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Updated: Feb 25, 2026

A Precision Medicine Tool for Measurement and Monitoring of Hemoglobin S in Sickle Cell Disease Patients Receiving Transfusion Therapy
How I manage sickle cell patients with high transcranial doppler results
John Brewin1, Banu Kaya2, Subarna Chakravorty3
1Department of Haematology, King's College London, London, UK.
Insights
Transcranial Doppler (TCD) effectively identifies stroke risk in children with sickle cell anaemia (SCA). TCD monitoring guides stroke prevention strategies, including transfusions or hydroxycarbamide therapy, improving patient outcomes.
Area of Science:
- Pediatric Hematology
- Neurology
- Medical Imaging
Background:
- Stroke is a severe complication in children with sickle cell anaemia (SCA).
- Transcranial Doppler (TCD) is a validated, non-invasive tool for assessing stroke risk.
- Current guidelines recommend TCD monitoring for stroke risk stratification in pediatric SCA patients.
Purpose of the Study:
- To outline an evidence-based algorithm for managing abnormal TCD velocities in children with SCA.
- To discuss the utility of TCD in primary stroke prevention and other clinical scenarios.
- To highlight the role of TCD in guiding therapeutic interventions for stroke risk reduction.
Main Methods:
- Review of randomized controlled trials demonstrating TCD efficacy in stroke risk stratification.
- Analysis of resource allocation for TCD monitoring programs.
- Discussion of alternative therapies like hydroxycarbamide and the need for frequent TCD follow-up.
Main Results:
- Chronic transfusion therapy is effective for stroke prevention based on TCD risk stratification.
- Hydroxycarbamide therapy can replace transfusions in select patients with careful TCD monitoring.
- TCD plays a crucial role in managing abnormal velocities and guiding treatment decisions.
Conclusions:
- TCD monitoring is essential for stroke risk assessment and prevention in children with SCA.
- An evidence-based algorithm can optimize the management of abnormal TCD findings.
- TCD has broader applications, including in Haemoglobin SC disease management.
Abstract:
Stroke is one of the most severe complications to affect children with sickle cell anaemia (SCA). Transcranial doppler (TCD) is an accurate and non-invasive method to determine stroke risk. Randomised controlled trials have demonstrated the efficacy of chronic transfusion therapy in stroke prevention based on risk stratification determined by TCD velocities. This has led to the regular use of TCD monitoring for children with SCA in order to determine stroke risk. Significant resource allocation is necessary to facilitate training, quality assurance and failsafe arrangements for non-attenders. In a subgroup of patients, chronic transfusions for primary stroke prevention can be replaced by hydroxycarbamide therapy, provided careful monitoring is undertaken; including repeat TCD studies at frequent intervals. The authors propose an evidence-based algorithm for the management of abnormal TCD velocities and discuss the role of this test in other clinical contexts, such as in Haemoglobin SC disease.
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