tetralogy /te·tral·o·gy/ (tĕ-tral´ah-je) a group or series of four.
tetralogy
tetralogy [tet-ral´ah-je]
tetralogy of Fallot a complex of congenital heart defects consisting of pulmonary stenosis, interventricular septal defect, hypertrophy of right ventricle, and dextroposition of the aorta. 
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Tetralogy of Fallot.
te·tral·o·gy (t -tr l  -j , -tr l-)n. A complex of four symptoms. |
tetralogy
[tetrol′əjē]
Etymology: Gk, tetra, four, logos, word
any group of four writings, symptoms, or other related factors. See also tetralogy of Fallot.
tetralogy [tet-ral´ah-je]
a group or series of four.
tetralogy of Fallot a congenital heart defect that combines four structural anomalies: obstruction to pulmonary flow; ventricular septal defect (abnormal opening between the right and left ventricles); dextroposition of the aorta (aortic opening overriding the septum and receiving blood from both ventricles); and right ventricular hypertrophy (increase of volume of the myocardium of the right ventricle).
Infants with this condition are sometimes referred to as blue babies because of the presence of cyanosis, an outstanding symptom. This is due to mixing of poorly oxygenated blood from the systemic circulation with oxygenated blood from the lungs, because of the position of the aorta. Other symptoms include clubbing of the ends of the fingers, hemoptysis, dyspnea on exertion, and a slight delay in growth and development.
Diagnosis is confirmed by electrocardiography, angiocardiography, and cardiac catheterization. These procedures demonstrate changes in the heart's electric impulses; defects in the ventricles, aorta, and pulmonary artery; and, from samplings of blood taken from the various chambers of the heart and great vessels, the oxygen content and pressure of the blood in these various areas.
Treatment involves surgical correction whenever possible. Without corrective surgery the prognosis is extremely poor for children who are deeply cyanotic and have dyspnea on slight exertion.
Before surgery, medical treatment is necessary to avoid complications and control dyspneic attacks. Since the hematocrit is high and polycythemia is common, efforts must be made to prevent dehydration and avoid the development of thrombi. Paroxysmal dyspnea, which often follows feeding or a spell of crying, usually can be relieved by placing the infant in knee-chest position, administering oxygen, or administering a mild sedative or morphine.
Surgical procedures for correction of the defects in the heart and great vessels vary according to the severity of symptoms and the age of the patient. In some cases an anastomosis of the arteries may be done as a temporary measure until more extensive surgery is feasible. In most cases open heart surgery is most successful in relieving symptoms and produces the most lasting benefits.
Infants with this condition are sometimes referred to as blue babies because of the presence of cyanosis, an outstanding symptom. This is due to mixing of poorly oxygenated blood from the systemic circulation with oxygenated blood from the lungs, because of the position of the aorta. Other symptoms include clubbing of the ends of the fingers, hemoptysis, dyspnea on exertion, and a slight delay in growth and development.
Diagnosis is confirmed by electrocardiography, angiocardiography, and cardiac catheterization. These procedures demonstrate changes in the heart's electric impulses; defects in the ventricles, aorta, and pulmonary artery; and, from samplings of blood taken from the various chambers of the heart and great vessels, the oxygen content and pressure of the blood in these various areas.
Treatment involves surgical correction whenever possible. Without corrective surgery the prognosis is extremely poor for children who are deeply cyanotic and have dyspnea on slight exertion.
Before surgery, medical treatment is necessary to avoid complications and control dyspneic attacks. Since the hematocrit is high and polycythemia is common, efforts must be made to prevent dehydration and avoid the development of thrombi. Paroxysmal dyspnea, which often follows feeding or a spell of crying, usually can be relieved by placing the infant in knee-chest position, administering oxygen, or administering a mild sedative or morphine.
Surgical procedures for correction of the defects in the heart and great vessels vary according to the severity of symptoms and the age of the patient. In some cases an anastomosis of the arteries may be done as a temporary measure until more extensive surgery is feasible. In most cases open heart surgery is most successful in relieving symptoms and produces the most lasting benefits.
Tetralogy of Fallot. The right ventricular outflow tract obstruction results in blood flowing from right to left across the ventricular septal defect. From Lissauer and Graham, 2002.
tetralogy
a group or series of four.
tetralogy of Fallot
a congenital defect of the heart that combines four structural anomalies: pulmonary stenosis (narrowing of the pulmonary artery); ventricular septal defect, or abnormal opening between the right and left ventricles; dextroposition of the aorta, in which the aortic opening overrides the septum and receives blood from both the right and left ventricles; and right ventricular hypertrophy, or increase of volume of the myocardium of the right ventricle.
This is almost always a lethal defect. There is poor exercise tolerance, dyspnea, often cyanosis. A loud murmur and a strong thrill are palpable on the left side.
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