Because the shunt is initially left to right there is normally no cyanosis.
With time, pulmonary hypertension and pulmonary vascular disease may develop, resulting in reversal of the flow, causing right ventricular hypertrophy, cyanosis, clubbing and polycythaemia.
Because the ductus joins the aorta distal to the left subclavian artery, the cyanosis does not affect the head and arms.
If the shunt is small and the pulmonary pressure is normal then if is possible for there to be survival, without symptoms, into adult life. However the chronic overloading of the left ventricle, as a result of flow from the aorta to pulmonary artery, may lead to cardiac failure.
Although systolic blood pressure may be sustained despite a left-to-right ductal shunt, the drop in diastolic blood pressure and localized vasoconstriction are believed to contribute to the clinical consequences of PDA (1,2,3)
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