Transcranial Doppler Screening in a Current Cohort of Children With Sickle Cell Anemia: Results From the DISPLACE

Julie Kanter1, Shannon Phillips2, Alyssa M Schlenz3

  • 1Division of Hematology and Oncology, University of Alabama Birmingham, Birmingham, AL.

Insights

Stroke prevention guidelines recommend transcranial Doppler (TCD) for children with sickle cell anemia (SCA), but implementation is poor. This study found low TCD screening rates, highlighting a critical gap in stroke risk identification for SCA patients.

Area of Science:

  • Pediatric Hematology
  • Neurology
  • Public Health

Background:

  • Stroke is a major complication in sickle cell anemia (SCA).
  • Transcranial Doppler (TCD) screening identifies children at high risk for stroke.
  • Current TCD screening implementation in SCA is suboptimal.

Purpose of the Study:

  • To assess baseline TCD screening implementation rates in a large cohort of children with SCA.
  • To identify factors influencing TCD implementation and report TCD results.
  • To inform strategies for improving stroke prevention in SCA.

Main Methods:

  • Analysis of data from Part 1 of the DISPLACE study, a 28-site assessment.
  • Inclusion of 5116 children with SCA eligible for TCD assessment.
  • Evaluation of TCD screening rates, characteristics, and results by age and site demographics.

Main Results:

  • Overall TCD screening rates were unsatisfactory, averaging 49.9% across sites.
  • Screening rates varied by region but were independent of site characteristics.
  • An abnormal TCD rate of 2.9% was observed, with a median age of 6.3 years for the first abnormal result.

Conclusions:

  • Real-world TCD screening practices for SCA patients show significant implementation gaps.
  • Findings from this large cohort provide critical data for improving stroke screening protocols.
  • The results underscore the need for enhanced clinical practice to improve stroke prevention in children with SCA.