Purpose:To establish reference values of the ratios of flow velocity in the middle cerebral artery (V MCA ) and the terminal portion of the internal carotid artery (V tICA ) to flow velocity in the extracranial portion of internal carotid artery (V ICA ) in children with sickle cell disease (SCD).
Materials and Methods:Institutional ethics committee approval and parental informed consent were obtained for this prospective HIPAAcompliant study. Sixty-eight children (38 female; mean age, 7.7 years Ϯ 3.3; range, 2-14 years) with HbSS genotype, without neurologic deficits and no history of stroke, were enrolled. Final study population comprised 56 (mean age 8.0 Ϯ 3.3 years, 26 females) children who underwent magnetic resonance (MR) angiography, which excluded intracranial arterial narrowing, transcranial color-coded duplex ultrasonography (US), and carotid US to determine V MCA /V ICA and V tICA /V ICA ratios from angle-corrected and uncorrected velocities. Tolerance interval estimates were used to calculate reference ranges and linear regression was used to quantify associations of Doppler parameters with age adjusted for hemoglobin and hematocrit.
Results:Reference ranges in centimeters per second for mean angle-corrected V MCA on the left and right sides were 62-198 and 69 -153; those for V tICA were 30 -196 and 36 -175; and those for V ICA were 18 -116 and 15-95, respectively. Reference ranges for mean angle-corrected V MCA /V ICA ratio on the left and right sides were 1.2-4.0 and 0.4 -3.4 and those for V tICA /V ICA ratio were 0.5-2.9 and 0.5-2.7, respectively. V MCA , V tICA , and V tICA /V ICA ratio were not age dependent, contrary to V ICA and V MCA /V ICA ratio, after controlling for hematocrit and hemoglobin.
Conclusion:The study provides reference limits for V MCA , V tICA , V ICA , and velocity ratios obtained from children with SCD. Note: This copy is for your personal, non-commercial use only. To order presentation-ready copies for distribution to your colleagues or clients, use the Radiology Reprints form at the end of this article.
Children with sickle cell disease (SCD) who develop intracranial arterial narrowing are at high risk of stroke (1). Transcranial Doppler ultrasonography (US) is a noninvasive method extensively used to detect narrowing based on flow velocity thresholds (1,2). Chronic transfusions can substantially reduce the risk of stroke in children with high velocities at transcranial Doppler US (1), yet even 70% of patients with high velocity who do not undergo transfusions do not develop stroke (3). Chronic transfusions are costly and associated with substantial morbidity and some mortality from transfusion-related infections, alloimmunization, and hemosiderosis (4,5). Children with high hyperemic velocity due to anemia may not have the same benefits from the transfusion therapy as those with arterial narrowing. Transcranial Doppler US screening should be improved since currently more patients may be exposed to substantial risk than the number that benefit from transfusion.False-po...