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Stroke prevention in the young child with sickle cell anaemia
Lara Roberts1, Sandra O'Driscoll, Moira C Dick
1Department of Paediatric Haematology, Kings College Hospital, Denmark Hill, London, SE5 9RS, UK.
Insights
Sickle cell anaemia (SCA) stroke risk is high in young children. Earlier transcranial Doppler (TCD) screening from age 2 can identify high-risk children, preventing strokes.
Area of Science:
- Pediatric Neurology
- Hematology
- Vascular Medicine
Background:
- Cerebrovascular disease and stroke are significant risks for children with sickle cell anaemia (SCA).
- Transcranial Doppler (TCD) ultrasound is effective in identifying children at high risk for stroke.
- Current UK guidelines recommend annual TCD screening starting at age 3, despite evidence of earlier stroke incidence.
Observation:
- A retrospective review analyzed stroke prevalence and TCD screening success in young children with SCA.
- Five stroke events were identified in children under 3 years old.
- TCD analysis proved equally successful in the 2-3 year age group compared to the 3-4 year group.
Findings:
- Stroke incidence peaks between ages 2 and 5 years, suggesting current screening ages may be too late.
- TCD screening is technically feasible and successful in children as young as 2 years old.
- Early TCD screening in children under 3 with SCA can detect stroke risks effectively.
Implications:
- Screening for stroke risk in children with SCA should commence earlier, at age 2 years.
- Infants with high-risk features of SCA may benefit from even earlier TCD screening attempts.
- Implementing earlier TCD screening can lead to timely interventions and stroke prevention in pediatric SCA patients.
Abstract:
Cerebrovascular disease resulting in stroke is a serious and preventable complication of sickle cell anaemia (SCA). Children at high risk of preventable stroke can be identified by transcranial Doppler ultrasound (TCD). Current guidelines in the UK recommend annual TCD screening from 3 years, although studies suggest an earlier peak incidence, between 2 and 5 years. A single centre retrospective review was undertaken to identify the prevalence of stroke and success of TCD screening in young children. We report five episodes of stroke in under 3s and outcome of TCD screening in children under 3, compared to over 3. TCD analysis was as successful in the 2-3-year age group as in the 3-4-year group. We therefore propose that all children with SCA should be offered TCD screening from the age of 2 years. Furthermore, infants with high risk features of SCA should undergo a first attempt at TCD screening even earlier.
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