by pulmonary valve stenosis. | |||
== | ===Atrial Septal Defect=== | ||
An [[atrial septal defect]] (ASD) is a hole in the wall (septum) that separates the two upper chambers of the heart (atria). This defect allows oxygen-rich blood from the left atrium to mix with oxygen-poor blood in the right atrium, potentially leading to increased blood flow to the lungs and further strain on the right side of the heart. | |||
==Diagnosis== | |||
The diagnosis of Trilogy of Fallot is typically made through a combination of physical examination, [[echocardiography]], and other imaging techniques such as [[cardiac MRI]] or [[CT scan]]. A heart murmur is often detected during a physical exam, prompting further investigation. | |||
==Treatment== | |||
Treatment for Trilogy of Fallot usually involves surgical intervention to correct the defects. This may include procedures to relieve the pulmonary stenosis, repair the atrial septal defect, and address any associated anomalies. In some cases, a [[balloon valvuloplasty]] may be performed to widen the pulmonary valve. | |||
==Prognosis== | |||
With appropriate surgical treatment, individuals with Trilogy of Fallot can lead relatively normal lives. However, they require regular follow-up with a cardiologist to monitor heart function and detect any potential complications. | |||
==Related pages== | |||
* [[Tetralogy of Fallot]] | * [[Tetralogy of Fallot]] | ||
* [[Congenital heart defect]] | * [[Congenital heart defect]] | ||
* [[Pulmonary valve stenosis]] | * [[Pulmonary valve stenosis]] | ||
==References== | |||
{{Reflist}} | |||
[[Category:Congenital heart defects]] | |||
[[Category:Cardiology]] | [[Category:Cardiology]] | ||
Revision as of 20:55, 9 February 2025
Congenital heart defect
Trilogy of Fallot is a rare congenital heart defect characterized by three primary cardiac anomalies: pulmonary valve stenosis, right ventricular hypertrophy, and an atrial septal defect. This condition is related to, but distinct from, the more well-known Tetralogy of Fallot.
Anatomy and Pathophysiology
Pulmonary Valve Stenosis

Pulmonary valve stenosis is a narrowing of the pulmonary valve opening, which restricts blood flow from the right ventricle to the pulmonary artery. This obstruction increases the workload on the right ventricle, leading to right ventricular hypertrophy.
Right Ventricular Hypertrophy

Right ventricular hypertrophy refers to the thickening of the muscular walls of the right ventricle. This occurs as a compensatory mechanism in response to the increased pressure required to overcome the obstruction caused by pulmonary valve stenosis.
Atrial Septal Defect
An atrial septal defect (ASD) is a hole in the wall (septum) that separates the two upper chambers of the heart (atria). This defect allows oxygen-rich blood from the left atrium to mix with oxygen-poor blood in the right atrium, potentially leading to increased blood flow to the lungs and further strain on the right side of the heart.
Diagnosis
The diagnosis of Trilogy of Fallot is typically made through a combination of physical examination, echocardiography, and other imaging techniques such as cardiac MRI or CT scan. A heart murmur is often detected during a physical exam, prompting further investigation.
Treatment
Treatment for Trilogy of Fallot usually involves surgical intervention to correct the defects. This may include procedures to relieve the pulmonary stenosis, repair the atrial septal defect, and address any associated anomalies. In some cases, a balloon valvuloplasty may be performed to widen the pulmonary valve.
Prognosis
With appropriate surgical treatment, individuals with Trilogy of Fallot can lead relatively normal lives. However, they require regular follow-up with a cardiologist to monitor heart function and detect any potential complications.
Related pages
References
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