Literature DB >> 8444244

Cerebrovascular accidents in sickle cell disease. Risk factors and blood transfusion influence. French Study Group on Sickle Cell Disease.

M de Montalembert1, P Beauvais, D Bachir, F Galacteros, R Girot.   

Abstract

This study presents a series of 34 sickle cell patients with one or more cerebrovascular accidents (CVA). Risk factors were studied in a subgroup of 19 patients whose clinical and biological characteristics were compared to those of a group of 444 sickle cell patients without CVA. The only risk factor discovered was a past history of purulent meningitis, which was significantly more frequent in sickle cell patients than in those without CVA (P < 0.0001). No biological or radiological factor affecting the risk of recurrence was found. The risk of recurrence, neurological defects or death after subsequent CVA justify long-term transfusion treatment in patients presenting with a second CVA. However our study shows that 10 patients who were not transfused after their first CVA had no recurrences, (median follow up = 7.9 years; 2-18 years), providing a basis for discussion on the indications of long-term transfusion therapy for sickle cell patients presenting with their first CVA.

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Year:  1993        PMID: 8444244     DOI: 10.1007/bf01956144

Source DB:  PubMed          Journal:  Eur J Pediatr        ISSN: 0340-6199            Impact factor:   3.183


  15 in total

1.  Recurrent cerebral ischemia during hypertransfusion therapy in sickle cell anemia.

Authors:  G R Buchanan; W P Bowman; S J Smith
Journal:  J Pediatr       Date:  1983-12       Impact factor: 4.406

2.  The natural history of stroke in sickle cell disease.

Authors:  D Powars; B Wilson; C Imbus; C Pegelow; J Allen
Journal:  Am J Med       Date:  1978-09       Impact factor: 4.965

3.  Commentary: sickle cell anemia, stroke, and transfusion.

Authors:  R A Seeler; J E Royal
Journal:  J Pediatr       Date:  1980-02       Impact factor: 4.406

4.  Cerebral blood flow in sickle cell cerebrovascular disease.

Authors:  P R Huttenlocher; J W Moohr; L Johns; F D Brown
Journal:  Pediatrics       Date:  1984-05       Impact factor: 7.124

5.  Sickle cell anemia and central nervous system infarction: a neuropathological study.

Authors:  S M Rothman; K H Fulling; J S Nelson
Journal:  Ann Neurol       Date:  1986-12       Impact factor: 10.422

6.  Effect of transfusion therapy on arteriographic abnormalities and on recurrence of stroke in sickle cell disease.

Authors:  M O Russell; H I Goldberg; A Hodson; H C Kim; J Halus; M Reivich; E Schwartz
Journal:  Blood       Date:  1984-01       Impact factor: 22.113

7.  Stroke associated with obstructive sleep apnea in a child with sickle cell anemia.

Authors:  P L Robertson; M S Aldrich; S M Hanash; G W Goldstein
Journal:  Ann Neurol       Date:  1988-06       Impact factor: 10.422

8.  Bone marrow transplantation in five children with sickle cell anaemia.

Authors:  C Vermylen; E Fernandez Robles; J Ninane; G Cornu
Journal:  Lancet       Date:  1988-06-25       Impact factor: 79.321

9.  High risk of recurrent stroke after discontinuance of five to twelve years of transfusion therapy in patients with sickle cell disease.

Authors:  W C Wang; E H Kovnar; I L Tonkin; R K Mulhern; J W Langston; S W Day; M J Schell; J A Wilimas
Journal:  J Pediatr       Date:  1991-03       Impact factor: 4.406

10.  Cerebral infarction in sickle cell anemia: mechanism based on CT and MRI.

Authors:  R J Adams; F T Nichols; V McKie; K McKie; P Milner; T E Gammal
Journal:  Neurology       Date:  1988-07       Impact factor: 9.910

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  3 in total

Review 1.  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

2.  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

Review 3.  Genetic, laboratory and clinical risk factors in the development of overt ischemic stroke in children with sickle cell disease.

Authors:  André Rolim Belisário; Célia Maria Silva; Cibele Velloso-Rodrigues; Marcos Borato Viana
Journal:  Hematol Transfus Cell Ther       Date:  2017-11-26
  3 in total

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