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Transcranial Doppler and Magnetic Resonance in Tanzanian Children With Sickle Cell Disease
BACKGROUND AND PURPOSE—: We determined prevalences of neurological complications, vascular abnormality, and infarction in Tanzanian children with sickle cell disease. METHODS—: Children with sickle cell disease were consecutively enrolled for transcranial Doppler; those with slightly elevated (>1...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Lippincott Williams & Wilkins
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6594727/ https://www.ncbi.nlm.nih.gov/pubmed/31195937 http://dx.doi.org/10.1161/STROKEAHA.118.018920 |
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author | Kija, Edward N. Saunders, Dawn E. Munubhi, Emmanuel Darekar, Angela Barker, Simon Cox, Timothy C.S. Mango, Mechris Soka, Deogratias Komba, Joyce Nkya, Deogratias A. Cox, Sharon E. Kirkham, Fenella J. Newton, Charles R.J.C. |
author_facet | Kija, Edward N. Saunders, Dawn E. Munubhi, Emmanuel Darekar, Angela Barker, Simon Cox, Timothy C.S. Mango, Mechris Soka, Deogratias Komba, Joyce Nkya, Deogratias A. Cox, Sharon E. Kirkham, Fenella J. Newton, Charles R.J.C. |
author_sort | Kija, Edward N. |
collection | PubMed |
description | BACKGROUND AND PURPOSE—: We determined prevalences of neurological complications, vascular abnormality, and infarction in Tanzanian children with sickle cell disease. METHODS—: Children with sickle cell disease were consecutively enrolled for transcranial Doppler; those with slightly elevated (>150 cm/s), low (<50 cm/s) or absent cerebral blood flow velocity (CBFv) were invited for brain magnetic resonance imaging and magnetic resonance angiography. RESULTS—: Of 200 children (median age 9; range 6–13 years; 105 [2.5%] boys), 21 (11%) and 15 (8%) had previous seizures and unilateral weakness, respectively. Twenty-eight (14%) had elevated and 39 (20%) had low/absent CBFv, all associated with lower hemoglobin level, but not higher indirect bilirubin level. On multivariable analysis, CBFv>150 cm/s was associated with frequent painful crises and low hemoglobin level. Absent/low CBFv was associated with low hemoglobin level and history of unilateral weakness. In 49 out of 67 children with low/absent/elevated transcranial Doppler undergoing magnetic resonance imaging, 43% had infarction, whereas 24 out of 48 (50%) magnetic resonance angiographies were abnormal. One had hemorrhagic infarction; none had microbleeds. Posterior circulation infarcts occurred in 14%. Of 11 children with previous seizure undergoing magnetic resonance imaging, 10 (91%) had infarction (5 silent) compared with 11 out of 38 (29%) of the remainder (P=0.003). Of 7 children with clinical stroke, 2 had recurrent stroke and 3 died; 4 out of 5 had absent CBFv. Of 193 without stroke, 1 died and 1 had a stroke; both had absent CBFv. CONCLUSIONS—: In one-third of Tanzanian children with sickle cell disease, CBFv is outside the normal range, associated with frequent painful crises and low hemoglobin level, but not hemolysis. Half have abnormal magnetic resonance angiography. African children with sickle cell disease should be evaluated with transcranial Doppler; those with low/absent/elevated CBFv should undergo magnetic resonance imaging/magnetic resonance angiography. |
format | Online Article Text |
id | pubmed-6594727 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Lippincott Williams & Wilkins |
record_format | MEDLINE/PubMed |
