Literature DB >> 2146901

Cerebral vessel stenosis in sickle cell disease: criteria for detection by transcranial Doppler.

R J Adams1, F T Nichols, R Aaslid, V C McKie, K McKie, E Carl, S Stephens, W O Thompson, P Milner, R Figueroa.   

Abstract

Ischemic stroke is a common and disabling complication of sickle cell disease (Hb SS). Most infarctions occur in the presence of intracranial stenotic lesions of the large vessels of the circle of Willis. Transcranial Doppler (TCD), by measuring flow velocity in these arterial segments, can detect focal stenosis on the basis of elevated flow velocity. We report the preliminary results of a prospective study to develop criteria for detection of stenotic lesions based on TCD and identification of patients with Hb SS at risk for stroke. Comparing the TCD findings from six patients with lesions demonstrated by angiography to those from 115 Hb SS children without stroke, we conclude: (a) middle cerebral (MCA), anterior cerebral (ACA), or internal carotid (ICA) artery mean velocities greater than 190 cm/s strongly suggest focal stenosis; (b) MCA or ACA mean velocities of 150 to 190 cm/s suggest abnormality but at present cannot be considered diagnostic of stenosis; (c) mean velocities up to 150 cm/s are possibly due to the effects of low hematocrit and/or young age, and cannot as yet be distinguished from velocity elevations due to vessel stenosis.

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Year:  1990        PMID: 2146901     DOI: 10.1097/00043426-199023000-00005

Source DB:  PubMed          Journal:  Am J Pediatr Hematol Oncol        ISSN: 0192-8562


  8 in total

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Review 2.  Screening children for sickle cell vasculopathy: guidelines for transcranial Doppler evaluation.

Authors:  Dorothy Bulas
Journal:  Pediatr Radiol       Date:  2005-02-10

3.  Lower Transcranial Doppler Flow Velocities in Sickle Cell Anemia Patients on Hydroxyurea: Myth or Fact.

Authors:  Sawsan M Moeen; Ahmad F Thabet; Hosam A Hasan; Medhat A Saleh
Journal:  Indian J Hematol Blood Transfus       Date:  2017-04-08       Impact factor: 0.900

4.  Original Research: Sickle cell anemia and pediatric strokes: Computational fluid dynamics analysis in the middle cerebral artery.

Authors:  Christian P Rivera; Alessandro Veneziani; Russell E Ware; Manu O Platt
Journal:  Exp Biol Med (Maywood)       Date:  2016-03-04

5.  Simple chronic transfusion therapy, a crucial therapeutic option for sickle cell disease, improves but does not normalize blood rheology: What should be our goals for transfusion therapy?

Authors:  Jon A Detterich
Journal:  Clin Hemorheol Microcirc       Date:  2018       Impact factor: 2.375

6.  Effects of age, gender, and hemisphere on cerebrovascular hemodynamics in children and young adults: Developmental scores and machine learning classifiers.

Authors:  Marie Arsalidou; Nikolay Skuratov; Evgeny Khalezov; Alexander Bernstein; Evgeny Burnaev; Maxim Sharaev
Journal:  PLoS One       Date:  2022-02-04       Impact factor: 3.240

7.  Risk factors for high cerebral blood flow velocity and death in Kenyan children with Sickle Cell Anaemia: role of haemoglobin oxygen saturation and febrile illness.

Authors:  Julie Makani; Fenella J Kirkham; Albert Komba; Tolulope Ajala-Agbo; Godfrey Otieno; Gregory Fegan; Thomas N Williams; Kevin Marsh; Charles R Newton
Journal:  Br J Haematol       Date:  2009-03-27       Impact factor: 6.998

8.  Haptoglobin, alpha-thalassaemia and glucose-6-phosphate dehydrogenase polymorphisms and risk of abnormal transcranial Doppler among patients with sickle cell anaemia in Tanzania.

Authors:  Sharon E Cox; Julie Makani; Deogratias Soka; Veline S L'Esperence; Edward Kija; Paula Dominguez-Salas; Charles R J Newton; Anthony A Birch; Andrew M Prentice; Fenella J Kirkham
Journal:  Br J Haematol       Date:  2014-02-21       Impact factor: 6.998

  8 in total

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