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Congenital Heart Disease: Tetralogy of Fallot, Animation

(USMLE topics, cardiology) Tetralogy of Fallot: Pathology, Etiology, Symptoms, Diagnosis and Treatment. Purchase a license to download a non-watermarked version of this video on AlilaMedicalMedia(dot)com Check out our new Alila Academy - AlilaAcademy(dot)com - complete video courses with quizzes, PDFs, and downloadable images. ©Alila Medical Media. All rights reserved. Voice by: Sue Stern. All images/videos by Alila Medical Media are for information purposes ONLY and are NOT intended to replace professional medical advice, diagnosis or treatment. Always seek the advice of a qualified healthcare provider with any questions you may have regarding a medical condition. Tetralogy of Fallot, or TOF, is a CONGENITAL heart disease, classically known as a combination of FOUR defects that disrupt the normal blood flow in the heart. In normal circulation, oxygen-poor blood from the body returns to the right side of the heart where it is pumped into the pulmonary artery and to the lungs. After being oxygenated, oxygen-RICH blood from the lungs returns to the left side of the heart to be pumped into the aorta and out to the body. Infants born with TOF are presented with 4 major structural defects: NARROWING of the PULMONARY output Ventricular septal defect: an OPENING in the interventricular septum Displacement of the aorta: it now connects to both ventricles and Hypertrophy of the right ventricle The 4 defects, however, are likely the result of a SINGLE incident during embryonic development – the MAL-alignment of the upper part of the ventricular septum, known as the conal septum, with the rest of it. As the conal septum moves rightward and anteriorly, it creates an opening in the septum; blocks the right ventricular outflow tract; and pulls the aorta over the ventricular septum. Finally, because the output to the lungs is obstructed, the right ventricle develops thicker muscle to push harder, resulting in right ventricular hypertrophy. The cause of TOF remains largely unknown but several genetic disorders and prenatal factors are thought to be associated with increased risks of this condition. Connected ventricles in TOF allow blood to flow from one side to the other. The DIRECTION of this flow, however, depends on the DEGREE of pulmonary tract obstruction. When the obstruction is minimal, the flow is LEFT-to-RIGHT, because the LEFT ventricular pressure is usually HIGHER. While some of the already oxygenated blood leaks back to the lungs, most of it goes the usual route to the aorta, and the baby appears “pink” as normal. However, in the long-term, if too much blood flows to the lungs, patients may develop congestive heart failure. On the other hand, when pulmonary stenosis is severe, blood in the right ventricle has to escape through the septal defect during ventricular contraction, and a RIGHT-to-LEFT shunt results. The MIXED blood, which is LOW in oxygen, is then pumped into the aorta and to the body, causing oxygen deprivation in body's tissues, or hypoxia. This may result in a BLUISH skin color, known as CYANOSIS. The greater the pulmonary obstruction, the more deoxygenated blood enters the systemic circulation, the more severe the symptoms. Children with TOF may develop acute episodes of hypoxia, known as "tet spells", during activities that demand more oxygen. These episodes are characterized by: shortness of breath, increased cyanosis, loss of consciousness, and may result in hypoxic brain injury and death. Tet spell is a medical emergency but simple procedures such as squatting and the knee chest position, which increase systemic vascular resistance and therefore decrease right-to-left shunting, can help to temporarily relieve symptoms. Diagnosis is by echocardiography and can be done prenatally. Treatment is usually by repair surgery within the first year of life. The surgery involves enlargement of the pulmonary tract and closure of the septal defect.