DISPLACE study shows poor quality of transcranial doppler ultrasound for stroke risk screening in sickle cell anemia

Kimberly A Davidow1, Robin E Miller1, Shannon M Phillips2

  • 1Department of Pediatrics, Lisa Dean Moseley Foundation Institute for Cancer and Blood Disorders, Nemours Children's Hospital, Delaware, Wilmington, DE.

Blood Advances
|April 26, 2024
PubMed

Insights

Standardizing transcranial Doppler (TCD) reporting is crucial for accurately screening children with sickle cell anemia (SCA) for stroke risk. Inconsistent TCD measurements hinder effective stroke prevention, necessitating improved quality assurance and training.

Area of Science:

  • Neurology
  • Pediatrics
  • Medical Imaging

Background:

  • Children with sickle cell anemia (SCA) face a heightened risk of stroke compared to their peers.
  • The Stroke Prevention Trial in Sickle Cell Anemia (STOP) established that transcranial Doppler (TCD) screening and red blood cell transfusions significantly reduce stroke risk by over 90%.
  • Accurate measurement of time-averaged mean maximum velocity (TAMMV) is critical for TCD screening, but adherence to STOP criteria has been challenging.

Purpose of the Study:

  • To evaluate the quality and accuracy of transcranial Doppler (TCD) and transcranial Doppler imaging (TCDi) reports in the context of sickle cell anemia (SCA) stroke risk assessment.
  • To identify inconsistencies in TCD/TCDi reporting practices across different institutions.

Main Methods:

  • A subanalysis of the DISPLACE study involving over 12,000 TCD/TCDi reports from 28 institutions.
  • Detailed review of 391 TCD reports to assess reporting quality and adherence to established criteria.
  • Analysis of variations in assessed vessels, velocity thresholds for abnormal results, and interpreter qualifications.

Main Results:

  • Significant variability was observed in the cerebral vessels assessed and the velocities used to define abnormal TCD/TCDi results.
  • In 52% of reviewed reports, it was unclear if the time-averaged mean maximum velocity (TAMMV) was the measured parameter.
  • Only 42% of reports clearly indicated that TAMMV was used for the interpretation of the examination as normal or abnormal.

Conclusions:

  • There are substantial inconsistencies in TCD/TCDi reporting for sickle cell anemia (SCA) stroke screening.
  • Standardization of TCD/TCDi reporting, specialized training for personnel, and robust quality assurance measures are urgently recommended.
  • Implementing these improvements is essential to ensure the appropriate and effective use of TCD/TCDi for potentially life-saving stroke prevention in SCA patients.