Literature DB >> 15162093

Sickle cell disease: primary stroke prevention.

Mehari Gebreyohanns1, Robert J Adams.   

Abstract

Stroke is an important and common complication of sickle cell disease (SCD), affecting children as well as adults. Clinically evident stroke, usually brain infarction, is usually associated with stenosis or occlusion of the intracranial arteries of the Circle of Willis, sometimes with formation of moyamoya (a Japanese word for "hazy" or "like a puff of smoke" that describes the appearance of a abnormal microvasculature on angiography believed secondary to internal carotid artery stenosis or occlusion and the resultant extensive collateralization). Several types of intracranial hemorrhage are observed but usually in older children and adults. Cerebrovascular diseases restricted to small vessels may go unrecognized but is associated with cognitive and learning problems. Prevention of recurrent stroke has been accomplished with chronic blood transfusion. A primary prevention strategy for clinical stroke, based on the Stroke Prevention in Sickle Cell Anemia Trial, has been tested in a randomized clinical trial. Over 2,000 young children with SCD were screened with transcranial Doppler ultrasound (TCD) to detect elevated blood flow velocity indicative of vessel disease and high risk of future stroke. Those randomized to standard care (no transfusion) had a 10%/year risk of stroke, which was reduced >90% with chronic transfusion. This approach is the only primary stroke prevention strategy so far tested in SCD in a randomized controlled trial. Silent lesions on magnetic resonance imaging are associated with an approximately 1.5%/year risk of clinical stroke and a trial is now starting in children with these lesions who do not meet Stroke Prevention in Sickle Cell Anemia Trial criteria for transfusion based on TCD. A controlled trial, based on intervention for nocturnal hypoxemia, is also underway. Hydroxyurea, bone marrow transplantation, antiplatelet, and antithrombotic agents may work but have not been tested in primary prevention in a systematic way. If early and repeated, TCD screening of children, as recommended by National Heart Lung and Blood Institute and the American Stroke Association, were implemented broadly the incidence of new strokes could be greatly reduced in these children.

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Mesh:

Year:  2004        PMID: 15162093

Source DB:  PubMed          Journal:  CNS Spectr        ISSN: 1092-8529            Impact factor:   3.790


  11 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.  Time-resolved 3D quantitative flow MRI of the major intracranial vessels: initial experience and comparative evaluation at 1.5T and 3.0T in combination with parallel imaging.

Authors:  Roland Bammer; Thomas A Hope; Murat Aksoy; Marcus T Alley
Journal:  Magn Reson Med       Date:  2007-01       Impact factor: 4.668

3.  Current therapy of sickle cell disease.

Authors:  Zakari Y Aliyu; Ashaunta R Tumblin; Gregory J Kato
Journal:  Haematologica       Date:  2006-01       Impact factor: 9.941

4.  Tonsilectomy in sickle cell diseases.

Authors:  Mehmet Rami Helvaci; Cumali Gokce; Ramazan Davran; Can Acipayam; Seckin Akkucuk; Mustafa Ugur
Journal:  Int J Clin Exp Med       Date:  2015-03-15

5.  Sickle cell diseases and ileus.

Authors:  Mehmet Rami Helvaci; Akin Aydogan; Seckin Akkucuk; Cem Oruc; Mustafa Ugur
Journal:  Int J Clin Exp Med       Date:  2014-09-15

6.  Acute chest syndrome in severity of sickle cell diseases.

Authors:  Mehmet Rami Helvaci; Can Acipayam; Akin Aydogan; Seckin Akkucuk; Cem Oruc; Cumali Gokce
Journal:  Int J Clin Exp Med       Date:  2014-12-15

7.  Optimal disease management and health monitoring in adults with sickle cell disease.

Authors:  Jo Howard; Swee Lay Thein
Journal:  Hematology Am Soc Hematol Educ Program       Date:  2019-12-06

Review 8.  Prospects for primary stroke prevention in children with sickle cell anaemia.

Authors:  Lori C Jordan; James F Casella; Michael R DeBaun
Journal:  Br J Haematol       Date:  2012-01-09       Impact factor: 6.998

9.  Ischemic infarction following an intra-cerebral hemorrhage in an adult sickle cell disease with angiographic Moyamoya.

Authors:  Praveen Kumar Gupta; Krishnan Pudukode Ramnath; Prabha Ramadorai; Abdulla Alajmi; Janaki Sudhakar Praharaju
Journal:  J Thromb Thrombolysis       Date:  2007-06-01       Impact factor: 2.300

10.  Characterization of inpatient moyamoya in the United States: 1988-2004.

Authors:  Darrin J Lee; David S Liebeskind
Journal:  Front Neurol       Date:  2011-07-04       Impact factor: 4.003

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