Paediatric Cardiac Surgery – What Parents Should Know About Congenital Heart Disease in Children

Paediatric Cardiac Surgery – What Parents Should Know About Congenital Heart Disease in Children
August 12 06:54 2016 Print This Article

Hearing the words “your child has a heart problem” is one of the most frightening moments a parent can face. It’s worth saying early, then, that this field has changed enormously over the past few decades – conditions that were once considered untreatable are now routinely fixed, often with a single procedure and a full recovery. Understanding what’s actually involved, and why timing and teamwork matter so much, can make an overwhelming diagnosis feel a lot more manageable.

What Is Congenital Heart Disease?

Congenital heart disease (CHD) refers to structural problems with the heart that are present from birth – a hole between chambers, a narrowed or malformed valve, or vessels that connect in the wrong place. It’s more common than most parents realise: globally, an estimated 1 in every 100 -110 live births has some form of congenital heart defect, and in India, the figure is generally cited at around 8 – 10 per 1,000 live births – which works out to well over 200,000 babies born with a heart defect in India each year. Of these, roughly one in five has a serious defect that needs intervention within the first year of life.

Not every defect needs surgery. Many small holes or mild valve issues are monitored and close or resolve on their own. But a meaningful proportion do require a procedure – either a catheter-based fix or open surgery – to allow a child to grow and develop normally.

Recognising the Warning Signs

Because babies can’t describe what’s wrong, parents and paediatricians rely on physical clues. Signs worth taking seriously include:

  • A bluish tinge to the lips, tongue, or nail beds (cyanosis) – a sign that oxygen-poor blood is circulating.
  • Rapid or laboured breathing, especially during feeds.
  • Poor weight gain or difficulty feeding– a baby’s heart working harder than it should burns calories that would otherwise go toward growth.
  • Sweating, unusually, during feeding rather than from heat.
  • Frequent colds, coughs, or chest infections that seem to recur more than expected.
  • A heart murmur picked up during a routine check-up – an extra or unusual sound heard through a stethoscope.

It’s worth knowing that heart murmurs are common and most are entirely harmless (“innocent” murmurs, caused by normal blood flow) – the vast majority of children with a murmur do not have structural heart disease. Still, any murmur in a newborn or infant is worth a paediatric cardiology opinion simply to rule out the minority that do signal something structural, since some defects go unrecognised at birth in a straightforward physical exam alone.

How Congenital Heart Disease Is Diagnosed

  • Pulse oximetry screening, now standard in many newborn units, measures blood oxygen levels non-invasively and can flag critical defects before a baby even shows symptoms.
  • Echocardiography (echo)– an ultrasound of the heart – is the primary tool for diagnosing structural defects and remains the single most useful test.
  • ECG and chest X-ray provide supporting information but have more limited standalone diagnostic value.
  • In select cases, fetal echocardiography during pregnancy can identify some defects before birth, allowing families and doctors to plan delivery and early care in advance.

Treatment: Not Every Defect Needs Open Surgery

Modern paediatric cardiac care has moved well beyond a one-size-fits-all surgical approach:

  • Watchful waiting is appropriate for many small defects, particularly small ventricular or atrial septal defects that have a real chance of closing spontaneously as a child grows.
  • Catheter-based (transcatheter) procedures– threading a thin tube through a blood vessel to close a hole or widen a narrowed valve – can treat certain defects without opening the chest at all, meaning shorter recovery and no visible scar.
  • Minimally invasive surgery, where feasible, uses smaller incisions than traditional open-heart approaches, which can mean less pain and a faster return to normal life.
  • Open-heart surgery remains necessary for more complex or combined defects, and outcomes here have improved dramatically. Advances in surgical technique, cardiopulmonary bypass management, and post-operative intensive care mean that the large majority of children who undergo surgery for congenital heart disease go on to lead active, normal lives.

