Defining stroke risk in children with sickle cell anaemia
- 8 March 2005
- journal article
- review article
- Published by Wiley in British Journal of Haematology
- Vol. 128 (6) , 751-766
- https://doi.org/10.1111/j.1365-2141.2004.05310.x
Abstract
Summary: 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.Keywords
This publication has 122 references indexed in Scilit:
- Is Chlamydia pneumoniae Infection Associated With Stroke in Children With Sickle Cell Disease?Pediatrics, 2004
- Nocturnal hypoxaemia and central-nervous-system events in sickle-cell diseaseThe Lancet, 2001
- Effects of a long-term transfusion regimen on sickle cell-related illnessesThe Journal of Pediatrics, 1994
- Stroke in a cohort of patients with homozygous sickle cell diseaseThe Journal of Pediatrics, 1992
- Stroke in a Tertiary Hospital in Saudi Arabia: A Study of 372 CasesEuropean Neurology, 1991
- Cerebrovascular accidents in children with sickle-cell disease and alpha-thalassemiaThe Journal of Pediatrics, 1988
- Measurement of regional cerebral blood flow, blood volume and oxygen metabolism in patients with sickle cell disease using positron emission tomography.Stroke, 1986
- Neurological complications of sickle cell anemiaJournal of Pediatric Hematology/Oncology, 1982
- Moyamoya in children with sickle cell anemia and cerebrovascular occlusionThe Journal of Pediatrics, 1978
- Transfusion therapy for cerebrovascular abnormalities in sickle cell diseaseThe Journal of Pediatrics, 1976