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Patent ductus arteriosus (PDA) is a medical condition in which the ductus arteriosus fails to close after birth: this allows a portion of oxygenated blood from the left heart to flow back to the lungs from the aorta, which has a higher blood pressure, to the pulmonary artery, which has a lower blood pressure.
The ductus arteriosus, also called the ductus Botalli, named after the Italian physiologist Leonardo Botallo, is a blood vessel in the developing fetus connecting the trunk of the pulmonary artery to the proximal descending aorta. It allows most of the blood from the right ventricle to bypass the fetus's fluid-filled non-functioning lungs.
If that ductus arteriosus doesn’t close off, then the baby is left with a patent ductus arteriosus, and this condition accounts for about 10% of all congenital heart defects, of which the vast majority, about 90%, are isolated heart defects, meaning there aren’t any additional congenital defects.
The ductus arteriosus connects at a junction point that has a low pressure zone (commonly called Bernoulli's principle) created by the inferior curvature (inner radius) of the artery. This low pressure region allows the artery to receive ( siphon ) the blood flow from the pulmonary artery which is under a higher pressure.
Because the aorta has lower pressure than the pulmonary artery, most of the blood flows across the ductus arteriosus away from the lungs. [1] Once the blood goes through the ductus arteriosus, it mixes with the blood from the aorta. This results in mixed blood oxygen saturation that supplies most of the structures of the lower half of the fetal ...
If the ductus arteriosus fails to close after birth, a condition known as patent ductus arteriosus can develop. This is a fairly common birth defect. This is a fairly common birth defect. Sufferers may have operations that leave them with no ligamentum arteriosum.
A labelled diagram showing a patent ductus arteriosus in relation to the great arteries and the heart. Items portrayed in this file ...
Eisenmenger syndrome or Eisenmenger's syndrome is defined as the process in which a long-standing left-to-right cardiac shunt caused by a congenital heart defect (typically by a ventricular septal defect, atrial septal defect, or less commonly, patent ductus arteriosus) causes pulmonary hypertension [1] [2] and eventual reversal of the shunt into a cyanotic right-to-left shunt.
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