HaematologyDr. Sukriti GuptaSickle Cell Disease

Senior Consultant, BMT, Haematology & Paediatric Haemato-Oncology, Artemis Hospitals, Gurugram

Part 11 of 11 in Diagnosis and Management of Sickle Cell Disease

Sickle Cell Disease in Pregnancy

November 9, 2025

Women with sickle cell disease who have generally done well and had infrequent pain crises up to childbearing age can and do become pregnant, but pregnancy in sickle cell disease still requires closer monitoring than a standard pregnancy, with visits to the obstetrician twice a month recommended through the third trimester.

Managing hydroxyurea and delivery planning

Hydroxyurea is generally held during pregnancy, since it is not considered safe for fetal development; good hydration and avoiding other stressful triggers are advised instead, alongside continued folic acid supplementation throughout. An elective caesarean section, typically planned at 36 to 37 weeks of gestation, is the preferred mode of delivery, minimising the additional stress that labour pain would add on top of the underlying disease. Betamethasone or dexamethasone is given beforehand to support fetal lung maturity, since delivery may need to happen earlier than planned if blood flow to the fetus becomes compromised at any point.

This article is based on a Jivo Masterclass session conducted by Dr. Sukriti Gupta, Senior Consultant, BMT, Haematology and Paediatric Haemato-Oncology, Artemis Hospitals, Gurugram. The article has been summarised with the assistance of an AI tool from the original masterclass recording. Watch the full Masterclass recording

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This guide is based on a live Jivo Masterclass — Dr. Sukriti Gupta taught doctors across Africa on November 9, 2025.

FROM THE LIVE Q&A

DR

Dr. Steven Cope (Cameroon)

For a positive diagnosis, is the hemoglobin S level the same across all countries?

SG

Dr. Sukriti Gupta

Patients carrying both sickle cell genes typically have a haemoglobin S level above 60%, and below that the manifestations are usually milder, seen more in sickle cell trait or a combination haemoglobinopathy such as HbSC or HbSE. There is a general tendency for higher HbS to mean more symptoms, but the correlation is not exact and cannot be relied on mathematically for any individual patient.

See all 9 questions from this masterclass →

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Frequently Asked Questions

What types of stroke are sickle cell patients most likely to suffer from, and how can it be prevented?

The middle and posterior cerebral artery territories are affected most commonly, similar to the pattern seen in adults, though the anterior territory can occasionally be involved too. Regular transcranial Doppler screening from two years of age is the key prevention tool: it uses ultrasound to measure blood flow velocity in the cerebral vessels and identifies children at higher risk of stroke early, so that preventive medication and closer monitoring can begin before a stroke actually happens.

What is your comment on the use of hydroxyurea in pregnancy, and what are the alternative options?

In pregnant women who have generally done well and had infrequent pain crises up to childbearing age, hydroxyurea is usually held during pregnancy since it is not a good option for fetal development. Good hydration and avoiding any other stressful conditions are advised instead, and folic acid supplementation must continue.

At what age do we commence hydroxyurea?

As early as the disease is detected, sometimes as young as two months of age.

What is the upper age limit for bone marrow transplant, and what are the cost implications for full match versus half match donors?

The best outcomes are under 16 years, 16 to 25 is still viable, and beyond 25 the risks rise and require much more detailed pre-transplant workup, including cardiac and kidney function assessment, though age is not always a fixed barrier if organ function is well preserved and the family is fully committed. A full-match sibling transplant typically costs around $24,000 to $25,000, rising for older patients closer to adult body weight, while a half-match or unrelated-donor transplant through a registry costs around $33,000 to $34,000, since registry and donor-related costs are higher even though complications are reduced.

In terms of treatment, how is gene therapy done, and is it possible for all patients?

Gene therapy uses the patient's own stem cells rather than a donor, mobilised and collected the same way as for a transplant, then modified in a laboratory using either a viral vector for gene addition or CRISPR-Cas9 editing to correct the underlying genetic change, a process that currently takes around six months. Because the cells being returned are the patient's own, recovery is generally faster than with a donor transplant, but the therapy currently has FDA approval only for patients aged 12 and older, and it remains expensive and not yet widely available outside the US, Europe and a handful of other countries.

Is hydroxyurea safe to continue during pregnancy for a woman with sickle cell disease?

No. Hydroxyurea is generally held during pregnancy since it is not considered safe for fetal development. Good hydration, avoiding stressful triggers and continued folic acid supplementation are advised instead.

What is the preferred mode of delivery for a woman with sickle cell disease?

An elective caesarean section, typically planned at 36 to 37 weeks of gestation, is preferred, since it avoids adding the stress of labour pain on top of the underlying disease and allows delivery to be moved earlier if needed.

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