Transcranial Doppler Screening in a Regional Care Network for Sickle Cell Disease in the United Kingdom

Paul Telfer1, Kerry Dwan, Andrea Simmons

  • 1*Center for Genomics and Child Health, Barts and The London School of Medicine, London †Liverpool Reviews and Implementation Group, University of Liverpool, Liverpool Departments of ‡Pediatrics §Neuroradiology, Royal London Hospital, Barts Health NHS Trust, London ∥Department of Pediatrics, Newham University Hospital, Barts Health NHS Trust, London ¶Newham Sickle Cell and Thalassemia Community Centre, London #Department of Pediatrics, Whipps Cross University Hospital, Barts Health NHS Trust, London **Department of Pediatrics, Basildon University Hospital NHS Trust, Basildon, Essex ††Department of Hematology, Queens Hospital, Romford NHS Trust, Romford, Essex, UK.

Insights

Transcranial Doppler ultrasound screening identifies a higher proportion of children at high risk for stroke than previously estimated. This screening can help identify children who may benefit from early intervention to prevent acute ischemic stroke.

Area of Science:

  • Pediatric Neurology
  • Neuroimaging
  • Cerebrovascular Disease

Background:

  • The prevalence and risk of stroke in children undergoing transcranial Doppler (TCD) ultrasound screening in the UK remain largely unknown.
  • Previous stroke risk assessment protocols may not fully capture the spectrum of risk in pediatric populations.
  • Accurate identification of high-risk children is crucial for timely intervention and stroke prevention.

Purpose of the Study:

  • To evaluate a clinician-led TCD ultrasound screening program in children using a modified STOP protocol.
  • To determine the proportion of children classified as high-risk for stroke based on specific velocity criteria.
  • To estimate the incidence of acute ischemic stroke (AIS) and acute hemorrhagic stroke in the screened cohort.

Main Methods:

  • A cohort of 542 children underwent 1653 TCD ultrasound scans over 2235 patient-years.
  • A modified STOP protocol was used for risk assessment, including abnormal velocities in the anterior cerebral artery and specific criteria for high-risk classification.
  • Follow-up data were collected to identify stroke events.

Main Results:

  • Fifty-eight children (10.7%) were identified as high-risk, with a significant proportion having high abnormal velocities or prior conditional scans.
  • Abnormal velocities were occasionally restricted to the anterior cerebral artery.
  • The incidence rates for all stroke, AIS, and acute hemorrhagic stroke were 0.27, 0.18, and 0.09 per 100 patient-years, respectively. Approximately 2 children per 1000 screened developed AIS.

Conclusions:

  • The modified risk assessment identified a higher proportion of high-risk children compared to previous estimates.
  • TCD ultrasound screening, particularly in children under six, can identify a substantial number of high-risk individuals.
  • The findings support the utility of TCD ultrasound screening in pediatric stroke prevention, with a low incidence of AIS in the screened population.