How Is Congenital Heart Disease Diagnosed in Newborns?

 Congenital heart disease in newborns is diagnosed using a combination of clinical examination and specialised testing.

The process begins with the Newborn Physical Examination, where clinicians listen for murmurs and assess circulation. Pulse oximetry is then used to measure oxygen levels, helping to detect hidden defects.

If a concern is identified, an echocardiogram is performed to confirm the diagnosis.

This step-by-step approach ensures that both obvious and subtle heart defects can be detected early.

Early diagnosis is critical in ensuring that babies receive the care they need as soon as possible.

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