Why Timing and Teamwork Matter So Much

Two things repeatedly come up in paediatric cardiac care as decisive factors in outcomes:

Timing. Some defects are safest to fix in the first days or weeks of life; others benefit from waiting until a child is a little older and stronger. Getting this timing right – neither rushing nor delaying – is one of the most consequential decisions a paediatric cardiac team makes, and it’s highly specific to each child’s particular defect and overall health.

Teamwork. A paediatric cardiac surgery case typically involves a paediatric cardiologist (diagnosis and long-term follow-up), a cardiac surgeon, a paediatric cardiac anaesthetist, perfusionists (who manage the heart-lung bypass machine during surgery), and a dedicated paediatric cardiac ICU team for recovery. The coordination between these specialists – not any single individual’s skill alone – is consistently what separates good outcomes from great ones.

Life After Surgery: What Parents Can Expect

A successful repair doesn’t always mean the story ends at discharge. Many children who’ve had congenital heart surgery need periodic follow-up with a paediatric cardiologist through childhood, and increasingly, this follow-up continues into adulthood – a growing recognition in the field that children who once wouldn’t have survived infancy are now living full adult lives and need ongoing, specialised cardiac care as adults, a discipline sometimes called Adult Congenital Heart Disease (ACHD). This is a genuinely new and expanding area of cardiology, a direct consequence of how much outcomes have improved over the past generation.

Day to day, most children recover to the point of full, unrestricted activity – including sport and exercise, in the majority of straightforward repairs – though this is always something to confirm with your child’s own cardiologist rather than assume.

Frequently Asked Questions

Is congenital heart disease always detected before or right after birth?+

Not always. While pulse oximetry screening and prenatal ultrasound catch many cases early, some defects – particularly milder ones – are only picked up later, sometimes when a murmur is noted at a routine check-up or when a child shows subtle signs like poor stamina during play.

Does a heart murmur mean my baby has a heart defect?+

Usually not. Heart murmurs are extremely common in infants and children, and the majority are “innocent” – a normal sound of blood flow rather than a sign of a structural problem. That said, any newborn murmur deserves a paediatric cardiology opinion to rule out the minority of cases that do need attention.

Will my child need more than one surgery?+

It depends entirely on the defect. Simple repairs are often a single, definitive procedure. More complex conditions – particularly certain combined defects – may be managed with a staged approach over a child’s early years. Your paediatric cardiac team will map this out based on your child’s specific anatomy.

Can a child live a normal life after heart surgery?+

In the majority of cases, yes. Advances in paediatric cardiac surgery mean most children go on to grow, play, and develop typically after a successful repair, with periodic cardiology follow-up rather than ongoing restriction.

What should I do if I notice symptoms like bluish lips or poor feeding in my baby?+

Don’t wait – these are signs worth an urgent paediatric evaluation. Even if the cause turns out to be unrelated to the heart, ruling out a cardiac cause quickly is always the safer path.

Does congenital heart disease run in families?+

There’s a modestly increased risk if a parent or sibling has had a congenital heart defect, and certain genetic conditions (such as Down syndrome) are associated with a higher likelihood of heart defects. However, most cases occur without any known family history or identifiable cause.

Stay Informed with Kauvery Hospital

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If your child has a heart murmur, symptoms that concern you, or a known congenital heart condition, book an appointment with Kauvery Hospital’s Paediatric Cardiology team for a thorough evaluation.

This article is for general health information and does not replace professional medical advice. Please consult a qualified paediatric cardiologist for guidance specific to your child.

Article Updated on 28th September 2026

Kauvery Hospital is globally known for its multidisciplinary services at all its Centers of Excellence, and for its comprehensive, Avant-Grade technology, especially in diagnostics and remedial care in heart diseases, transplantation, vascular and neurosciences medicine. Located in the heart of Trichy (Tennur, Royal Road and Alexandria Road (Cantonment), Chennai, Hosur, Salem, Tirunelveli and Bengaluru, the hospital also renders adult and pediatric trauma care.

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