spelling | pubmed-65947272019-07-22 Transcranial Doppler and Magnetic Resonance in Tanzanian Children With Sickle Cell Disease Kija, Edward N. Saunders, Dawn E. Munubhi, Emmanuel Darekar, Angela Barker, Simon Cox, Timothy C.S. Mango, Mechris Soka, Deogratias Komba, Joyce Nkya, Deogratias A. Cox, Sharon E. Kirkham, Fenella J. Newton, Charles R.J.C. Stroke Original Contributions BACKGROUND AND PURPOSE—: We determined prevalences of neurological complications, vascular abnormality, and infarction in Tanzanian children with sickle cell disease. METHODS—: Children with sickle cell disease were consecutively enrolled for transcranial Doppler; those with slightly elevated (>150 cm/s), low (<50 cm/s) or absent cerebral blood flow velocity (CBFv) were invited for brain magnetic resonance imaging and magnetic resonance angiography. RESULTS—: Of 200 children (median age 9; range 6–13 years; 105 [2.5%] boys), 21 (11%) and 15 (8%) had previous seizures and unilateral weakness, respectively. Twenty-eight (14%) had elevated and 39 (20%) had low/absent CBFv, all associated with lower hemoglobin level, but not higher indirect bilirubin level. On multivariable analysis, CBFv>150 cm/s was associated with frequent painful crises and low hemoglobin level. Absent/low CBFv was associated with low hemoglobin level and history of unilateral weakness. In 49 out of 67 children with low/absent/elevated transcranial Doppler undergoing magnetic resonance imaging, 43% had infarction, whereas 24 out of 48 (50%) magnetic resonance angiographies were abnormal. One had hemorrhagic infarction; none had microbleeds. Posterior circulation infarcts occurred in 14%. Of 11 children with previous seizure undergoing magnetic resonance imaging, 10 (91%) had infarction (5 silent) compared with 11 out of 38 (29%) of the remainder (P=0.003). Of 7 children with clinical stroke, 2 had recurrent stroke and 3 died; 4 out of 5 had absent CBFv. Of 193 without stroke, 1 died and 1 had a stroke; both had absent CBFv. CONCLUSIONS—: In one-third of Tanzanian children with sickle cell disease, CBFv is outside the normal range, associated with frequent painful crises and low hemoglobin level, but not hemolysis. Half have abnormal magnetic resonance angiography. African children with sickle cell disease should be evaluated with transcranial Doppler; those with low/absent/elevated CBFv should undergo magnetic resonance imaging/magnetic resonance angiography. Lippincott Williams & Wilkins 2019-07 2019-06-14 /pmc/articles/PMC6594727/ /pubmed/31195937 http://dx.doi.org/10.1161/STROKEAHA.118.018920 Text en © 2019 The Authors. Stroke is published on behalf of the American Heart Association, Inc., by Wolters Kluwer Health, Inc. This is an open access article under the terms of the Creative Commons Attribution (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution, and reproduction in any medium, provided that the original work is properly cited. |
spellingShingle | Original Contributions Kija, Edward N. Saunders, Dawn E. Munubhi, Emmanuel Darekar, Angela Barker, Simon Cox, Timothy C.S. Mango, Mechris Soka, Deogratias Komba, Joyce Nkya, Deogratias A. Cox, Sharon E. Kirkham, Fenella J. Newton, Charles R.J.C. Transcranial Doppler and Magnetic Resonance in Tanzanian Children With Sickle Cell Disease |
title | Transcranial Doppler and Magnetic Resonance in Tanzanian Children With Sickle Cell Disease |
title_full | Transcranial Doppler and Magnetic Resonance in Tanzanian Children With Sickle Cell Disease |
title_fullStr | Transcranial Doppler and Magnetic Resonance in Tanzanian Children With Sickle Cell Disease |
title_full_unstemmed | Transcranial Doppler and Magnetic Resonance in Tanzanian Children With Sickle Cell Disease |
title_short | Transcranial Doppler and Magnetic Resonance in Tanzanian Children With Sickle Cell Disease |
title_sort | transcranial doppler and magnetic resonance in tanzanian children with sickle cell disease |
topic | Original Contributions |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6594727/ https://www.ncbi.nlm.nih.gov/pubmed/31195937 http://dx.doi.org/10.1161/STROKEAHA.118.018920 |
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