CardiologyDr. Aseem R. SrivastavaCongenital Heart Disease

Chief - Paediatric Cardio Thoracic and Vascular Surgery (CTVS), Artemis Hospitals, Gurgaon, India

Series overview · 14 articles

Correct Timing for Congenital Heart Surgery

August 6, 2026

The right time for congenital heart surgery in a child is decided by the natural history of the specific heart condition, meaning how quickly it is likely to cause death or serious harm if left untreated, rather than by a fixed rule about age or weight. Dr. Aseem R. Srivastava, Chief of Paediatric CTVS and Adult Congenital Heart Diseases at Artemis Hospitals, Gurgaon, shared a detailed breakdown of correct surgical timing across the common congenital heart conditions during a Jivo Masterclass session.

Why "wait until the child is bigger" is the wrong default

There is a common misunderstanding, not just in India but in the US, Europe and the Middle East, that children need to reach a certain age or weight before congenital heart surgery can be offered. This is incorrect, because while surgical mortality may look better in an older, bigger child, the children who die during a delayed waiting period are simply not counted in that comparison. The correct approach is to base timing on the natural history of each specific condition, weighing the risk of waiting against the risk of surgery.

A wide range of recommended timings

Across the conditions covered in this series, an atrial septal defect is the one heart condition where waiting, until around 3 to 4 years of age, is genuinely the right approach. Most other congenital heart conditions, including transposition of the great arteries, patent ductus arteriosus with symptoms, coarctation of the aorta, truncus arteriosus and complex conditions with pulmonary stenosis, need treatment at diagnosis or within the first year of life, and delaying surgery in these cases raises the risk of the child becoming inoperable or dying while waiting.

A complete guide to this series

This series draws directly on Dr. Srivastava's Jivo Masterclass session to walk through the recommended timing for atrial septal defect, ventricular septal defect, AV canal defect, Tetralogy of Fallot, TAPVR, transposition of the great arteries, PDA, coarctation of the aorta, truncus arteriosus, complex TGA with pulmonary stenosis, late-presenting congenital heart disease, what makes a strong paediatric cardiac programme, and the cost of congenital heart surgery in India. Jivo works with Artemis Hospitals and Dr. Aseem R. Srivastava to connect doctors and families across Africa with timely congenital heart surgery in India, including through a dedicated womb-to-world programme for babies diagnosed before birth.

Atrial Septal Defect (ASD): Why the Best Age to Close It Is 3 to 4 Years | Ventricular Septal Defect (VSD): When Small Holes Close on Their Own and When Surgery Can't Wait | AV Canal Defect: Why Surgery Is Needed by 3 to 4 Months of Age | Tetralogy of Fallot: Timing of Repair and Why Waiting Is Dangerous | Total Anomalous Pulmonary Venous Return (TAPVR): Why Surgery Cannot Wait | Transposition of the Great Arteries (TGA): Why Timing Is a Matter of Days | Patent Ductus Arteriosus (PDA): When to Close and How | Coarctation of the Aorta: Why Immediate Surgery Prevents Death and Lifelong Hypertension | Truncus Arteriosus: Why Newborns Need Surgery at Diagnosis | TGA with VSD and Pulmonary Stenosis: Rastelli and Nikaidoh Procedures | Late-Presenting Congenital Heart Disease: What to Do When Diagnosis Comes Too Late | What Makes a Good Paediatric Cardiac Surgery Programme | Cost of Congenital Heart Surgery in India

This article is based on a Jivo Masterclass session conducted by Dr. Aseem R. Srivastava, Chief, Paediatric CTVS and Adult Congenital Heart Diseases, Artemis Hospitals, Gurgaon, India. The article has been summarised with the assistance of an AI tool from the original masterclass recording. Watch the full Masterclass recording

This guide is based on a live Jivo Masterclass — Dr. Aseem R. Srivastava taught doctors across Africa on August 31, 2025.

Watch the full recording, or read the guide above.

FROM THE LIVE Q&A

DR

Dr. Aoke (Ethiopia)

What is the correct timing for a patient with transposition of the great arteries (TGA), VSD, and LVOT obstruction? Also, since we live in a resource-limited country where diagnosis is sometimes made late, and patients may then ask for treatment abroad after a late diagnosis, what is your recommendation for handling late presenters, especially with simple shunt lesions?

