Literature DB >> 15755278

Defining stroke risk in children with sickle cell anaemia.

Carolyn Hoppe1.   

Abstract

Sickle cell anaemia (SCA) is the most common cause of childhood stroke, occurring with the highest frequency before the age of 6 years. Despite the relative frequency of stroke in SCA, few predictors of risk exist. Anaemia, leucocytosis, hypertension, silent infarction, and history of acute chest syndrome are well-documented risk factors for ischaemic stroke in SCA. Recent data suggest that other environmental and genetic factors, many unrelated to SCA, influence the development of cerebrovascular disease. Non-invasive assessment of individual stroke risk using transcranial Doppler ultrasonography has provided a means of selecting and prophylactically treating SCA children at highest risk. With the ultimate goal of preventing stroke, the information gained from the studies reviewed here may lead to improved prediction of stroke so that clinical trials to assess risk-based therapy may be carried out on selected children with SCA.

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Year:  2005        PMID: 15755278     DOI: 10.1111/j.1365-2141.2004.05310.x

Source DB:  PubMed          Journal:  Br J Haematol        ISSN: 0007-1048            Impact factor:   6.998


  8 in total

1.  Frequent red cell transfusions reduced vascular endothelial activation and thrombogenicity in children with sickle cell anemia and high stroke risk.

Authors:  Hyacinth I Hyacinth; Robert J Adams; Jenifer H Voeks; Jacqueline M Hibbert; Beatrice E Gee
Journal:  Am J Hematol       Date:  2013-11-28       Impact factor: 10.047

2.  White matter has impaired resting oxygen delivery in sickle cell patients.

Authors:  Yaqiong Chai; Adam M Bush; Julie Coloigner; Aart J Nederveen; Benita Tamrazi; Chau Vu; Soyoung Choi; Thomas D Coates; Natasha Lepore; John C Wood
Journal:  Am J Hematol       Date:  2019-02-21       Impact factor: 10.047

3.  Stroke Prevention Trial in Sickle Cell Anemia (STOP): extended follow-up and final results.

Authors:  Margaret T Lee; Sergio Piomelli; Suzanne Granger; Scott T Miller; Shannon Harkness; Donald J Brambilla; Robert J Adams
Journal:  Blood       Date:  2006-08-01       Impact factor: 22.113

4.  Abnormal transcranial Döppler ultrasonography in children with sickle cell disease.

Authors:  Ana Claudia Celestino Bezerra Leite; Raquel Vasconcellos Carvalhaes de Oliveira; Patrícia Gomes de Moura; Célia Maria Silva; Clarisse Lobo
Journal:  Rev Bras Hematol Hemoter       Date:  2012

5.  Morphological and functional platelet abnormalities in Berkeley sickle cell mice.

Authors:  Arun S Shet; Thomas J Hoffmann; Marketa Jirouskova; Christin A Janczak; Jacqueline R M Stevens; Adewole Adamson; Narla Mohandas; Elizabeth A Manci; Therese Cynober; Barry S Coller
Journal:  Blood Cells Mol Dis       Date:  2008-04-18       Impact factor: 3.039

6.  Association of laboratory markers and cerebral blood flow among sickle cell anemia children.

Authors:  Corynne Stéphanie Ahouéfa Adanho; Sètondji Cocou Modeste Alexandre Yahouédéhou; Sânzio Silva Santana; Camilo Vieira; Rayra Pereira Santiago; Jeanne Machado de Santana; Thassila Nogueira Pitanga; Milena Magalhães Aleluia; Vítor Valério Maffili; Ivana Paula Ribeiro Leite; Dalila Luciola Zanette; Isa Menezes Lyra; Marilda Souza Goncalves
Journal:  Front Pediatr       Date:  2022-08-26       Impact factor: 3.569

7.  Primary stroke prevention for sickle cell disease in north-east Italy: the role of ethnic issues in establishing a Transcranial Doppler screening program.

Authors:  Raffaella Colombatti; Giorgio Meneghetti; Mario Ermani; Marta Pierobon; Laura Sainati
Journal:  Ital J Pediatr       Date:  2009-06-22       Impact factor: 2.638

Review 8.  Prevalence of Stroke in Asian Patients with Sickle Cell Anemia: A Systematic Review and Meta-Analysis.

Authors:  Sandip Kuikel; Robin Rauniyar; Sanjeev Kharel; Anil Bist; Subarna Giri; Sahil Thapaliya; Sunanda Paudel
Journal:  Neurol Res Int       Date:  2021-06-03
  8 in total

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