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CHAPTER 47 Doppler Sonography of the Brain in Children 1599

Cerebrovascular Disease: Indicators in

Children With Sickle Cell Disease 66,67

Maximum velocity, OA ≥ 35 cm/sec

TAMM velocity, MCA ≥ 170 cm/sec

RI in OA ≤ 0.6

Velocity in OA greater than velocity in ipsilateral MCA

Maximum velocity in PCA, vertebral, or basilar arteries

greater than or equal to MCA velocity

Turbulence

Visualization of PCA or ACA without visualization of MCA

Any RI < 0.3

Maximum MCA PSV ≥ 200 cm/sec

A

ACA, Anterior cerebral artery; MCA, middle cerebral artery; OA,

ophthalmic artery; PCA, posterior cerebral artery; PSV, peak systolic

velocity; RI, resistive index, TAMM, time-averaged mean of the

maximum.

Data from Seibert JJ, Miller SF, Kirby RS, et al. Cerebrovascular

disease in symptomatic and asymptomatic patients with sickle cell

anemia: screening with duplex transcranial Doppler US—correlation

with MR imaging and MR angiography. Radiology. 1993;189(2):457-

466 66 ; Seibert JJ, Glasier CM, Kirby RS, et al. Transcranial Doppler,

MRA, and MRI as a screening examination for cerebrovascular

disease in patients with sickle cell anemia: an 8-year study. Pediatr

Radiol. 1998;28(3):138-142. 67

B

FIG. 47.5 Abnormal Ophthalmic Artery (OA) Flow in 16-Year-Old

Boy With Sickle Cell Disease. Patient had his irst left cerebrovascular

accident (CVA, stroke) at age 7 years. Spectral Doppler ultrasound

waveforms through the eye show increased diastolic low in both OAs.

(A) Increased velocity in the right OA with maximum velocity of 66 cm/

sec; (B) reversed low in the left OA.

Siegel et al. 68 compared transtemporal TCD to neurologic

examination and also found a maximum low in the MCA of

more than 200 cm/sec or less than 100 cm/sec (including no

low) as signiicant for disease. Verlhac et al. 63 studied SCD with

duplex Doppler imaging with a 3-MHz transducer transtemporally

and suboccipitally, as well as with MRA and MRI. Arteriography

was performed in patients with suspected stenosis on TCD

sonography. hey found that patients with a mean velocity greater

than 190 cm/sec had stenosis on arteriography. Kogutt et al. 69

evaluated symptomatic SCD patients and found 91% sensitivity

and 22% speciicity of TCD using MRA as the reference standard.

Abnormal TCD values were (1) maximum and mean velocity

(V max and V mean ) greater than 2 standard deviations (SD) from

normal values reported by Adams et al. 65,70 in SCD: V max MCA

> 168 ± −38 cm/sec and V mean MCA 115 ± −31 cm/sec, and V max

ACA 138 ± 34 cm/sec and V mean ACA 94 ± 28 cm/sec; (2) RI <

0.40; and (3) V max MCA < V max ACA (Fig. 47.12).

Screening sickle cell patients with the nonimaging pulsed

Doppler ultrasound technique involves scanning the patient

transtemporally to evaluate the MCA, bifurcation, DICA, ACA,

and PCA. he OA can be evaluated through the orbit. he basilar

and vertebral arteries can be evaluated from the occipital approach.

he PSV, EDV, TAMM velocity, and RI of each of these vessels

should be measured at least twice to obtain the most accurate

measurement. 71 he MCA should be tracked from the peripheral

branch to the bifurcation with velocities obtained every 2 mm.

Optimizing the tracing is crucial in identifying regions of stenosis.

72 Color Doppler low imaging (TCDI) can also be used

to screen SCD patients. his technique is faster to learn, allows

for quicker vessel identiication, and improves gate placement.

Because image-based probes tend to be larger than nonimaging

probes, however, optimizing the tracing may be more diicult

and can result in slightly lower velocities than those obtained

by nonimaging methods. 20,21

he Stroke Prevention Trial in Sickle Cell Anemia (STOP)

study led by Robert Adams showed that regular transfusion of

children at risk for stroke (based on Doppler sonography) could

prevent CVA. 19,72-75 Adams studied children age 2 to 16 years,

from 14 medical centers, who had MCA mean velocities higher

than 200 cm/sec and were at risk of developing stroke. Half

received blood transfusions every 3 to 4 weeks, enough to lower

sickle cell hemoglobin to below 30%. Ater 1 year, the transfusions

Text continued on p. 1604.

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