Literature DB >> 21700785

Sickle cell disease: reference values and interhemispheric differences of nonimaging transcranial Doppler blood flow parameters.

M Arkuszewski1, J Krejza, R Chen, J L Kwiatkowski, R Ichord, R Zimmerman, K Ohene-Frempong, L Desiderio, E R Melhem.   

Abstract

BACKGROUND AND
PURPOSE: TCD screening is widely used to identify children with SCD at high risk of stroke. Those with high mean flow velocities in major brain arteries have increased risk of stroke. Thus, our aim was to establish reference values of interhemispheric differences and ratios of blood flow Doppler parameters in the tICA, MCA, and ACA as determined by conventional TCD in children with sickle cell anemia.
MATERIALS AND METHODS: Reference limits of blood flow parameters were established on the basis of a consecutive cohort of 56 children (mean age, 100 ± 40 months; range, 29-180 months; 30 females) free of neurologic deficits and intracranial stenosis detectable by MRA, with blood flow velocities <170 cm/s by conventional TCD. Reference limits were estimated by using tolerance intervals, within which are included with a probability of .90 of all possible data values from 95% of a population.
RESULTS: Average peak systolic velocities were significantly higher in the right hemisphere in the MCA and ACA (185 ± 28 cm/s versus 179 ± 27 and 152 ± 30 cm/s versus 143 ± 34 cm/s respectively). Reference limits for left-to-right differences in the mean flow velocities were the following: -43 to 33 cm/s for the MCA; -49 to 38 cm/s for the ACA, and -38 to 34 cm/s for the tICA, respectively. Respective reference limits for left-to-right velocity ratios were the following: 0.72 to 1.25 cm/s for the MCA; 0.62 to 1.39 cm/s for the ACA, and 0.69 to 1.27 cm/s for the tICA. Flow velocities in major arteries were inversely related to age and Hct or Hgb.
CONCLUSIONS: The study provides reference intervals of TCD flow velocities and their interhemispheric differences and ratios that may be helpful in identification of intracranial arterial stenosis in children with SCD undergoing sonographic screening for stroke prevention.

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Mesh:

Year:  2011        PMID: 21700785      PMCID: PMC7964337          DOI: 10.3174/ajnr.A2529

Source DB:  PubMed          Journal:  AJNR Am J Neuroradiol        ISSN: 0195-6108            Impact factor:   3.825


  42 in total

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Authors:  J Krejza; Z Mariak; E R Melhem; R J Bert
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Review 2.  Reference intervals: an update.

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5.  Fundamental importance of arterial oxygen content in the regulation of cerebral blood flow in man.

Authors:  M M Brown; J P Wade; J Marshall
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6.  Cell-free hemoglobin limits nitric oxide bioavailability in sickle-cell disease.

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7.  Long-term stroke risk in children with sickle cell disease screened with transcranial Doppler.

Authors:  R J Adams; V C McKie; E M Carl; F T Nichols; R Perry; K Brock; K McKie; R Figueroa; M Litaker; S Weiner; D Brambilla
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8.  The natural history of conditional transcranial Doppler flow velocities in children with sickle cell anaemia.

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9.  Cerebral hyperemia, stroke, and transfusion in sickle cell disease.

Authors:  I Prohovnik; S G Pavlakis; S Piomelli; J Bello; J P Mohr; S Hilal; D C De Vivo
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2.  Age-Related Changes of Normal Cerebral and Cardiac Blood Flow in Children and Adults Aged 7 Months to 61 Years.

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Journal:  J Am Heart Assoc       Date:  2016-01-04       Impact factor: 5.501

3.  Implementation of a Process for Initial Transcranial Doppler Ultrasonography in Children With Sickle Cell Anemia.

Authors:  Lori E Crosby; Naomi E Joffe; Blair Davis; Charles T Quinn; Lisa Shook; Darice Morgan; Kenya Simmons; Karen A Kalinyak
Journal:  Am J Prev Med       Date:  2016-07       Impact factor: 5.043

4.  The significance of inadequate transcranial Doppler studies in children with sickle cell disease.

Authors:  Simon Greenwood; Colin Deane; Oliver L Rees; Ben Freedman; Suresh Kumar; Naser Ben Ramadan; Sarah Wilkinson; Grant Marais; Julie Lord; Subarna Chakravorty; Susan E Height; Kate Gardner; David C Rees
Journal:  PLoS One       Date:  2017-07-25       Impact factor: 3.240

5.  MRI detection of brain abnormality in sickle cell disease.

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  5 in total

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