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Neurology Research Programs: Stroke Research In Sickle Cell Disease
   
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Stop StudySTOP Study

In 1997, the Stroke Prevention Trial in Sickle Cell Anemia (STOP) proved that transcranial Doppler (TCD) ultrasound screening and chronic transfusion could reduce the annual incidence of first clinical stroke in high-risk children from about 10% per year to about 1% per year. This led to recommendations for TCD screening of all children with sickle cell disease (SCD) and transfusions for those with abnormal TCD velocities. In this study led by the Medical College of Georgia and New England Research Institutes, 130 children ages 2-16 were randomly assigned to receive either transfusions or standard care. The National Heart, Lung, and Blood Institute funded the study

Children with time-averaged maximum mean (TAMM) velocities of 200 cm/sec or higher in the middle cerebral artery (MCA) or distal internal carotid artery (dICA) were eligible for the study. These blood vessels were chosen because blockage of the MCA and dICA is the most frequent cause of brain infarction in these patients.

If a clinic were following 200 children with SCD without stroke, about one child would have a stroke each year. This is a 0.5% incidence rate. Transfusing all 200 patients could prevent the first stroke, but this would not be an optimal use of resources. With the STOP strategy, about 10 patients are treated each year to prevent one stroke. Better prediction methods could further reduce the number of patients needing to be treated to prevent the first stroke.

   
  © 2003 MCG

Questions and Comments to Bill Hamilton 


  February 02, 2004


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