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Published in: Annals of Hematology 10/2009

01-10-2009 | Original Article

Stroke prevention in the young child with sickle cell anaemia

Authors: Lara Roberts, Sandra O’Driscoll, Moira C. Dick, Sue E. Height, Colin Deane, David E. Goss, Keith Pohl, David C. Rees

Published in: Annals of Hematology | Issue 10/2009

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Abstract

Cerebrovascular disease resulting in stroke is a serious and preventable complication of sickle cell anaemia (SCA). Children at high risk of preventable stroke can be identified by transcranial Doppler ultrasound (TCD). Current guidelines in the UK recommend annual TCD screening from 3 years, although studies suggest an earlier peak incidence, between 2 and 5 years. A single centre retrospective review was undertaken to identify the prevalence of stroke and success of TCD screening in young children. We report five episodes of stroke in under 3s and outcome of TCD screening in children under 3, compared to over 3. TCD analysis was as successful in the 2–3-year age group as in the 3–4-year group. We therefore propose that all children with SCA should be offered TCD screening from the age of 2 years. Furthermore, infants with high risk features of SCA should undergo a first attempt at TCD screening even earlier.
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Metadata
Title
Stroke prevention in the young child with sickle cell anaemia
Authors
Lara Roberts
Sandra O’Driscoll
Moira C. Dick
Sue E. Height
Colin Deane
David E. Goss
Keith Pohl
David C. Rees
Publication date
01-10-2009
Publisher
Springer-Verlag
Published in
Annals of Hematology / Issue 10/2009
Print ISSN: 0939-5555
Electronic ISSN: 1432-0584
DOI
https://doi.org/10.1007/s00277-009-0757-z

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