AR

Dr. Aseem R. Srivastava

For TGA with VSD and LVOT obstruction, these kids essentially have pulmonary stenosis with a VSD, and timing depends on the kid's oxygen saturation — they will need a Rastelli or a Nikaidoh operation, both requiring an implant, and the intent is to give the biggest implant possible since a smaller implant means an earlier return for a change. If saturations are above 75% and the kid is growing and doing well, they can wait and have surgery at around one year of age; if saturations are less than 75% with significant failure to thrive, they should come for surgery at any age or weight. On late presenters: we are also a resource-limited country — four or five surgeons doing this work for half of India — and face the same problem of kids coming late every day. My suggestion is education programmes, including pulse oximeter screening at birth, 1 month, and 6 months, referring for an echo early if abnormal. Late-presenting PDAs and cyanotic conditions apart from TGA are usually still operable, even if at slightly higher risk, but VSD shunt lesions can become inoperable if too late — however, even when a kid looks clinically inoperable, we always offer a cardiac catheterisation to confirm, since a significant proportion will still turn out to be operable, if high risk. And even an inoperable VSD child, with good, appropriately timed medical management (diuretics, pulmonary vasodilators), can still survive 25–35 years, whereas without that care they will die much earlier.

See all 2 questions from this masterclass →

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Frequently Asked Questions

What is the average cost of ASD closure?

Approximately 5,500 USD.

What is the correct timing for a patient with transposition of the great arteries (TGA), VSD, and LVOT obstruction? Also, since we live in a resource-limited country where diagnosis is sometimes made late, and patients may then ask for treatment abroad after a late diagnosis, what is your recommendation for handling late presenters, especially with simple shunt lesions?

For TGA with VSD and LVOT obstruction, these kids essentially have pulmonary stenosis with a VSD, and timing depends on the kid's oxygen saturation — they will need a Rastelli or a Nikaidoh operation, both requiring an implant, and the intent is to give the biggest implant possible since a smaller implant means an earlier return for a change. If saturations are above 75% and the kid is growing and doing well, they can wait and have surgery at around one year of age; if saturations are less than 75% with significant failure to thrive, they should come for surgery at any age or weight. On late presenters: we are also a resource-limited country — four or five surgeons doing this work for half of India — and face the same problem of kids coming late every day. My suggestion is education programmes, including pulse oximeter screening at birth, 1 month, and 6 months, referring for an echo early if abnormal. Late-presenting PDAs and cyanotic conditions apart from TGA are usually still operable, even if at slightly higher risk, but VSD shunt lesions can become inoperable if too late — however, even when a kid looks clinically inoperable, we always offer a cardiac catheterisation to confirm, since a significant proportion will still turn out to be operable, if high risk. And even an inoperable VSD child, with good, appropriately timed medical management (diuretics, pulmonary vasodilators), can still survive 25–35 years, whereas without that care they will die much earlier.

Does a child need to reach a certain age or weight before congenital heart surgery is possible?

No. This is a common misunderstanding in India as well as the US, Europe, and the Middle East. Surgical mortality may appear lower in an older, bigger child, but that comparison never counts the children who die during the waiting period. The right approach is to base timing on the natural history of each specific heart condition, weighing the risk of waiting against the risk of surgery.

What determines the correct timing for congenital heart surgery?

Timing is decided by the natural history of the specific heart condition, meaning how quickly it is likely to cause death or serious harm if left untreated, rather than by a fixed rule about the child's age or weight.

Which congenital heart condition is the one exception where waiting is the right approach?

An atrial septal defect. It is the one heart condition in this series where waiting, until the child is around 3 to 4 years old, is genuinely the correct strategy rather than a compromise.

Which congenital heart conditions require treatment within the first year of life?

Most conditions covered in this series, including transposition of the great arteries, patent ductus arteriosus with symptoms, coarctation of the aorta, truncus arteriosus, and complex conditions involving pulmonary stenosis, need treatment at diagnosis or within the first year of life. Delaying surgery in these cases raises the risk of the child becoming inoperable or dying while waiting.

Who leads the paediatric cardiac programme behind this masterclass series?

Dr. Aseem R. Srivastava, Chief of Paediatric CTVS and Adult Congenital Heart Diseases at Artemis Hospitals, Gurgaon, who shared this breakdown of surgical timing during a Jivo Masterclass session.

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