Cerebral infarcts and cerebrovascular disease in neurologically intact Tanzanian children with sickle cell anaemia
Cerebral infarcts and cerebrovascular disease in neurologically intact Tanzanian children with sickle cell anaemia
Introduction:Children and adolescents with sickle cell anemia (SCA) without history of neurological manifestations remain at risk of stroke and require cost effective screening as evidence-based stroke prevention interventions are developed. Although there are data on the prevalence of Transcranial Doppler (TCD) abnormality, there are relatively few studies on the prevalence of silent cerebral infarction (SCI) on magnetic resonance imaging (MRI) and vasculopathy on MR angiography (MRA), paricularly in Africa, where the burden of disease is greatest. In this study in Africa, we determined the prevalence of SCI on MRI and cerebral vasculopathy on MRA, and explored associations with age, sex, internal carotid/middle cerebral artery (ICA/MCA) and basilar cerebral blood flow velocities (CBFV) on TCD, and hematological variables.Patients and methods:We prospectively studied children with homozygous SCA (HbSS) without prior clinically overt stroke or TIA or seizures. Clinical information and blood for full blood count was collected for all patients. All were offered TCD using non-imaging equipment (Compumedics) and MRI and MRA of intracranial arteries on a Philips 1.5 Tesla scanner. MRA was graded as 1 Turbulence, 2 Stenosis, 3 Occlusion, 4 Occlusion with collaterals (moyamoya). Imaging was reviewed by 2 neuroradiologists (MJ and DS) and consensus was reached.Results:Within a period of 12 months, 395 children with SCA were recruited. Mean age was 12.7+/-4 (range 5-19 years); 199 (50.4%) were male. Mean hemoglobin was 7.6±1.1 (range 4.1-13.5) g/dl. 381 had TCD, of whom 227 (57%) have had brain MRI and MRA so far.Only 14/395 (3.5%) of patients had abnormal CBFV, 8 (2%) with maximum CBFV 200cm/sec).Prevalence of silent cerebral infarction was 29% (65/227) and was similar in males (30%; 34/114) and females (28%; 31/110) but was lower in children aged
1089-1089
Mwakatika, Mboka Mwakatika
0d273411-2ad5-46ff-a85d-4f4b91e220d2
Saunders, Dawn E
9d877417-e3ee-493d-9477-a66b47c3455d
Makani, Julie
76a145a7-02fc-43ea-a1df-3a52d2004e48
Kirkham, Fenella Jane
1dfbc0d5-aebe-4439-9fb2-dac6503bcd58
29 November 2018
Mwakatika, Mboka Mwakatika
0d273411-2ad5-46ff-a85d-4f4b91e220d2
Saunders, Dawn E
9d877417-e3ee-493d-9477-a66b47c3455d
Makani, Julie
76a145a7-02fc-43ea-a1df-3a52d2004e48
Kirkham, Fenella Jane
1dfbc0d5-aebe-4439-9fb2-dac6503bcd58
Mwakatika, Mboka Mwakatika, Saunders, Dawn E, Makani, Julie and Kirkham, Fenella Jane
(2018)
Cerebral infarcts and cerebrovascular disease in neurologically intact Tanzanian children with sickle cell anaemia.
Blood, 132 (Supplement 1), .
(doi:10.1182/blood-2018-99-119056).
Abstract
Introduction:Children and adolescents with sickle cell anemia (SCA) without history of neurological manifestations remain at risk of stroke and require cost effective screening as evidence-based stroke prevention interventions are developed. Although there are data on the prevalence of Transcranial Doppler (TCD) abnormality, there are relatively few studies on the prevalence of silent cerebral infarction (SCI) on magnetic resonance imaging (MRI) and vasculopathy on MR angiography (MRA), paricularly in Africa, where the burden of disease is greatest. In this study in Africa, we determined the prevalence of SCI on MRI and cerebral vasculopathy on MRA, and explored associations with age, sex, internal carotid/middle cerebral artery (ICA/MCA) and basilar cerebral blood flow velocities (CBFV) on TCD, and hematological variables.Patients and methods:We prospectively studied children with homozygous SCA (HbSS) without prior clinically overt stroke or TIA or seizures. Clinical information and blood for full blood count was collected for all patients. All were offered TCD using non-imaging equipment (Compumedics) and MRI and MRA of intracranial arteries on a Philips 1.5 Tesla scanner. MRA was graded as 1 Turbulence, 2 Stenosis, 3 Occlusion, 4 Occlusion with collaterals (moyamoya). Imaging was reviewed by 2 neuroradiologists (MJ and DS) and consensus was reached.Results:Within a period of 12 months, 395 children with SCA were recruited. Mean age was 12.7+/-4 (range 5-19 years); 199 (50.4%) were male. Mean hemoglobin was 7.6±1.1 (range 4.1-13.5) g/dl. 381 had TCD, of whom 227 (57%) have had brain MRI and MRA so far.Only 14/395 (3.5%) of patients had abnormal CBFV, 8 (2%) with maximum CBFV 200cm/sec).Prevalence of silent cerebral infarction was 29% (65/227) and was similar in males (30%; 34/114) and females (28%; 31/110) but was lower in children aged
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Published date: 29 November 2018
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Local EPrints ID: 446088
URI: http://eprints.soton.ac.uk/id/eprint/446088
ISSN: 0006-4971
PURE UUID: f62c7ae8-2bf1-44ad-8a1d-ceb8fbf9ad9c
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Date deposited: 20 Jan 2021 17:31
Last modified: 13 Dec 2021 02:49
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Author:
Mboka Mwakatika Mwakatika
Author:
Dawn E Saunders
Author:
Julie Makani
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